CN106653887A - Back-junction back-contact solar cell - Google Patents
Back-junction back-contact solar cell Download PDFInfo
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Abstract
本发明提供了一种背结背接触太阳能电池,包括,基片;复合在所述基片前表面的复合层;复合在所述基片背表面的隧穿氧化物层;复合在所述隧穿氧化物层上的P型掺杂半导体层和N型掺杂半导体层;设置在所述P型掺杂半导体层上的正电极;设置在所述N型掺杂半导体层上的负电极。本发明提出了一种采用隧穿氧化层钝化接触结构的背结背接触太阳能电池,采用隧穿氧化层钝化接触结构,这种结构避免了金属电极和衬底的直接接触,有效的减小了载流子在金属接触界面的复合,提高了电池的开压;而且由于金属接触不会带来复合的增加,金属接触可以覆盖发射极和背场的绝大部分面积,避免了载流子的横向运输,有利于降低串联电阻,进一步提高电池效率。The invention provides a back-junction and back-contact solar cell, comprising: a substrate; a composite layer compounded on the front surface of the substrate; a tunnel oxide layer compounded on the back surface of the substrate; A P-type doped semiconductor layer and an N-type doped semiconductor layer on the oxide layer; a positive electrode arranged on the P-type doped semiconductor layer; a negative electrode arranged on the N-type doped semiconductor layer. The present invention proposes a back-junction and back-contact solar cell adopting a tunneling oxide layer passivation contact structure. The tunneling oxide layer passivation contact structure is adopted. This structure avoids direct contact between the metal electrode and the substrate, and effectively reduces the The recombination of carriers at the metal contact interface is reduced, and the opening voltage of the battery is increased; and because the metal contact does not bring about an increase in recombination, the metal contact can cover most of the area of the emitter and the back field, avoiding the current carrying The lateral transport of the electrons is beneficial to reduce the series resistance and further improve the battery efficiency.
Description
技术领域technical field
本发明属于太阳能电池技术领域,涉及一种背结背接触太阳能电池,尤其涉及一种背面采用隧穿氧化层钝化接触结构的背结背接触太阳能电池。The invention belongs to the technical field of solar cells, and relates to a back-junction and back-contact solar cell, in particular to a back-junction and back-contact solar cell with a tunnel oxide layer passivation contact structure on the back.
背景技术Background technique
太阳能电池又称为“太阳能芯片”或“光电池”,是一种利用太阳光直接发电的光电半导体薄片,是通过光电效应或者光化学效应直接把光能转化成电能的装置。太阳能电池只要被满足一定照度条件的光照到,瞬间就可输出电压及在有回路的情况下产生电流。在物理学上称为太阳能光伏(Photovoltaic,缩写为PV),简称光伏。太阳能电池的工作原理就是,太阳光照在半导体p-n结上,形成新的空穴-电子对,在p-n结内建电场的作用下,光生空穴流向p区,光生电子流向n区,接通电路后就产生电流。A solar cell, also known as a "solar chip" or a "photovoltaic cell", is a photoelectric semiconductor sheet that uses sunlight to directly generate electricity. It is a device that directly converts light energy into electrical energy through the photoelectric effect or photochemical effect. As long as the solar cell is illuminated by light that meets a certain illuminance condition, it can output voltage instantly and generate current when there is a loop. In physics, it is called solar photovoltaic (Photovoltaic, abbreviated as PV), or photovoltaic for short. The working principle of a solar cell is that when sunlight shines on the p-n junction of a semiconductor, new hole-electron pairs are formed. Under the action of the built-in electric field of the p-n junction, the photo-generated holes flow to the p-region, and the photo-generated electrons flow to the n-region, turning on the circuit Then a current is generated.
随着全社会对环境问题的日益关注,太阳能电池作为一种可以直接将太阳能转化为电能的装备,越来越得到人们的关注,同样的太阳能电池的种类的也越来越多。太阳能电池就是利用PN结的光伏效应将光能直接转换为电能的,传统的太阳能电池发射极作在电池的前表面,在电池的前面和背面都有电极,入射的光子激发出电子空穴对,电子空穴对被位于电池前表面的PN结分离开来,通过电极引出到外电路。As the whole society pays more and more attention to environmental issues, solar cells, as a device that can directly convert solar energy into electrical energy, are getting more and more attention from people, and there are more and more types of solar cells. Solar cells use the photovoltaic effect of the PN junction to directly convert light energy into electrical energy. The emitter of a traditional solar cell is made on the front surface of the cell, and there are electrodes on the front and back of the cell. The incident photons excite electron-hole pairs. , the electron-hole pairs are separated by the PN junction located on the front surface of the battery, and are drawn out to the external circuit through the electrodes.
相比于传统太阳能电池,新型的背结背接触电池具有取得更高转换效率的潜能,逐渐成为产业化高效电池的主要研发方向。背结背接触电池,又名背接触指交叉(interdigitated backcontact,IBC)太阳能电池(简称IBC电池),这种电池将发射极和背场全部作在了电池的背面,减小了遮光损失,而且由于电极作在了电池的背表面,不用再考虑遮光,所以电极可以做的很宽,这大大减小了串联电阻,这些特性都可以提高电池的转换效率。但是包括背结背接触太阳能电池在内的绝大部分电池都没有解决的一个问题就是,金属和衬底形成欧姆接触以后,会在接触表面引入大量的界面态,这使得该表面的载流子复合速率明显增大,这会大大降低电池的性能。而通常的解决方案,就是尽量减小金属和衬底的接触面积,可是这又会引起载流子的横向运输,增加串联电阻,又会降低电池的性能。Compared with traditional solar cells, the new back-junction and back-contact cells have the potential to achieve higher conversion efficiency, and have gradually become the main research and development direction of industrialized high-efficiency cells. Back-junction back-contact battery, also known as interdigitated backcontact (IBC) solar cell (referred to as IBC battery), this kind of battery has all the emitter and back field on the back of the battery, which reduces the shading loss, and Since the electrodes are made on the back surface of the battery, there is no need to consider shading, so the electrodes can be made very wide, which greatly reduces the series resistance, and these characteristics can improve the conversion efficiency of the battery. However, a problem that most solar cells, including back-junction and back-contact solar cells, have not solved is that after the metal and the substrate form an ohmic contact, a large number of interface states will be introduced on the contact surface, which makes the carrier on the surface The recombination rate increases significantly, which can greatly reduce the performance of the battery. The usual solution is to minimize the contact area between the metal and the substrate, but this will cause the lateral transport of carriers, increase the series resistance, and reduce the performance of the battery.
因此,如何找到一种更合适的背结背接触电池,能够具有较好的电池性能,同时技术方案简单易于实现,已成为领域内诸多一线研发人员亟待解决的问题。Therefore, how to find a more suitable back-junction and back-contact battery, which can have better battery performance, and at the same time the technical solution is simple and easy to implement, has become an urgent problem to be solved by many front-line researchers in the field.
发明内容Contents of the invention
有鉴于此,本发明要解决的技术问题在于提供一种背结背接触太阳能电池,特别是一种采用隧穿氧化层钝化接触结构的背结背接触太阳能电池,本发明提供的背面采用隧穿氧化层钝化接触结构的背结背接触太阳能电池具有较高的电池性能,而且技术方案简单易于实现。In view of this, the technical problem to be solved by the present invention is to provide a back-junction and back-contact solar cell, especially a back-junction and back-contact solar cell using a tunnel oxide layer passivation contact structure. The back-junction and back-contact solar cell with passivation contact structure through the oxide layer has high cell performance, and the technical solution is simple and easy to realize.
本发明提供了一种背结背接触太阳能电池,包括:The invention provides a back junction back contact solar cell, comprising:
基片;Substrate;
复合在所述基片前表面的复合层;a composite layer composited on the front surface of the substrate;
复合在所述基片背表面的隧穿氧化物层;a tunnel oxide layer compounded on the back surface of the substrate;
复合在所述隧穿氧化物层上的P型掺杂半导体层和N型掺杂半导体层;a P-type doped semiconductor layer and an N-type doped semiconductor layer compounded on the tunnel oxide layer;
设置在所述P型掺杂半导体层上的正电极;a positive electrode disposed on the P-type doped semiconductor layer;
设置在所述N型掺杂半导体层上的负电极。a negative electrode disposed on the N-type doped semiconductor layer.
优选的,所述基片前表面的复合层包括:Preferably, the composite layer on the front surface of the substrate comprises:
复合在所述基片前表面上的前场区;a front field region compounded on the front surface of the substrate;
复合在所述前场区上的前表面钝化层;a front surface passivation layer compounded on the front field region;
复合在所述前表面钝化层上的减反射层。An anti-reflection layer compounded on the front surface passivation layer.
优选的,所述P型掺杂半导体层和N型掺杂半导体层相邻交替复合在所述隧穿氧化物层上,和/或所述P型掺杂半导体层和N型掺杂半导体层相隔交替复合在所述隧穿氧化物层上;Preferably, the P-type doped semiconductor layer and the N-type doped semiconductor layer are adjacently and alternately compounded on the tunnel oxide layer, and/or the P-type doped semiconductor layer and the N-type doped semiconductor layer Alternately composited on the tunnel oxide layer;
所述P型掺杂半导体层的宽度与所述N型掺杂半导体层的宽度比为(2~10):1。The ratio of the width of the P-type doped semiconductor layer to the width of the N-type doped semiconductor layer is (2˜10):1.
优选的,所述P型掺杂半导体层和N型掺杂半导体层相邻交替复合在所述隧穿氧化物层上时,所述正电极的宽度小于所述P型掺杂半导体层的宽度,所述负电极的宽度小于所述N型掺杂半导体层的宽度,且所述正电极不与所述N型掺杂半导体层相接触,所述负电极不与所述P型掺杂半导体层相接触。Preferably, when the P-type doped semiconductor layer and the N-type doped semiconductor layer are alternately compounded on the tunnel oxide layer, the width of the positive electrode is smaller than the width of the P-type doped semiconductor layer , the width of the negative electrode is smaller than the width of the N-type doped semiconductor layer, and the positive electrode is not in contact with the N-type doped semiconductor layer, and the negative electrode is not in contact with the P-type doped semiconductor layer layers are in contact.
优选的,所述基片前表面的复合层具有绒面陷光结构。Preferably, the composite layer on the front surface of the substrate has a suede light-trapping structure.
优选的,所述基片前表面具有绒面陷光结构。Preferably, the front surface of the substrate has a textured light trapping structure.
优选的,所述基片的材质包括轻掺杂的硅材料,所述轻掺杂的掺杂浓度为1013~1017cm-3;所述掺杂的类型为N型;Preferably, the material of the substrate includes lightly doped silicon material, the doping concentration of the lightly doped is 10 13 ~ 10 17 cm -3 ; the type of doping is N type;
所述硅材料包括单晶硅、多晶硅和硅薄膜中的一种或多种;The silicon material includes one or more of single crystal silicon, polycrystalline silicon and silicon thin film;
所述掺杂的材质包括硼、磷、镓和砷中的一种或多种;The doped material includes one or more of boron, phosphorus, gallium and arsenic;
所述基片的少子寿命大于等于500μs;所述基片的电阻率为1~50Ω·c m;The minority carrier lifetime of the substrate is greater than or equal to 500 μs; the resistivity of the substrate is 1 to 50 Ω·cm;
所述基片的厚度为50~300μm。The thickness of the substrate is 50-300 μm.
优选的,所述隧穿氧化物层的材质为绝缘材料;Preferably, the material of the tunnel oxide layer is an insulating material;
所述绝缘材料包括二氧化硅、二氧化钛、氧化铝和氮化硅中的一种或多种;The insulating material includes one or more of silicon dioxide, titanium dioxide, aluminum oxide and silicon nitride;
所述隧穿氧化物层的厚度为0.3~2nm。The thickness of the tunnel oxide layer is 0.3-2 nm.
优选的,所述P型掺杂半导体层和N型掺杂半导体层的半导体材质各自包括微晶硅、多晶硅和非晶硅中的一种或多种;所述掺杂的材质各自包括硼、磷、镓和砷中的一种或多种;Preferably, the semiconductor materials of the P-type doped semiconductor layer and the N-type doped semiconductor layer each include one or more of microcrystalline silicon, polycrystalline silicon, and amorphous silicon; each of the doped materials includes boron, One or more of phosphorus, gallium and arsenic;
所述掺杂的浓度各自为1018~1021cm-3;The doping concentrations are each 10 18 to 10 21 cm -3 ;
所述P型掺杂半导体层和N型掺杂半导体层的厚度各自选自5nm~500nm。The thicknesses of the P-type doped semiconductor layer and the N-type doped semiconductor layer are each selected from 5 nm to 500 nm.
优选的,所述前场区为在基片前表面上,通过扩散磷形成的高掺杂区域;Preferably, the front field region is a highly doped region formed by diffusing phosphorus on the front surface of the substrate;
所述前场区的厚度为0.5~2μm;The thickness of the front field region is 0.5-2 μm;
所述前表面钝化层包括氧化硅层、氮化硅层、氧化硅和氮化硅叠层或碳化硅层;The front surface passivation layer includes a silicon oxide layer, a silicon nitride layer, a stack of silicon oxide and silicon nitride or a silicon carbide layer;
所述前表面钝化层的厚度为50~100nm;The thickness of the front surface passivation layer is 50-100nm;
所述减反射层的材质包括氮化硅、ITO、氧化硅和氧化钛中的一种或多种;The material of the antireflection layer includes one or more of silicon nitride, ITO, silicon oxide and titanium oxide;
所述减反射层的厚度为40~100nm。The thickness of the anti-reflection layer is 40-100 nm.
本发明提供了一种背结背接触太阳能电池,包括,基片;复合在所述基片前表面的复合层;复合在所述基片背表面的隧穿氧化物层;复合在所述隧穿氧化物层上的P型掺杂半导体层和N型掺杂半导体层;设置在所述P型掺杂半导体层上的正电极;设置在所述N型掺杂半导体层上的负电极。与现有技术相比,本发明针对金属和衬底形成欧姆接触以后,会在接触表面引入大量的界面态,这使得该表面的载流子复合速率明显增大,降低电池的性能的缺陷,提出了一种采用隧穿氧化层钝化接触结构的背结背接触太阳能电池。本发明采用隧穿氧化层钝化接触结构,这种结构避免了金属电极和衬底的直接接触,有效的减小了载流子在金属接触界面的复合,提高了电池的开压;而且由于金属接触不会带来复合的增加,金属接触可以覆盖发射极和背场的绝大部分面积,避免了载流子的横向运输,有利于降低串联电阻,进一步提高电池效率。而且本发明采用的制备工艺和现有的太阳能电池制备工艺兼容性良好,而且相较于传统背接触电池工艺更简单,生产成本更低。The invention provides a back-junction and back-contact solar cell, comprising: a substrate; a composite layer compounded on the front surface of the substrate; a tunnel oxide layer compounded on the back surface of the substrate; A P-type doped semiconductor layer and an N-type doped semiconductor layer on the oxide layer; a positive electrode arranged on the P-type doped semiconductor layer; a negative electrode arranged on the N-type doped semiconductor layer. Compared with the prior art, the present invention will introduce a large number of interface states on the contact surface after forming an ohmic contact between the metal and the substrate, which will significantly increase the carrier recombination rate on the surface and reduce the performance of the battery. A back-junction and back-contact solar cell with a passivated contact structure using a tunnel oxide layer is proposed. The present invention adopts a tunneling oxide layer passivation contact structure, which avoids the direct contact between the metal electrode and the substrate, effectively reduces the recombination of carriers at the metal contact interface, and improves the opening voltage of the battery; and because The metal contact will not increase the recombination. The metal contact can cover most of the area of the emitter and the back field, avoiding the lateral transport of carriers, which is conducive to reducing the series resistance and further improving the battery efficiency. Moreover, the preparation process adopted by the present invention has good compatibility with the existing solar cell preparation process, and is simpler and lower in production cost than the traditional back contact cell process.
实验结果表明,本发明提供的背面采用隧穿氧化层钝化接触结构的背结背接触太阳能电池,电池效率能够达到22%。Experimental results show that the back junction and back contact solar cell with tunnel oxide layer passivation contact structure on the back provided by the present invention can reach 22% cell efficiency.
附图说明Description of drawings
图1为本发明实施例1提供的背结背接触太阳能电池的结构示意简图;Fig. 1 is a schematic structural diagram of a back-junction and back-contact solar cell provided in Example 1 of the present invention;
图2为本发明实施例2提供的背结背接触太阳能电池的结构示意简图;Fig. 2 is a schematic structural diagram of a back-junction and back-contact solar cell provided in Example 2 of the present invention;
图3为本发明实施例3提供的隧穿氧化层钝化接触结构的背结背接触太阳能电池的I-V特性曲线。FIG. 3 is an I-V characteristic curve of a back-junction back-contact solar cell with a tunnel oxide layer passivation contact structure provided by Example 3 of the present invention.
具体实施方式detailed description
为了进一步了解本发明,下面结合实施例对本发明的优选实施方案进行描述,但是应当理解,这些描述只是为进一步说明本发明的特征和优点而不是对本发明专利要求的限制。In order to further understand the present invention, the preferred embodiments of the present invention are described below in conjunction with the examples, but it should be understood that these descriptions are only for further illustrating the features and advantages of the present invention rather than limiting the patent requirements of the present invention.
本发明所有原料,对其来源没有特别限制,在市场上购买的或按照本领域技术人员熟知的常规方法制备的即可。All raw materials in the present invention have no particular limitation on their sources, they can be purchased from the market or prepared according to conventional methods well known to those skilled in the art.
本发明所有原料,对其纯度没有特别限制,本发明优选采用分析纯或太阳能电池制备领域常规的纯度要求。The purity of all raw materials in the present invention is not particularly limited, and the present invention preferably adopts analytical purity or conventional purity requirements in the field of solar cell preparation.
本发明所有原料,其牌号和简称均属于本领域常规牌号和简称,每个牌号和简称在其相关用途的领域内均是清楚明确的,本领域技术人员根据牌号、简称以及相应的用途,能够从市售中购买得到或常规方法制备得到。All raw materials of the present invention, their grades and abbreviations belong to the conventional grades and abbreviations in this field, and each grade and abbreviation are all clear and definite in the field of its related use. Those skilled in the art can according to the grades, abbreviations and corresponding uses, It can be purchased from commercial sources or prepared by conventional methods.
本发明提供了一种背结背接触太阳能电池,包括:The invention provides a back junction back contact solar cell, comprising:
基片;Substrate;
复合在所述基片前表面的复合层;a composite layer composited on the front surface of the substrate;
复合在所述基片背表面的隧穿氧化物层;a tunnel oxide layer compounded on the back surface of the substrate;
复合在所述隧穿氧化物层上的P型掺杂半导体层和N型掺杂半导体层;a P-type doped semiconductor layer and an N-type doped semiconductor layer compounded on the tunnel oxide layer;
设置在所述P型掺杂半导体层上的正电极;a positive electrode disposed on the P-type doped semiconductor layer;
设置在所述N型掺杂半导体层上的负电极。a negative electrode disposed on the N-type doped semiconductor layer.
本发明对所述背结背接触太阳能电池的定义和概念没有特别限制,以本领域技术人员熟知的背结背接触太阳能电池(IBC电池)的定义和概念即可,本领域技术人员可以根据实际应用情况、复合情况以及产品性能进行选择和调整。The present invention is not particularly limited to the definition and concept of the back-junction back-contact solar cell, and the definition and concept of the back-junction back-contact solar cell (IBC cell) well known to those skilled in the art can be used. Those skilled in the art can Application conditions, composite conditions and product performance are selected and adjusted.
本发明对所述基片没有特别限制,以本领域技术人员熟知的背结背接触太阳能电池的基片或衬底即可,本领域技术人员可以根据实际应用情况、复合情况以及产品性能进行选择和调整,本发明所述基片的材质优选包括轻掺杂的硅材料,所述掺杂的类型优选为N型。The present invention has no special restrictions on the substrate, and the substrate or substrate of the back-junction and back-contact solar cell well known to those skilled in the art can be selected according to the actual application situation, composite situation and product performance. And adjustment, the material of the substrate in the present invention preferably includes lightly doped silicon material, and the doping type is preferably N-type.
本发明对所述轻掺杂的硅材料的掺杂浓度没有特别限制,以本领域技术人员熟知的轻掺杂的硅材料的掺杂浓度即可,本领域技术人员可以根据实际应用情况、复合情况以及产品性能进行选择和调整,本发明所述轻掺杂的硅材料的掺杂浓度优选为1013~1017cm-3,更优选为1013~1016cm-3,最优选为1014~1015cm-3。The present invention has no special limitation on the doping concentration of the lightly doped silicon material, the doping concentration of the lightly doped silicon material well known to those skilled in the art can be used, and those skilled in the art can combine The doping concentration of the lightly doped silicon material in the present invention is preferably 10 13 to 10 17 cm -3 , more preferably 10 13 to 10 16 cm -3 , most preferably 10 14 ~ 10 15 cm -3 .
本发明对所述轻掺杂的硅材料的硅材料没有特别限制,以本领域技术人员熟知的轻掺杂的硅材料的硅材料即可,本领域技术人员可以根据实际应用情况、复合情况以及产品性能进行选择和调整,本发明所述硅材料优选包括单晶硅、多晶硅和硅薄膜中的一种或多种,更优选为单晶硅、多晶硅或硅薄膜。The present invention is not particularly limited to the silicon material of the lightly doped silicon material, and the silicon material of the lightly doped silicon material well-known to those skilled in the art can be used. Those skilled in the art can select according to the actual application situation, compounding situation and The product performance is selected and adjusted. The silicon material in the present invention preferably includes one or more of single crystal silicon, polycrystalline silicon and silicon thin film, more preferably single crystal silicon, polycrystalline silicon or silicon thin film.
本发明对所述轻掺杂的硅材料的掺杂材料没有特别限制,以本领域技术人员熟知的掺杂材料即可,本领域技术人员可以根据实际应用情况、复合情况以及产品性能进行选择和调整,本发明所述掺杂的材质优选包括硼、磷、镓和砷中的一种或多种,更优选为硼、磷、镓或砷。In the present invention, the doping material of the lightly doped silicon material is not particularly limited, and the doping material well-known to those skilled in the art can be used, and those skilled in the art can select and select according to actual application conditions, compounding conditions, and product performance. Adjustment, the doped material in the present invention preferably includes one or more of boron, phosphorus, gallium and arsenic, more preferably boron, phosphorus, gallium or arsenic.
本发明对所述基片的性能参数没有特别限制,以本领域技术人员熟知的背结背接触太阳能电池的基片常规性能参数即可,本领域技术人员可以根据实际应用情况、复合情况以及产品性能进行选择和调整,本发明所述基片的少子寿命优选大于等于500μs,更优选大于等于800μs,最优选大于等于1000μs;所述基片的电阻率优选为1~50Ω·cm,更优选为10~40Ω·cm,最优选为20~30Ω·cm。The present invention has no special limitation on the performance parameters of the substrate, and the conventional performance parameters of the substrate of the back-junction and back-contact solar cell well known to those skilled in the art can be used. performance is selected and adjusted, the minority carrier lifetime of the substrate of the present invention is preferably greater than or equal to 500 μs, more preferably greater than or equal to 800 μs, most preferably greater than or equal to 1000 μs; the resistivity of the substrate is preferably 1 to 50 Ω cm, more preferably 10 to 40Ω·cm, most preferably 20 to 30Ω·cm.
本发明对所述基片的厚度没有特别限制,以本领域技术人员熟知的背结背接触太阳能电池的基片常规厚度即可,本领域技术人员可以根据实际应用情况、复合情况以及产品性能进行选择和调整,本发明所述基片的厚度优选为50~300μm,更优选为100~250μm,最优选为150~200μm。The present invention has no special limitation on the thickness of the substrate, the conventional thickness of the substrate of the back-junction and back-contact solar cell well known to those skilled in the art can be used, and those skilled in the art can make the thickness according to the actual application situation, composite situation and product performance. Selection and adjustment, the thickness of the substrate of the present invention is preferably 50-300 μm, more preferably 100-250 μm, most preferably 150-200 μm.
本发明对所述复合的方式没有特别限制,以本领域技术人员熟知的太阳能电池的常规复合方式即可,本领域技术人员可以根据实际应用情况、复合情况以及产品性能进行选择和调整,本发明所述复合优选为掺杂、沉积、蒸镀、氧化、涂覆、溶胶凝胶和刻蚀中的一种或多种,更优选为生长、掺杂、沉积、蒸镀、氧化、涂覆、溶胶凝胶或刻蚀。The present invention has no special limitation on the compounding method, and the conventional compounding method of solar cells well known to those skilled in the art can be used. Those skilled in the art can select and adjust according to actual application conditions, compounding conditions and product performance. The present invention The recombination is preferably one or more of doping, deposition, evaporation, oxidation, coating, sol-gel and etching, more preferably growth, doping, deposition, evaporation, oxidation, coating, Sol gel or etch.
本发明对所述基片前表面的定义没有特别限制,以本领域技术人员熟知的基片前表面的定义即可,本领域技术人员可以根据实际应用情况、复合情况以及产品性能进行选择和调整,本发明所述基片的前表面,即是指基片的受光面方向或是太阳电池的受光面的方向的表面;所述基片的背表面,即是指基片的背光面方向或是太阳电池的背光面的方向的表面。The definition of the front surface of the substrate is not particularly limited in the present invention, the definition of the front surface of the substrate well known to those skilled in the art can be used, and those skilled in the art can select and adjust according to the actual application situation, composite situation and product performance The front surface of the substrate in the present invention refers to the direction of the light-receiving surface of the substrate or the surface of the direction of the light-receiving surface of the solar cell; the back surface of the substrate refers to the direction of the backlight surface of the substrate or It is the surface in the direction of the backlight side of the solar cell.
本发明对所述基片前表面的结构没有特别限制,以本领域技术人员熟知的基片前表面的结构即可,本领域技术人员可以根据实际应用情况、复合情况以及产品性能进行选择和调整,本发明所述基片的前表面具有陷光结构,更优选为具有绒面陷光结构。In the present invention, the structure of the front surface of the substrate is not particularly limited, and the structure of the front surface of the substrate well-known to those skilled in the art can be used, and those skilled in the art can select and adjust according to actual application conditions, composite conditions, and product performance. , The front surface of the substrate of the present invention has a light-trapping structure, more preferably has a textured light-trapping structure.
本发明对所述基片前表面的复合层的整体结构没有特别限制,以本领域技术人员熟知的基片前表面的复合层的整体结构即可,本领域技术人员可以根据实际应用情况、复合情况以及产品性能进行选择和调整,本发明所述基片的前表面的复合层具有陷光结构,更优选为具有绒面陷光结构。本发明所述基片前表面与所述基片前表面的复合层具有相同的陷光结构。The present invention has no particular limitation on the overall structure of the composite layer on the front surface of the substrate. The overall structure of the composite layer on the front surface of the substrate well known to those skilled in the art will suffice. Those skilled in the art can combine According to the situation and product performance, the composite layer on the front surface of the substrate in the present invention has a light-trapping structure, more preferably a suede light-trapping structure. In the present invention, the front surface of the substrate and the composite layer on the front surface of the substrate have the same light-trapping structure.
本发明中,前表面的陷光结构是通过各向异性腐蚀硅表面的方法制备的,其结构为许多正立的或者是倒立的金字塔结构,前场扩散区(前场区)、前表面钝化层和减反射层都是在这种绒面陷光结构上形成的。本发明对所述陷光结构的形成方式没有特别限制,以本领域技术人员熟知的陷光结构的形成方式即可,本领域技术人员可以根据实际应用情况、复合情况以及产品性能进行选择和调整,本发明所述陷光结构可以通过化学腐蚀或干法刻蚀的方法形成。In the present invention, the light-trapping structure on the front surface is prepared by anisotropically etching the silicon surface, and its structure is many upright or inverted pyramid structures, the front field diffusion area (front field area), the front surface blunt Both the chemical layer and the anti-reflection layer are formed on this suede light-trapping structure. The present invention has no special limitation on the formation method of the light trapping structure, and the formation method of the light trapping structure well known to those skilled in the art can be selected and adjusted according to the actual application situation, composite situation and product performance. , The light trapping structure of the present invention can be formed by chemical etching or dry etching.
本发明对所述基片前表面的复合层的组成没有特别限制,以本领域技术人员熟知的基片前表面的常规复合层组成即可,本领域技术人员可以根据实际应用情况、复合情况以及产品性能进行选择和调整,本发明所述基片前表面的复合层优选包括:The composition of the composite layer on the front surface of the substrate is not particularly limited in the present invention, and the composition of the conventional composite layer on the front surface of the substrate well-known to those skilled in the art can be used. Those skilled in the art can according to actual application conditions, composite conditions and Product performance is selected and adjusted, and the composite layer on the front surface of the substrate of the present invention preferably includes:
复合在所述基片前表面上的前场区;a front field region compounded on the front surface of the substrate;
复合在所述前场区上的前表面钝化层;a front surface passivation layer compounded on the front field region;
复合在所述前表面钝化层上的减反射层。An anti-reflection layer compounded on the front surface passivation layer.
本发明对所述前场区没有特别限制,以本领域技术人员熟知的太阳能电池的前场区即可,本领域技术人员可以根据实际应用情况、复合情况以及产品性能进行选择和调整,本发明所述前场区优选为重掺杂区,所述掺杂的类型优选为N型。The present invention has no special restrictions on the front field area, and the front field area of solar cells well known to those skilled in the art can be used. Those skilled in the art can select and adjust according to actual application conditions, composite conditions and product performance. The present invention The front field region is preferably a heavily doped region, and the doping type is preferably N-type.
本发明对所述前场区的掺杂浓度没有特别限制,以本领域技术人员熟知的常规重掺杂浓度即可,本领域技术人员可以根据实际应用情况、复合情况以及产品性能进行选择和调整,本发明所述前场区的掺杂浓度优选为1017~1019cm-3,更优选为1017~1018cm-3,最优选为1018~1019cm-3。In the present invention, the doping concentration of the front field region is not particularly limited, and the conventional heavy doping concentration well known to those skilled in the art can be used, and those skilled in the art can select and adjust it according to actual application conditions, compounding conditions, and product performance. In the present invention, the doping concentration of the front field region is preferably 10 17 to 10 19 cm -3 , more preferably 10 17 to 10 18 cm -3 , most preferably 10 18 to 10 19 cm -3 .
本发明对所述前场区的掺杂材料没有特别限制,以本领域技术人员熟知的掺杂材料即可,本领域技术人员可以根据实际应用情况、复合情况以及产品性能进行选择和调整,本发明所述前场区的掺杂材质优选为磷掺杂。本发明对所述前场区的掺杂方式没有特别限制,以本领域技术人员熟知的掺杂方式即可,本领域技术人员可以根据实际应用情况、复合情况以及产品性能进行选择和调整,本发明所述前场区的掺杂方式优选为在基片前表面上,通过扩散磷形成这种重掺杂的区域。In the present invention, the doping material of the front field region is not particularly limited, and the doping material well-known to those skilled in the art can be used. Those skilled in the art can select and adjust according to the actual application situation, compounding situation and product performance. In the invention, the doping material of the front field region is preferably phosphorus doped. In the present invention, the doping method of the front field region is not particularly limited, and the doping method known to those skilled in the art can be used. Those skilled in the art can select and adjust according to the actual application situation, compounding situation and product performance. The doping method of the front field region in the invention is preferably to form such a heavily doped region by diffusing phosphorus on the front surface of the substrate.
本发明对所述前场区的厚度没有特别限制,以本领域技术人员熟知的背结背接触太阳能电池的前场区常规厚度即可,本领域技术人员可以根据实际应用情况、复合情况以及产品性能进行选择和调整,本发明所述前场区的厚度优选为0.5~2μm,更优选为0.8~1.8μm,最优选为1~1.5μm。The present invention has no special limitation on the thickness of the front field region, and the conventional thickness of the front field region of the back-junction and back-contact solar cell well known to those skilled in the art is sufficient. The performance is selected and adjusted. The thickness of the front field region in the present invention is preferably 0.5-2 μm, more preferably 0.8-1.8 μm, and most preferably 1-1.5 μm.
本发明对所述前表面钝化层没有特别限制,以本领域技术人员熟知的太阳能电池的前表面钝化层即可,本领域技术人员可以根据实际应用情况、复合情况以及产品性能进行选择和调整,本发明前表面钝化层优选包括氧化硅层、氮化硅层、氧化硅和氮化硅叠层或碳化硅层,更优选为氧化硅层、氮化硅层或氧化硅和氮化硅的叠层。The present invention is not particularly limited to the front surface passivation layer, the front surface passivation layer of the solar cell well-known to those skilled in the art can be used, and those skilled in the art can select and select according to the actual application situation, composite situation and product performance. Adjustment, the front surface passivation layer of the present invention preferably includes a silicon oxide layer, a silicon nitride layer, a stack of silicon oxide and silicon nitride or a silicon carbide layer, more preferably a silicon oxide layer, a silicon nitride layer or silicon oxide and nitride stack of silicon.
本发明对所述前表面钝化层的性能参数没有特别限制,以本领域技术人员熟知的常规前表面钝化层的性能参数即可,本领域技术人员可以根据实际应用情况、复合情况以及产品性能进行选择和调整。The present invention has no special limitation on the performance parameters of the front surface passivation layer, and the performance parameters of the conventional front surface passivation layer well known to those skilled in the art will suffice. performance options and adjustments.
本发明对所述前表面钝化层的厚度没有特别限制,以本领域技术人员熟知的背结背接触太阳能电池的前表面钝化层的常规厚度即可,本领域技术人员可以根据实际应用情况、复合情况以及产品性能进行选择和调整,本发明所述前表面钝化层的厚度优选为50~100nm,更优选为60~90nm,最优选为70~80nm。The present invention has no special limitation on the thickness of the front surface passivation layer, the conventional thickness of the front surface passivation layer of the back junction back contact solar cell well known to those skilled in the art can be used, those skilled in the art can according to the actual application situation , recombination and product performance are selected and adjusted. The thickness of the front surface passivation layer in the present invention is preferably 50-100 nm, more preferably 60-90 nm, and most preferably 70-80 nm.
本发明对所述减反射层没有特别限制,以本领域技术人员熟知的太阳能电池的减反射层即可,本领域技术人员可以根据实际应用情况、复合情况以及产品性能进行选择和调整,本发明所述减反射层优选为具有减反射作用膜层,其材质具体更优选包括氮化硅、ITO、氧化硅和氧化钛中的一种或多种,更优选为氮化硅、ITO、氧化硅或氧化钛,最优选为氮化硅或ITO。In the present invention, the anti-reflection layer is not particularly limited, and the anti-reflection layer of a solar cell well-known to those skilled in the art can be used. Those skilled in the art can select and adjust according to actual application conditions, composite conditions, and product performance. The present invention The anti-reflection layer is preferably a film layer with an anti-reflection effect, and its material is more preferably one or more of silicon nitride, ITO, silicon oxide and titanium oxide, more preferably silicon nitride, ITO, silicon oxide or titanium oxide, most preferably silicon nitride or ITO.
本发明对所述减反射层的厚度没有特别限制,以本领域技术人员熟知的背结背接触太阳能电池的减反射层常规厚度即可,本领域技术人员可以根据实际应用情况、复合情况以及产品性能进行选择和调整,本发明所述减反射层的厚度优选为40~100nm,更优选为50~90nm,最优选为60~80nm。The present invention has no special limitation on the thickness of the anti-reflection layer, and the conventional thickness of the anti-reflection layer of the back-junction back-contact solar cell well known to those skilled in the art can be used. The performance is selected and adjusted. The thickness of the anti-reflection layer in the present invention is preferably 40-100 nm, more preferably 50-90 nm, and most preferably 60-80 nm.
本发明提供的电池的前表面依次设计有前场扩散区(前场区)、前表面钝化层和减反射层,更进一步的均与基片前表面具有相同的绒面陷光结构。其中减反射层位于电池的最前面,可以为氮化硅、氧化钛材料构成的薄膜。前表面钝化层在减反射层和衬底之间,起到钝化电池前表面的作用,可以为氮化硅、氧化硅的材料构成的薄膜。前场区是通过在衬底的前表面进行磷扩散,在衬底的前表面形成一个重掺的N型区,特别是在制完绒面陷光结构之后,对前表面进行磷扩散形成的,掺杂浓度要比衬底高,在1017cm-3到1019cm-3之间。其作用为形成一个指向衬底内部的电场,减小少数载流子在表面的浓度,从而降低表面复合速率。The front surface of the battery provided by the present invention is sequentially designed with a front field diffusion area (front field area), a front surface passivation layer and an anti-reflection layer, and furthermore, all have the same suede light trapping structure as the front surface of the substrate. Wherein the anti-reflection layer is located at the front of the battery, and may be a thin film made of silicon nitride or titanium oxide. The front surface passivation layer is between the anti-reflection layer and the substrate, and plays the role of passivating the front surface of the battery, and can be a thin film made of silicon nitride or silicon oxide. The front field region is formed by phosphorous diffusion on the front surface of the substrate to form a heavily doped N-type region on the front surface of the substrate, especially after the textured light-trapping structure is fabricated, and phosphorous is diffused on the front surface. , the doping concentration is higher than that of the substrate, between 10 17 cm -3 and 10 19 cm -3 . Its function is to form an electric field pointing to the inside of the substrate, reducing the concentration of minority carriers on the surface, thereby reducing the surface recombination rate.
本发明对所述基片背表面的隧穿氧化物层(隧穿氧化层)没有特别限制,以本领域技术人员熟知的隧穿氧化物层即可,本领域技术人员可以根据实际应用情况、复合情况以及产品性能进行选择和调整,本发明所述隧穿氧化层的材质优选为绝缘材料,即所述隧穿氧化物绝缘介质层,其材质更具体优选包括二氧化硅、二氧化钛、氧化铝和氮化硅中的一种或多种,更优选为二氧化硅、二氧化钛、氧化铝或氮化硅,最优选为二氧化硅或氧化铝。The present invention has no particular limitation on the tunneling oxide layer (tunneling oxide layer) on the back surface of the substrate, and the tunneling oxide layer well-known to those skilled in the art will suffice. Composite conditions and product performance are selected and adjusted. The material of the tunneling oxide layer in the present invention is preferably an insulating material, that is, the tunneling oxide insulating dielectric layer. More specifically, its material preferably includes silicon dioxide, titanium dioxide, aluminum oxide and one or more of silicon nitride, more preferably silicon dioxide, titanium dioxide, aluminum oxide or silicon nitride, most preferably silicon dioxide or aluminum oxide.
本发明对所述隧穿氧化物层的厚度没有特别限制,以本领域技术人员熟知的背结背接触太阳能电池的前场区常规厚度即可,本领域技术人员可以根据实际应用情况、复合情况以及产品性能进行选择和调整,本发明所述隧穿氧化物层的厚度优选为0.3~2nm,更优选为0.5~1.8nm,更优选为0.7~1.6nm,最优选为1.0~1.5nm。In the present invention, the thickness of the tunneling oxide layer is not particularly limited, and the conventional thickness of the front field region of the back-junction and back-contact solar cell well known to those skilled in the art is sufficient. and product performance are selected and adjusted. The thickness of the tunnel oxide layer in the present invention is preferably 0.3-2 nm, more preferably 0.5-1.8 nm, more preferably 0.7-1.6 nm, and most preferably 1.0-1.5 nm.
本发明对所述隧穿氧化物层的复合方式没有特别限制,本领域技术人员可以根据实际应用情况、复合情况以及产品性能进行选择和调整,本发明所述隧穿氧化物层的复合方式优选为湿法氧化或原子层沉积等技术得到。The present invention has no special limitation on the compounding method of the tunneling oxide layer. Those skilled in the art can select and adjust according to the actual application situation, compounding situation and product performance. The compounding method of the tunneling oxide layer in the present invention is preferably It is obtained by techniques such as wet oxidation or atomic layer deposition.
本发明基片的背表面形成掺杂半导体层之前,在衬底的底部先形成一层很薄的隧穿氧化层,该隧穿氧化层主要是起到化学钝化的作用,因此该氧化层应该和衬底有一个良好的界面;而且由于载流子要通过隧穿的方式通过该氧化层,为了使载流子可以很容易的隧穿该氧化层,从而获得一个比较小的串联电阻,该氧化层要报,厚度在0.5~2nm之间。本发明提供的隧穿氧化层可以覆盖衬底的整个背表面,可以覆盖衬底的局部背表面,优选为全部覆盖。Before the doped semiconductor layer is formed on the back surface of the substrate of the present invention, a very thin tunnel oxide layer is formed on the bottom of the substrate. The tunnel oxide layer mainly plays the role of chemical passivation, so the oxide layer There should be a good interface with the substrate; and since the carriers pass through the oxide layer by tunneling, in order for the carriers to easily tunnel through the oxide layer, a relatively small series resistance is obtained. The oxide layer should be reported, with a thickness between 0.5 and 2 nm. The tunnel oxide layer provided by the present invention can cover the entire back surface of the substrate, can cover a part of the back surface of the substrate, preferably completely.
本发明对所述复合在所述隧穿氧化物层上的P型掺杂半导体层没有特别限制,以本领域技术人员熟知的背结背接触太阳能电池的P型掺杂半导体层即可,本领域技术人员可以根据实际应用情况、复合情况以及产品性能进行选择和调整。The present invention has no special limitation on the P-type doped semiconductor layer compounded on the tunnel oxide layer, and the P-type doped semiconductor layer of the back-junction and back-contact solar cell well known to those skilled in the art can be used. Those skilled in the art can make selections and adjustments according to actual application conditions, composite conditions and product performance.
本发明对所述P型掺杂半导体层的半导体材质没有特别限制,以本领域技术人员熟知的背结背接触太阳能电池的P型掺杂半导体层的半导体材质即可,本领域技术人员可以根据实际应用情况、复合情况以及产品性能进行选择和调整,本发明所述P型掺杂半导体层的半导体材质优选各自包括微晶硅、多晶硅和非晶硅中的一种或多种,更优选为微晶硅、多晶硅或非晶硅。The present invention is not particularly limited to the semiconductor material of the P-type doped semiconductor layer, and the semiconductor material of the P-type doped semiconductor layer of the back-junction and back-contact solar cell well known to those skilled in the art can be used. Those skilled in the art can according to The actual application situation, composite situation and product performance are selected and adjusted, and the semiconductor material of the P-type doped semiconductor layer in the present invention preferably includes one or more of microcrystalline silicon, polycrystalline silicon and amorphous silicon, more preferably Microcrystalline silicon, polycrystalline silicon or amorphous silicon.
本发明对所述P型掺杂半导体层的掺杂的材质没有特别限制,以本领域技术人员熟知的背结背接触太阳能电池的P型掺杂半导体层的掺杂的材质即可,本领域技术人员可以根据实际应用情况、复合情况以及产品性能进行选择和调整,本发明所述P型掺杂半导体层的掺杂的材质优选各自包括硼、磷、镓和砷中的一种或多种,更优选为硼、磷、镓或砷,最优选为硼。The present invention has no special limitation on the doping material of the P-type doped semiconductor layer, and the doping material of the P-type doped semiconductor layer of the back-junction back-contact solar cell well known to those skilled in the art can be used. A skilled person can select and adjust according to actual application conditions, composite conditions and product performance. The doped material of the P-type doped semiconductor layer in the present invention preferably includes one or more of boron, phosphorus, gallium and arsenic. , more preferably boron, phosphorus, gallium or arsenic, most preferably boron.
本发明对所述P型掺杂半导体层的掺杂浓度没有特别限制,以本领域技术人员熟知的常规掺杂浓度即可,本领域技术人员可以根据实际应用情况、复合情况以及产品性能进行选择和调整,本发明所述P型掺杂半导体层的掺杂浓度优选为1018~1021cm-3,更优选为1018~1020cm-3,最优选为1019~1021cm-3。The present invention has no special limitation on the doping concentration of the P-type doped semiconductor layer, and the conventional doping concentration well known to those skilled in the art can be used, and those skilled in the art can choose according to the actual application situation, compounding situation and product performance. and adjustment, the doping concentration of the P-type doped semiconductor layer in the present invention is preferably 10 18 to 10 21 cm -3 , more preferably 10 18 to 10 20 cm -3 , most preferably 10 19 to 10 21 cm -3 3 .
本发明对所述P型掺杂半导体层的复合方式和掺杂方式没有特别限制,以本领域技术人员熟知的复合方式和掺杂方式即可,本领域技术人员可以根据实际应用情况、复合情况以及产品性能进行选择和调整,本发明所述P型掺杂半导体层优选为P型掺杂半导体层直接在隧穿氧化层上形成,可以采用PECVD工艺生长,并进行原位掺杂的方式形成,也可以先用PECVD生长半导体层,然后用扩散的方式进行掺杂。The present invention has no special restrictions on the compounding and doping methods of the P-type doped semiconductor layer, and the compounding and doping methods known to those skilled in the art can be used. And the product performance is selected and adjusted, the P-type doped semiconductor layer of the present invention is preferably formed directly on the tunnel oxide layer by the P-type doped semiconductor layer, which can be grown by PECVD process and formed by in-situ doping , the semiconductor layer can also be grown by PECVD first, and then doped by diffusion.
本发明对所述P型掺杂半导体层的厚度没有特别限制,以本领域技术人员熟知的背结背接触太阳能电池的前场区常规厚度即可,本领域技术人员可以根据实际应用情况、复合情况以及产品性能进行选择和调整,本发明所述P型掺杂半导体层的厚度优选为5nm~500nm,更优选为50nm~450nm,更优选为100nm~400nm,最优选为200nm~300nm。In the present invention, the thickness of the P-type doped semiconductor layer is not particularly limited, and the conventional thickness of the front field region of the back-junction and back-contact solar cell well known to those skilled in the art can be used. Those skilled in the art can combine The thickness of the P-type doped semiconductor layer in the present invention is preferably 5nm-500nm, more preferably 50nm-450nm, more preferably 100nm-400nm, and most preferably 200nm-300nm.
本发明对所述复合在所述隧穿氧化物层上的N型掺杂半导体层没有特别限制,以本领域技术人员熟知的背结背接触太阳能电池的N型掺杂半导体层即可,本领域技术人员可以根据实际应用情况、复合情况以及产品性能进行选择和调整。In the present invention, there is no special limitation on the N-type doped semiconductor layer compounded on the tunnel oxide layer, and the N-type doped semiconductor layer of the back-junction and back-contact solar cell well known to those skilled in the art can be used. Those skilled in the art can make selections and adjustments according to actual application conditions, composite conditions and product performance.
本发明对所述N型掺杂半导体层的半导体材质没有特别限制,以本领域技术人员熟知的背结背接触太阳能电池的N型掺杂半导体层的半导体材质即可,本领域技术人员可以根据实际应用情况、复合情况以及产品性能进行选择和调整本发明所述N型掺杂半导体层的半导体材质优选各自包括微晶硅、多晶硅和非晶硅中的一种或多种,更优选为微晶硅、多晶硅或非晶硅。The present invention is not particularly limited to the semiconductor material of the N-type doped semiconductor layer, and the semiconductor material of the N-type doped semiconductor layer of the back-junction and back-contact solar cell well known to those skilled in the art can be used. Those skilled in the art can according to The actual application situation, composite situation and product performance are selected and adjusted. The semiconductor material of the N-type doped semiconductor layer of the present invention preferably includes one or more of microcrystalline silicon, polycrystalline silicon and amorphous silicon, more preferably microcrystalline silicon. crystalline silicon, polycrystalline silicon or amorphous silicon.
本发明对所述N型掺杂半导体层的掺杂的材质没有特别限制,以本领域技术人员熟知的背结背接触太阳能电池的N型掺杂半导体层的掺杂的材质即可,本领域技术人员可以根据实际应用情况、复合情况以及产品性能进行选择和调整本发明所述N型掺杂半导体层的掺杂的材质优选各自包括硼、磷、镓和砷中的一种或多种,更优选为硼、磷、镓或砷,最优选为磷。The present invention has no particular limitation on the doped material of the N-type doped semiconductor layer, and the doped material of the N-type doped semiconductor layer of the back-junction back-contact solar cell well known to those skilled in the art can be used. The skilled person can select and adjust the doped material of the N-type doped semiconductor layer in the present invention according to the actual application situation, composite situation and product performance, preferably each including one or more of boron, phosphorus, gallium and arsenic, More preferred is boron, phosphorous, gallium or arsenic, most preferred is phosphorous.
本发明对所述N型掺杂半导体层的掺杂浓度没有特别限制,以本领域技术人员熟知的常规掺杂浓度即可,本领域技术人员可以根据实际应用情况、复合情况以及产品性能进行选择和调整,本发明所述N型掺杂半导体层的掺杂浓度优选为1018~1021cm-3,更优选为1018~1020cm-3,最优选为1019~1021cm-3。In the present invention, the doping concentration of the N-type doped semiconductor layer is not particularly limited, and the conventional doping concentration well known to those skilled in the art can be used, and those skilled in the art can choose according to the actual application situation, compounding situation and product performance. and adjustment, the doping concentration of the N-type doped semiconductor layer in the present invention is preferably 10 18 to 10 21 cm -3 , more preferably 10 18 to 10 20 cm -3 , most preferably 10 19 to 10 21 cm -3 3 .
本发明对所述N型掺杂半导体层的复合方式和掺杂方式没有特别限制,以本领域技术人员熟知的复合方式和掺杂方式即可,本领域技术人员可以根据实际应用情况、复合情况以及产品性能进行选择和调整,本发明所述N型掺杂半导体层优选为N型掺杂半导体层直接在隧穿氧化层上形成,可以采用PECVD工艺生长,并进行原位掺杂的方式形成,也可以先用PECVD生长半导体层,然后用扩散的方式进行掺杂。The present invention has no special restrictions on the compounding and doping methods of the N-type doped semiconductor layer, and the compounding and doping methods known to those skilled in the art can be used. and product performance selection and adjustment, the N-type doped semiconductor layer in the present invention is preferably formed directly on the tunnel oxide layer, and can be grown by PECVD process and formed by in-situ doping , the semiconductor layer can also be grown by PECVD first, and then doped by diffusion.
本发明对所述N型掺杂半导体层的厚度没有特别限制,以本领域技术人员熟知的背结背接触太阳能电池的前场区常规厚度即可,本领域技术人员可以根据实际应用情况、复合情况以及产品性能进行选择和调整,本发明所述N型掺杂半导体层的厚度优选为5nm~500nm,更优选为50nm~450nm,更优选为100nm~400nm,最优选为200nm~300nm。In the present invention, the thickness of the N-type doped semiconductor layer is not particularly limited, and the conventional thickness of the front field region of the back-junction and back-contact solar cell well known to those skilled in the art can be used. Those skilled in the art can combine The thickness of the N-type doped semiconductor layer in the present invention is preferably 5nm-500nm, more preferably 50nm-450nm, more preferably 100nm-400nm, most preferably 200nm-300nm.
本发明对所述P型掺杂半导体层和N型掺杂半导体层的设置关系没有特别限制,以本领域技术人员熟知的背结背接触太阳能电池的P型掺杂半导体层和N型掺杂半导体层的设置关系即可,本领域技术人员可以根据实际应用情况、复合情况以及产品性能进行选择和调整,本发明所述P型掺杂半导体层和N型掺杂半导体层优选相邻交替复合在所述隧穿氧化物层上,和/或所述P型掺杂半导体层和N型掺杂半导体层相隔交替复合在所述隧穿氧化物层上,更优选相邻交替复合在所述隧穿氧化物层上,或相隔交替复合在所述隧穿氧化物层上。The present invention has no special limitation on the arrangement relationship between the P-type doped semiconductor layer and the N-type doped semiconductor layer. The setting relationship of the semiconductor layer is enough, and those skilled in the art can select and adjust according to the actual application situation, compounding situation and product performance. The P-type doped semiconductor layer and the N-type doped semiconductor layer in the present invention are preferably alternately compounded adjacent to each other. On the tunnel oxide layer, and/or the P-type doped semiconductor layer and the N-type doped semiconductor layer are alternately compounded on the tunnel oxide layer, more preferably adjacent alternately compounded on the on the tunneling oxide layer, or alternately compounded on the tunneling oxide layer.
本发明所述相隔交替即是指,交替分布且两者之间存在一定的空隙,即插指状分布。Alternate intervals in the present invention refer to alternate distribution with a certain gap between them, that is, finger-like distribution.
本发明对所述P型掺杂半导体层和N型掺杂半导体层的宽度关系没有特别限制,以本领域技术人员熟知的背结背接触太阳能电池的P型掺杂半导体层和N型掺杂半导体层的宽度关系即可,本领域技术人员可以根据实际应用情况、复合情况以及产品性能进行选择和调整,本发明所述P型掺杂半导体层的宽度与所述N型掺杂半导体层的宽度比优选为(2~10):1,更优选为(3~9):1,更优选为(4~8):1,最优选为(5~7):1。The present invention has no particular limitation on the width relationship between the P-type doped semiconductor layer and the N-type doped semiconductor layer. The width relationship of the semiconductor layer is sufficient, and those skilled in the art can select and adjust according to the actual application situation, composite situation and product performance. The width of the P-type doped semiconductor layer in the present invention and the width of the N-type doped semiconductor layer The width ratio is preferably (2-10):1, more preferably (3-9):1, more preferably (4-8):1, most preferably (5-7):1.
特别的,当所述P型掺杂半导体层和N型掺杂半导体层相邻交替复合在所述隧穿氧化物层上时,由于正电极不能和背场区接触,负电极不能和发射极区接触,所述正电极的宽度小于所述P型掺杂半导体层的宽度,所述负电极的宽度小于所述N型掺杂半导体层的宽度,且所述正电极不与所述N型掺杂半导体层相接触,所述负电极不与所述P型掺杂半导体层相接触。In particular, when the P-type doped semiconductor layer and the N-type doped semiconductor layer are alternately compounded on the tunnel oxide layer, since the positive electrode cannot be in contact with the back field region, the negative electrode cannot be in contact with the emitter The width of the positive electrode is smaller than the width of the P-type doped semiconductor layer, the width of the negative electrode is smaller than the width of the N-type doped semiconductor layer, and the positive electrode is not in contact with the N-type doped semiconductor layer. The doped semiconductor layer is in contact, and the negative electrode is not in contact with the P-type doped semiconductor layer.
本发明还包括设置在所述P型掺杂半导体层上的正电极以及设置在所述N型掺杂半导体层上的负电极。The present invention also includes a positive electrode arranged on the P-type doped semiconductor layer and a negative electrode arranged on the N-type doped semiconductor layer.
本发明对所述正电极和负电极的形成方式没有特别限制,以本领域技术人员熟知的电极形成方式即可,本领域技术人员可以根据实际应用情况、复合情况以及产品性能进行选择和调整,本发明所述电极的形成方式优选采用丝网印刷、溅射或金属蒸法形成。The present invention has no special limitation on the formation method of the positive electrode and the negative electrode, and the electrode formation method known to those skilled in the art can be used. Those skilled in the art can select and adjust according to the actual application situation, composite situation and product performance. The electrode of the present invention is preferably formed by screen printing, sputtering or metal vaporization.
本发明的衬底的背面N型掺杂半导体层和P型掺杂半导体层可以连接在一起,也可以用一条沟槽将它们分离开来,优选呈插指状交替分布,两种类型的掺杂半导体层与衬底之间有一层很薄的隧穿氧化层。呈插指状分布的N型掺杂半导体层和P型掺杂半导体层构成电池的发射极区与背场区。The N-type doped semiconductor layer and the P-type doped semiconductor layer on the back side of the substrate of the present invention can be connected together, or they can be separated by a trench, preferably alternately distributed in the form of interpolated fingers, and the two types of doped There is a very thin tunnel oxide layer between the hetero-semiconductor layer and the substrate. The N-type doped semiconductor layer and the P-type doped semiconductor layer distributed in the shape of fingers constitute the emitter region and the back field region of the battery.
其中,P型掺杂半导体层可以采用PECVD方法进行成长并进行原位掺杂,掺杂杂质优选为硼,厚度为5~500nm之间,掺杂浓度在1017cm-3~1021cm-3之间。N型掺杂半导体层采用和P型掺杂半导体层一样的工艺制备,掺杂杂质优选为磷。厚度和掺杂浓度和P型掺杂半导体层相近。但是N型掺杂半导体层的宽度要比P型掺杂半导体层的宽度小,P型掺杂半导体层的宽度和N型掺杂半导体层宽度之比应该在2~10之间。Among them, the P-type doped semiconductor layer can be grown by PECVD method and in-situ doped, the doping impurity is preferably boron, the thickness is between 5 and 500 nm, and the doping concentration is between 10 17 cm -3 and 10 21 cm - between 3 . The N-type doped semiconductor layer is prepared by the same process as the P-type doped semiconductor layer, and the doped impurity is preferably phosphorus. The thickness and doping concentration are similar to those of the P-type doped semiconductor layer. However, the width of the N-type doped semiconductor layer is smaller than that of the P-type doped semiconductor layer, and the ratio of the width of the P-type doped semiconductor layer to the width of the N-type doped semiconductor layer should be between 2 and 10.
本发明的正负电极,都是在电池的背面形成的,其中正电极从发射极区也就是P型掺杂半导体层引出,负电极从背场区也就是N型掺杂半导体层引出。The positive and negative electrodes of the present invention are all formed on the back of the battery, wherein the positive electrode is drawn from the emitter region, that is, the P-type doped semiconductor layer, and the negative electrode is drawn from the back field region, that is, the N-type doped semiconductor layer.
如果发射极区和背场区是分离的,则正负电极可以完全覆盖发射极区和背场区,如果发射极区和背场区是连接在一起的,那么正负电极可以覆盖发射极区和背场区的绝大部分,但是正电极不能和背场区接触,负电极不能和发射极区接触,当然正负电极之间也要隔离开来。If the emitter area and the back field area are separated, the positive and negative electrodes can completely cover the emitter area and the back field area, and if the emitter area and the back field area are connected together, then the positive and negative electrodes can cover the emitter area And most of the back field area, but the positive electrode cannot be in contact with the back field area, and the negative electrode cannot be in contact with the emitter area. Of course, the positive and negative electrodes should also be isolated.
本发明上述步骤提供了该背面采用隧穿氧化层钝化接触结构的背结背接触太阳能电池,首先作为背结背接触太阳能电池,该结构的太阳能电池,前表面没有金属栅线,所以没有遮光损失,发射区和背场,正负电极都在电池的背面,因此金属电极可以几乎覆盖电池的整个背面,这极大地减小电池的串联电阻,而且正负电极都作在背面,对于电池片之间的互联要简单很多。The above steps of the present invention provide a back-junction and back-contact solar cell with a tunnel oxide layer passivation contact structure on the back, firstly as a back-junction and back-contact solar cell, the solar cell with this structure has no metal grid lines on the front surface, so there is no shading Loss, emission area and back field, the positive and negative electrodes are on the back of the battery, so the metal electrode can cover almost the entire back of the battery, which greatly reduces the series resistance of the battery, and both the positive and negative electrodes are on the back, for the battery sheet The interconnection between them is much simpler.
而且本发明采用了隧穿氧化层钝化接触结构,通过采用隧穿氧化层钝化接触结构有效的减小了金属接触界面的载流子复合,该结构避免了金属电极直接和和衬底接触,大大减小载流子在金属接触界面的复合,不用为了降低界面复合而减小金属接触面积,可以使金属接触面几乎覆盖整个电池背面,从而减少了载流子的横向运输,可以进一步降低电池的串联电阻,提高电池的效率。本发明将该结构应用到背结背接触太阳能电池上,使得背结背接触电池的优点得到了最大程度的发挥。而且本发明采用的制备工艺和现有的太阳能电池制备工艺兼容性良好,甚至可以进一步简化电池的制备工艺,降低生产成本。Moreover, the present invention adopts a tunneling oxide layer passivation contact structure, which effectively reduces the carrier recombination of the metal contact interface by adopting the tunneling oxide layer passivation contact structure, and this structure avoids direct contact between the metal electrode and the substrate , greatly reducing the recombination of carriers at the metal contact interface, without reducing the metal contact area in order to reduce interface recombination, the metal contact surface can almost cover the entire back of the battery, thereby reducing the lateral transport of carriers, which can further reduce The series resistance of the battery increases the efficiency of the battery. The invention applies the structure to the back-junction and back-contact solar cell, so that the advantages of the back-junction and back-contact solar cell are maximized. Moreover, the preparation process adopted by the present invention has good compatibility with the existing solar cell preparation process, and can even further simplify the cell preparation process and reduce production costs.
实验结果表明,本发明提供的背面采用隧穿氧化层钝化接触结构的背结背接触太阳能电池,电池效率能够达到22%。Experimental results show that the back junction and back contact solar cell with tunnel oxide layer passivation contact structure on the back provided by the present invention can reach 22% cell efficiency.
为了进一步说明本发明,以下结合实施例对本发明提供的一种背结背接触太阳能电池进行详细描述,但是应当理解,这些实施例是在以本发明技术方案为前提下进行实施,给出了详细的实施方式和具体的操作过程,只是为进一步说明本发明的特征和优点,而不是对本发明权利要求的限制,本发明的保护范围也不限于下述的实施例。In order to further illustrate the present invention, a back-junction and back-contact solar cell provided by the present invention will be described in detail below in conjunction with examples, but it should be understood that these examples are implemented on the premise of the technical solution of the present invention, and detailed The embodiments and the specific operation process are only to further illustrate the features and advantages of the present invention, rather than to limit the claims of the present invention, and the scope of protection of the present invention is not limited to the following examples.
实施例1Example 1
参见图1,图1为本发明实施例1提供的背结背接触太阳能电池的结构示意简图。其中,101为衬底(基片),102为隧穿氧化物层,103为N型掺杂半导体层,104为P型掺杂半导体层,105为正电极,106为负电极,107为前场区,108为减反射层,109为前表面钝化层,110为整体的绒面陷光结构。Referring to FIG. 1 , FIG. 1 is a schematic structural diagram of a back-junction and back-contact solar cell provided by Embodiment 1 of the present invention. Among them, 101 is the substrate (substrate), 102 is the tunnel oxide layer, 103 is the N-type doped semiconductor layer, 104 is the P-type doped semiconductor layer, 105 is the positive electrode, 106 is the negative electrode, and 107 is the front electrode. In the field area, 108 is an anti-reflection layer, 109 is a passivation layer on the front surface, and 110 is an overall suede light-trapping structure.
由图1可知,P型掺杂半导体层和N型掺杂半导体层呈插指状交替分布,P型掺杂半导体层和N型掺杂半导体层之间通过一个沟道隔离开来,彼此之间是绝缘的。其中P型掺杂半导体层作为发射极要比作为背场区域的N型掺杂半导体层宽。It can be seen from Fig. 1 that the P-type doped semiconductor layer and the N-type doped semiconductor layer are alternately distributed in the shape of interpolated fingers, and the P-type doped semiconductor layer and the N-type doped semiconductor layer are separated by a trench. The room is insulated. Wherein the P-type doped semiconductor layer as the emitter is wider than the N-type doped semiconductor layer as the back field region.
该种结构的太阳能电池的具体制备方法如下:The concrete preparation method of the solar cell of this kind structure is as follows:
在厚度为100微米的N型单晶硅片的前表面用氢氧化钠溶液腐蚀的方法,制备出金字塔形的绒面结构,氢氧化钠的浓度为1%,腐蚀时间为5min,温度为60℃。在制备绒面上,采用离子注入的方式,注入砷原子,在前表面形成一个N型掺杂区,掺杂浓度为1017cm-3,掺杂深度为2微米。形成前表面N型掺杂区之后,再在前表面采用等离子体增强化学气相沉积的方法,沉积一层厚度为20纳米的氧化硅作为钝化层,然后载在钝化层的上面采用溅射的方式沉积一层200纳米后的ITO作为减反射层。然后采用热氧氧化的方法,在硅片的背面形成一层厚度为2nm的隧穿氧化层,在形成隧穿氧化层之后,采用硬掩膜遮挡的方式,采用LPCVD的方法,在隧穿氧化层上面形成交替分布的N型掺杂的多晶硅和P型掺杂的多晶硅,N型掺杂多晶硅宽度为800微米,厚度为100nm,掺杂浓度为1019cm-3,P型掺杂多晶硅的宽度为200微米,厚度为100nm,掺杂浓度为1019cm-3。N型掺杂多晶硅和P型掺杂多晶硅之间有一个宽度为40微米的空隙。在形成N型掺杂多晶硅和P型掺杂多晶硅之后,再采用丝网印刷的方法,在作为发射极的P型掺杂多晶硅和作为背场的N型掺杂多晶硅上形成金属接触,金属要覆盖整个掺杂多晶硅层,正电极和负电极之间也有一个40微米的空隙,最后得到背面采用隧穿氧化层钝化接触结构的背结背接触太阳能电池。A pyramid-shaped suede structure is prepared by corroding the front surface of an N-type single crystal silicon wafer with a thickness of 100 microns with a sodium hydroxide solution. The concentration of sodium hydroxide is 1%, the etching time is 5 minutes, and the temperature is 60 ℃. On the textured surface, arsenic atoms were implanted by ion implantation to form an N-type doped region on the front surface with a doping concentration of 10 17 cm -3 and a doping depth of 2 microns. After forming the N-type doped region on the front surface, a layer of silicon oxide with a thickness of 20 nanometers is deposited on the front surface as a passivation layer by plasma-enhanced chemical vapor deposition, and then placed on the passivation layer by sputtering A layer of 200nm ITO was deposited as an anti-reflection layer by the way. Then, a layer of tunnel oxide layer with a thickness of 2nm is formed on the back of the silicon wafer by thermal oxygen oxidation method. N-type doped polysilicon and P-type doped polysilicon are alternately distributed on the layer, the N-type doped polysilicon has a width of 800 microns, a thickness of 100nm, and a doping concentration of 10 19 cm -3 , and the P-type doped polysilicon The width is 200 microns, the thickness is 100 nm, and the doping concentration is 10 19 cm -3 . There is a gap with a width of 40 microns between the N-type doped polysilicon and the P-type doped polysilicon. After forming N-type doped polysilicon and P-type doped polysilicon, the screen printing method is used to form metal contacts on the P-type doped polysilicon used as the emitter and the N-type doped polysilicon used as the back field. Covering the entire doped polysilicon layer, there is also a 40 micron gap between the positive electrode and the negative electrode, and finally a back-junction back-contact solar cell with a tunnel oxide passivation contact structure on the back is obtained.
对本发明实施例1制备的背结背接触太阳能电池的性能进行表征。测试采用标准测试条件(SRC),测试电池的I-V特性曲线。The performance of the back-junction back-contact solar cell prepared in Example 1 of the present invention was characterized. The test uses standard test conditions (SRC) to test the I-V characteristic curve of the battery.
测试结果表明,本发明制备的背结背接触太阳能电池的平均性能参数如下:开路电压为660mV,短路电流密度为41.4mA,填充因子为78.8%,效率为21.2%。The test results show that the average performance parameters of the back junction and back contact solar cells prepared by the invention are as follows: the open circuit voltage is 660mV, the short circuit current density is 41.4mA, the filling factor is 78.8%, and the efficiency is 21.2%.
实施例2Example 2
参见图2,图2为本发明实施例2提供的背结背接触太阳能电池的结构示意简图。其中,101为衬底(基片),102为隧穿氧化物层,103为N型掺杂半导体层,104为P型掺杂半导体层,105为正电极,106为负电极,107为前场区,108为减反射层,109为前表面钝化层,110为整体的绒面陷光结构。Referring to FIG. 2 , FIG. 2 is a schematic structural diagram of a back-junction and back-contact solar cell provided by Embodiment 2 of the present invention. Among them, 101 is the substrate (substrate), 102 is the tunnel oxide layer, 103 is the N-type doped semiconductor layer, 104 is the P-type doped semiconductor layer, 105 is the positive electrode, 106 is the negative electrode, and 107 is the front electrode. In the field area, 108 is an anti-reflection layer, 109 is a passivation layer on the front surface, and 110 is an overall suede light-trapping structure.
由图2可知,P型掺杂半导体层和N型掺杂半导体层也可以如图2所示是连接在一起的,虽然连接在一起,但是P型掺杂半导体层和N型掺杂半导体层会形成一个PN结,电池正常工作时,PN结是处于反偏状态,因此不会造成漏电。As can be seen from Figure 2, the P-type doped semiconductor layer and the N-type doped semiconductor layer can also be connected together as shown in Figure 2, although they are connected together, the P-type doped semiconductor layer and the N-type doped semiconductor layer A PN junction will be formed. When the battery is working normally, the PN junction is in a reverse bias state, so it will not cause leakage.
本发明提供的太阳能电池的正负电极都是在电池的背面形成的,其中正电极从P型掺杂半导体层引出,负电极从N型掺杂半导体层引出。如图1所示,如果P型掺杂半导体层和N型掺杂半导体层是分离了,那么电极可以完全覆盖P型掺杂半导体层和N型掺杂半导体层。如图2所示如果P型掺杂半导体层和N型掺杂半导体层是连接在一起的,那么金属电极就只能覆盖掺杂半导体层的大部分,同时要保证正电极不和N型掺杂半导体层接触,负电极不和P型掺杂半导体层接触。The positive and negative electrodes of the solar cell provided by the present invention are all formed on the back of the cell, wherein the positive electrode is drawn from the P-type doped semiconductor layer, and the negative electrode is drawn from the N-type doped semiconductor layer. As shown in FIG. 1 , if the P-type doped semiconductor layer and the N-type doped semiconductor layer are separated, the electrodes can completely cover the P-type doped semiconductor layer and the N-type doped semiconductor layer. As shown in Figure 2, if the P-type doped semiconductor layer and the N-type doped semiconductor layer are connected together, then the metal electrode can only cover most of the doped semiconductor layer, and at the same time, it must be ensured that the positive electrode is not mixed with the N-type doped semiconductor layer. The doped semiconductor layer is in contact with the negative electrode, and the negative electrode is not in contact with the P-type doped semiconductor layer.
该种结构的太阳能电池的制备方法如下:The preparation method of the solar cell of this kind structure is as follows:
在厚度为100微米的N型单晶硅片的前表面用氢氧化钠溶液腐蚀的方法,制备出金字塔形的绒面结构,氢氧化钠的浓度为1%,腐蚀时间为5min,温度为60℃。在制备绒面上,采用离子注入的方式,注入砷原子,在前表面形成一个N型掺杂区,掺杂浓度为1017cm-3,掺杂深度为2微米。形成前表面N型掺杂区之后,再在前表面采用等离子体增强化学气相沉积的方法,沉积一层厚度为20纳米的氧化硅作为钝化层,然后载在钝化层的上面采用溅射的方式沉积一层200纳米后的ITO作为减反射层。然后采用热氧氧化的方法,在硅片的背面形成一层厚度为2nm的隧穿氧化层,在形成隧穿氧化层之后,采用硬掩膜遮挡的方式,采用LPCVD的方法,在隧穿氧化层上面形成交替分布的N型掺杂的多晶硅和P型掺杂的多晶硅,N型掺杂多晶硅宽度为800微米,厚度为100nm,掺杂浓度为1019cm-3,P型掺杂多晶硅的宽度为200微米,厚度为100nm,掺杂浓度为1019cm-3。N型掺杂多晶硅和P型掺杂多晶硅直接接触,两者之间形成一个PN结。在形成N型掺杂多晶硅和P型掺杂多晶硅之后,再采用丝网印刷的方法,在作为发射极的N型掺杂多晶硅上形成正电极,在作为背场的N型掺杂多晶硅上形成负电极,金属部分地覆盖掺杂多晶硅层,正电极和负电极之间有一个40微米的空隙,最后得到背面采用隧穿氧化层钝化接触结构的背结背接触太阳能电池。A pyramid-shaped suede structure is prepared by corroding the front surface of an N-type single crystal silicon wafer with a thickness of 100 microns with a sodium hydroxide solution. The concentration of sodium hydroxide is 1%, the etching time is 5 minutes, and the temperature is 60 ℃. On the textured surface, arsenic atoms were implanted by ion implantation to form an N-type doped region on the front surface with a doping concentration of 10 17 cm -3 and a doping depth of 2 microns. After forming the N-type doped region on the front surface, a layer of silicon oxide with a thickness of 20 nanometers is deposited on the front surface as a passivation layer by plasma-enhanced chemical vapor deposition, and then placed on the passivation layer by sputtering A layer of 200nm ITO was deposited as an anti-reflection layer by the way. Then, a layer of tunnel oxide layer with a thickness of 2nm is formed on the back of the silicon wafer by thermal oxygen oxidation method. N-type doped polysilicon and P-type doped polysilicon are alternately distributed on the layer, the N-type doped polysilicon has a width of 800 microns, a thickness of 100 nm, and a doping concentration of 10 19 cm -3 , and the P-type doped polysilicon The width is 200 microns, the thickness is 100 nm, and the doping concentration is 10 19 cm -3 . N-type doped polysilicon is in direct contact with P-type doped polysilicon, and a PN junction is formed between them. After forming N-type doped polysilicon and P-type doped polysilicon, the positive electrode is formed on the N-type doped polysilicon as the emitter, and the positive electrode is formed on the N-type doped polysilicon as the back field by screen printing. For the negative electrode, the metal partially covers the doped polysilicon layer, and there is a gap of 40 microns between the positive electrode and the negative electrode. Finally, a back-junction back-contact solar cell with a tunnel oxide layer passivation contact structure is obtained on the back.
对本发明实施例2制备的背结背接触太阳能电池的性能进行表征。测试采用标准测试条件(SRC),测试电池的I-V特性曲线。The performance of the back-junction back-contact solar cell prepared in Example 2 of the present invention was characterized. The test uses standard test conditions (SRC) to test the I-V characteristic curve of the battery.
测试结果表明,本发明制备的背结背接触太阳能电池的平均性能参数如下:开路电压为660mV,短路电流密度为42mA,填充因子为78.0%,效率为21.6%。The test results show that the average performance parameters of the back junction and back contact solar cells prepared by the invention are as follows: the open circuit voltage is 660mV, the short circuit current density is 42mA, the filling factor is 78.0%, and the efficiency is 21.6%.
实施例3Example 3
太阳能电池的制备方法如下:The preparation method of the solar cell is as follows:
在厚度为100微米的N型单晶硅片的前表面用氢氧化钠溶液腐蚀的方法,制备出金字塔形的绒面结构,氢氧化钠的浓度为1%,腐蚀时间为5min,温度为60℃。在制备绒面上,采用离子注入的方式,注入砷原子,在前表面形成一个N型掺杂区,掺杂浓度为1017cm-3,掺杂深度为2微米。形成前表面N型掺杂区之后,再在前表面采用等离子体增强化学气相沉积的方法,沉积一层厚度为20纳米的氧化硅作为钝化层,然后载在钝化层的上面采用溅射的方式沉积一层200纳米后的ITO作为减反射层。然后采用热氧氧化的方法,在硅片的背面形成一层厚度为2nm的隧穿氧化层,在形成隧穿氧化层之后,采用LPCVD的方法,在隧穿氧化层上面生长一层N型掺杂的多晶硅,然后通过光刻的方法,将背场区的多晶硅保护起来,然后通过RIE刻蚀的方法,将没有被保护住的多晶硅腐蚀掉,从而形成背场。然后采用LPCVD的方法,生长一层P型掺杂的多晶硅,还是通过同样的光刻和RIE刻蚀的方法形成电池的发射极区。A pyramid-shaped suede structure is prepared by corroding the front surface of an N-type single crystal silicon wafer with a thickness of 100 microns with a sodium hydroxide solution. The concentration of sodium hydroxide is 1%, the etching time is 5 minutes, and the temperature is 60 ℃. On the textured surface, arsenic atoms were implanted by ion implantation to form an N-type doped region on the front surface with a doping concentration of 10 17 cm -3 and a doping depth of 2 microns. After forming the N-type doped region on the front surface, a layer of silicon oxide with a thickness of 20 nanometers is deposited on the front surface as a passivation layer by plasma-enhanced chemical vapor deposition, and then placed on the passivation layer by sputtering A layer of 200nm ITO was deposited as an anti-reflection layer by the way. Then use thermal oxygen oxidation method to form a tunnel oxide layer with a thickness of 2nm on the back of the silicon wafer. After forming the tunnel oxide layer, use LPCVD to grow a layer of N-type doped oxide on the tunnel oxide layer. Doped polysilicon, and then protect the polysilicon in the back field region by photolithography, and then etch the unprotected polysilicon by RIE etching method, thereby forming the back field. Then use the LPCVD method to grow a layer of P-type doped polysilicon, and form the emitter region of the battery through the same photolithography and RIE etching method.
N型掺杂多晶硅宽度为800微米,厚度为100nm,掺杂浓度为1019cm-3,P型掺杂多晶硅的宽度为200微米,厚度为100nm,掺杂浓度为1019cm-3。N型掺杂多晶硅和P型掺杂多晶硅直接接触,两者之间形成一个PN结。在形成N型掺杂多晶硅和P型掺杂多晶硅之后,再采用丝网印刷的方法,在作为发射极的N型掺杂多晶硅上形成正电极,在作为背场的N型掺杂多晶硅上形成负电极,金属部分地覆盖掺杂多晶硅层,正电极和负电极之间有一个40微米的空隙,最后得到背面采用隧穿氧化层钝化接触结构的背结背接触太阳能电池。N-type doped polysilicon has a width of 800 microns, a thickness of 100 nm, and a doping concentration of 10 19 cm -3 , and a P-type doped polysilicon has a width of 200 microns, a thickness of 100 nm, and a doping concentration of 10 19 cm -3 . N-type doped polysilicon is in direct contact with P-type doped polysilicon, and a PN junction is formed between them. After forming N-type doped polysilicon and P-type doped polysilicon, the positive electrode is formed on the N-type doped polysilicon as the emitter, and the positive electrode is formed on the N-type doped polysilicon as the back field by screen printing. For the negative electrode, the metal partially covers the doped polysilicon layer, and there is a gap of 40 microns between the positive electrode and the negative electrode. Finally, a back-junction back-contact solar cell with a tunnel oxide layer passivation contact structure is obtained on the back.
对本发明实施例3制备的背结背接触太阳能电池的性能进行表征。测试采用标准测试条件(SRC),测试电池的I-V特性曲线。The performance of the back-junction back-contact solar cell prepared in Example 3 of the present invention was characterized. The test uses standard test conditions (SRC) to test the I-V characteristic curve of the battery.
参见图3,图3为本发明实施例3提供的隧穿氧化层钝化接触结构的背结背接触太阳能电池的I-V特性曲线。Referring to FIG. 3 , FIG. 3 is an I-V characteristic curve of a back-junction back-contact solar cell with a tunnel oxide layer passivation contact structure provided by Embodiment 3 of the present invention.
由图3可知,本发明制备的背结背接触太阳能电池的平均性能参数如下:开路电压为662mV,短路电流密度为42.4mA,填充因子为78.5%,效率为22.0%。It can be seen from Fig. 3 that the average performance parameters of the back junction and back contact solar cells prepared by the present invention are as follows: the open circuit voltage is 662mV, the short circuit current density is 42.4mA, the fill factor is 78.5%, and the efficiency is 22.0%.
以上对本发明提供的一种背面采用隧穿氧化层钝化接触结构的背结背接触太阳能电池进行了详细的介绍,本文中应用了具体个例对本发明的原理及实施方式进行了阐述,以上实施例的说明只是用于帮助理解本发明的方法及其核心思想,包括最佳方式,并且也使得本领域的任何技术人员都能够实践本发明,包括制造和使用任何装置或系统,和实施任何结合的方法。应当指出,对于本技术领域的普通技术人员来说,在不脱离本发明原理的前提下,还可以对本发明进行若干改进和修饰,这些改进和修饰也落入本发明权利要求的保护范围内。本发明专利保护的范围通过权利要求来限定,并可包括本领域技术人员能够想到的其他实施例。如果这些其他实施例具有不是不同于权利要求文字表述的结构要素,或者如果它们包括与权利要求的文字表述无实质差异的等同结构要素,那么这些其他实施例也应包含在权利要求的范围内。A back-junction back-contact solar cell with a tunnel oxide layer passivation contact structure on the back provided by the present invention has been introduced in detail above. In this paper, a specific example has been used to illustrate the principle and implementation of the present invention. The above implementation The description of the example is only used to help understand the method and its core idea of the present invention, including the best mode, and also enables anyone skilled in the art to practice the present invention, including making and using any device or system, and implementing any combination Methods. It should be pointed out that for those skilled in the art, without departing from the principles of the present invention, some improvements and modifications can be made to the present invention, and these improvements and modifications also fall within the protection scope of the claims of the present invention. The patentable scope of the invention is defined by the claims, and may include other examples that occur to those skilled in the art. Such other examples are intended to be within the scope of the claims if they have structural elements that do not differ from the literal language of the claims, or if they include equivalent structural elements with insubstantial differences from the literal language of the claims.
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