CN107195699A - One kind passivation contact solar cell and preparation method - Google Patents
One kind passivation contact solar cell and preparation method Download PDFInfo
- Publication number
- CN107195699A CN107195699A CN201710564575.XA CN201710564575A CN107195699A CN 107195699 A CN107195699 A CN 107195699A CN 201710564575 A CN201710564575 A CN 201710564575A CN 107195699 A CN107195699 A CN 107195699A
- Authority
- CN
- China
- Prior art keywords
- crystalline silicon
- type crystalline
- layer
- solar cell
- preparation
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 238000002161 passivation Methods 0.000 title claims abstract description 39
- 238000002360 preparation method Methods 0.000 title claims abstract description 20
- 229910021419 crystalline silicon Inorganic materials 0.000 claims abstract description 69
- 239000000758 substrate Substances 0.000 claims abstract description 48
- 229920005591 polysilicon Polymers 0.000 claims abstract description 44
- 229910021420 polycrystalline silicon Inorganic materials 0.000 claims abstract description 43
- 229910052751 metal Inorganic materials 0.000 claims abstract description 29
- 239000002184 metal Substances 0.000 claims abstract description 29
- 238000000034 method Methods 0.000 claims description 28
- 229910021417 amorphous silicon Inorganic materials 0.000 claims description 17
- 230000003647 oxidation Effects 0.000 claims description 13
- 238000007254 oxidation reaction Methods 0.000 claims description 13
- 238000000137 annealing Methods 0.000 claims description 12
- -1 phosphonium ion Chemical class 0.000 claims description 9
- 229910004205 SiNX Inorganic materials 0.000 claims description 6
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 6
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 6
- 229910052710 silicon Inorganic materials 0.000 claims description 6
- 239000010703 silicon Substances 0.000 claims description 6
- 229910052709 silver Inorganic materials 0.000 claims description 6
- 239000004332 silver Substances 0.000 claims description 6
- 238000000151 deposition Methods 0.000 claims description 5
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical group O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 4
- 239000012670 alkaline solution Substances 0.000 claims description 4
- 238000001505 atmospheric-pressure chemical vapour deposition Methods 0.000 claims description 4
- 238000005468 ion implantation Methods 0.000 claims description 4
- 238000004518 low pressure chemical vapour deposition Methods 0.000 claims description 4
- 229910017604 nitric acid Inorganic materials 0.000 claims description 4
- 125000004437 phosphorous atom Chemical group 0.000 claims description 4
- 239000007864 aqueous solution Substances 0.000 claims description 3
- 238000004140 cleaning Methods 0.000 claims description 3
- 230000008021 deposition Effects 0.000 claims description 3
- 238000002513 implantation Methods 0.000 claims description 3
- 229910052698 phosphorus Inorganic materials 0.000 claims description 3
- 239000011574 phosphorus Substances 0.000 claims description 3
- 238000012545 processing Methods 0.000 claims description 3
- 229910052796 boron Inorganic materials 0.000 claims description 2
- 238000010884 ion-beam technique Methods 0.000 claims description 2
- 150000002500 ions Chemical class 0.000 claims description 2
- 238000000623 plasma-assisted chemical vapour deposition Methods 0.000 claims description 2
- 238000007650 screen-printing Methods 0.000 claims description 2
- 239000011159 matrix material Substances 0.000 claims 16
- 239000011248 coating agent Substances 0.000 claims 4
- 238000000576 coating method Methods 0.000 claims 4
- 230000015572 biosynthetic process Effects 0.000 claims 3
- 239000012528 membrane Substances 0.000 claims 3
- 229910052681 coesite Inorganic materials 0.000 claims 2
- 229910052906 cristobalite Inorganic materials 0.000 claims 2
- 239000000377 silicon dioxide Substances 0.000 claims 2
- 229910052682 stishovite Inorganic materials 0.000 claims 2
- 229910052905 tridymite Inorganic materials 0.000 claims 2
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 claims 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims 1
- 239000004411 aluminium Substances 0.000 claims 1
- 229910052782 aluminium Inorganic materials 0.000 claims 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 229910052593 corundum Inorganic materials 0.000 claims 1
- 239000013078 crystal Substances 0.000 claims 1
- 235000008216 herbs Nutrition 0.000 claims 1
- 229910052738 indium Inorganic materials 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 238000006385 ozonation reaction Methods 0.000 claims 1
- 239000005297 pyrex Substances 0.000 claims 1
- 210000002268 wool Anatomy 0.000 claims 1
- 229910001845 yogo sapphire Inorganic materials 0.000 claims 1
- 230000006798 recombination Effects 0.000 abstract description 5
- 238000005215 recombination Methods 0.000 abstract description 5
- 238000010521 absorption reaction Methods 0.000 abstract description 2
- 230000009286 beneficial effect Effects 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 9
- 229910004298 SiO 2 Inorganic materials 0.000 description 8
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 7
- 238000005245 sintering Methods 0.000 description 4
- 239000005388 borosilicate glass Substances 0.000 description 3
- 239000000969 carrier Substances 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 101001073212 Arabidopsis thaliana Peroxidase 33 Proteins 0.000 description 2
- 101001123325 Homo sapiens Peroxisome proliferator-activated receptor gamma coactivator 1-beta Proteins 0.000 description 2
- 102100028961 Peroxisome proliferator-activated receptor gamma coactivator 1-beta Human genes 0.000 description 2
- 229910052581 Si3N4 Inorganic materials 0.000 description 2
- UORVGPXVDQYIDP-UHFFFAOYSA-N borane Chemical compound B UORVGPXVDQYIDP-UHFFFAOYSA-N 0.000 description 2
- 239000008367 deionised water Substances 0.000 description 2
- 229910021641 deionized water Inorganic materials 0.000 description 2
- 238000013461 design Methods 0.000 description 2
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 2
- 230000005641 tunneling Effects 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 229910001316 Ag alloy Inorganic materials 0.000 description 1
- 229910000085 borane Inorganic materials 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 239000007943 implant Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005457 optimization Methods 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 239000002210 silicon-based material Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10F—INORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
- H10F77/00—Constructional details of devices covered by this subclass
- H10F77/30—Coatings
- H10F77/306—Coatings for devices having potential barriers
- H10F77/311—Coatings for devices having potential barriers for photovoltaic cells
- H10F77/315—Coatings for devices having potential barriers for photovoltaic cells the coatings being antireflective or having enhancing optical properties
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10F—INORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
- H10F10/00—Individual photovoltaic cells, e.g. solar cells
- H10F10/10—Individual photovoltaic cells, e.g. solar cells having potential barriers
- H10F10/14—Photovoltaic cells having only PN homojunction potential barriers
- H10F10/146—Back-junction photovoltaic cells, e.g. having interdigitated base-emitter regions on the back side
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10F—INORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
- H10F71/00—Manufacture or treatment of devices covered by this subclass
- H10F71/121—The active layers comprising only Group IV materials
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10F—INORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
- H10F71/00—Manufacture or treatment of devices covered by this subclass
- H10F71/129—Passivating
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10F—INORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
- H10F77/00—Constructional details of devices covered by this subclass
- H10F77/20—Electrodes
- H10F77/206—Electrodes for devices having potential barriers
- H10F77/211—Electrodes for devices having potential barriers for photovoltaic cells
- H10F77/219—Arrangements for electrodes of back-contact photovoltaic cells
- H10F77/227—Arrangements for electrodes of back-contact photovoltaic cells for emitter wrap-through [EWT] photovoltaic cells, e.g. interdigitated emitter-base back-contacts
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/50—Photovoltaic [PV] energy
- Y02E10/546—Polycrystalline silicon PV cells
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/50—Photovoltaic [PV] energy
- Y02E10/547—Monocrystalline silicon PV cells
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
- Y02P70/50—Manufacturing or production processes characterised by the final manufactured product
Landscapes
- Photovoltaic Devices (AREA)
Abstract
本发明涉及一种钝化接触的背结太阳能电池及制备方法,包括N型晶体硅基体,前表面从内到外依次为隧穿氧化层、本征多晶硅层、局部掺杂的n+多晶硅区域、钝化减反膜和n+金属电极,所述n+金属电极设置在所述局部掺杂的n+多晶硅区域上;所述N型晶体硅基体的背表面从内到外依次为p+掺杂区域、钝化膜和p+金属电极,所述p+金属电极设置在所述p+掺杂区域上。其有益效果是:N型晶体硅基体前表面采用局部的n+掺杂多晶硅钝化层,相对于整面n+多晶硅层覆盖的背结电池,不仅可以减少多晶硅层对入射光的无效吸收,提升电池的短路电流,并且可以实现前表面的钝化接触,大大降低了电池前表面的复合速率,提升了开路电压和短路电流。
The invention relates to a passivated contact back-junction solar cell and a preparation method thereof, comprising an N-type crystalline silicon substrate, and the front surface is sequentially composed of a tunnel oxide layer, an intrinsic polysilicon layer, a locally doped n+ polysilicon region, A passivation anti-reflection film and an n+ metal electrode, the n+ metal electrode is arranged on the locally doped n+ polysilicon region; the back surface of the N-type crystalline silicon substrate is a p+ doped region, passivation a chemical film and a p+ metal electrode, and the p+ metal electrode is arranged on the p+ doped region. Its beneficial effects are: the front surface of the N-type crystalline silicon substrate adopts a local n+ doped polysilicon passivation layer. Compared with the back junction cell covered by the entire n+ polysilicon layer, it can not only reduce the ineffective absorption of incident light by the polysilicon layer, but also improve the efficiency of the battery. The short-circuit current can be achieved, and the passivation contact of the front surface can be realized, which greatly reduces the recombination rate of the front surface of the battery, and improves the open-circuit voltage and short-circuit current.
Description
技术领域technical field
本发明涉及太阳能电池技术领域,具体涉及一种钝化接触太阳能电池及制备方法。The invention relates to the technical field of solar cells, in particular to a passivated contact solar cell and a preparation method.
背景技术Background technique
晶硅太阳能电池的表面钝化一直是设计和优化的重中之重。从早期的仅有背电场钝化,到正面氮化硅钝化,再到背面引入诸如氧化硅、氧化铝、氮化硅等介质层的钝化局部开孔接触的PERC/PERL设计。虽然这一结构暂时缓解了背面钝化的问题,但并未根除背面钝化的问题,开孔处的高复合速率依然存在,而且使工艺进一步复杂。PERC以及PERL结构的电池虽然已经拥有相对完善的表面钝化结构,不过将背面的接触范围限制在开孔区域,除了增加了工艺的复杂度外,开孔的过程采用不同的工艺还会对周围的硅材料造成不同程度的损伤,这也额外地增加了金属接触区域的复合。由于开孔限制了载流子的传输路径,使之偏离垂直于接触面的最短路径并拥堵在开口处,增大了填充因子的损失。近几年来,一种既能实现整面钝化,且无需开孔接触的技术成为机构研究的热点,这就是钝化接触(PassivatedContact)技术。Surface passivation of crystalline silicon solar cells has always been a top priority in design and optimization. From the early passivation of only the back electric field, to the passivation of silicon nitride on the front, and then to the PERC/PERL design of the passivation local opening contact of the dielectric layer such as silicon oxide, aluminum oxide, and silicon nitride on the back. Although this structure temporarily alleviates the problem of back passivation, it does not eradicate the problem of back passivation. The high recombination rate at the opening still exists, and it further complicates the process. Although the PERC and PERL structure batteries already have a relatively complete surface passivation structure, the contact range on the back is limited to the opening area. In addition to increasing the complexity of the process, the opening process uses different processes and will also affect the surrounding area. The silicon material causes varying degrees of damage, which additionally increases the recombination of the metal contact area. Since the opening restricts the transport path of carriers, it deviates from the shortest path perpendicular to the contact surface and congests at the opening, which increases the loss of fill factor. In recent years, a technology that can achieve passivation on the entire surface without opening contact has become a research hotspot in institutions, which is Passivated Contact technology.
N型背结电池,是在N型衬底硅片下,前表面形成n+掺杂区域,背表面形成p+发射极,前接触电池的受光面(前表面)存在一个n+/n结(前表面场)。但是,它的掺杂浓度和结深无法形成很好的欧姆接触,导致串联电阻增加影响最终的填充因子和转化效率。如何让前表面场可以有效抑制光生载流子在前表面的复合,使得更多的光生载流子到达背面的发射极,是目前背结电池电池转换效率提升的一个巨大挑战。The N-type back-junction cell is under the N-type substrate silicon wafer, the front surface forms an n+ doped region, the back surface forms a p+ emitter, and there is an n+/n junction (front surface) on the light-receiving surface (front surface) of the front contact cell. field). However, its doping concentration and junction depth cannot form a good ohmic contact, resulting in an increase in series resistance and affecting the final fill factor and conversion efficiency. How to make the front surface field can effectively suppress the recombination of photo-generated carriers on the front surface so that more photo-generated carriers can reach the emitter on the back is a huge challenge to improve the conversion efficiency of back-junction cells.
发明内容Contents of the invention
本发明的目的在于克服现有技术的不足,提供一种局部钝化接触的背结太阳能电池及制备方法。The object of the present invention is to overcome the deficiencies of the prior art, and provide a back junction solar cell with local passivation contact and a preparation method.
本发明的提提供的一种局部钝化接触的背结太阳能电池,其技术方案为:A kind of back junction solar cell with partial passivation contact provided by the present invention, its technical scheme is:
一种钝化接触太阳能电池,包括N型晶体硅基体,其特征在于:所述N型晶体硅基体的前表面从内到外依次为隧穿氧化层、本征多晶硅层、局部掺杂的n+多晶硅区域、钝化减反膜和n+金属电极,所述n+金属电极设置在所述局部掺杂的n+多晶硅区域上;所述N型晶体硅基体的背表面从内到外依次为p+掺杂区域、钝化膜和p+金属电极,所述p+金属电极设置在所述p+掺杂区域上。A passivated contact solar cell, comprising an N-type crystalline silicon substrate, characterized in that: the front surface of the N-type crystalline silicon substrate is sequentially composed of a tunnel oxide layer, an intrinsic polysilicon layer, and locally doped n+ A polysilicon region, a passivation anti-reflection film and an n+ metal electrode, the n+ metal electrode is arranged on the locally doped n+ polysilicon region; the back surface of the N-type crystalline silicon substrate is p+ doped sequentially from the inside to the outside region, a passivation film and a p+ metal electrode, the p+ metal electrode is arranged on the p+ doped region.
本发明还提供了一种钝化接触太阳能电池的制备方法,包括以下步骤:The present invention also provides a method for preparing a passivated contact solar cell, comprising the following steps:
(1)、分别对N型晶体硅基体的前表面和背表面进行掺杂处理,所述N型晶体硅基体前表面的掺杂处理方式为:在N型晶体硅基体的前表面生长隧穿氧化层,并在隧穿氧化层上生长本征多晶硅层或本征非晶硅层,然后在本征多晶硅层或本征非晶硅层上,选择性地局部注入磷离子;所述N型晶体硅基体背表面的掺杂处理方式为:采用APCVD的方式沉积硼硅玻璃,或采用离子注入的方式注入硼离子;(1) Perform doping treatment on the front surface and the back surface of the N-type crystalline silicon substrate respectively, the doping treatment method of the front surface of the N-type crystalline silicon substrate is: grow tunneling on the front surface of the N-type crystalline silicon substrate oxide layer, and grow an intrinsic polysilicon layer or an intrinsic amorphous silicon layer on the tunnel oxide layer, and then selectively locally implant phosphorus ions on the intrinsic polysilicon layer or the intrinsic amorphous silicon layer; the N-type The doping treatment method of the back surface of the crystalline silicon substrate is: depositing borosilicate glass by APCVD, or implanting boron ions by ion implantation;
(2)、将N型晶体硅基体采用弱碱性溶液进行选择清洗,去除非注入区域的本征多晶硅层或本征非晶硅层,再进行退火处理;退火完成后,在硅片前表面形成局部掺杂的n+多晶硅层,在硅片背表面形成p+掺杂的发射极;(2) Selectively clean the N-type crystalline silicon substrate with a weak alkaline solution to remove the intrinsic polysilicon layer or intrinsic amorphous silicon layer in the non-implanted area, and then perform annealing treatment; Form a locally doped n+ polysilicon layer, and form a p+ doped emitter on the back surface of the silicon wafer;
(3)、在N型晶体硅基体的前表面形成钝化减反膜,在N型晶体硅基体的背表面形成钝化膜;(3), forming a passivation anti-reflection film on the front surface of the N-type crystalline silicon substrate, and forming a passivation film on the back surface of the N-type crystalline silicon substrate;
(4)、在N型晶体硅基体的前表面形成与n+掺杂区相欧姆接触接触的n+金属电极,在N型晶体硅基体的背表面形成与p+掺杂区相欧姆接触的p+金属电极,完成太阳能电池的制作。(4), forming an n+ metal electrode in ohmic contact with the n+ doped region on the front surface of the N-type crystalline silicon substrate, and forming a p+ metal electrode in ohmic contact with the p+ doped region on the back surface of the N-type crystalline silicon substrate , to complete the production of solar cells.
其中,步骤(1)中,前表面隧穿氧化层为SiO2,厚度为1-3nm,SiO2的生长方法为高温热氧化法、硝酸氧化法、臭氧氧化法或CVD沉积法。Wherein, in step (1), the tunnel oxide layer on the front surface is SiO 2 with a thickness of 1-3nm, and the growth method of SiO 2 is high temperature thermal oxidation, nitric acid oxidation, ozone oxidation or CVD deposition.
其中,步骤(1)中,在前表面隧穿氧化层上生长本征多晶硅层或本征非晶硅层的方法是:将N型晶体硅基体放入LPCVD设备中,在前表面隧穿氧化层上生长本征多晶硅层或本征非晶硅层。Wherein, in step (1), the method for growing an intrinsic polysilicon layer or an intrinsic amorphous silicon layer on the front surface tunnel oxide layer is: put the N-type crystalline silicon substrate into the LPCVD equipment, and tunnel the oxide layer on the front surface An intrinsic polysilicon layer or an intrinsic amorphous silicon layer is grown on the layer.
其中,步骤(1)中,在本征多晶硅层或者本征非晶硅层上,采用离子注入掩膜,选择性地注入磷原子,其磷原子的注入剂量为1×1015cm-2~8×1015cm-2。Wherein, in step (1), phosphorus atoms are selectively implanted on the intrinsic polysilicon layer or intrinsic amorphous silicon layer using an ion implantation mask, and the implantation dose of phosphorus atoms is 1×10 15 cm -2 ~ 8×10 15 cm -2 .
其中,步骤(1)中,在本征多晶硅层或本征非晶硅层上注入磷离子时,在N型晶体硅基体前表面和离子束之间设置掩膜,掩膜上设置线条状开口,线条状开口宽度为200~2000um。Wherein, in step (1), when implanting phosphorus ions on the intrinsic polysilicon layer or the intrinsic amorphous silicon layer, a mask is set between the front surface of the N-type crystalline silicon substrate and the ion beam, and a line-shaped opening is set on the mask , the width of the line-shaped opening is 200-2000um.
其中,步骤(2)中,所述弱碱性溶液为浓度1%的KOH水溶液,退火处理的峰值温度为800~1100℃,退火时间为30~200min,环境气源为N2和O2。Wherein, in step (2), the weak alkaline solution is 1% KOH aqueous solution, the peak temperature of the annealing treatment is 800-1100° C., the annealing time is 30-200 min, and the ambient gas source is N 2 and O 2 .
其中,步骤(3)中,钝化减反膜的制备方法是,在N型晶体硅基体的前表面利用PECVD设备沉积一层厚度为60-80nm的SiNx介质膜;钝化膜的制备方法是,在N型晶体硅基体的背表面利用ALD设备先沉积一层厚度为2-10nm的Al2O3介质膜,然后在Al2O3介质膜上再沉积一层厚度为40~80nm的SiNx介质膜。Wherein, in the step (3), the preparation method of the passivation antireflection film is to utilize PECVD equipment to deposit a layer of SiN x dielectric film with a thickness of 60-80nm on the front surface of the N-type crystalline silicon substrate; the preparation method of the passivation film Yes, use ALD equipment to deposit a layer of Al 2 O 3 dielectric film with a thickness of 2-10nm on the back surface of the N-type crystalline silicon substrate, and then deposit a layer of Al 2 O 3 dielectric film with a thickness of 40-80nm on the Al 2 O 3 dielectric film SiN x dielectric film.
其中,步骤(4)中,金属电极的制备方法是,通过丝网印刷的方法在N型晶体硅基体的前表面n+掺杂区域上印刷银浆,在背表面p+掺杂区域上印刷银铝浆,然后进行烧结处理。Wherein, in step (4), the preparation method of the metal electrode is to print silver paste on the n+ doped region of the front surface of the N-type crystalline silicon substrate by screen printing, and print silver aluminum on the p+ doped region of the back surface. slurry, followed by sintering.
其中,进行步骤(1)之前,对N型晶体硅基体的前表面和背表面作制绒处理;N型晶体硅基体的电阻率为0.5~15Ω·cm;N型晶体硅基体的厚度为50~300μm。Wherein, before step (1), the front surface and the back surface of the N-type crystalline silicon substrate are subjected to texturing treatment; the resistivity of the N-type crystalline silicon substrate is 0.5 to 15 Ω cm; the thickness of the N-type crystalline silicon substrate is 50 ~300μm.
本发明的实施包括以下技术效果:Implementation of the present invention comprises following technical effect:
本发明提供的一种钝化接触太阳能电池,通过将N型晶体硅基体前表面采用局部的n+掺杂多晶硅钝化层,相对于整面n+多晶硅层覆盖的背结电池,不仅可以减少多晶硅层对入射光的无效吸收,从而提升电池的短路电流,并且可以实现前表面的钝化接触,大大降低了电池前表面的复合速率,提升了开路电压和短路电流。采用本发明掺杂处理方式制备的背结太阳能电池在完成前后表面的钝化膜覆盖后其隐开路电压(Implied Voc)可达700mV以上,暗饱和电流密度J0<20fA cm-2,印刷电极制成背结接触电池后,其短波段的内量子效率达98%以上。In the passivated contact solar cell provided by the present invention, by using a local n+ doped polysilicon passivation layer on the front surface of the N-type crystalline silicon substrate, compared with the back junction cell covered by the entire n+ polysilicon layer, not only the polysilicon layer can be reduced The ineffective absorption of incident light can increase the short-circuit current of the battery, and can realize the passivation contact of the front surface, greatly reducing the recombination rate of the front surface of the battery, and increasing the open-circuit voltage and short-circuit current. After the back-junction solar cell prepared by the doping treatment method of the present invention is covered with a passivation film on the front and rear surfaces, the implied open circuit voltage (Implied Voc) can reach more than 700mV, the dark saturation current density J 0 <20fA cm -2 , and the printed electrode After the back-junction contact cell is made, the internal quantum efficiency in the short-wave band can reach more than 98%.
附图说明Description of drawings
图1为本发明实施例中钝化接触太阳能电池的制备方法步骤一后的电池结构截面示意图。FIG. 1 is a schematic cross-sectional view of the cell structure after step 1 of the method for preparing a passivated contact solar cell in an embodiment of the present invention.
图2为本发明实施例中钝化接触太阳能电池的制备方法步骤二后的电池结构截面示意图。2 is a schematic cross-sectional view of the cell structure after step 2 of the method for preparing a passivated contact solar cell in an embodiment of the present invention.
图3为本发明实施例中钝化接触太阳能电池的制备方法步骤三后的电池结构截面示意图。3 is a schematic cross-sectional view of the cell structure after step 3 of the method for preparing a passivated contact solar cell in an embodiment of the present invention.
图4为本发明实施例中钝化接触太阳能电池的制备方法步骤四后的电池结构截面示意图。4 is a schematic cross-sectional view of the cell structure after step 4 of the method for preparing a passivated contact solar cell in an embodiment of the present invention.
图5为本发明实施例中钝化接触太阳能电池的制备方法步骤五后的电池结构截面示意图。5 is a schematic cross-sectional view of the cell structure after step five of the method for preparing a passivated contact solar cell in an embodiment of the present invention.
图6为本发明实施例中钝化接触太阳能电池的制备方法步骤六后的电池结构截面示意图。6 is a schematic cross-sectional view of the cell structure after step six of the method for preparing a passivated contact solar cell in an embodiment of the present invention.
图7为本发明实施例中钝化接触太阳能电池的制备方法步骤七后的电池结构截面示意图。7 is a schematic cross-sectional view of the cell structure after step 7 of the method for preparing a passivated contact solar cell in an embodiment of the present invention.
图8为本发明实施例中钝化接触太阳能电池的制备方法步骤八后的电池结构截面示意图。FIG. 8 is a schematic cross-sectional view of the cell structure after Step 8 of the method for preparing a passivated contact solar cell in an embodiment of the present invention.
具体实施方式detailed description
下面将结合实施例以及附图对本发明加以详细说明,需要指出的是,所描述的实施例仅旨在便于对本发明的理解,而对其不起任何限定作用。The present invention will be described in detail below in conjunction with the embodiments and the accompanying drawings. It should be noted that the described embodiments are only intended to facilitate the understanding of the present invention, rather than limiting it in any way.
参见图1至图8所示,本实施例提供的一种钝化接触太阳能电池的制备方法,包括以下步骤:Referring to Figures 1 to 8, a method for preparing a passivated contact solar cell provided in this embodiment includes the following steps:
(1)、选择N型晶体硅基体10,并对N型晶体硅基体10的前表面和背表面作制绒处理;N型晶体硅基体10的电阻率为0.5~15Ω·cm,优选1~5Ω·cm;N型晶体硅基体10的厚度为50~300μm,优选120~200μm;完成本步骤后的电池结构如图1所示。(1), select the N-type crystalline silicon substrate 10, and do texture processing to the front surface and the back surface of the N-type crystalline silicon substrate 10; the resistivity of the N-type crystalline silicon substrate 10 is 0.5~15Ω·cm, preferably 1~ 5Ω·cm; the thickness of the N-type crystalline silicon substrate 10 is 50-300 μm, preferably 120-200 μm; the battery structure after this step is shown in FIG. 1 .
(2)、将步骤(1)处理后的N型晶体硅基体10放入APCVD(常压化学气相沉积)机台中,使用气体为硼烷,在背表面形成一层硼硅玻璃(BSG)24,如图2所示。(2), put the N-type crystalline silicon substrate 10 processed in step (1) into an APCVD (atmospheric pressure chemical vapor deposition) machine, use gas as borane, and form a layer of borosilicate glass (BSG) 24 on the back surface ,as shown in picture 2.
(3)、在步骤(2)处理后的N型晶体硅基体10前表面生长一层隧穿氧化层15,本实施例中隧穿氧化层15是SiO2层。生长隧穿氧化层15的方法有硝酸氧化法、高温热氧化法、干式臭氧氧化法及湿式臭氧氧化法。本实施例采用湿式臭氧氧化法,将N型晶体硅基体10放入去离子水中,然后在去离子水中通入臭氧,使得臭氧浓度达到20-50ppm,反应温度30-50℃,时间为5-20min,生长的隧穿氧化层15的厚度为1-3nm。完成本步骤后的电池结构如图3所示。(3) A tunnel oxide layer 15 is grown on the front surface of the N-type crystalline silicon substrate 10 after the treatment in step (2). In this embodiment, the tunnel oxide layer 15 is a SiO 2 layer. The methods for growing the tunneling oxide layer 15 include nitric acid oxidation, high temperature thermal oxidation, dry ozone oxidation and wet ozone oxidation. This embodiment adopts the wet ozone oxidation method, put the N-type crystalline silicon substrate 10 into deionized water, and then pass ozone into the deionized water, so that the ozone concentration reaches 20-50ppm, the reaction temperature is 30-50°C, and the time is 5- After 20 minutes, the thickness of the grown tunnel oxide layer 15 is 1-3 nm. The structure of the battery after this step is shown in FIG. 3 .
(4)、将步骤(3)处理后的N型晶体硅基体10放入LPCVD设备(低压化学气相沉积)中,在其前表面生长本征多晶硅层26,本征多晶硅层的厚度为大于100nm。完成本步骤后的电池结构如图4所示。(4), the N-type crystalline silicon substrate 10 processed in step (3) is put into LPCVD equipment (low pressure chemical vapor deposition), and the intrinsic polysilicon layer 26 is grown on its front surface, and the thickness of the intrinsic polysilicon layer is greater than 100nm . The battery structure after completing this step is shown in FIG. 4 .
(5)、将步骤(4)处理后的N型晶体硅基体10放入离子注入设备,硅片前表面与离子源之间设置掩膜夹具,掩膜上设置有线条状开口,开口宽度为200~2000um。在本征多晶硅层26上选择性注入磷原子,形成注入区域28,注入剂量为1×1015cm-2~8×1015cm-2,优选1×1015cm-2~3×10cm-2。完成本步骤后的电池结构如图5所示。(5), put the N-type crystalline silicon substrate 10 processed in step (4) into the ion implantation equipment, a mask fixture is set between the front surface of the silicon wafer and the ion source, and a linear opening is arranged on the mask, and the opening width is 200~2000um. Phosphorus atoms are selectively implanted on the intrinsic polysilicon layer 26 to form the implanted region 28, and the implantation dose is 1×10 15 cm −2 to 8×10 15 cm −2 , preferably 1×10 15 cm −2 to 3×10 cm −2 2 . The battery structure after this step is shown in FIG. 5 .
(6)、将步骤(5)处理后的N型晶体硅基体10放入清洗设备,采用浓度为1%的KOH水溶液进行选择性清洗,去除未注入区域的本征多晶硅和非晶硅层,最后进行烘干;然后将N型晶体硅基体10放入退火炉中进行高温退火。退火处理的峰值温度为800~1100℃,退火时间为30~200min,环境气源为N2和O2。退火处理后,本征多晶硅层非掺杂区域26转化为本征多晶硅层12,注入区域28转化为n+掺杂多晶硅区域13。完成本步骤后的电池结构如图6所示。(6), put the N-type crystalline silicon substrate 10 processed in step (5) into cleaning equipment, and use KOH aqueous solution with a concentration of 1% for selective cleaning to remove the intrinsic polysilicon and amorphous silicon layers in the non-implanted regions, Finally, drying is carried out; then the N-type crystalline silicon substrate 10 is put into an annealing furnace for high-temperature annealing. The peak temperature of the annealing treatment is 800-1100° C., the annealing time is 30-200 minutes, and the ambient gas source is N 2 and O 2 . After the annealing treatment, the non-doped region 26 of the intrinsic polysilicon layer is transformed into the intrinsic polysilicon layer 12 , and the implanted region 28 is transformed into the n+ doped polysilicon region 13 . The structure of the battery after this step is shown in FIG. 6 .
(7)、在步骤(6)处理后的N型晶体硅基体10的前表面生长钝化减反膜14,在N型晶体硅基体10的背表面生长钝化膜18。前表面的钝化减反膜14是SiNx膜,其厚度为60-80nm,背表面的钝化膜18是SiO2、SiNx或Al2O3介质膜中一种或多种,利用ALD设备先沉积一层厚度为2-10nm的Al2O3介质膜,然后在Al2O3介质膜上再沉积一层厚度为40~80nm的SiNx介质膜。完成本步骤后的电池结构如图7所示。(7) A passivation antireflection film 14 is grown on the front surface of the N-type crystalline silicon substrate 10 after step (6), and a passivation film 18 is grown on the back surface of the N-type crystalline silicon substrate 10 . The passivation anti-reflection film 14 on the front surface is a SiNx film with a thickness of 60-80nm, and the passivation film 18 on the back surface is one or more of SiO 2 , SiN x or Al 2 O 3 dielectric films, using ALD The equipment first deposits a layer of Al 2 O 3 dielectric film with a thickness of 2-10nm, and then deposits a layer of SiN x dielectric film with a thickness of 40-80nm on the Al 2 O 3 dielectric film. The battery structure after completing this step is shown in FIG. 7 .
(8)、在N型晶体硅基体10的背表面使用银浆印刷p+金属电极22并进行烘干,在N型晶体硅基体10的前表面使用掺铝银浆印刷n+金属电极20并进行烘干。银浆及掺铝银浆均采用现有N型电池工艺中常用的型号。完成本步骤后的电池结构如图8所示。(8), use silver paste to print p+ metal electrode 22 on the back surface of N-type crystalline silicon substrate 10 and dry it, and use aluminum-doped silver paste to print n+ metal electrode 20 on the front surface of N-type crystalline silicon substrate 10 and bake it Dry. Both the silver paste and the aluminum-doped silver paste are commonly used in the existing N-type battery technology. The battery structure after completing this step is shown in FIG. 8 .
(9)、将步骤(8)处理后的N型晶体硅基体10传送入带式烧结炉进行烧结,烧结峰值温度为850-950℃,即完成一种钝化接触太阳能电池的制备。(9) Transfer the N-type crystalline silicon substrate 10 treated in step (8) into a belt sintering furnace for sintering. The sintering peak temperature is 850-950° C., that is, the preparation of a passivated contact solar cell is completed.
优选地,所述N型晶体硅基体的前表面为N型晶体硅表面;或,所述N型晶体硅基体的前表面为在N型晶体硅前表面隧穿氧化层上生长本征多晶硅层或者本征非晶硅层;当所述N型晶体硅基体的前表面为在N型晶体硅前表面隧穿氧化层上生长本征多晶硅层或者本征非晶硅层时,所述N型前表面隧穿氧化层为SiO2,厚度为1-3nm,SiO2的生长方法为高温热氧化法、硝酸氧化法、臭氧氧化法或CVD沉积法。Preferably, the front surface of the N-type crystalline silicon substrate is an N-type crystalline silicon surface; or, the front surface of the N-type crystalline silicon substrate is an intrinsic polysilicon layer grown on a tunnel oxide layer on the front surface of the N-type crystalline silicon Or an intrinsic amorphous silicon layer; when the front surface of the N-type crystalline silicon substrate is an intrinsic polysilicon layer or an intrinsic amorphous silicon layer grown on the tunnel oxide layer on the front surface of the N-type crystalline silicon, the N-type The tunnel oxide layer on the front surface is SiO 2 with a thickness of 1-3nm. The growth method of SiO 2 is high temperature thermal oxidation, nitric acid oxidation, ozone oxidation or CVD deposition.
参见图8所示,本实施例的一种背接触太阳能电池,包括N型晶体硅基体10,N型晶体硅基体10的前表面从内到外依次为隧穿氧化层15、本征多晶硅层12、正表面n+掺杂多晶硅区域13、钝化减反膜14和n+金属电极20;N型晶体硅基体10的背表面从内到外依次为背表面p+掺杂区域16、钝化膜18和p+金属电极22,掺杂区域包括正表面n+掺杂多晶硅区域13和背表面p+掺杂区域16,正表面n+掺杂多晶硅区域13上设置有n+金属电极20,背表面p+掺杂区域16上设置有p+金属电极22。Referring to FIG. 8 , a back-contact solar cell of this embodiment includes an N-type crystalline silicon substrate 10, and the front surface of the N-type crystalline silicon substrate 10 is sequentially composed of a tunnel oxide layer 15 and an intrinsic polysilicon layer from the inside to the outside. 12. The n+ doped polysilicon region 13 on the front surface, the passivation anti-reflection film 14 and the n+ metal electrode 20; the back surface of the N-type crystalline silicon substrate 10 is the back surface p+ doped region 16 and the passivation film 18 from inside to outside. and p+ metal electrode 22, the doped region comprises a front surface n+ doped polysilicon region 13 and a back surface p+ doped region 16, the front surface n+ doped polysilicon region 13 is provided with an n+ metal electrode 20, and the back surface p+ doped region 16 A p+ metal electrode 22 is provided on it.
优选地,p+金属电极22是银铝背面电极,n+金属电极2020是银合金正面电极。钝化膜18是SiO2、SiNx或Al2O3介质膜中一种或多种,前表面的钝化减反膜14是SiNx膜,其厚度为60-80nm,钝化膜18是SiO2、SiNx或Al2O3介质膜中一种或多种,其Al2O3介质膜为2-10nm,SiNx介质膜厚度为60-80nm。p+金属电极22包括背面主栅和背面副栅(图中未示出),背面主栅和背面副栅构成H型栅线,其中背面主栅宽0.5-3mm,等间距设置3-6根,背面副栅宽20-60um。n+金属电极20包括正面主栅和正面副栅(图中未示出),正面主栅和正面副栅构成H型栅线,其中正面主栅宽0.5-3mm,等间距设置3-6根,正面副栅宽20-60um。Preferably, the p+ metal electrode 22 is a silver aluminum back electrode, and the n+ metal electrode 2020 is a silver alloy front electrode. The passivation film 18 is one or more of SiO 2 , SiN x or Al 2 O 3 dielectric films, the passivation anti-reflection film 14 on the front surface is a SiNx film, and its thickness is 60-80nm, and the passivation film 18 is SiO 2. One or more of SiNx or Al 2 O 3 dielectric films, the thickness of the Al 2 O 3 dielectric film is 2-10nm, and the thickness of the SiNx dielectric film is 60-80nm. The p+ metal electrode 22 includes a rear main grid and a rear auxiliary grid (not shown in the figure), and the rear main grid and the rear auxiliary grid form an H-shaped grid line, wherein the rear main grid is 0.5-3 mm wide, and 3-6 are arranged at equal intervals. The sub-gate width on the back is 20-60um. The n+ metal electrode 20 includes a front main grid and a front sub-grid (not shown in the figure), and the front main grid and the front sub-grid form an H-shaped grid line, wherein the front main grid is 0.5-3 mm wide, and 3-6 are arranged at equal intervals. The width of the front sub-gate is 20-60um.
上述结构的钝化接触太阳能电池在完成前后表面的钝化膜覆盖后,经测试,其隐开路电压(Implied Voc)可达700mV以上,暗饱和电流密度J0<20fA cm-2,印刷电极制成的背接触电池后,其短波段的内量子效率达95%以上。After the passivation contact solar cell with the above structure is covered with the passivation film on the front and rear surfaces, its implied open circuit voltage (Implied Voc) can reach more than 700mV after testing, and the dark saturation current density J 0 <20fA cm -2 . After the back contact battery is completed, the internal quantum efficiency in the short-wave band can reach more than 95%.
最后应当说明的是,以上实施例仅用以说明本发明的技术方案,而非对本发明保护范围的限制,尽管参照较佳实施例对本发明作了详细地说明,本领域的普通技术人员应当理解,可以对本发明的技术方案进行修改或者等同替换,而不脱离本发明技术方案的实质和范围。Finally, it should be noted that the above embodiments are only used to illustrate the technical solutions of the present invention, rather than limiting the protection scope of the present invention, although the present invention has been described in detail with reference to the preferred embodiments, those of ordinary skill in the art should understand , the technical solution of the present invention may be modified or equivalently replaced without departing from the spirit and scope of the technical solution of the present invention.
Claims (10)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201710564575.XA CN107195699B (en) | 2017-07-12 | 2017-07-12 | A kind of passivation contact solar cell and preparation method thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201710564575.XA CN107195699B (en) | 2017-07-12 | 2017-07-12 | A kind of passivation contact solar cell and preparation method thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN107195699A true CN107195699A (en) | 2017-09-22 |
| CN107195699B CN107195699B (en) | 2023-04-14 |
Family
ID=59883494
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201710564575.XA Active CN107195699B (en) | 2017-07-12 | 2017-07-12 | A kind of passivation contact solar cell and preparation method thereof |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN107195699B (en) |
Cited By (42)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108447918A (en) * | 2018-03-29 | 2018-08-24 | 晶澳(扬州)太阳能科技有限公司 | Doping structure and preparation method of passivation contact polysilicon thin film |
| CN108511534A (en) * | 2018-05-18 | 2018-09-07 | 通威太阳能(安徽)有限公司 | A kind of back side film layer structure and preparation method thereof promoting PERC battery efficiencies and yield |
| CN108695410A (en) * | 2018-06-11 | 2018-10-23 | 苏州宝澜环保科技有限公司 | A kind of N-shaped polysilicon solar cell and its manufacturing method |
| CN108922936A (en) * | 2018-07-31 | 2018-11-30 | 晶澳(扬州)太阳能科技有限公司 | A kind of MWT solar battery and preparation method thereof |
| CN108987505A (en) * | 2018-07-31 | 2018-12-11 | 晶澳(扬州)太阳能科技有限公司 | A kind of solar battery and preparation method thereof |
| CN109065639A (en) * | 2018-06-22 | 2018-12-21 | 晶澳(扬州)太阳能科技有限公司 | N-type crystalline silicon solar battery and preparation method, photovoltaic module |
| CN109524480A (en) * | 2018-11-26 | 2019-03-26 | 东方日升(常州)新能源有限公司 | A kind of p-type crystal silicon solar battery and preparation method thereof of local contact passivation |
| CN109671790A (en) * | 2018-12-25 | 2019-04-23 | 浙江晶科能源有限公司 | A kind of N-type double-sided solar battery and preparation method thereof |
| CN109713082A (en) * | 2018-12-29 | 2019-05-03 | 浙江晶科能源有限公司 | A kind of passivation method of polysilicon film in solar cell |
| CN109713065A (en) * | 2018-12-28 | 2019-05-03 | 泰州中来光电科技有限公司 | A kind of passivation solar battery of type metal electrode and preparation method thereof |
| CN109755343A (en) * | 2017-11-03 | 2019-05-14 | 上海神舟新能源发展有限公司 | The tunnel oxide of emitter junction selective exposure is passivated PERC battery preparation method |
| CN109841693A (en) * | 2019-02-25 | 2019-06-04 | 泰州隆基乐叶光伏科技有限公司 | A kind of passivation contact structures and solar battery |
| CN109994570A (en) * | 2018-11-27 | 2019-07-09 | 东方日升(常州)新能源有限公司 | A kind of preparation method of high-efficiency P-type passivation contact crystalline silicon solar cell |
| CN110098279A (en) * | 2018-01-30 | 2019-08-06 | 上海凯世通半导体股份有限公司 | The production method of solar battery |
| CN110137270A (en) * | 2019-04-17 | 2019-08-16 | 天津爱旭太阳能科技有限公司 | A kind of preparation method of selectivity front passivation PERC solar battery |
| CN110137274A (en) * | 2019-05-24 | 2019-08-16 | 通威太阳能(安徽)有限公司 | A kind of p-type high-efficiency battery and preparation method thereof of passivation on double surfaces contact |
| CN110289319A (en) * | 2019-05-14 | 2019-09-27 | 江苏顺风光电科技有限公司 | Preparation method of selective emitter monocrystalline PERC cell combined with tunnel oxide layer |
| CN110491953A (en) * | 2019-09-11 | 2019-11-22 | 南京爱通智能科技有限公司 | A kind of efficient crystal silicon photovoltaic battery structure and preparation method thereof |
| CN110610998A (en) * | 2019-09-24 | 2019-12-24 | 苏州腾晖光伏技术有限公司 | A kind of crystalline silicon solar cell with front local passivation contact and preparation method thereof |
| CN110838528A (en) * | 2019-10-29 | 2020-02-25 | 协鑫集成科技股份有限公司 | A post-doped N-type contact passivation battery |
| CN110931603A (en) * | 2019-12-11 | 2020-03-27 | 晶澳(扬州)太阳能科技有限公司 | Solar cell and preparation method thereof |
| CN110993744A (en) * | 2019-12-26 | 2020-04-10 | 浙江晶科能源有限公司 | Preparation method of P-type passivated contact battery |
| CN110983289A (en) * | 2019-12-04 | 2020-04-10 | 江苏杰太光电技术有限公司 | A method for preparing passivation contact structure based on LPCVD secondary ion implantation |
| CN111009593A (en) * | 2019-11-08 | 2020-04-14 | 江苏杰太光电技术有限公司 | A method for preparing partial polysilicon thin film passivation contact based on PVD technology |
| CN111063761A (en) * | 2018-10-17 | 2020-04-24 | 晶澳太阳能有限公司 | Preparation process of solar cell |
| CN111063759A (en) * | 2018-10-17 | 2020-04-24 | 晶澳太阳能有限公司 | Preparation process of solar cell |
| CN111063760A (en) * | 2018-10-17 | 2020-04-24 | 晶澳太阳能有限公司 | A kind of preparation process of solar cell |
| CN111180551A (en) * | 2020-01-02 | 2020-05-19 | 浙江晶科能源有限公司 | Selective emitter solar cell and preparation method thereof |
| CN111416017A (en) * | 2020-03-26 | 2020-07-14 | 泰州中来光电科技有限公司 | A kind of preparation method of passivation contact solar cell |
| CN111628050A (en) * | 2020-06-11 | 2020-09-04 | 常州时创能源股份有限公司 | Method for realizing electronic local passivation contact, crystalline silicon solar cell and preparation method thereof |
| CN111725359A (en) * | 2020-06-17 | 2020-09-29 | 泰州中来光电科技有限公司 | A kind of preparation method of passivation contact solar cell |
| CN112701174A (en) * | 2020-12-29 | 2021-04-23 | 泰州中来光电科技有限公司 | Back emitter passivation contact battery and preparation method, assembly and system thereof |
| CN112885924A (en) * | 2021-02-05 | 2021-06-01 | 泰州隆基乐叶光伏科技有限公司 | Solar cell and manufacturing method thereof |
| WO2021203813A1 (en) * | 2020-04-08 | 2021-10-14 | 浙江正泰太阳能科技有限公司 | P-type passivating contact solar cell and preparation method therefor |
| CN113611755A (en) * | 2021-08-06 | 2021-11-05 | 无锡琨圣智能装备股份有限公司 | Local passivation contact IBC battery structure and preparation method thereof |
| CN113875025A (en) * | 2019-03-29 | 2021-12-31 | 新加坡国立大学 | Solar cell and solar cell manufacturing method |
| CN114068740A (en) * | 2021-11-23 | 2022-02-18 | 浙江爱旭太阳能科技有限公司 | Solar cell and battery pack |
| WO2023072165A1 (en) * | 2021-10-27 | 2023-05-04 | 天合光能股份有限公司 | Passivated contact solar cell |
| EP4064367A4 (en) * | 2019-11-20 | 2023-12-06 | Zhejiang Jinko Solar Co., Ltd. | PARTIAL TUNNELING OF AN OXIDE LAYER PASSIVATION CONTACT STRUCTURE OF A PHOTOVOLTAIC CELL AND PHOTOVOLTAIC MODULE |
| US11901467B2 (en) | 2020-10-30 | 2024-02-13 | Zhejiang Jinko Solar Co., Ltd. | Solar cell |
| US20250151453A1 (en) * | 2024-03-29 | 2025-05-08 | Trina Solar Co., Ltd. | Solar cell |
| WO2025145811A1 (en) * | 2024-01-05 | 2025-07-10 | 通威太阳能(眉山)有限公司 | Solar cell, manufacturing method therefor and photovoltaic module |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20070169808A1 (en) * | 2006-01-26 | 2007-07-26 | Kherani Nazir P | Solar cell |
| JP3201880U (en) * | 2015-09-08 | 2016-01-07 | 元晶太陽能科技股▲ふん▼有限公司Tsec Corporation | Solar cell structure with locally deactivated heterojunction |
| CN105895738A (en) * | 2016-04-26 | 2016-08-24 | 泰州中来光电科技有限公司 | A passivated contact N-type solar cell and its preparation method, component and system |
| CN206864484U (en) * | 2017-07-12 | 2018-01-09 | 泰州中来光电科技有限公司 | One kind passivation contact solar cell |
-
2017
- 2017-07-12 CN CN201710564575.XA patent/CN107195699B/en active Active
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20070169808A1 (en) * | 2006-01-26 | 2007-07-26 | Kherani Nazir P | Solar cell |
| JP3201880U (en) * | 2015-09-08 | 2016-01-07 | 元晶太陽能科技股▲ふん▼有限公司Tsec Corporation | Solar cell structure with locally deactivated heterojunction |
| CN105895738A (en) * | 2016-04-26 | 2016-08-24 | 泰州中来光电科技有限公司 | A passivated contact N-type solar cell and its preparation method, component and system |
| CN206864484U (en) * | 2017-07-12 | 2018-01-09 | 泰州中来光电科技有限公司 | One kind passivation contact solar cell |
Cited By (52)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN109755343A (en) * | 2017-11-03 | 2019-05-14 | 上海神舟新能源发展有限公司 | The tunnel oxide of emitter junction selective exposure is passivated PERC battery preparation method |
| CN110098279A (en) * | 2018-01-30 | 2019-08-06 | 上海凯世通半导体股份有限公司 | The production method of solar battery |
| CN108447918A (en) * | 2018-03-29 | 2018-08-24 | 晶澳(扬州)太阳能科技有限公司 | Doping structure and preparation method of passivation contact polysilicon thin film |
| CN108511534A (en) * | 2018-05-18 | 2018-09-07 | 通威太阳能(安徽)有限公司 | A kind of back side film layer structure and preparation method thereof promoting PERC battery efficiencies and yield |
| CN108695410A (en) * | 2018-06-11 | 2018-10-23 | 苏州宝澜环保科技有限公司 | A kind of N-shaped polysilicon solar cell and its manufacturing method |
| CN108695410B (en) * | 2018-06-11 | 2020-08-04 | 广东德九新能源有限公司 | N-type polycrystalline silicon solar cell and manufacturing method thereof |
| CN109065639A (en) * | 2018-06-22 | 2018-12-21 | 晶澳(扬州)太阳能科技有限公司 | N-type crystalline silicon solar battery and preparation method, photovoltaic module |
| CN108922936A (en) * | 2018-07-31 | 2018-11-30 | 晶澳(扬州)太阳能科技有限公司 | A kind of MWT solar battery and preparation method thereof |
| CN108987505A (en) * | 2018-07-31 | 2018-12-11 | 晶澳(扬州)太阳能科技有限公司 | A kind of solar battery and preparation method thereof |
| CN111063760A (en) * | 2018-10-17 | 2020-04-24 | 晶澳太阳能有限公司 | A kind of preparation process of solar cell |
| CN111063761A (en) * | 2018-10-17 | 2020-04-24 | 晶澳太阳能有限公司 | Preparation process of solar cell |
| CN111063759A (en) * | 2018-10-17 | 2020-04-24 | 晶澳太阳能有限公司 | Preparation process of solar cell |
| CN109524480B (en) * | 2018-11-26 | 2021-03-23 | 东方日升(常州)新能源有限公司 | Local contact passivated P-type crystalline silicon solar cell and preparation method thereof |
| CN109524480A (en) * | 2018-11-26 | 2019-03-26 | 东方日升(常州)新能源有限公司 | A kind of p-type crystal silicon solar battery and preparation method thereof of local contact passivation |
| CN109994570A (en) * | 2018-11-27 | 2019-07-09 | 东方日升(常州)新能源有限公司 | A kind of preparation method of high-efficiency P-type passivation contact crystalline silicon solar cell |
| CN109994570B (en) * | 2018-11-27 | 2021-04-30 | 东方日升(常州)新能源有限公司 | Preparation method of efficient P-type passivated contact crystalline silicon solar cell |
| CN109671790A (en) * | 2018-12-25 | 2019-04-23 | 浙江晶科能源有限公司 | A kind of N-type double-sided solar battery and preparation method thereof |
| CN109713065B (en) * | 2018-12-28 | 2023-10-31 | 泰州中来光电科技有限公司 | Passivation solar cell with printed metal electrode and preparation method thereof |
| CN109713065A (en) * | 2018-12-28 | 2019-05-03 | 泰州中来光电科技有限公司 | A kind of passivation solar battery of type metal electrode and preparation method thereof |
| CN109713082A (en) * | 2018-12-29 | 2019-05-03 | 浙江晶科能源有限公司 | A kind of passivation method of polysilicon film in solar cell |
| CN109841693A (en) * | 2019-02-25 | 2019-06-04 | 泰州隆基乐叶光伏科技有限公司 | A kind of passivation contact structures and solar battery |
| CN113875025A (en) * | 2019-03-29 | 2021-12-31 | 新加坡国立大学 | Solar cell and solar cell manufacturing method |
| CN110137270A (en) * | 2019-04-17 | 2019-08-16 | 天津爱旭太阳能科技有限公司 | A kind of preparation method of selectivity front passivation PERC solar battery |
| CN110289319A (en) * | 2019-05-14 | 2019-09-27 | 江苏顺风光电科技有限公司 | Preparation method of selective emitter monocrystalline PERC cell combined with tunnel oxide layer |
| CN110137274A (en) * | 2019-05-24 | 2019-08-16 | 通威太阳能(安徽)有限公司 | A kind of p-type high-efficiency battery and preparation method thereof of passivation on double surfaces contact |
| CN110491953A (en) * | 2019-09-11 | 2019-11-22 | 南京爱通智能科技有限公司 | A kind of efficient crystal silicon photovoltaic battery structure and preparation method thereof |
| CN110610998A (en) * | 2019-09-24 | 2019-12-24 | 苏州腾晖光伏技术有限公司 | A kind of crystalline silicon solar cell with front local passivation contact and preparation method thereof |
| CN110838528B (en) * | 2019-10-29 | 2021-07-06 | 协鑫集成科技股份有限公司 | A post-doped N-type contact passivation battery |
| CN110838528A (en) * | 2019-10-29 | 2020-02-25 | 协鑫集成科技股份有限公司 | A post-doped N-type contact passivation battery |
| CN111009593A (en) * | 2019-11-08 | 2020-04-14 | 江苏杰太光电技术有限公司 | A method for preparing partial polysilicon thin film passivation contact based on PVD technology |
| CN111009593B (en) * | 2019-11-08 | 2021-09-07 | 江苏杰太光电技术有限公司 | A method for preparing partial polysilicon thin film passivation contact based on PVD technology |
| EP4064367A4 (en) * | 2019-11-20 | 2023-12-06 | Zhejiang Jinko Solar Co., Ltd. | PARTIAL TUNNELING OF AN OXIDE LAYER PASSIVATION CONTACT STRUCTURE OF A PHOTOVOLTAIC CELL AND PHOTOVOLTAIC MODULE |
| CN110983289A (en) * | 2019-12-04 | 2020-04-10 | 江苏杰太光电技术有限公司 | A method for preparing passivation contact structure based on LPCVD secondary ion implantation |
| CN110983289B (en) * | 2019-12-04 | 2022-06-28 | 江苏杰太光电技术有限公司 | A method for preparing passivation contact structure based on LPCVD secondary ion implantation |
| CN110931603A (en) * | 2019-12-11 | 2020-03-27 | 晶澳(扬州)太阳能科技有限公司 | Solar cell and preparation method thereof |
| CN110993744A (en) * | 2019-12-26 | 2020-04-10 | 浙江晶科能源有限公司 | Preparation method of P-type passivated contact battery |
| CN111180551A (en) * | 2020-01-02 | 2020-05-19 | 浙江晶科能源有限公司 | Selective emitter solar cell and preparation method thereof |
| CN111416017A (en) * | 2020-03-26 | 2020-07-14 | 泰州中来光电科技有限公司 | A kind of preparation method of passivation contact solar cell |
| WO2021203813A1 (en) * | 2020-04-08 | 2021-10-14 | 浙江正泰太阳能科技有限公司 | P-type passivating contact solar cell and preparation method therefor |
| CN111628050B (en) * | 2020-06-11 | 2021-08-03 | 常州时创能源股份有限公司 | Method for realizing electronic local passivation contact, crystalline silicon solar cell and preparation method thereof |
| CN111628050A (en) * | 2020-06-11 | 2020-09-04 | 常州时创能源股份有限公司 | Method for realizing electronic local passivation contact, crystalline silicon solar cell and preparation method thereof |
| CN111725359A (en) * | 2020-06-17 | 2020-09-29 | 泰州中来光电科技有限公司 | A kind of preparation method of passivation contact solar cell |
| US11901467B2 (en) | 2020-10-30 | 2024-02-13 | Zhejiang Jinko Solar Co., Ltd. | Solar cell |
| CN112701174A (en) * | 2020-12-29 | 2021-04-23 | 泰州中来光电科技有限公司 | Back emitter passivation contact battery and preparation method, assembly and system thereof |
| CN112885924A (en) * | 2021-02-05 | 2021-06-01 | 泰州隆基乐叶光伏科技有限公司 | Solar cell and manufacturing method thereof |
| CN113611755A (en) * | 2021-08-06 | 2021-11-05 | 无锡琨圣智能装备股份有限公司 | Local passivation contact IBC battery structure and preparation method thereof |
| WO2023072165A1 (en) * | 2021-10-27 | 2023-05-04 | 天合光能股份有限公司 | Passivated contact solar cell |
| WO2023072164A1 (en) * | 2021-10-27 | 2023-05-04 | 天合光能股份有限公司 | Solar cell |
| CN114068740A (en) * | 2021-11-23 | 2022-02-18 | 浙江爱旭太阳能科技有限公司 | Solar cell and battery pack |
| WO2025145811A1 (en) * | 2024-01-05 | 2025-07-10 | 通威太阳能(眉山)有限公司 | Solar cell, manufacturing method therefor and photovoltaic module |
| US20250151453A1 (en) * | 2024-03-29 | 2025-05-08 | Trina Solar Co., Ltd. | Solar cell |
| US20250311476A1 (en) * | 2024-03-29 | 2025-10-02 | Trina Solar Co., Ltd. | Solar cell |
Also Published As
| Publication number | Publication date |
|---|---|
| CN107195699B (en) | 2023-04-14 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN107195699B (en) | A kind of passivation contact solar cell and preparation method thereof | |
| CN111416017B (en) | Preparation method of passivated contact solar cell | |
| CN115207137A (en) | A kind of combined passivation back contact battery and preparation method thereof | |
| CN108110065A (en) | A kind of back contact solar cell and preparation method thereof | |
| CN115498057B (en) | Combined passivation back contact solar cell and preparation method thereof based on laser diffusion | |
| CN106374009A (en) | A passivated contact IBC battery and its preparation method, assembly and system | |
| CN111628049A (en) | Method for realizing local hole passivation contact, crystalline silicon solar cell and preparation method thereof | |
| CN110265494A (en) | A kind of partial back field TOPCon solar cell and its preparation method | |
| CN102623517B (en) | Back contact type crystalline silicon solar cell and production method thereof | |
| CN108538962A (en) | A kind of preparation method of the IBC batteries of passivation contact | |
| CN107968127A (en) | One kind passivation contact N-type solar cell and preparation method, component and system | |
| CN110739367A (en) | A kind of preparation method of N-type TOPCon solar cell | |
| CN105489671A (en) | N-type double-sided solar cell and preparation method thereof | |
| CN114256385B (en) | TBC back contact solar cell and preparation method thereof | |
| CN105895738A (en) | A passivated contact N-type solar cell and its preparation method, component and system | |
| US20130061926A1 (en) | Solar cell element and method for producing the same, and solar cell module | |
| CN107845692A (en) | A kind of preparation method of modified back side tunnel oxidation passivation contact high-efficiency battery | |
| CN205564789U (en) | Passivation contact N type solar cell and subassembly and system thereof | |
| CN206864484U (en) | One kind passivation contact solar cell | |
| CN102800738A (en) | Interdigital back contact type solar cell and preparation method thereof | |
| CN108123046A (en) | A kind of perovskite/n-type crystalline silicon stacked solar cell, cascade solar cell and its manufacturing method | |
| CN108039374A (en) | The preparation method of N-shaped double-side solar cell | |
| CN111244230A (en) | Preparation method of back junction solar cell with passivated metal contact | |
| CN103904141B (en) | Low surface concentration is lightly doped the preparation method of district's selective emitting electrode structure | |
| CN105576083A (en) | N-type double-side solar cell based on APCVD technology and preparation method thereof |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PB01 | Publication | ||
| PB01 | Publication | ||
| SE01 | Entry into force of request for substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| GR01 | Patent grant | ||
| GR01 | Patent grant |