CN105826405A - Mono-crystalline silicon double-sided solar cell and preparation method thereof - Google Patents
Mono-crystalline silicon double-sided solar cell and preparation method thereof Download PDFInfo
- Publication number
- CN105826405A CN105826405A CN201610331351.XA CN201610331351A CN105826405A CN 105826405 A CN105826405 A CN 105826405A CN 201610331351 A CN201610331351 A CN 201610331351A CN 105826405 A CN105826405 A CN 105826405A
- Authority
- CN
- China
- Prior art keywords
- pyramid
- solar cell
- double
- preparation
- silicon
- 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.)
- Pending
Links
- 238000002360 preparation method Methods 0.000 title claims abstract description 21
- 229910021421 monocrystalline silicon Inorganic materials 0.000 title abstract description 36
- 239000000758 substrate Substances 0.000 claims abstract description 34
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims abstract description 26
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 26
- 239000010703 silicon Substances 0.000 claims abstract description 26
- 229910052581 Si3N4 Inorganic materials 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 14
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 claims description 14
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 12
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 12
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 12
- 229910052814 silicon oxide Inorganic materials 0.000 claims description 10
- 238000000926 separation method Methods 0.000 claims description 8
- WGTYBPLFGIVFAS-UHFFFAOYSA-M tetramethylammonium hydroxide Chemical compound [OH-].C[N+](C)(C)C WGTYBPLFGIVFAS-UHFFFAOYSA-M 0.000 claims description 8
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 7
- 230000004888 barrier function Effects 0.000 claims description 7
- 229910052709 silver Inorganic materials 0.000 claims description 7
- 239000004332 silver Substances 0.000 claims description 7
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 5
- 238000000623 plasma-assisted chemical vapour deposition Methods 0.000 claims description 5
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 4
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 4
- 229910021419 crystalline silicon Inorganic materials 0.000 claims description 4
- 238000000151 deposition Methods 0.000 claims description 4
- 239000011521 glass Substances 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 claims description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 3
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 3
- 229910052782 aluminium Inorganic materials 0.000 claims description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 3
- 229910052802 copper Inorganic materials 0.000 claims description 3
- 239000010949 copper Substances 0.000 claims description 3
- 230000008021 deposition Effects 0.000 claims description 3
- 229910017604 nitric acid Inorganic materials 0.000 claims description 3
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 2
- 229910045601 alloy Inorganic materials 0.000 claims description 2
- 239000000956 alloy Substances 0.000 claims description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 2
- 239000007864 aqueous solution Substances 0.000 claims description 2
- 229910052793 cadmium Inorganic materials 0.000 claims description 2
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 claims description 2
- 239000013043 chemical agent Substances 0.000 claims description 2
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052737 gold Inorganic materials 0.000 claims description 2
- 239000010931 gold Substances 0.000 claims description 2
- 239000011133 lead Substances 0.000 claims description 2
- 239000000463 material Substances 0.000 claims description 2
- 229910052751 metal Inorganic materials 0.000 claims description 2
- 239000002184 metal Substances 0.000 claims description 2
- 150000002739 metals Chemical class 0.000 claims description 2
- 229910052759 nickel Inorganic materials 0.000 claims description 2
- 229910010271 silicon carbide Inorganic materials 0.000 claims description 2
- 239000010936 titanium Substances 0.000 claims description 2
- 229910052719 titanium Inorganic materials 0.000 claims description 2
- 229910052725 zinc Inorganic materials 0.000 claims description 2
- 239000011701 zinc Substances 0.000 claims description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical compound [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims 3
- 238000007704 wet chemistry method Methods 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
- 241000628997 Flos Species 0.000 claims 1
- 239000010408 film Substances 0.000 claims 1
- MRNHPUHPBOKKQT-UHFFFAOYSA-N indium;tin;hydrate Chemical compound O.[In].[Sn] MRNHPUHPBOKKQT-UHFFFAOYSA-N 0.000 claims 1
- 239000013081 microcrystal Substances 0.000 claims 1
- 239000005297 pyrex Substances 0.000 claims 1
- 239000000377 silicon dioxide Substances 0.000 claims 1
- 239000010409 thin film Substances 0.000 claims 1
- 210000002268 wool Anatomy 0.000 claims 1
- 238000002161 passivation Methods 0.000 abstract description 25
- 238000010521 absorption reaction Methods 0.000 abstract description 6
- 238000006243 chemical reaction Methods 0.000 abstract description 5
- 230000003287 optical effect Effects 0.000 abstract description 5
- 230000006798 recombination Effects 0.000 abstract description 4
- 238000005215 recombination Methods 0.000 abstract description 4
- 239000010410 layer Substances 0.000 description 50
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 14
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 8
- 238000009792 diffusion process Methods 0.000 description 8
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 8
- 239000011574 phosphorus Substances 0.000 description 8
- 229910052698 phosphorus Inorganic materials 0.000 description 8
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 7
- 229910052796 boron Inorganic materials 0.000 description 7
- 239000012535 impurity Substances 0.000 description 7
- 229910021417 amorphous silicon Inorganic materials 0.000 description 5
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- ILAHWRKJUDSMFH-UHFFFAOYSA-N boron tribromide Chemical compound BrB(Br)Br ILAHWRKJUDSMFH-UHFFFAOYSA-N 0.000 description 4
- 239000005388 borosilicate glass Substances 0.000 description 4
- 238000005468 ion implantation Methods 0.000 description 4
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 4
- 239000005360 phosphosilicate glass Substances 0.000 description 4
- 239000002356 single layer Substances 0.000 description 4
- 239000012670 alkaline solution Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 238000010248 power generation Methods 0.000 description 2
- 238000007650 screen-printing Methods 0.000 description 2
- 238000005245 sintering Methods 0.000 description 2
- 230000005540 biological transmission Effects 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 229910021424 microcrystalline silicon Inorganic materials 0.000 description 1
- 238000001000 micrograph Methods 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 238000012876 topography 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
- H10F77/70—Surface textures, e.g. pyramid structures
- H10F77/703—Surface textures, e.g. pyramid structures of the semiconductor bodies, e.g. textured active layers
-
- 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
-
- 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
- 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
- H10F77/00—Constructional details of devices covered by this subclass
- H10F77/70—Surface textures, e.g. pyramid structures
-
- 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
本发明公开了一种单晶硅双面太阳电池,属于太阳电池技术领域,在单晶硅衬底的正面依次形成正面金字塔形绒面、正面掺杂发射结、正面钝化减反介质层以及正面电极,在单晶硅衬底的背面依次形成背面金字塔形绒面、背表面场、背面钝化减反介质层以及背面电极,其特征在于:所述背面金字塔形绒面为分离型金字塔形绒面,金字塔结构仅部分地覆盖单晶硅衬底,金字塔结构分散地分布在硅衬底上,被金字塔结构覆盖的区域占背面硅衬底的20%‑90%。同时,本发明还公开了一种单晶硅双面太阳电池的制备方法。本发明可优化双面太阳电池的少数载流子表面复合和光学吸收特性,提高量子转换效率。
The invention discloses a monocrystalline silicon double-sided solar cell, which belongs to the technical field of solar cells. A front pyramid-shaped suede surface, a front doped emitter junction, a front passivation antireflection medium layer and a front surface of a single crystal silicon substrate are sequentially formed. The front electrode, on the back of the single crystal silicon substrate, forms the back pyramid-shaped suede, the back surface field, the back passivation anti-reflection medium layer and the back electrode in sequence, and it is characterized in that: the back pyramid-shaped suede is a separated pyramid shape On the suede surface, the pyramid structure only partially covers the single crystal silicon substrate, and the pyramid structure is scattered on the silicon substrate, and the area covered by the pyramid structure accounts for 20%-90% of the silicon substrate on the back side. At the same time, the invention also discloses a preparation method of a single-crystal silicon double-sided solar cell. The invention can optimize the minority carrier surface recombination and optical absorption characteristics of the double-sided solar cell, and improve the quantum conversion efficiency.
Description
技术领域 technical field
本发明涉及一种太阳电池及其制备方法,尤其涉及一种单晶硅双面太阳电池及其制备方法,属于太阳电池技术领域。 The invention relates to a solar cell and a preparation method thereof, in particular to a single crystal silicon double-sided solar cell and a preparation method thereof, belonging to the technical field of solar cells.
背景技术 Background technique
追求提高电池转换效率,同时降低甚至维持制造成本及是业界不断追求的目标和提高自身竞争力之所在。相对于单面受光的传统晶体硅太阳电池,双面太阳电池利用正、背两个受光面,可以获得更高的光电流密度,很大程度地提高发电功率。根据安装地面和环境,基于双面太阳电池的光伏发电系统可以获得10至30%的功率增益。 The pursuit of improving battery conversion efficiency while reducing or even maintaining manufacturing costs is the goal that the industry is constantly pursuing and where it can improve its own competitiveness. Compared with traditional crystalline silicon solar cells that receive light on one side, double-sided solar cells use two light-receiving surfaces, the front and the back, to obtain higher photocurrent densities and greatly increase power generation. Depending on the installation ground and environment, a photovoltaic power generation system based on bifacial solar cells can achieve a power gain of 10 to 30%.
双面太阳电池结构包括:正、背面的绒面形貌结构、pn结发射极、钝化减反介质层、正、背面电极等。其中,背面的绒面可以有效地提高地面和环境反射光在双面电池背面的吸收,是双面太阳电池的重要结构。目前双面太阳电池的背面都采用与正面类似的绒面形貌结构,即制绒获得的金字塔分布紧密,相互交叠。虽然这种紧密分布的金字塔有利于最大限度地吸收直射光,但不一定是漫反射光的最佳光吸收结构,并且较高的表面积会带来少数载流子复合。因此,双面太阳电池的背面结构有待进一步优化。 The structure of double-sided solar cells includes: front and back textured surface structures, pn junction emitters, passivation anti-reflection dielectric layers, front and back electrodes, etc. Among them, the suede on the back can effectively improve the absorption of ground and ambient reflected light on the back of the double-sided solar cell, which is an important structure of the double-sided solar cell. At present, the back of the double-sided solar cell adopts a texture structure similar to that of the front, that is, the pyramids obtained by texture are closely distributed and overlap each other. Although such densely distributed pyramids are good for maximizing the absorption of direct light, they are not necessarily the optimal light-absorbing structure for diffuse reflection light, and the higher surface area will bring minority carrier recombination. Therefore, the back structure of double-sided solar cells needs to be further optimized.
发明内容 Contents of the invention
本发明针对现有技术中存在的上述技术问题,提供一种单晶硅双面太阳电池,优化太阳电池少数载流子表面负荷和光学吸收特性,提高量子转换效率。 The present invention aims at the above-mentioned technical problems existing in the prior art, and provides a monocrystalline silicon double-sided solar cell, which optimizes the minority carrier surface load and optical absorption characteristics of the solar cell, and improves the quantum conversion efficiency.
本发明的另一方面,提供一种单晶硅双面太阳电池的制备方法,提高太阳电池的转换效率和生产效率。 Another aspect of the present invention provides a method for preparing a monocrystalline silicon double-sided solar cell, which improves the conversion efficiency and production efficiency of the solar cell.
为此,本发明采用如下技术方案: For this reason, the present invention adopts following technical scheme:
一种单晶硅双面太阳电池,在单晶硅衬底(100)的正面依次形成正面金字塔形绒面(101)、正面掺杂发射结(102)、正面钝化减反介质层(103)以及正面电极(104),在单晶硅衬底的背面依次形成背面金字塔形绒面(105)、背表面场(106)、背面钝化减反介质层(107)以及背面电极(108),其特征在于:所述背面金字塔形绒面(105)为分离型金字塔形绒面,金字塔结构(105a)仅部分地覆盖单晶硅衬底,金字塔结构(105a)分散地分布在硅衬底上,被金字塔结构(105a)覆盖的区域占背面硅衬底的20%-90%。 A monocrystalline silicon double-sided solar cell, in which a front pyramid-shaped suede surface (101), a front doped emitter junction (102), and a front passivation anti-reflection dielectric layer (103) are sequentially formed on the front surface of a single crystal silicon substrate (100). ) and the front electrode (104), on the back of the single crystal silicon substrate sequentially form the back pyramid-shaped suede (105), the back surface field (106), the back passivation anti-reflection dielectric layer (107) and the back electrode (108) , characterized in that: the back pyramid-shaped suede (105) is a separated pyramid-shaped suede, the pyramid structure (105a) only partially covers the monocrystalline silicon substrate, and the pyramid structure (105a) is dispersedly distributed on the silicon substrate On the top, the area covered by the pyramid structure (105a) accounts for 20%-90% of the back silicon substrate.
进一步地,单个金字塔结构(105a)的底边长是1-7μm。 Further, the base length of a single pyramid structure (105a) is 1-7 μm.
进一步地,所述正面钝化减反介质层(103)和背面钝化减反介质层(107)分别为由氧化硅、氮化硅、氮氧化硅、氧化铝、碳化硅、非晶硅、微晶硅、氧化铟锡或者氧化钛为材料组成的单层膜或多层膜。 Further, the front passivation anti-reflection dielectric layer (103) and the back passivation anti-reflection dielectric layer (107) are respectively made of silicon oxide, silicon nitride, silicon oxynitride, aluminum oxide, silicon carbide, amorphous silicon, Microcrystalline silicon, indium tin oxide or titanium oxide is a single-layer film or multi-layer film composed of materials.
进一步地,所述正面电极(104)、背面电极(108)为银、铝、铜、镍、钛、锡、铅、镉、金、锌的一种或多种金属或其合金。 Further, the front electrode (104) and the back electrode (108) are one or more metals of silver, aluminum, copper, nickel, titanium, tin, lead, cadmium, gold, zinc or alloys thereof.
本发明的另一方面,提供一种单晶硅双面太阳电池的制备方法,用于制备所述单晶硅双面太阳电池,包括如下步骤: Another aspect of the present invention provides a method for preparing a single-crystal silicon double-sided solar cell, which is used to prepare the single-crystal silicon double-sided solar cell, comprising the following steps:
S1:在单晶硅衬底表面制绒; S1: Texturing on the surface of a single crystal silicon substrate;
S2:正面掺杂形成发射结; S2: The front side is doped to form an emitter junction;
S3:去除背面含杂质玻璃层; S3: removing the impurity-containing glass layer on the back;
S4:湿化学法制备背面分离金字塔形貌结构,并去除背面掺杂层; S4: Wet chemical method to prepare the back separation pyramid structure, and remove the doping layer on the back;
S5:背面掺杂形成背表面场; S5: Back doping forms a back surface field;
S6:制备正面、背面钝化减反介质层; S6: preparing front and back passivation anti-reflection medium layers;
S7:制备正面、背面电极。 S7: preparing front and back electrodes.
在步骤S4中,湿化学法制备背面分离金字塔形貌结构所采用的化学药剂有氢氧化钠、氢氧化钾、四甲基氢氧化铵、硝酸、磷酸、氢氟酸、乙醇、异丙醇或乙二醇中的一种或两种以上混合的水溶液;制备温度是60至80℃,时间是10-900秒。 In step S4, the chemical agents used to prepare the rear separation pyramid structure by wet chemical method include sodium hydroxide, potassium hydroxide, tetramethylammonium hydroxide, nitric acid, phosphoric acid, hydrofluoric acid, ethanol, isopropanol or One or two or more mixed aqueous solutions of ethylene glycol; the preparation temperature is 60 to 80°C, and the time is 10-900 seconds.
进一步地,在步骤S2和S3之间,还可以包括如下步骤:S2-1:正面沉积阻挡层。 Further, between steps S2 and S3, the following steps may also be included: S2-1: depositing a barrier layer on the front side.
进一步地,在步骤S5和S6之间,还包括如下步骤:S5-1:使用氢氟酸去除正面的氧化硅、磷硅玻璃和背面的硼硅玻璃。 Further, between steps S5 and S6, the following steps are also included: S5-1: using hydrofluoric acid to remove silicon oxide, phosphosilicate glass on the front and borosilicate glass on the back.
本发明的单晶硅双面太阳电池,通过在电池的背面设置分离型金字塔形绒面,减少太阳电池背面绒面的表面积,明显地降低光生少数载流子在背表面的复合;正面入射的长波长光在背表面的反射增加,透射减小,重新被太阳电池吸收;同时,背面覆有减反介质层,背面的光学反射没有明显增加,保证背面的光学吸收特性。因此,通过背面分离金字塔形貌结构,可以优化双面太阳电池的少数载流子表面复合和光学吸收特性,提高量子转换效率。 The monocrystalline silicon double-sided solar cell of the present invention reduces the surface area of the back surface of the solar cell by arranging a separate pyramid-shaped textured surface on the back side of the battery, and significantly reduces the recombination of photogenerated minority carriers on the back surface; The reflection of long-wavelength light on the back surface increases, the transmission decreases, and is absorbed by the solar cell again; at the same time, the back is covered with an anti-reflection medium layer, and the optical reflection on the back does not increase significantly, ensuring the optical absorption characteristics of the back. Therefore, the minority carrier surface recombination and optical absorption properties of double-sided solar cells can be optimized to improve the quantum conversion efficiency by separating the pyramidal topography on the back side.
本发明的单晶硅双面太阳电池的制备方法,仅仅增加一道湿化学方法制备背面分离金字塔形貌结构,工艺相对简单,适合于低成本、大批量、稳定的工业制造。 The preparation method of the monocrystalline silicon double-sided solar cell of the present invention only needs to add a wet chemical method to prepare the rear separation pyramid structure, the process is relatively simple, and it is suitable for low-cost, large-volume, and stable industrial manufacturing.
附图说明 Description of drawings
图1为本发明的单晶硅双面太阳电池的结构示意图; Fig. 1 is the structural representation of monocrystalline silicon double-sided solar cell of the present invention;
图2为本发明的分离型金字塔形绒面的显微镜照片; Fig. 2 is the micrograph of separation type pyramidal suede of the present invention;
其中,100为单晶硅衬底,101为正面金字塔形绒面,102为正面掺杂发射结,103为正面钝化减反介质层,104为正面电极,105为背面金字塔形绒面,105a为金字塔结构,106为背表面场,107为背面钝化减反介质层,108为背面电极,109为未被金字塔结构覆盖的区域;图中相应的产品结构仅为示意图,未按比例绘制。 Among them, 100 is a single crystal silicon substrate, 101 is a pyramid-shaped suede surface on the front side, 102 is a doped emitter junction on the front side, 103 is a passivation anti-reflection dielectric layer on the front side, 104 is a front electrode, 105 is a pyramid-shaped suede surface on the back side, 105a 106 is the back surface field, 107 is the passivation anti-reflection dielectric layer on the back, 108 is the back electrode, and 109 is the area not covered by the pyramid structure; the corresponding product structure in the figure is only a schematic diagram and is not drawn to scale.
具体实施方式 detailed description
为了使本技术领域的人员更好的理解本发明方案,下面将结合本发明实施例中的附图,对本发明实施例中的技术方案进行清楚、完整的描述。 In order to enable those skilled in the art to better understand the solutions of the present invention, the technical solutions in the embodiments of the present invention will be clearly and completely described below in conjunction with the drawings in the embodiments of the present invention.
实施例1: Example 1:
本实施例是本发明应用于P型单晶硅的情形。如图1所示,在P型单晶硅衬底100的正面依次形成正面金字塔形绒面101、正面磷掺杂发射结102、正面钝化减反介质层103以及正面电极104,在P型单晶硅衬底的背面依次形成背面分离型金字塔形绒面105、背面硼掺杂形成的硼掺杂背表面场106、背面钝化减反介质层107以及背面电极108,其中,如图2所示,背面分离型金字塔形绒面105中,金字塔结构105a仅部分地覆盖单晶硅衬底,金字塔结构105a分散地分布在单晶硅衬底的背面,留下一些未被金字塔结构覆盖的区域109。 This embodiment is the case where the present invention is applied to P-type single crystal silicon. As shown in FIG. 1 , a front pyramid-shaped textured surface 101, a front phosphorus-doped emitter junction 102, a front passivation anti-reflection dielectric layer 103, and a front electrode 104 are sequentially formed on the front surface of a P-type single crystal silicon substrate 100. The rear side of the single crystal silicon substrate is sequentially formed with a back separated pyramid-shaped textured surface 105, a boron-doped back surface field 106 formed by boron doping on the back side, a back passivation anti-reflection dielectric layer 107, and a back electrode 108, wherein, as shown in FIG. 2 As shown, in the back separation type pyramid-shaped suede 105, the pyramid structure 105a only partially covers the single crystal silicon substrate, and the pyramid structure 105a is scatteredly distributed on the back side of the single crystal silicon substrate, leaving some not covered by the pyramid structure. Area 109.
在本实施例中,被金字塔结构105a覆盖的区域占整个背面硅衬底的85%,单个金字塔结构105a的底边长是5μm;正面钝化减反介质层103为由氮化硅制成的单层膜,膜厚70至80nm;背面钝化减反介质层107为由氧化铝和氮化硅制成的双层膜,其中,氧化铝膜厚20至30nm和氮化硅膜厚50至70nm。正面电极104和背面电极108均为银栅电极。 In this embodiment, the area covered by the pyramid structure 105a accounts for 85% of the entire backside silicon substrate, and the base length of a single pyramid structure 105a is 5 μm; the front passivation anti-reflection dielectric layer 103 is made of silicon nitride Single-layer film with a film thickness of 70 to 80 nm; the back passivation anti-reflection dielectric layer 107 is a double-layer film made of aluminum oxide and silicon nitride, wherein the film thickness of aluminum oxide is 20 to 30 nm and the film thickness of silicon nitride is 50 to 50 nm. 70nm. Both the front electrode 104 and the back electrode 108 are silver grid electrodes.
实施例2: Example 2:
本实施例与实施例1的不同之处在于:背面分离型金字塔形绒面105中,被金字塔结构105a覆盖的区域占整个背面硅衬底的50%,单个金字塔结构105a的底边长是7μm。正面钝化减反介质层103为由氮氧化硅制成的单层膜,膜厚70至80nm;背面钝化减反介质层107为由氧化钛和氧化硅制成的双层膜,其中,氧化钛膜厚20至30nm和氧化硅膜厚50至70nm。正面电极104和背面电极108均为铜电极。 The difference between this embodiment and Embodiment 1 is: in the back separated pyramid-shaped suede 105, the area covered by the pyramid structure 105a accounts for 50% of the entire back silicon substrate, and the base length of a single pyramid structure 105a is 7 μm . The front passivation anti-reflection medium layer 103 is a single-layer film made of silicon oxynitride with a film thickness of 70 to 80 nm; the back passivation anti-reflection medium layer 107 is a double-layer film made of titanium oxide and silicon oxide, wherein, The titanium oxide film has a thickness of 20 to 30 nm and the silicon oxide film has a thickness of 50 to 70 nm. Both the front electrode 104 and the back electrode 108 are copper electrodes.
实施例3: Example 3:
本实施例是本发明应用于N型单晶硅的情形。如图1所示,在N型单晶硅衬底100的正面依次形成正面金字塔形绒面101、正面掺硼掺杂发射结102、正面钝化减反介质层103以及正面电极104,在N型单晶硅衬底的背面依次形成背面分离型金字塔形绒面105、背面磷掺杂形成的磷掺杂背表面场106、背面钝化减反介质层107以及背面电极108,其中,背面分离型金字塔形绒面105中,金字塔结构105a仅部分地覆盖单晶硅衬底,金字塔结构105a分散地分布在单晶硅衬底的背面,被金字塔结构105a覆盖的区域占整个背面硅衬底的30%,单个金字塔结构105a的底边长是2μm。 This embodiment is a case where the present invention is applied to N-type single crystal silicon. As shown in FIG. 1, a front pyramid-shaped textured surface 101, a front boron-doped emitter junction 102, a front passivation anti-reflection dielectric layer 103, and a front electrode 104 are sequentially formed on the front surface of an N-type single crystal silicon substrate 100. The rear side of the monocrystalline silicon substrate is sequentially formed with a rear separated pyramid-shaped textured surface 105, a phosphorus-doped rear surface field 106 formed by doping the rear phosphorus, a rear passivation anti-reflection dielectric layer 107, and a rear electrode 108, wherein the rear separation In the type pyramid-shaped suede surface 105, the pyramid structure 105a only partially covers the single crystal silicon substrate, and the pyramid structures 105a are scatteredly distributed on the back side of the single crystal silicon substrate, and the area covered by the pyramid structure 105a accounts for the whole back side of the silicon substrate. 30%, the base length of a single pyramid structure 105a is 2 μm.
在本实施例中,正面钝化减反介质层103为由由氧化铝和氮化硅制成的双层膜,其中,氧化铝膜厚20至30nm和氮化硅膜厚50至70nm;背面钝化减反介质层107为氮化硅制成的单层膜,膜厚70至80nm;正面电极104和背面电极108均为银栅电极。 In this embodiment, the front passivation anti-reflection dielectric layer 103 is a double-layer film made of aluminum oxide and silicon nitride, wherein the thickness of the aluminum oxide film is 20 to 30 nm and the thickness of the silicon nitride film is 50 to 70 nm; The passivation anti-reflection medium layer 107 is a single-layer film made of silicon nitride with a film thickness of 70 to 80 nm; both the front electrode 104 and the back electrode 108 are silver grid electrodes.
实施例4: Example 4:
本实施例与实施例3的不同之处在于:背面分离型金字塔形绒面105中,被金字塔结构105a覆盖的区域占整个背面硅衬底的65%,单个金字塔结构105a的底边长是4μm。正面钝化减反介质层103为由由氧化铟锡和非晶硅制成的双层膜,其中,氧化铟锡膜厚60至80nm和非晶硅膜厚5至20nm;背面钝化减反介质层107为氧化铟锡和非晶硅制成的双层膜,其中,氧化铟锡膜厚60至80nm和非晶硅膜厚5至20nm;正面电极104和背面电极108均为银电极。 The difference between this embodiment and Embodiment 3 is: in the back separated pyramid-shaped suede 105, the area covered by the pyramid structure 105a accounts for 65% of the entire back silicon substrate, and the base length of a single pyramid structure 105a is 4 μm . The front passivation anti-reflection dielectric layer 103 is a double-layer film made of indium tin oxide and amorphous silicon, wherein the thickness of the indium tin oxide film is 60 to 80 nm and the thickness of the amorphous silicon film is 5 to 20 nm; The dielectric layer 107 is a double-layer film made of indium tin oxide and amorphous silicon, wherein the film thickness of indium tin oxide is 60-80 nm and the film thickness of amorphous silicon is 5-20 nm; the front electrode 104 and the back electrode 108 are both silver electrodes.
实施例5: Example 5:
一种单晶硅双面太阳电池的制备方法,用于制备实施例1所述的P单晶硅双面太阳电池,包括如下步骤: A method for preparing a monocrystalline silicon double-sided solar cell, for preparing the P single-crystalline silicon double-sided solar cell described in Example 1, comprising the steps of:
S1:在单晶硅衬底表面制绒:使用含氢氧化钠和异丙醇的碱性制绒液,温度是80℃,对p型单晶硅衬底100表面进行制绒,形成正面金字塔形绒面101,同时去除硅片切割损伤层; S1: Texturing on the surface of a single crystal silicon substrate: Use an alkaline texturing solution containing sodium hydroxide and isopropanol at a temperature of 80°C to texture the surface of the p-type single crystal silicon substrate 100 to form a front pyramid Shape the suede 101, and remove the silicon wafer cutting damage layer at the same time;
S2:正面掺杂形成发射结:进行磷掺杂形成正面掺杂发射结102,磷掺杂可以采用三氯氧磷源的管式炉扩散、离子注入或涂覆含磷杂质层的扩散,扩散方阻是40至200Ω/□; S2: Front doping to form an emitter junction: Phosphorus doping is performed to form a front doped emitter junction 102. Phosphorus doping can be diffused in a tube furnace with a phosphorus oxychloride source, ion implantation, or diffusion by coating a phosphorus-containing impurity layer. Square resistance is 40 to 200Ω/□;
S2-1:正面沉积阻挡层:采用PECVD在正面沉淀氧化硅薄膜的工艺阻挡层,厚度是50至300nm; S2-1: Deposition barrier layer on the front side: use PECVD to deposit a process barrier layer of silicon oxide film on the front side, with a thickness of 50 to 300 nm;
S3:去除背面含杂质玻璃层:使用氢氟酸去除背面的磷硅玻璃层; S3: Removing the impurity-containing glass layer on the back: using hydrofluoric acid to remove the phosphosilicate glass layer on the back;
S4:湿化学法制备背面分离型金字塔形绒面,并去除背面掺杂:使用含四甲基氢氧化铵和异丙醇的碱性药液,温度是80℃,时间是10至900s,制备形成背面分离型金字塔形绒面105,同时去除背面磷掺杂层; S4: Preparation of back-separated pyramid-shaped suede by wet chemical method, and removal of doping on the back: using an alkaline solution containing tetramethylammonium hydroxide and isopropanol, the temperature is 80°C, and the time is 10 to 900s. Forming the rear separated pyramid-shaped suede 105, while removing the phosphorus-doped layer on the rear;
S5:背面掺杂形成背表面场:进行硼掺杂形成背表面场106,硼掺杂可以采用三溴化硼源的管式炉扩散、离子注入或涂覆含硼杂质层的扩散,扩散方阻是60至200Ω/□; S5: back surface doping to form back surface field: perform boron doping to form back surface field 106, boron doping can adopt tube furnace diffusion of boron tribromide source, ion implantation or diffusion of coating boron-containing impurity layer, the diffusion method Resistance is 60 to 200Ω/□;
S5-1:使用氢氟酸去除正面的氧化硅、磷硅玻璃和背面的硼硅玻璃; S5-1: Use hydrofluoric acid to remove silicon oxide, phosphosilicate glass on the front and borosilicate glass on the back;
S6:制备正面、背面钝化减反介质层:采用PECVD制备正面氮化硅103和背面氧化铝/氮化硅的钝化减反介质层107;正面氮化硅厚度是70至80nm,背面氧化铝厚度是20至30nm,氮化硅厚度是50至70nm; S6: Preparation of front and back passivation anti-reflection dielectric layers: PECVD is used to prepare front-side silicon nitride 103 and rear-side aluminum oxide/silicon nitride passivation anti-reflection dielectric layer 107; Aluminum thickness is 20 to 30nm, silicon nitride thickness is 50 to 70nm;
S7:制备正、背面电极:采用丝网印刷分别在正、背面制备含银栅线电极104和108,并进行高温烧结,烧结温度是850至900℃。 S7: Preparing front and back electrodes: using screen printing to prepare silver-containing grid wire electrodes 104 and 108 on the front and back sides, respectively, and sintering at a high temperature at a temperature of 850 to 900°C.
当然,在步骤S4中,也可以采用含硝酸和氢氟酸的酸性药液制备背面分离型金字塔形绒面。 Certainly, in step S4, an acid solution containing nitric acid and hydrofluoric acid may also be used to prepare the back-separated pyramid-shaped suede.
实施例2的制备方法参照实施例1的制备方法。 The preparation method of embodiment 2 refers to the preparation method of embodiment 1.
实施例6: Embodiment 6:
一种单晶硅双面太阳电池的制备方法,用于制备实施例3所述的N单晶硅双面太阳电池,包括如下步骤: A method for preparing a monocrystalline silicon double-sided solar cell, which is used to prepare the N single-crystalline silicon double-sided solar cell described in Example 3, comprising the steps of:
S1:在单晶硅衬底表面制绒:使用含氢氧化钠和异丙醇的碱性制绒液,温度是80℃,对n型单晶硅衬底100表面进行制绒,形成正面绒面形貌101,同时去除硅片切割损伤层; S1: Texturing on the surface of the single crystal silicon substrate: use an alkaline texturing solution containing sodium hydroxide and isopropanol at a temperature of 80°C to make texturing on the surface of the n-type single crystal silicon substrate 100 to form a front texture Surface morphology 101, while removing the silicon wafer cutting damage layer;
S2:正面掺杂形成发射结:进行硼掺杂形成正面硼掺杂发射结102,磷掺杂可以采用三溴化硼源的管式炉扩散、离子注入或涂覆含硼杂质层的扩散,扩散方阻是60至200Ω/□; S2: front-side doping to form an emitter junction: perform boron doping to form a front-side boron-doped emitter junction 102, phosphorus doping can be diffused in a tube furnace with a boron tribromide source, ion implantation or diffusion coated with a boron-containing impurity layer, Diffusion square resistance is 60 to 200Ω/□;
S2-1:正面沉积阻挡层:采用PECVD在正面沉淀氧化硅薄膜的工艺阻挡层,厚度是50至300nm; S2-1: Deposition barrier layer on the front side: use PECVD to deposit a process barrier layer of silicon oxide film on the front side, with a thickness of 50 to 300 nm;
S3:去除背面含杂质玻璃层:使用氢氟酸去除背面的硼硅玻璃层; S3: remove the impurity glass layer on the back: use hydrofluoric acid to remove the borosilicate glass layer on the back;
S4:湿化学法制备背面分离型金字塔形绒面,并去除背面掺杂:使用含四甲基氢氧化铵和异丙醇的碱性药液,温度是80℃,时间是10至900s,制备背面金字塔形绒面105,同时去除背面硼掺杂层; S4: Preparation of back-separated pyramid-shaped suede by wet chemical method, and removal of doping on the back: using an alkaline solution containing tetramethylammonium hydroxide and isopropanol, the temperature is 80°C, and the time is 10 to 900s. Pyramidal suede 105 on the back side, while removing the boron doped layer on the back side;
S5:背面掺杂形成背表面场:进行磷掺杂形成背表面场106,磷掺杂可以采用三氯氧磷源的管式炉扩散、离子注入或涂覆含磷杂质层的扩散,扩散方阻是40至200Ω/□; S5: Doping on the back to form a back surface field: Phosphorus doping is performed to form a back surface field 106. The phosphorus doping can be diffused in a tube furnace with phosphorus oxychloride source, ion implantation or diffusion coated with a phosphorus-containing impurity layer. The diffusion method Resistance is 40 to 200Ω/□;
S5-1:使用氢氟酸去除正面的氧化硅、硼硅玻璃和背面的磷硅玻璃; S5-1: Use hydrofluoric acid to remove silicon oxide, borosilicate glass on the front and phosphosilicate glass on the back;
S6:制备正面、背面钝化减反介质层:采用PECVD制备正面氧化铝/氮化硅,103和背面氮化硅的钝化减反介质层107;正面氧化铝厚度是20至30nm,氮化硅厚度是50至70nm;背面氮化硅厚度是70至80nm; S6: Preparation of the front and back passivation anti-reflection dielectric layers: PECVD is used to prepare the passivation anti-reflection dielectric layer 107 of the front aluminum oxide/silicon nitride, 103 and the back silicon nitride; the thickness of the front aluminum oxide is 20 to 30 nm, The thickness of silicon is 50 to 70nm; the thickness of silicon nitride on the back is 70 to 80nm;
S7:制备正、背面电极:采用丝网印刷分别在正、背面制备含银栅线电极104和108,并进行高温烧结,烧结温度是850至900℃。 S7: Preparing front and back electrodes: using screen printing to prepare silver-containing grid wire electrodes 104 and 108 on the front and back sides, respectively, and sintering at a high temperature at a temperature of 850 to 900°C.
实施例4的制备方法参照实施例3的制备方法。 The preparation method of embodiment 4 refers to the preparation method of embodiment 3.
显然,所描述的实施例仅仅是本发明的部分实施例,而不是全部的实施例。基于本发明中的实施例,本领域普通技术人员在没有做出创造性劳动前提下所获得的所有其他实施例,都应当属于本发明保护的范围。 Apparently, the described embodiments are only some, not all, embodiments of the present invention. Based on the embodiments of the present invention, all other embodiments obtained by persons of ordinary skill in the art without making creative efforts shall fall within the protection scope of the present invention.
Claims (8)
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201610331351.XA CN105826405A (en) | 2016-05-17 | 2016-05-17 | Mono-crystalline silicon double-sided solar cell and preparation method thereof |
| PCT/CN2016/098553 WO2017197811A1 (en) | 2016-05-17 | 2016-09-09 | Double-sided monocrystalline silicon solar cell and manufacturing method thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201610331351.XA CN105826405A (en) | 2016-05-17 | 2016-05-17 | Mono-crystalline silicon double-sided solar cell and preparation method thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN105826405A true CN105826405A (en) | 2016-08-03 |
Family
ID=56530894
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201610331351.XA Pending CN105826405A (en) | 2016-05-17 | 2016-05-17 | Mono-crystalline silicon double-sided solar cell and preparation method thereof |
Country Status (2)
| Country | Link |
|---|---|
| CN (1) | CN105826405A (en) |
| WO (1) | WO2017197811A1 (en) |
Cited By (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106952974A (en) * | 2017-03-31 | 2017-07-14 | 浙江晶科能源有限公司 | A kind of preparation method of P-type black silicon bifacial battery |
| WO2017197811A1 (en) * | 2016-05-17 | 2017-11-23 | 常州天合光能有限公司 | Double-sided monocrystalline silicon solar cell and manufacturing method thereof |
| CN107887453A (en) * | 2017-10-10 | 2018-04-06 | 横店集团东磁股份有限公司 | A kind of two-sided aluminum oxide p-type PERC solar cells and preparation method |
| CN108336156A (en) * | 2018-03-12 | 2018-07-27 | 南昌大学 | A kind of crystal silicon double-side solar cell structure with HAC-D features |
| CN108336155A (en) * | 2018-03-12 | 2018-07-27 | 南昌大学 | A kind of HAC-D crystal silicon double-side solar cell structure |
| CN108336157A (en) * | 2018-03-12 | 2018-07-27 | 南昌大学 | A kind of double-side solar cell structure of local amorphous silicon emitter crystalline silicon back surface field |
| CN108461553A (en) * | 2018-03-12 | 2018-08-28 | 南昌大学 | A kind of double-side solar cell structure with local amorphous silicon/crystalline silicon heterojunction characteristic |
| CN108807565A (en) * | 2018-07-13 | 2018-11-13 | 苏州太阳井新能源有限公司 | A kind of passivation contact electrode structure, applicable solar cell and production method |
| CN109346535A (en) * | 2018-09-14 | 2019-02-15 | 江苏林洋光伏科技有限公司 | Method for fabricating selective texture and emitter of silicon solar cell by laser |
| CN109638103A (en) * | 2018-06-05 | 2019-04-16 | 中智(泰兴)电力科技有限公司 | Two-sided differential textured structure for single crystal silicon heterojunction solar cell and preparation method |
| CN110071183A (en) * | 2019-05-10 | 2019-07-30 | 苏州腾晖光伏技术有限公司 | A kind of solar battery and preparation method thereof |
| CN112635591A (en) * | 2020-12-22 | 2021-04-09 | 泰州隆基乐叶光伏科技有限公司 | Preparation method of solar cell and solar cell |
| CN114678446A (en) * | 2022-03-25 | 2022-06-28 | 江苏润阳世纪光伏科技有限公司 | Low-cost contact passivation full-back electrode solar cell and preparation method thereof |
| CN115020503A (en) * | 2021-08-04 | 2022-09-06 | 上海晶科绿能企业管理有限公司 | Solar cell, preparation method thereof and photovoltaic module |
| CN116504877A (en) * | 2023-05-08 | 2023-07-28 | 安徽华晟新能源科技有限公司 | Heterojunction battery and its preparation method |
| CN115241299B (en) * | 2022-07-27 | 2023-10-31 | 浙江晶科能源有限公司 | Solar cell and photovoltaic module |
| US11843071B2 (en) | 2021-08-04 | 2023-12-12 | Shanghai Jinko Green Energy Enterprise Management Co., Ltd. | Solar cell, manufacturing method thereof, and photovoltaic module |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108336176A (en) * | 2018-03-12 | 2018-07-27 | 南昌大学 | A kind of Si bases local emitter double-side solar cell structure |
| CN109950352B (en) * | 2019-04-23 | 2024-11-08 | 通威太阳能(成都)有限公司 | A solar cell using an amorphous silicon passivation layer and a method for manufacturing the same |
| CN109980022B (en) * | 2019-04-24 | 2024-12-06 | 通威太阳能(成都)有限公司 | A P-type tunneling oxide passivation contact solar cell and its preparation method |
| CN112038438B (en) * | 2019-06-04 | 2025-02-25 | 阜宁阿特斯阳光电力科技有限公司 | A lightly doped substrate, a substrate with a selective emitter, a solar cell, and a preparation method and application thereof |
| CN112993079A (en) * | 2019-12-02 | 2021-06-18 | 阜宁阿特斯阳光电力科技有限公司 | Preparation method of photovoltaic cell and photovoltaic cell |
| CN113078232B (en) * | 2019-12-17 | 2025-09-05 | 苏州阿特斯阳光电力科技有限公司 | N-type battery structure and preparation method thereof |
| CN113990980B (en) * | 2020-07-09 | 2024-08-16 | 嘉兴阿特斯技术研究院有限公司 | Solar cell and preparation method thereof |
| CN112349816B (en) * | 2020-11-19 | 2022-05-17 | 江苏大学 | A high-efficiency and low-cost N-type TOPCon cell preparation method based on PECVD technology |
| CN112599636B (en) * | 2020-12-07 | 2023-08-01 | 浙江晶科能源有限公司 | A kind of preparation method of crystalline silicon solar cell and crystalline silicon solar cell |
| CN114649438B (en) * | 2020-12-17 | 2024-05-10 | 浙江爱旭太阳能科技有限公司 | Preparation method of N-type HIBC solar cell |
| CN113782625A (en) * | 2021-01-06 | 2021-12-10 | 宣城睿晖宣晟企业管理中心合伙企业(有限合伙) | Heterojunction battery and preparation method thereof |
| CN113540269B (en) * | 2021-09-14 | 2022-04-12 | 浙江晶科能源有限公司 | Solar cell and preparation method thereof, photovoltaic module |
| CN114447156A (en) * | 2022-01-27 | 2022-05-06 | 环晟光伏(江苏)有限公司 | A method for laser grooving on the front surface of electroplating cells |
| CN116435403B (en) * | 2023-02-28 | 2024-09-17 | 六智韬新能源科技(上海)有限公司 | Flexible monocrystalline silicon piece, flexible solar cell and preparation method of flexible monocrystalline silicon piece and flexible solar cell |
| CN116613224B (en) * | 2023-07-20 | 2023-09-29 | 天合光能股份有限公司 | Solar cell, manufacturing method thereof, photovoltaic module and photovoltaic system |
| CN117153910A (en) * | 2023-08-22 | 2023-12-01 | 天合光能股份有限公司 | Heterojunction solar cell, manufacturing method thereof, photovoltaic module and photovoltaic system |
| CN118382310B (en) * | 2024-06-21 | 2024-12-20 | 淮安捷泰新能源科技有限公司 | Perovskite/silicon laminated solar cell and preparation method thereof |
| CN119584718B (en) * | 2024-12-02 | 2025-09-02 | 隆基绿能科技股份有限公司 | Solar cell, photovoltaic module and semiconductor substrate |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2149155B1 (en) * | 2007-05-07 | 2010-10-27 | Georgia Tech Research Corporation | Formation of high quality back contact with screen-printed local back surface field |
| CN204315603U (en) * | 2014-10-30 | 2015-05-06 | 广东爱康太阳能科技有限公司 | A kind of polished backside crystal silicon solar batteries |
| CN105047742A (en) * | 2015-09-07 | 2015-11-11 | 中国东方电气集团有限公司 | Double-sided N-type crystalline silicon cell and preparation method thereof |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104350607B (en) * | 2012-06-13 | 2018-01-12 | 三菱电机株式会社 | Solar cell and its manufacture method |
| KR101976420B1 (en) * | 2013-03-06 | 2019-05-09 | 엘지전자 주식회사 | Solar cell and method for manufacturing the same |
| CN103489951B (en) * | 2013-09-05 | 2015-11-11 | 西南科技大学 | Two-sided black crystalline silicon high-efficiency solar cell |
| CN105826405A (en) * | 2016-05-17 | 2016-08-03 | 常州天合光能有限公司 | Mono-crystalline silicon double-sided solar cell and preparation method thereof |
-
2016
- 2016-05-17 CN CN201610331351.XA patent/CN105826405A/en active Pending
- 2016-09-09 WO PCT/CN2016/098553 patent/WO2017197811A1/en not_active Ceased
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2149155B1 (en) * | 2007-05-07 | 2010-10-27 | Georgia Tech Research Corporation | Formation of high quality back contact with screen-printed local back surface field |
| CN204315603U (en) * | 2014-10-30 | 2015-05-06 | 广东爱康太阳能科技有限公司 | A kind of polished backside crystal silicon solar batteries |
| CN105047742A (en) * | 2015-09-07 | 2015-11-11 | 中国东方电气集团有限公司 | Double-sided N-type crystalline silicon cell and preparation method thereof |
Cited By (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2017197811A1 (en) * | 2016-05-17 | 2017-11-23 | 常州天合光能有限公司 | Double-sided monocrystalline silicon solar cell and manufacturing method thereof |
| CN106952974B (en) * | 2017-03-31 | 2019-06-11 | 浙江晶科能源有限公司 | Preparation method of P-type black silicon double-sided battery |
| CN106952974A (en) * | 2017-03-31 | 2017-07-14 | 浙江晶科能源有限公司 | A kind of preparation method of P-type black silicon bifacial battery |
| CN107887453B (en) * | 2017-10-10 | 2019-03-15 | 横店集团东磁股份有限公司 | A kind of double-sided alumina P-type PERC solar cell and production method |
| CN107887453A (en) * | 2017-10-10 | 2018-04-06 | 横店集团东磁股份有限公司 | A kind of two-sided aluminum oxide p-type PERC solar cells and preparation method |
| CN108336156A (en) * | 2018-03-12 | 2018-07-27 | 南昌大学 | A kind of crystal silicon double-side solar cell structure with HAC-D features |
| CN108336155A (en) * | 2018-03-12 | 2018-07-27 | 南昌大学 | A kind of HAC-D crystal silicon double-side solar cell structure |
| CN108336157A (en) * | 2018-03-12 | 2018-07-27 | 南昌大学 | A kind of double-side solar cell structure of local amorphous silicon emitter crystalline silicon back surface field |
| CN108461553A (en) * | 2018-03-12 | 2018-08-28 | 南昌大学 | A kind of double-side solar cell structure with local amorphous silicon/crystalline silicon heterojunction characteristic |
| CN109638103A (en) * | 2018-06-05 | 2019-04-16 | 中智(泰兴)电力科技有限公司 | Two-sided differential textured structure for single crystal silicon heterojunction solar cell and preparation method |
| CN108807565A (en) * | 2018-07-13 | 2018-11-13 | 苏州太阳井新能源有限公司 | A kind of passivation contact electrode structure, applicable solar cell and production method |
| CN108807565B (en) * | 2018-07-13 | 2024-04-16 | 苏州太阳井新能源有限公司 | Passivation contact electrode structure, solar cell applicable to passivation contact electrode structure and manufacturing method of passivation contact electrode structure |
| CN109346535A (en) * | 2018-09-14 | 2019-02-15 | 江苏林洋光伏科技有限公司 | Method for fabricating selective texture and emitter of silicon solar cell by laser |
| CN110071183A (en) * | 2019-05-10 | 2019-07-30 | 苏州腾晖光伏技术有限公司 | A kind of solar battery and preparation method thereof |
| CN112635591A (en) * | 2020-12-22 | 2021-04-09 | 泰州隆基乐叶光伏科技有限公司 | Preparation method of solar cell and solar cell |
| US11843071B2 (en) | 2021-08-04 | 2023-12-12 | Shanghai Jinko Green Energy Enterprise Management Co., Ltd. | Solar cell, manufacturing method thereof, and photovoltaic module |
| US11824136B2 (en) | 2021-08-04 | 2023-11-21 | Shanghai Jinko Green Energy Enterprise Management Co., Ltd. | Solar cell, manufacturing method thereof, and photovoltaic module |
| CN115020503A (en) * | 2021-08-04 | 2022-09-06 | 上海晶科绿能企业管理有限公司 | Solar cell, preparation method thereof and photovoltaic module |
| US11929449B2 (en) | 2021-08-04 | 2024-03-12 | Shanghai Jinko Green Energy Enterprise Management Co., Ltd. | Solar cell, manufacturing method thereof, and photovoltaic module |
| US12132138B2 (en) | 2021-08-04 | 2024-10-29 | Shanghai Jinko Green Energy Enterprise Management Co., Ltd. | Solar cell, manufacturing method thereof, and photovoltaic module |
| CN114678446A (en) * | 2022-03-25 | 2022-06-28 | 江苏润阳世纪光伏科技有限公司 | Low-cost contact passivation full-back electrode solar cell and preparation method thereof |
| CN115241299B (en) * | 2022-07-27 | 2023-10-31 | 浙江晶科能源有限公司 | Solar cell and photovoltaic module |
| CN116504877A (en) * | 2023-05-08 | 2023-07-28 | 安徽华晟新能源科技有限公司 | Heterojunction battery and its preparation method |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2017197811A1 (en) | 2017-11-23 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN105826405A (en) | Mono-crystalline silicon double-sided solar cell and preparation method thereof | |
| CN105826411B (en) | Monocrystalline silicon double-side solar cell and preparation method thereof | |
| CN103489934B (en) | Local aluminum back surface field solar cell of a kind of transparent two sides and preparation method thereof | |
| WO2022105192A1 (en) | Pecvd technology-based preparation method for high-efficiency low-cost n-type topcon battery | |
| CN101937944A (en) | Preparation method of double-sided passivated crystalline silicon solar cell | |
| CN102208486A (en) | Preparation method of MWT (Metal Wrap Through) solar cell | |
| CN104934500A (en) | Method for preparing back-surface passivation crystalline silicon solar cell with selective emitter | |
| CN103887347A (en) | Double-face P-type crystalline silicon battery structure and manufacturing method thereof | |
| WO2023093604A1 (en) | Solar cell and preparation method for solar cell | |
| CN106684160A (en) | Back-junction back-contact solar cell | |
| CN105122461B (en) | Manufacturing method of solar cell | |
| CN218585997U (en) | Solar cell of P-type silicon | |
| WO2015118935A1 (en) | Photoelectric conversion element and solar cell module provided with same | |
| CN103594534B (en) | Aluminum emitter stage back junction back contact crystalline silicon solar cell and manufacture method thereof | |
| CN109585600A (en) | A kind of production method of the efficient crystal silicon solar batteries of two-sided PERC | |
| CN205900558U (en) | Monocrystalline silicon double-sided solar cell | |
| CN111524982A (en) | Solar cell | |
| CN108461554A (en) | Full back-contact heterojunction solar battery and preparation method thereof | |
| CN205900556U (en) | A single crystal silicon double-sided solar cell | |
| CN204315603U (en) | A kind of polished backside crystal silicon solar batteries | |
| CN119604059A (en) | A P-type double-sided passivated selective contact TOPCon battery structure and preparation method | |
| CN119153568A (en) | Back contact solar cell and preparation method thereof | |
| CN102403398A (en) | Method for manufacturing solar cell | |
| CN103943693A (en) | A P-type silicon substrate back contact solar cell structure and preparation method | |
| CN103646991A (en) | Preparation method of P-type crystal silicon double-sided cell |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| RJ01 | Rejection of invention patent application after publication |
Application publication date: 20160803 |
|
| RJ01 | Rejection of invention patent application after publication |