CN103594534B - Aluminum emitter stage back junction back contact crystalline silicon solar cell and manufacture method thereof - Google Patents
Aluminum emitter stage back junction back contact crystalline silicon solar cell and manufacture method thereof Download PDFInfo
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- 229910052782 aluminium Inorganic materials 0.000 title claims abstract description 14
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 title claims abstract description 14
- 229910021419 crystalline silicon Inorganic materials 0.000 title claims abstract description 14
- 238000000034 method Methods 0.000 title claims description 18
- 238000004519 manufacturing process Methods 0.000 title abstract description 13
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims abstract description 34
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 34
- 239000010703 silicon Substances 0.000 claims abstract description 34
- 239000000758 substrate Substances 0.000 claims abstract description 27
- 238000002161 passivation Methods 0.000 claims abstract description 14
- 238000004140 cleaning Methods 0.000 claims abstract description 8
- 238000005245 sintering Methods 0.000 claims abstract description 5
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 claims description 24
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 24
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 18
- 238000009792 diffusion process Methods 0.000 claims description 12
- 238000007650 screen-printing Methods 0.000 claims description 10
- 229910052581 Si3N4 Inorganic materials 0.000 claims description 9
- 239000011259 mixed solution Substances 0.000 claims description 9
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 claims description 9
- 239000000243 solution Substances 0.000 claims description 9
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 7
- 229910052698 phosphorus Inorganic materials 0.000 claims description 7
- 239000011574 phosphorus Substances 0.000 claims description 7
- 238000005498 polishing Methods 0.000 claims description 7
- 238000007639 printing Methods 0.000 claims description 6
- 239000000126 substance Substances 0.000 claims description 6
- 238000002360 preparation method Methods 0.000 claims description 5
- 229910004205 SiNX Inorganic materials 0.000 claims description 4
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical group ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 claims description 4
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 3
- 238000005229 chemical vapour deposition Methods 0.000 claims description 3
- 238000001035 drying Methods 0.000 claims description 3
- 229910021421 monocrystalline silicon Inorganic materials 0.000 claims description 3
- 229910052709 silver Inorganic materials 0.000 claims description 3
- 239000004332 silver Substances 0.000 claims description 3
- 229910019213 POCl3 Inorganic materials 0.000 claims description 2
- 239000003513 alkali Substances 0.000 claims description 2
- 238000005553 drilling Methods 0.000 claims description 2
- 239000002002 slurry Substances 0.000 claims description 2
- 238000005530 etching Methods 0.000 abstract description 2
- 238000000151 deposition Methods 0.000 abstract 1
- 235000012431 wafers Nutrition 0.000 description 7
- 239000000969 carrier Substances 0.000 description 4
- XGCTUKUCGUNZDN-UHFFFAOYSA-N [B].O=O Chemical compound [B].O=O XGCTUKUCGUNZDN-UHFFFAOYSA-N 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 239000012670 alkaline solution Substances 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 229910052755 nonmetal Inorganic materials 0.000 description 2
- RLOWWWKZYUNIDI-UHFFFAOYSA-N phosphinic chloride Chemical group ClP=O RLOWWWKZYUNIDI-UHFFFAOYSA-N 0.000 description 2
- 238000005215 recombination Methods 0.000 description 2
- 230000006798 recombination Effects 0.000 description 2
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- 229910004012 SiCx Inorganic materials 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000005468 ion implantation Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 239000002210 silicon-based material Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 230000004083 survival effect Effects 0.000 description 1
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- H10F10/146—Back-junction photovoltaic cells, e.g. having interdigitated base-emitter regions on the back side
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Abstract
本发明公开了一种铝发射极背结背接触晶体硅太阳电池及其制造方法,该电池包括前表面与背表面均覆盖有N型掺杂层的板状的N型硅衬底,在 N型掺杂层外覆盖有钝化层,背表面的N型硅衬底上间隔地嵌入有P型掺杂层,P型掺杂层上方连接有电池正极,背表面N型掺杂层中还嵌入有电池负极。其制造方法包括织构化处理、掺杂层制作、开孔、刻蚀、清洗、沉积、烧结等步骤。本发明具有低成本和可量产的优点。
The invention discloses an aluminum emitter back-junction back-contact crystalline silicon solar cell and a manufacturing method thereof. The passivation layer is covered outside the N-type doped layer on the back surface, and P-type doped layers are embedded at intervals on the N-type silicon substrate on the back surface. Embedded with the negative terminal of the battery. The manufacturing method includes the steps of texturing, doping layer making, opening, etching, cleaning, depositing, sintering and the like. The invention has the advantages of low cost and mass production.
Description
技术领域technical field
本发明涉及一种太阳能电池的结构及制造方法,具体涉及一种铝发射极背结背接触晶体硅太阳电池及其制造方法。The invention relates to a structure and a manufacturing method of a solar cell, in particular to an aluminum emitter back-junction back-contact crystalline silicon solar cell and a manufacturing method thereof.
背景技术Background technique
太阳能电池可将太阳能直接转化成电能,是利用太阳能资源的有效方式,由于在使用中不会产生任何有害物质,所以近几年来太阳能电池在解决能源与环境问题方面倍受青睐,有着极好的市场前景。太阳能也被誉为是最理想的能源,是解决人类社会赖以生存和发展的重要资源。Solar cells can directly convert solar energy into electrical energy, which is an effective way to utilize solar energy resources. Since no harmful substances are produced during use, solar cells have been favored in solving energy and environmental problems in recent years. market expectation. Solar energy is also known as the most ideal energy source and an important resource for the survival and development of human society.
目前主流的太阳能电池材料是用P型硅衬底,通过高温磷扩散来形成pn 结。然而P型晶硅电池受体内硼氧对的影响存在光致衰减的现象,而N型硅材料相对于P型硅材料来说,由于其对金属杂质和许多非金属缺陷不敏感同时体内较少的硼氧对,所以性能的稳定性要高于P 型晶硅电池;同时由于N 型电池的少子寿命更高,这为制备更高效的太阳电池奠定了基础。The current mainstream solar cell material uses a P-type silicon substrate to form a pn junction through high-temperature phosphorus diffusion. However, there is a phenomenon of light-induced attenuation due to the influence of boron-oxygen pairs in the P-type crystalline silicon cell, and the N-type silicon material is relatively insensitive to metal impurities and many non-metal defects due to its insensitivity to metal impurities and many non-metal defects. There are fewer boron-oxygen pairs, so the stability of performance is higher than that of P-type crystalline silicon cells; at the same time, due to the higher minority carrier lifetime of N-type cells, this lays the foundation for the preparation of more efficient solar cells.
背结背接触太阳电池早在1977 年开始进入人们的视线,直到现在仍然是太阳电池行业研究的热点。相对于常规的硅电池,背结背接触太阳电池的优势很明显,主要可以表现在以下几个方面:(1)背结背接触太阳电池以N型晶体硅作为衬底,少子寿命高,适用于制备高效电池,特别适用于于背结背接触太阳电池这种pn 结在背表面的电池结构,因为产生于前表面的光生载流子必须要迁移到电池背表面的pn 结才能被利用,较高的少子寿命是减少光生载流子在太阳电池表面和体内复合的保证;(2)N型基体的硼含量极低,因此由硼氧对造成的光致衰减没有P型基体材料明显,对封装后组件的效率提升更为明显;(3)背结背接触太阳电池的正面没有电极,减少了遮光面积,增加了光生电流,电池的正负电极呈交指状的分布在电池的背面;(4)背结背接触太阳电池易于封装,和常规电池相比,无需把前一片的负极交叉接到后一片的正极,易于操作。Back-junction and back-contact solar cells began to come into people's sight as early as 1977, and it is still a research hotspot in the solar cell industry until now. Compared with conventional silicon cells, the advantages of back-junction and back-contact solar cells are obvious, mainly in the following aspects: (1) Back-junction and back-contact solar cells use N-type crystalline silicon as the substrate, which has a high minority carrier life and is suitable for It is suitable for the preparation of high-efficiency cells, especially suitable for back-junction and back-contact solar cells, which have a pn junction on the back surface of the cell structure, because the photo-generated carriers generated on the front surface must migrate to the pn junction on the back surface of the cell to be utilized. A higher minority carrier lifetime is the guarantee to reduce the recombination of photogenerated carriers on the surface and in the body of the solar cell; (2) The boron content of the N-type substrate is extremely low, so the light-induced attenuation caused by the boron-oxygen pair is not as obvious as that of the P-type substrate material, The improvement of the efficiency of the packaged components is more obvious; (3) There is no electrode on the front of the back junction solar cell, which reduces the shading area and increases the photo-generated current. The positive and negative electrodes of the cell are distributed on the back of the cell in a finger shape ; (4) Back-junction and back-contact solar cells are easy to package. Compared with conventional batteries, there is no need to cross the negative electrode of the previous sheet to the positive electrode of the latter sheet, which is easy to operate.
发明内容Contents of the invention
发明目的:为了克服现有技术中存在的不足,本发明提供一种铝发射极背结背接触晶体硅太阳电池及其制造方法,该方法安全可靠与传统的太阳电池生产线兼容,适合于目前太阳电池的产线升级。Purpose of the invention: In order to overcome the deficiencies in the prior art, the present invention provides an aluminum emitter back-junction back-contact crystalline silicon solar cell and its manufacturing method, which is safe, reliable and compatible with traditional solar cell production lines, and is suitable for current solar Battery production line upgrade.
技术方案:为解决上述技术问题,本发明提供的铝发射极背结背接触晶体硅太阳电池,包括板状的N型硅衬底,在所述N型硅衬底的前表面和背表面覆盖有N型掺杂层,所述N型掺杂层外覆盖有钝化层,所述背表面的N型硅衬底上间隔地嵌入有P型掺杂层,所述P型掺杂层上方连接有电池正极,所述背表面N型掺杂层中嵌入有电池负极。Technical solution: In order to solve the above-mentioned technical problems, the aluminum emitter back-junction back-contact crystalline silicon solar cell provided by the present invention includes a plate-shaped N-type silicon substrate covered on the front surface and the back surface of the N-type silicon substrate. There is an N-type doped layer, the N-type doped layer is covered with a passivation layer, the N-type silicon substrate on the back surface is embedded with P-type doped layers at intervals, above the P-type doped layer The positive pole of the battery is connected, and the negative pole of the battery is embedded in the N-type doped layer on the back surface.
优选的,所述N型掺杂层的方阻值为30-120ohm/sq。Preferably, the square resistance of the N-type doped layer is 30-120 ohm/sq.
优选的,所述N型硅衬底前表面的钝化层为SiNx钝化层,背表面的钝化层是SiO2、SiOx/SiNx、Al2O3/SiNx或SiCx钝化层。Preferably, the passivation layer on the front surface of the N-type silicon substrate is a SiNx passivation layer, and the passivation layer on the back surface is a SiO 2 , SiOx/SiNx, Al 2 O 3 /SiNx or SiCx passivation layer.
本发明同时提出上述铝发射极背结背接触晶体硅太阳电池的制方法,包括以下步骤:The present invention simultaneously proposes a method for manufacturing the above-mentioned aluminum emitter back-junction back-contact crystalline silicon solar cell, comprising the following steps:
(1)用碱性溶液对N型硅片进行双面织构化处理;(1) Double-sided texturing of N-type silicon wafers with alkaline solution;
(2)N型硅片双面制作n型掺杂层,掺杂层的方阻在30-120ohm/sq;(2) N-type doped layers are made on both sides of N-type silicon wafers, and the square resistance of the doped layers is 30-120ohm/sq;
(3)对N型硅片背面p+图案化区域进行局部开孔,去除该区域的PSG;(3) Partially open the p + patterned area on the back of the N-type silicon wafer to remove the PSG in this area;
(4)对N型硅片图案化的p+区域进行抛光刻蚀,去除p+图案化区域上的n型掺杂层;(4) Polishing and etching the patterned p + region of the N-type silicon wafer to remove the n-type doped layer on the p + patterned region;
(5)去除其它区域的PSG,并进行湿法清洗;(5) Remove PSG from other areas and perform wet cleaning;
(6)在硅片前表面和背表面沉积钝化层;(6) Deposit a passivation layer on the front and back surfaces of the silicon wafer;
(7)背面p+图案化区域介质膜开孔;(7) Dielectric film openings in the p+ patterned area on the back;
(8)丝网印刷背面电极、烧结。(8) Screen printing back electrode, sintering.
优选的,所述步骤2)中掺杂层可以通过POCl3扩散、离子注入或固态源扩散的方法制作。Preferably, the doped layer in step 2) can be fabricated by POCl3 diffusion, ion implantation or solid state source diffusion.
优选的,所述步骤3)中的开孔方法为腐蚀性浆料开孔或者激光开孔。Preferably, the method of opening holes in the step 3) is opening holes with corrosive slurry or laser opening.
优选的,所述步骤4)中图案化P+区域抛光的方法是采用对硅和PSG具有选择性刻蚀的碱性溶液。Preferably, the method for polishing the patterned P+ region in step 4) is to use an alkaline solution that can selectively etch silicon and PSG.
优选的,所述步骤7)中背面介质膜开孔的方式为印刷腐蚀性浆料或者采用激光开膜;如果采用可烧穿介质膜的铝浆,则跳过该步骤。Preferably, in step 7), the method of opening the dielectric film on the back side is to print corrosive paste or use laser to open the film; if aluminum paste that can burn through the dielectric film is used, this step is skipped.
有益效果:发明采用基体材料为N型晶体硅片,其少子寿命高并且光致衰减小,对制备电池和封装组件都有优势;采用钝化膜钝化电池的前后表面能有效的降低表面少数载流子的复合速率,提高表面少子寿命,而在正反两面制备减反射膜的目的则是为了减少光子的反射,增加对光子的吸收,增加光生电流进而增加电池最终的转换效率。电池的正、负电极均制作于的背面,减少了遮光面积,增加了光生电流,能更好的收集硅片产生的电流,同时在金属与硅片之间形成良好的欧姆接触;采用丝网印刷Al浆料或者溅射铝的方法形成背面的发射极能够减化工艺步骤,降低成本与时间;所有的工艺步骤均在现有的工艺条件下完成,不需要增加任何设备就能制造出高效的背结背接触太阳电池。Beneficial effects: the invention adopts N-type crystalline silicon chip as the base material, which has high minority carrier life and small light-induced attenuation, which has advantages for the preparation of batteries and packaging components; the use of passivation film passivation on the front and rear surfaces of the battery can effectively reduce the surface minority The recombination rate of carriers improves the lifetime of minority carriers on the surface, and the purpose of preparing anti-reflection coatings on both sides is to reduce the reflection of photons, increase the absorption of photons, increase the photogenerated current and increase the final conversion efficiency of the battery. Both the positive and negative electrodes of the battery are made on the back of the battery, which reduces the shading area, increases the photo-generated current, and can better collect the current generated by the silicon wafer, while forming a good ohmic contact between the metal and the silicon wafer; using silk screen The method of printing Al paste or sputtering aluminum to form the emitter on the back can reduce the process steps, reduce cost and time; all process steps are completed under the existing process conditions, and high-efficiency back-junction back-contact solar cells.
附图说明Description of drawings
图1 本发明的实施例一的结构示意图;Fig. 1 is a schematic structural diagram of Embodiment 1 of the present invention;
图2是本发明的实施例一的工序图;Fig. 2 is a process diagram of Embodiment 1 of the present invention;
图中各标号:N 型硅衬底1、氮化硅薄膜2、N型掺杂层3、P 型掺杂层4、电池正极5、电池负极6。Each label in the figure: N-type silicon substrate 1 , silicon nitride film 2 , N-type doped layer 3 , P-type doped layer 4 , battery positive electrode 5 , and battery negative electrode 6 .
具体实施方式detailed description
实施例一Embodiment one
本实施例的铝发射极背结背接触晶体硅太阳电池的结构如图1所示,包括N 型硅衬底1、氮化硅薄膜2、N型掺杂层3、P 型掺杂层4、电池的正极5、电池的负极6。其中 N型硅衬底1为板状,在N型硅衬底1的前表面和背表面覆盖有N型掺杂层3,N型掺杂层外覆盖有钝化层,该钝化层为氮化硅薄膜2,背表面的N型硅衬底1上间隔地嵌入有P型掺杂层4,P型掺杂层上方连接有电池正极5,所述背表面N型掺杂层3中嵌入有电池负极6。The structure of the aluminum emitter back-junction and back-contact crystalline silicon solar cell of this embodiment is shown in Figure 1, including an N-type silicon substrate 1, a silicon nitride film 2, an N-type doped layer 3, and a P-type doped layer 4 , the positive pole 5 of the battery, and the negative pole 6 of the battery. Wherein the N-type silicon substrate 1 is plate-shaped, and the front surface and the back surface of the N-type silicon substrate 1 are covered with an N-type doped layer 3, and the N-type doped layer is covered with a passivation layer, and the passivation layer is Silicon nitride film 2, P-type doped layers 4 are embedded at intervals on the N-type silicon substrate 1 on the back surface, and the positive electrode 5 of the battery is connected above the P-type doped layer, and the N-type doped layer 3 on the back surface The negative electrode 6 of the battery is embedded.
上述新型背结背接触结构N型硅太阳能电池的制备方法的工序如下:The procedure of the preparation method of the above-mentioned novel back-junction and back-contact structure N-type silicon solar cell is as follows:
(1)选择N 型硅衬底,且N型硅衬底的电阻率在3-5ohm.cm,少子寿命大于300us ;(1) Choose an N-type silicon substrate, and the resistivity of the N-type silicon substrate is 3-5ohm.cm, and the minority carrier lifetime is greater than 300us;
(2)采用氢氧化钠溶液对N型单晶硅衬底的表面制备出金字塔形状的陷光结构,后用盐酸和氢氟酸的混合溶液进行化学清洗;氢氧化钠溶液的浓度范围0.5%;盐酸和氢氟酸混合溶液中,盐酸:氢氟酸配比为1:2.5;盐酸和氢氟酸混合溶液的浓度为1.1%;(2) Use sodium hydroxide solution to prepare a pyramid-shaped light-trapping structure on the surface of the N-type single crystal silicon substrate, and then perform chemical cleaning with a mixed solution of hydrochloric acid and hydrofluoric acid; the concentration range of the sodium hydroxide solution is 0.5% ; In hydrochloric acid and hydrofluoric acid mixed solution, hydrochloric acid: hydrofluoric acid ratio is 1:2.5; The concentration of hydrochloric acid and hydrofluoric acid mixed solution is 1.1%;
(3)使用扩散炉管进行双面磷扩散,磷源采用的是POCl3,温度为840℃,方阻要求为70ohm/sq;(3) Diffusion furnace tubes are used for double-sided phosphorus diffusion. The phosphorus source is POCl 3 , the temperature is 840°C, and the square resistance requirement is 70ohm/sq;
(4)采用印刷Merck浆料的方法去除背面p+图案化区域的PSG;(4) Use the method of printing Merck paste to remove the PSG in the p + patterned area on the back;
(5)采用有机碱溶液对p+图案化区域进行抛光,抛光后去除PSG;(5) Polishing the p + patterned area with an organic alkali solution, and removing PSG after polishing;
(6)采用等离子化学气相沉积的方法在扩散面制备75nm 厚的氮化硅薄膜,背面制备130nm厚的氮氧化硅薄膜;(6) A 75nm thick silicon nitride film is prepared on the diffusion surface by plasma chemical vapor deposition, and a 130nm thick silicon nitride oxide film is prepared on the back;
(7)制备电极区:(7) Prepare the electrode area:
a)开槽:采用Merck开孔方法对发射极区域重新进行开槽,去除氮氧化硅层,开槽宽度为200μm,完成后进行化学清洗并烘干;a) Grooving: The emitter area is regrooved by the Merck hole opening method to remove the silicon oxynitride layer. The groove width is 200 μm. After completion, chemical cleaning and drying are carried out;
b)采用丝网印刷的方法进行对准并在未开孔区域印刷银浆细栅;b) Align by screen printing and print silver paste fine grids in the unopened areas;
c)采用丝网印刷的方法进行对准并在开孔区域印刷铝浆细栅;c) Align by screen printing and print a fine grid of aluminum paste in the opening area;
d)采用丝网印刷的方法进行印刷主栅;d) printing the main grid by screen printing;
e)烧结。e) Sintering.
本实施例中的电池按工序顺序排列的各种半成品状态如图2所示。Various semi-finished states of the battery in this embodiment are arranged according to the process sequence as shown in FIG. 2 .
实施例二Embodiment two
本实施例的铝发射极背结背接触晶体硅太阳电池结构与实施例一相同,采用的制造方法不同:The structure of the aluminum emitter back-junction back-contact crystalline silicon solar cell of this embodiment is the same as that of Embodiment 1, but the manufacturing method adopted is different:
(1)选择N 型硅衬底,且N 型硅衬底的电阻率在3-5ohm.cm,少子寿命大于300us ;(1) Choose an N-type silicon substrate, and the resistivity of the N-type silicon substrate is 3-5ohm.cm, and the minority carrier lifetime is greater than 300us;
(2)采用氢氧化钠溶液对N 型单晶硅衬底的表面制备出金字塔形状的陷光结构,后用盐酸和氢氟酸的混合溶液进行化学清洗;氢氧化钠溶液的浓度范围0.5% ;盐酸和氢氟酸混合溶液中,盐酸:氢氟酸配比为1:2.5 ;盐酸和氢氟酸混合溶液的浓度为1.1% ;(2) Use sodium hydroxide solution to prepare a pyramid-shaped light-trapping structure on the surface of the N-type single crystal silicon substrate, and then perform chemical cleaning with a mixed solution of hydrochloric acid and hydrofluoric acid; the concentration range of the sodium hydroxide solution is 0.5% ; In hydrochloric acid and hydrofluoric acid mixed solution, hydrochloric acid: hydrofluoric acid ratio is 1:2.5; The concentration of hydrochloric acid and hydrofluoric acid mixed solution is 1.1%;
(3)使用扩散炉管进行双面磷扩散,磷源采用的是POCl3温度为840℃,方阻要求为50ohm/sq;(3) Diffusion furnace tubes are used for double-sided phosphorus diffusion. The phosphorus source is POCl 3 with a temperature of 840°C and a square resistance requirement of 50ohm/sq;
(4)采用者激光的方法去除背面p+区域的PSG;(4) Using the laser method to remove the PSG in the p + region on the back;
(5)采用化学方法对背面p+区域进行抛光,抛光后去除PSG;(5) Chemically polish the p + region on the back, and remove PSG after polishing;
(6)采用等离子化学气相沉积的方法在扩散面制备80nm 厚的氮化硅薄膜,背面制备130nm厚的氮氧化硅薄膜;(6) Prepare a silicon nitride film with a thickness of 80nm on the diffusion surface by plasma chemical vapor deposition, and a silicon nitride oxide film with a thickness of 130nm on the back;
(7)制备电极区:(7) Prepare the electrode area:
a)开槽:采用激光开孔方法对发射极区域重新进行开槽,去除氮氧化硅层,开槽宽度为200μm,完成后进行化学清洗并烘干;a) Grooving: The emitter area is regrooved by laser drilling method to remove the silicon oxynitride layer. The groove width is 200 μm. After completion, chemical cleaning and drying are carried out;
b)采用丝网印刷的方法进行对准并在未开孔区域印刷银浆细栅;b) Align by screen printing and print a silver paste fine grid in the unopened area;
c)采用丝网印刷的方法进行对准并在开孔区域印刷烧穿型铝浆细栅;c) Align by screen printing and print a burn-through aluminum paste fine grid in the opening area;
d)采用丝网印刷的方法进行印刷主栅;d) printing the main grid by screen printing;
e)烧结。e) Sintering.
本发明为量产高效晶硅太阳能电池提供了一种新的生产模式理念,适用性及可操作性强,隐含着巨大的使用价值。The invention provides a new production mode concept for mass production of high-efficiency crystalline silicon solar cells, has strong applicability and operability, and implies huge use value.
以上述依据本发明的理想实施例为启示,通过上述的说明内容,相关工作人员完全可以在不偏离本项发明技术思想的范围内,进行多样的变更以及修改。本项发明的技术性范围并不局限于说明书上的内容,必须要根据权利要求范围来确定其技术性范围。Inspired by the above-mentioned ideal embodiment according to the present invention, through the above-mentioned description content, relevant workers can make various changes and modifications within the scope of not departing from the technical idea of the present invention. The technical scope of the present invention is not limited to the content in the specification, but must be determined according to the scope of the claims.
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| CN113328012B (en) * | 2021-06-24 | 2023-10-03 | 浙江爱旭太阳能科技有限公司 | Method for manufacturing PERC battery with reduced recombination rate and PERC battery |
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| CN203674224U (en) * | 2013-11-27 | 2014-06-25 | 奥特斯维能源(太仓)有限公司 | Aluminium emitting electrode back-junction-back contact crystalline silicon solar cell |
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