WO2020057264A1 - Photopile et procédé de préparation associé - Google Patents
Photopile et procédé de préparation associé Download PDFInfo
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- WO2020057264A1 WO2020057264A1 PCT/CN2019/098440 CN2019098440W WO2020057264A1 WO 2020057264 A1 WO2020057264 A1 WO 2020057264A1 CN 2019098440 W CN2019098440 W CN 2019098440W WO 2020057264 A1 WO2020057264 A1 WO 2020057264A1
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- silicon wafer
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- laser
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- 238000002360 preparation method Methods 0.000 title claims abstract description 11
- 238000000034 method Methods 0.000 claims abstract description 46
- 238000005498 polishing Methods 0.000 claims abstract description 28
- 238000002161 passivation Methods 0.000 claims abstract description 21
- 238000000137 annealing Methods 0.000 claims abstract description 19
- 238000000151 deposition Methods 0.000 claims abstract description 9
- 238000007639 printing Methods 0.000 claims abstract description 8
- 238000005245 sintering Methods 0.000 claims abstract description 4
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 90
- 229910052710 silicon Inorganic materials 0.000 claims description 89
- 239000010703 silicon Substances 0.000 claims description 89
- 239000000243 solution Substances 0.000 claims description 35
- 239000005360 phosphosilicate glass Substances 0.000 claims description 32
- 238000009792 diffusion process Methods 0.000 claims description 19
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 14
- 229910052698 phosphorus Inorganic materials 0.000 claims description 14
- 239000011574 phosphorus Substances 0.000 claims description 14
- 229910052782 aluminium Inorganic materials 0.000 claims description 10
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 10
- 239000002003 electrode paste Substances 0.000 claims description 9
- 238000004519 manufacturing process Methods 0.000 claims description 9
- 229910018072 Al 2 O 3 Inorganic materials 0.000 claims description 7
- 239000013585 weight reducing agent Substances 0.000 claims description 7
- 230000005684 electric field Effects 0.000 claims description 6
- 229910052581 Si3N4 Inorganic materials 0.000 claims description 4
- 239000003513 alkali Substances 0.000 claims description 4
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 claims description 4
- 238000005553 drilling Methods 0.000 claims description 3
- 239000012670 alkaline solution Substances 0.000 claims 1
- 238000001035 drying Methods 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 abstract description 18
- 238000002310 reflectometry Methods 0.000 abstract description 16
- 230000005540 biological transmission Effects 0.000 abstract description 4
- 238000002834 transmittance Methods 0.000 abstract description 3
- 235000012431 wafers Nutrition 0.000 description 75
- 238000005530 etching Methods 0.000 description 13
- 230000008569 process Effects 0.000 description 12
- 238000010304 firing Methods 0.000 description 9
- 239000002253 acid Substances 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 7
- 239000000654 additive Substances 0.000 description 6
- 238000005516 engineering process Methods 0.000 description 6
- 238000001039 wet etching Methods 0.000 description 5
- 230000000996 additive effect Effects 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 230000008021 deposition Effects 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 238000007517 polishing process Methods 0.000 description 4
- 238000010521 absorption reaction Methods 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000007650 screen-printing Methods 0.000 description 3
- 230000009286 beneficial effect Effects 0.000 description 2
- 238000000623 plasma-assisted chemical vapour deposition Methods 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 230000006798 recombination Effects 0.000 description 2
- 238000005215 recombination Methods 0.000 description 2
- 230000004580 weight loss Effects 0.000 description 2
- 101001073212 Arabidopsis thaliana Peroxidase 33 Proteins 0.000 description 1
- 101001123325 Homo sapiens Peroxisome proliferator-activated receptor gamma coactivator 1-beta Proteins 0.000 description 1
- 102100028961 Peroxisome proliferator-activated receptor gamma coactivator 1-beta Human genes 0.000 description 1
- 229910004205 SiNX Inorganic materials 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- HIVGXUNKSAJJDN-UHFFFAOYSA-N [Si].[P] Chemical compound [Si].[P] HIVGXUNKSAJJDN-UHFFFAOYSA-N 0.000 description 1
- XNRNVYYTHRPBDD-UHFFFAOYSA-N [Si][Ag] Chemical compound [Si][Ag] XNRNVYYTHRPBDD-UHFFFAOYSA-N 0.000 description 1
- 229910021419 crystalline silicon Inorganic materials 0.000 description 1
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 229910021421 monocrystalline silicon Inorganic materials 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L31/18—Processes or apparatus specially adapted for the manufacture or treatment of these devices or of parts thereof
- H01L31/1804—Processes or apparatus specially adapted for the manufacture or treatment of these devices or of parts thereof comprising only elements of Group IV of the Periodic Table
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L31/02—Details
- H01L31/0216—Coatings
- H01L31/02161—Coatings for devices characterised by at least one potential jump barrier or surface barrier
- H01L31/02167—Coatings for devices characterised by at least one potential jump barrier or surface barrier for solar cells
- H01L31/02168—Coatings for devices characterised by at least one potential jump barrier or surface barrier for solar cells the coatings being antireflective or having enhancing optical properties for the solar cells
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L31/04—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices
- H01L31/06—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices characterised by potential barriers
- H01L31/068—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices characterised by potential barriers the potential barriers being only of the PN homojunction type, e.g. bulk silicon PN homojunction solar cells or thin film polycrystalline silicon PN homojunction solar cells
- H01L31/0682—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices characterised by potential barriers the potential barriers being only of the PN homojunction type, e.g. bulk silicon PN homojunction solar cells or thin film polycrystalline silicon PN homojunction solar cells back-junction, i.e. rearside emitter, solar cells, e.g. interdigitated base-emitter regions back-junction cells
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L31/18—Processes or apparatus specially adapted for the manufacture or treatment of these devices or of parts thereof
- H01L31/186—Particular post-treatment for the devices, e.g. annealing, impurity gettering, short-circuit elimination, recrystallisation
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L31/18—Processes or apparatus specially adapted for the manufacture or treatment of these devices or of parts thereof
- H01L31/186—Particular post-treatment for the devices, e.g. annealing, impurity gettering, short-circuit elimination, recrystallisation
- H01L31/1868—Passivation
-
- 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
Definitions
- the invention relates to the field of crystalline silicon solar cells, in particular to a method for preparing a high-efficiency SE-PERC solar cell.
- SE-PERC solar cell is one of the most popular high-efficiency cells on the market. It combines frontal laser heavy doping technology (SE) and local contact back passivation technology (PERC), which greatly improves the efficiency of solar cells.
- SE-PERC solar cells include back electrode, back electric field, SiNx / Al 2 O 3 stack, P-type silicon, N ++ layer, N + layer, silicon oxide, silicon nitride, and positive electrode in order from bottom to top.
- the N ++ layer passes the front laser.
- One is the acid etching method, and the preparation process is: texturing-diffusion-front laser-acid etching polishing-de-PSG-annealing-back deposition Passivation film-deposition antireflection film-backside laser opening-back electrode, back electric field and positive electrode printing-firing annealing;
- the other is alkaline etching method, its preparation process is: texturing-diffusion-front laser-go PSG on the back-Alkaline etching polishing on the back-PSG on the front-Annealing-Passivation film on the back-Antireflection film on the front-Laser aperture on the back-Back electrode, back electric field and positive electrode printing-firing annealing.
- the method of etching polishing affects its efficiency; although the process of acid polishing is simple, its back reflectivity is low, the light transmission loss is large, and the conversion efficiency is low; The back reflectance has been improved, but the solar cell conversion efficiency has not been greatly improved, so it is necessary to improve the preparation method of the SE-PERC cell.
- a technical problem to be solved by the present invention is to provide a method for preparing a solar cell, which can effectively improve the back reflectivity of a solar cell without affecting the frontal square resistance, and effectively improve the conversion efficiency of the solar cell.
- a technical problem to be solved by the present invention is to provide a high-efficiency SE-PERC solar cell with high conversion efficiency.
- the present invention provides a method for preparing a solar cell.
- the method includes:
- the method may further include:
- step (12) The silicon wafer obtained in step (11) is fired at a high temperature to form a back electrode, an aluminum back electric field, and a positive electrode.
- a high-efficiency SE-PERC solar cell can be manufactured.
- the square resistance of the silicon wafer after phosphorus diffusion is 90-200 ⁇ / sq, especially 90-150 ⁇ / sq; in step (5), the square resistance of the silicon wafer heavily doped region
- the undoped region has a square resistance value of 25-75 ⁇ / sq, particularly 25-45 ⁇ / sq.
- the square resistance of the laser heavily doped region on the front surface of the silicon wafer after annealing is 60-100 ⁇ / sq, particularly 60-80 ⁇ / sq.
- step (4) the weight of the silicon wafer is reduced to 0.3-0.5 g; the reflectivity of the back surface of the silicon wafer after polishing is 30-55%.
- a HF solution is used to remove the phosphosilicate glass, and the mass concentration of the HF solution is 3-10%.
- the passivation film is an Al 2 O 3 / SiN x film; its thickness is 110-150 nm.
- the anti-reflection film is a silicon nitride film; its thickness is 65-80 nm; after the anti-reflection film is deposited, the front refractive index of the silicon wafer is 2-2.5.
- the porosity is 3-10%.
- the sintering temperature is 300-900 ° C.
- the present invention also discloses a high-efficiency SE-PERC solar cell, which is prepared by using the above preparation method.
- the invention is prepared through processes such as texturing, diffusion, back PSG removal, alkali polishing, front doping, PSG removal on the front, annealing, passivation film deposition, antireflection film deposition, back hole opening, electrode printing, and sintering annealing.
- a high conversion efficiency SE-PERC solar cell is implemented; the beneficial effects of implementing the present invention are as follows:
- the present invention effectively improves the reflectivity of the back surface of the solar cell through alkaline polishing on the back surface, which significantly reduces the long-wavelength transmittance, thereby reducing light transmission loss, increasing the current density Jsc, and thereby improving the conversion efficiency of the SE-PERC solar cell. .
- the present invention effectively prevents the problem of rising square resistance caused by loosening of the surface phosphorus in the traditional alkali polishing process, and prevents poor and low silver-silicon contact after electrode printing Battery conversion efficiency issues.
- the solar cell conversion efficiency can be improved to ⁇ 21.95%.
- the invention provides a method for preparing a high-efficiency SE-PERC solar cell.
- the method includes:
- wet etching is used to form a suede on both sides of the silicon wafer. Specifically, 800 pcs of single crystal silicon wafer is taken. Wet etching is used to form a suede with an inverted pyramid structure.
- the weight of the silicon wafer is reduced by 0.4-0.8g, preferably 0.5-0.7g; after texturing, the reflectivity of the silicon wafer is 9-13%, preferably 10-12%, and further preferably 9 -10%; Controlling the reflectivity of the silicon wafer after texturing is beneficial for controlling the solar cell's reflectivity to sunlight in the later stage, effectively increasing the solar cell's absorption of sunlight, and improving the solar cell's conversion efficiency.
- the square resistance of the silicon wafer after diffusion is 90-200 ⁇ / sq, preferably 90-150 ⁇ / sq, and further preferably 120-150 ⁇ / sq;
- the surface square resistance of the silicon wafer can reduce the surface doping concentration, which can not only improve the short-wave effect of the battery and increase the short-circuit current; but also reduce the dark saturation current caused by surface recombination and increase the open-circuit voltage; optimize battery performance.
- the phosphosilicate glass on the back of the wafer can be removed by using HCl solution, HNO 3 solution or HF solution; preferably, the phosphosilicate glass on the back of the wafer is removed by HF solution; in some embodiments, the mass concentration of the HF solution is 3% -10%.
- the HF solution can quickly remove the phosphosilicate glass on the back of the silicon wafer; preventing the reaction time from being too long and causing damage to the silicon wafer.
- the back surface of the silicon wafer may be polished by using KOH or NaOH solution containing additives; in some embodiments, the back surface of the silicon wafer is polished in a polishing tank containing a KOH (containing additive) solution; further preferably, the quality of the KOH solution
- the concentration is 5% -20%, and more preferably 10-20%.
- KOH solution has strong alkalinity, and the polishing effect is more obvious.
- the weight loss of the silicon wafer during polishing is 0.3-0.5 g; the reflectivity of the back surface of the silicon wafer after polishing is 30-55%, and more preferably 40-55%.
- Alkali polishing can effectively improve the reflectivity on the back of the silicon wafer, significantly reducing the long-wavelength transmittance, thereby reducing light transmission loss, increasing the current density Jsc, and thereby improving the conversion efficiency of the SE-PERC solar cell.
- the mixed solution of HF and HNO 3 is used to polish the back surface of the silicon wafer; however, the back reflectivity after polishing is low, generally lower than 30. %; Reduces the absorption of sunlight, reduces the current density, and reduces the conversion efficiency of solar cells.
- the invention adopts a KOH solution containing additives for polishing, which can effectively improve the reflectivity of the back surface of the solar cell.
- Tier laser is used for front-side doping; laser doping increases the doping concentration of the electrode region; reduces the ohmic contact between the silver paste and the silicon wafer, thereby increasing the fill factor; and improving the performance of the solar cell.
- the difference between the square resistance of the heavily doped region and the undoped region of the silicon wafer is 25-75 ⁇ / sq, preferably 25-45 ⁇ / sq, and more preferably 30- 45 ⁇ / sq; the square resistance of the heavily doped electrode region can improve the solar cell conversion efficiency within this range.
- the method for manufacturing a solar cell of the present disclosure may further include the following steps.
- the phosphosilicate glass on the front side of the wafer can be removed by using HCl solution, HNO 3 solution or HF solution; in some embodiments, the phosphosilicate glass on the front side of the wafer is removed by HF solution; the mass concentration of the HF solution is 3% -10%.
- the HF solution can quickly remove the phosphosilicate glass on the front surface of the silicon wafer; it prevents the wafer from being damaged due to the long reaction time.
- laser heavy doping uses phosphorus-silicon glass produced during the phosphorus diffusion process as a doping source, and the phosphorus in the phosphorus-silica glass layer is advanced to the depth of the silicon wafer by laser irradiation to form a heavy doping.
- Miscellaneous region that is, laser re-doping directly after phosphorus doping can ensure a higher concentration of the doping source, which can minimize the square resistance of the heavily doped region, improve the ohmic contact between the electrode and the substrate, and improve Solar cell conversion efficiency.
- the present invention adopts a completely different technical route.
- the process of removing phosphorous silicon glass on the back surface and polishing the back surface is carried out; then, the front surface is heavily doped with laser; Glass, which reduces the phosphorus source during the laser heavy doping process, is not good for improving the conversion efficiency of solar cells.
- the present invention overcomes this prejudice through research.
- the square resistance of the laser heavily doped region on the front side of the silicon wafer is 60-100 ⁇ / sq, particularly 60-80 ⁇ / sq;
- the polishing process is placed before the laser heavy doping process, which effectively prevents the problem of loose phosphorus on the surface of the laser heavily doped region during the traditional alkaline polishing process; it ensures the low square resistance of the heavily doped region; thereby improving ohmic contact; The conversion efficiency of solar cells.
- annealing is performed using hot oxygen; in some embodiments, the temperature after annealing is controlled at 500-800 ° C; preferably 500-600 ° C.
- the annealing process can effectively oxidize the silicon wafer and play a role of passivation, which can reduce the junction region recombination, increase the open circuit voltage, and improve the product yield.
- the passivation film is an Al 2 O 3 / SiN x film; the passivation film may be deposited using PECVD; in some embodiments, the deposition thickness is 110-150 nm.
- the passivation film can effectively reduce the back surface of the silicon wafer, increase the open circuit voltage, and improve the conversion efficiency of the solar cell.
- the anti-reflection film is a silicon nitride film; the anti-reflection film can be deposited by a PECVD method; in some embodiments, the thickness is 65-80 nm; the front side of the silicon wafer is refracted after the anti-reflection film is deposited The rate is 2-2.5; the front anti-reflection film can effectively improve the solar energy absorption rate and improve the conversion efficiency of solar cells.
- Dier laser is used to open the passivation film on the back surface, so that the aluminum and silicon form an ohmic contact, and the opening rate is controlled between 3% and 10%.
- step (12) The silicon wafer obtained in step (11) is fired at a high temperature to form a back electrode, an aluminum back electric field, and a positive electrode to obtain a high-efficiency SE-PERC solar cell finished product.
- the firing temperature is 300-900 ° C, preferably 300-600 ° C.
- Frontal laser use Dier laser for frontal doping, and decrease the square resistance of silicon wafer to 30 ⁇ / sq;
- Annealing use hot oxygen for annealing treatment and control the temperature at 500 °C;
- an Al 2 O 3 / SiN x film is deposited on the back surface, and the thickness of the passivation film is 110 nm;
- a SiN x film is deposited on the front side, the thickness of the anti-reflection film is controlled at 65 nm, and the refractive index is 2.05;
- Paste printing Back screen paste and aluminum paste are printed on the back of the silicon wafer by screen printing process; positive electrode paste is printed on the front side and dried;
- Frontal laser use Dier laser for frontal doping, and the square resistance drop of the silicon wafer is controlled to 45 ⁇ / sq;
- Annealing use hot oxygen for annealing treatment and control the temperature at 550 ° C;
- the SiN x film is deposited on the front side, the thickness of the antireflection film is controlled at 80 nm, and the refractive index is 2.11;
- Paste printing Back screen paste and aluminum paste are printed on the back of the silicon wafer by screen printing process; positive electrode paste is printed on the front side and dried;
- Frontal laser use Dier laser for frontal doping, and the square resistance drop of the silicon wafer is controlled to 45 ⁇ / sq;
- Annealing use hot oxygen for annealing treatment and control the temperature at 550 ° C;
- an Al 2 O 3 / SiN x film is deposited on the back surface, and the thickness of the passivation film is 135 nm;
- a SiN x film is deposited on the front side, the thickness of the anti-reflection film is controlled at 80 nm, and the refractive index is 2.15;
- (10) Backside laser use Dir laser to open the passivation film on the back side, and the opening rate is controlled to 3.5%;
- Paste printing Back screen paste and aluminum paste are printed on the back of the silicon wafer by screen printing process; positive electrode paste is printed on the front side and dried;
- the SE-PERC solar cell efficiency in the present invention is above 21%. Compared with traditional SE-PERC solar cells, the efficiency has been significantly improved.
- step (1) and step (2) are the same as Embodiment 3 of the present invention; step (3) is the same as step (5) of Embodiment 3 of the present invention; step (4) is Use HF / HNO 3 solution (ratio 1: 2) to perform acid etching polishing and PSG removal on silicon wafers.
- the weight loss of the etching is controlled to 0.35g, and the reflectance is controlled to 20% -30%.
- Step (5)- Step (11) is the same as step (6) -step (12) of Embodiment 3 of the present invention.
- step (1) and step (2) are the same as the embodiment 3 of the present invention
- step (3) is the same as the step (5) of the embodiment 3
- Steps (3) and (4) in Embodiment 3 of the present invention are respectively the same
- Steps (6)-(12) are the same as Steps (6)-(12) in Embodiment 3 of the present invention.
- Example 3 500 solar cells in Example 3, Comparative Example 1, and Comparative Example 2 were produced and tested for performance.
- the test results are shown in Table 2.
- Table 2 As can be seen from Table 2, compared with the traditional preparation method, the preparation method of the present invention can effectively improve the efficiency of the solar cell, and its gain can reach 0.8-1%.
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Abstract
La présente invention concerne une photopile et un procédé de préparation associé. Le procédé comprend des étapes de texturation, de diffusion, d'élimination du PSG sur le côté arrière, de polissage alcalin, de dopage lourd sur le côté avant, de retrait du PSG sur le côté avant, de recuit, de dépôt d'un film de passivation, de dépôt d'un film antireflet, de perforation sur le côté arrière, d'impression, de frittage et de recuit d'électrode. La réflectivité côté arrière de la photopile est efficacement réduite par polissage alcalin sur le côté arrière, de telle sorte que la transmittance dans une bande de longueur d'onde est considérablement réduite, ce qui permet de réduire la perte de transmission de lumière et d'augmenter une densité de courant électrique Jsc, puis d'améliorer l'efficacité de conversion d'une photopile SE-PERC.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201811080648.9A CN109449248A (zh) | 2018-09-17 | 2018-09-17 | 一种高效率se-perc太阳能电池的制备方法 |
CN201811080648.9 | 2018-09-17 |
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WO2020057264A1 true WO2020057264A1 (fr) | 2020-03-26 |
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PCT/CN2019/098440 WO2020057264A1 (fr) | 2018-09-17 | 2019-07-30 | Photopile et procédé de préparation associé |
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WO (1) | WO2020057264A1 (fr) |
Cited By (2)
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