CN111564530B - Novel crystalline silicon PERC battery front oxide layer preparation process - Google Patents
Novel crystalline silicon PERC battery front oxide layer preparation process Download PDFInfo
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- 238000002360 preparation method Methods 0.000 title claims abstract description 40
- 101001073212 Arabidopsis thaliana Peroxidase 33 Proteins 0.000 title claims abstract description 14
- 101001123325 Homo sapiens Peroxisome proliferator-activated receptor gamma coactivator 1-beta Proteins 0.000 title claims abstract description 14
- 102100028961 Peroxisome proliferator-activated receptor gamma coactivator 1-beta Human genes 0.000 title claims abstract description 14
- 229910021419 crystalline silicon Inorganic materials 0.000 title claims abstract description 13
- 238000000034 method Methods 0.000 claims abstract description 27
- 229910052581 Si3N4 Inorganic materials 0.000 claims abstract description 18
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 claims abstract description 18
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 claims abstract description 18
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 16
- 238000000623 plasma-assisted chemical vapour deposition Methods 0.000 claims abstract description 16
- 229910052814 silicon oxide Inorganic materials 0.000 claims abstract description 16
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims abstract description 15
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 15
- 239000010703 silicon Substances 0.000 claims abstract description 15
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims abstract description 13
- 238000005530 etching Methods 0.000 claims abstract description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 9
- 210000004027 cell Anatomy 0.000 claims abstract description 8
- 238000004140 cleaning Methods 0.000 claims abstract description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 3
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 3
- 239000007789 gas Substances 0.000 claims abstract description 3
- 229910002804 graphite Inorganic materials 0.000 claims abstract description 3
- 239000010439 graphite Substances 0.000 claims abstract description 3
- 210000002381 plasma Anatomy 0.000 claims abstract description 3
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 6
- 238000010926 purge Methods 0.000 claims description 6
- 230000035484 reaction time Effects 0.000 claims description 6
- 238000002161 passivation Methods 0.000 abstract description 6
- 238000009792 diffusion process Methods 0.000 abstract description 3
- 230000003647 oxidation Effects 0.000 description 7
- 238000007254 oxidation reaction Methods 0.000 description 7
- 239000000758 substrate Substances 0.000 description 4
- 229910017107 AlOx Inorganic materials 0.000 description 3
- 239000003513 alkali Substances 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 238000002310 reflectometry Methods 0.000 description 2
- 230000003685 thermal hair damage Effects 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000006388 chemical passivation reaction Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000010849 ion bombardment Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000001465 metallisation Methods 0.000 description 1
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- 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
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- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
- C23C16/22—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the deposition of inorganic material, other than metallic material
- C23C16/30—Deposition of compounds, mixtures or solid solutions, e.g. borides, carbides, nitrides
- C23C16/34—Nitrides
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- C23C16/455—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating characterised by the method used for introducing gases into reaction chamber or for modifying gas flows in reaction chamber
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- C23C16/45525—Atomic layer deposition [ALD]
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Abstract
The invention relates to the field of crystalline silicon PERC battery passivation. A novel crystalline silicon PERC cell front oxide layer preparation process is carried out according to the process procedures of cleaning and texturing, diffusion and junction making, back etching, double-sided aluminum oxide preparation, front silicon nitride film preparation, back laser grooving and front and back electrode preparation; in the preparation process of the double-sided aluminum oxide, a silicon wafer is inserted into an aluminum flower basket, TMA and water vapor are circularly introduced, and a layer of 3-5nm aluminum oxide film is respectively prepared on the front surface and the back surface of the silicon wafer; in the preparation process of the front silicon nitride film, a silicon wafer with double-sided alumina is put into a graphite boat, silicon nitride is prepared in a tubular PECVD (plasma enhanced chemical vapor deposition), NH3 and N2 gases are introduced, a radio frequency source is switched on, the front alumina film layer is knocked off by high-energy plasmas, and meanwhile, a silicon oxide layer is formed.
Description
Technical Field
The invention relates to the field of crystalline silicon PERC battery passivation.
Background
At present, the passivation of the front surface of the PERC cell uses a silicon oxide passivation technology, the back surface uses aluminum oxide as a basic passivation film, in the specific preparation process, the front silicon oxide layer is realized by thermal oxidation, the back aluminum oxide is deposited by ALD and PECVD methods, the preparation of the front silicon oxide layer and the preparation of the back aluminum oxide layer are independently carried out, the equipment cost is high, and in the thermal oxidation process of the front silicon oxide layer, the thermal damage of the silicon substrate caused by high temperature is serious.
Disclosure of Invention
The technical problem to be solved by the invention is as follows: how to avoid the thermal oxidation process in the preparation process of the front silicon oxide layer and avoid the thermal damage of the silicon substrate caused by the high-temperature process.
The technical scheme adopted by the invention is as follows: a novel crystalline silicon PERC cell front oxide layer preparation process is carried out according to the process procedures of cleaning and texturing, diffusion and junction making, back etching, double-sided aluminum oxide preparation, front silicon nitride film preparation, back laser grooving and front and back electrode preparation; in the preparation process of the double-sided aluminum oxide, a silicon wafer is inserted into an aluminum flower basket, TMA and water vapor are circularly introduced, and a layer of 3-5nm aluminum oxide film is respectively prepared on the front surface and the back surface of the silicon wafer; in the preparation process of the front silicon nitride film, a silicon wafer with double-sided alumina is put into a graphite boat, silicon nitride is prepared in a tubular PECVD (plasma enhanced chemical vapor deposition), NH3 and N2 gases are introduced, a radio frequency source is switched on, the front alumina film layer is knocked off by high-energy plasmas, and meanwhile, a silicon oxide layer is formed.
The specific process of the double-sided alumina preparation process comprises the following steps: preparing a double-sided alumina film layer with the thickness of 3-5nm and the refractive index of 1.6-1.65 by using ALD equipment, wherein TMA and H2O are periodically introduced in the preparation process, the TMA introduction flow rate is 15-20sccm, the reaction time is 2.5-3.5s, and the purging time is 6-8 s; H2O was introduced at a flow rate of 15-20sccm for 32 cycles with a reaction time of 2.5-3.5s and a purge time of 10-15 s.
The specific process of the front silicon nitride film preparation process comprises the following steps: preparing silicon nitride in a tubular PECVD (plasma enhanced chemical vapor deposition), firstly performing pretreatment, and introducing NH3 and N2, wherein the pressure in the tube is 2000-2500mTorr, the temperature is 400-450 ℃, the power is 12000-14000W, the pulse on-off ratio is 1:10, NH3/N2= 1: 1-3: 1, and the time is 180-250 s; then NH3 and SiH4 are introduced, the pressure is 1000-2000mTorr, the temperature is 450-500 ℃, the power is 11000-13000W, the pulse on-off ratio is 1:12, the introduced SiH4/NH3 = 1/4-1/10, and the time is 550-650 s.
The invention has the beneficial effects that: the process technology for preparing the crystalline silicon PERC cell not only reduces the conventional PERC preparation process and the manufacturing cost, but also improves the performance of the crystalline silicon cell. In the preparation process of the aluminum oxide, the chemical passivation effect of the silicon oxide formed on the surface of the silicon substrate is far better than that of the silicon oxide prepared by thermal oxidation. The invention utilizes the characteristics and adopts the process technology for preparing the double-sided aluminum oxide to simultaneously realize the passivation of the SiOx and the AlOx on the front surface and the back surface of the battery through one procedure. The method has the advantages of low cost and simple process, avoids damage of high-temperature thermal oxidation to the silicon wafer, and solves the problem that metal burning-through is difficult in the metallization process of the front surface aluminum oxide. Most importantly, the front oxide layer formed by AlOx preparation has an order of magnitude lower surface defect density than a thermally oxidized silicon oxide layer.
Detailed Description
The front surface of the battery of the embodiment is sequentially provided with a silicon oxide layer, a silicon nitride layer and a positive electrode; the back surface is sequentially provided with an aluminum oxide layer, a silicon nitride layer and a back electrode.
In the invention, silicon oxide on the front surface of the crystalline silicon PERC cell is formed by using positive PECVD ion bombardment after double-sided aluminum oxide deposition. The preparation method comprises the following steps:
cleaning and texturing by adopting the prior process. The texture etching uses alkali texture etching, the etching amount is controlled to be 0.4-0.6g, and the reflectivity is 7% -12%.
And (4) diffusion and junction making by adopting the existing process.
And etching by adopting the existing process. And (3) using alkali etching, wherein the etching amount is controlled to be 0.14-0.17g, and the reflectivity is 35% -45%.
And (3) preparing double-sided alumina. And preparing a double-sided aluminum oxide film layer with the thickness of 3-5nm and the refractive index of 1.6-1.65 by using ALD equipment. In the preparation process, TMA and H2O are periodically introduced, wherein the TMA introduction flow is 15-20sccm, the reaction time is 2.5-3.5s, and the purging time is 6-8 s; H2O was introduced at a flow rate of 15-20sccm for 32 cycles with a reaction time of 2.5-3.5s and a purge time of 10-15 s.
And preparing a front silicon nitride film. Preparing silicon nitride in a tubular PECVD (plasma enhanced chemical vapor deposition), firstly performing pretreatment, and introducing NH3 and N2, wherein the pressure in the tube is 2000-2500mTorr, the temperature is 400-450 ℃, the power is 12000-14000W, the pulse on-off ratio is 1:10, NH3/N2= 1: 1-3: 1, and the time is 180-250 s; then NH3 and SiH4 are introduced, the pressure is 1000-2000mTorr, the temperature is 450-500 ℃, the power is 11000-13000W, the pulse on-off ratio is 1:12, the introduced SiH4/NH3 = 1/4-1/10, and the time is 550-650 s.
The preparation of the back silicon nitride film adopts the prior art.
And (3) laser film opening is carried out on the back surface, and the existing process is adopted.
The front and back electrodes are prepared by the existing process.
The invention provides a novel preparation process of a front oxide layer of a crystalline silicon PERC battery, which is characterized in that an etched silicon wafer is subjected to double-sided alumina preparation, then a front surface alumina layer is removed through pretreatment of positive PECVD (plasma enhanced chemical vapor deposition), and a silicon oxide layer in contact with a silicon substrate is reserved. The preparation process has the advantages of simple process, low cost and excellent battery performance. The front oxidation layer formed by AlOx preparation is higher than the silicon oxide layer grown by thermal oxidation, the surface defect density is lower by one order of magnitude, and the conversion efficiency of the battery is improved by nearly 0.3 percent.
Claims (3)
1. A novel crystalline silicon PERC battery front oxide layer preparation process is characterized in that: the method comprises the following steps of cleaning and texturing, diffusing and knotting, back etching, double-sided aluminum oxide preparation, front silicon nitride film preparation, back laser grooving and front and back electrode preparation; in the preparation process of the double-sided aluminum oxide, a silicon wafer is inserted into an aluminum flower basket, TMA and water vapor are circularly introduced, and a layer of 3-5nm aluminum oxide film is respectively prepared on the front surface and the back surface of the silicon wafer; in the preparation process of the front silicon nitride film, a silicon wafer with double-sided alumina is put into a graphite boat, silicon nitride is prepared in a tubular PECVD (plasma enhanced chemical vapor deposition), NH3 and N2 gases are introduced, a radio frequency source is switched on, the front alumina film layer is knocked off by high-energy plasmas, and meanwhile, a silicon oxide layer is formed.
2. The process of claim 1 for preparing a novel crystalline silicon PERC cell pre-oxide layer, wherein: the specific process of the double-sided alumina preparation process comprises the following steps: preparing a double-sided alumina film layer with the thickness of 3-5nm and the refractive index of 1.6-1.65 by using ALD equipment, wherein TMA and H2O are periodically introduced in the preparation process, the TMA introduction flow rate is 15-20sccm, the reaction time is 2.5-3.5s, and the purging time is 6-8 s; H2O was introduced at a flow rate of 15-20sccm for 32 cycles with a reaction time of 2.5-3.5s and a purge time of 10-15 s.
3. The process of claim 1 for preparing a novel crystalline silicon PERC cell pre-oxide layer, wherein: the specific process of the front silicon nitride film preparation process comprises the following steps: preparing silicon nitride in a tubular PECVD (plasma enhanced chemical vapor deposition), firstly performing pretreatment, and introducing NH3 and N2, wherein the pressure in the tube is 2000-2500mTorr, the temperature is 400-450 ℃, the power is 12000-14000W, the pulse on-off ratio is 1:10, NH3/N2= 1: 1-3: 1, and the time is 180-250 s; then NH3 and SiH4 are introduced, the pressure is 1000-2000mTorr, the temperature is 450-500 ℃, the power is 11000-13000W, the pulse on-off ratio is 1:12, the introduced SiH4/NH3 = 1/4-1/10, and the time is 550-650 s.
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