CN103746008A - Antireflection layer for solar cell and preparing process of antireflection layer - Google Patents
Antireflection layer for solar cell and preparing process of antireflection layer Download PDFInfo
- Publication number
- CN103746008A CN103746008A CN201410031087.9A CN201410031087A CN103746008A CN 103746008 A CN103746008 A CN 103746008A CN 201410031087 A CN201410031087 A CN 201410031087A CN 103746008 A CN103746008 A CN 103746008A
- Authority
- CN
- China
- Prior art keywords
- layer
- reflection layer
- antireflection layer
- reflection
- solar cell
- 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
- 238000000034 method Methods 0.000 title claims abstract description 17
- CMIHHWBVHJVIGI-UHFFFAOYSA-N gadolinium(III) oxide Inorganic materials [O-2].[O-2].[O-2].[Gd+3].[Gd+3] CMIHHWBVHJVIGI-UHFFFAOYSA-N 0.000 claims abstract description 29
- 238000000137 annealing Methods 0.000 claims abstract description 22
- 238000009792 diffusion process Methods 0.000 claims abstract description 18
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 10
- 238000000151 deposition Methods 0.000 claims abstract description 8
- 238000005229 chemical vapour deposition Methods 0.000 claims abstract description 6
- 235000012239 silicon dioxide Nutrition 0.000 claims abstract description 5
- 239000000377 silicon dioxide Substances 0.000 claims abstract description 5
- 229910052681 coesite Inorganic materials 0.000 claims abstract description 4
- 229910052906 cristobalite Inorganic materials 0.000 claims abstract description 4
- 229910052682 stishovite Inorganic materials 0.000 claims abstract description 4
- 229910052905 tridymite Inorganic materials 0.000 claims abstract description 4
- 229940075613 gadolinium oxide Drugs 0.000 claims description 26
- 229910001938 gadolinium oxide Inorganic materials 0.000 claims description 26
- 229910021419 crystalline silicon Inorganic materials 0.000 claims description 23
- 229910004298 SiO 2 Inorganic materials 0.000 claims description 15
- 238000002360 preparation method Methods 0.000 claims description 15
- 239000007789 gas Substances 0.000 claims description 11
- 238000004519 manufacturing process Methods 0.000 claims description 8
- 238000006243 chemical reaction Methods 0.000 claims description 6
- 239000011261 inert gas Substances 0.000 claims description 6
- 230000001590 oxidative effect Effects 0.000 claims description 6
- 238000005554 pickling Methods 0.000 claims description 5
- 229910052688 Gadolinium Inorganic materials 0.000 claims description 4
- 230000008021 deposition Effects 0.000 claims description 4
- 238000001704 evaporation Methods 0.000 claims description 4
- 230000008020 evaporation Effects 0.000 claims description 4
- 239000002243 precursor Substances 0.000 claims description 4
- 239000012159 carrier gas Substances 0.000 claims description 3
- UIWYJDYFSGRHKR-UHFFFAOYSA-N gadolinium atom Chemical compound [Gd] UIWYJDYFSGRHKR-UHFFFAOYSA-N 0.000 claims description 3
- 229910052757 nitrogen Inorganic materials 0.000 claims description 3
- 150000002902 organometallic compounds Chemical class 0.000 claims description 3
- 229910021421 monocrystalline silicon Inorganic materials 0.000 claims description 2
- 229910021420 polycrystalline silicon Inorganic materials 0.000 claims description 2
- 239000000126 substance Substances 0.000 claims description 2
- 239000012808 vapor phase Substances 0.000 claims 1
- 229910052710 silicon Inorganic materials 0.000 abstract description 4
- 239000010703 silicon Substances 0.000 abstract description 3
- 238000002488 metal-organic chemical vapour deposition Methods 0.000 description 10
- 239000000463 material Substances 0.000 description 9
- 239000000758 substrate Substances 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 4
- 229910052698 phosphorus Inorganic materials 0.000 description 4
- 239000011574 phosphorus Substances 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 3
- 230000005684 electric field Effects 0.000 description 3
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- 229910010413 TiO 2 Inorganic materials 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 238000005530 etching Methods 0.000 description 2
- 230000031700 light absorption Effects 0.000 description 2
- CUJRVFIICFDLGR-UHFFFAOYSA-N acetylacetonate Chemical compound CC(=O)[CH-]C(C)=O CUJRVFIICFDLGR-UHFFFAOYSA-N 0.000 description 1
- 125000005595 acetylacetonate group Chemical group 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- -1 etching Chemical compound 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000005693 optoelectronics Effects 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10F—INORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
- H10F77/00—Constructional details of devices covered by this subclass
- H10F77/30—Coatings
- H10F77/306—Coatings for devices having potential barriers
- H10F77/311—Coatings for devices having potential barriers for photovoltaic cells
- H10F77/315—Coatings for devices having potential barriers for photovoltaic cells the coatings being antireflective or having enhancing optical properties
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10F—INORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
- H10F71/00—Manufacture or treatment of devices covered by this subclass
- H10F71/121—The active layers comprising only Group IV materials
-
- 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
Description
技术领域 technical field
本发明属于半导体领域,尤其涉及光电类材料的应用领域,具体涉及一种减反射层及其制备工艺。 The present invention belongs to the field of semiconductors, in particular to the application field of optoelectronic materials, and in particular to an anti-reflection layer and its preparation process.
背景技术 Background technique
减反射层对于太阳能电池非常重要,它可以通过减少太阳能电池反射光来增加太阳能电池光吸收,提高太阳能电池的短路电流,从而提高太阳能电池的光电转换效率。而传统的减反射材料存在着难以克服的缺陷,如SiO2、MgF2等减反射材料折射率太低,而TiO2禁带宽度太窄,寻求一种高性能的减反射材料成为目前光伏产业研究的热点。 The anti-reflection layer is very important for solar cells. It can increase the light absorption of solar cells by reducing the reflected light of solar cells, increase the short-circuit current of solar cells, and thus improve the photoelectric conversion efficiency of solar cells. However, traditional anti-reflection materials have insurmountable defects, such as SiO 2 , MgF 2 and other anti-reflection materials whose refractive index is too low, and the band gap of TiO 2 is too narrow. Seeking a high-performance anti-reflection material has become the current photovoltaic industry research hotspot.
发明内容 Contents of the invention
本发明的目的在于提供一种太阳能电池的减反射层,该减反射层采用新的减反射材料,该减反射材料具有与Si晶格失配率低、禁带宽度大、折射率高、稳定性好等优点,可用于取代传统的SiO2、MgF2、 TiO2等减反射材料,本发明同时提供该减反射层的制备工艺。 The object of the present invention is to provide a kind of anti-reflection layer of solar cell, and this anti-reflection layer adopts new anti-reflection material, and this anti-reflection material has low lattice mismatch ratio with Si, wide band gap, high refractive index, stable It can be used to replace traditional anti-reflection materials such as SiO 2 , MgF 2 , TiO 2 , etc., and the invention also provides a preparation process for the anti-reflection layer.
为实现本发明的上述目的所采用的技术方案是:一种太阳能电池用减反射层,其特征是该减反射层是由氧化钆(Gd2O3)构成。 The technical solution adopted to achieve the above object of the present invention is: an anti-reflection layer for solar cells, characterized in that the anti-reflection layer is made of gadolinium oxide (Gd 2 O 3 ).
本发明的减反射层可应用于单晶硅、多晶硅太阳能电池的减反层中。 The anti-reflection layer of the invention can be applied to the anti-reflection layer of monocrystalline silicon and polycrystalline silicon solar cells.
上述太阳能电池用减反射层的制备工艺,其特征是在P型晶体硅的制作中,当P型晶体硅完成HF酸酸洗工序后,采用有机化学气相沉积方法(MOCVD)在N型扩散层上沉积氧化钆减反射层,并进行退火处理,在减反射层与N型扩散层之间形成SiO2缓冲层,完成减反射层的制备。 The preparation process of the above-mentioned antireflection layer for solar cells is characterized in that in the production of P-type crystalline silicon, after the P-type crystalline silicon has completed the HF acid pickling process, organic chemical vapor deposition (MOCVD) is used on the N-type diffusion layer An anti-reflection layer of gadolinium oxide is deposited on it, and annealing is performed to form a SiO 2 buffer layer between the anti-reflection layer and the N-type diffusion layer to complete the preparation of the anti-reflection layer.
所沉积的氧化钆减反射层的最佳厚度为70~140nm。 The optimum thickness of the deposited gadolinium oxide antireflection layer is 70-140nm.
在氧化钆的MOCVD沉积方法中,前驱体为钆的有机金属化合物,腔室的反应温度为300~700℃,沉积时间为15~30min,蒸发温度为100~250℃,压力为2~10mbar,载气为Ar和O2的混合气体。 In the MOCVD deposition method of gadolinium oxide, the precursor is an organometallic compound of gadolinium, the reaction temperature of the chamber is 300-700°C, the deposition time is 15-30min, the evaporation temperature is 100-250°C, and the pressure is 2-10mbar. The carrier gas is a mixed gas of Ar and O2 .
所述的退火处理形成SiO2缓冲层的工艺为:将沉积有氧化钆减反射层的电池片放入通有惰性气体或氧化气体的退火炉中,控制退火温度为300~800℃,退火时间为0.5~4小时,在减反射层与N型扩散层之间形成1nm 左右的SiO2薄层(缓冲层)。 The annealing process to form the SiO2 buffer layer is as follows: put the battery sheet deposited with the gadolinium oxide anti-reflection layer into an annealing furnace with an inert gas or an oxidizing gas, control the annealing temperature to 300-800°C, and the annealing time For 0.5 to 4 hours, a thin SiO 2 layer (buffer layer) of about 1 nm is formed between the anti-reflection layer and the N-type diffusion layer.
所述的惰性气体或氧化气体为Ar、N2、N2O或H2中的任一种。 The inert gas or oxidizing gas is any one of Ar, N 2 , N 2 O or H 2 .
本发明的上述技术方案中,在P型晶体硅的制作过程中,当经过P型晶体硅衬底清洗、制绒、扩散磷、边缘刻蚀、HF酸洗剂洗涤后,采用有机化学气相沉积方法(MOCVD)在晶硅片上沉积氧化钆减反射层,并进行退火处理,在减反射层与N型扩散层之间形成SiO2缓冲层,完成减反射层的制备,然后进行电极以及电场的制作,完成晶硅电池的制备。 In the above-mentioned technical scheme of the present invention, in the production process of P-type crystalline silicon, after cleaning the P-type crystalline silicon substrate, texturizing, diffusing phosphorus, edge etching, and HF pickling agent washing, organic chemical vapor deposition is used to Method (MOCVD) Deposit gadolinium oxide anti-reflection layer on the crystalline silicon wafer, and perform annealing treatment, form a SiO 2 buffer layer between the anti-reflection layer and the N-type diffusion layer, complete the preparation of the anti-reflection layer, and then perform electrode and electric field The fabrication of crystalline silicon cells is completed.
Gd2O3常温下与Si一样,都呈立方相结构,其介电常数较高,K(Gd2O3) =14~22,与Si有非常近的晶格匹配常数(a(Gd2O3)=10.812A;2a(Si)=10.862A),晶格失配率很低,可以在Si上生长出高质量的薄膜, Gd2O3有较高的热力学稳定性(>1000℃)、较大的带隙宽度(5.9ev)以及较高的折射率(1.9),是制备减反射层的理想材料。 Gd 2 O 3 has the same cubic phase structure as Si at room temperature, and its dielectric constant is high, K(Gd 2 O 3 ) =14~22, and it has a very close lattice matching constant with Si (a(Gd 2 O 3 )=10.812A; 2a(Si)=10.862A), the lattice mismatch rate is very low, high-quality films can be grown on Si, and Gd 2 O 3 has high thermodynamic stability (>1000℃ ), large bandgap width (5.9ev) and high refractive index (1.9), it is an ideal material for preparing anti-reflection layer.
本发明将氧化钆做为制备太阳能电池的减反射层的减反射材料,在太阳能电池的制作中,首先在P型硅HF酸洗剂洗涤后沉积氧化钆减反射层,然后在惰性气体保护环境或氧化气体保护环境下进行退火处理,在减反射层和晶硅电池之间生成了SiO2缓冲层。氧化钆减反射层由MOCVD方法制备,获得的减反射层与晶硅衬底晶格匹配性好,缺陷密度低、折射率高、热稳定性能好、禁带宽度大,保证了电池的减反射效果。 The present invention uses gadolinium oxide as the anti-reflection material for the anti-reflection layer of the solar cell. In the manufacture of the solar cell, the gadolinium oxide anti-reflection layer is first deposited after being washed with P-type silicon HF pickling agent, and then the anti-reflection layer is deposited in an inert gas protection environment. Or annealing treatment is carried out under the protection environment of oxidizing gas, and a SiO 2 buffer layer is formed between the anti-reflection layer and the crystalline silicon cell. The gadolinium oxide anti-reflection layer is prepared by MOCVD. The obtained anti-reflection layer has good lattice matching with the crystalline silicon substrate, low defect density, high refractive index, good thermal stability, and large forbidden band width, which ensures the anti-reflection of the battery Effect.
附图说明 Description of drawings
图1为含有氧化钆减反射层的P型晶体硅太阳能电池的结构示意图; Fig. 1 is the structural representation of the P-type crystalline silicon solar cell that contains gadolinium oxide anti-reflection layer;
图2为含有氧化钆减反射层的P型晶体硅太阳能电池制备流程图。 Fig. 2 is a flow chart of the preparation of a P-type crystalline silicon solar cell containing a gadolinium oxide anti-reflection layer.
具体实施方式 Detailed ways
下面结合附图和具体实施的例子对本发明做进一步详细的描述,然而所述的实施例不应以限制的方式解释。 The present invention will be described in further detail below in conjunction with the accompanying drawings and specific implementation examples, but the described embodiments should not be interpreted in a limiting manner.
本发明的太阳能电池的减反射层及其制备工艺,是在P型晶体硅完成HF酸洗剂工序后,采用有机化学气相沉积(MOCVD)方法沉积氧化钆减反射层。在氧化钆MOCVD沉积方法中,前驱体为钆的有机金属化合物,腔室的反应温度为300~700℃,沉积时间为15~30min,蒸发温度为100~250℃,压力为2~10mbar,载气为Ar和O2的混合气体。然后进行退火处理形成SiO2缓冲层,完成减反射层的制备。退火处理形成SiO2缓冲层的工艺为:将沉积有氧化钆-氧化铝减反射层的电池片放入通有惰性气体或氧化气体的退火炉中,控制退火温度为300~800℃,退火时间为0.5~4小时,在减反射层与N型扩散层之间形成1nm 左右的SiO2缓冲层。 The anti-reflection layer of the solar cell and its preparation process of the present invention is to deposit the anti-reflection layer of gadolinium oxide by organic chemical vapor deposition (MOCVD) after the HF pickling agent process is completed on the P-type crystalline silicon. In the MOCVD deposition method of gadolinium oxide, the precursor is an organometallic compound of gadolinium, the reaction temperature of the chamber is 300-700°C, the deposition time is 15-30min, the evaporation temperature is 100-250°C, and the pressure is 2-10mbar. The gas is a mixed gas of Ar and O2 . Then perform an annealing treatment to form a SiO 2 buffer layer to complete the preparation of the anti-reflection layer. The annealing process to form the SiO2 buffer layer is as follows: put the battery sheet deposited with the gadolinia-alumina anti-reflection layer into an annealing furnace with an inert gas or an oxidizing gas, control the annealing temperature to 300-800°C, and the annealing time For 0.5 to 4 hours, a SiO 2 buffer layer of about 1 nm is formed between the anti-reflection layer and the N-type diffusion layer.
具体实施例如下: Specific examples are as follows:
从图2给出的含有氧化钆减反射层的P型晶体硅太阳能电池制备流程图中可以看出,其制备P型晶体硅太阳能电池的流程如下: It can be seen from the flow chart of the preparation of a P-type crystalline silicon solar cell containing a gadolinium oxide anti-reflection layer given in Figure 2 that the process for preparing a P-type crystalline silicon solar cell is as follows:
a、使用HF和HC1对P型晶体硅衬底进行清洗制绒,以便去除机械损伤层、油污以及金属杂质,同时在表面形成起伏不平的绒面,以便增加表面积进而增加光吸收;然后将P型晶硅衬底放入扩散室内,通入磷源,使磷元素扩散进入P型晶硅表面,形成N层,即形成PN结;然后使用HNO3和HF的混合液体进行周边刻蚀,去掉边缘沉积的N层,以便使电池片与外界绝缘;然后去磷硅玻璃,即用HF洗掉扩散过程中形成的二氧化硅等物质。以上为太阳能电池制备过程中的常规工艺,在此不做赘述。 a. Use HF and HC1 to clean and texture the P-type crystalline silicon substrate in order to remove the mechanical damage layer, oil stains and metal impurities, and at the same time form an uneven texture on the surface to increase the surface area and increase light absorption; then P Type crystalline silicon substrate is placed in the diffusion chamber, and a phosphorus source is introduced to diffuse phosphorus into the surface of P-type crystalline silicon to form an N layer, that is, a PN junction; then use a mixed liquid of HNO 3 and HF to perform peripheral etching to remove The N layer deposited on the edge in order to insulate the battery sheet from the outside world; then the phosphorous silicon glass is removed, that is, the silicon dioxide and other substances formed during the diffusion process are washed away with HF. The above is the conventional process in the solar cell manufacturing process, which will not be repeated here.
b、完成以上步骤后,将P型晶硅电池片迅速放入MOCVD反应腔室中,在N型扩散层一侧的N型扩散层上用MOCVD方法沉积氧化钆减反射层,其厚度控制在70~140nm范围内,在氧化钆减反射层的制备工艺中,前驱体为乙酰丙酮釓Gd(acac)3,腔室的反应温度为300~700℃,沉积时间为15~30min,蒸发温度为100~250℃,压力为2~10mbar,载气为Ar和O2的混合气体。 b. After completing the above steps, quickly put the P-type crystalline silicon cell into the MOCVD reaction chamber, and deposit a gadolinium oxide anti-reflection layer on the N-type diffusion layer on the side of the N-type diffusion layer by MOCVD, and its thickness is controlled at In the range of 70-140nm, in the preparation process of gadolinium oxide anti-reflection layer, the precursor is acetylacetonate Gd(acac) 3 , the reaction temperature of the chamber is 300-700°C, the deposition time is 15-30min, and the evaporation temperature is 100~250℃, the pressure is 2~10mbar, the carrier gas is the mixed gas of Ar and O2 .
c、沉积完氧化钆减反射层之后,进行退火处理,在减反射层与N型扩散层之间生成SiO2缓冲层。将电池片放入通有Ar、N2、N2O或H2中的任一种的退火炉中,退火温度设定在300~800℃范围内,退火时间控制在0.5~4小时范围内,使减反射层与N型扩散层之间形成1nm 左右的SiO2薄层(SiO2缓冲层),至此,完成了减反射层的制备。 c. After the gadolinium oxide anti-reflection layer is deposited, annealing is performed to form a SiO 2 buffer layer between the anti-reflection layer and the N-type diffusion layer. Put the cell into an annealing furnace with any one of Ar, N 2 , N 2 O or H 2 , set the annealing temperature in the range of 300-800°C, and control the annealing time in the range of 0.5-4 hours , so that a thin SiO 2 layer (SiO 2 buffer layer) of about 1nm is formed between the anti-reflection layer and the N-type diffusion layer. So far, the preparation of the anti-reflection layer is completed.
d、在电池背光侧制备铝背电场和金属栅状背电极,在向光侧(含减反射层一侧)制备金属栅线前电极,经过烘干、烧结工序后,制成完整的带有氧化钆减反射层的晶体硅太阳电池。 d. Prepare an aluminum back electric field and a metal grid-shaped back electrode on the backlight side of the battery, and prepare a metal grid wire front electrode on the light-facing side (including the anti-reflection layer side). After drying and sintering, a complete battery with A crystalline silicon solar cell with gadolinium oxide anti-reflection layer.
从图1所示的带有氧化钆减反射层的P型晶体硅太阳能电池的结构示意图中可以看出,在P型晶硅衬底1上扩散磷,形成N扩散层2,然后在N扩散层2上采用MOCVD方法在其表面沉积了一层氧化钆减反射层3,氧化钆减反射层3经退火处理,形成SiO2缓冲层4,SiO2缓冲层4位于减反射层3与N型扩散层2之间,最后在P型衬底1上再丝网印刷铝背电场5及金属栅线背电极6,在减反射层3上丝网印刷金属栅线前电极7,从而制成了带有氧化釓减反射层的晶硅太阳能电池。
It can be seen from the structural diagram of a P-type crystalline silicon solar cell with a gadolinium oxide anti-reflection layer shown in Figure 1 that phosphorus is diffused on a P-type crystalline silicon substrate 1 to form an
所述的有机化学气相沉积方法(MOCVD),为本领域内普通专业技术人员的常识,不再重述。 The organic chemical vapor deposition method (MOCVD) is the common knowledge of those skilled in the art and will not be repeated here.
以上是对本发明的说明而非限定,基于本发明思想的其他实施方式,均在本发明的保护范围之内。 The above is an illustration but not a limitation of the present invention, and other implementations based on the idea of the present invention are within the protection scope of the present invention.
Claims (7)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201410031087.9A CN103746008A (en) | 2014-01-23 | 2014-01-23 | Antireflection layer for solar cell and preparing process of antireflection layer |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201410031087.9A CN103746008A (en) | 2014-01-23 | 2014-01-23 | Antireflection layer for solar cell and preparing process of antireflection layer |
Publications (1)
Publication Number | Publication Date |
---|---|
CN103746008A true CN103746008A (en) | 2014-04-23 |
Family
ID=50503015
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201410031087.9A Pending CN103746008A (en) | 2014-01-23 | 2014-01-23 | Antireflection layer for solar cell and preparing process of antireflection layer |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN103746008A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107240612A (en) * | 2017-06-06 | 2017-10-10 | 界首市七曜新能源有限公司 | Mono-crystalline silicon solar plate |
CN108538932A (en) * | 2018-04-01 | 2018-09-14 | 格润智能光伏南通有限公司 | A kind of photovoltaic glass |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101499492A (en) * | 2008-02-02 | 2009-08-05 | 财团法人工业技术研究院 | Transparent solar cell module |
CN102856328A (en) * | 2012-10-10 | 2013-01-02 | 友达光电股份有限公司 | Solar cell and manufacturing method thereof |
CN103178135A (en) * | 2013-02-26 | 2013-06-26 | 友达光电股份有限公司 | Solar cell and manufacturing method thereof |
-
2014
- 2014-01-23 CN CN201410031087.9A patent/CN103746008A/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101499492A (en) * | 2008-02-02 | 2009-08-05 | 财团法人工业技术研究院 | Transparent solar cell module |
CN102856328A (en) * | 2012-10-10 | 2013-01-02 | 友达光电股份有限公司 | Solar cell and manufacturing method thereof |
CN103178135A (en) * | 2013-02-26 | 2013-06-26 | 友达光电股份有限公司 | Solar cell and manufacturing method thereof |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107240612A (en) * | 2017-06-06 | 2017-10-10 | 界首市七曜新能源有限公司 | Mono-crystalline silicon solar plate |
CN107240612B (en) * | 2017-06-06 | 2019-02-12 | 界首市七曜新能源有限公司 | Monocrystalline silicon solar panel |
CN108538932A (en) * | 2018-04-01 | 2018-09-14 | 格润智能光伏南通有限公司 | A kind of photovoltaic glass |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN103632935B (en) | The Boron diffusion method of N type silicon chip, crystal silicon solar energy battery and preparation method thereof | |
CN110137274A (en) | A kind of p-type high-efficiency battery and preparation method thereof of passivation on double surfaces contact | |
CN102598311A (en) | Solar cell and method for manufacturing such a solar cell | |
RU2456709C2 (en) | Solar cell and method and apparatus for making said solar cell | |
CN105355707A (en) | Efficient crystalline silicon solar cell and preparation method therefor | |
CN106653942A (en) | N-type monocrystalline silicon double-sided cell manufacturing method | |
CN103219427A (en) | Method for realizing single-sided texturing of high-light-trapping nano structure | |
CN102005508B (en) | A method for continuously preparing PN junctions and antireflection films for crystalline silicon solar cells | |
WO2023202132A1 (en) | Solar cell and manufacturing method therefor | |
CN106409926A (en) | Multilayer passivation film of crystalline-silicon battery and manufacturing method thereof | |
CN106711280A (en) | Method of making N-type double-sided battery | |
CN104009116A (en) | Manufacturing method of diamond line cutting polycrystalline silicon wafer battery | |
CN106328736B (en) | A kind of anti-LID black silicon solars high-efficiency battery and its production method | |
CN103531657A (en) | Preparation method for polycrystal/monocrystal-like solar cell selective emitting electrode structure | |
CN104091839B (en) | A kind of manufacture method of the antireflective coating for solar battery sheet | |
CN102254960A (en) | Passivation layer for p-type silicon surface of crystalline silicon solar cell and preparation method thereof | |
CN103746008A (en) | Antireflection layer for solar cell and preparing process of antireflection layer | |
CN103746006A (en) | Passivating layer of crystalline silicon solar cell and passivating process thereof | |
CN101499502A (en) | Crystalline silicon solar cell and its passivation method | |
CN105244417B (en) | Crystalline silicon solar cell and preparation method thereof | |
CN103762279B (en) | The manufacture method, N-type silicon solar cell and preparation method thereof of the selectivity back surface field of N-type silicon solar cell | |
CN116072748B (en) | Photovoltaic cell based on CuAlO2/Si and preparation method | |
CN110047950A (en) | A kind of solar cell and preparation method thereof with passivation layer structure | |
CN113571411B (en) | Manufacturing method of N-type TOPCon solar cell | |
CN116364793A (en) | Preparation method of monocrystalline silicon-based composite suede structure |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C02 | Deemed withdrawal of patent application after publication (patent law 2001) | ||
WD01 | Invention patent application deemed withdrawn after publication |
Application publication date: 20140423 |