钝化
退火(玻璃)
兴奋剂
原位
材料科学
太阳能电池
分析化学(期刊)
结晶
硅
纳米技术
光电子学
化学
图层(电子)
有机化学
复合材料
作者
Wookjin Choi,Keeya Madani,Ying-Yuan Huang,Aditi Jain,Young‐Woo Ok,Vijaykumar D. Upadhyaya Min Gu Kang,Sung‐Jin Choi,A. Rohatgi
标识
DOI:10.1109/pvsc43889.2021.9518759
摘要
This paper presents fabrication and optimization of p+ passivating contact (p+ poly-Si/SiOx/c-Si) for high efficiency p-TOPCon solar cells. The p+ passivating contacts were formed by (i) in-situ doped p+ poly-Si via LPCVD and (ii) ex-situ doping of intrinsic poly-Si via APCVD boron diffusion. We studied the relationship between the passivation quality of this contact as a function of boron diffusion profile varied by altering (i) the crystallization annealing temperature, and (ii) the APCVD precursor gas flow ratio $\left( {{\emptyset _{{B_2}{H_6}}}/{\emptyset _{Si{H_4}}}} \right).$ In-situ doping resulted in higher B concentration in poly-Si, which improves field induced passivation, as well as in Si absorber near the interface, which enhances Auger recombination to degrade passivation. This trade-off resulted in lower optimum annealing temperature for in-situ process (875°C vs 950°C). However, process optimization resulted in excellent passivation with comparable iVoc and J0 for both in-situ (719mV/6.3fAcm -2 ) and ex-situ doped (716mV/6.6fAcm -2 ) un-metallized p-TOPCon. Greater than 22.0% screen-printed large area (244.32cm 2 ) bifacial p-TOPCon solar cells were fabricated by replacing LBSF of p-PERC cells with 270 nm p + TOPCon junction with ~10% metal coverage on the rear side. TOPCon cells gave 0.4% higher efficiency than their PERC counterpart.
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