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CO-DIFFUSION FOR P-TYPE PERT SOLAR CELLS USING APCVD BSG LAYERS AS BORON DOPING SOURCE

机译:使用APCVD BSG层作为硼掺杂源的P型Pert太阳能电池共扩散

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In this work, we investigate boron-doped back surface field (BSF) formation from borosilicate glass (BSG) deposited by atmospheric pressure chemical vapor deposition (APCVD). Carrier lifetime samples with different boron concentration in the BSG are exposed to high-temperature processes with varying temperature and gas atmospheres. The development aims at producing p-type Si-based passivated emitter and rear totally diffused (PERT) cells in a POCl_3 co-diffusion process. Our experiments confirm the critical impact of the O_2 concentration on boron diffusion from APCVD BSG layers. For different peak temperatures Si surface oxidation formation need to be balanced carefully. Moderate diffusion temperatures of 875°C (30 min) yield a BSF doping with R_(sh) = 131 Ω/sq and a recombination current density of J_(0, BSF) = 21 fA/cm~2 (planar surface, AlO_x/SiN_x-passivation). Finally, 156 mm sized PERT cells fabricated from p-type Czochralski-grown Si wafers using the developed co-diffusion process show peak efficiencies of 20.6%, confirming the feasibility of our co-diffusion approach.
机译:在这项工作中,我们调查从通过常压化学气相沉积(APCVD)来沉积硼硅酸盐玻璃(BSG)硼掺杂的背表面场(BSF)的形成。与在BSG不同硼浓度载流子寿命的样品被暴露于高温工艺具有不同的温度和气体环境。发展的目的是在一个POCl_3共扩散法生产Si系p型钝化发射极和背面完全扩散(PERT)细胞。我们的实验确认O_2浓度对硼扩散从APCVD BSG层临界冲击。对于不同的峰值温度的Si的表面氧化形成需要仔细平衡。的875℃(30分钟)得到具有R_(SH)一个BSF掺杂适度扩散温度= 131Ω/□和J_(0,BSF)= 21 FA /厘米〜2(平面表面,AlO_x的复合电流密度/ SiN_x钝化)。最后,156毫米尺寸PERT细胞中使用的20.6%的发达共扩散过程显示最高效率,证实了我们共同扩散方法的可行性从p型切克劳斯基法生长的Si晶片制成。

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