Study of the passivation mechanism of c-Si by Al2O3 using in situ infrared spectroscopy

Rohan P. Chaukulkar, W. Nemeth, A. Dameron, P. Stradins, S. Agarwal
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引用次数: 1

Abstract

We present an in situ attenuated total reflection Fourier transform infrared (ATR-FTIR) spectroscopy study of the passivation mechanism in the surface passivation of Si solar cells by Al2O3 thin films deposited via atomic layer deposition (ALD) using TMA and O3 as precursors. The IR measurements suggest that during the annealing stage, the Si-H bonding near the interface decreases. We have used D-terminated c-Si internal-reflection crystals to differentiate the residual H atoms that may migrate from ALD Al2O3 films versus the residual D atoms present at the Al2O3/c-Si interface after ALD. Within the sensitivity of the ATR-FTIR spectroscopy setup of ~1012 cm-2 for Si-H bonds, we do not detect any migration of H from Al2O3 to the c-Si interface. Therefore, we conclude that the migration of O, and the subsequent restructuring of the interface during the annealing step, primarily contributes toward the chemical passivation of the Al2O3/c-Si interface.
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用原位红外光谱研究Al2O3钝化c-Si的机理
本文采用原位衰减全反射傅立叶变换红外(ATR-FTIR)光谱研究了以TMA和O3为前驱体,通过原子层沉积(ALD)沉积Al2O3薄膜对硅太阳能电池表面钝化的机理。红外测量表明,在退火阶段,界面附近的Si-H键减少。我们使用D端c-Si内反射晶体来区分ALD Al2O3薄膜中可能迁移的残余H原子与ALD后Al2O3/c-Si界面上存在的残余D原子。在ATR-FTIR光谱设置的~1012 cm-2的Si-H键灵敏度范围内,我们没有检测到H从Al2O3到c-Si界面的任何迁移。因此,我们得出结论,O的迁移以及随后在退火步骤中界面的重组是导致Al2O3/c-Si界面化学钝化的主要原因。
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