钝化
等离子体增强化学气相沉积
非晶硅
材料科学
光电子学
氧化硅
太阳能电池
硅
无定形固体
拉曼光谱
退火(玻璃)
化学气相沉积
晶体硅
傅里叶变换红外光谱
化学工程
图层(电子)
分析化学(期刊)
纳米技术
氧化物
物理
化学
复合材料
结晶学
光学
氮化硅
冶金
有机化学
工程类
作者
Mickaël Lozac’h,Shota Nunomura,Hitoshi Sai,Koji Matsubara
标识
DOI:10.1016/j.solmat.2018.05.004
摘要
Abstract A stacked layer of ultrathin hydrogenated silicon oxide (SiOx:H) and hydrogenated amorphous silicon (a-Si:H) has been developed to passivate the crystalline silicon (c-Si) surface (see graphical abstract). Silicon oxide has the advantage of excellent optical and passivation properties. The SiOx:H layer is deposited on the c-Si surface by atomic layer deposition (ALD), with its thickness precisely controlled below 2 nm. The a-Si:H layer is deposited on the SiOx:H layer by plasma-enhanced chemical vapor deposition (PECVD) with a specific doping property, i.e. intrinsic, n- or p-type. The samples are then annealed in the range of 100 °C to 950 °C to study the fundamental passivation properties. We find that a combination of an ultrathin SiOx:H and (p) a-Si:H layers shows a favorable passivation compared to a neat (p) a-Si:H layer. The effective minority carrier lifetime, measured by quasi-steady-state photoconductance (QSSPC), is ~ 0.5 ms after low temperature annealing at 300 °C. The passivation property is discussed in terms of hydrogen concentration, bond configurations, stoichiometry x of SiOx:H, and material microstructure, characterized by Fourier transform infra-red (FTIR) and Raman spectroscopy. It is suggested that a reorganization of both the SiOx:H, and the (p) a-Si:H layers, associated with hydrogen diffusion, plays an important role in improving the passivation.
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