Cross-sectional profile of photocarrier mobility in thin-film solar cells via multimolecular recombination and charge extraction by linearly increasing voltage (cs-p-CELIV)

光伏 材料科学 电子迁移率 光电子学 有机太阳能电池 载流子寿命 太阳能电池 薄膜 硅 光伏系统 光学 纳米技术 物理 聚合物 电气工程 复合材料 工程类
作者
Noah B. Stocek,Miguel J. Young,Reg Bauld,Tianhao Ouyang,Giovanni Fanchini
出处
期刊:Journal of Applied Physics [American Institute of Physics]
卷期号:135 (4)
标识
DOI:10.1063/5.0174799
摘要

The ability to spatially resolve the carrier mobility profile along the cross section of micrometer-thin solar cells is vital, both for fundamental studies in photovoltaics and as quality control for reproducibly obtaining high conversion efficiencies in commercial solar cell modules. Presently, no technique capable of such an endeavor is available to the best of our knowledge. Here, we introduce a novel method capable of profiling the carrier mobility along the z axis in thin-film photovoltaics. Our setup is based on the integration of photogenerated charge extraction by linearly increasing voltage (p-CELIV) with a scanning confocal optical microscope (SCOM) toward a confocal and cross-sectional p-CELIV (cs-p-CELIV) system. As monomolecular recombination of excess carriers is the most frequent radiative pathway for electrons and holes in solar cells at low power density of illumination, while multimolecular recombination dominates at high power, enhanced multimolecular recombination occurs at the SCOM focal plane. Thus, the cs-p-CELIV signal provides enhanced information on the mobility of all of the cross-sectional layers except the focal plane. By scanning the focal plane along the z axis, the mobility profile can be derived. To demonstrate our technique, we use it to investigate the carrier mobility in three hydrogenated amorphous silicon (a-Si:H) solar cells. The mobility profiles obtained by cs-p-CELIV correlate well with well-known depletion layer effects and the H content profile in a-Si:H, which is measured independently. Our findings are in excellent agreement with models suggesting a critical role of Si–H bonding in locally determining the carrier mobility in a-Si:H.
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