材料科学
光电子学
兴奋剂
硫系化合物
能量转换效率
离子
钝化
电导率
载流子寿命
宽禁带半导体
工作职能
带偏移量
电子
图层(电子)
电子迁移率
二极管
光电效应
锂(药物)
量子隧道
纳米技术
接受者
阻挡层
电子能带结构
工作(物理)
多激子产生
作者
Jun-Cai Zhang,Jing-Dong Zhang,Lingjie Liu,Jie Huang,Jin-Rui Cai,Hui Li,Li-Mei Lin,G N Chen
摘要
The efficiency of Sb2(S,Se)3 solar cells is primarily limited by severe back-interface non-radiative recombination due to unfavorable band alignment and defects, thus making low-cost, stable, and suitably bandgap-matched PbS a promising inorganic HTL to address this issue. Nevertheless, its intrinsically low conductivity, coupled with the tunable surface electronic structure of Sb2(S,Se)3, results in a significant energy level mismatch and thus a high hole transport barrier at the Sb2(S,Se)3/PbS interface. This work presents a facile ion doping strategy (IDS) by doping of lithium ions (Li+) into the PbS lattice. The IDS increases the carrier concentration, enhances the p-type conductivity of PbS, optimizes its energy level position, and simultaneously passivates the interface defects, suppressing non-radiative recombination. The interface level alignment of Sb2(S,Se)3/PbS is optimized, significantly reducing the valence band offset barrier for hole transport from 0.21 to 0.14 eV, greatly promoting the extraction and transport of holes across the interface. Ultimately, the photoelectric conversion efficiency (PCE) of the FTO/CdS/Sb2(S,Se)3/Li-PbS/carbon device reaches 9.36% (Voc = 0.53 V, Jsc = 27.80 mA/cm2, FF = 63.86%), significantly outperforming the champion unmodified device (PCE = 7.41%). This work provides an efficient solution for HTL modification in chalcogenide solar cells.
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