材料科学
碳化
能量转换效率
钙钛矿(结构)
电导率
阴极
化学工程
电极
生物量(生态学)
复合材料
多孔性
碳纤维
光电子学
化学
扫描电子显微镜
复合数
地质学
工程类
海洋学
物理化学
作者
Haichao Liu,Yahong Xie,Peng Wei,Wei Wang,Huamei Chen,Cong Geng,Qiang Yue
标识
DOI:10.1016/j.jallcom.2020.155851
摘要
Abstract Hole transporting material (HTM)-free carbon-based perovskite solar cells (C–PSCs) have attracted widespread attention for their notable characteristics of excellent long-term stability and low cost. However, the power conversion efficiency (PCE) of C–PSCs is significantly lower than that of HTM-based PSCs. This is mostly due to the unexpected electron recombination happening at the interface of perovskite/carbon. In this study, biomass-based carbon materials were obtained from discarded soybean dregs with sufficient pore size and good conductivity through programmed temperature carbonization and KOH activation processes. Composites of KOH-activated soybean dregs carbon and conductive carbon were used as the counter electrodes (CEs) of C–PSCs, the electrode interface performance was significantly improved and a PCE of 12.05% was obtained, which was 50% higher than that of pure carbon-based C–PSCs. Through long-term stability tests, it was found that the efficiency of the unpackaged cell did not decrease in after 960 h in the air.
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