材料科学
钙钛矿(结构)
钝化
串联
能量转换效率
带隙
钙钛矿太阳能电池
光电子学
硅
纳米技术
化学工程
工程类
复合材料
图层(电子)
作者
Sanlong Wang,Hongrui Sun,Jing Wang,Xin Ge,Yucheng Li,Diannan Li,Qian Huang,Xiaona Du,Ying Zhao,Xiaodan Zhang
标识
DOI:10.1002/aenm.202400151
摘要
Abstract Tandem solar cells combining perovskite and silicon have witnessed rapid development in recent years. However, the top cell, utilizing wide‐bandgap perovskite as absorbers generally suffer significant open‐circuit voltage ( V OC ) deficit, particularly for inorganic perovskite, which poses a considerable obstacle to enhancing the power conversion efficiency (PCE). Here, a modulation strategy by using 2,6‐pyridinedicarboxamide (PC), the crystallization kinetics of inorganic perovskite film can be effectively regulated, specifically manifested as a relatively longer annealing time in the air, resulting in sufficient growth for the inorganic perovskite grains. Additionally, PC can effectively in situ passivate uncoordinated Pb 2+ , suppressing the non‐radiative recombination of charge carriers. Eventually, a record PCE of 22.07% is achieved based on n–i–p inorganic perovskite solar cells (IPSCs), which also demonstrate the highest V OC above 1.34 V (1.71 eV of bandgap). More importantly, the unencapsulated IPSCs show enhanced thermal stability and photostability. Furthermore, the n–i–p IPSCs are also applied to inorganic perovskite/silicon tandem solar cells (IPTSCs), a PCE of 27.27% and an impressive V OC of 2.024 V are obtained.
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