钙钛矿(结构)
钝化
开路电压
能量转换效率
材料科学
带隙
光电子学
碘化物
化学工程
电压
纳米技术
化学
无机化学
结晶学
电气工程
工程类
图层(电子)
作者
Xixi Yu,Huxue He,Yunuo Hui,Hua Wang,Xing Zhu,Shaoyuan Li,Tao Zhu
标识
DOI:10.3389/fchem.2024.1441057
摘要
High-performance wide-bandgap (WBG) perovskite solar cells are used as top cells in perovskite/silicon or perovskite/perovskite tandem solar cells, which possess the potential to overcome the Shockley-Queisser limitation of single-junction perovskite solar cells (PSCs). However, WBG perovskites still suffer from severe nonradiative recombination and large open-circuit voltage (Voc) losses, which restrict the improvement of PSC performance. Herein, we introduce 3,3′-diethyl-oxacarbo-cyanine iodide (DiOC 2 (3)) and multifunctional groups (C=N, C=C, C-O-C, C-N) into perovskite precursor solutions to simultaneously passivate deep level defects and reduce recombination centers. The multifunctional groups in DiOC 2 (3) coordinate with free Pb 2+ at symmetric sites, passivating Pb vacancy defects, effectively suppressing nonradiative recombination, and maintaining considerable stability. The results reveal that the power conversion efficiency (PCE) of the 1.68 eV WBG perovskite solar cell with an inverted structure increases from 18.51% to 21.50%, and the Voc loss is only 0.487 V. The unpackaged device maintains 95% of its initial PCE after 500 h, in an N 2 environment at 25°C.
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