钝化
结晶
钙钛矿(结构)
材料科学
能量转换效率
卤化物
硫氰酸盐
化学工程
成核
离子
光电子学
纳米技术
无机化学
化学
有机化学
工程类
图层(电子)
作者
Xiaogang Wang,Hao Huang,Shuxian Du,Peng Cui,Zhineng Lan,Yingying Yang,Luyao Yan,Jun Ji,Benyu Liu,Shujie Qu,Qiang Zhang,Xiaopeng Yue,Xing Zhao,Meicheng Li
出处
期刊:Solar RRL
[Wiley]
日期:2022-10-06
卷期号:6 (12)
被引量:6
标识
DOI:10.1002/solr.202200717
摘要
Further performance enhancement of perovskite solar cells (PSCs) is limited by the defect‐assisted recombination losses. The approaches employed to decrease the losses contain defect passivation, perovskite crystallization control, interface engineering, etc. Herein, a new material of acetamidine thiocyanate (AASCN) via a facile method is synthesized, which exhibits dual functions combining a cation with passivation and an anion with crystallization. The iodine vacancies in the perovskite can be effectively passivated through hydrogen bonds formed by the NH bonds of the polar cation AA + . Furthermore, the pseudo‐halide anion SCN − can coordinate the Pb–I octahedrons, improving the perovskite film crystallization. Through vaporing the AASCN on perovskite films during the secondary crystal growth process, the defects mitigation and crystallization improvement are synergistically achieved. As a consequence, the FA 0.25 MA 0.75 PbI 3 PSCs with AASCN achieve a power conversion efficiency of 23.17%, which is higher than that (21.43%) of untreated PSCs. In detail, the open‐circuit voltage has also a significant advancement from 1.095 to 1.167 V after the AASCN treatment. The design and synthesization of the multifunctional materials are supposed to provide a feasible approach for the performance improvement of PSCs.
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