甲脒
成核
结晶度
材料科学
结晶
三碘化物
钝化
面(心理学)
离子
带隙
结合能
选择性
钙钛矿(结构)
能量转换效率
相(物质)
无机化学
化学工程
化学物理
结晶学
化学
纳米技术
物理化学
光电子学
催化作用
电解质
复合材料
色素敏化染料
人格
电极
有机化学
物理
五大性格特征
核物理学
图层(电子)
生物化学
社会心理学
心理学
工程类
作者
Shengwen Li,Junmin Xia,Zhaorui Wen,Hao Gu,Jia Guo,Chao Liang,Hui Pan,Xingzhu Wang,Shi Chen
标识
DOI:10.1002/advs.202300056
摘要
Formamidinium lead triiodide (α-FAPbI3 ) has been widely used in high-efficiency perovskite solar cells due to its small band gap and excellent charge-transport properties. Recently, some additives show facet selectivity to generate a (001) facet-dominant film during crystallization. However, the mechanism to realize such (001) facet selectivity is not fully understood. Here, the authors attempted to use three ammonia salts NH4 X (X are pseudohalide anions) to achieve better (001) facet selectivity in perovskite crystallization and improved crystallinity. After addition, the (001) facet dominance is generally increased with the best effect from SCN- anions. The theoretical calculation revealed three mechanisms of such improvements. First, pseudohalide anions have larger binding energy than the iodine ion to bind the facets including (110), (210), and (111), slowing down the growth of these facets. The large binding energy also reduces nucleation density and improves crystallinity. Second, pseudohalide ions improve phase purity by increasing the formation energies of the δ-phase and other hexagonal polytypes, retarding the α- to δ-phase transition. Third, the strong binding of these anions can also effectively passivate the iodine vacancies and suppress nonradiative recombination. As a result, the devices show a power conversion efficiency of 24.11% with a Voc of 1.181 V.
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