材料科学
钙钛矿(结构)
硫脲
铋
带隙
卤化物
路易斯酸
结晶度
无机化学
结晶
结晶学
化学
催化作用
有机化学
光电子学
冶金
复合材料
作者
Qiaoying Jia,Cong Li,Weiye Tian,Malin B. Johansson,Erik M. J. Johansson,Rusen Yang
标识
DOI:10.1021/acsami.0c14512
摘要
Bismuth halide perovskites have recently been considered a potential alternative to lead halide analogues due to their low toxicity and high stability. However, the layered flake structure and wide band gap limit their applications in perovskite solar cells (PSCs). We herein show that large-grained all-inorganic bismuth-based perovskites with a narrow band gap can be obtained from a Lewis acid–base adduct reaction under ambient conditions. Thiourea (CH4N2S) is utilized as a Lewis base to interact with BiI3, confirmed with infrared (IR) spectra. The strong coordination between thiourea and the Bi3+ center could slow down the perovskite crystallization and promote the preferred orientation of the perovskite crystals with a hexagonal phase. The morphology of the perovskite films varies dramatically with an increase of molar ratio of BiI3 and thiourea in the precursor. The perovskites derived from a BiI3/thiourea ratio of 1:2 display extrathick grains, higher surface coverage, extended light absorption, higher crystallinity, and similar air stability compared to the pristine sample. The power conversion efficiency (PCE) of the thiourea-induced bismuth perovskite solar cells is significantly enhanced due to the higher surface coverage and the broader absorption of the perovskite film.
科研通智能强力驱动
Strongly Powered by AbleSci AI