卤化物
碘化物
钙钛矿(结构)
胶体
化学
相(物质)
离解(化学)
光化学
溴化物
化学工程
材料科学
无机化学
结晶学
物理化学
有机化学
工程类
作者
Nathaniel Hiott,Jishnudas Chakkamalayath,Prashant V. Kamat
标识
DOI:10.1021/acsmaterialslett.3c00729
摘要
The photostability of lead halide perovskites is an important criterion for their utilization in light harvesting applications. Colloidal two-dimensional mixed halide perovskites offer a convenient approach to probe photoinduced transformations using spectroscopy tools. We employed suspensions of colloidal 2D methylammonium lead halide perovskite platelets with butylammonium and octylammonium as organic spacer cations. Upon irradiation of the mixed halide perovskite (BAOAMAPb 2 (Br 3.5 I 3.5 )) colloidal platelet suspension, we observe a phase transformation, as seen from the formation of bromide rich domains (BAOAMAPb 2 Br 7 ) and an iodide complex (PbI 3 – ). Unlike in the case of 3D mixed halide films, we did not observe the formation of iodide rich domains as part of the photoinduced phase segregation process. Instead, we observed the dissociation of the BAOAMAPb 2 I 7 to form an iodide complex, PbI 3 – . Interestingly, this photoinduced phase transformation was reversible, as the products which were confined in the colloidal core restored the original mixed halide phase upon storage in dark. The spectroscopic measurements that characterize excited states of different colloidal methylammonium lead halide perovskites and kinetics of photoinduced transformation and their dark recovery are presented. These new phototransformations of colloidal perovskite platelets provide new insights into the processes that dictate their overall photostability.
科研通智能强力驱动
Strongly Powered by AbleSci AI