光致发光
光催化
卤化物
材料科学
带隙
钙钛矿(结构)
微秒
光化学
无机化学
作者
Hang Yin,Junsheng Chen,Peng Guan,Daoyuan Zheng,Qingkun Kong,Songqiu Yang,Panwang Zhou,Bin Yang,Tönu Pullerits,Ke-Li Han
标识
DOI:10.1002/ange.202108133
摘要
Lead-free halide perovskites have triggered interest in the field of optoelectronics and photocatalysis because of their low toxicity, and tunable optical and charge-carrier properties. From an application point of view, it is desirable to develop stable multifunctional lead-free halide perovskites. We have developed a series of Cs2PtxSn1−xCl6 perovskites (0≤x≤1) with high stability, which show switchable photoluminescence and photocatalytic functions by varying the amount of Pt4+ substitution. A Cs2PtxSn1−xCl6 solid solution with a dominant proportion of Pt4+ shows broadband photoluminescence with a lifetime on the microsecond timescale. A Cs2PtxSn1−xCl6 solid solution with a small amount of Pt4+ substitution exhibits photocatalytic hydrogen evolution activity. An optical spectroscopy study reveals that the switch between photoluminescence and photocatalysis functions is controlled by sub-band gap states. Our finding provides a new way to develop lead-free multifunctional halide perovskites with high stability.
科研通智能强力驱动
Strongly Powered by AbleSci AI