甲脒
三碘化物
量子点
钙钛矿(结构)
材料科学
光电子学
带隙
光致发光
卤化物
化学物理
纳米技术
化学
电解质
电极
无机化学
物理化学
色素敏化染料
结晶学
作者
Karim A. Elmestekawy,Adam D. Wright,Kilian B. Lohmann,Juliane Borchert,Michael B. Johnston,Laura M. Herz
出处
期刊:ACS Nano
[American Chemical Society]
日期:2022-05-24
卷期号:16 (6): 9640-9650
被引量:13
标识
DOI:10.1021/acsnano.2c02970
摘要
Lead halide perovskites are leading candidates for photovoltaic and light-emitting devices, owing to their excellent and widely tunable optoelectronic properties. Nanostructure control has been central to their development, allowing for improvements in efficiency and stability, and changes in electronic dimensionality. Recently, formamidinium lead triiodide (FAPbI3) has been shown to exhibit intrinsic quantum confinement effects in nominally bulk thin films, apparent through above-bandgap absorption peaks. Here, we show that such nanoscale electronic effects can be controlled through partial replacement of the FA cation with Cs. We find that Cs-cation exchange causes a weakening of quantum confinement in the perovskite, arising from changes in the bandstructure, the length scale of confinement, or the presence of δH-phase electronic barriers. We further observe photon emission from quantum-confined regions, highlighting their potential usefulness to light-emitting devices and single-photon sources. Overall, controlling this intriguing quantum phenomenon will allow for its suppression or enhancement according to need.
科研通智能强力驱动
Strongly Powered by AbleSci AI