Controlling Intrinsic Quantum Confinement in Formamidinium Lead Triiodide Perovskite through Cs Substitution

被引:15
|
作者
Elmestekawy, Karim A. [1 ]
Wright, Adam D. [1 ]
Lohmann, Kilian B. [1 ]
Borchert, Juliane [1 ]
Johnston, Michael B. [1 ]
Herz, Laura M. [1 ,2 ]
机构
[1] Univ Oxford, Dept Phys, Clarendon Lab, Oxford OX1 3PU, England
[2] Tech Univ Munich, Inst Adv Study, D-85748 Garching, Germany
基金
英国工程与自然科学研究理事会;
关键词
perovskites; mixed-cation perovskite; FAPbI3; quantum confinement; absorption coefficient; photoluminescence; time-resolved photoluminescence; CHARGE-CARRIER DYNAMICS; MIXED-HALIDE PEROVSKITES; ELECTRONIC-PROPERTIES; PHOTOLUMINESCENCE; METHYLAMMONIUM; STABILIZATION; PERFORMANCE; MOBILITIES; TRIHALIDE; IMPACT;
D O I
10.1021/acsnano.2c02970
中图分类号
O6 [化学];
学科分类号
0703 ;
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 delta H-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.
引用
收藏
页码:9640 / 9650
页数:11
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