钙钛矿(结构)
激子
卤化物
材料科学
微晶
微观结构
光电子学
化学物理
凝聚态物理
电子
化学
物理
结晶学
无机化学
量子力学
冶金
作者
Giulia Grancini,Ajay Ram Srimath Kandada,Jarvist M. Frost,Alex J. Barker,Michele De Bastiani,Marina Gandini,Sergio Marras,Guglielmo Lanzani,Aron Walsh,Annamaria Petrozza
出处
期刊:Nature Photonics
[Nature Portfolio]
日期:2015-08-17
卷期号:9 (10): 695-701
被引量:249
标识
DOI:10.1038/nphoton.2015.151
摘要
Solar cells based on hybrid inorganic-organic halide perovskites have demonstrated high power conversion efficiencies in a range of architectures. The existence and stability of bound electron-hole pairs in these materials, and their role in the exceptional performance of optoelectronic devices, remains a controversial issue. Here we demonstrate, through a combination of optical spectroscopy and multiscale modeling as a function of the degree of polycrystallinity and temperature, that the electron-hole interaction is sensitive to the microstructure of the material. The long-range order is disrupted by polycrystalline disorder and the variations in electrostatic potential found for smaller crystals suppress exciton formation, while larger crystals of the same composition demonstrate an unambiguous excitonic state. We conclude that fabrication procedures and morphology strongly influence perovskite behaviour, with both free carrier and excitonic regimes possible, with strong implications for optoelectronic devices.
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