材料科学
外延
薄膜
化学气相沉积
晶体生长
沉积(地质)
基质(水族馆)
分析化学(期刊)
光电子学
化学工程
脉冲激光沉积
气相
金属有机气相外延
物理气相沉积
单晶
光致发光
钙钛矿(结构)
作者
Zihao Liu,Tomonori Matsushita,M. Sotome,Takashi Kondo
出处
期刊:European Quantum Electronics Conference
日期:2021-06-21
标识
DOI:10.1109/cleo/europe-eqec52157.2021.9541870
摘要
Metal halide perovskites have shown high potential for opto-electronic devices due to their excellent properties: strong light absorption, long carrier lifetime, and moderate mobilities. The power conversion efficiencies of the perovskite solar cells have reached 25.5%, which are comparable to crystalline Si ones. Most of the current perovskite devices are polycrystalline thin films made by spin-coating. To further enhance the performance of perovskite devices, single crystals and epitaxial growth are necessary. Compared with spin-coating, vapor phase deposition has higher controllability. We have been focusing on the epitaxial growth of crystalline all-perovskite heterostructures using physical vapour phase deposition technique. We have tried to grow CH 3 NH 3 PbI 3 thin films on the CH 3 NH 3 PbBr 3 single crystals by co-evaporation of CH 3 NH 3 I and PbI 2 [1] . However, we obtained only Br-rich CH 3 NH 3 Pb(BrI) 3 alloy epitaxial thin films due to the ion inter-diffusion. Recently, the inter-diffusion free CH(NH 2 ) 2 PbI 3 film was reported to be grown on CH 3 NH 3 Pb(BrCl) 3 alloy substrates by solution method [2] . Inspired by this, here we report the vapor phase epitaxial growth of perovskite thin films by changing the organic cations and its effect on the ion inter-diffusion.
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