钙钛矿(结构)
结晶度
纳米晶
化学
光电流
超快激光光谱学
锡
相(物质)
正交晶系
量子点
纳米技术
化学工程
光谱学
材料科学
光电子学
结晶学
晶体结构
物理
工程类
有机化学
量子力学
作者
Feng Liu,Chao Ding,Yaohong Zhang,Teresa S. Ripollés,Taichi Kamisaka,Taro Toyoda,Shuzi Hayase,Takashi Minemoto,Kenji Yoshino,Songyuan Dai,Masatoshi Yanagida,Hidenori Noguchi,Qing Shen
摘要
Organic–inorganic hybrid perovskite solar cells have demonstrated unprecedented high power conversion efficiencies in the past few years. Now, the universal instability of the perovskites has become the main barrier for this kind of solar cells to realize commercialization. This situation can be even worse for those tin-based perovskites, especially for CsSnI3, because upon exposure to ambient atmosphere the desired black orthorhombic phase CsSnI3 would promptly lose single crystallinity and degrade to the inactive yellow phase, followed by irreversible oxidation into metallic Cs2SnI6. By alloying CsSnI3 with CsPbI3, we herein report the synthesis of alloyed perovskite quantum dot (QD), CsSn1–xPbxI3, which not only can be phase-stable for months in purified colloidal solution but also remains intact even directly exposed to ambient air, far superior to both of its parent CsSnI3 and CsPbI3 QDs. Ultrafast transient absorption spectroscopy studies reveal that the photoexcited electrons in the alloyed QDs can be injected into TiO2 nanocrystals at a fast rate of 1.12 × 1011 s–1, which enables a high photocurrent generation in solar cells.
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