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胶体合成用于太阳能电池的空气稳定合金 CsSnPbI 钙钛矿纳米晶体。

Colloidal Synthesis of Air-Stable Alloyed CsSnPbI Perovskite Nanocrystals for Use in Solar Cells.

机构信息

Faculty of Informatics and Engineering, The University of Electro-Communications , 1-5-1 Chofugaoka, Chofu, Tokyo 182-8585, Japan.

Faculty of Life Science and Systems Engineering, Kyushu Institute of Technology , 2-4 Hibikino, Wakamatsu-ku, Kitakyushu, Fukuoka 808-0196, Japan.

出版信息

J Am Chem Soc. 2017 Nov 22;139(46):16708-16719. doi: 10.1021/jacs.7b08628. Epub 2017 Nov 13.

Abstract

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 CsSnI, because upon exposure to ambient atmosphere the desired black orthorhombic phase CsSnI would promptly lose single crystallinity and degrade to the inactive yellow phase, followed by irreversible oxidation into metallic CsSnI. By alloying CsSnI with CsPbI, we herein report the synthesis of alloyed perovskite quantum dot (QD), CsSnPbI, 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 CsSnI and CsPbI QDs. Ultrafast transient absorption spectroscopy studies reveal that the photoexcited electrons in the alloyed QDs can be injected into TiO nanocrystals at a fast rate of 1.12 × 10 s, which enables a high photocurrent generation in solar cells.

摘要

有机-无机杂化钙钛矿太阳能电池在过去几年中展示了前所未有的高光能量转换效率。如今,钙钛矿普遍的不稳定性已成为这类太阳能电池实现商业化的主要障碍。对于锡基钙钛矿来说,这种情况可能更糟,尤其是对于 CsSnI,因为暴露在环境气氛中,所需的黑正交相 CsSnI 会迅速失去单晶性并降解为非活性的黄色相,随后不可逆地氧化成金属 CsSnI。通过将 CsSnI 与 CsPbI 合金化,我们在此报告了合金钙钛矿量子点(QD)CsSnPbI 的合成,它不仅可以在纯化的胶体溶液中稳定数月,而且即使直接暴露在环境空气中也保持完整,远远优于其母体 CsSnI 和 CsPbI QDs。超快瞬态吸收光谱研究表明,合金量子点中的光激发电子可以以 1.12×10 s 的快速速率注入 TiO 纳米晶中,这使得太阳能电池中产生了高的光电流。

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