| Literature DB >> 29091445 |
Feng Liu1, Chao Ding1, Yaohong Zhang1, Teresa S Ripolles2, Taichi Kamisaka1, Taro Toyoda1,3, Shuzi Hayase2,3, Takashi Minemoto4,3, Kenji Yoshino5,3, Songyuan Dai6, Masatoshi Yanagida7,8, Hidenori Noguchi7,8, Qing Shen1,3.
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 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.Entities:
Year: 2017 PMID: 29091445 DOI: 10.1021/jacs.7b08628
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419