锡
钙钛矿(结构)
碘化物
材料科学
带隙
八面体
热稳定性
晶体结构
纳米技术
光电子学
无机化学
化学
结晶学
冶金
有机化学
作者
W.S. Park,Youjin Reo,Wonryeol Yang,Hamin Choi,Seungju Jeon,Bogyu Lim,Ao Liu,Huihui Zhu,Yong‐Young Noh
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2024-04-29
卷期号:9 (5): 2436-2445
被引量:3
标识
DOI:10.1021/acsenergylett.4c00620
摘要
Two-dimensional (2D) layered perovskites have garnered significant research interest within the perovskite community due to their potential as semiconducting materials characterized by high structural stability and favorable optoelectrical properties. Among various contenders, 2D Dion–Jacobson (DJ) perovskites featuring diammonium organic spacers stand out for their exceptional stability. This stability is attributed to the robust hydrogen bonding of the spacer, which leads to a shorter distance between the inorganic octahedral cage layers. In this study, we highlight the remarkable structural stability of 2D DJ perovskite in Sn2+ perovskite thin-film transistors, achieved through the incorporation of 3-(aminomethyl)piperidinium tin iodide (3AMPSnI4) and 4-(aminomethyl)piperidinium tin iodide (4AMPSnI4). The varying positions of the aminomethyl group determine the distortion of the crystal lattice, impacting their respective optical and electrical properties. The relatively low distortion 3AMPSnI4 demonstrates transistor performance with a 10-fold increase in field-effect mobility and 2 orders of magnitude improvement in the on/off current ratio through high film quality with grain size exceeding 10 μm and narrower bandgap. Moreover, the stability of both the film and device under ambient air exposure is markedly improved, with 2D DJ perovskites retaining their crystal structure for over 24 h, presenting a notable enhancement compared to 2D Ruddlesden–Popper perovskites.
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