材料科学
钙钛矿(结构)
凝聚态物理
场效应晶体管
电荷(物理)
薄膜
晶体管
化学物理
光电子学
纳米技术
化学工程
电压
电气工程
物理
量子力学
工程类
作者
Sile Hu,Bing Tang,Stephen V. Kershaw,Nicholas A. Kotov,Rogach Andrey
标识
DOI:10.1021/acsami.3c19200
摘要
Chiral halide perovskite materials promise both superior light response and the capability to distinguish circularly polarized emissions, which are especially common in the fluorescence spectra of organic chiral materials. Herein, thin-film field-effect transistors (FETs) based on chiral quasi-two-dimensional perovskites are explored, and the temperature dependence of the charge carrier transport mechanism over the broad temperature range (80–300 K) is revealed. A typical p-type charge transport behavior is observed for both left-handed (S-C6H5(CN2)2NH3)2(CH3NH3)n−1PbnI3n+1 and right-handed (R-C6H5(CN2)2NH3)2(CH3NH3)n−1PbnI3n+1 chiral perovskites, with maximum carrier mobilities of 1.7 × 10–5 cm2 V–1 s–1 and 2.5 × 10–5 cm2 V–1 s–1 at around 280 K, respectively. The shallow traps with smaller activation energy (0.03 eV) hinder the carrier transport over the lower temperature regime (80–180 K), while deep traps with 1 order of magnitude larger activation energy than the shallow traps moderate the charge carrier transport in the temperature range of 180–300 K. From the charge carrier mechanism point of view, impurity scattering is established as the dominant factor from 80 K until around 280 K, while phonon scattering becomes predominant up to room temperature. Responsivities of 0.15 A W–1 and 0.14 A W–1 for left-handed and right-handed chiral perovskite FET devices are obtained.
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