异质结
钙钛矿(结构)
材料科学
X射线光电子能谱
介孔材料
量子点
电子顺磁共振
光电子学
光催化
量子产额
纳米技术
化学工程
化学
物理
光学
结晶学
核磁共振
催化作用
荧光
工程类
生物化学
作者
Zhongliang Dong,Zhijie Zhang,Ying Jiang,Yaoqing Chu,Jiayue Xu
标识
DOI:10.1016/j.cej.2021.133762
摘要
Heterojunction engineering, especially S-scheme heterojunction, has been recognized as a promising way to explore photocatalysts with boosted charge separation and CO2 photoreduction. Herein, we develop a CsPbBr3@mesoporous TiO2 beads (MTB) S-scheme heterojunction by embedding CsPbBr3 perovskite quantum dots (QDs) into the pores of MTB. The intimate interfacial interaction and staggered band structures promised the S-scheme charge transfer route, as confirmed by X-ray photoelectron spectra (XPS), electron spin resonance (ESR), etc. The 0.15CsPbBr3@MTB (15 wt% of CsPbBr3) hybrid exhibited a remarkable yield of 145.28 μmol g−1h−1 for CO2 photoreduction under simulated sunlight irradiation, which was 4.64 and 3.49-fold enhancement than the pristine MTB and CsPbBr3, respectively. This study provides useful guide towards the design of perovskite-based heterojunctions for photocatalytic applications.
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