分解水
光催化
钙钛矿(结构)
制氢
铋
带隙
材料科学
辐照
氢
相(物质)
水溶液
紫外线
化学工程
纳米技术
光化学
催化作用
化学
光电子学
物理化学
结晶学
物理
有机化学
工程类
核物理学
冶金
生物化学
作者
Antonio J. Chacón-García,Herme G. Baldoví,Artem A. Babaryk,Antonio Rodríguez‐Diéguez,Sergio Navalón,Yolanda Pérez,Hermenegildo Garcı́a,Patricia Horcajada
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2023-11-24
卷期号:17 (5): 4593-4601
被引量:5
标识
DOI:10.1007/s12274-023-6254-1
摘要
Organic–inorganic hybrid perovskites have gained great attention as promising photocatalysts for hydrogen generation. However, due to their poor stability in water, the use of aqueous hydrohalic acid solutions is specifically required for an efficient hydrogen evolution. Herein, three novel photoactive lead-free hybrid perovskites based on bismuth and triazolium cations (denoted as IEF-15, IEF-16, and IEF-17 (IEF stands for IMDEA energy frameworks)) were synthesized and fully characterized (structural, compositional, optical, etc.). Further, these solids were proposed as photocatalysts for the challenging gas phase overall water splitting (OWS) reaction. Accordingly, IEF-16 thin films exhibited a remarkable photocatalytic activity in both H and O evolution, as a consequence of its appropriate bandgap and energy-band alignment, achieving hydrogen evolution rates of 846 and 360μmol⋅g after 24 h under ultraviolet–visible (UV–vis) irradiation or simulated solar irradiation, respectively. This study additionally highlights the remarkable structural and photochemical stability of IEF-16 under different operational conditions (i.e. water volume, irradiation and temperature), paving the way for green hydrogen production from OWS using perovskite-based photocatalysts.
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