非阻塞I/O
异质结
材料科学
光催化
半导体
X射线光电子能谱
可见光谱
光电子学
工作职能
吸收(声学)
光化学
太阳能燃料
化学工程
催化作用
纳米技术
化学
工程类
复合材料
生物化学
图层(电子)
作者
Zhongliao Wang,Bei Cheng,Liuyang Zhang,Jiaguo Yu,Haiyan Tan
出处
期刊:Solar RRL
[Wiley]
日期:2021-08-17
卷期号:6 (1)
被引量:118
标识
DOI:10.1002/solr.202100587
摘要
Artificial photosynthesis by CO 2 photoreduction is an ideal channel for mitigating the greenhouse effect and energy crises. Nevertheless, its efficiency is still low due to severe charge recombination and sluggish kinetics. Herein, an S‐scheme BiOBr/NiO heterojunction, composed of two kinds of p‐type semiconductors, exhibits enhanced CO 2 photoreduction activity. Enhanced light absorption and specific surface area are attributable to NiO nanosheets with hierarchical porous structures. Results from in situ irradiated X‐ray photoelectron spectroscopy and work function calculation manifest that the photoexcited electrons transfer from BiOBr to NiO via the S‐scheme mechanism. And charge separation and a strong redox ability are simultaneously realized. In situ diffuse reflectance infrared Fourier transform spectra unveil complex intermediates in CO 2 photoreduction. This work presents a novel understanding for the CO 2 photoreduction mechanism of S‐scheme heterojunctions built by p‐type semiconductors by integrating in situ monitoring techniques with density functional theory calculation.
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