光催化
价带
可见光谱
氧化还原
降级(电信)
价(化学)
辐照
材料科学
光化学
光电子学
化学工程
化学
无机化学
催化作用
带隙
有机化学
物理
计算机科学
电信
核物理学
工程类
作者
Jiaqi Zhao,Li‐Zhu Wu,Tierui Zhang
出处
期刊:Chem
[Elsevier]
日期:2024-03-27
卷期号:10 (4): 1046-1048
标识
DOI:10.1016/j.chempr.2024.03.018
摘要
The balance between oxidation potential and spectral response range is a critical consideration in photocatalysis. In this issue of Chem, Zhu and co-workers present a general approach in which Fe3+ additives initiate the generation of intra-valence band holes in organic conjugated molecular crystals under visible-light irradiation. This approach significantly enhances the oxidation potential for photocatalytic pollutant degradation. The balance between oxidation potential and spectral response range is a critical consideration in photocatalysis. In this issue of Chem, Zhu and co-workers present a general approach in which Fe3+ additives initiate the generation of intra-valence band holes in organic conjugated molecular crystals under visible-light irradiation. This approach significantly enhances the oxidation potential for photocatalytic pollutant degradation. Generation of holes from intra-valence band for enhanced oxidation potentials under visible lightGuo et al.ChemFebruary 19, 2024In BriefThis study presents a novel approach for initiating intra-valence band hole generation in organic conjugated molecular crystals under visible light irradiation. Among five representative organic conjugated particles, the oxidation potentials of intra-valence band holes can reach up to 3.85 V vs. RHE. These holes couple with carbonyl groups, forming hole-coupled carbonyl sites (–C=O+) with a long lifetime of 84.5 ns. The high-energy photogenerated holes exhibit scalable oxidation capabilities, such as the degradation of organic pollutants in water under natural sunlight conditions. Full-Text PDF
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