氨
氧化还原
可见光谱
价带
光催化
半导体
化学
光化学
带隙
纳米技术
材料科学
无机化学
催化作用
光电子学
有机化学
作者
Min Chen,Changbin Zhang,Hong He
标识
DOI:10.1021/acs.est.0c02589
摘要
Excessive emission of ammonia (NH3) gives rise to a number of negative effects on the environment and human health. Photocatalysis is an efficient method to eliminate gaseous NH3; however, photocatalytic oxidation (PCO) of NH3 in the visible light region has not been achieved to date. Herein, we test a set of typical visible-light-sensitive photocatalysts (N-TiO2, g-C3N4, and Ag3PO4) for NH3 oxidation and reveal for the first time that the semiconductor Ag3PO4 can harness visible light to realize ambient NH3 oxidation. Combining the activity testing results with the photochemical properties of samples, we confirm that photoexcited holes are responsible for triggering the initial key step of NH3 oxidation (NH3 to •NH2), and therefore, the redox potential of photoexcited holes plays the decisive role in the reaction. We propose that an active visible light photocatalyst for NH3 oxidation requires both a suitable band gap for visible light response and a low valence band edge associated with a high oxidation potential for activating NH3 to •NH2. Our findings provide new insights into the PCO of pollutants under visible light and will benefit future design of more efficient visible-light-sensitive photocatalysts.
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