异质结
光催化
材料科学
铋
可见光谱
氮氧化物
载流子
半导体
光电子学
限制
吸收(声学)
纳米技术
化学工程
催化作用
化学
复合材料
有机化学
冶金
机械工程
生物化学
工程类
燃烧
作者
Qin Geng,Hongtao Xie,Wenjing Ji,Yizhao Li,Si Chen,Bangwei Deng,Ruiben Jin,Fan Dong
标识
DOI:10.1021/acs.jpcc.4c01980
摘要
Given the environmental hazards posed by low-concentration NOx emissions, visible-light-driven photocatalytic technologies have been widely studied for the removal of NOx. Constrained by the insufficient light absorption range and rapid recombination of carriers of an individual photocatalyst, the construction of heterojunctions has emerged as a promising strategy to bolster photocatalytic reaction kinetics. However, traditional approaches for fabricating heterojunctions frequently result in interfaces that are loosely connected and poorly contacted, greatly limiting the photocatalytic performance of the heterojunctions. Therefore, in this research, a BiOI/Bi5O7I p-n heterojunction was successfully constructed through an in situ phase transformation approach, demonstrating exceptional photocatalytic performance in the purification of NO under visible light irradiation. Benefiting from the interfacial electric field formed at the tightly formed heterojunction interface, significant suppression of carrier recombination and improved separation efficiency were achieved, as evidenced by both in situ DRIFTS and theoretical calculations. This strategy can also inspire the utilization of in situ heterojunction construction to modulate the electronic structure of conventional bismuth-based semiconductors, enhance charge transfer at the interface, and improve the photocatalytic activity.
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