Semiconductor-cocatalyst interfacial electron transfer in actual photocatalytic reaction

IF 15.7 1区 化学 Q1 CHEMISTRY, APPLIED
Jiazang Chen
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引用次数: 0

Abstract

ABSTRACT

Semiconductor-cocatalyst interfacial electron transfer has widely been considered as a fast step occurring on picosecond-microsecond timescale in photocatalytic reaction. However, the formed potential barriers severely slow this interfacial electronic process by thermionic emission. Although trap-assisted charge recombination can transfer electrons from semiconductor to cocatalyst and can even be evident under weak illumination, the parallel connection with thermionic emission makes the photocatalytic photon utilization encounter a minimum along the variation of light intensity. By this cognition, the light-intensity-dependent photocatalytic behaviors can be predicted by simulating the photoinduced semiconductor-cocatalyst interfacial electron transfer that mainly determines the reaction rate. We then propose a (photo)electrochemical method to evaluate the time constants for occurring this interfacial electronic process in actual photocatalytic reaction without relying on extremely high photon flux that is required to generate discernible optical signal in common instrumental methods based on ultrafast pulse laser. The evaluated decisecond-second timescale can accurately guide us to develop certain strategies to facilitate this rate-determining step to improve photon utilization.
实际光催化反应中半导体-助催化剂界面电子转移
摘要半导体-助催化剂界面电子转移被广泛认为是光催化反应中发生在皮秒-微秒时间尺度上的快速步骤。然而,形成的势垒严重减缓了热电子发射的界面电子过程。尽管陷阱辅助电荷复合可以将电子从半导体转移到助催化剂上,并且在弱光照下也能明显地实现,但与热离子发射的平行连接使得光催化光子利用率随着光强的变化而减小。通过这种认知,可以通过模拟主要决定反应速率的光诱导半导体-助催化剂界面电子转移来预测依赖于光强的光催化行为。然后,我们提出了一种(光)电化学方法来评估实际光催化反应中发生该界面电子过程的时间常数,而不依赖于基于超快脉冲激光的常见仪器方法中产生可识别光信号所需的极高光子通量。评估的决策秒-秒时间尺度可以准确地指导我们制定某些策略来促进这一速率决定步骤,以提高光子利用率。
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来源期刊
Chinese Journal of Catalysis
Chinese Journal of Catalysis 工程技术-工程:化工
CiteScore
25.80
自引率
10.30%
发文量
235
审稿时长
1.2 months
期刊介绍: The journal covers a broad scope, encompassing new trends in catalysis for applications in energy production, environmental protection, and the preparation of materials, petroleum chemicals, and fine chemicals. It explores the scientific foundation for preparing and activating catalysts of commercial interest, emphasizing representative models.The focus includes spectroscopic methods for structural characterization, especially in situ techniques, as well as new theoretical methods with practical impact in catalysis and catalytic reactions.The journal delves into the relationship between homogeneous and heterogeneous catalysis and includes theoretical studies on the structure and reactivity of catalysts.Additionally, contributions on photocatalysis, biocatalysis, surface science, and catalysis-related chemical kinetics are welcomed.
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