Improved photocatalytic activity and durability of AgTaO3/AgBr heterojunction: The relevance of phase and electronic structure

IF 5.062
Fang Wang , Tingting Wang , Junyu Lang, Yiguo Su, Xiaojing Wang
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引用次数: 15

Abstract

AgTaO3/AgBr heterojunction was constructed for visible light driven photocatalytic purpose in order to investigate the relevance of phase conversion, electronic structure and photocatalytic properties. The result indicated that AgBr grafted on AgTaO3 to form AgTaO3/AgBr heterojunction gave intense visible light absorption, which exhibits highly enhanced photocatalytic performance than their individual counterpart. Theoretical and experimental investigation showed that the matched electronic structure between AgTaO3 and AgBr induced an efficient transfer of photogenerated electrons from AgBr to AgTaO3, leading to efficient charge separation and the subsequent improved photocatalytic activity. Partial AgBr converted to AgBr/Ag during the photocatalytic process, leading to the construction of ternary AgTaO3/AgBr/Ag photocatalyst. Because of the surface plasmon resonance effect of Ag, the resulting AgTaO3/AgBr/Ag exhibited wide range absorption and improved charge separation efficiency, which showed high durability and superior photocatalytic activity toward methyl orange degradation. On the basis of spin resonance measurement and trapping experiment, it is expected that photogenerated electrons, O2, and OH active species dominate the photodegradation of methyl orange.

Abstract Image

提高AgTaO3/AgBr异质结的光催化活性和耐久性:相和电子结构的相关性
构建AgTaO3/AgBr异质结用于可见光驱动的光催化目的,以研究其相变、电子结构与光催化性能的相关性。结果表明,AgBr接枝在AgTaO3上形成的AgTaO3/AgBr异质结具有较强的可见光吸收能力,其光催化性能比单独接枝的AgTaO3/AgBr具有较强的光催化性能。理论和实验研究表明,AgTaO3和AgBr之间匹配的电子结构诱导了光生电子从AgBr向AgTaO3的有效转移,从而实现了有效的电荷分离,从而提高了AgTaO3的光催化活性。在光催化过程中,部分AgBr转化为AgBr/Ag,构建了三元AgTaO3/AgBr/Ag光催化剂。由于Ag的表面等离子体共振效应,制备的AgTaO3/AgBr/Ag具有较宽的吸收范围和较高的电荷分离效率,对甲基橙的降解具有较高的耐久性和优异的光催化活性。根据自旋共振测量和俘获实验,预计光生电子、O2−和OH活性物质主导甲基橙的光降解。
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来源期刊
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审稿时长
2.8 months
期刊介绍: The Journal of Molecular Catalysis A: Chemical publishes original, rigorous, and scholarly full papers that examine the molecular and atomic aspects of catalytic activation and reaction mechanisms in homogeneous catalysis, heterogeneous catalysis (including supported organometallic catalysis), and computational catalysis.
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