Photogenerated carriers transfer in Pd/TiO2-AgO heterojunction and its photocatalytic behaviors on oxidative dehydrogenation of ethane to ethylene

IF 5.3 2区 化学 Q1 CHEMISTRY, APPLIED
Liming Zhou , Xiaomeng Zhao , Dongting Li , Pengyuan Qiu , Siyang Tang , Hairong Yue , Changjun Liu , Shan Zhong , Kui Ma , Bin Liang
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引用次数: 0

Abstract

Photocatalytic oxidative dehydrogenation of ethane to ethylene with a high selectivity is an attractive reaction. In this study, different types of heterojunctions between Pd/TiO2 and a second metal oxide semiconductor were designed and synthesized to realize high activity conversion of C2H6 to C2H4. Pd/TiO2-AgO heterojunction was proved with best reaction performance. The addition of AgO facilitated the activation of reactant molecules. It enhanced directional transfer of electron-hole pairs and separation efficiency of photogenerated carriers. Pd/TiO2-5 % AgO heterojunction was proved with the best separation ability of photogenerated carriers and the largest number of surface hydroxyl groups. Detailed charge transfer path and reaction mechanism were proposed and discussed.

Abstract Image

钯/二氧化钛-氧化银异质结中的光生载流子转移及其在乙烷氧化脱氢制乙烯过程中的光催化行为
光催化氧化脱氢将乙烷高选择性地转化为乙烯是一种极具吸引力的反应。本研究设计并合成了 Pd/TiO2 与第二种金属氧化物半导体之间不同类型的异质结,以实现 C2H6 向 C2H4 的高活性转化。结果表明,Pd/TiO2-AgO 异质结的反应性能最佳。AgO 的加入促进了反应物分子的活化。它增强了电子-空穴对的定向转移和光生载流子的分离效率。实验证明,Pd/TiO2-5 % AgO 异质结的光生载流子分离能力最强,表面羟基数量最多。提出并讨论了详细的电荷转移路径和反应机理。
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来源期刊
Catalysis Today
Catalysis Today 化学-工程:化工
CiteScore
11.50
自引率
3.80%
发文量
573
审稿时长
2.9 months
期刊介绍: Catalysis Today focuses on the rapid publication of original invited papers devoted to currently important topics in catalysis and related subjects. The journal only publishes special issues (Proposing a Catalysis Today Special Issue), each of which is supervised by Guest Editors who recruit individual papers and oversee the peer review process. Catalysis Today offers researchers in the field of catalysis in-depth overviews of topical issues. Both fundamental and applied aspects of catalysis are covered. Subjects such as catalysis of immobilized organometallic and biocatalytic systems are welcome. Subjects related to catalysis such as experimental techniques, adsorption, process technology, synthesis, in situ characterization, computational, theoretical modeling, imaging and others are included if there is a clear relationship to catalysis.
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