Electronic structure and enhanced photoelectrocatalytic performance of RuxZn1-xO/Ti electrodes

被引:35
作者
Shao, Yanqun [1 ,2 ]
Feng, Keke [1 ]
Guo, Jie [1 ]
Zhang, Rongrong [1 ]
He, Sijiang [1 ]
Wei, Xinli [1 ]
Lin, Yuting [1 ]
Ye, Zhanghao [1 ]
Chen, Kongfa [1 ]
机构
[1] Fuzhou Univ, Coll Mat Sci & Engn, Fuzhou 350108, Peoples R China
[2] Fuzhou Univ, Coll Zhicheng, Fuzhou 350002, Peoples R China
基金
中国国家自然科学基金;
关键词
RuxZn1-xO/Ti electrode; first-principles calculation; electric collector; photoelectric synergistic catalysis; POT MULTICOMPONENT SYNTHESIS; DOPED ZNO; PHOTOCATALYTIC DEGRADATION; OPTICAL-PROPERTIES; CATALYTIC-PROPERTIES; AQUEOUS-SOLUTION; 1ST PRINCIPLES; OXIDATION; EFFICIENT; RUO2;
D O I
10.1007/s40145-021-0486-x
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Modification is one of the most important and effective methods to improve the photoelectrocatalytic (PEC) performance of ZnO. In this paper, the RuxZn1-xO/Ti electrodes were prepared by thermal decomposition method and the effect of Ru content on those electrodes' electronic structure was analyzed through the first-principles calculation. Various tests were also performed to observe the microstructures and PEC performance. The results showed that as the Ru4+ transferred into ZnO lattice and replaced a number of Zn2+, the conduction band of ZnO moved downward and the valence band went upward. The number of photogenerated electron-hole pairs increased as the impurity levels appeared in the band gap. In addition, ZnO nanorods exhibited a smaller grain size and a rougher surface under the effect of Ru. Meanwhile, the RuO2 nanoparticles on the surface of ZnO nanorods acted as the electron-transfer channel, helping electrons transfer to the counter electrode and delaying the recombination of the electron-hole pairs. Specifically, the RuxZn1-xO/Ti electrodes with 9.375 mol% Ru exhibited the best PEC performance with a rhodamine B (RhB) removal rate of 97%, much higher than the combination of electrocatalysis (EC, 12%) and photocatalysis (PC, 50%), confirming the synergy of photoelectrocatalysis.
引用
收藏
页码:1025 / 1041
页数:17
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