Effect of Surface Plasmon Resonance and the Heterojunction on Photoelectrochemical Activity of Metal-Loaded TiO2 Electrodes under Visible Light Irradiation

被引:2
|
作者
Chang, Chia-Yu [1 ,2 ]
Yamakata, Akira [1 ,3 ]
Tseng, Wenjea J. [2 ]
机构
[1] Toyota Technol Inst, Grad Sch Engn, Photochem React Lab, Nagoya, Aichi 4688511, Japan
[2] Natl Chung Hsing Univ, Dept Mat Sci & Engn, Taichung 402, Taiwan
[3] Okayama Univ, Grad Sch Nat Sci Technol, Okayama 7008530, Japan
关键词
HYDROGEN-PRODUCTION; RAMAN-SPECTRA; ANATASE TIO2; WATER; PHOTOCATALYSIS; PHOTODEPOSITION; CATALYSTS; TEMPERATURE; PERFORMANCE; FABRICATION;
D O I
10.1021/acs.jpcc.2c02649
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
This study examines the influence of surface plasmon resonance (SPR) and the semiconducting heterojunction on the photoelectrochemical (PEC) activity of metal-loaded TiO2 electrodes under visible light irradiation. Different metal nanoparticles (including Au, Ag, Rh, and Cu) have been selected deliberately and deposited on the TiO2 electrode layers via photodeposition and subsequent annealing at 300 degrees C. UV-vis spectra show an increased absorbance in the visible light region with the metal loading. X-ray photon spectroscopy reveals the formation of CuO, Ag2O, and Ru2O3 after annealing, while only Au remains in its metallic state. The PEC activity increases in the ascending order of Cu < Au < Rh < Ag. This is consistent with the electrochemical impedance measurement where the Ag-loaded TiO2 electrode shows the lowest charge transfer resistance together with the highest ion diffusion rate. Our findings suggest that the presence of semiconducting p-n heterojunctions with associated oxygen-vacancy defects facilitates the enhanced PEC activity by reducing the electron-hole recombination in addition to the SPR effect.
引用
收藏
页码:12450 / 12459
页数:10
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