Study of PdO species on surface of TiO2 for photoreduction of CO2 into CH4

被引:19
|
作者
Zhao, Qiao [1 ,2 ]
Li, Hanbo [1 ,2 ]
Zhang, Lixin [1 ,2 ]
Cao, Yaan [1 ]
机构
[1] Nankai Univ, TEDA Appl Phys Inst, Key Lab Weak Light Nonlinear Photon, Minist Educ, Tianjin 300457, Peoples R China
[2] Nankai Univ, Sch Phys, Tianjin 300457, Peoples R China
基金
中国国家自然科学基金;
关键词
TiO2; CO2; Photoreduction; CH4; PdO; Inactivation; ENHANCED PHOTOCATALYTIC ACTIVITY; CARBON-DIOXIDE; REDUCTION; ENERGY; HETEROSTRUCTURE; DECOMPOSITION; NANOPARTICLES; COPPER; IONS;
D O I
10.1016/j.jphotochem.2019.112032
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
Different percentage of PdO composited TiO2 photocatalysts (TiO2-PdOX%, X >= 1.5) are prepared using the sol-gel way. It can be revealed that the inducted Pd ions play a role of PdO surface species instead of entering into the TiO2 crystal lattice determined by the characterization measurements of X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and High-resolution transmission electron microscopy (HRTEM). The behaviors of photogenerated electron-hole pairs and band structure of the synthesized TiO2-PdOX% (X >= 1.5) photocatalysts are investigated by Photoluminescence (PL), PL lifetime decay curves, XPS valence band (VB) spectra, the density-functional theory (DFT) calculation and UV-vis diffuse reflectance spectra. The TiO2-PdOX% (X >= 1.5) photocatalysts exhibit higher activity for conversion of CO2 to CH4 than pristine TiO2 due to the presence of PdO. The inactivation mechanism for TiO2-PdOX% photoreduction is also discussed. This work can further explain the influence of surface species on photocatalytic performance.
引用
收藏
页数:8
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