Surface oxygen vacancies on WO3 contributed to enhanced photothermo-synergistic effect

被引:94
作者
Li, Yingying
Wang, Changhua
Zheng, Han
Wan, Fangxu
Yu, Fei
Zhang, Xintong [1 ]
Liu, Yichun
机构
[1] Northeast Normal Univ, Sch Phys, Ctr Adv Optoelect Mat Res, 5268 Renmin St, Changchun 130024, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Phase transition in WO3; Photothermocatalytic; Visible-NIR response; Oxygen vacancy; WO3; LIGHT-DRIVEN THERMOCATALYSIS; TIO2; PHOTOCATALYSIS; ISOTOPIC EXCHANGE; LATTICE OXYGEN; OXIDATION; HYDROGEN; CATALYST; BENZENE; NANOCOMPOSITES; PURIFICATION;
D O I
10.1016/j.apsusc.2016.07.042
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
Photothermooxidation has demonstrated a high efficiency in the removal of volatile organic compounds in air. Among photothermocatalysts, attention is presently focused on composites of noble metal/metal oxide or metal oxide/metal oxide. Instead, in this work, we present a case of single oxide WO3 subjected to hydrogen treatment as photothermocatalyst. With the increase of hydrogen treatment temperature, the color of WO3 changes from yellow to blue to dark blue and a phase transition from WO3 to W0232 to WO2 is accompanied, suggesting an increase of concentration of oxygen vacancy. Photothermocatalytic test against degradation of gaseous acetaldehyde at 60 degrees C under UV light shows that WO3-x sample with low concentration of oxygen vacancy displays the most significant synergetic effect between photocatalysis and thermocatalysis. Its photothermocatalytic activity in terms of CO2 evolution rate is 5.2 times higher than that of photocatalytic activity. However, WO3 -W02.72 and WO2 with high degree of oxygen deficiency show insignificant synergetic effect between photocatalysis and thermocatalysis. The reason for the different synergistic effect over above samples is believed to lie in balance between decreased activation energy of lattice oxygen and recombination of photogenerated electrons and holes induced by oxygen deficiency. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:654 / 661
页数:8
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