Strain-assisted in-situ formed oxygen defective WO3 film for photothermal-synergistic reverse water gas shift reaction and single-particle study

光致发光 水煤气变换反应 材料科学 光热治疗 氧气 催化作用 粒子(生态学) 粒径 解吸 载流子 化学工程 吸附 纳米技术 光化学 化学 光电子学 物理化学 有机化学 工程类 地质学 海洋学
作者
Yayang Xu,Mu Liu,Fengxia Tong,Fahao Ma,Xiangyun He,Zeyan Wang,Peng Wang,Yuanyuan Liu,Hefeng Cheng,Ying Dai,Zhaoke Zheng,Baibiao Huang
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:433: 134199-134199 被引量:22
标识
DOI:10.1016/j.cej.2021.134199
摘要

Among the reactions about CO2 conversion, the reverse water gas shift (RWGS) reaction is an efficient method to convert CO2 to CO. Herein, by the assistance of strain and introduction of light and reactant, in-situ formed oxygen defective WO3 film was synthesized, as an effective catalyst for reverse water gas shift reaction with an intense photothermal-synergistic effect. Furthermore, the in-situ single-particle Time-Resolved Photoluminescence (TRPL) and Photoluminescence (PL) spectrum were used to explore the details during the reaction, and prolonged charge carrier lifetime and significantly enhanced Photoluminescence intensities were observed in the in-situ single-particle study. Notably, the production rate of CO for WO3 film is almost 10 times that of powder, which means that WO3 film has an intense photothermal-synergistic effect. As proved by the results of CO2 temperature-programmed desorption (TPD) and CO2 adsorption, the oxygen vacancies are beneficial to the capture and activation of CO2, boosting the process of the reverse water gas shift. Meanwhile, lattice strain arising from the thermal expansion during the reaction could assist the in-situ formation of oxygen defects, enhance charge separation and regulate the electrical structure. All of this contribute to the synergy effect in photothermal reaction. Our work may provide a novel strategy for reasonable design of catalyst and illuminate the behavior of carriers in single-particle level.
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