Tuning oxygen vacancies via photoinduced defect engineering in plasma pre-treated TiO2 for efficient solar-light-driven oxidation of trace methane
文献类型: 外文期刊
作者: Qiyu Zhang;Jiakang Duan;Zhiping Zhu;Li Rong;Xiaochang Lin;Hongmin Dong;Dezhao Liu
作者机构:
关键词: Oxygen vacancy;Photocatalytic methane oxidation;Photoinduced defect engineering;Plasma treatment
期刊名称: Chemical Engineering Journal
ISSN: 1385-8947
年卷期: 2024 年 497 卷
页码:
收录情况: SCIE(2024版) ; ; EI(2024版)
摘要: Photocatalysis employing cost-effective commercial titanium dioxide offers an ideal solution for eliminating trace methane emissions from livestock and poultry farming. However, significant challenges such as the rapid recombination of photogenerated carriers, a limited light absorption spectrum, and weak adsorption capabilities considerably hinder the effectiveness of titanium dioxide in the photocatalytic treatment of trace methane. This study proposes a novel approach to activate plasma pre-treated N-doped commercial anatase TiO2 into dual-defect TiO2 (N-doped TiO2-x) featuring stable and controllable oxygen vacancies (OV) through photoinduced defect engineering. Characterizations of the photocatalyst confirm the successful creation of surface defects, further evaluated through solar-light-driven CH4 (ppm level) removal investigations. The yield of this N-doped TiO2-x in converting CH4 is 4.84 μmol h−1, 44 times greater than that of unmodified TiO2, significantly outperforming previous studies. UV–Vis diffuse reflection spectra, and photoluminescence indicate that the modified commercial anatase TiO2 possesses a narrower band gap, efficient photogenerated carrier separation, and enhanced charge transfer. Furthermore, density functional theory (DFT) calculations demonstrate that the synergistic effects of oxygen vacancies and N doping enhance the adsorption and activation of both O2 and CH4 in the rate-determining step of the reaction. This innovative strategy holds considerable promise for modifying various materials for more efficient photocatalytic applications.
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