F-doped CeO2 supported Co-based nanoparticles for enhanced photocatalytic H2 evolution from ammonia borane

被引:16
|
作者
Song, Jin [1 ]
Wu, Fenglong [1 ]
Lu, Yulun [1 ]
Zhang, Xinyan [1 ]
机构
[1] Hetao Coll, Dept Ecol & Resource Engn, Bayan Nur 015000, Peoples R China
基金
中国国家自然科学基金;
关键词
Doping; F-CeO; 2; Photocatalytic; H; evolution; Ammonia borane; CATALYTIC HYDROGEN EVOLUTION; METAL NANOPARTICLES; HIGH-EFFICIENCY; HYDROLYSIS; SURFACE; PERFORMANCE; GENERATION; SHELL; OXIDE; NI;
D O I
10.1016/j.ijhydene.2022.12.219
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
Doping as a common mean to generate defects to boost the catalytic performance of metal oxide semiconductor-based materials has aroused great interest. However, doping usually requires high temperatures and is time consuming. Herein, we report a facile strategy for the preparation of F doped CeO2 (F-CeO2) with assistance of the electrostatic attraction between F- and CeO2 with oxygen vacancies at room temperature, then F-CeO2 acts as superior support of metal Co nanoparticles (NPs) for efficient hydrolysis of NH3BH3 under light irradiation. The activity of Co/F-CeO2 is significantly enhanced and Co/F-CeO2-0.6 exhibited highest catalytic activity with TOF value 92.8 min-1 which increases 47% compared with Co/CeO2. Experimental and characterization results show the enhanced performance attributes to high efficiency photogenerated carrier separation and boosting adsorption capacity of H2O and NH3BH3 over Co/F-CeO2 due to F doped into CeO2 crys-tallites. Furthermore, theory calculations further confirm that the band gap of F-CeO2 becomes smaller and F-CeO2 is more favorable the adsorption for H2O and NH3BH3 than pure CeO2. This work offers a facile and time efficiency strategy to realize controllable element doped in metal oxide under ambient, and gives deep insights into the structure-activity relationship of catalyst between defect engineering and photocatalytic performance.(c) 2022 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:13202 / 13212
页数:11
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