Oxygen-Deficient BiOBr as a Highly Stable Photocatalyst for Efficient CO2 Reduction into Renewable Carbon-Neutral Fuels

被引:134
作者
Kong, Xin Ying [1 ]
Lee, W. P. Cathie [1 ]
Ong, Wee-Jun [1 ,2 ]
Chai, Siang-Piao [1 ]
Mohamed, Abdul Rahman [3 ]
机构
[1] Monash Univ, Sch Engn, Chem Engn Discipline, Multidisciplinary Platform Adv Engn, Jalan Lagoon Selatan, Bandar Sunway 47500, Selangor, Malaysia
[2] ASTAR, IMRE, 2 Fusionopolis Way, Innovis 138634, Singapore
[3] Univ Sains Malaysia, Sch Chem Engn, Low Carbon Econ LCE Grp, Engn Campus, Nibong Tebal 14300, Pulau Pinang, Malaysia
关键词
bismuth oxybromide; CO2; reduction; oxygen deficiency; photocatalysis; solar energy; VISIBLE-LIGHT ABSORPTION; BISMUTH OXYBROMIDE; 001; FACETS; RICH TIO2; DIOXIDE; VACANCY; NANOPARTICLES; DISSOCIATION; MICROSPHERES; DEGRADATION;
D O I
10.1002/cctc.201600782
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
A highly facile one-pot ethylene glycol-assisted solvothermal process was employed to fabricate bismuth oxybromide (BiOBr) with oxygen-deficient defects. These defects played an indispensable role for superior photocatalytic CO2 reduction, in which the as-prepared sample demonstrated a remarkable improvement of 3.3 and 5.7-fold for CH4 production over pristine BiOBr and P25, respectively. The enhancement could be attributed to the presence of oxygen vacancies, which acted as the active sites for CO2 adsorption and activation. In addition, the oxygen-deficiency-induced defect states could effectively trap photogenerated electrons, thus improving the separation of the electron-hole pairs and significantly slow down the recombination rate of charge carriers. On top of that, oxygen-deficient BiOBr exhibited long term stability (>50 hours of catalytic reaction) for CO2 photoreduction under simulated solar light, where no reducing agent or any post-treatment was needed to regenerate the oxygen vacancies.
引用
收藏
页码:3074 / 3081
页数:8
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