Facile Synthesis of Co@TiO2/C Hybrid Catalyst and Its Application to Photocatalytic Reduction of CO2 under Visible-Light Irradiation

被引:0
作者
Xu, Yong [1 ]
Fu, Zi-Cheng [1 ]
Fu, Wen-Fu [1 ,2 ]
Liu, Su [2 ]
Fu, Wen-Fu [1 ,2 ]
机构
[1] Chinese Acad Sci, Tech Inst Phys & Chem, Beijing 100190, Peoples R China
[2] Yunnan Normal Univ, Coll Chem & Chem Engn, Kunming 650092, Yunnan, Peoples R China
来源
PROCEEDINGS OF 2019 IEEE 2ND INTERNATIONAL CONFERENCE ON RENEWABLE ENERGY AND POWER ENGINEERING (REPE 2019) | 2019年
关键词
Co@TiO2/C hybrid catalyst; photocatalysis; visible light; CO2; reduction; CO; TIO2; SELECTIVITY; COCATALYST; COMPLEX; TITANIA; SYSTEM;
D O I
10.1109/repe48501.2019.9025148
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Solar-light-driven reduction of CO2 into energy-rich carbon-based products has attracted wide attention, with specific importance attached to the development of highly efficient catalysts and the establishing new photocataytic systems. Herein, we develop a facile approach to embed Co nanoparticles to hollow TiO2 nanorods (HTONR) to form a hybrid catalyst (Co/HTONR) by one-step calcination of a self-assembly of cobalt(II) and tetrabutyl titanate. After coating with a carbon nanolayer, the photocatalytic activity of the material towards CO2-to-CO conversion was boosted, CO generation rate of up to 54,000 mu mol h(-1) g(-1) was observed in the first hour of reaction. The average production rate of 28,500 mu mol h(-1) g(-1) with a selectivity of 78.1% for the transformation can be achieved even though the irradiation time was prolonged to 3 h. The excellent efficiency was partially attributed to the carbon nanolayer improving the electron transmission properties and accordingly enhanced the catalytic activities comparison to that of Co@TiO2. Additionally, the introduction of hollow TiO2 nanorods increases the local CO2 concentration owing to its adsorption. And existence of -OH group on the surface of TiO2 facilitated the key kinetic step of proton transfer during CO2 photoreduction, which is further confirmed by an investigation of catalytic efficiencies as a function of amount of H2O.
引用
收藏
页码:166 / 171
页数:6
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