The photoelectric catalytic reduction of CO2 to methanol on CdSeTe NSs/TiO2 NTs

被引:45
作者
Li, Peiqiang [1 ]
Zhang, Jun [1 ]
Wang, Huying [1 ]
Jing, Hua [1 ]
Xu, Jinfeng [1 ]
Sui, Xiaona [1 ]
Hu, Haitao [1 ]
Yin, Hongzong [1 ]
机构
[1] Shandong Agr Univ, Coll Chem & Mat Sci, Tai An 271018, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
TIO2; NANOPARTICLES; NANOTUBE ARRAYS; CARBON-DIOXIDE; HYDROGENATION; CONVERSION; FUELS; GAP;
D O I
10.1039/c3cy00978e
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
The CdSeTe nanosheet (CdSeTe NS)/TiO2 nanotube (TiO2 NT) photoelectrocatalyst was obtained by the hydrothermal method by loading CdSeTe NSs onto TiO2 NTs which were prepared by an anodic oxidation method. The SEM and TEM results show that CdSeTe had a flaky structure with a large size of 300-400 nm and a small size of about 100 nm, which distributed on the TiO2 NT surface uniformly. The HRTEM and XRD characterization revealed that the CdSeTe NSs grew along the (100) and (002) orientations. Measured by UV-vis DRS and XPS, the energy band gap of the TiO2 NTs was narrowed from 3.20 eV to 1.48 eV by the introduction of the CdSeTe NSs, of which the conduction band and valence band are located at -0.46 eV and 1.02 eV, respectively. In the photoelectrocatalytic reduction CO2 process, the current density had a significant improvement after the decoration with the CdSeTe NSs, increasing from 0.31 mA cm(-2) to 4.50 mA cm(-2) at -0.8 V. Methanol was the predominant photoelectrocatalytic reduction product identified by chromatography, and it reached 1166.77 mu mol L-1 after 5 h. In addition, the mechanism of the high efficiency photoelectrocatalytic reduction of CO2 to methanol was explained from the following aspects: energy band matching, high efficiency electron transmission and the stability of the catalyst.
引用
收藏
页码:1070 / 1077
页数:8
相关论文
共 35 条
[1]   Investigations of the metal-oxide semiconductors promising for photoelectrochemical conversion of solar energy [J].
Aroutiounian, VM ;
Arakelyan, VM ;
Shahnazaryan, GE .
SOLAR ENERGY MATERIALS AND SOLAR CELLS, 2005, 89 (2-3) :153-163
[2]  
Balaraman E, 2011, NAT CHEM, V3, P609, DOI [10.1038/NCHEM.1089, 10.1038/nchem.1089]
[3]   Selective solar-driven reduction of CO2 to methanol using a catalyzed p-GaP based photoelectrochemical cell [J].
Barton, Emily E. ;
Rampulla, David M. ;
Bocarsly, Andrew B. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2008, 130 (20) :6342-+
[4]   Luminescence of Polyethylene Glycol Coated CdSeTe/ZnS and InP/ZnS Nanoparticles in the Presence of Copper Cations [J].
Beaune, Gregory ;
Tamang, Sudarsan ;
Bernardin, Aude ;
Bayle-Guillemaud, Pascale ;
Fenel, Daphna ;
Schoehn, Guy ;
Vinet, Francoise ;
Reiss, Peter ;
Texier, Isabelle .
CHEMPHYSCHEM, 2011, 12 (12) :2247-2254
[5]  
Berndt ME, 1996, GEOLOGY, V24, P351, DOI 10.1130/0091-7613(1996)024<0351:ROCDSO>2.3.CO
[6]  
2
[7]   Hydrothermal Treatment of a Hematite Film Leads to Highly Oriented Faceted Nanostructures with Enhanced Photocurrents [J].
Bora, Debajeet K. ;
Braun, Artur ;
Erni, Rolf ;
Fortunato, Giuseppino ;
Graule, Thomas ;
Constable, Edwin C. .
CHEMISTRY OF MATERIALS, 2011, 23 (08) :2051-2061
[8]   Development of Molecular Electrocatalysts for CO2 Reduction and H2 Production/Oxidation [J].
Dubois, M. Rakowski ;
Dubois, Daniel L. .
ACCOUNTS OF CHEMICAL RESEARCH, 2009, 42 (12) :1974-1982
[9]   Combustion synthesis of CuO-ZnO-ZrO2 catalysts for the hydrogenation of carbon dioxide to methanol [J].
Guo, Xiaoming ;
Mao, Dongsen ;
Wang, Song ;
Wu, Guisheng ;
Lu, Guanzhong .
CATALYSIS COMMUNICATIONS, 2009, 10 (13) :1661-1664