Enhanced photocatalytic water splitting activity of carbon-modified TiO2 composite materials synthesized by a green synthetic approach

被引:107
作者
Parayil, Sreenivasan Koliyat [1 ]
Kibombo, Harrison S. [1 ]
Wu, Chia-Ming [1 ]
Peng, Rui [1 ]
Baltrusaitis, Jonas [2 ]
Koodali, Ranjit T. [1 ]
机构
[1] Univ S Dakota, Dept Chem, Vermillion, SD 57069 USA
[2] Univ Iowa, Dept Chem, Iowa City, IA 52246 USA
关键词
TiO2; Sucrose; Pyrolysis; Carbonization; Photocatalysis; Hydrogen evolution; LOW-TEMPERATURE PREPARATION; CO-DOPED TIO2; NANOCRYSTALLINE TIO2; HYDROGEN GENERATION; HYDROTHERMAL METHOD; CHARGE SEPARATION; SURFACE; SEMICONDUCTOR; TITANIA; ANATASE;
D O I
10.1016/j.ijhydene.2012.02.067
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
We report a green and facile approach for the preparation of carbon-modified (C-modified) TiO2 composite materials by hydrothermal synthesis followed by pyrolytic treatment. The resultant materials were characterized by powder X-ray diffraction (XRD), nitrogen physisorption studies, Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), diffuse reflectance spectroscopy (DRS), photoluminescence (PL) spectroscopy, and transmission electron microscopy (TEM). The photocatalytic performances of these materials were evaluated by calculating the amount of hydrogen evolved from the decomposition of water under solar simulated irradiation conditions. An improvement was achieved from no H-2 evolution at all with the bare TiO2, to an evolution of 0.21 mL g(-1) h(-1) from a composite material modified with an optimum carbon loading of 3.62%. These results suggested that the interaction of carbon with predominantly rutile form of TiO2 can promote shallow trapping of photogenerated electrons in the oxygen vacancies. This phenomenon consequently enhances the photocatalytic activity by minimizing charge carrier recombination, a characteristic demonstrated by fluorescence quenching of the TiO2 emission. Copyright (C) 2012, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:8257 / 8267
页数:11
相关论文
共 66 条
[1]   Preparation, Characterization of Sulfur-Doped Nanosized TiO2 and Photocatalytic Degradation of Methylene Blue Under Visible Light [J].
Ang, Thiam Peng ;
Law, Jia Yan ;
Han, Yi-Fan .
CATALYSIS LETTERS, 2010, 139 (1-2) :77-84
[2]  
Briggs D., 1983, Practical Surface Analysis: by Auger and X-ray Photoelectron Spectroscopy
[3]   Carbon and nitrogen co-doped TiO2 with enhanced visible-light photocatalytic activity [J].
Chen, Daimei ;
Jiang, Zhongyi ;
Geng, Jiaqing ;
Wang, Qun ;
Yang, Dong .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2007, 46 (09) :2741-2746
[4]   THE ROLE OF METAL-ION DOPANTS IN QUANTUM-SIZED TIO2 - CORRELATION BETWEEN PHOTOREACTIVITY AND CHARGE-CARRIER RECOMBINATION DYNAMICS [J].
CHOI, WY ;
TERMIN, A ;
HOFFMANN, MR .
JOURNAL OF PHYSICAL CHEMISTRY, 1994, 98 (51) :13669-13679
[5]   Nitrogen-doped TiO2 from TiN and its visible light photoelectrochemical properties [J].
Cui, Xiaoli ;
Ma, Ming ;
Zhang, Wei ;
Yang, Yanchao ;
Zhang, Zhuangjian .
ELECTROCHEMISTRY COMMUNICATIONS, 2008, 10 (03) :367-371
[6]   ELECTRONIC BAND-STRUCTURE OF TITANIUM-DIOXIDE [J].
DAUDE, N ;
GOUT, C ;
JOUANIN, C .
PHYSICAL REVIEW B, 1977, 15 (06) :3229-3235
[7]   Theory of carbon doping of titanium dioxide [J].
Di Valentin, C ;
Pacchioni, G ;
Selloni, A .
CHEMISTRY OF MATERIALS, 2005, 17 (26) :6656-6665
[8]   Dynamics of Localized Charges in Dopamine-Modified TiO2 and their Effect on the Formation of Reactive Oxygen Species [J].
Dimitrijevic, Nada M. ;
Rozhkova, Elena ;
Rajh, Tijana .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2009, 131 (08) :2893-2899
[9]   Light-induced charge separation and redox chemistry at the surface of TiO2/host-guest hybrid nanoparticles [J].
Dimitrijevic, NM ;
Rajh, T ;
Saponjic, ZV ;
de la Garza, L ;
Tiede, DM .
JOURNAL OF PHYSICAL CHEMISTRY B, 2004, 108 (26) :9105-9110
[10]   Revealing the nature of trapping sites in nanocrystalline titanium dioxide by selective surface modification [J].
Dimitrijevic, NM ;
Saponjic, ZV ;
Bartels, DM ;
Thurnauer, MC ;
Tiede, DM ;
Rajh, T .
JOURNAL OF PHYSICAL CHEMISTRY B, 2003, 107 (30) :7368-7375