Nonaqueous synthesis of CoOx/TiO2 nanocomposites showing high photocatalytic activity of hydrogen generation

被引:48
作者
Wang, Yu-Fen [1 ]
Hsieh, Meng-Chun [1 ]
Lee, Jyh-Fu [2 ]
Yang, Chia-Min [1 ,3 ]
机构
[1] Natl Tsing Hua Univ, Dept Chem, Hsinchu 30013, Taiwan
[2] Natl Synchrotron Radiat Res Ctr, Hsinchu 30076, Taiwan
[3] Natl Tsing Hua Univ, Frontier Res Ctr Fundamental & Appl Sci Matters, Hsinchu 30013, Taiwan
关键词
p-n diode-type photocatalyst; CoOx/TiO2; nanocomposite; Nonaqueous synthesis; Photocatalytic hydrogen production; WATER; NANOMATERIALS; DEGRADATION; ADSORPTION; CHEMISTRY; CATALYSTS; DEVELOP; BIOMASS; COBALT; OXYGEN;
D O I
10.1016/j.apcatb.2013.05.073
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
This paper describes a nonaqueous sol-gel preparation of p-n diode-type CoOx/TiO2 nanocomposites for photocatalytic hydrogen generation. Characterization results suggested that the nanocomposites consisted of highly crystalline anatase nanoparticles and Co3O4-like species. They showed composition-dependent activity for hydrogen production under ultraviolet light irradiation with methanol as a sacrificial agent. The nanocomposite with the optimum composition exhibited superior photocatalytic activity and a hydrogen evolution rate of 2.17 mmol g(-1) h(-1). In comparison, the hydrogen evolution rates for the reference photocatalysts Degussa P25 and sodium tantalite measured under the same conditions were 20 mu mol g(-1) and 410 mu mol g(-1), respectively. The stability and the concentration-dependent hydrogen production with methanol or ethanol as sacrificial agent were also studied. In addition, the nanocomposite was capable of producing hydrogen, albeit in small amount, in the sacrificial agent-free conditions in the phosphate-buffered solutions. The results show not only the uniqueness of the nonaqueous synthesis for highly active CoOx/TiO2 heterojunction photocatalysts, but also the possibility to further improve the photocatalytic activity of CoOx/TiO2 through surface engineering. (c) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:626 / 632
页数:7
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