A strategy for in-situ synthesis of well-defined core-shell Au@TiO2 hollow spheres for enhanced photocatalytic hydrogen evolution

被引:54
作者
Ngaw, Chee Keong [1 ]
Xu, Qingchi [2 ]
Tan, Timothy T. Y. [2 ]
Hu, Peng [4 ]
Cao, Shaowen [3 ]
Loo, Joachim S. C. [4 ]
机构
[1] Nanyang Technol Univ, Energy Res Inst, Interdisciplinary Grad Sch, Singapore 639798, Singapore
[2] Nanyang Technol Univ, Sch Chem & Biomed Engn, Solar Fuels Lab, Singapore 627459, Singapore
[3] Wuhan Univ Technol, State Key Lab Adv Technol Mat Synth & Proc, Wuhan 430070, Peoples R China
[4] Nanyang Technol Univ, Sch Mat Sci & Engn, Solar Fuels Lab, Singapore 639798, Singapore
基金
新加坡国家研究基金会;
关键词
Hollow spheres; Core-shell; Titanium dioxide; Gold nanoparticles; Photocatalytic hydrogen evolution; Surface plasmonic resonance; SURFACE-PLASMON RESONANCE; MESOPOROUS TANTALUM OXIDE; GOLD NANOPARTICLES; LIGHT-DRIVEN; 001; FACETS; TIO2; NANOCOMPOSITES; CARBON; SIZE; NANOSTRUCTURES;
D O I
10.1016/j.cej.2014.07.059
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
This work reports a simple strategy to prepare Au@TiO2 core-shell hollow spheres with well-defined morphology by combining an in-situ hydrothermal reduction technique with the adsorption of Ti4+ ions onto carbon spheres via a hard template strategy. H-2 evolution measurements suggest that the prepared Au@TiO2-2 (2.0 wt%) hollow spheres exhibited remarkable H-2 evolution activity (7 times) compared to Au-P25 under ultra violet irradiation. The enhanced photocatalytic efficiencies are attributed to the large surface area of Au@TiO2, with the encapsulated Au NPs acting as co-catalyst. In addition, an enhanced surface plasmonic resonance (SPR) effect by the Au NPs resulted in better light absorption of the hollow structure. This synthesis strategy can also be extended to other types of core-shell hollow composites (Pt@TiO2 and Au@Fe2O3). This would open a new avenue for the development of well-defined core-shell hollow structures for various applications, including hydrogen generation. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:112 / 121
页数:10
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