Room-temperature synthesis of cuprous oxide and its heterogeneous nanostructures for photocatalytic applications

被引:23
|
作者
Zhu, Hongmei [1 ]
Li, Yi [2 ]
Jiang, Xuchuan [2 ]
机构
[1] Univ South China, Sch Mech Engn, Hengyang 421001, Hunan, Peoples R China
[2] Monash Univ, Dept Chem Engn, Clayton, Vic 3800, Australia
基金
澳大利亚研究理事会;
关键词
Cuprous oxide (Cu2O); Nanospheres; Octahedrons; Nanowires; Heterogeneous nanostructures; Photocatalysis; REDUCED GRAPHENE OXIDE; ONE-POT SYNTHESIS; CU2O NANOCRYSTALS; HYDROTHERMAL SYNTHESIS; CONTROLLABLE SYNTHESIS; SHAPE EVOLUTION; GOLD NANORODS; NANOPARTICLES; GROWTH; EFFICIENT;
D O I
10.1016/j.jallcom.2018.09.092
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 study represents a facile but effective room-temperature strategy for the synthesis of shape/size-controlled cuprous oxide (Cu2O) nanoparticles under mild conditions. The proposed synthesis method offers several advantages/novelties including: room-temperature processing, simple operation procedures, controllable shape and size, high yield, and available for scaling up. The effects of the pertinent variables on the particle formation and growth have been investigated, such as concentration of copper ions (Cu2+), surfactants, reducing agents, and the molar ratios among variables. The composition, microstructure and optical properties were then characterized using advanced techniques. It was found that the use of different surfactants may result in significant morphology changes from spheres to octahedrons and/or wires under the reported conditions. To enhance photocatalytic performance in dye degradation, the Cu2O nanoparticles could be further surface decorated by titanium dioxide (TiO2) to form heterogeneous nanocomposites that can improve the electron-hole separation. This study may be useful to develop simple but general approaches to obtain cuprous/copper oxides and other hybrid semiconductor nanostructures with structure and functional control for catalysis and sensing applications. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:447 / 459
页数:13
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