Interfacial Hydrothermal Synthesis of Cu@Cu2O Core-Shell Microspheres with Enhanced Visible-Light-Driven Photocatalytic Activity

被引:217
|
作者
Ai, Zhihui [1 ,2 ]
Zhang, Lizhi [1 ]
Lee, Shuncheng [2 ]
Ho, Wingkei [2 ]
机构
[1] Cent China Normal Univ, Coll Chem, Minist Educ, Key Lab Pesticide & Chem Biol, Wuhan 430079, Peoples R China
[2] Hong Kong Polytech Univ, Res Ctr Environm Technol & Management, Dept Civil & Struct Engn, Hong Kong, Hong Kong, Peoples R China
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2009年 / 113卷 / 49期
基金
美国国家科学基金会;
关键词
ONE-POT SYNTHESIS; CHARGE SEPARATION; REDUCTION ROUTE; CU2O NANOCUBES; NANOCRYSTALS; NANOPARTICLES; NANOWIRES; IRRADIATION; FABRICATION; CONVERSION;
D O I
10.1021/jp9083647
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
In this Study, core-shell Cu@Cu2O microspheres were synthesized with an interfacial hydrothermal method. The resulting products were systematically characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, high-resolution transmission electron microscopy, and X-ray photoelectron spectroscopy. A core-shell Cu@Cu2O microsphere formation mechanism, which involved the in situ transformation of Cu to Cu2O, was proposed on the basis of the characterization results. That is, pure Cu microspheres were first formed through the reduction of copper(II) acetylacetonate. Then Surface Cu was oxidatively tran;formed to a Cu2O shell, resulting in the Cu@Cu2O core-shell structure. The content of Cu2O shell in thin composite microspheres increased with prolonged reaction time. The as-prepared Cu@Cu2O core-shell microspheres exhibited enhanced photocatalytic activity as compared to Cu2O on the degradation of gaseous nitrogen monoxide under visible light irradiation. The reasons for visible-light-driven photocatalytic activity enhancement on Cu@Cu2O core-shell microspheres were discussed. These Cu@Cu2O microspheres are ideal candidates for fundamental studies as well as catalytic, electronic, and magnetic applications.
引用
收藏
页码:20896 / 20902
页数:7
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