Facile synthesis of CeO2 hollow structures with controllable morphology by template-engaged etching of Cu2O and their visible light photocatalytic performance

被引:88
|
作者
Fang, Siman [1 ,2 ]
Xin, Yongji [2 ]
Ge, Lei [1 ,2 ]
Han, Changcun [2 ]
Qiu, Ping [2 ]
Wu, Linen [2 ]
机构
[1] China Univ Petr, Coll Sci, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China
[2] China Univ Petr Being, Coll Sci, Dept Mat Sci & Engn, Beijing 102249, Peoples R China
基金
美国国家科学基金会;
关键词
CeO2 hollow structure; Template-engaged; Morphology-controlled; Photocatalysis; WATER; MICROSPHERES; EVOLUTION; SPHERES; XPS; NANOSTRUCTURES; DECOMPOSITION; NANOCRYSTALS; OXYNITRIDE; REDUCTION;
D O I
10.1016/j.apcatb.2015.05.051
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
The novel ceria (CeO2) hollow structures with uniform cubic, polyhedral and sphere shapes were successfully synthesized by template-engaged coordinating etching of shape-controlled Cu2O crystals. The obtained samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microcopy (TEM), high resolution of transmission electron microcopy (HRTEM), X-ray photoelectron spectroscopy (XPS), electron spin resonance (ESR) and photoluminescence spectroscopy (PL). The photocatalytic oxygen evolution via water oxidation was investigated for CeO2 hollow structures with varied shapes under visible light irradiation. The photocatalytic results indicate that polyhedral CeO2 nanocages show the highest photocatalytic activity, in contrast with spherical CeO2 hollow structure and cubic CeO2 hollow structure. The excellent catalytic activity can be attributed to the unique properties of the polyhedral CeO2 nanocages, including efficient light refection through the inner shells, more active sites for enhancing separation efficiency of charge carriers. It is expected that this study could provide helpful results for designing and exploration of novel hollow structures with tunable photocatalytic performance. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:458 / 467
页数:10
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