材料科学
降级(电信)
X射线光电子能谱
锰
无机化学
催化氧化
氧化物
光催化
作者
Zhiming Li,Xiaolin Guo,Fei Tao,Renxian Zhou
出处
期刊:RSC Advances
[The Royal Society of Chemistry]
日期:2018-07-16
卷期号:8 (45): 25283-25291
被引量:14
摘要
We synthesized four CeO2–MnOx mixed oxides with different morphologies using simple hydrothermal methods. The catalytic activity for chlorobenzene (CB) degradation decreases in the following order: rod-CeO2–MnOx > plate-CeO2–MnOx > polyhedra-CeO2–MnOx > cube-CeO2–MnOx. CeO2 and MnOx in the mixed oxides are highly dispersed and two new phases of both todorokite (S.G.: P2/m:b) and vernadite (S.G.: I4/m) with a special tunnel-like structure are found. Both rod-CeO2–MnOx and plate-CeO2–MnOx exhibit increased lattice microstrains generated from lattice distortion and defects; further, there are more oxygen vacancies and more MnOx (Mn4+ and Mn2+) species on the surface, particularly when compared to cube-CeO2–MnOx. Therefore, this promotes deeper oxidation activity for CB. Moreover, the strong interaction between CeO2 and MnOx also promotes the redox ability of CeO2–MnOx mixed oxides, while their oxygen storage capacity (OSC) properties are not only intrinsic to their structures but also limited to their surfaces and by their particle sizes.
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