Li Zhiming, Guo Xiaolin, Tao Fei, Zhou Renxian
Institute of Catalysis, Zhejiang University Hangzhou 310028 PR China
RSC Adv. 2018 Jul 16;8(45):25283-25291. doi: 10.1039/c8ra04010a.
We synthesized four CeO-MnO mixed oxides with different morphologies using simple hydrothermal methods. The catalytic activity for chlorobenzene (CB) degradation decreases in the following order: rod-CeO-MnO > plate-CeO-MnO > polyhedra-CeO-MnO > cube-CeO-MnO . CeO and MnO in the mixed oxides are highly dispersed and two new phases of both todorokite (S.G.: 2/:) and vernadite (S.G.: 4/) with a special tunnel-like structure are found. Both rod-CeO-MnO and plate-CeO-MnO exhibit increased lattice microstrains generated from lattice distortion and defects; further, there are more oxygen vacancies and more MnO (Mn and Mn) species on the surface, particularly when compared to cube-CeO-MnO . Therefore, this promotes deeper oxidation activity for CB. Moreover, the strong interaction between CeO and MnO also promotes the redox ability of CeO-MnO 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.
我们采用简单的水热法合成了四种不同形貌的CeO-MnO混合氧化物。对氯苯(CB)降解的催化活性按以下顺序降低:棒状CeO-MnO>片状CeO-MnO>多面体CeO-MnO>立方状CeO-MnO。混合氧化物中的CeO和MnO高度分散,发现了具有特殊隧道状结构的钙锰矿(空间群:2/:)和水钠锰矿(空间群:4/)这两个新相。棒状CeO-MnO和片状CeO-MnO均表现出由晶格畸变和缺陷产生的晶格微应变增加;此外,与立方状CeO-MnO相比,其表面有更多的氧空位和更多的MnO(Mn和Mn)物种。因此,这促进了对CB的深度氧化活性。此外,CeO和MnO之间的强相互作用也促进了CeO-MnO混合氧化物的氧化还原能力,而它们的储氧能力(OSC)特性不仅取决于其结构,还受限于其表面和粒径。