Crystal-facet-dependent activity and N2 yield of Ag/CeO2 catalysts for catalytic oxidation of N, N-Dimethylformamide

催化作用 脱氢 纳米棒 氧气 金属 离解(化学) 产量(工程) 吸附 无机化学 化学 材料科学 晶体结构 结晶学 物理化学 纳米技术 有机化学 冶金
作者
Xiaohan Guo,Chenxiao Dong,Meixingzi Gao,Dongsheng Ye,Qiguang Dai,Wangcheng Zhan,Zhiqiang Wang,Li Wang,Aiyong Wang,Yun Guo,Yanglong Guo
出处
期刊:Applied Catalysis B-environmental [Elsevier]
卷期号:341: 123286-123286 被引量:13
标识
DOI:10.1016/j.apcatb.2023.123286
摘要

Shape-controlled CeO2 with different exposed crystal facets, CeO2 nanorods (110) and (100), nanocubes (100) and nano-octahedrons (111), were prepared as supports of Ag and then the catalytic oxidation of N, N-dimethylformamide (DMF) was investigated. Ag/CeO2 nanorod (Ag/r-Ce) catalyst exhibits better dispersion of Ag species due to the abundant oxygen vacancies of CeO2 (110) with outstanding anchoring effect, meanwhile, more Ag-O-Ce interfaces and Ag+ species are achieved because of the strong metal-support interaction and easy migration of oxygen species between Ag and CeO2 (110). Ag/r-Ce catalyst exhibits excellent catalytic activity (T90 =158 °C), 100% yield of CO2 at 240 °C, 80% yield of N2 in the temperature range of 237–400 °C, unexceptionable H2O-resistance, high stability at 240 °C for 120 h. In situ DRIFTS reveals that the dissociation of (O)C-N bond is firstly involved in DMF oxidation, and then the stepwise and repeated dehydrogenation of -N(CH3)2 and the insertion reaction of surface lattice oxygen occurs. Meanwhile the formed -HCO is completely oxidized into CO2 and H2O by surface adsorbed oxygen species and the two adjacent -NH2 species combines into N2.
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