Metal organic framework-templated fabrication of exposed surface defect-enriched Co3O4 catalysts for efficient toluene oxidation

被引:70
作者
Han, Dawei [1 ,2 ]
Ma, Xiuyun [2 ,5 ]
Yang, Xueqin [4 ]
Xiao, Menglan [2 ,5 ]
Sun, Hua [2 ,5 ]
Ma, Lingjuan [1 ]
Yu, Xiaolin [2 ,5 ]
Ge, Maofa [2 ,3 ,5 ]
机构
[1] Qufu Normal Univ, Sch Chem & Chem Engn, Qufu 273165, Shandong, Peoples R China
[2] Chinese Acad Sci, Inst Chem, CAS Res Educ Ctr Excellence Mol Sci, Beijing Natl Lab Mol Sci BNLMS,State Key Lab Stru, Beijing 100190, Peoples R China
[3] Chinese Acad Sci, Inst Urban Environm, Ctr Excellence Reg Atmospher Environm, Xiamen 361021, Peoples R China
[4] Henan Agr Univ, Coll Forestry, Zhengzhou 450002, Peoples R China
[5] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
MOF; Co3O4; catalyst; Toluene oxidation; Promoting effect; LOW-TEMPERATURE; COBALT OXIDE; CO; PERFORMANCE; COMBUSTION; PRECURSOR; MN;
D O I
10.1016/j.jcis.2021.06.139
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
Exposed surface defect-enriched Co3O4 catalysts derived from metal organic framework (MOF) were fabricated by the promotion of surface Mn species for toluene oxidation. The incorporation of Mn species into Co3O4 surface lattice could give rise to the local lattice distortion in spinel structure, resulting in highly exposed surface defect rather than bulk defect. More Co3+ species were also exposed on the surface of MnOx/Co3O4 samples owing to the electron transfer from Co to Mn species by the occupation of surface Mn in octahedral Co3+ sites. Accordingly, the low-temperature reducibility and high mobility of lattice oxygen were significantly improved in virtue of the highly exposed surface defect and predominately surface Co3+ sites, thus promoting the catalytic activity and stability for toluene oxidation. Moreover, the toluene conversion decreased with the increase of weight hourly space velocity (WHSV). In situ DRIFTS results confirmed the continuous oxidation process for toluene degradation, and the conversion of benzoate into maleic anhydride should be the rate-controlling step. (C) 2021 Elsevier Inc. All rights reserved.
引用
收藏
页码:695 / 705
页数:11
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