Selective oxygen species for the oxidative coupling of methane

被引:82
|
作者
Kim, Ilho [1 ]
Lee, Gihoon [1 ]
Bin Na, Hyon [1 ]
Ha, Jeong-Myeong [2 ]
Jung, Ji Chul [1 ]
机构
[1] Myongji Univ, Dept Chem Engn, Yongin 17058, South Korea
[2] Korea Inst Sci & Technol, Clean Energy Res Ctr, Seoul 02792, South Korea
来源
MOLECULAR CATALYSIS | 2017年 / 435卷
基金
新加坡国家研究基金会;
关键词
Selective oxygen species; Methane conversion; Oxidative coupling; Perovskite catalyst; Electrophilic lattice oxygen; SYNTHESIS GAS; CATALYTIC CONVERSION; C-2; HYDROCARBONS; SURFACE; OXIDES; ACTIVATION; MODEL; FUELS; MG;
D O I
10.1016/j.mcat.2017.03.012
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
Herein, we attempt to identify selective oxygen species for the oxidative coupling of methane using lanthanum-based perovskite catalysts (LaXO3, X = Al, Fe, or Ni), which are well-known not only as stoichiometric materials with simple and definite structures but also as materials with outstanding catalytic activities in various methane conversion reactions. The catalytic activities of LaXO3 in the presence or absence of oxygen clearly demonstrated that surface lattice oxygen species are responsible for the selective conversion of methane. More importantly, electrophilic (LaAlO3), moderate (LaFeO3), and nucle-ophilic (LaNiO3) lattice oxygen species selectively catalyze the oxidative coupling of methane to C-2 hydrocarbons, the direct partial oxidation of methane to carbon monoxide, and the methane combustion to carbon dioxide, respectively. In addition, adsorbed oxygen species originating from gas-phase oxygen play roles both in converting methane to CO. and in filling surface lattice oxygen vacancies, which are caused by the reaction of lattice oxygen and methane. Finally, we concluded that electrophilic lattice oxygen species and the facile filling of surface lattice oxygen vacancies by gas-phase oxygen are key factors for the systematic design of efficient catalysts for the oxidative coupling of methane. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:13 / 23
页数:11
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