Selective oxygen species for the oxidative coupling of methane

Authors
Kim, IlhoLee, GihoonBin Na, HyonHa, Jeong-MyeongJung, Ji Chul
Issue Date
2017-07
Publisher
ELSEVIER SCIENCE BV
Citation
MOLECULAR CATALYSIS, v.435, pp.13 - 23
Abstract
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.
Keywords
SYNTHESIS GAS; CATALYTIC CONVERSION; C-2 HYDROCARBONS; SURFACE; OXIDES; ACTIVATION; MODEL; FUELS; MG; SYNTHESIS GAS; CATALYTIC CONVERSION; C-2 HYDROCARBONS; SURFACE; OXIDES; ACTIVATION; MODEL; FUELS; MG; Selective oxygen species; Methane conversion; Oxidative coupling; Perovskite catalyst; Electrophilic lattice oxygen
ISSN
2468-8231
URI
https://pubs.kist.re.kr/handle/201004/122575
DOI
10.1016/j.mcat.2017.03.012
Appears in Collections:
KIST Article > 2017
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