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Generating C4 Alkenes in Solid Oxide Fuel Cells via Cofeeding H2 and n-Butane Using a Selective Anode Electrocatalyst
Author(s) -
Xiaoyu Yan,
Ying Yang,
Yimin Zeng,
Babak Shalchi Amirkhiz,
JingLi Luo,
Ning Yan
Publication year - 2020
Publication title -
acs applied materials and interfaces
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.535
H-Index - 228
eISSN - 1944-8252
pISSN - 1944-8244
DOI - 10.1021/acsami.9b20918
Subject(s) - materials science , anode , oxide , chemical engineering , dehydrogenation , butane , catalysis , faraday efficiency , electrode , organic chemistry , metallurgy , chemistry , engineering
Solid oxide fuel cells (SOFCs) offer opportunities for the application as both power sources and chemical reactors. Yet, it remains a grand challenge to simultaneously achieve high efficiency of transforming higher hydrocarbons to value-added products and of generating electricity. To address it, we here present an ingenious approach of nanoengineering the triple-phase boundary of an SOFC anode, featuring abundant Co 7 W 6 @WO x core-shell nanoparticles dispersed on the surface of black La 0.4 Sr 0.6 TiO 3 . We also developed a cofeeding strategy, which is centered on concurrently feeding the SOFC anode with H 2 and chemical feedstock. Such combined optimizations enable effective (electro)catalytic dehydrogenation of n -butane to butenes and 1,3-butadiene. The C4 alkene yield is higher than 50% while the peak power density of the SOFC reached 212 mW/cm 2 at 650 °C. In addition, coke formation is largely suppressed and little CO/CO 2 is produced in this process. While this work shows new possibility of chemical-electricity coupling in SOFCs, it might also open bona fide avenues toward the electrocatalytic synthesis of chemicals at higher temperatures.

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