| Literature DB >> 33369393 |
Lili Lin1,2, Qiaolin Yu1, Mi Peng1, Aowen Li3, Siyu Yao1, Shuheng Tian1, Xi Liu4, Ang Li5, Zheng Jiang6, Rui Gao7,8,9, Xiaodong Han5, Yong-Wang Li7,8, Xiao-Dong Wen7,8, Wu Zhou3,10, Ding Ma1.
Abstract
Methanol-water reforming is a promising solution for H2 production/transportation in stationary and mobile hydrogen applications. Developing inexpensive catalysts with sufficiently high activity, selectivity, and stability remains challenging. In this paper, nickel-supported over face-centered cubic (fcc) phase α-MoC has been discovered to exhibit extraordinary hydrogen production activity in the aqueous-phase methanol reforming reaction. Under optimized condition, the hydrogen production rate of 2% Ni/α-MoC is about 6 times higher than that of conventional noble metal 2% Pt/Al2O3 catalyst. We demonstrate that Ni is atomically dispersed over α-MoC via carbon bridge bonds, forming a Ni1-Cx motif on the carbide surface. Such Ni1-Cx motifs can effectively stabilize the isolated Ni1 sites over the α-MoC substrate, rendering maximized active site density and high structural stability. In addition, the synergy between Ni1-Cx motif and α-MoC produces an active interfacial structure for water dissociation, methanol activation, and successive reforming processes with compatible activity.Entities:
Year: 2020 PMID: 33369393 DOI: 10.1021/jacs.0c10776
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419