| Literature DB >> 30412314 |
Zhongxin Chen1,2, Cuibo Liu1, Xiaoxu Zhao1,2, Huan Yan1, Jing Li1, Pin Lyu1, Yonghua Du3, Shibo Xi3, Kai Chi4, Xiao Chi1, Haisen Xu1, Xing Li1,2, Wei Fu1, Kai Leng1, Stephen J Pennycook2,5, Shuai Wang4, Kian Ping Loh1,2.
Abstract
Confined catalysis in a 2D system is of particular interest owing to the facet control of the catalysts and the anisotropic kinetics of reactants, which suppress side reactions and improve selectivity. Here, a 2D-confined system consisting of intercalated Pt nanosheets within few-layered graphene is demonstrated. The strong metal-substrate interaction between the Pt nanosheets and the graphene leads to the quasi-2D growth of Pt with a unique (100)/(111)/(100) faceted structure, thus providing excellent catalytic activity and selectivity toward one-carbon (C1) products for the glycerol oxidation reaction. A hierarchically porous graphene architecture, grown on carbon cloth, is used to fabricate the confined catalyst bed in order to enhance the mass-diffusion limitation in interface-confined reactions. Owing to its unique 3D porous structure, this graphene-confined Pt catalyst exhibits an extraordinary mass activity of 2910 mA mgPt -1 together with a formate selectivity of 79% at 60 °C. This paves the way toward rational designs of heterogeneous catalysts for energy-related applications.Entities:
Keywords: confined catalysis; electrocatalysis; glycerol oxidation; graphene; platinum nanosheets
Year: 2018 PMID: 30412314 DOI: 10.1002/adma.201804763
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849