Affiliation:
1. Key Laboratory of Green Chemistry and Technology of Ministry of Education College of Chemistry Sichuan University Chengdu 610064 China
2. School of Basic Medical Sciences Ningxia Medical University Yinchuan 750004 China
3. School of Chemistry and Chemical Engineering Shanghai Jiao Tong University Shanghai 200240 China
Abstract
AbstractThe development of active and selective metal electrocatalysts for complete ethanol oxidation reaction (EOR) into desired C1 products is extremely promising for practical application of direct ethanol fuel cells. Despite some encouraging achievements, their activity and selectivity remain unsatisfactory. In this work, it is reported that 2D PtRhPb mesoporous nanosheets (MNSs) with anisotropic structure and surface‐clean metal site perform perfectly for complete EOR electrocatalysis in both three‐electrode and two‐electrode systems. Different to the traditional routes, a selective etching strategy is developed to produce surface‐clean mesopores while retaining parent anisotropy quasi‐single‐crystalline structure without the mesopore‐forming surfactants. This method also allows the general synthesis of surface‐clean mesoporous metals with other compositions and structures. When being performed for alkaline EOR electrocatalysis, the best PtRhPb MNSs deliver remarkably high activity (7.8 A mg−1) and superior C1 product selectivity (70% of Faradaic efficiency), both of which are much better than reported electrocatalysts. High performance is assigned to multiple structural and compositional synergies that not only stabilized key OHads intermediate by surface‐clean mesopores but also separated the chemisorption of two carbons in ethanol by adjacent Pt and Rh sites, which facilitate the oxidation cleavage of stable C─C bond for complete EOR electrocatalysis.
Funder
National Key Research and Development Program of China
Sichuan Province Science and Technology Support Program
Cited by
1 articles.
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