Facile synthesis of composition-tunable PtRh nanosponges for methanol oxidation reaction

被引:75
作者
Lu, Qingqing [1 ,2 ]
Huang, Jianshe [1 ]
Han, Ce [1 ]
Sun, Litai [1 ,2 ]
Yang, Xiurong [1 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Electroanalyt Chem, Changchun 130022, Jilin, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
Platinum; Rhodium; Nanosponges; Electrocatalyst; Methanol oxidation reaction; ONE-STEP SYNTHESIS; ENHANCED ELECTROCATALYTIC PERFORMANCE; REDUCED GRAPHENE OXIDE; HIGH-SURFACE-AREA; ETHANOL ELECTROOXIDATION; FUEL-CELLS; OXYGEN REDUCTION; EFFICIENT ELECTROCATALYSTS; SUPERIOR ELECTROCATALYSTS; RH NANOPARTICLES;
D O I
10.1016/j.electacta.2018.02.021
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Currently, the synthesis of desired Pt-based electrocatalysts for methanol oxidation reaction (MOR) remains a challenge in terms of controlling the particle morphology, composition, and electrochemical property. In this study, we present a rapid and facile method for the formation of bimetallic PtRh nanosponges (NSs) by the co-reduction of two metallic precursors using sodium borohydride at room temperature in the absence of any surfactant. Their compositions can be directly tuned by changing the ratio between Pt and Rh precursors. PtRh NSs were obtained in a high yield of three-dimensional (3D) foam-like nanostructure with interconnected pores. Interestingly, the electrocatalytic performance of as-synthesized PtRh NSs was composition-dependent, and they exhibited remarkably improved methanol oxidation activity as compared to Pt NSs and commercial Pt/C catalyst. PtRh NSs were also found to be much more stable as evidenced by the chronoamperometric measurement. Their superior electrochemical properties are ascribed to the 3D porous nanostructure, alloy effect, and clean particle surface. This work provides a simple and effective method to prepare highly active electrocatalysts toward MOR in acid medium. (c) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:305 / 311
页数:7
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