Improved activity and stability of Ag-Rh network-like nanoalloy as support-free electrocatalyst for oxygen reduction in alkaline fuel cells

被引:9
作者
Bhuvanendran, Narayanamoorthy [1 ]
Balaji, Subramanian [2 ]
Zhang, Weiqi [1 ]
Xu, Qian [1 ]
Pasupathi, Sivakumar [3 ]
Su, Huaneng [1 ]
机构
[1] Jiangsu Univ, Inst Energy Res, 301 Xuefu Rd, Zhenjiang 212013, Jiangsu, Peoples R China
[2] Sri Chandrasekharendra Saraswathi Viswa Mahavidya, Fac Sci, Dept Chem, Enathur 631561, Kanchipuram, India
[3] Univ Western Cape, HySA Syst Competence Ctr, South African Inst Adv Mat Chem, ZA-7535 Bellville, South Africa
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
CATHODE ELECTROCATALYST; POLYCRYSTALLINE SILVER; DIRECT METHANOL; CARBON; CATALYSTS; NANOPARTICLES; PERFORMANCE; PLATINUM; MODEL; ELECTROOXIDATION;
D O I
10.1063/1.5119054
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
In this study, a simple and environmentally amicable synthesis procedure for support-free silver-rhodium (Ag-Rh) bimetallic network-like nanoalloy was used to catalyze an oxygen reduction reaction in an alkaline medium. The support-free network-like morphology of Ag-Rh nanoalloy exhibits a higher electrochemical surface area (ECSA) of 65.6 m(2)/g than carbon (VC) supported Ag-Rh (23.8 m(2)/g). In comparison to the reported benchmark Ag-based electrocatalysts, it presents an improved mass and specific activity of 971.1mA/mg and 1.45mA/cm(2), respectively. Based on the durability test, the support-free Ag-Rh catalyst retains similar to 70% of its initial ECSA after 7000 potential cycles, and Ag-Rh/VC possesses only 20% after 5000 potential cycles due to the surface oxidation of carbon support. Hence, the superior electrocatalytic performance attributed to the support-free morphology and alloy formation with Rh was clearly demonstrated, which could potentially be the choice of the cathodic electrocatalyst for alkaline fuel cells.
引用
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页数:9
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