Formic acid decomposition-inhibited intermetallic Pd3Sn2 nanonetworks for efficient formic acid electrooxidation

被引:33
|
作者
Li, Fumin [1 ]
Xue, Qi [2 ]
Ma, Ge [3 ]
Li, Shuni [1 ]
Hu, Mancheng [1 ]
Yao, Hongchang [4 ]
Wang, Xin [3 ]
Chen, Yu [2 ]
机构
[1] Shaanxi Normal Univ, Sch Chem & Chem Engn, Key Lab Macromol Sci Shaanxi Prov, Xian 710062, Peoples R China
[2] Shaanxi Normal Univ, Sch Mat Sci & Engn, Key Lab Appl Surface & Colloid Chem, Minist Educ, Xian 710062, Peoples R China
[3] South China Normal Univ, Int Acad Optoelect Zhaoqing, Guangzhou 510631, Guangdong, Peoples R China
[4] Zhengzhou Univ, Coll Chem & Mol Engn, Zhengzhou 450001, Peoples R China
基金
中国国家自然科学基金;
关键词
Direct formic acid fuel cells; Intermetallic Pd-Sn compounds; Nanonetworks; Formic acid decomposition; Formic acid electrooxidation; ETHANOL OXIDATION REACTION; ONE-STEP SYNTHESIS; ELECTROCHEMICAL OXIDATION; ELECTROCATALYTIC ACTIVITY; CATALYTIC PERFORMANCE; ALLOY NANOPARTICLES; WO2.72; NANORODS; TIN; SEMIHYDROGENATION; NANOCATALYSTS;
D O I
10.1016/j.jpowsour.2019.227615
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Inhibiting formic acid decomposition on Pd-based electrocatalysts is a major challenge for realizing the commercialization of direct formic acid fuel cells (DFAFCs). Inspired by the catalytic characteristics of formic acid decomposition/electrooxidation on Pd-based materials, here we synthesize intermetallic bimetallic Pd-Sn nanonetworks (NNWs) to deal with this problem. Compared to commercial Pd black with high catalytic activity, the strong Pd-Sn electronic interaction in intermetallic Pd3Sn2 NNWs induces the complete inhibition of formic acid decomposition at 80 degrees C. Parallelly, Pd3Sn2 NNWs exhibit mass activity of 448 A g(pd)(1-) for formic acid electrooxidation due to Pd-Sn synergistic effect, which is 2.1 times higher than that of commercial Pd black. The stable intermetallic structure and three-dimensionally interconnected architecture endow Pd3Sn2 NNWs with better electrochemical and electrocatalytic durability, suggesting promising cost-effective anode catalysts for DFAFCs.
引用
收藏
页数:9
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