Nickel -supported PdM (M = Au and Ag) nanodendrites as formate oxidation (electro)catalytic anodes for direct fuel cells and hydrogen generation at room temperature

被引:10
作者
Pan, Bowei [1 ,2 ]
Shan, Shuang [1 ,2 ]
Wang, Junpeng [1 ,2 ]
Tang, Quan [1 ,2 ]
Guo, Longfei [1 ,2 ]
Jin, Tao [1 ,2 ]
Wang, Qiao [1 ,2 ]
Li, Zhen [1 ,2 ]
Usman, Muhammad [1 ,2 ]
Chen, Fuyi [1 ,2 ]
机构
[1] Northwestern Polytech Univ, State Key Lab Solidificat Proc, Xian 710072, Peoples R China
[2] Northwestern Polytech Univ, Sch Mat Sci & Engn, Xian 710072, Peoples R China
基金
中国国家自然科学基金;
关键词
FORMIC-ACID; CARBON-DIOXIDE; NANOPARTICLES; PALLADIUM; CATALYSTS; ELECTRODE; ETHANOL; PAPER;
D O I
10.1039/d2nr06637h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The study provides a proof of concept for the first time that unique palladium-gold (PdAu) and palladium-silver (PdAg) nanodendrites are bifunctional catalytic active sites for formate oxidation reactions (FORs) and formate dehydrogenation reactions (FDRs). The unique nanodendritic structure was developed via a simple galvanic displacement reaction for the direct growth of PdAu and PdAg nanodendrites on a nickel foam (PdAu/NiNF and PdAg/NiNF). These PdAu/NiNF and PdAg/NiNF electrodes exhibited 2.32 and 1.59 times higher specific activity than that of the commercial Pd/C electrode and promising stability toward FORs. Moreover, the PdAu/NiNF and PdAg/NiNF nanodendrites were also highly active and selective catalysts for hydrogen generation from a formate solution with turnover frequency (TOF) values of 311 h(-1) and 287 h(-1) respectively. Impressively, a passive air-breathing formate fuel cell with PdAu/NiNF used as an anode can yield an open-circuit voltage of 1.12 V and a peak power density of 21.7 mW cm(-2), which outperforms most others reported in the literature. PdAu and PdAg nanodendritic catalysts supported on a nickel foam demonstrate an open structure and uniform catalyst distribution and offer a promising nanoalloy for air-breathing formate fuel cells and on-site chemical hydrogen production systems.
引用
收藏
页码:7032 / 7043
页数:12
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