Metal-Organic-Framework-Derived Co-Fe Bimetallic Oxygen Reduction Electrocatalysts for Alkaline Fuel Cells

被引:193
作者
Xiong, Yin [1 ]
Yang, Yao [1 ]
DiSalvo, Francis J. [1 ]
Abruna, Hector D. [1 ]
机构
[1] Cornell Univ, Baker Lab, Dept Chem & Chem Biol, Ithaca, NY 14853 USA
基金
美国国家科学基金会;
关键词
DOPED CARBON ELECTROCATALYSTS; COBALT OXIDE; ENHANCED ACTIVITY; ACTIVE-SITES; EFFICIENT; CATALYSTS; PERFORMANCE; EVOLUTION; CATHODE; NANOPARTICLES;
D O I
10.1021/jacs.9b03561
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The oxygen reduction reaction (ORR) is considered the cornerstone for regenerative energy conversion devices involving fuel cells and electrolyzers. The development of non-precious-metal electrocatalysts is of paramount importance for their large-scale commercialization. Here, Co-Fe binary alloy embedded bimetallic organic frameworks (BMOF)s based on carbon nanocomposites have been designed with a compositionally optimized template, by a facile host-guest strategy, for ORR in alkaline media. The electrocatalyst exhibits promising electrocatalytic activity for ORR with a half-wave potential of 0.89 V in 0.1 M NaOH, comparable to state-of-the-art Pt/C electrocatalysts. More importantly, it exhibits robust durability after 30 000 potential cycles. Scanning transmission electron microscopy (STEM) and quantitative energy-dispersive Xray (EDX) spectroscopy suggest that the Co-Fe alloy nanoparticles have a homogeneous elemental distribution of Co and Fe at the atomic-scale optimized BMOF and Co/Fe ratio of 9:1. The long-term durability is attributed to its ability to maintain its structural and compositional integrity after the cycling process, as evidenced by STEM-EDX analysis. This work provides valuable insights into the design and fabrication of novel platinum-group-metals-free highly active ORR electrocatalysts in alkaline media.
引用
收藏
页码:10744 / 10750
页数:7
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