Electrocatalytic Oxygen Evolution by Hierarchically Structured Cobalt-Iron Composites

被引:0
|
作者
Gao, Dandan [1 ]
Liu, Rongji [1 ]
Liu, Si [1 ]
Greiner, Simon [1 ,2 ]
Anjass, Montaha [1 ,2 ,3 ]
Biskupek, Johannes [4 ]
Kaiser, Ute [4 ]
Braun, Hanna [5 ]
Jacob, Timo [2 ,3 ,5 ]
Streb, Carsten [1 ,2 ,3 ]
机构
[1] Ulm Univ, Inst Inorgan Chem 1, D-89081 Ulm, Germany
[2] Helmholtz Inst Ulm, Electrochem Energy Storage HIU, D-89081 Ulm, Germany
[3] Karlsruhe Inst Technol, D-76021 Karlsruhe, Germany
[4] Ulm Univ, Cent Facil Electron Microscopy, Electron Microscopy Mat Sci, D-89081 Ulm, Germany
[5] Ulm Univ, Inst Electrochem, D-89081 Ulm, Germany
关键词
electrocatalysis; composite; oxygen evolution reaction; electrodeposition; nanostructure; copper foam; WATER OXIDATION; NICKEL PHOSPHATE; EFFICIENT; CRYSTALLINE; NANOSHEETS; CATALYST; FILM; ELECTRODEPOSITION; HYDROGEN; SULFATE;
D O I
10.1021/acsami.1c03618
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The development of scalable routes to highly active and efficient oxygen evolution reaction (OER) electrocatalysts based on earth-abundant materials is crucial for post-fossil fuel energy schemes. Here, we demonstrate how commercial copper foam electrodes can be functionalized for water oxidation using a facile electrodeposition process. The resulting composite electrode features hierarchically structured cobalt-iron-based catalyst particles, which offer channel-like structures for the transport of electrolyte and release of oxygen gas bubbles. We report high electrocatalytic OER performance as demonstrated by high current densities at low overpotentials (293 mV at j = 50 mA cm(-2)) and long-term stability under technologically relevant alkaline conditions (>24 h in 1.0 M aqueous KOH).
引用
收藏
页码:19048 / 19054
页数:7
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