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Co-Doped Nanoporous Fe3P Self-Supported Electrodes for Enhanced Alkaline Hydrogen Evolution
Nana Yang1, Ning Mi1, Lin Lei1
1School of Materials Engineering, Longdong University, Qingyang 745000, China.
Cobalt-doped nanoporous iron phosphide (np-Co-Fe3P) significantly enhances alkaline hydrogen evolution reaction (HER) performance. This advanced electrocatalyst achieves a low overpotential of 70 mV, outperforming its undoped counterpart.
Area of Science:
- Materials Science
- Electrochemistry
- Catalysis
Background:
- Transition-metal phosphides are key non-noble metal electrocatalysts for hydrogen evolution.
- Improving their efficiency in alkaline media remains a critical challenge.
Purpose of the Study:
- To fabricate a Co-doped nanoporous Fe3P electrode for enhanced alkaline hydrogen evolution reaction (HER).
- To investigate the effects of Co doping and nanoporous structure on HER performance.
Main Methods:
- Fabrication of Co-doped nanoporous Fe3P via melt spinning and electrochemical dealloying.
- Structural and chemical characterization using X-ray photoelectron spectroscopy (XPS).
- Electrochemical testing of HER performance in 1.0 M KOH.
Main Results:
- Successfully synthesized a 3D nanoporous Fe3P framework with incorporated Co.
- Co doping modified the local chemical environment of Fe and P, enhancing catalytic activity.
- The np-Co-Fe3P electrode achieved 10 mA cm-2 at only 70 mV overpotential, significantly lower than np-Fe3P (199 mV).
- np-Co-Fe3P exhibited a lower Tafel slope (94 mV dec-1), reduced charge-transfer resistance, and higher double-layer capacitance (109.4 mF cm-2).
Conclusions:
- Co incorporation and dealloying-induced nanoporous architecture effectively enhance alkaline HER performance.
- This strategy offers a promising pathway for developing advanced non-noble metal electrocatalysts.
- The developed np-Co-Fe3P shows great potential for efficient hydrogen production in alkaline electrolytes.
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