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Synthesis of Platinum-nickel Nanowires and Optimization for Oxygen Reduction Performance
Published on: April 27, 2018
A Superior and Stable Electrocatalytic Oxygen Evolution Reaction by One-Dimensional FeCoP Colloidal Nanostructures
Lakshya Kumar1, Bindu Antil1, Ankur Kumar1
1Nanochemistry Laboratory, Department of Chemistry, University of Delhi, North campus, Delhi 110007, India.
Transition metal phosphides (FeCoP) show great promise as electrocatalysts for the oxygen evolution reaction (OER). This study developed FeCoP nanorods with exceptional activity and stability for OER applications.
Area of Science:
- Materials Science
- Electrochemistry
- Catalysis
Background:
- Transition metal phosphides (TMPs) are promising electrocatalysts for the oxygen evolution reaction (OER).
- Their stability, conductivity, and ability to form active oxy-hydroxide species contribute to their catalytic potential.
- Non-noble metal catalysts are sought after for cost-effectiveness.
Purpose of the Study:
- To develop a novel, high-performance electrocatalyst for OER.
- To investigate the structure-activity relationship of a rod-shaped FeCoP electrocatalyst.
- To understand the mechanism behind the enhanced OER performance.
Main Methods:
- A "one-pot" colloidal synthesis approach was used to create rod-shaped FeCoP electrocatalysts.
- Electrochemical performance was evaluated using techniques like cyclic voltammetry.
- Material characterization included X-ray photoelectron spectroscopy, X-ray diffraction, Raman, and infrared spectroscopy.
Main Results:
- The FeCoP electrocatalyst demonstrated excellent OER activity with a current density of 950 mA cm-2 and a low Tafel slope of 54 mV dec-1.
- Ultralow OER overpotentials of 230 and 260 mV were achieved at 50 and 100 mA cm-2, respectively.
- Superior catalytic stability was observed over 10,000 cycles and 60 hours at 50 mA cm-2.
Conclusions:
- The developed FeCoP nanorods are highly efficient and stable electrocatalysts for OER.
- The enhanced performance is attributed to a high number of active sites facilitating in situ surface formation and adsorption of reactive species.
- This work highlights the potential of non-noble metal TMPs for efficient oxygen evolution catalysis.
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