Abstract
Medium/high-entropy alloy (MEA/HEA) catalysts have emerged as ideal candidates as multi-functional catalysts owing to their synergistic effects of multiple metal components on the boosted catalytic activity. However, the facile preparation and screening of suitable MEAs element to achieve high catalytic performance still remain challenging. In this work, we successfully synthesized a MoCoCu-P MEA electrocatalyst for water splitting electrocatalysis through a feasible electrodeposition method. The as-prepared MEA demonstrated an overpotential of 276.1 mV (j=10 mA/cm²) for OER with a Tafel slope of 38.3 mV/dec, coupled with an overpotential of 64.7 mV for HER (j=10 mA/cm²) with a Tafel slope of 87.7 mV/dec. Employed in an overall water electrolysis cell, MEA achieved a nearly 100% Faradaic efficiency and superior stability over than 50 hours at a high current density of 50 mA/cm2. X-ray photoelectron spectroscopy (XPS) analysis verify that high-valence Co and Mo are the most active sites for OER, while electron-rich Cu at the presence of P is responsible for the boosted HER in the MoCoCu-P MEA. This study not only provides a feasible electrodeposition strategy to obtain MEA catalysts with high activity and excellent stability, but also sheds fundamental lights on the identification of the active sites in MEA catalysis.
| Original language | English |
|---|---|
| Article number | 174332 |
| Journal | Journal of Alloys and Compounds |
| Volume | 988 |
| DOIs | |
| State | Published - 15 Jun 2024 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Keywords
- Active sites
- Hydrogen evolution reaction
- Medium-entropy alloy
- One-step electrodeposition
- Overall water electrolysis cell
- Oxygen evolution reaction
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