Abstract
To address the poor conductivity and insufficient HER activity of NiFe-LDH, this study proposes a synergistic strategy integrating transition metal doping and phosphorization engineering. This approach enables in-situ fabrication of a self-supporting NiFeCrPX/NF heterojunction catalyst. Cr3+ incorporation optimizes the Ni/Fe active centers and facilitates formation of a NiFeCr-LTH precursor, which converts into a multiphase Ni2P–FeP2–Cr12P7 heterojunction during phosphorization. This heterostructure elevates bulk conductivity and accelerates interfacial charge-transfer kinetics. Consequently, NiFeCrPX/NF exhibits outstanding bifunctional performance, achieving 100 mA cm−2 at low overpotentials of 210 mV for HER and 247 mV for OER in alkaline electrolyte. Moreover, it drives overall water splitting at 10 mA cm−2 with only 1.57 V and sustains stable operation for over 100 h. This study provides a design strategy for efficient dual-function electrocatalysts via synergistic transition metal doping and heterojunction engineering.
| Original language | English |
|---|---|
| Article number | 156616 |
| Journal | International Journal of Hydrogen Energy |
| Volume | 258 |
| DOIs | |
| State | Published - 7 Aug 2026 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Keywords
- Bifunctional electrocatalyst
- NiFe-LDH
- NiFeCrP/NF
- Overall water splitting
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