Work

Dual‐Molten‐Salt Etching Strategy Enables Built‐in Electric Field in Mo‐ MX ene/ N i F e S e Heterostructure for Superior OER Performance

Year: 2026
Type: article
Abstract: Transition metal selenides have emerged as potential catalysts for the oxygen evolution reaction, yet their practical implementation faces two fundamental challenges: irreversible nanoparticle aggregation under operational conditions and unfavorable adsorption energetics for critical oxygen intermediates. Herein, a strategy that integrates dual‐molten‐salt etching with hydrothermal selenization has been developed to tightly anchor FeNiSe nanoparticles onto a porous Mo‐based MXene substrate (Mo‐MXene/NiFeSe). The hierarchical porous architecture of Mo‐MXene/NiFeSe facilitates rapid mass and charge transport. The NiFeSe nanoparticles are chemically anchored within the conductive Mo‐MXene matrix via in‐situ formed Mo–O–Fe/Ni bonds, effectively preventing agglomeration during the catalytic process. Additionally, the work function gradient between Mo‐MXene and NiFeSe induces charge redistribution, creating a built‐in electric field that optimizes intermediate adsorption kinetics and enhances charge transport efficiency. Therefore, Mo‐MXene/NiFeSe achieves an ultralow overpotential of 231 mV to reach current density of 10 mA cm −2 and sustain 91% of its initial current density over 55 h in alkaline electrolyte. Density functional theory (DFT) calculations reveal that the adsorption free energy of *OOH for Mo‐MXene/NiFeSe is significantly reduced, effectively lowering the kinetic barrier of the rate‐determining step. This work provides both fundamental insights into built‐in electric field‐enhanced catalysis and a practical strategy for developing high‐performance and durable oxygen evolution reaction electrocatalysts.
Language: English
Field: Energy
Open Access status: hybrid
Estimated APC paid: $3,000
OpenAlex ID: W7126182735
FWCI: 6.21
Cites: 48
Cited by: 7
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