Abstract
Developing low-cost and durable bifunctional electrocatalysts for overall water splitting is crucial for scalable green hydrogen production. Herein, we report a dual-cation-doped Ru,Mn–CoTe2 catalyst with a porous nanosheet architecture, synthesized via a Mo-assisted route followed by in situ tellurization and controlled Ru incorporation. The inclusion of Mo during precursor formation directs the evolution of a sheet-like CoMnMo–LDH, while its removal during tellurization generates abundant pores and defect sites favorable for Ru anchoring. The advances in synergistic dual doping and directed structural engineering are evidenced by DFT calculations, which confirm an optimized hydrogen adsorption energy (ΔGH* = −0.081 eV) for HER and a low OER overpotential of 0.54 V. The Ru,Mn–CoTe2 exhibits outstanding bifunctional activity, requiring only 39 mV for HER and 220 mV for OER to reach 10 mA cm−2 in 1.0 M KOH. An electrolyzer cell also demonstrates an exceptional cell voltage of 1.69 V to achieve a current density of 0.5 A cm−2 in 1.0 M KOH at 60 °C, along with prospective stability, sustaining 600 h of continuous operation. This work establishes a rational dual-doping and structural-engineering strategy for designing highly active, stable, and scalable telluride-based catalysts for industrial water electrolysis and sustainable hydrogen generation.
| Original language | English |
|---|---|
| Pages (from-to) | 7143-7156 |
| Number of pages | 14 |
| Journal | Materials Horizons |
| Volume | 13 |
| Issue number | 14 |
| DOIs | |
| State | Published - 2026.07.20 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
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SDG 9 Industry, Innovation, and Infrastructure
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Investigators from Jeonbuk National University Report New Data on Structural Engineering (Synergistic Dual Doping and Directed Structural Engineering of 2d Cobalt Tellurium Nanoarchitectures for Practical-level Overall Water Splitting)
Kim, H., Kim, N. H., Tran, D. T., Kim, H.-G. & Kim, D. H.
26.06.29
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