High-current density alkaline water/seawater splitting by Mo and Fe co-doped Ni3S2:Invariant active sites with accelerated water dissociation kinetics
A cost-effective and durable electrocatalyst for alkaline seawater splitting is essential for producing green hydrogen at industrial-grade current densities. Herein, we report a one-step hydrothermal synthesis of Mo and Fe co-doped Ni3S2 (Mo, Fe-Ni3S2) nanoarrays. X-ray diffraction (XRD) and X-ray p...
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Published in | Applied catalysis. B, Environmental Vol. 361; p. 124698 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier B.V
01.02.2025
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Subjects | |
Online Access | Get full text |
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Summary: | A cost-effective and durable electrocatalyst for alkaline seawater splitting is essential for producing green hydrogen at industrial-grade current densities. Herein, we report a one-step hydrothermal synthesis of Mo and Fe co-doped Ni3S2 (Mo, Fe-Ni3S2) nanoarrays. X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) confirm the invariant active sites such as Ni-S, Mo and Fe. Experimental and theoretical analyses demonstrate Mo and Fe doping significantly reduces the Gibbs free energy of the rate-determining step, enhancing water-dissociation kinetics and electrocatalytic activity. Optimized Mo, Fe-Ni3S2 exhibits exceptional performance in 1.0 M KOH, requiring only 186 mV and 59 mV to attain 10 mA cm−2 for OER and HER. Notably, for OER, an overpotential of only 253 mV is required at 200 mA cm−2. A two-electrode water splitting system using Mo, Fe-Ni3S2 as both cathode and anode exhibits robust stability in natural seawater electrolysis for 100 h without significant degradation, highlighting its potential for low-cost hydrogen production from seawater.
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•Mo, Fe-Ni3S2 was prepared by a facile one-step hydrothermal method.•Mo and Fe doping reduces Gibbs free energy for OER steps and water decomposition.•OER overpotential of Mo, Fe-Ni3S2 is 234 mV at 100 mA/cm² and 253 mV at 200 mA/cm².•Mo, Fe-Ni3S2 catalyst shows excellent performance in alkaline seawater electrolysis. |
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ISSN: | 0926-3373 |
DOI: | 10.1016/j.apcatb.2024.124698 |