Abstract
Electrocatalytic seawater splitting offers a promising avenue for cost-effective and environmentally friendly hydrogen production. However, the activity of catalysts has significantly degraded at high-salinity conditions, preventing commercial-scale practical applications. Here, we demonstrate that iron-doped nickel-based electrocatalysts with low doping concentration exhibit an outstanding performance for the oxygen evolution reaction (OER) in seawater, particularly at high-salinity conditions. Notably, the OER catalysts present only a marginal increase in overpotential of ∼5 mV as the sodium chloride concentration in the electrolyte increases from 0 M to saturation. Furthermore, the low iron-doped electrocatalysts sustain consistent oxygen generation over 100 h of operation in a saturated seawater electrolyte. Supported by first-principles calculations, we unravel that low-concentration iron doping in Ni-based catalysts can mitigate chloride ion adsorption, thereby amplifying the OER activity in saturated seawater electrolytes, which is in contrast with high iron-doped electrocatalysts. Our work provides a useful perspective on designing catalysts for electrolytic seawater OER, potentially paving the way for large-scale implementation of seawater splitting technologies.
Original language | English |
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Pages (from-to) | 15581-15590 |
Number of pages | 10 |
Journal | ACS Catalysis |
Volume | 13 |
Issue number | 23 |
DOIs | |
Publication status | Published - 1 Dec 2023 |
Keywords
- high-salinity condition
- hydrogen production
- non-noble-metal electrocatalysts
- oxygen evolution reaction
- seawater splitting
ASJC Scopus subject areas
- Catalysis
- General Chemistry