A Mo-guided self-reconstructed highly active NiOOH catalyst for a durable alkaline oxygen evolution reaction

Alkaline water electrolysis (AWE) is vital for green hydrogen production but suffers from sluggish oxygen evolution reaction (OER) kinetics and poor electrode stability. Here, a facile and feasible Mo-guided self-reconstruction strategy was developed to construct an outstanding pure nickel-based OER electrocatalyst (γ-NiOOH<sub>Mo-SR</sub>/NF). Benefiting from the <i>in situ</i> generated abundant high-valent Ni sites and interfacial hydrogen-bonding network, γ-NiOOH<sub>Mo-SR</sub>/NF exhibited excellent OER activity and impressive long-term stability over 1100 h at 1.0 A cm<sup>-2</sup>, even exceeding 100 h at 3.0 A cm<sup>-2</sup>, outperforming most reported non-precious metal catalysts. <i>In situ</i> spectroscopic studies confirmed that the interfacial hydrogen-bonding network promoted OH<sup>-</sup> transport and suppressed local acidification, thereby endowing γ-NiOOH<sub>Mo-SR</sub>/NF with superior OER performance. The present work is instructive for designing highly efficient Ni-based OER electrocatalysts.

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Publication Details

Journal
Chemical Communications
Published
2025-11-25
DOI
https://doi.org/10.1039/d5cc06040k
Citations
2
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
0.73
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article

A Mo-guided self-reconstructed highly active NiOOH catalyst for a durable alkaline oxygen evolution reaction

Yuan He, Zhanwei Chen, Zhi‐Min Liao, Shaowei Yang et al.
2 citations
Chemical Communications
Electrocatalysts for Energy Conversion
0.73
article

A Mo-guided self-reconstructed highly active NiOOH catalyst for a durable alkaline oxygen evolution reaction

Yuan He, Zhanwei Chen, Zhi‐Min Liao, Shaowei Yang, Hao Jiang, Hepeng Zhang, He Zhi
article en
2 citations

Abstract

Alkaline water electrolysis (AWE) is vital for green hydrogen production but suffers from sluggish oxygen evolution reaction (OER) kinetics and poor electrode stability. Here, a facile and feasible Mo-guided self-reconstruction strategy was developed to construct an outstanding pure nickel-based OER electrocatalyst (γ-NiOOH<sub>Mo-SR</sub>/NF). Benefiting from the <i>in situ</i> generated abundant high-valent Ni sites and interfacial hydrogen-bonding network, γ-NiOOH<sub>Mo-SR</sub>/NF exhibited excellent OER activity and impressive long-term stability over 1100 h at 1.0 A cm<sup>-2</sup>, even exceeding 100 h at 3.0 A cm<sup>-2</sup>, outperforming most reported non-precious metal catalysts. <i>In situ</i> spectroscopic studies confirmed that the interfacial hydrogen-bonding network promoted OH<sup>-</sup> transport and suppressed local acidification, thereby endowing γ-NiOOH<sub>Mo-SR</sub>/NF with superior OER performance. The present work is instructive for designing highly efficient Ni-based OER electrocatalysts.

Chemical CommunicationsVol. 62(1)
Northwestern Polytechnical University (CN)
Openalex Percentile: Top 27%
Electrocatalysts for Energy Conversion
0.73
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