generation of Ni/Fe hydroxide layers by anodic etching of a Ni/Fe film for efficient oxygen evolution reaction

Commercial applications of electrolytic water splitting require cost-efficient and active oxygen evolution catalysts. Nickel-iron (NiFe)-based compounds have attracted significant attention as oxygen evolution reaction (OER) catalysts due to their high catalytic activity. We develop a simple and eas...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:New journal of chemistry 2022-10, Vol.46 (42), p.249-2496
Hauptverfasser: Li, Ling, Wu, Jing, Huang, Lieyuan, Lan, Gaoli, Wang, Naxiang, Zhang, Hui, Chen, Xin, Ge, Xingbo
Format: Artikel
Sprache:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Commercial applications of electrolytic water splitting require cost-efficient and active oxygen evolution catalysts. Nickel-iron (NiFe)-based compounds have attracted significant attention as oxygen evolution reaction (OER) catalysts due to their high catalytic activity. We develop a simple and easily controlled method by combining anodic fluoridation and cyclic voltammetry (CV) treatment to convert NiFe alloy to Ni/Fe hydroxide. A cracked layer structure of Ni/Fe hydroxide formed on the surface during the fluoridation of NiFe alloy and the CV process in KOH. The Ni/Fe hydroxide exhibits considerable OER activity with an onset potential of 1.47 V vs. RHE and a Tafel slope of 47 mV dec −1 in 0.1 M KOH. The electrode also shows an acceptable stability in alkaline media. The results indicate that anodic fluoridation and CV treatment are promising methods to form active layer structures of hydroxide on transition metals and their alloys, further increasing the electrocatalytic activity of the catalyst. A Ni/Fe hydroxide electrocatalyst was fabricated via a simple and easily controlled method by combining anodic fluoridation and cyclic voltammetry (CV) treatment as an efficient catalyst for the OER.
ISSN:1144-0546
1369-9261
DOI:10.1039/d1nj05775h