Rapid synthesis of sea urchin-like Ni(OH)@Ni(Fe)OOH electrocatalysts for the oxygen evolution reaction
Exploring highly active, low-cost electrocatalysts for the oxygen evolution reaction (OER) is of great significance but still a major challenge. Herein, we synthesized Ni(OH) 2 @Ni(Fe)OOH with a sea urchin-like structure on a nickel foam via a simple hydrothermal and subsequent soaking process. Expe...
Gespeichert in:
Veröffentlicht in: | New journal of chemistry 2024-09, Vol.48 (37), p.1638-16386 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Exploring highly active, low-cost electrocatalysts for the oxygen evolution reaction (OER) is of great significance but still a major challenge. Herein, we synthesized Ni(OH)
2
@Ni(Fe)OOH with a sea urchin-like structure on a nickel foam
via
a simple hydrothermal and subsequent soaking process. Experimental results indicate that incorporation of Fe into Ni(OH)
2
is favorable for modulating the electronic structure as well as achieving faster electron transfer and improved intrinsic activity, thereby leading to excellent OER activity. The optimized Ni(OH)
2
@Ni(Fe)OOH electrocatalyst exhibits superior OER activity with overpotentials of 245 and 310 mV at 10 and 100 mA cm
−2
, respectively, and a small Tafel slope of 40.7 mV dec
−1
and high stability over 100 h, which is more than that of benchmark RuO
2
and several control samples without the introduction of Fe. More importantly, the overall water splitting system using Ni(OH)
2
@Ni(Fe)OOH-100 as the anode and Pt/C as the cathode only requires a cell voltage of 1.54 V to afford a current density of 10 mA cm
−2
. This work not only demonstrates the key factor of Fe doping, but also offers a new path for the development of NiFe-based OER catalysts.
A sea urchin-like Ni(OH)
2
@Ni(Fe)OOH-100 electrocatalyst was successfully grown on a Ni foam through a hydrothermal and subsequent soaking process and exhibits excellent activity toward the OER. |
---|---|
ISSN: | 1144-0546 1369-9261 |
DOI: | 10.1039/d4nj03135k |