Overall water electrolysis on a graphdiyne-iron oxyhydroxide heterostructure

Water electrolysis provides an effective method for energy efficient hydrogen production. The challenge in this field is how to synthesize electrocatalysts with high activity and stability in water electrolysis reactions. Herein, a new heterostructure of graphdiyne-iron oxyhydroxide was synthesized...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2023-05, Vol.11 (18), p.9824-9828
Hauptverfasser: Chen, Xi, Zhang, Danyan, Zheng, Xuchen, Zhang, Chao, Gao, Yang, Xing, Chengyu, Chen, Siao, Wu, Han, Xue, Yurui, Li, Yuliang
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Water electrolysis provides an effective method for energy efficient hydrogen production. The challenge in this field is how to synthesize electrocatalysts with high activity and stability in water electrolysis reactions. Herein, a new heterostructure of graphdiyne-iron oxyhydroxide was synthesized by controlled growth of GDY films on the surface of FeOOH nanowires (FeOOH@GDY). An interface structure with an electron-donor (GDY) and electron-acceptor (Fe) was formed, which showed the obvious incomplete charge transfer between GDY and Fe atoms at the interfaces. This produces infinite active sites which guarantee excellent catalytic activity. The GDY grown on the surfaces of oxyhydroxides endows the electrocatalyst with high stability. These unique and fascinating properties make FeOOH@GDY show excellent catalytic activities toward overall water splitting (OWS) with a small cell voltage of 1.43 V at 10 mA cm −2 under ambient conditions and excellent long-term stability. The incomplete charge transfer between graphdiyne and metal atoms at the interface structures endows the catalyst with excellent catalytic activity.
ISSN:2050-7488
2050-7496
DOI:10.1039/d3ta01176c