Coordination compound-derived La-doped FeS2/N-doped carbon (NC) as an efficient electrocatalyst for the oxygen evolution reaction

By annealing/sulfuring of coordination compound (CC) precursors, [LaxFe1−x(H2O)8Fe(CN)6]·2hmt (x = 0, 0.33 and 0.5) (hmt = hexamethylenetetramine), FeS2/N-doped carbon (NC), La-doped FeS2/NC-0.33 and La-doped FeS2/NC-0.5 were synthesized. All of them can electrolyze the oxygen evolution reaction (OE...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:CrystEngComm 2022-04, Vol.24 (22), p.4049-4056
Hauptverfasser: Xuan Ao Ma, Yang, Hai, Gong, Yun
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:By annealing/sulfuring of coordination compound (CC) precursors, [LaxFe1−x(H2O)8Fe(CN)6]·2hmt (x = 0, 0.33 and 0.5) (hmt = hexamethylenetetramine), FeS2/N-doped carbon (NC), La-doped FeS2/NC-0.33 and La-doped FeS2/NC-0.5 were synthesized. All of them can electrolyze the oxygen evolution reaction (OER). Among them, the optimum sample La-doped FeS2/NC-0.33 shows a low overpotential (η) of 217/239 mV at 30/50 mA cm−2, which is comparable and even superior to commercial RuO2 and many iron sulfide-based catalysts reported previously. Furthermore, La-doped FeS2/NC-0.33 exhibits long-term OER activity with the transformation of FeS2 → FeOOH over 60 h electrolysis at 20 mA cm−2. In addition, density functional theory (DFT) simulations reveal that the rate-determining steps on La-doped FeS2 and FeS2 (200) surfaces are the formation of O2 and Fe*–OH, respectively, and La-doped FeS2 exhibits a less ΔGmax value of 1.585 eV with a smaller η value of 0.355 V, which is attributed to their different d-band centers before and after La-doping.
ISSN:1466-8033
DOI:10.1039/d2ce00431c