Strongly Coupled Architectures of Cobalt Phosphide Nanoparticles Assembled on Graphene as Bifunctional Electrocatalysts for Water Splitting

Efficient bifunctional electrocatalysts for both the cathodic hydrogen evolution reaction (HER) and anodic oxygen evolution reaction (OER) are crucial for water splitting in a sustainable energy system. A strategy for fabricating strongly coupled cobalt phosphide (CoP)/graphene (G) architectures com...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:ChemElectroChem 2016-05, Vol.3 (5), p.719-725
Hauptverfasser: Huang, Huawei, Yu, Chang, Yang, Juan, Zhao, Changtai, Han, Xiaotong, Liu, Zhibin, Qiu, Jieshan
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Efficient bifunctional electrocatalysts for both the cathodic hydrogen evolution reaction (HER) and anodic oxygen evolution reaction (OER) are crucial for water splitting in a sustainable energy system. A strategy for fabricating strongly coupled cobalt phosphide (CoP)/graphene (G) architectures composed of CoP nanoparticles and G is described. Benefiting from synergetic effects of a dual support system of CoP for electroactive sites and G to enhance charge transfer, low overpotentials of 120 mV for the HER (0.5 m H2SO4) and 292 mV for the OER (1 m KOH) are required to achieve current densities of 10 mA cm−2. The as‐prepared CoP/G composites, which serve as bifunctional catalysts for both HER and OER in complete water splitting, can generate a current density of 10 mA cm−2 at 1.626 V. The present strategy provides a novel and efficient method for configuring high‐efficiency electrocatalysts for energy‐related storage and conversion devices. Power of two: Strongly coupled architectures (CoP/G) composed of CoP nanoparticles anchored on graphene sheets have been synthesized and exhibit enhanced performances for the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER; see figure).
ISSN:2196-0216
2196-0216
DOI:10.1002/celc.201600001