Metal–Organic Framework-Derived Co3ZnC/Co Embedded in Nitrogen-Doped Carbon Nanotube-Grafted Carbon Polyhedra as a High-Performance Electrocatalyst for Water Splitting
Source abstract
Abstract
The development of efficient, low-cost, and stable electrocatalysts for overall water splitting is of great significance for energy conversion. Transition-metal carbides (TMCs) with high catalytic activity and low cost have attracted great interests. Nevertheless, utilizing an efficient catalyst for overall water splitting is still a challenging issue for TMCs. Herein, we report the synthesis of a high-performance electrocatalyst comprising Co 3 ZnC and Co nanoparticles embedded in a nitrogen-doped carbon nanotube-grafted carbon polyhedral (Co 3 ZnC/Co-NCCP) by the pyrolysis of bimetallic zeolitic imidazolate frameworks in a reductive atmosphere of Ar/H 2 . The Co 3 ZnC/Co-NCCP exhibits remarkable electrochemical activity in catalyzing both the oxygen evolution reaction and hydrogen evolution reaction, in terms of low overpotential and excellent stability. Furthermore, the Co 3 ZnC/Co-NCCP catalyst leads to a highly performed overall water splitting in the 1 M KOH electrolyte, delivering a current density of 10 mA cm –2 at a low applied external potential of 1.65 V and shows good stability without obvious deactivation after 10 h operation. The present strategy opens a new avenue to the design of efficient electrocatalysts in electrochemical applications.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Electrocatalysts for Energy Conversion · Advanced battery technologies research · Advancements in Battery Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Advanced Research Institute for Multidisciplinary Science, Beijing Institute of Technology, Beijing 100081, P. R. China
State Key Laboratory of Advanced Chemical Power Sources, Zunyi 563000, P. R. China
Funding
Beijing Institute of Technology · National Natural Science Foundation of China
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