Related Experiment Video
Updated: Dec 11, 2025

Synthesis of Metal Nanoparticles Supported on Carbon Nanotube with Doped Co and N Atoms and its Catalytic Applications in Hydrogen Production
Published on: December 6, 2021
Interfacial Engineering of Bimetallic Carbide and Cobalt Encapsulated in Nitrogen-Doped Carbon Nanotubes for
Kun Wang1, Zhenjiang Lu1, Yizhao Li1,2
1Key Laboratory of Energy Materials Chemistry, Ministry of Education, Key Laboratory of Advanced Functional Materials, Autonomous Region, Institute of Applied Chemistry, College of Chemistry, Xinjiang University, Urumqi, Xinjiang, 830046, P. R. China.
Abstract:
Heterojunction engineering is a fundamental strategy to develop efficient electrocatalysts for the oxygen reduction reaction by tuning electronic properties through interfacial cooperation. In this study, a heterojunction electrocatalyst consisting of bimetallic carbide Co3 ZnC and cobalt encapsulated within N-doped carbon nanotubes (Co3 ZnC/Co@NCNTs) is synthesized by a facile two-step ion exchange-thermolysis pathway. Co3 ZnC/Co@NCNTs effectively promotes interfacial charge transport between the different components with optimizes adsorption and desorption of intermediate products at the heterointerface. In situ-grown N-doped carbon nanotubes (NCNTs) not only improve the electrical conductivity but also suppress the oxidation of transition metal nanoparticles in alkaline media. Moreover, the abundant nitrogen types (pyridinic N, Co-Nx , and graphitic nitrogen) in the carbon skeleton provide more active sites for oxygen adsorption. Benefitting from this optimized structure, Co3 ZnC/Co@NCNTs hybrid not only demonstrates excellent oxygen reduction activity, with a half-wave potential of 0.83 V and fast mass transport with limited current density of 6.23 mA cm-2 , but also exhibits superior stability and methanol tolerance, which surpass those of commercial Pt/C catalysts. This work provides an effective heterostructure for interfacial electronic modulation to improve electrocatalytic performance.

