文献类型：期刊文献

英文题名：Production of Self-Supporting Hollow Carbon Nanofiber Membranes with Co/Co2P Heterojunctions via Continuous Coaxial Co-Spinning for Efficient Overall Water Splitting

作者：Duan, Ruidan[1];Ding, Jianhang[1];Fan, Jiawei[1];Zhuang, Linzhou[1,2]

机构：[1]East China Univ Sci & Technol, Sch Chem Engn, State Key Lab Chem Engn, Shanghai 200237, Peoples R China;[2]East China Univ Sci & Technol, Shanghai Key Lab Multiphase Mat Chem Engn, Shanghai 200237, Peoples R China

年份：2025

卷号：15

期号：7

外文期刊名：COATINGS

收录：;EI(收录号：20253018861369);WOS:【SCI-EXPANDED(收录号:WOS:001553302500001)】；

基金：This work was supported by research funding provided by National Natural Science Foundation of China (Grant Nos. 22378119 and 22208092).

语种：英文

外文关键词：water electrolysis; self-supporting hollow carbon nanofibers; continuous coaxial co-spinning; heterojunction engineering; transition metal phosphides

摘要：To address mass transport limitations in carbon nanofiber membrane electrodes for overall water splitting, a self-supporting nitrogen-doped hollow carbon nanofiber membrane embedded with Co/Co2P heterojunctions (Co/Co2P-NCNFs-H) was fabricated via continuous coaxial electrospinning. The architecture features uniform hollow channels (200-250 nm diameter, 30-50 nm wall thickness) and a high specific surface area (254 m2 g-1), as confirmed by SEM, TEM, and BET analysis. The Co/Co2P heterojunction was uniformly dispersed on nitrogen-doped hollow carbon nanofibers through electrospinning, leverages interfacial electronic synergy to accelerate charge transfer and optimize the hydrogen evolution reaction (HER) and the oxygen evolution reaction (OER). Electrochemical tests demonstrated exceptional catalytic activity, achieving current densities of 100 mA cm-2 at ultralow overpotentials of 405.6 mV (OER) and 247.9 mV (HER) in 1.0 M KOH-surpassing most reported transition metal catalysts for both half-reactions. Moreover, the electrode exhibited robust long-term stability, maintaining performance for nearly 20 h at 0.6 V (vs. Ag/AgCl) (OER) and over 250 h at -1.5 V (vs. Ag/AgCl) (HER), attributed to the mechanical integrity of the hollow architecture and strong metal-carbon interactions. This work demonstrates that integrating hollow nanostructures (enhanced mass transport) and heterojunction engineering (optimized electronic configurations) creates a scalable strategy for designing efficient bifunctional catalysts, offering significant promise for sustainable hydrogen production via water electrolysis.