Biomass-derived self-supported porous carbon membrane embedded with Co nanoparticles as an advanced electrocatalyst for efficient and robust hydrogen evolution reaction

过电位 电催化剂 材料科学 化学工程 可逆氢电极 法拉第效率 制氢 纳米颗粒 电化学 阴极 碳纤维 分解水 碳化 电极 纳米技术 催化作用 化学 工作电极 复合材料 有机化学 物理化学 工程类 复合数 光催化 扫描电子显微镜
作者
Shixiong Min,Yan Duan,Yanan Li,Fang Wang
出处
期刊:Renewable Energy [Elsevier]
卷期号:155: 447-455 被引量:25
标识
DOI:10.1016/j.renene.2020.03.164
摘要

Powderous transition metal-based electrocatalysts have been widely studied for hydrogen evolution reaction (HER), but their practical application still remains challenging due to the tedious slurry-based electrode assembly process and unavoidable stability decay at high current density. Herein, a self-supported H2 evolution cathode based on pomelo peel (PP)-derived porous carbon (PPDC) membrane with embedded Co nanoparticles ([email protected]) is developed by direct carbonization of Co-adsorbed PP (Co2+-PP). Benefiting from the large surface areas, the abundant open and interconnected pores, the highly graphitic PPDC membrane, and the highly dispersed Co nanoparticles, the self-supported [email protected] electrode demonstrates superior electrocatalytic performance for HER in 1.0 M KOH solution, with overpotentials of 154 and 264 mV at current densities of 10 and 100 mA cm−2, respectively. In addition, owing to the good structural integrity, the [email protected] electrode exhibits an excellent cycling stability for 2000 cycles and a stable current density of ∼100 mA cm−2 at a constant overpotential of 265 mV over 12 h with a nearly 100% Faradaic efficiency (FE) and H2 production rate of 1.56 mmol h−1. Therefore, this work provides a versatile and effective strategy for development of high-performance self-supported electrodes at low cost for large-scale H2 production from electrochemical water splitting.
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