材料科学
异质结
析氧
无定形固体
电催化剂
电化学
化学工程
纳米技术
分解水
电解
电极
基质(水族馆)
金属有机骨架
无定形碳
催化作用
光电子学
化学
物理化学
结晶学
光催化
工程类
电解质
生物化学
海洋学
吸附
地质学
作者
Guangyao Zhou,Xue Zhou,Jing Li,Wei‐Ran Huang,Huan Pang,Songtao Zhang,Jun Yang,Lin Xu,Yawen Tang
出处
期刊:Small
[Wiley]
日期:2024-09-18
标识
DOI:10.1002/smll.202404598
摘要
Abstract The endowment of metal organic frameworks (MOF) with superior electrocatalytic performance without compromising their structural/compositional superiorities is of great significance for the development of renewable energy devices, yet remains a grand challenge. Herein, a deliberate partial amorphization strategy is developed to construct a heterostructured electrocatalyst consisting of crystalline Co‐MOF and amorphous Co‐S nanoflake arrays aligned on the carbon cloth (CC) substrate (abbreviated as Co‐MOF/Co‐S@CC hereafter) through a rapid sulfuration method. The simultaneous implement of crystalline‐amorphous (c‐a) heterostructure and nanoflake arrayed architecture on CC substrate renders the Co‐MOF/Co‐S@CC with abundant and tight active sites, accelerated charge transfer rate, regulated electronic structures, and reinforced structural stability. As such, the obtained Co‐MOF/Co‐S@CC electrode demonstrates outstanding electrochemical hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) performances with the overpotentials of 64 and 217 mV at 10 mA cm −2 , respectively. Moreover, a two‐electrode electrolyzer assembled by Co‐MOF/Co‐S@CC electrodes exhibits the lower cell voltages and larger current densities than those of Pt/C and RuO 2 counterparts, excellent reversibility and prominent long‐term stability, representing a great prospect for feasible H 2 production. This adopted concept of c‐a heterostructure for electronic regulation may bring about insightful inspiration for designing high‐performance electrocatalysts for sustainable energy systems.
科研通智能强力驱动
Strongly Powered by AbleSci AI