过电位
析氧
材料科学
电催化剂
催化作用
电解质
分解水
金属有机骨架
碳纳米管
化学工程
纳米技术
电子转移
化学
电极
光催化
光化学
电化学
吸附
物理化学
有机化学
工程类
作者
Mengya Wang,Dawei Liu,Katam Srinivas,Hesheng Yu,Fei Ma,Ziheng Zhang,Yu Wu,Xinsheng Li,Yue Wang,Yuanfu Chen
标识
DOI:10.1016/j.ijhydene.2023.10.212
摘要
The efficiency of electrolytic water splitting is hampered by the slow kinetics of the oxygen evolution reaction (OER). Addressing this challenge, we present a novel catalyst with rich Ni3S4/FeNi2S4 heterostructures anchored metal-organic framework-derived nanosheets interconnected by carbon nanotubes (NiFe–S@CNT). The NiFe–S@CNT electrocatalyst shows an ultralow overpotential of 246 mV at a current density of 10 mA/cm2 (η10), surpassing the benchmark RuO2 (η10 = 291 mV) as well as many reported sulfide electrocatalysts. The strong heterointerface interaction between Ni3S4 and FeNi2S4 induce synergistic effects, modifying the electronic structure of active sites and generating a large number of lattice defects. Additionally, the carbon nanotubes skeleton facilitates efficient electron transfer and enhances electrical conductivity during the catalytic process. Moreover, the metal-organic framework derivative inherits a porous structure, aiding in electrolyte penetration and efficient bubble release. This study provides a facile and scalable strategy to develop nonprecious transition-metal-based OER catalysts with abundant heterointerfaces and active sites for efficient water splitting.
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