Constructing a Hetero-interface Composed of Oxygen Vacancy-Enriched Co3O4 and Crystalline–Amorphous NiFe-LDH for Oxygen Evolution Reaction

电催化剂 塔菲尔方程 纳米片 无定形固体 催化作用 氧气 材料科学 结晶学 析氧 化学 化学工程 纳米技术 物理化学 有机化学 冶金 工程类 生物化学 电化学 电极
作者
Junjun Lv,Linmeng Wang,Rushuo Li,Kaiyue Zhang,Danfeng Zhao,Yaqiong Li,Xiangjun Li,Xiubing Huang,Ge Wang
出处
期刊:ACS Catalysis [American Chemical Society]
卷期号:11 (23): 14338-14351 被引量:265
标识
DOI:10.1021/acscatal.1c03960
摘要

The development of high-performance electrocatalysts is a highly efficient strategy to optimize the sluggish kinetic property of the oxygen evolution reaction (OER). Herein, we synthesize a kind of nickel foam (NF)-supported electrocatalyst composed of a one-dimensional Co3O4 nanowire as the core and a two-dimensional NiFe-LDH nanosheet as the shell (denoted as NiFe-60/Co3O4@NF). Fluorine is introduced into the precursor Co(OH)F of Co3O4, which results in improved thermal stability and significantly increased regularly distributed oxygen vacancies, while the electrochemically deposited NiFe-LDH nanosheets possess a crystalline/amorphous hybrid structure. As a result, the hetero-interface mainly constituting Ni species from NiFe-LDH and Co3O4 from Co(OH)F contributes to the interaction between Co and Fe species and facilitates the electron transfer. Simultaneously, the interaction between oxygen vacancies in Co3O4 and coordinatively unsaturated Fe species in the amorphous area in NiFe-LDH is also determined, finally completing the electron backtracking. Benefiting from these factors, only low overpotentials of 221 and 257 mV are required to deliver the current densities of 100 and 500 mA cm–2, respectively, with a quite small Tafel slope of 34.6 mV dec–1 during OER for the well-designed NiFe-60/Co3O4@NF electrocatalyst.
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