Nanosheet-assembled transition metal sulfides nanoflowers derived from CoMo-MOF for efficient oxygen evolution reaction

析氧 过电位 纳米片 纳米花 过渡金属 化学工程 材料科学 催化作用 分解水 金属有机骨架 硫化镍 硫化物 纳米技术 无机化学 化学 电极 电化学 物理化学 吸附 光催化 工程类 冶金 生物化学
作者
Shudi Yu,Dongmei Liu,Cheng Wang,Jie Li,Rui Yu,Yong Wang,Jiongting Yin,Xiaomei Wang,Yukou Du
出处
期刊:Journal of Colloid and Interface Science [Elsevier BV]
卷期号:653: 1464-1477 被引量:27
标识
DOI:10.1016/j.jcis.2023.10.006
摘要

Oxygen evolution reaction (OER) is a multi-electron transfer process, whose intrinsic sluggish dynamic restricts the whole process of overall water splitting (OWS). To address this issue, a porous transition metal sulfide (TMS) catalyst with rich heterojunctions was prepared by vulcanization and trace Fe doping of CoMo-based metal–organic framework (MOF). In this work, the nanoflower composed of ultrathin 2D nanosheets anchored on a nickel foam presents a layered interface that contributes to the exposure of active regions. The resulting electrode denoted as Fe@CoMo2S4/Ni3S2/NF required a low overpotential (η10 = 167 mV @ 10 mA cm−2, η50 = 260 mV @ 50 mA cm−2) in 1.0 M KOH for OER and a small cell voltage (E = 1.513 V @ 10 mA cm−2) to power OWS when coupled with commercial Pt/C. It also exhibited splendid morphological and chemical stability with virtually invariant polarization curve and flower-like appearance after 1000 CV cycles, as well as long-term durability over 100 h with a constant current density of 10 mA cm−2. This work revealed the multi-anionic regulation mechanism in the surface reconstruction of sulfide electrocatalysts, and verified that Co/Mo/Ni-based oxysulfide was the true active substance of OER, which inspired the understanding and design of multi-anionic regulated electrocatalysts.
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