镍
脱氢
化学工程
催化作用
电化学
氢氧化物
拉曼光谱
纳米颗粒
材料科学
动力学
相(物质)
纳米技术
化学
电极
冶金
有机化学
物理化学
工程类
物理
光学
量子力学
作者
J. Wang,Wenru Zhao,Hui Yu,Wei Wang,Yipu Xu,Liu‐Liu Shen,Guirong Zhang,Donghai Mei
标识
DOI:10.1016/j.apcatb.2024.124086
摘要
Nickel-based materials are promising electrocatalysts for anodic oxidation of 5-hydroxymethylfurfural (HMF) to value-added 2, 5-furandicarboxylic acid (FDCA). However, their catalytic efficiency is impeded by the sluggish phase transformation of Ni(II) hydroxide to the active Ni(III) oxyhydroxide. Herein, we demonstrate for the first time that the phase transformation kinetics and the HMF oxidation activity of nickel nanoparticles can be modulated by creating self-assemblies with different particle aggregation structures: ordered nanoarrays, disordered nanoarrays, and random aggregates. Notably, the nanoparticle assembly featuring an ordered nanoarray structure exhibits the highest activity, achieving 99.8% HMF conversion and 99.2% FDCA yield at 1.36 V. In situ Raman spectroscopy and electrochemical analysis reveal that the ordered nanoarray effectively accelerates the transformation kinetics, attributed to the reduced dehydrogenation barrier of Ni(II) hydroxide as confirmed by density functional theory calculations. This work contributes new insights into the structure-performance relationship of Ni-based catalysts, offering valuable guidance for designing high-performing electrocatalysts.
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