化学
电催化剂
过电位
对苯二甲酸
苯甲醇
偏苯三甲酸
金属有机骨架
镍
背景(考古学)
无机化学
配体(生物化学)
催化作用
活动站点
解吸
有机化学
电化学
聚酯纤维
物理化学
分子
电极
古生物学
生物化学
受体
吸附
生物
作者
Wenli Su,Xingzi Zheng,Wei Xiong,Ying Ouyang,Zhe Zhang,Weijie Zeng,Haotian Duan,Xingyu Chen,Peiyuan Su,Zemin Sun,Mengwei Yuan
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2024-06-26
卷期号:63 (27): 12572-12581
被引量:9
标识
DOI:10.1021/acs.inorgchem.4c01507
摘要
The kinetics of electrocatalytic reactions are closely related to the number and intrinsic activity of the active sites. Open active sites offer easy access to the substrate and allow for efficient desorption and diffusion of reaction products without significant hindrance. Metal-organic frameworks (MOFs) with open active sites show great potential in this context. To increase the density of active sites, trimesic acid was utilized as a ligand to anchor more Ni sites and in situ construct the nickel foam-loaded Ni-based trimesic MOF electrocatalyst (Ni-TMA-MOF/NF). When tested as an electrocatalyst for benzyl alcohol oxidation, Ni-TMA-MOF/NF exhibited lower overpotential and superior durability compared to Ni foam-loaded Ni-based terephthalic MOF electrocatalyst (Ni-PTA-MOF/NF) and Ni(OH)
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