二茂铁
电化学
金属有机骨架
催化作用
组合化学
材料科学
齿合度
纳米技术
化学
电极
金属
有机化学
物理化学
吸附
冶金
作者
Yujing Nie,Yijiang Li,Junwei Li,Leniu Chen,Xudong Wang,Tao Chen,Zhixiong Cai
标识
DOI:10.1016/j.colsurfa.2023.132742
摘要
Metal-organic frameworks (MOFs) exhibit structural diversity and functional tunability, rendering them a versatile platform for a wide range of applications. Specifically, defects or function groups induced by exotic ligands is an efficient strategy to adjust the catalytic performance. In this study, we explore the impact of incorporating ferrocene derivatives into two Ni-based MOFs and examine their suitability as potential glucose sensors. One strategy involves introducing bidentate 1,1′-ferrocenedicarboxylic acid (1,1′-Fc) into the 3D Ni-1,4-benzenedicarboxylic acid MOF (Fc-Ni-BDC) using a simple single-step hydrothermal method. Another approach involves encapsulating ferrocenemethylamine (Fc-NH2) inside the cavity of 2D conductive Ni-HHTP MOF (HHTP=2,3,6,7,10,11-hexahydroxytriphenylene) driven by electrostatic attraction to form Fc-Ni-HHTP. On account of the synergy between ferrocene derivatives and MOFs, the hybrid MOFs demonstrated remarkable electrochemical performance, characterized by pronounced electrocatalytic reactivity towards glucose oxidation. It is showed that the doped ferrocene derivatives act as electron donors to the MOF active sites, modifying the electronic structure and facilitating the kinetics of the reactions, then an augmentation in the catalytic efficiency has been achieved. This work demonstrates a simple strategy to improve MOF-based electrochemical sensors by incorporating metallocene ligands.
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