Introducing a Synergistic Ligand Containing an Exotic Metal in Metal–Organic Framework Nanoarrays Enabling Superior Electrocatalytic Water Oxidation Performance

过电位 塔菲尔方程 化学 金属有机骨架 金属 计时安培法 电子转移 化学工程 配体(生物化学) 吸附 电流密度 解吸 无机化学 电极 光化学 电化学 物理化学 有机化学 循环伏安法 物理 工程类 受体 量子力学 生物化学
作者
Ye Tan,Chong Lin,Xiao He,Junjie Zou,Chunpei Yan,Jingyang Tian
出处
期刊:Inorganic Chemistry [American Chemical Society]
卷期号:61 (29): 11432-11441 被引量:7
标识
DOI:10.1021/acs.inorgchem.2c01756
摘要

Designing and fabricating well-aligned metal-organic framework nanoarrays (MOF NAs) with high electrocatalytic activity and durability for water oxidation at large current density remain huge challenges. Here the vertical NiFc-MOF NAs constructed from agaric-like nanosheets were fabricated by introducing a ligand containing an exotic Fe atom to coordinate with Ni ion using Ni(OH)2 NAs as a self-sacrificing template. The NiFc-MOF NAs exhibited superior water oxidation performance with a very low overpotential of 161 mV at the current density of 10 mA cm-2. Chronoamperometry was tested at an overpotential of 250 mV, which delivered an initial industrial-grade current density of 702 mA cm-2 and still remained at 694 mA cm-2 after 24 h. Furthermore, it possessed fast reaction kinetics with a small Tafel slope of 29.5 mV dec-1. The superior electrocatalytic performance can be ascribed to the structural advantage of vertically grown agaric-like NAs and the synergistic electron coupling between Ni and Fe atoms, namely, electron transfer from Ni to Fe atoms in NiFc-MOF NAs. The exposed density and valence state of active Ni sites were synchronously increased. Furthermore, the energy barrier for the adsorption/desorption of oxygenated intermediates was ultimately optimized for water oxidation. This work provides a novelty orientation to accelerate electrocatalytic performance of MOF NAs by introducing self-sacrificing templates containing one metal and synergistic ligand containing dissimilar metal.
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