铜
碳纳米管
氧气
金属
析氧
碳纤维
金属有机骨架
化学工程
化学
材料科学
无机化学
纳米技术
冶金
电化学
复合材料
有机化学
物理化学
电极
复合数
吸附
工程类
作者
Yashu Liu,Wei Zi,Zehang Li,Shilin Wu,Shan Qiao,Hongbo Zhou
标识
DOI:10.1016/j.ijhydene.2024.03.007
摘要
To reveal the oxygen evolution reaction (OER) catalytic performance and structure-activity relationship of copper-iron-based metal-organic frameworks (MOFs) at the molecular level, new types of Cu–Fe MOF based materials, Cu2Fe/CNT and {CuFe2}n/CNT (CNT: carbon nanotube), were synthesized and studied. The results showed that the two materials exhibited different catalytic activities, with the former showing lower activity (Overpotential at the current density of 10 mA cm−2: η10 = 450 mV, Tafel slope: 92.4 mV dec−1) and the latter showing much higher activity (η10 = 370 mV, Tafel slope: 64.8 mV dec−1). Further analysis revealed that the performance difference was due to ligand rearrangement between metals in Cu2Fe/CNT, which affected the exposure of active metal sites. Meanwhile, the unique three-dimensional MOF structure of {CuFe2}n/CNT significantly increased the electrochemical surface area (ECSA), enhancing the electrochemical performance. This study demonstrates how the intricate ligand rearrangement effects in non-precious metal catalysts can greatly influence their performance. Understanding and rationally tuning these coordination interactions is crucial for designing high-performance non-noble metal electrocatalysts.
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