析氧
化学
催化作用
氢氧化物
化学工程
热液循环
氧气
钴
电极
异质结
分解水
氢
电流密度
工作(物理)
水热反应
纳米技术
氢氧化钴
联轴节(管道)
制氢
无机化学
电催化剂
过渡金属
电池电压
燃料电池
电流(流体)
反应条件
水热合成
电压
作者
Zhongjie Song,Yuhao Wang,Nannan Zhang,Jun Yu,Zhengying Wu,Yukou Du
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2026-08-25
卷期号:65 (35): 20631-20641
被引量:1
标识
DOI:10.1021/acs.inorgchem.6c03462
摘要
The development of highly efficient oxygen evolution reaction (OER) electrode materials has attracted widespread attention. In this work, we prepared MIL-101(Fe) using the traditional hydrothermal and oil bath method to coat a layer of NiCo-LDH (nickel cobalt layered double hydroxide (LDH)) on its surface, forming an MOF (metal-organic framework)/LDH heterostructure. The core-shell heterostructure and synergistic effect among Co, Ni, and Fe atoms give the catalyst an excellent OER catalytic performance. Specifically, it requires overpotentials of 216 and 247 mV to reach current densities of 10 and 50 mA·cm-2, respectively. Chronopotentiometry shows that it can maintain a current density of 100 mA·cm-2 for over 100 h. In overall water-splitting tests, it only requires an applied voltage of 1.52 V to reach 10 mA·cm-2 and exhibits stability for over 100 h at 100 mA·cm-2. Furthermore, this work identified 3 h as the optimal oil bath time and revealed that the synergistic coupling of MOF and LDH facilitates the shift of the OER mechanism to the LOM (lattice oxygen mechanism) pathway. This work ingeniously constructs a material with a core-shell structure, realizing performance enhancement through the synergistic effects among multiple metals and making a beneficial contribution to promote the development of green hydrogen production.
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