Iridium incorporated cobalt-based hydroxide on nickel-contained carbon nanofibers renders highly efficient oxygen evolution reaction

被引:2
|
作者
Xu, Jiaqi [1 ]
Cao, Shoufu [2 ]
Zhong, Mengxiao [1 ]
Chen, Xiaojie [1 ]
Li, Weimo [1 ]
Yan, Su [1 ]
Wang, Ce [1 ]
Wang, Zhaojie [2 ]
Lu, Xiaoqing [2 ]
Lu, Xiaofeng [1 ]
机构
[1] Jilin Univ, Alan G MacDiarmid Inst, Coll Chem, Changchun 130012, Peoples R China
[2] China Univ Petr, Sch Mat Sci & Engn, Qingdao 266580, Peoples R China
基金
中国国家自然科学基金;
关键词
Electrospinning; Iridium incorporation; Oxygen evolution reaction; Core-sheath structure; Ni-contained carbon nanofibers; BETA-CO(OH)(2); WATER; IR; BATTERIES;
D O I
10.1016/j.seppur.2023.124638
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The construction of high-performance oxygen evolution reaction (OER) electrocatalysts is crucial for energy applications. Here, we demonstrate a reliable route to incorporate iridium (Ir) into cobalt (Co)-based hydroxide derived from ZIF-67 on the surface of Ni-contained carbon nanofibers (denoted as Ni-CNFs/Ir-Co(OH)2) as an electrocatalyst to boost its alkaline OER property. The optimized Ni-CNFs/Ir-Co(OH)2 sample exhibits an extraordinary OER activity with an overpotential of only 240 mV to reach 10 mA cm-2, much lower than that of commercial IrO2 electrocatalyst (331 mV). The theoretical results illustrate the highly active Co sites of Iredge-Co (OH)2 for OER. Furthermore, the distinct nanofibrous architecture of Ni-CNFs endows with a desirable electrical conductivity of the catalyst, thus the Ni-CNFs/Ir-Co(OH)2 sample presents a desirable durability for OER testing. In addition, a total water electrolyzer is built by using the prepared Ni-CNFs/Ir-Co(OH)2 and Pt/C as electrodes, which requires only 1.50 V at 10 mA cm-2, superior to the value of Pt/C||IrO2 cell (1.62 V). This study puts forward an effective route to explore superior OER electrocatalysts by engineering the electronic structure of metal hydroxide for energy applications.
引用
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页数:8
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