Modulation of morphology and electronic structure of cobalt thiophenedicarboxylic coordination polymer via ligand exchange for high-performance oxygen evolution reaction and supercapacitor

被引:1
|
作者
Wang, Hong [1 ,2 ]
Wu, Shuai [1 ,2 ]
Zhao, Peihua [1 ]
Wang, Chao [1 ,2 ]
Guo, Li [1 ,2 ]
Wang, Yanzhong [1 ,2 ]
机构
[1] North Univ China, Sch Mat Sci & Engn, Taiyuan 030051, Peoples R China
[2] North Univ China, Shanxi Key Lab Efficient Hydrogen Storage & Prod T, Taiyuan 030051, Peoples R China
基金
中国国家自然科学基金;
关键词
MOFs; Ferrocenedicarboxylic acid; Oxygen evolution reaction (OER); Supercapacitors; METAL-ORGANIC FRAMEWORK; EFFICIENT; NANOPARTICLES; NANOSHEETS; CATALYSTS;
D O I
10.1016/j.jcis.2024.07.071
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Rationally designing metal organic frameworks (MOFs) as an ideal dual-function material for water electrolysis and supercapacitors is of great significance for energy storage and conversion. Herein, we successfully synthesized the nanoneedle-like structure CoNi-MOF by partially replacing 2, 5-thiophenedicarboxylic acid (TDA) with 1, 1 '-Ferrocenedicarboxylate (Fc). The exchange of Fc ligand can modulate the morphology and electronic structure of CoNi-TDA, thus exposing the abundant active sites and improving the electrical conductivity. The asprepared CoNi-TDA/0.2Fc exhibited a low overpotential of 236 mV at 10 mA cm-2 for oxygen evolution reaction (OER) and a low Tafel slope of 40.44 mV dec- 1. Additionally, CoNi-TDA/0.2Fc demonstrated a notable specific capacitance of 1409 F g-1 at 1 A/g and excellent stability, maintaining a capacitance retention of 96.54 % after 20,000 cycles. The study proposes a new strategy to modulate the morphology and electronic structure of MOFs via the ligand exchange for high-performance energy storage and conversion device.
引用
收藏
页码:712 / 720
页数:9
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