化学
电化学
超级电容器
配体(生物化学)
连接器
电容
金属有机骨架
拓扑(电路)
钴
氧化亚铁硫杆菌
电极
金属
纳米棒
化学工程
纳米技术
无机化学
铜
材料科学
物理化学
有机化学
受体
生物浸出
生物化学
数学
吸附
组合数学
计算机科学
工程类
操作系统
作者
Richa Rajak,Mohit Saraf,Shaikh M. Mobin
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2020-01-16
卷期号:59 (3): 1642-1652
被引量:59
标识
DOI:10.1021/acs.inorgchem.9b02762
摘要
A new Na/Co-based heterometallic metal-organic framework, [Na2Co(SDCA)(μ2-OH)2(μ2-H2O)2(Azopy)]n (where Azopy = 4,4'-Azopyridine and SDCA = 2,5'-thiophenedicarboxylic acid) (1) with nanorod-shaped morphology was synthesized using mixed-ligand approach via slow-diffusion technique under ambient conditions. The crystal structure study demonstrates the proportion of Co(II) and Na(I) metal node to be 1:2 and the acquired coordination network reveals as a 3D architecture. Topologically, the 4-c Na(I) ion directs in situ assembly of 4-c SDCA linker and 6-c Co(II) ion, resulting in the formation of 4,4,6-c net with a topology named as smm3. Additionally, 1 was incorporated as a binder-free material for a glassy carbon electrode (1-GCE) to explore its supercapacitor performance, which reveals a high specific capacitance of 321.8 F g-1 at 4 A g-1 and notable rate performance (∼78.9% of initial capacitance up to 16 A g-1) as well as excellent cycling stability (retains 97.4% after 5000 cycles). The demonstrated strategy of employing different heterometallic clusters with mixed ligands markedly increases MOF's complexity and induces synergistic properties, which is highly favorable for electrochemical applications. Hence, the present approach can be extended to build a wide range of MOFs and synergistically enhanced electrochemical performance can be achieved.
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