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A facile morphology tunable strategy of Zn-MOF derived hierarchically carbon materials with enhanced supercapacitive performance through the solvent effect.

Authors :
Miao R
Sun C
Li J
Sun Y
Chen Y
Pan J
Tang Y
Wan P
Source :
Dalton transactions (Cambridge, England : 2003) [Dalton Trans] 2022 Dec 06; Vol. 51 (47), pp. 18213-18223. Date of Electronic Publication: 2022 Dec 06.
Publication Year :
2022

Abstract

Metal-organic framework (MOF) derived porous carbon materials have been widely applied as active materials for supercapacitors due to their large specific surface area and ordered pore structure. This paper presents a facile and effective strategy to regulate the morphology of a zinc-based metal-organic framework (Zn-trimesic acid, Zn-BTC) by adjusting the ethanol content in a solvent, which can effectively change the pore structure of Zn-BTC derived porous carbon (PC). The optimal PC prepared in 50% ethanol displays a rodlike structure with a large specific surface area (SSA) of 1930 m <superscript>2</superscript> g <superscript>-1</superscript> and an average pore size of 2.9 nm. This material shows an excellent rate performance with 78.8% capacitance retention when the current density increases from 1 A g <superscript>-1</superscript> to 100 A g <superscript>-1</superscript> and outstanding electrochemical stability with only 2.2% decline of capacitance after 200 000 cycles at 50 A g <superscript>-1</superscript> . Moreover, the assembled symmetrical capacitor shows a high energy density of 16.09 W h kg <superscript>-1</superscript> at 698 W kg <superscript>-1</superscript> and 11.89 W h kg <superscript>-1</superscript> at a high power density of 41.56 kW kg <superscript>-1</superscript> . This method would provide a new pathway for the preparation of carbon materials with an adjustable pore size for high-performance supercapacitors.

Details

Language :
English
ISSN :
1477-9234
Volume :
51
Issue :
47
Database :
MEDLINE
Journal :
Dalton transactions (Cambridge, England : 2003)
Publication Type :
Academic Journal
Accession number :
36399001
Full Text :
https://doi.org/10.1039/d2dt02624d