Imidazole linker‐induced covalent triazine framework–ZIF hybrids for confined hollow carbon super‐heterostructures toward a long‐life supercapacitor

Abstract Carbon super‐heterostructures with high nitrogen contents from the covalent hybrid precursors of covalent triazine frameworks (CTFs) and zeolitic imidazolic frameworks (ZIFs) are scarcely explored because of CTF's ordered structure and toxic superacid that dissolves or destabilizes the...

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Main Authors: Madagonda M. Vadiyar, Ji‐Young Kim, Jee‐Hwan Bae, Kyung‐Wan Nam
Format: Article
Language:English
Published: Wiley 2023-10-01
Series:Carbon Energy
Subjects:
Online Access:https://doi.org/10.1002/cey2.344
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author Madagonda M. Vadiyar
Ji‐Young Kim
Jee‐Hwan Bae
Kyung‐Wan Nam
author_facet Madagonda M. Vadiyar
Ji‐Young Kim
Jee‐Hwan Bae
Kyung‐Wan Nam
author_sort Madagonda M. Vadiyar
collection DOAJ
description Abstract Carbon super‐heterostructures with high nitrogen contents from the covalent hybrid precursors of covalent triazine frameworks (CTFs) and zeolitic imidazolic frameworks (ZIFs) are scarcely explored because of CTF's ordered structure and toxic superacid that dissolves or destabilizes the metal nodes. To solve this problem, herein, we report a straightforward two‐step pathway for the covalent hybridization of disordered CTF (d–CTF)–ZIF composites via preincorporation of an imidazole (IM) linker into ordered CTFs, followed by the imidazole‐site‐specific covalent growth of ZIFs. Direct carbonization of these synthesized d–CTF−IM−ZIF hybrids results in unique hollow carbon super‐heterostructures with ultrahigh nitrogen content (>18.6%), high specific surface area (1663 m2 g−1), and beneficial trace metal (Co/Zn NPs) contents for promoting the redox pseudocapacitance. As proof of concept, the obtained carbon super‐heterostructure (Co–Zn–NCSNH–800) is used as a positive electrode in an asymmetric supercapacitor, demonstrating a remarkable energy density of 61 Wh kg−1 and extraordinary cyclic stability of 97% retention after 30,000 cycles at the cell level. Our presynthetic modifications of CTF and their covalent hybridization with ZIF crystals pave the way toward new design strategies for synthesizing functional porous carbon materials for promising energy applications.
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spelling doaj.art-803a76c1d20046cd86459458a8e3869f2023-11-22T22:45:00ZengWileyCarbon Energy2637-93682023-10-01510n/an/a10.1002/cey2.344Imidazole linker‐induced covalent triazine framework–ZIF hybrids for confined hollow carbon super‐heterostructures toward a long‐life supercapacitorMadagonda M. Vadiyar0Ji‐Young Kim1Jee‐Hwan Bae2Kyung‐Wan Nam3Department of Energy and Materials Engineering Dongguk University Seoul South KoreaAdvanced Analysis & Data Center Korea Institute of Science and Technology (KIST) Seoul South KoreaAdvanced Analysis & Data Center Korea Institute of Science and Technology (KIST) Seoul South KoreaDepartment of Energy and Materials Engineering Dongguk University Seoul South KoreaAbstract Carbon super‐heterostructures with high nitrogen contents from the covalent hybrid precursors of covalent triazine frameworks (CTFs) and zeolitic imidazolic frameworks (ZIFs) are scarcely explored because of CTF's ordered structure and toxic superacid that dissolves or destabilizes the metal nodes. To solve this problem, herein, we report a straightforward two‐step pathway for the covalent hybridization of disordered CTF (d–CTF)–ZIF composites via preincorporation of an imidazole (IM) linker into ordered CTFs, followed by the imidazole‐site‐specific covalent growth of ZIFs. Direct carbonization of these synthesized d–CTF−IM−ZIF hybrids results in unique hollow carbon super‐heterostructures with ultrahigh nitrogen content (>18.6%), high specific surface area (1663 m2 g−1), and beneficial trace metal (Co/Zn NPs) contents for promoting the redox pseudocapacitance. As proof of concept, the obtained carbon super‐heterostructure (Co–Zn–NCSNH–800) is used as a positive electrode in an asymmetric supercapacitor, demonstrating a remarkable energy density of 61 Wh kg−1 and extraordinary cyclic stability of 97% retention after 30,000 cycles at the cell level. Our presynthetic modifications of CTF and their covalent hybridization with ZIF crystals pave the way toward new design strategies for synthesizing functional porous carbon materials for promising energy applications.https://doi.org/10.1002/cey2.344asymmetric supercapacitordefective covalent triazine frameworkshollow carbon super‐heterostructureslinker defect
spellingShingle Madagonda M. Vadiyar
Ji‐Young Kim
Jee‐Hwan Bae
Kyung‐Wan Nam
Imidazole linker‐induced covalent triazine framework–ZIF hybrids for confined hollow carbon super‐heterostructures toward a long‐life supercapacitor
Carbon Energy
asymmetric supercapacitor
defective covalent triazine frameworks
hollow carbon super‐heterostructures
linker defect
title Imidazole linker‐induced covalent triazine framework–ZIF hybrids for confined hollow carbon super‐heterostructures toward a long‐life supercapacitor
title_full Imidazole linker‐induced covalent triazine framework–ZIF hybrids for confined hollow carbon super‐heterostructures toward a long‐life supercapacitor
title_fullStr Imidazole linker‐induced covalent triazine framework–ZIF hybrids for confined hollow carbon super‐heterostructures toward a long‐life supercapacitor
title_full_unstemmed Imidazole linker‐induced covalent triazine framework–ZIF hybrids for confined hollow carbon super‐heterostructures toward a long‐life supercapacitor
title_short Imidazole linker‐induced covalent triazine framework–ZIF hybrids for confined hollow carbon super‐heterostructures toward a long‐life supercapacitor
title_sort imidazole linker induced covalent triazine framework zif hybrids for confined hollow carbon super heterostructures toward a long life supercapacitor
topic asymmetric supercapacitor
defective covalent triazine frameworks
hollow carbon super‐heterostructures
linker defect
url https://doi.org/10.1002/cey2.344
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