Improving the performance of an anionic MOF by counter cation replacement as electrode material in a full cell setup of a potassium ion capacitor.


Journal

RSC advances
ISSN: 2046-2069
Titre abrégé: RSC Adv
Pays: England
ID NLM: 101581657

Informations de publication

Date de publication:
17 Apr 2023
Historique:
received: 16 03 2023
accepted: 12 04 2023
medline: 24 4 2023
pubmed: 24 4 2023
entrez: 24 04 2023
Statut: epublish

Résumé

Potassium-based energy storage devices are attracting increasing attention as an alternative to lithium and sodium systems. In addition, metal-organic frameworks (MOFs) can be considered as promising electrode materials for this type of device due to their advantageous properties. Herein, the anionic MOF JUMP-1 and its analog with pre-loading of potassium cations, namely JUMP-1(K), were synthesized and characterized. The anionic framework of JUMP-1 is found to be extremely stable towards the exchange of the dimethylammonium cations by potassium ions. These MOFs were tested in composite electrodes in combination with conventional organic electrolytes as anode materials in a potassium-based system, including the full cell assembly of a potassium ion capacitor (KIC). The results show the significant improvement in capacity between the pristine JUMP-1 and the potassium-exchanged analog JUMP-1(K) as electrode materials. KICs containing JUMP-1(K) coupled with activated carbon (AC) display a promising stability over 4000 cycles. According to the results from these studies, the composite MOF electrode with the potassium-exchange analog JUMP-1(K) presents a promising approach, for which the electrochemical performance compared to the pristine anionic MOF is significantly enhanced.

Identifiants

pubmed: 37091608
doi: 10.1039/d3ra01746j
pii: d3ra01746j
pmc: PMC10113920
doi:

Types de publication

Journal Article

Langues

eng

Pagination

12277-12284

Informations de copyright

This journal is © The Royal Society of Chemistry.

Déclaration de conflit d'intérêts

There are no conflicts to declare.

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Auteurs

Chalita Aphirakaramwong (C)

Institut für Technische Chemie und Umweltchemie, Friedrich-Schiller-Universität Jena Jena Germany andrea.balducci@uni-jena.de.
Center of Excellence for Energy Storage Technology (CEST), Department of Chemical and Biomolecular Engineering, School of Energy Science and Engineering, Vidyasirimedhi Institute of Science and Technology Rayong 21210 Thailand.

Oluseun Akintola (O)

Institut für Anorganische und Analytische Chemie, Friedrich-Schiller-Universität Jena Jena Germany sekr.plass@uni-jena.de.

Christian T Plass (CT)

Institut für Festkörperphysik, Friedrich-Schiller-Universität Jena Jena Germany.

Montree Sawangphruk (M)

Center of Excellence for Energy Storage Technology (CEST), Department of Chemical and Biomolecular Engineering, School of Energy Science and Engineering, Vidyasirimedhi Institute of Science and Technology Rayong 21210 Thailand.

Winfried Plass (W)

Institut für Anorganische und Analytische Chemie, Friedrich-Schiller-Universität Jena Jena Germany sekr.plass@uni-jena.de.

Andrea Balducci (A)

Institut für Technische Chemie und Umweltchemie, Friedrich-Schiller-Universität Jena Jena Germany andrea.balducci@uni-jena.de.
Center for Energy and Environmental Chemistry Jena (CEEC Jena) Jena Germany.

Classifications MeSH