Coexistence of Redox‐Active Metal and Ligand Sites in Copper‐Based Two‐Dimensional Conjugated Metal–Organic Frameworks as Active Materials for Battery‐Supercapacitor Hybrid Systems

Two-dimensional (2D) conjugated metal-organic frameworks (c-MOFs) are promising materials for supercapacitor (SC) electrodes due to their high electrochemically accessible surface area coupled with superior electrical conductivity compared to traditional MOFs. In this work, porous and non-porous HHB-Cu (HHB=hexahydroxybenzene), derived through surfactant-assisted synthesis are studied as representative 2D c-MOF models with different characteristics, showing diverse reversible redox reactions with Na<sup>+</sup> and Li<sup>+</sup> in aqueous (10 M NaNO<sub>3</sub>) and organic (1.0 M LiPF<sub>6</sub> in ethylene carbonate and dimethyl carbonate) electrolytes, respectively. These redox activities were here deployed to design negative electrodes for hybrid SCs (HSCs), combining the battery-like property of HHB-Cu at the negative electrode and the high capacitance and robust cyclic stability of activated carbon (AC) at the positive electrodes. In the organic electrolyte, porous HHB-Cu-based HSC achieves a maximum cell specific capacity (C<sub>s</sub>) of 22.1 mAh g<sup>-1</sup> at 0.1 A g<sup>-1</sup>, specific energy (Es) of 15.55 Wh kg<sup>-1</sup> at specific power (Ps) of 70.49 W kg<sup>-1</sup>, and 77 % cyclic stability after 3000 gravimetric charge-discharge (GCD) cycles at 1 A g<sup>-1</sup> (specific metrics calculated on the mass of both electrode materials). In the aqueous electrolyte, porous HHB-Cu-based HSC displays a C<sub>s</sub> of 13.9 mAh g<sup>-1</sup> at 0.1 A g<sup>-1</sup>, Es of 6.13 Wh kg<sup>-1</sup> at 44.05 W kg<sup>-1</sup>, and 72.3 % C<sub>s</sub> retention after 3000 GCD cycles. The non-porous sample, interesting for its superior electrical conductivity despite its limited surface area compared to its porous counterpart, shows lower Es performance but better rate capability compared to the porous one. This study indicates the potential of assembling a battery-SC hybrid system by rationally exploiting the battery-like behavior of 2D c-MOFs and the electrochemical double-layer capacitance of AC.

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Publication Details

Journal
ChemSusChem
Published
2024-09-20
DOI
https://doi.org/10.1002/cssc.202401454
Citations
3
Primary Topic
Supercapacitor Materials and Fabrication
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article
Field-Weighted Citation Impact
0.35

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article

Coexistence of Redox‐Active Metal and Ligand Sites in Copper‐Based Two‐Dimensional Conjugated Metal–Organic Frameworks as Active Materials for Battery‐Supercapacitor Hybrid Systems

Valentina Mastronardi, Sebastiano Bellani, Minghao Yu, Ahiud Morag et al.
3 citations
ChemSusChem
Supercapacitor Materials and Fabrication
0.35
article

Coexistence of Redox‐Active Metal and Ligand Sites in Copper‐Based Two‐Dimensional Conjugated Metal–Organic Frameworks as Active Materials for Battery‐Supercapacitor Hybrid Systems

Valentina Mastronardi, Sebastiano Bellani, Minghao Yu, Ahiud Morag, Francesco Bonaccorso, Sanjay Thorat, Marilena Isabella Zappia, Renhao Dong⧫, Samaneh Vaez, Lea Pasquale, Hossein Beydaghi, Jaya‐Kumar Panda, Agnese Gamberini, Matteo Abruzzese, Xinliang Feng, Zhiyong Wang, Ahmad Bagheri
article en
3 citations

Abstract

Two-dimensional (2D) conjugated metal-organic frameworks (c-MOFs) are promising materials for supercapacitor (SC) electrodes due to their high electrochemically accessible surface area coupled with superior electrical conductivity compared to traditional MOFs. In this work, porous and non-porous HHB-Cu (HHB=hexahydroxybenzene), derived through surfactant-assisted synthesis are studied as representative 2D c-MOF models with different characteristics, showing diverse reversible redox reactions with Na<sup>+</sup> and Li<sup>+</sup> in aqueous (10 M NaNO<sub>3</sub>) and organic (1.0 M LiPF<sub>6</sub> in ethylene carbonate and dimethyl carbonate) electrolytes, respectively. These redox activities were here deployed to design negative electrodes for hybrid SCs (HSCs), combining the battery-like property of HHB-Cu at the negative electrode and the high capacitance and robust cyclic stability of activated carbon (AC) at the positive electrodes. In the organic electrolyte, porous HHB-Cu-based HSC achieves a maximum cell specific capacity (C<sub>s</sub>) of 22.1 mAh g<sup>-1</sup> at 0.1 A g<sup>-1</sup>, specific energy (Es) of 15.55 Wh kg<sup>-1</sup> at specific power (Ps) of 70.49 W kg<sup>-1</sup>, and 77 % cyclic stability after 3000 gravimetric charge-discharge (GCD) cycles at 1 A g<sup>-1</sup> (specific metrics calculated on the mass of both electrode materials). In the aqueous electrolyte, porous HHB-Cu-based HSC displays a C<sub>s</sub> of 13.9 mAh g<sup>-1</sup> at 0.1 A g<sup>-1</sup>, Es of 6.13 Wh kg<sup>-1</sup> at 44.05 W kg<sup>-1</sup>, and 72.3 % C<sub>s</sub> retention after 3000 GCD cycles. The non-porous sample, interesting for its superior electrical conductivity despite its limited surface area compared to its porous counterpart, shows lower Es performance but better rate capability compared to the porous one. This study indicates the potential of assembling a battery-SC hybrid system by rationally exploiting the battery-like behavior of 2D c-MOFs and the electrochemical double-layer capacitance of AC.

ChemSusChemVol. 18(4)
Politecnico di Torino (IT), Italian Institute of Technology (IT), BeDimensional (Italy) (IT), Max Planck Institute of Microstructure Physics (DE), Institut de Recherche et d’Innovation (FR), Technische Universität Dresden (DE), University of Hong Kong (HK)
European Commission, Istituto Italiano di Tecnologia, HORIZON EUROPE Framework Programme
Openalex Percentile: Top 51%
Supercapacitor Materials and Fabrication
0.35
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