Sub-nanopores enabling optimized ion storage performance of carbon cathodes for Zn-ion hybrid supercapacitors

[Display omitted] •Sub-nanopores are verified to be capable of promoting the desolvation of [Zn(H2O)6]2 + to optimize the ion storage performance of the carbon cathodes in ZHSs.•A new strategy is proposed to study the dehydration behaviors of [Zn(H2O)6]2 + in carbon cathodes.•Superior electrochemica...

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Veröffentlicht in:Journal of colloid and interface science 2024-09, Vol.669, p.766-774
Hauptverfasser: Kang, Fulian, Li, Yang, Zheng, Zhiyuan, Peng, Xinya, Rong, Jianhua, Dong, Liubing
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Sprache:eng
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Zusammenfassung:[Display omitted] •Sub-nanopores are verified to be capable of promoting the desolvation of [Zn(H2O)6]2 + to optimize the ion storage performance of the carbon cathodes in ZHSs.•A new strategy is proposed to study the dehydration behaviors of [Zn(H2O)6]2 + in carbon cathodes.•Superior electrochemical performance especially exceptional fast charge/discharge ability is realized for carbon cathodes of ZHSs. Aqueous Zn-ion hybrid supercapacitors (ZHSs) are attracting significant attention as a promising electrochemical energy storage system. However, carbon cathodes of ZHSs exhibit unsatisfactory ion storage performance due to the large size of hydrated Zn-ions (e.g., [Zn(H2O)6]2+), which encumbers compact ion arrangement and rapid ion transport at the carbon-electrolyte interfaces. Herein, a porous carbon material (HMFC) with abundant sub-nanopores is synthesized to optimize the ion storage performance of the carbon cathode in ZHSs, in which the sub-nanopores effectively promote the dehydration of hydrated Zn-ions and thus optimize the ion storage performance of the carbon cathode in ZHSs. A novel strategy is proposed to study the dehydration behaviors of hydrated Zn-ions in carbon cathodes, including quantitatively determining the desolvation activation energy of hydrated Zn-ions and in-situ monitoring active water content at the carbon-electrolyte interface. The sub-nanopores-induced desolvation effect is verified, and its coupling with large specific surface area and hierarchically porous structure endows the HMFC cathode with improved electrochemical performance, including a 53 % capacity increase compared to the carbon cathode counterpart without sub-nanopores, fast charge/discharge ability that can output 46.0 Wh/kg energy within only 4.4 s, and 98.2 % capacity retention over 20,000 charge/discharge cycles. This work provides new insights into the rational design of porous carbon cathode materials toward high-performance ZHSs.
ISSN:0021-9797
1095-7103
DOI:10.1016/j.jcis.2024.05.048