<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Tordi P</submitter><funding>Interdisciplinary Thematic Institute SysChem</funding><funding>Italian Ministry of Research</funding><funding>Department of Chemistry "Ugo Schiff", University of Florence, Italy</funding><funding>European Union</funding><funding>National Recovery and Resilience Plan</funding><funding>Institut Universitaire de France</funding><funding>CSGI (Consorzio Interuniversitario per lo Sviluppo dei Sistemi a Grande Interfase)</funding><funding>European Commission</funding><funding>NextGenerationEU</funding><pagination>e2503937</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12372438</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>21(33)</volume><pubmed_abstract>The development of sustainable, high-performance gel polymer electrolytes (GPEs) is crucial for next-generation energy storage; however, existing materials often exhibit limited mechanical stability, suboptimal ionic transport, or environmental drawbacks. Here, for the first time gelatin-alginate organohydrogels  crosslinked with Cu&lt;sup>2+&lt;/sup> and Mn&lt;sup>2+&lt;/sup> are used as GPEs for supercapacitors, in combination with Li&lt;sup>+&lt;/sup> incorporation to enhance ionic conductivity and transport. Small-Angle X-ray Scattering (SAXS) reveals that the choice of the crosslinking cation governs the nanoscale organization of the polymer network-reflected in distinct correlation lengths-which in turn critically influences ionic transport, mechanical stability, and electrochemical performance. Cu&lt;sup>2+&lt;/sup>-crosslinked gels achieve the highest areal capacitance (591.8 mF cm&lt;sup>-2&lt;/sup>), energy density (82.2 µWh cm&lt;sup>-2&lt;/sup>), and power density (1957.8 µW cm&lt;sup>-2&lt;/sup>), whereas Mn&lt;sup>2+&lt;/sup>-crosslinked gels exhibit superior cycling stability (88.3% retention over 5000 cycles). Li&lt;sup>+&lt;/sup> incorporation increases the mechanical flexibility of Mn-based gels-reducing the compressive modulus by over 60%-enhancing ion mobility and charge storage. Conversely, Cu-based gels maintain structural integrity while exhibiting improved conductivity. These findings demonstrate how biopolymer-based GPEs, designed through nanoscale engineering and ion doping, achieve an optimal balance of mechanical robustness and electrochemical performance. By combining scalability and exceptional energy storage capabilities, these materials establish a new paradigm for flexible supercapacitors and sustainable energy technologies.</pubmed_abstract><journal>Small (Weinheim an der Bergstrasse, Germany)</journal><pubmed_title>Ionically Tunable Gel Electrolytes Based on Gelatin-Alginate Biopolymers for High-Performance Supercapacitors.</pubmed_title><pmcid>PMC12372438</pmcid><funding_grant_id>ANR-10-IDEX-0002</funding_grant_id><funding_grant_id>ProgettoDipartimentidiEccellenza2023-2027</funding_grant_id><funding_grant_id>B83C22004890007</funding_grant_id><pubmed_authors>Ciesielski A</pubmed_authors><pubmed_authors>Montes-Garcia V</pubmed_authors><pubmed_authors>Bonini M</pubmed_authors><pubmed_authors>Tordi P</pubmed_authors><pubmed_authors>Tamayo A</pubmed_authors><pubmed_authors>Samori P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Ionically Tunable Gel Electrolytes Based on Gelatin-Alginate Biopolymers for High-Performance Supercapacitors.</name><description>The development of sustainable, high-performance gel polymer electrolytes (GPEs) is crucial for next-generation energy storage; however, existing materials often exhibit limited mechanical stability, suboptimal ionic transport, or environmental drawbacks. Here, for the first time gelatin-alginate organohydrogels  crosslinked with Cu&lt;sup>2+&lt;/sup> and Mn&lt;sup>2+&lt;/sup> are used as GPEs for supercapacitors, in combination with Li&lt;sup>+&lt;/sup> incorporation to enhance ionic conductivity and transport. Small-Angle X-ray Scattering (SAXS) reveals that the choice of the crosslinking cation governs the nanoscale organization of the polymer network-reflected in distinct correlation lengths-which in turn critically influences ionic transport, mechanical stability, and electrochemical performance. Cu&lt;sup>2+&lt;/sup>-crosslinked gels achieve the highest areal capacitance (591.8 mF cm&lt;sup>-2&lt;/sup>), energy density (82.2 µWh cm&lt;sup>-2&lt;/sup>), and power density (1957.8 µW cm&lt;sup>-2&lt;/sup>), whereas Mn&lt;sup>2+&lt;/sup>-crosslinked gels exhibit superior cycling stability (88.3% retention over 5000 cycles). Li&lt;sup>+&lt;/sup> incorporation increases the mechanical flexibility of Mn-based gels-reducing the compressive modulus by over 60%-enhancing ion mobility and charge storage. Conversely, Cu-based gels maintain structural integrity while exhibiting improved conductivity. These findings demonstrate how biopolymer-based GPEs, designed through nanoscale engineering and ion doping, achieve an optimal balance of mechanical robustness and electrochemical performance. By combining scalability and exceptional energy storage capabilities, these materials establish a new paradigm for flexible supercapacitors and sustainable energy technologies.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Aug</publication><modification>2026-05-08T06:53:45.671Z</modification><creation>2026-04-07T23:31:30.646Z</creation></dates><accession>S-EPMC12372438</accession><cross_references><pubmed>40528667</pubmed><doi>10.1002/smll.202503937</doi></cross_references></HashMap>