<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>21(36)</volume><submitter>Li H</submitter><pubmed_abstract>The exploration of innovative and high-efficiency energy storage materials is crucial for advancing high-performance supercapacitors. In this study, a novel composite material is synthesized, comprising multilayered MXene (Ti&lt;sub>3&lt;/sub>C&lt;sub>2&lt;/sub>T&lt;sub>x&lt;/sub>) nanoparticles integrated with porous NiCo&lt;sub>2&lt;/sub>Se&lt;sub>4&lt;/sub> nanosheets. The accordion-like nanostructure of MXene and its strong interfacial interactions enhance the surface area and cycling stability of the nanocomposite. Additionally, substituting selenium (Se) for Ni-Co-based hydroxides modulates orbital hybridization with the corresponding metal cations, significantly improving electrochemical activity and reducing the adsorption/desorption energy barrier for electrolyte ions. The synergistic interaction between these two materials enabled the composite electrode to achieve a high specific capacity of 796.25 C g&lt;sup>-1&lt;/sup> at 1 A g&lt;sup>-1&lt;/sup> while maintaining over 90% of its initial capacity after 8000 cycles. Furthermore, the as-fabricated asymmetric hybrid capacitor, employing activated carbon as the negative electrode, delivered an energy density of 64.36 Wh kg&lt;sup>-1&lt;/sup> at a power density of 0.8 kW kg&lt;sup>-1&lt;/sup>, surpassing the performance of most previously reported hybrid capacitors. The developed composite structure holds significant potential for integration into various electrochemical devices, such as batteries, sensors, and electrolyzers.</pubmed_abstract><journal>Small (Weinheim an der Bergstrasse, Germany)</journal><pagination>e04350</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12423915</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Selenized Binary Transition Metals-MXene Composite for High-Performance Asymmetric Hybrid Capacitors.</pubmed_title><pmcid>PMC12423915</pmcid><pubmed_authors>Li H</pubmed_authors><pubmed_authors>Kalaiyarasan G</pubmed_authors><pubmed_authors>Cao X</pubmed_authors><pubmed_authors>Kim W</pubmed_authors><pubmed_authors>Koo B</pubmed_authors><pubmed_authors>Ko MJ</pubmed_authors><pubmed_authors>Ali M</pubmed_authors><pubmed_authors>Lee D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Selenized Binary Transition Metals-MXene Composite for High-Performance Asymmetric Hybrid Capacitors.</name><description>The exploration of innovative and high-efficiency energy storage materials is crucial for advancing high-performance supercapacitors. In this study, a novel composite material is synthesized, comprising multilayered MXene (Ti&lt;sub>3&lt;/sub>C&lt;sub>2&lt;/sub>T&lt;sub>x&lt;/sub>) nanoparticles integrated with porous NiCo&lt;sub>2&lt;/sub>Se&lt;sub>4&lt;/sub> nanosheets. The accordion-like nanostructure of MXene and its strong interfacial interactions enhance the surface area and cycling stability of the nanocomposite. Additionally, substituting selenium (Se) for Ni-Co-based hydroxides modulates orbital hybridization with the corresponding metal cations, significantly improving electrochemical activity and reducing the adsorption/desorption energy barrier for electrolyte ions. The synergistic interaction between these two materials enabled the composite electrode to achieve a high specific capacity of 796.25 C g&lt;sup>-1&lt;/sup> at 1 A g&lt;sup>-1&lt;/sup> while maintaining over 90% of its initial capacity after 8000 cycles. Furthermore, the as-fabricated asymmetric hybrid capacitor, employing activated carbon as the negative electrode, delivered an energy density of 64.36 Wh kg&lt;sup>-1&lt;/sup> at a power density of 0.8 kW kg&lt;sup>-1&lt;/sup>, surpassing the performance of most previously reported hybrid capacitors. The developed composite structure holds significant potential for integration into various electrochemical devices, such as batteries, sensors, and electrolyzers.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-06-03T02:28:34.257Z</modification><creation>2026-04-23T03:10:02.026Z</creation></dates><accession>S-EPMC12423915</accession><cross_references><pubmed>40697043</pubmed><doi>10.1002/smll.202504350</doi></cross_references></HashMap>