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<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.1039/D4TA07393B</dc:identifier><dc:language>eng</dc:language><dc:creator>Alvira, Darío</dc:creator><dc:creator>Antorán, Daniel</dc:creator><dc:creator>Darjazi, Hamideh</dc:creator><dc:creator>Elia, Giuseppe Antonio</dc:creator><dc:creator>Gerbaldi, Claudio</dc:creator><dc:creator>Sebastian, Victor</dc:creator><dc:creator>Manyà, Joan J.</dc:creator><dc:title>High performing and sustainable hard carbons for Na-ion batteries through acid-catalysed hydrothermal carbonisation of vine shoots</dc:title><dc:identifier>ART-2024-142566</dc:identifier><dc:description>This study investigates the synthesis of hard carbons via acid-assisted hydrothermal carbonisation (HTC) of vine shoots, followed by thermal annealing, to be used as Na-ion battery anodes. Various carbons with diverse pore structures, ordering degrees, 2D morphologies, and chemical compositions are obtained using 2 mol dm-3 solutions of HNO3, HCl, H2SO4, or H3PO4 as the hydrothermal media. Compared to standard ester-based liquid electrolytes, the use of a diglyme-based electrolyte (NaPF6/DGM) substantially boosts both the initial coulombic efficiency (ICE) and the specific capacity, particularly evident with the highly ordered and porous H3PO4-1000 and HCl-1000 carbons. These materials exhibit outstanding performance, storing 200 mAh g-1 at 2 A g-1 and showing ICE values of 68% and 77%, respectively. The improved stability and capacity are attributed to the formation of a more stable and thinner solid electrolyte interface (SEI), along with sodium storage into graphitic regions through a solvent co-intercalation reaction. While ester-based electrolytes limit hard carbon mesoporosity and require the promotion of turbostratic domains, ether-based electrolytes enable the development of more ordered and porous carbons, enhancing transport kinetics, sodium storage capacity, and electrode stability. Overall, acid-catalysed HTC offers a sustainable pathway for tailoring hard carbon based electrodes, repurposing biomass residues into valuable materials for green and low-cost energy storage applications.</dc:description><dc:date>2024</dc:date><dc:source>http://zaguan.unizar.es/record/150458</dc:source><dc:doi>10.1039/D4TA07393B</dc:doi><dc:identifier>http://zaguan.unizar.es/record/150458</dc:identifier><dc:identifier>oai:zaguan.unizar.es:150458</dc:identifier><dc:relation>info:eu-repo/grantAgreement/ES/DGA/T22-23R</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MICINN/PDC2022-133866-I00</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MICINN/PID2021-127847OB-I00</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MCINN/PID2022-137218OB-I00</dc:relation><dc:identifier.citation>Journal of Materials Chemistry A 13, 4 (2024), 2730-2741</dc:identifier.citation><dc:rights>by-nc</dc:rights><dc:rights>https://creativecommons.org/licenses/by-nc/4.0/deed.es</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

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