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dc.contributor.authorFOTIUS, J. A. A.
dc.contributor.authorFACURE, M. H. M.
dc.contributor.authorCORREA, D. S.
dc.contributor.authorCARRILHO, E.
dc.contributor.authorBARUD, H. da S.
dc.contributor.authorOLIVEIRA, H. P. de
dc.date.accessioned2025-05-28T19:53:47Z-
dc.date.available2025-05-28T19:53:47Z-
dc.date.created2025-05-28
dc.date.issued2025
dc.identifier.citationJournal of Materials Research, 2025.
dc.identifier.urihttp://www.alice.cnptia.embrapa.br/alice/handle/doc/1176126-
dc.descriptionThe promising application of MXenes in energy storage-based solutions is seriously afected by stacking processes that reduce available active sites for charge accumulation. Incorporating MXene into biopolymer templates represents a promising strategy to avoid aggregation of active electrochemical compounds, resulting in the optimization of the specifc capacitance and energy/power density. Herein, the production of Ti3C2Tx/alginate composites is explored as a part of a strategy to reduce the aggregation degree in MXene while preserving the electrical output performance of the overall electrode. By efectively incorporating MXene into sodium alginate-based electrodes, the energy density and power density of a 2-electrode device were 10.2 Wh kg–1 and 1724.1 W kg–1, respectively. This paper highlights a competitive device prototype with a reduced MXene content compared to a pure MXene electrode, signifcantly lowering the final cost of the resulting supercapacitor due to the lower density of the active electrochemical fller.
dc.language.isoeng
dc.rightsopenAccess
dc.subjectSustainable energy
dc.subjectFaradaic processes
dc.subjectHybrid supercapacitors
dc.titleTi3C2Tx MXene/alginate‑based electrodes for supercapacitors.
dc.typeArtigo de periódico
dc.format.extent216 p.
riaa.ainfo.id1176126
riaa.ainfo.lastupdate2025-05-28
dc.identifier.doi10.1557/s43578-025-01588-6
dc.contributor.institutionUNIVERSIDADE FEDERAL DO VALE DO SÃO FRANCISCO; UNIVERSIDADE DE SÃO PAULO; DANIEL SOUZA CORREA, CNPDIA; UNIVERSIDADE DE SÃO PAULO; UNIVERSITY OF ARARAQUARA; UNIVERSIDADE FEDERAL DO VALE DO SÃO FRANCISCO.
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