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http://www.alice.cnptia.embrapa.br/alice/handle/doc/1176126
Title: | Ti3C2Tx MXene/alginate‑based electrodes for supercapacitors. |
Authors: | FOTIUS, J. A. A.![]() ![]() FACURE, M. H. M. ![]() ![]() CORREA, D. S. ![]() ![]() CARRILHO, E. ![]() ![]() BARUD, H. da S. ![]() ![]() OLIVEIRA, H. P. de ![]() ![]() |
Affiliation: | UNIVERSIDADE 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. |
Date Issued: | 2025 |
Citation: | Journal of Materials Research, 2025. |
Pages: | 16 p. |
Description: | The 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. |
Keywords: | Sustainable energy Faradaic processes Hybrid supercapacitors |
DOI: | 10.1557/s43578-025-01588-6 |
Type of Material: | Artigo de periódico |
Access: | openAccess |
Appears in Collections: | Artigo em periódico indexado (CNPDIA)![]() ![]() |
Files in This Item:
File | Description | Size | Format | |
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P-Ti3C2Tx-MXene-alginatebased-electrodes.pdf | 3.22 MB | Adobe PDF | ![]() View/Open |