Influence of Multiwalled Carbon Nanotubes as Additives in Biomass-Derived Carbons for Supercapacitor Applications

Glucose-derived carbon/carbon nanotube (CNT) hybrid materials were prepared by hydrothermal carbonization of glucose in the presence of CNTs and subsequent carbonization, physical activation, or chemical activation. The proportion of CNTs added during the hydrothermal polymerization of glucose was v...

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Detalles Bibliográficos
Autores: Rey Raap, Natalia, Enterría, Marina, Martins, José Inácio, Pereira, Manuel Fernando R, Figueiredo, José Luís
Tipo de recurso: artículo
Estado:Versión aceptada para publicación
Fecha de publicación:2019
País:España
Institución:Consejo Superior de Investigaciones Científicas (CSIC)
Repositorio:DIGITAL.CSIC. Repositorio Institucional del CSIC
OAI Identifier:oai:digital.csic.es:10261/414825
Acceso en línea:http://hdl.handle.net/10261/414825
https://api.elsevier.com/content/abstract/scopus_id/85061260475
Access Level:acceso abierto
Palabra clave:oxygen functionalities
electric double-layer capacitor
glucose-derived carbons
high porosity
hydrothermal carbons
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Descripción
Sumario:Glucose-derived carbon/carbon nanotube (CNT) hybrid materials were prepared by hydrothermal carbonization of glucose in the presence of CNTs and subsequent carbonization, physical activation, or chemical activation. The proportion of CNTs added during the hydrothermal polymerization of glucose was varied to ascertain the optimum dose to maximize the performance of the carbon hybrids in supercapacitor applications. Both the thermal treatment applied and the addition of CNTs lead to changes in the textural and chemical properties of the activated carbons. It was observed that samples bearing CNTs exhibit higher number of nucleation centers for glucose oligomers to polymerize, and consequently, the behavior of the hydrothermal carbon toward activation differs according to the activating agent employed. Moreover, the initial chemical speciation dominated by acidic groups shifts to more basic functionalities (quinones and carbonyl groups) with the addition of CNTs. The effect of the different physicochemical properties of the prepared carbons on their electrochemical behavior was evaluated. The addition of 2 wt % of CNTs and subsequent chemical activation leads to electrode materials yielding 206 F g-1 and 78% of capacitance retention up to 0.8 V and 20 A g-1 and high rate cyclability (97% after 5000 cycles). The outstanding performance is ascribed to the high surface area, narrow mesopores, and phenol/carbonyl surface functionalities, which enhance molecular diffusion, the amount of stored energy, and electronic transportation, respectively.