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1.
ACS Omega ; 3(8): 9246-9255, 2018 Aug 31.
Artículo en Inglés | MEDLINE | ID: mdl-30197998

RESUMEN

Using reduced graphene oxide (r-GO) as a multifunctional conductive binder, a simple, cost-effective, and environmentally friendly approach is developed to fabricate activated carbon/reduced graphene oxide (AC/r-GO) composite electrodes for supercapacitors with outstanding performance. In such a composite, r-GO provides several much needed critical functions: r-GO not only serves as the binder material improving the AC particle/particle cohesion and electrode-film/substrate adhesion but also improves the electrical conductivity of the composite and provides additional surfaces for ion adsorption. Furthermore, during electrode fabrication, initial GO precursor functions as an effective dispersant for AC, resulting in a stable electrode material slurry. Employing characterization by advanced microscopy techniques, we show that AC and r-GO assemble into an interconnected network structure, resulting in a composite with high specific capacitance, excellent rate capability, and long cycling life stability. Such high-performance electrodes coupled with their relatively simple, scalable, and low-cost fabrication process thereby provide a clear pathway toward large-scale implementation of supercapacitors.

2.
ACS Nano ; 10(1): 747-54, 2016 Jan 26.
Artículo en Inglés | MEDLINE | ID: mdl-26714196

RESUMEN

The contribution of subnanometer pores in carbon electrodes to the charge-storage mechanism in supercapacitors has been the subject of intense debate for over a decade. Here, we provide a model system based on graphene oxide, which employs interlayer constrictions as a model for pore sizes that can be both controllably tuned and studied in situ during supercapacitor device use. Correlating electrochemical performance and in situ tuning of interlayer constrictions, we observe a peak in specific capacitance when interlayer constriction size reaches the diameters of unsolvated ions, supporting the hypothesized link between loss of ion solvation shell and anomalous capacitance increase for subnanometer pores.

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