2017
DOI: 10.1016/j.jallcom.2017.06.231
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Facile synthesis of mesoporous carbon from furfuryl alcohol-butanol system by EISA process for supercapacitors with enhanced rate capability

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Cited by 20 publications
(20 citation statements)
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“…Both XRD and Raman results concluded that the synthesized carbon material is more of graphitic nature, which is expected to improve the charge‐transfer rate characteristics of electrode material in delivering good electrochemical performance as graphitic nature enhances the electrical conductivity of carbon material. The N 2 adsorption‐desorption isotherm in Figure 4A clearly exhibits a type IV isotherm, characteristics of mesoporous nature of the carbon material and a slight sharp raise of N 2 uptake at low relative pressure (<0.3 P/Po), reveals the presence of micropores . The specific surface area and pore volume of GPCS carbon material is around 1246 m 2 g ‐1 and 0.86 cm 3 g ‐1 , respectively.…”
Section: Resultsmentioning
confidence: 95%
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“…Both XRD and Raman results concluded that the synthesized carbon material is more of graphitic nature, which is expected to improve the charge‐transfer rate characteristics of electrode material in delivering good electrochemical performance as graphitic nature enhances the electrical conductivity of carbon material. The N 2 adsorption‐desorption isotherm in Figure 4A clearly exhibits a type IV isotherm, characteristics of mesoporous nature of the carbon material and a slight sharp raise of N 2 uptake at low relative pressure (<0.3 P/Po), reveals the presence of micropores . The specific surface area and pore volume of GPCS carbon material is around 1246 m 2 g ‐1 and 0.86 cm 3 g ‐1 , respectively.…”
Section: Resultsmentioning
confidence: 95%
“…The N 2 adsorption-desorption isotherm in Figure 4A clearly exhibits a type IV isotherm, characteristics of mesoporous nature of the carbon material and a slight sharp raise of N 2 uptake at low relative pressure (<0.3 P/Po), reveals the presence of micropores. 12,16 The specific surface area and pore volume of GPCS carbon material is around 1246 m 2 g -1 and 0.86 cm 3 g -1 , respectively. The pore size distribution of carbon is obtained by 2D-NLDFT and is presented in Figure 4B.…”
Section: Resultsmentioning
confidence: 99%
“…The degree of graphitization as well as the ordered and disordered structures of mesoporous carbon materials was characterized by Raman spectroscopy. The Raman spectra of the CMK‐8 (x) materials in Figure B exhibit two distinct broad peaks at approximately 1350 and 1590 cm −1 , corresponding to the D band (due to structural defects and partially disordered amorphous carbon) and G band (sp 2 bonded carbon‐carbon stretching), respectively . The I D /I G ratio between the intensities of the D and G bands is normally employed to estimate the degree of graphitization .…”
Section: Resultsmentioning
confidence: 99%
“…In their work Nanaji et al [151] demonstrated that utilizing FA as an alternative source of carbon precursor (for the first time) a smart, efficient and cost-effective methodology employing a modified evaporation induced self-assembly (EISA), strategy was used to synthesise mesoporous carbon (MC), which exhibited excellent textural parameters, employed in super-capacitors. They showed that the resulting carbon synthesised with the modified EISA method exhibited a higher specific surface area with large pore volume and more ordered graphitic carbon.…”
Section: Sundry Applicationsmentioning
confidence: 99%