2012
DOI: 10.1007/s10008-012-1850-0
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Supercapacitors based on carbide-derived carbons synthesised using HCl and Cl2 as reactants

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Cited by 49 publications
(82 citation statements)
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“…Yushin and coworkers [11] established that the mesopores in SiC-CDC allowed for a greatly increased specific surface area up to 2430 m 2 g À1 and peaking specific capacitance 170 F g À1 , in aqueous electrolytes, thus nearly doubling the previously reported values [12]. Simon and coworkers showed that evaluation of the ordered mesoporous SiC-CDC as an electrode material for supercapacitors terminates as respectable gravimetric capacitance 80 F g À1 in non-aqueous electrolyte, nearly 40 F g À1 lower than that established for TiC-CDC or Mo 2 C-CDC based supercapacitors [5,9,[14][15][16]. High capacity retention (up to 1 V s À1 ) at high cyclation rate has been demonstrated compared to other high specific surface area porous carbons, explained by the quick mass-transfer processes in mesopores and bigger micropores [5,9,[14][15][16].…”
Section: Introductionmentioning
confidence: 67%
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“…Yushin and coworkers [11] established that the mesopores in SiC-CDC allowed for a greatly increased specific surface area up to 2430 m 2 g À1 and peaking specific capacitance 170 F g À1 , in aqueous electrolytes, thus nearly doubling the previously reported values [12]. Simon and coworkers showed that evaluation of the ordered mesoporous SiC-CDC as an electrode material for supercapacitors terminates as respectable gravimetric capacitance 80 F g À1 in non-aqueous electrolyte, nearly 40 F g À1 lower than that established for TiC-CDC or Mo 2 C-CDC based supercapacitors [5,9,[14][15][16]. High capacity retention (up to 1 V s À1 ) at high cyclation rate has been demonstrated compared to other high specific surface area porous carbons, explained by the quick mass-transfer processes in mesopores and bigger micropores [5,9,[14][15][16].…”
Section: Introductionmentioning
confidence: 67%
“…Simon and coworkers showed that evaluation of the ordered mesoporous SiC-CDC as an electrode material for supercapacitors terminates as respectable gravimetric capacitance 80 F g À1 in non-aqueous electrolyte, nearly 40 F g À1 lower than that established for TiC-CDC or Mo 2 C-CDC based supercapacitors [5,9,[14][15][16]. High capacity retention (up to 1 V s À1 ) at high cyclation rate has been demonstrated compared to other high specific surface area porous carbons, explained by the quick mass-transfer processes in mesopores and bigger micropores [5,9,[14][15][16]. Systematic analysis of electrochemical impedance data showed a low intrinsic resistance of CDC based systems, high ion accessibility to the microporous-mesoporous hierarchical structure, and thus a remarkably low relaxation time of the system, evidencing that the use of such hierarchical porous carbons for high power supercapacitors is very promising [5,8,[13][14][15][16].…”
Section: Introductionmentioning
confidence: 97%
“…After drying under vacuum, the pure Al layer (2 μm) was deposited onto one side of the CDC by the magnetron sputtering method. [19][20][21] The electrolyte used was prepared from pure acetonitrile (AN, H 2 O <20 ppm), and from dry (C 2 H 5 ) 3 CH 3 NBF 4 (Stella Chemifa). The two-electrode standard Al test cell (HS Test Cell, Hohsen Corporation) with two identical electrodes (geometric area of about 2.0 cm 2 ) was completed inside a glove box (Labmaster sp, MBraun; O 2 and H 2 O concentrations lower than 0.1 ppm) and all electrochemical experiments were carried out at temperature T = 20…”
mentioning
confidence: 99%
“…The specific surface area, micropore surface area (S micro ), micropore volume (V micro ) and total pore volume (V tot ) and other parameters for porous carbon materials were calculated according to the Brunauer-Emmett-Teller and t-plot method. The pore size distribution was determined using non local density functional theory assuming a slit-shaped pores model [7][8][9]13,16]. …”
Section: Physical Characterizationmentioning
confidence: 99%
“…In the present work, activated carbons (ACs) were synthesised from D-glucose by using HTC method followed by pyrolysis and activation with carbon dioxide at 900 °C with different activation step lengths to prepare carbon materials with variable specific surface area, pore size distribution and optimal ratio of micro-and mesopores for supercapacitor application [5][6][7][8][9][10][11][12][13][14][15][16]. Synthesised carbon materials were noted as GDAC (glucose derived activated carbon).…”
Section: Introductionmentioning
confidence: 99%