2006
DOI: 10.1016/j.carbon.2005.07.029
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Superior electric double layer capacitors using ordered mesoporous carbons

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Cited by 719 publications
(379 citation statements)
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“…On the other hand, 200-220 F g −1 seems to be the upper limit for this type of electrolyte [24][25][26][27][28][29][30][31][32][33]. This limit is in agreement with the expected value based on 1500-1600 m 2 g −1 as a realistic upper-bound for the specific surface area of templated mesoporous carbons (see Section 3.1).…”
Section: Specific Capacitance At Low Current Densitysupporting
confidence: 86%
See 2 more Smart Citations
“…On the other hand, 200-220 F g −1 seems to be the upper limit for this type of electrolyte [24][25][26][27][28][29][30][31][32][33]. This limit is in agreement with the expected value based on 1500-1600 m 2 g −1 as a realistic upper-bound for the specific surface area of templated mesoporous carbons (see Section 3.1).…”
Section: Specific Capacitance At Low Current Densitysupporting
confidence: 86%
“…Recently, some authors have emphasized the ability of new advanced mesoporous carbons to store large amounts of energy with faster charge propagation than that achieved by microporous carbons [23][24][25][26][27][28][29][30][31][32]. It has been reported that the former suit the size of the electrolyte ions and enhance the EDLC performance at high rate.…”
Section: Evolution Of Electrical Capacitance With Current Densitymentioning
confidence: 99%
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“…[2][3][4][5][8][9][10][11][12] Understanding the influence of different mesoporous materials (ordered or disordered arrangement) on ion diffusion behavior is fundamental to enhancing EDLC's performance. However, in the past, the diverse and uncontrollable intrinsic microporous structure of physically or chemically activated carbons has made it impossible to precisely investigate the relations between mesoporous textures and ion diffusion behavior.…”
Section: Introductionmentioning
confidence: 99%
“…Figure 2(b) shows the FE-SEM image obtained through the hydrothermal synthesis at 180 ℃ for 36 h. It can be known that the aspect ratio of the nanowire has increased by about two folds compared to the experiment implemented at 150 ℃. Further, it can be ascertained that the nanowire can be easily synthesized when the supply of sufficient heat energy is maintained [6][7][8][9][10][11]. Figure 2(c) shows the FE-SEM image obtained by finally synthesizing the LTO powders, synthesized at 150 ℃ for 36 h using the hydrothermal synthesis method, at 700 ℃ for 6 h in the box furnace.…”
Section: Resultsmentioning
confidence: 99%