2018
DOI: 10.1007/s10854-018-9039-7
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Enhanced electrochemical performances of heteroatom-enriched carbon with hierarchical pores prepared by trehalose as a pore-forming agent and a simple one-step carbonization/activation process for supercapacitors

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Cited by 9 publications
(9 citation statements)
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“…HDC 2 delivers an energy density of 8.4 Wh kg À1 at a power density of 150 W kg À1 and retains an energy density of 7 Wh kg À1 at a high power density of 6000 W kg À1 , higher than other HDCs in this work and many previously reported carbonbased supercapacitors. [24,[33][34][35][36][37][38][39]…”
Section: Electrochemical Performancementioning
confidence: 99%
“…HDC 2 delivers an energy density of 8.4 Wh kg À1 at a power density of 150 W kg À1 and retains an energy density of 7 Wh kg À1 at a high power density of 6000 W kg À1 , higher than other HDCs in this work and many previously reported carbonbased supercapacitors. [24,[33][34][35][36][37][38][39]…”
Section: Electrochemical Performancementioning
confidence: 99%
“…For example, the presence of boron 3 , nitrogen 4 , phosphorus 5 , or sulfur 6 can confer acid/alkali properties to carbon materials and improve the Faraday interaction between electrolyte ions and functional groups, thereby increasing the specific capacitance through the pseudo capacitance effect. 7 Among the various heteroatoms, the presence of nitrogen and oxygen atoms can not only enhance the surface tension, wettability, and hydrophilicity of the electrode, but also elevate the inhomogeneity arising from moderate structural defects. In addition, the electron donor characteristics of the carbon matrix can also be optimized.…”
Section: Introductionmentioning
confidence: 99%
“…34−37 Inspired by the phenomenon of the well-known cation ion intercalation of graphite cathodes in potassium-ion batteries, 38−40 we believe that increasing interplanar spacings of the carbon layers is a smart route to exploit adequately the active sites inside the catalysts because the wider spacings make it easier for oxygen molecules to travel through the interior of the carbon layers. 28,29 In this way, special structural trehalose with an underlying layered structure seems to be the ideal carbon source for Fe−N−C due to its broad interplanar spacings after carbonization, 41 by a raid of abundant pores for dispersing of Fe ions in it. 42,43 Herein, using trehalose as structure forming template, a novel candied haws-like Fe−N−C catalyst (CH-FeNC), composed of trehalose, PANI, and ZIF8 precursors, was fabricated first by a two-step synthesis strategy via raw material morphology and structure design and controllable pyrolysis carbonization.…”
Section: Introductionmentioning
confidence: 99%