Hierarchically structured carbon replica of hybrid layered double hydroxideElectronic supplementary information (ESI) available: 13C NMR spectra, N2 adsorption-desorption isotherm, variation of the voltammetric charge. See DOI: 10.1039/c0nj00630k
A hierarchically structured carbon replica with a tri-modal distribution of porosity was prepared by pyrolysis of a three-dimensionally ordered macroporous (3-DOM) organic-inorganic hybrid layered double hydroxide (LDH). By an original inverse opal method involving LDH platelet regeneration, macropo...
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creator | Prévot, Vanessa Géraud, Erwan Stimpfling, Thomas Ghanbaja, Jaafar Leroux, Fabrice |
description | A hierarchically structured carbon replica with a tri-modal distribution of porosity was prepared by pyrolysis of a three-dimensionally ordered macroporous (3-DOM) organic-inorganic hybrid layered double hydroxide (LDH). By an original inverse opal method involving LDH platelet regeneration, macroporous Mg
2
Al-vinyl benzene sulfonate (VBS) was synthesized and subsequently submitted to a moderate thermal treatment to induce the VBS
in situ
polymerization. Successive steps of carbonization and demineralization were conducted to yield to a carbon replica. A thermal treatment under inert atmosphere ensures the carbonization of the organic part and the simultaneous decomposition of the LDH into oxide and mixed oxide particles. The latter acts as a porogen agent during the acid-leaching step, which induces the removal of the inorganic part. The samples upon carbonization and the capacitive properties of the resulting carbon replica were thoroughly characterized using powder X-ray diffraction (PXRD), Fourier-transform infra-red (FTIR) and
13
C nuclear magnetic resonance (NMR) spectroscopy, field-emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM) and Brunauer-Emmet-Teller (BET) analysis of the nitrogen adsorption isotherm. 3-DOM carbon replicas exhibit poor capacitive behaviour in aqueous electrolyte, explained by a high ionic resistivity present in the porosity. Even though this electrical disruptive effect can be explained on the basis of the macroporosity of the disconnected carbon 3-DOM, this allows us to envisage other applications for this approach in order to obtain tri-modal carbon-based materials.
Using a template approach, a 3-DOM LDH hybrid compound intercalated with VBS monomer has been successfully prepared and used to produce a hierarchically micro/meso/macroporous carbonaceous replica. |
doi_str_mv | 10.1039/c0nj00630k |
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2
Al-vinyl benzene sulfonate (VBS) was synthesized and subsequently submitted to a moderate thermal treatment to induce the VBS
in situ
polymerization. Successive steps of carbonization and demineralization were conducted to yield to a carbon replica. A thermal treatment under inert atmosphere ensures the carbonization of the organic part and the simultaneous decomposition of the LDH into oxide and mixed oxide particles. The latter acts as a porogen agent during the acid-leaching step, which induces the removal of the inorganic part. The samples upon carbonization and the capacitive properties of the resulting carbon replica were thoroughly characterized using powder X-ray diffraction (PXRD), Fourier-transform infra-red (FTIR) and
13
C nuclear magnetic resonance (NMR) spectroscopy, field-emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM) and Brunauer-Emmet-Teller (BET) analysis of the nitrogen adsorption isotherm. 3-DOM carbon replicas exhibit poor capacitive behaviour in aqueous electrolyte, explained by a high ionic resistivity present in the porosity. Even though this electrical disruptive effect can be explained on the basis of the macroporosity of the disconnected carbon 3-DOM, this allows us to envisage other applications for this approach in order to obtain tri-modal carbon-based materials.
Using a template approach, a 3-DOM LDH hybrid compound intercalated with VBS monomer has been successfully prepared and used to produce a hierarchically micro/meso/macroporous carbonaceous replica.</description><identifier>ISSN: 1144-0546</identifier><identifier>EISSN: 1369-9261</identifier><identifier>DOI: 10.1039/c0nj00630k</identifier><language>eng</language><creationdate>2011-01</creationdate><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids></links><search><creatorcontrib>Prévot, Vanessa</creatorcontrib><creatorcontrib>Géraud, Erwan</creatorcontrib><creatorcontrib>Stimpfling, Thomas</creatorcontrib><creatorcontrib>Ghanbaja, Jaafar</creatorcontrib><creatorcontrib>Leroux, Fabrice</creatorcontrib><title>Hierarchically structured carbon replica of hybrid layered double hydroxideElectronic supplementary information (ESI) available: 13C NMR spectra, N2 adsorption-desorption isotherm, variation of the voltammetric charge. See DOI: 10.1039/c0nj00630k</title><description>A hierarchically structured carbon replica with a tri-modal distribution of porosity was prepared by pyrolysis of a three-dimensionally ordered macroporous (3-DOM) organic-inorganic hybrid layered double hydroxide (LDH). By an original inverse opal method involving LDH platelet regeneration, macroporous Mg
2
Al-vinyl benzene sulfonate (VBS) was synthesized and subsequently submitted to a moderate thermal treatment to induce the VBS
in situ
polymerization. Successive steps of carbonization and demineralization were conducted to yield to a carbon replica. A thermal treatment under inert atmosphere ensures the carbonization of the organic part and the simultaneous decomposition of the LDH into oxide and mixed oxide particles. The latter acts as a porogen agent during the acid-leaching step, which induces the removal of the inorganic part. The samples upon carbonization and the capacitive properties of the resulting carbon replica were thoroughly characterized using powder X-ray diffraction (PXRD), Fourier-transform infra-red (FTIR) and
13
C nuclear magnetic resonance (NMR) spectroscopy, field-emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM) and Brunauer-Emmet-Teller (BET) analysis of the nitrogen adsorption isotherm. 3-DOM carbon replicas exhibit poor capacitive behaviour in aqueous electrolyte, explained by a high ionic resistivity present in the porosity. Even though this electrical disruptive effect can be explained on the basis of the macroporosity of the disconnected carbon 3-DOM, this allows us to envisage other applications for this approach in order to obtain tri-modal carbon-based materials.
Using a template approach, a 3-DOM LDH hybrid compound intercalated with VBS monomer has been successfully prepared and used to produce a hierarchically micro/meso/macroporous carbonaceous replica.</description><issn>1144-0546</issn><issn>1369-9261</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqFkM1Lw0AQxYMoWD8u3oXxptDU3aZG6rVW2oMVrPcy3Z2Y1U02zG6K-cc9u0XFg6Cnecz7zcxjkuREioEU2fhSifpFiDwTrztJT2b5OB0Pc7kbtRyNUnE1yveTA-8jI-V1LnvJ-8wQI6vSKLS2Ax-4VaFl0qCQ164GpsZGE1wBZbdmo8FiR1tAu3ZtKXY1uzejaWpJBXa1UeDbprFUUR2QOzB14bjCYOK68-lyfgG4QWMxTt-AzCawuH8E32ynsQ-LIaD2jpstn2r6lmC8CyVx1YcNsvlcF1PFHmycDVhVFDgeVyXyMw1gSQS3D_N44td3jpK9Aq2n4696mJzeTZ8ms5S9WjVsqhh79YNn__tnf_mrRhfZBxqdhx4</recordid><startdate>20110101</startdate><enddate>20110101</enddate><creator>Prévot, Vanessa</creator><creator>Géraud, Erwan</creator><creator>Stimpfling, Thomas</creator><creator>Ghanbaja, Jaafar</creator><creator>Leroux, Fabrice</creator><scope/></search><sort><creationdate>20110101</creationdate><title>Hierarchically structured carbon replica of hybrid layered double hydroxideElectronic supplementary information (ESI) available: 13C NMR spectra, N2 adsorption-desorption isotherm, variation of the voltammetric charge. See DOI: 10.1039/c0nj00630k</title><author>Prévot, Vanessa ; Géraud, Erwan ; Stimpfling, Thomas ; Ghanbaja, Jaafar ; Leroux, Fabrice</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-rsc_primary_c0nj00630k3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Prévot, Vanessa</creatorcontrib><creatorcontrib>Géraud, Erwan</creatorcontrib><creatorcontrib>Stimpfling, Thomas</creatorcontrib><creatorcontrib>Ghanbaja, Jaafar</creatorcontrib><creatorcontrib>Leroux, Fabrice</creatorcontrib></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Prévot, Vanessa</au><au>Géraud, Erwan</au><au>Stimpfling, Thomas</au><au>Ghanbaja, Jaafar</au><au>Leroux, Fabrice</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hierarchically structured carbon replica of hybrid layered double hydroxideElectronic supplementary information (ESI) available: 13C NMR spectra, N2 adsorption-desorption isotherm, variation of the voltammetric charge. See DOI: 10.1039/c0nj00630k</atitle><date>2011-01-01</date><risdate>2011</risdate><volume>35</volume><issue>1</issue><spage>169</spage><epage>177</epage><pages>169-177</pages><issn>1144-0546</issn><eissn>1369-9261</eissn><abstract>A hierarchically structured carbon replica with a tri-modal distribution of porosity was prepared by pyrolysis of a three-dimensionally ordered macroporous (3-DOM) organic-inorganic hybrid layered double hydroxide (LDH). By an original inverse opal method involving LDH platelet regeneration, macroporous Mg
2
Al-vinyl benzene sulfonate (VBS) was synthesized and subsequently submitted to a moderate thermal treatment to induce the VBS
in situ
polymerization. Successive steps of carbonization and demineralization were conducted to yield to a carbon replica. A thermal treatment under inert atmosphere ensures the carbonization of the organic part and the simultaneous decomposition of the LDH into oxide and mixed oxide particles. The latter acts as a porogen agent during the acid-leaching step, which induces the removal of the inorganic part. The samples upon carbonization and the capacitive properties of the resulting carbon replica were thoroughly characterized using powder X-ray diffraction (PXRD), Fourier-transform infra-red (FTIR) and
13
C nuclear magnetic resonance (NMR) spectroscopy, field-emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM) and Brunauer-Emmet-Teller (BET) analysis of the nitrogen adsorption isotherm. 3-DOM carbon replicas exhibit poor capacitive behaviour in aqueous electrolyte, explained by a high ionic resistivity present in the porosity. Even though this electrical disruptive effect can be explained on the basis of the macroporosity of the disconnected carbon 3-DOM, this allows us to envisage other applications for this approach in order to obtain tri-modal carbon-based materials.
Using a template approach, a 3-DOM LDH hybrid compound intercalated with VBS monomer has been successfully prepared and used to produce a hierarchically micro/meso/macroporous carbonaceous replica.</abstract><doi>10.1039/c0nj00630k</doi><tpages>9</tpages></addata></record> |
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source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
title | Hierarchically structured carbon replica of hybrid layered double hydroxideElectronic supplementary information (ESI) available: 13C NMR spectra, N2 adsorption-desorption isotherm, variation of the voltammetric charge. See DOI: 10.1039/c0nj00630k |
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