A Controllable Self-Assembly Method for Large-Scale Synthesis of Graphene Sponges and Free-Standing Graphene Films

A simple method to prepare large‐scale graphene sponges and free‐standing graphene films using a speed vacuum concentrator is presented. During the centrifugal evaporation process, the graphene oxide (GO) sheets in the aqueous suspension are assembled to generate network‐linked GO sponges or a serie...

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Veröffentlicht in:Advanced functional materials 2010-06, Vol.20 (12), p.1930-1936
Hauptverfasser: Liu, Fei, Seo, Tae Seok
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container_title Advanced functional materials
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creator Liu, Fei
Seo, Tae Seok
description A simple method to prepare large‐scale graphene sponges and free‐standing graphene films using a speed vacuum concentrator is presented. During the centrifugal evaporation process, the graphene oxide (GO) sheets in the aqueous suspension are assembled to generate network‐linked GO sponges or a series of multilayer GO films, depending on the temperature of a centrifugal vacuum chamber. While sponge‐like bulk GO materials (GO sponges) are produced at 40 °C, uniform free‐standing GO films of size up to 9 cm2 are generated at 80 °C. The thickness of GO films can be controlled from 200 nm to 1 µm based on the concentration of the GO colloidal suspension and evaporation temperature. The synthesized GO films exhibit excellent transparency, typical fluorescent emission signal, and high flexibility with a smooth surface and condensed density. Reduced GO sponges and films with less than 5 wt% oxygen are produced through a thermal annealing process at 800 °C with H2/Ar flow. The structural flexibility of the reduced GO sponges, which have a highly porous, interconnected, 3D network, as well as excellent electrochemical properties of the reduced GO film with respect to electrode kinetics for the [Fe(CN)6]3−/4− redox system, are demonstrated. Large‐scale graphene oxide (GO) sponges or free‐standing large‐area GO films are generated from a GO suspension in a speed vacuum concentrator simply by controlling the chamber temperature. While the reduced GO sponge shows a high structural flexibility, the GO film and its reduced form demonstrate excellent photoluminescence and electrochemical properties.
doi_str_mv 10.1002/adfm.201000287
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During the centrifugal evaporation process, the graphene oxide (GO) sheets in the aqueous suspension are assembled to generate network‐linked GO sponges or a series of multilayer GO films, depending on the temperature of a centrifugal vacuum chamber. While sponge‐like bulk GO materials (GO sponges) are produced at 40 °C, uniform free‐standing GO films of size up to 9 cm2 are generated at 80 °C. The thickness of GO films can be controlled from 200 nm to 1 µm based on the concentration of the GO colloidal suspension and evaporation temperature. The synthesized GO films exhibit excellent transparency, typical fluorescent emission signal, and high flexibility with a smooth surface and condensed density. Reduced GO sponges and films with less than 5 wt% oxygen are produced through a thermal annealing process at 800 °C with H2/Ar flow. The structural flexibility of the reduced GO sponges, which have a highly porous, interconnected, 3D network, as well as excellent electrochemical properties of the reduced GO film with respect to electrode kinetics for the [Fe(CN)6]3−/4− redox system, are demonstrated. Large‐scale graphene oxide (GO) sponges or free‐standing large‐area GO films are generated from a GO suspension in a speed vacuum concentrator simply by controlling the chamber temperature. 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Funct. Mater</addtitle><description>A simple method to prepare large‐scale graphene sponges and free‐standing graphene films using a speed vacuum concentrator is presented. During the centrifugal evaporation process, the graphene oxide (GO) sheets in the aqueous suspension are assembled to generate network‐linked GO sponges or a series of multilayer GO films, depending on the temperature of a centrifugal vacuum chamber. While sponge‐like bulk GO materials (GO sponges) are produced at 40 °C, uniform free‐standing GO films of size up to 9 cm2 are generated at 80 °C. The thickness of GO films can be controlled from 200 nm to 1 µm based on the concentration of the GO colloidal suspension and evaporation temperature. The synthesized GO films exhibit excellent transparency, typical fluorescent emission signal, and high flexibility with a smooth surface and condensed density. Reduced GO sponges and films with less than 5 wt% oxygen are produced through a thermal annealing process at 800 °C with H2/Ar flow. The structural flexibility of the reduced GO sponges, which have a highly porous, interconnected, 3D network, as well as excellent electrochemical properties of the reduced GO film with respect to electrode kinetics for the [Fe(CN)6]3−/4− redox system, are demonstrated. Large‐scale graphene oxide (GO) sponges or free‐standing large‐area GO films are generated from a GO suspension in a speed vacuum concentrator simply by controlling the chamber temperature. While the reduced GO sponge shows a high structural flexibility, the GO film and its reduced form demonstrate excellent photoluminescence and electrochemical properties.</description><subject>Density</subject><subject>electrode</subject><subject>Electrodes</subject><subject>Evaporation</subject><subject>Flexibility</subject><subject>Graphene</subject><subject>Self assembly</subject><subject>speed vacuum concentrator</subject><subject>Sponges</subject><subject>thin films</subject><subject>Three dimensional</subject><issn>1616-301X</issn><issn>1616-3028</issn><issn>1616-3028</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNqFkM1PgzAYh4nRxDm9eu7NE7NAS9mRbIKazY9sftyajr7dUKDYsij_vSyY6c1Tf33zPG_y_hzn3MMjD2P_UkhVjnzcZexH7MAZeKEXukH3Odxn7_XYObH2DWOPsYAMHBOjia4ao4tCrApACyiUG1sL5apo0RyajZZIaYNmwqzBXWRiB7VVswGbW6QVSo2oN1B101pXa7BIVBIlBjq46WJerX-RJC9Ke-ocKVFYOPt5h85TcrWcXLuz-_RmEs_cLKCUuQAhgQhCGgmPRuBLrHwgK0kZUUQAkRQHivlSAiEZE5EkkIGfSSVUJAiBYOhc9Htroz-2YBte5jaD7tAK9NbyKMIho3SMO3LUk5nR1hpQvDZ5KUzLPcx33fJdt3zfbSeMe-EzL6D9h-bxNJn_dd3ezW0DX3tXmHcesoBR_nKX8mD5eJtOn8f8IfgGn22O0A</recordid><startdate>20100623</startdate><enddate>20100623</enddate><creator>Liu, Fei</creator><creator>Seo, Tae Seok</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SP</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>20100623</creationdate><title>A Controllable Self-Assembly Method for Large-Scale Synthesis of Graphene Sponges and Free-Standing Graphene Films</title><author>Liu, Fei ; Seo, Tae Seok</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3557-ee64e8e658a158e2d0f2e4bd574f4ae4d503f72dde44c7a8d4ece2cdfaf8a44e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Density</topic><topic>electrode</topic><topic>Electrodes</topic><topic>Evaporation</topic><topic>Flexibility</topic><topic>Graphene</topic><topic>Self assembly</topic><topic>speed vacuum concentrator</topic><topic>Sponges</topic><topic>thin films</topic><topic>Three dimensional</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Fei</creatorcontrib><creatorcontrib>Seo, Tae Seok</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><collection>Electronics &amp; Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Advanced functional materials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Fei</au><au>Seo, Tae Seok</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Controllable Self-Assembly Method for Large-Scale Synthesis of Graphene Sponges and Free-Standing Graphene Films</atitle><jtitle>Advanced functional materials</jtitle><addtitle>Adv. Funct. Mater</addtitle><date>2010-06-23</date><risdate>2010</risdate><volume>20</volume><issue>12</issue><spage>1930</spage><epage>1936</epage><pages>1930-1936</pages><issn>1616-301X</issn><issn>1616-3028</issn><eissn>1616-3028</eissn><abstract>A simple method to prepare large‐scale graphene sponges and free‐standing graphene films using a speed vacuum concentrator is presented. During the centrifugal evaporation process, the graphene oxide (GO) sheets in the aqueous suspension are assembled to generate network‐linked GO sponges or a series of multilayer GO films, depending on the temperature of a centrifugal vacuum chamber. While sponge‐like bulk GO materials (GO sponges) are produced at 40 °C, uniform free‐standing GO films of size up to 9 cm2 are generated at 80 °C. The thickness of GO films can be controlled from 200 nm to 1 µm based on the concentration of the GO colloidal suspension and evaporation temperature. The synthesized GO films exhibit excellent transparency, typical fluorescent emission signal, and high flexibility with a smooth surface and condensed density. Reduced GO sponges and films with less than 5 wt% oxygen are produced through a thermal annealing process at 800 °C with H2/Ar flow. The structural flexibility of the reduced GO sponges, which have a highly porous, interconnected, 3D network, as well as excellent electrochemical properties of the reduced GO film with respect to electrode kinetics for the [Fe(CN)6]3−/4− redox system, are demonstrated. Large‐scale graphene oxide (GO) sponges or free‐standing large‐area GO films are generated from a GO suspension in a speed vacuum concentrator simply by controlling the chamber temperature. While the reduced GO sponge shows a high structural flexibility, the GO film and its reduced form demonstrate excellent photoluminescence and electrochemical properties.</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><doi>10.1002/adfm.201000287</doi><tpages>7</tpages></addata></record>
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source Wiley Online Library Journals Frontfile Complete
subjects Density
electrode
Electrodes
Evaporation
Flexibility
Graphene
Self assembly
speed vacuum concentrator
Sponges
thin films
Three dimensional
title A Controllable Self-Assembly Method for Large-Scale Synthesis of Graphene Sponges and Free-Standing Graphene Films
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