2009
DOI: 10.1021/cm9006603
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Hydrothermal Dehydration for the “Green” Reduction of Exfoliated Graphene Oxide to Graphene and Demonstration of Tunable Optical Limiting Properties

Abstract: This work reports a simple, clean, and controlled hydrothermal dehydration route to convert graphene oxide (GO) to stable graphene solution. The hydrothermally treated GO was characterized using UV-visible absorption spectroscopy, atomic force microscopy, Raman spectroscopy, X-ray photoemission spectroscopy, and solid state 13 C NMR spectra. Compared to chemical reduction processes using hydrazine, the present "water-only" route has the combined advantages of removing oxygen functional groups from GO and repai… Show more

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Cited by 1,470 publications
(826 citation statements)
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“…The Raman spectrum from graphite showed the characteristic dominant presented in the literature [45] , thereby confirming that our synthesis method results in the formation of CCG.…”
Section: Dispersion Stabilitysupporting
confidence: 88%
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“…The Raman spectrum from graphite showed the characteristic dominant presented in the literature [45] , thereby confirming that our synthesis method results in the formation of CCG.…”
Section: Dispersion Stabilitysupporting
confidence: 88%
“…Raman spectroscopy is a widely used method for the characterisation (and identification) of carbon materials such as graphite and its conversion via exfoliation to GO and reduction to graphene [43,44,45,46] . The Raman spectrum from graphite showed the characteristic dominant presented in the literature [45] , thereby confirming that our synthesis method results in the formation of CCG.…”
Section: Dispersion Stabilitymentioning
confidence: 99%
“…2) indicate the existence of ether C-O (B286.7 eV) and ester C( ¼ O)O (B288.6 eV) bonds, in addition to the dominant C ¼ C bonds (B284.5 eV 20 ). Under present solvothermal synthesis conditions, reactions are expected 14,21 between/among the OH, COOH and epoxy bond functional groups of adjacent graphene sheets to generate aromatic ether and ester bonds between the sheets mainly at the edges 13,16,17 . The existence of a significant amount of C-O carbon (B3.7 at%), C ¼ O carbon (B1.6 at%) and C( ¼ O)O ester carbonyl carbon (B1.7 at%) is consistent with the observed corresponding peak for the C-O bonds in infrared spectra ( Supplementary Fig.…”
Section: Synthesismentioning
confidence: 98%
“…The condensation/cross-linking of the functional groups during synthesis, such as OH, COOH and epoxy groups that are mainly located on GO sheets edges, is expected to covalently interconnect the sheets, thereby forming a monolithic 3D chemically linked network 13,16,17 , though no direct evidence is available yet. The subsequent annealing step would remove most of the functional groups, partially restoring p-conjugation and increasing electrical conductivity 18,19 .…”
Section: Synthesismentioning
confidence: 99%
“…This red shift shows the reduction of GO and arises from the restoration of a π-conjugation network of reduced GO. In addition, the disappearance of the weak absorption peak at 300 nm vouches for the elimination of oxygen groups in reduced GO [23][24][25]. Figure 3C and D (inset) shows the UV-vis spectra and Tauc plot of the MgO-GO2 and MgO-GO3 sample produced by MgO doped-GO at 180°C and 210°C, respectively.…”
Section: Linear Optical Propertiesmentioning
confidence: 95%