2019
DOI: 10.1016/j.apsusc.2018.12.096
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Effective reduction of graphene oxide via a hybrid microwave heating method by using mildly reduced graphene oxide as a susceptor

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Cited by 55 publications
(14 citation statements)
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“…Microwaves are effectively absorbed by π-electrons that cause very rapid warming of GO (several hundreds of degrees in few seconds) that results in the breaking of weakest bonds [ 127 ]. According to this principle, r-GO domains with sp 2 carbon network and free π-electrons heat faster than GO-ones that minimize the efficiency of this method [ 128 , 129 ]. When chemically reduced or simultaneously exfoliated and reduced, the quality of r-GO is low and oxygen content is as high as in the case of the conventional thermal method [ 54 , 127 ].…”
Section: Go/rgo: Properties Reduction Methods and Characterizatimentioning
confidence: 99%
“…Microwaves are effectively absorbed by π-electrons that cause very rapid warming of GO (several hundreds of degrees in few seconds) that results in the breaking of weakest bonds [ 127 ]. According to this principle, r-GO domains with sp 2 carbon network and free π-electrons heat faster than GO-ones that minimize the efficiency of this method [ 128 , 129 ]. When chemically reduced or simultaneously exfoliated and reduced, the quality of r-GO is low and oxygen content is as high as in the case of the conventional thermal method [ 54 , 127 ].…”
Section: Go/rgo: Properties Reduction Methods and Characterizatimentioning
confidence: 99%
“…The two sub-peaks are located at 532.6 eV and 533.6 eV, corresponding to the C-O and C-O-C/C-OH groups. 32,33 The peak intensities of the C-O-C/C-OH group and C-O group in LIG samples are basically equal, which is due to the relatively higher carbon content in LIG. Correspondingly, the C-O group peak in the N-LIG sample is slightly stronger than the C-O-C/C-OH group peak, which also confirms that the carbon content in N-LIG is slightly lower.…”
Section: Characterization Of N-lig Materialsmentioning
confidence: 97%
“…In Figure 4A, the peaks of C1s (286.2 eV) and O1s (534.2 eV) are observed in the XPS spectra of acid T300, T300-GO and T300-GO-ATP. [28,29] In addition, N1s (~399.8 eV) peaks are found in T300-GO and T300-GO-ATP, indicating that an amidation reaction took place between T300 and GO or between GO and ATP ( Figure 3A). [30] A Si2P peak was found at 104.3 eV, which verifies that the Si-OH of ATP reacted with the oxygen functional groups on T300-GO to generate T300-GO-ATP, ensuring superior thermal stability even at −196 C. In Figure 4B, compared with the C1s spectrum of Acid T300, T300-GO has C N and O C N peak at 284.9 and 287.3 eV.…”
Section: Surface Topography Of T300-go-atpmentioning
confidence: 99%