2016
DOI: 10.1039/c6ra24386j
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Sodium storage in fluorine-rich mesoporous carbon fabricated by low-temperature carbonization of polyvinylidene fluoride with a silica template

Abstract: A fluorine-rich mesoporous carbon is prepared by low-temperature carbonization of polyvinylidene fluoride with a silica template, exhibiting excellent sodium anodic performances.

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Cited by 20 publications
(12 citation statements)
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“…It can also be found that the characteristic peak of O 1s at 532 eV decreases significantly in FMG, suggesting that large amounts of oxygen functional groups are removed under the interaction with HF molecules. The phenomenon is similar to Feng’s work in which a F- and N-codoped graphene was fabricated through a hydrothermal route and is attributed to the deoxidation reaction and the substitution reaction of F atoms with oxygen functional groups. , The deconvoluted O 1s spectra of MG and FMG are shown in Figure b,c, in which the peaks at 532.1 and 533.6 eV belong to carbonyl (−C–O–C−) and hydroxyl (−OH) groups, respectively . Based on an integral area calculation, it is found that the ratio between carbonyl groups and hydroxyl groups decreases from 4.66 for MG to 2.82 for FMG, indicating that the carbonyl groups are more apt to be diminished and replaced during the F-doping process.…”
Section: Results and Discussionsupporting
confidence: 81%
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“…It can also be found that the characteristic peak of O 1s at 532 eV decreases significantly in FMG, suggesting that large amounts of oxygen functional groups are removed under the interaction with HF molecules. The phenomenon is similar to Feng’s work in which a F- and N-codoped graphene was fabricated through a hydrothermal route and is attributed to the deoxidation reaction and the substitution reaction of F atoms with oxygen functional groups. , The deconvoluted O 1s spectra of MG and FMG are shown in Figure b,c, in which the peaks at 532.1 and 533.6 eV belong to carbonyl (−C–O–C−) and hydroxyl (−OH) groups, respectively . Based on an integral area calculation, it is found that the ratio between carbonyl groups and hydroxyl groups decreases from 4.66 for MG to 2.82 for FMG, indicating that the carbonyl groups are more apt to be diminished and replaced during the F-doping process.…”
Section: Results and Discussionsupporting
confidence: 81%
“…33,34 The deconvoluted O 1s spectra of MG and FMG are shown in Figure 2b,c, in which the peaks at 532.1 and 533.6 eV belong to carbonyl (−C−O− C−) and hydroxyl (−OH) groups, respectively. 35 Based on an integral area calculation, it is found that the ratio between carbonyl groups and hydroxyl groups decreases from 4.66 for MG to 2.82 for FMG, indicating that the carbonyl groups are more apt to be diminished and replaced during the F-doping process. Figure 2d depicts the F 1s spectrum.…”
Section: Resultsmentioning
confidence: 99%
“…Conversely, the C–F (covalent) peak at 290.8 eV disappeared, as shown in Table 1 . Instead, a peak at 288.09 eV indicating a C–F (semi-ionic) bond emerged [ 40 ]. For the F 1s spectra shown in Figure 1 b, the peak at 687.9 eV corresponding to the C–F (covalent) bond vanished [ 41 ].…”
Section: Resultsmentioning
confidence: 99%
“…Heteroatom doping is also a useful strategy that could broaden the interlamellar spacing of layered MTs, providing large channels for ion transfer, and increasing the storage sites for ions; further this can reduce the bad gap between the valence band and conduction band, thereby promoting faster electron transport. 120–122 However, the related research has not been investigated, we can introduce cations and anions into MTs to further improve their performance. In addition, the work on composite is mainly restricted to traditional carbon materials; the emerging MXenes 2D materials with large interlayer spacing, high metallic conductivity, hydrophilic surface, and outstanding mechanical property, 123–125 can also be an excellent conductive matrix.…”
Section: Discussionmentioning
confidence: 99%