2015
DOI: 10.1016/j.diamond.2015.10.030
|View full text |Cite
|
Sign up to set email alerts
|

Water-dispersible carbon nanotube prepared by non-destructive functionalization technique of admicellar polymerization

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
7
0

Year Published

2016
2016
2023
2023

Publication Types

Select...
7

Relationship

1
6

Authors

Journals

citations
Cited by 12 publications
(7 citation statements)
references
References 31 publications
0
7
0
Order By: Relevance
“…The loading mass of PAA in the PAA-SWNT film was revealed by thermogravimetric analysis (TGA) (Figure f). The weight percentage of PAA in the PAA-SWNT was around 10% …”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…The loading mass of PAA in the PAA-SWNT film was revealed by thermogravimetric analysis (TGA) (Figure f). The weight percentage of PAA in the PAA-SWNT was around 10% …”
Section: Resultsmentioning
confidence: 99%
“…The weight percentage of PAA in the PAA-SWNT was around 10%. 41 The electrochemical performances of Li−S battery with our designed carbon interlayer were evaluated by coin-type half cell (2032R type) and presented in Figure 3. Figure 3a shows the initial discharge−charge curves of the pure sulfur cathode, the sulfur cathode with a SWNT interlayer, and the sulfur cathode with a PAA-SWNT interlayer.…”
Section: ■ Results and Discussionmentioning
confidence: 99%
“…We used XRD spectroscopy to examine the difference in chemical periodicity upon grafting CNT–COOH with U moieties ( Figure 3 ). The characteristic peaks of CNT–COOH and CNT–U appeared at values of 2 θ of 26°, 29°, 43°, and 45°, assigned to the distinguishable (002), (220), (100), and (101) planes, respectively [ 24 , 25 , 28 ]. Interestingly, the XRD pattern of CNT–U featured a broad peak at 18°–19° that was not present for CNT–COOH.…”
Section: Resultsmentioning
confidence: 99%
“…The resulting mixture was heated under reflux at 80 °C with vigorous stirring for 24 h. The crude product was subjected to PTFE filtration (Poly(tetrafluoroethylene) membrane, Merck KGaA, Darmstadt, Germany) and centrifugation (3000 rpm, 5 min) to produce CNT–U. Fourier transform infrared (FTIR) spectroscopy ( Figure S2 ): 3200–3400 cm −1 (NH stretching), 1650 (C=O) cm −1 [ 22 , 23 ]; Raman spectroscopy ( Figure S3 ): 1580 cm −1 (intense G band; Raman-allowed phonon high-frequency mode), 1350 cm −1 (disordered-induced D band, presumably originating from defects in the curved graphene sheets and tube ends [ 24 , 25 ]).…”
Section: Methodsmentioning
confidence: 99%
“…Admicellar polymerization was first employed modifying CNT in order to enhance their dispersion inside a polyacrylonitrile matrix . Of particular note, water‐soluble polymers polyacrylic acid (PAA) and polyvinyl acetate (PVAc) and copolymer of PAA and PVAc have been used to prepare water‐dispersed CNT by admicellar polymerization . These same polymers, PAA and PVAc, were selected to prepare water‐dispersed CNT in this study.…”
Section: Introductionmentioning
confidence: 99%