2018
DOI: 10.1002/pc.24976
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Poly(3,4‐Propylenedioxythiophene) Capsulated Yolk–Shell Carbon Spheres for High‐Performance Electrochemical Capacitors

Abstract: In this article, the yolk–shell structure of resin‐based carbon spheres (YRFC) and the solid structure of resin‐based carbon spheres (SRFC) were prepared by condensation polymerization, and then novel spherical composites of poly(3,4‐propylenedioxythiophene)/YRFC (PProDOT/YRFC) and PProDOT/SRFC were obtained by in situ chemical oxidative polymerization. The prepared composites were characterized by Fourier transform infrared spectroscopy (FTIR), ultraviolet–visible absorption spectra (UV–vis), Raman, X‐ray dif… Show more

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Cited by 10 publications
(5 citation statements)
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“…PProDOT/YRFC showed a SC retention of 87.3% after 10 000 charge/discharge cycles, owing to its uniformly dispersible fluffy structure. 53 Kim et al , reported ternary silver/manganese oxide/polyaniline (Ag/MnO 2 /PANI) thin films which exhibited a SC of 800 F g −1 and a cycling stability of up to 83% compared to the pure PANI polymer (66%). 54 A hierarchical N-doped porous carbon fiber@Cu (NPCF@Cu) composite based supercapacitor was reported by Hui et al , where a SC of 210 F g −1 was achieved by NPCF@Cu-10 higher than NPCF@Cu-0 (130 F g −1 ) and NPCF-10 (105 F g −1 ) at a discharge current density of 50 F g −1 .…”
Section: Resultsmentioning
confidence: 99%
“…PProDOT/YRFC showed a SC retention of 87.3% after 10 000 charge/discharge cycles, owing to its uniformly dispersible fluffy structure. 53 Kim et al , reported ternary silver/manganese oxide/polyaniline (Ag/MnO 2 /PANI) thin films which exhibited a SC of 800 F g −1 and a cycling stability of up to 83% compared to the pure PANI polymer (66%). 54 A hierarchical N-doped porous carbon fiber@Cu (NPCF@Cu) composite based supercapacitor was reported by Hui et al , where a SC of 210 F g −1 was achieved by NPCF@Cu-10 higher than NPCF@Cu-0 (130 F g −1 ) and NPCF-10 (105 F g −1 ) at a discharge current density of 50 F g −1 .…”
Section: Resultsmentioning
confidence: 99%
“…The absorption at 1500 and 1384 cm −1 correspond to the CC and C–C stretching in the thiophene ring of PProDOT, indicating a successful polymerization. 107,108 It can be seen that dopant influences the position of the absorption band. Particularly, the ClO 4 − dopant shifts the corresponding characteristic absorption bands towards higher wavenumbers (C–O–C bond stretching vibration band; 1055 and 1173 cm −1 , C–S–C bonds vibration band; 777, 879, and 947 cm −1 , the CC and C–C stretching band in polythiophene ring; 1504 and 1323 cm −1 ) probably due to different interaction of electrolyte ions with the polaronic structure of the polymeric unit, and absorption intensity decrease.…”
Section: Resultsmentioning
confidence: 99%
“…The absorption at 1500 and 1384 cm −1 correspond to the CC and C-C stretching in the thiophene ring of PProDOT, indicating a successful polymerization. 107,108 It can be seen that dopant influences the position of the absorption band.…”
Section: Structural and Chemical Analysismentioning
confidence: 99%
“…4A, 4D, and 4G) of these species can be deconvoluted in five or four peaks, being C-C/ C=C, C-S/C-N=C-N + /C-S + /C=C-O, C=N + /C-O-C, and π-π interactions. [36][37][38] The S2p spectra (Figs. 4B, 4E, and 4H) of these species can be deconvoluted in three or two peaks assigned to S2p 3/2 and S2p 1/2 (S + ), indicating that the S atoms have valencies of 2 and 1, which is in accordance with its structure.…”
Section: Resultsmentioning
confidence: 99%
“…4B, 4E, and 4H) of these species can be deconvoluted in three or two peaks assigned to S2p 3/2 and S2p 1/2 (S + ), indicating that the S atoms have valencies of 2 and 1, which is in accordance with its structure. 36,[39][40][41] The N1s spectra (Figs. 4C, 4F, and 4I) of these species can be deconvoluted in four peaks, being =N-, -N-H/-N-C, -N + -H, and =N + -H. [42][43][44] According to the XPS results and related literature, 37,45,46 the interactive forces, including H-bonding and Coulomb force between the two polymers and rutin, were likely to appear in the MIP electropolymerization process (Scheme 1).…”
Section: Resultsmentioning
confidence: 99%