2020
DOI: 10.1007/s00339-019-3271-8
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On the mechanism of conductivity enhancement in PEDOT:PSS/PVA blend fiber induced by UV-light irradiation

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Cited by 19 publications
(27 citation statements)
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“…30,31 In general, pristine PEDOT:PSS lms usually contains both benzoid and quinoid structural conformation. 23,32 In a benzoid (coiled) conformation, the C a -C b between two thiophene rings in the PEDOT chain is similar to s bond, which usually has a low density of conjugated p-electrons. Whereas in the case of quinoid (linear) conformation, adjacent thiophene rings nearly lie on the same plane resulting in the delocalization of conjugated p-electrons throughout the PEDOT chain.…”
Section: Resultsmentioning
confidence: 99%
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“…30,31 In general, pristine PEDOT:PSS lms usually contains both benzoid and quinoid structural conformation. 23,32 In a benzoid (coiled) conformation, the C a -C b between two thiophene rings in the PEDOT chain is similar to s bond, which usually has a low density of conjugated p-electrons. Whereas in the case of quinoid (linear) conformation, adjacent thiophene rings nearly lie on the same plane resulting in the delocalization of conjugated p-electrons throughout the PEDOT chain.…”
Section: Resultsmentioning
confidence: 99%
“…Whereas in the case of quinoid (linear) conformation, adjacent thiophene rings nearly lie on the same plane resulting in the delocalization of conjugated p-electrons throughout the PEDOT chain. 23,32 Therefore, if the dominant conformation exists in PEDOT lms is in the form of quinoid (linear) structure will lead to increased conjugated length of PEDOT chain, thereby resulting in enhanced conductivity of the sample. In case of thiophene rings, UV irradiation leads to the red shi of the peak as shown in Fig.…”
Section: Resultsmentioning
confidence: 99%
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“…This is because Figure S3 shows 2.0% and 2.5% EMIM:TFSI-DMSO, films with a less significant red shift than films with NaBH 4 treated films. The quinoid structure as shown in Figure 3a has restricted rotation around the sp 2 carbon double bond on the thiophene backbone thereby adopting a planer structure with more crystalline packing relative to the benzoid (Figure 3b) structure in which more thiophene units adopt a helical structure with lower molecular ordering that impedes hopping of charge carriers (polarons) within and between the polymer chains [32,33].…”
Section: Mechanisms For the Improved Electrical Conductivity Of Emim:mentioning
confidence: 99%
“…The most significant utilization of this instrumental technique was in determining the Raman red shift at 1440 cm -1 which indicates the benzoid to quinoid conformational change in PEDOT chains. [298][299][300] The spectra were run from 300 nm to 1900 nm. The Raman spectra were measured using a Renishaw inVia Raman system.…”
Section: Raman Spectroscopymentioning
confidence: 99%