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Synthesis of Highly Conductive Poly(3-hexylthiophene) by Chemical Oxidative Polymerization Using Surfactant Templates

Poly(3-hexylthiophene) (P3HT) was systematically synthesized by chemical oxidative polymerization in chloroform with ferric chloride (FeCl(3)) as the oxidizing agent and various surfactants of the shape templates. The effects of 3HT: FeCl(3) mole ratios, polymerization times, and surfactant types an...

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Autores principales: Kesornsit, Sanhanut, Direksilp, Chatrawee, Phasuksom, Katesara, Thummarungsan, Natlita, Sakunpongpitiporn, Phimchanok, Rotjanasuworapong, Kornkanok, Sirivat, Anuvat, Niamlang, Sumonman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9503232/
https://www.ncbi.nlm.nih.gov/pubmed/36146004
http://dx.doi.org/10.3390/polym14183860
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author Kesornsit, Sanhanut
Direksilp, Chatrawee
Phasuksom, Katesara
Thummarungsan, Natlita
Sakunpongpitiporn, Phimchanok
Rotjanasuworapong, Kornkanok
Sirivat, Anuvat
Niamlang, Sumonman
author_facet Kesornsit, Sanhanut
Direksilp, Chatrawee
Phasuksom, Katesara
Thummarungsan, Natlita
Sakunpongpitiporn, Phimchanok
Rotjanasuworapong, Kornkanok
Sirivat, Anuvat
Niamlang, Sumonman
author_sort Kesornsit, Sanhanut
collection PubMed
description Poly(3-hexylthiophene) (P3HT) was systematically synthesized by chemical oxidative polymerization in chloroform with ferric chloride (FeCl(3)) as the oxidizing agent and various surfactants of the shape templates. The effects of 3HT: FeCl(3) mole ratios, polymerization times, and surfactant types and concentrations on the electrical conductivity, particle shape and size were systematically investigated. Furthermore, dodecylbenzenesulfonic acid (DBSA), p-toluenesulfonic acid (PTSA), sodium dodecyl sulfate (SDS), and sodium dioctyl sulfosuccinate (AOT) were utilized as the surfactant templates. The P3HT synthesized with DBSA at 6 CMC, where CMC stands for the Critical Micelle Concentration of surfactant, provided a higher electrical conductivity than those with PTSA, SDS and AOT. The highest electrical conductivity of P3HT using DBSA was 16.21 ± 1.55 S cm(−1) in which the P3HT particle shape was spherical with an average size of 1530 ± 227 nm. The thermal analysis indicated that the P3HT synthesized with the surfactants yielded higher stability and char yields than that of P3HT without. The P3HT_DBSA electrical conductivity was further enhanced by de-doping and doping with HClO(4). At the 10:1 doping mole ratio, the electrical conductivity of dP3HT_DBSA increased by one order of magnitude relative to P3HT_DBSA prior to the de-doping. The highest electrical conductivity of dP3HT_DBSA obtained was 172 ± 5.21 S cm(−1) which is the highest value relative to previously reported.
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spelling pubmed-95032322022-09-24 Synthesis of Highly Conductive Poly(3-hexylthiophene) by Chemical Oxidative Polymerization Using Surfactant Templates Kesornsit, Sanhanut Direksilp, Chatrawee Phasuksom, Katesara Thummarungsan, Natlita Sakunpongpitiporn, Phimchanok Rotjanasuworapong, Kornkanok Sirivat, Anuvat Niamlang, Sumonman Polymers (Basel) Article Poly(3-hexylthiophene) (P3HT) was systematically synthesized by chemical oxidative polymerization in chloroform with ferric chloride (FeCl(3)) as the oxidizing agent and various surfactants of the shape templates. The effects of 3HT: FeCl(3) mole ratios, polymerization times, and surfactant types and concentrations on the electrical conductivity, particle shape and size were systematically investigated. Furthermore, dodecylbenzenesulfonic acid (DBSA), p-toluenesulfonic acid (PTSA), sodium dodecyl sulfate (SDS), and sodium dioctyl sulfosuccinate (AOT) were utilized as the surfactant templates. The P3HT synthesized with DBSA at 6 CMC, where CMC stands for the Critical Micelle Concentration of surfactant, provided a higher electrical conductivity than those with PTSA, SDS and AOT. The highest electrical conductivity of P3HT using DBSA was 16.21 ± 1.55 S cm(−1) in which the P3HT particle shape was spherical with an average size of 1530 ± 227 nm. The thermal analysis indicated that the P3HT synthesized with the surfactants yielded higher stability and char yields than that of P3HT without. The P3HT_DBSA electrical conductivity was further enhanced by de-doping and doping with HClO(4). At the 10:1 doping mole ratio, the electrical conductivity of dP3HT_DBSA increased by one order of magnitude relative to P3HT_DBSA prior to the de-doping. The highest electrical conductivity of dP3HT_DBSA obtained was 172 ± 5.21 S cm(−1) which is the highest value relative to previously reported. MDPI 2022-09-15 /pmc/articles/PMC9503232/ /pubmed/36146004 http://dx.doi.org/10.3390/polym14183860 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kesornsit, Sanhanut
Direksilp, Chatrawee
Phasuksom, Katesara
Thummarungsan, Natlita
Sakunpongpitiporn, Phimchanok
Rotjanasuworapong, Kornkanok
Sirivat, Anuvat
Niamlang, Sumonman
Synthesis of Highly Conductive Poly(3-hexylthiophene) by Chemical Oxidative Polymerization Using Surfactant Templates
title Synthesis of Highly Conductive Poly(3-hexylthiophene) by Chemical Oxidative Polymerization Using Surfactant Templates
title_full Synthesis of Highly Conductive Poly(3-hexylthiophene) by Chemical Oxidative Polymerization Using Surfactant Templates
title_fullStr Synthesis of Highly Conductive Poly(3-hexylthiophene) by Chemical Oxidative Polymerization Using Surfactant Templates
title_full_unstemmed Synthesis of Highly Conductive Poly(3-hexylthiophene) by Chemical Oxidative Polymerization Using Surfactant Templates
title_short Synthesis of Highly Conductive Poly(3-hexylthiophene) by Chemical Oxidative Polymerization Using Surfactant Templates
title_sort synthesis of highly conductive poly(3-hexylthiophene) by chemical oxidative polymerization using surfactant templates
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9503232/
https://www.ncbi.nlm.nih.gov/pubmed/36146004
http://dx.doi.org/10.3390/polym14183860
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