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PEDOT:PSS/graphene quantum dots films with enhanced thermoelectric properties via strong interfacial interaction and phase separation

The typical conductive polymer of PEDOT:PSS has recently attracted intensive attention in thermoelectric conversion because of its low cost and low thermal conductivity as well as high electrical conductivity. However, compared to inorganic counterparts, the relatively poor thermoelectric performanc...

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Autores principales: Du, Fei-Peng, Cao, Nan-Nan, Zhang, Yun-Fei, Fu, Ping, Wu, Yan-Guang, Lin, Zhi-Dong, Shi, Run, Amini, Abbas, Cheng, Chun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5915444/
https://www.ncbi.nlm.nih.gov/pubmed/29691433
http://dx.doi.org/10.1038/s41598-018-24632-4
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author Du, Fei-Peng
Cao, Nan-Nan
Zhang, Yun-Fei
Fu, Ping
Wu, Yan-Guang
Lin, Zhi-Dong
Shi, Run
Amini, Abbas
Cheng, Chun
author_facet Du, Fei-Peng
Cao, Nan-Nan
Zhang, Yun-Fei
Fu, Ping
Wu, Yan-Guang
Lin, Zhi-Dong
Shi, Run
Amini, Abbas
Cheng, Chun
author_sort Du, Fei-Peng
collection PubMed
description The typical conductive polymer of PEDOT:PSS has recently attracted intensive attention in thermoelectric conversion because of its low cost and low thermal conductivity as well as high electrical conductivity. However, compared to inorganic counterparts, the relatively poor thermoelectric performance of PEDOT:PSS has greatly limited its development and high-tech applications. Here, we report a dramatic enhancement in the thermoelectric performance of PEDOT:PSS by constructing unique composite films with graphene quantum dots (GQDs). At room temperature, the electrical conductivity and Seebeck coefficient of PEDOT:PSS/GQDs reached to 7172 S/m and 14.6 μV/K, respectively, which are 30.99% and 113.2% higher than those of pristine PEDOT:PSS. As a result, the power factor of the optimized PEDOT:PSS/GQDs composite is 550% higher than that of pristine PEDOT:PSS. These significant improvements are attributed to the ordered alignment of PEDOT chains on the surface of GQDs, originated from the strong interfacial interaction between PEDOT:PSS and GQDs and the separation of PEDOT and PSS phases. This study evidently provides a promising route for PEDOT:PSS applied in high-efficiency thermoelectric conversion.
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spelling pubmed-59154442018-04-30 PEDOT:PSS/graphene quantum dots films with enhanced thermoelectric properties via strong interfacial interaction and phase separation Du, Fei-Peng Cao, Nan-Nan Zhang, Yun-Fei Fu, Ping Wu, Yan-Guang Lin, Zhi-Dong Shi, Run Amini, Abbas Cheng, Chun Sci Rep Article The typical conductive polymer of PEDOT:PSS has recently attracted intensive attention in thermoelectric conversion because of its low cost and low thermal conductivity as well as high electrical conductivity. However, compared to inorganic counterparts, the relatively poor thermoelectric performance of PEDOT:PSS has greatly limited its development and high-tech applications. Here, we report a dramatic enhancement in the thermoelectric performance of PEDOT:PSS by constructing unique composite films with graphene quantum dots (GQDs). At room temperature, the electrical conductivity and Seebeck coefficient of PEDOT:PSS/GQDs reached to 7172 S/m and 14.6 μV/K, respectively, which are 30.99% and 113.2% higher than those of pristine PEDOT:PSS. As a result, the power factor of the optimized PEDOT:PSS/GQDs composite is 550% higher than that of pristine PEDOT:PSS. These significant improvements are attributed to the ordered alignment of PEDOT chains on the surface of GQDs, originated from the strong interfacial interaction between PEDOT:PSS and GQDs and the separation of PEDOT and PSS phases. This study evidently provides a promising route for PEDOT:PSS applied in high-efficiency thermoelectric conversion. Nature Publishing Group UK 2018-04-24 /pmc/articles/PMC5915444/ /pubmed/29691433 http://dx.doi.org/10.1038/s41598-018-24632-4 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Du, Fei-Peng
Cao, Nan-Nan
Zhang, Yun-Fei
Fu, Ping
Wu, Yan-Guang
Lin, Zhi-Dong
Shi, Run
Amini, Abbas
Cheng, Chun
PEDOT:PSS/graphene quantum dots films with enhanced thermoelectric properties via strong interfacial interaction and phase separation
title PEDOT:PSS/graphene quantum dots films with enhanced thermoelectric properties via strong interfacial interaction and phase separation
title_full PEDOT:PSS/graphene quantum dots films with enhanced thermoelectric properties via strong interfacial interaction and phase separation
title_fullStr PEDOT:PSS/graphene quantum dots films with enhanced thermoelectric properties via strong interfacial interaction and phase separation
title_full_unstemmed PEDOT:PSS/graphene quantum dots films with enhanced thermoelectric properties via strong interfacial interaction and phase separation
title_short PEDOT:PSS/graphene quantum dots films with enhanced thermoelectric properties via strong interfacial interaction and phase separation
title_sort pedot:pss/graphene quantum dots films with enhanced thermoelectric properties via strong interfacial interaction and phase separation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5915444/
https://www.ncbi.nlm.nih.gov/pubmed/29691433
http://dx.doi.org/10.1038/s41598-018-24632-4
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