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Femtosecond Optical Annealing Induced Polymer Melting and Formation of Solid Droplets

Interaction between femtosecond laser pulses with polymeric thin films induced transient optical annealing of the polymer molecules. Melting of the polymer films took place during the transient annealing process, so that a solid-liquid-solid phase transition process was observed. Ultrafast cooling o...

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Detalles Bibliográficos
Autores principales: Yang, Jinghui, Huang, Cuiying, Zhang, Xinping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6402037/
https://www.ncbi.nlm.nih.gov/pubmed/30960112
http://dx.doi.org/10.3390/polym11010128
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author Yang, Jinghui
Huang, Cuiying
Zhang, Xinping
author_facet Yang, Jinghui
Huang, Cuiying
Zhang, Xinping
author_sort Yang, Jinghui
collection PubMed
description Interaction between femtosecond laser pulses with polymeric thin films induced transient optical annealing of the polymer molecules. Melting of the polymer films took place during the transient annealing process, so that a solid-liquid-solid phase transition process was observed. Ultrafast cooling of the melting polymer produced solidified droplets. Microscopic and spectroscopic characterization revealed that the polymer molecules were rearranged with preferable H-aggregation to reach the lowest formation energy during the melting process. Intermolecular coupling was enhanced due to the modified molecular arrangement. This observation of melting of polymeric semiconductors due to the interaction with femtosecond light pulses is potentially important for better understanding laser-matter interactions and for exploring organic optoelectronic devices through special material processing.
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spelling pubmed-64020372019-04-02 Femtosecond Optical Annealing Induced Polymer Melting and Formation of Solid Droplets Yang, Jinghui Huang, Cuiying Zhang, Xinping Polymers (Basel) Article Interaction between femtosecond laser pulses with polymeric thin films induced transient optical annealing of the polymer molecules. Melting of the polymer films took place during the transient annealing process, so that a solid-liquid-solid phase transition process was observed. Ultrafast cooling of the melting polymer produced solidified droplets. Microscopic and spectroscopic characterization revealed that the polymer molecules were rearranged with preferable H-aggregation to reach the lowest formation energy during the melting process. Intermolecular coupling was enhanced due to the modified molecular arrangement. This observation of melting of polymeric semiconductors due to the interaction with femtosecond light pulses is potentially important for better understanding laser-matter interactions and for exploring organic optoelectronic devices through special material processing. MDPI 2019-01-13 /pmc/articles/PMC6402037/ /pubmed/30960112 http://dx.doi.org/10.3390/polym11010128 Text en © 2019 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Yang, Jinghui
Huang, Cuiying
Zhang, Xinping
Femtosecond Optical Annealing Induced Polymer Melting and Formation of Solid Droplets
title Femtosecond Optical Annealing Induced Polymer Melting and Formation of Solid Droplets
title_full Femtosecond Optical Annealing Induced Polymer Melting and Formation of Solid Droplets
title_fullStr Femtosecond Optical Annealing Induced Polymer Melting and Formation of Solid Droplets
title_full_unstemmed Femtosecond Optical Annealing Induced Polymer Melting and Formation of Solid Droplets
title_short Femtosecond Optical Annealing Induced Polymer Melting and Formation of Solid Droplets
title_sort femtosecond optical annealing induced polymer melting and formation of solid droplets
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6402037/
https://www.ncbi.nlm.nih.gov/pubmed/30960112
http://dx.doi.org/10.3390/polym11010128
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