Study on the growth of functional crystals guided by coalescence and stacking behaviors of P(VDF-TrFE) ferroelectric lamellar crystals

碩士 === 國立成功大學 === 材料科學及工程學系 === 107 === The unique polarity of P(VDF-TrFE) crystalline phase below curie transition temperature is attributed to the lattice packing of all-trans molecular segments, which allocates most of substituted fluorine atoms on one side of molecular segments and hydrogen atom...

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Main Authors: Chia-HungPan, 潘嘉宏
Other Authors: jrjeng Ruan
Format: Others
Language:zh-TW
Published: 2019
Online Access:http://ndltd.ncl.edu.tw/handle/ab7q2d
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spelling ndltd-TW-107NCKU51591002019-10-26T06:24:20Z http://ndltd.ncl.edu.tw/handle/ab7q2d Study on the growth of functional crystals guided by coalescence and stacking behaviors of P(VDF-TrFE) ferroelectric lamellar crystals P(VDF-TrFE)鐵電性板晶的融合及排列行為對功能性晶相分佈的影響 Chia-HungPan 潘嘉宏 碩士 國立成功大學 材料科學及工程學系 107 The unique polarity of P(VDF-TrFE) crystalline phase below curie transition temperature is attributed to the lattice packing of all-trans molecular segments, which allocates most of substituted fluorine atoms on one side of molecular segments and hydrogen atoms on the other side. In this study, the growth habits and stacking behavior of crystalline lamellae within thin films were explored. The coalescence of lamellar crystals has been identified to occur during the secondary crystallization above Curie temperature. It is viewed that, for the residue amorphous fractions in between lamellar crystals, the further crystallization above Curie temperature causes the assembly and coalescence of present lamellar crystal. With the presence of a limited fraction of amorphous poly(methyl methacrylate) (PMMA), the continuous coalescence and growth of lamellar crystals eventually result in regular stacking arrays. Furthermore, the shrinkage and deformation of the PMMA domains is observed as a result of continuous lamellae growth above the Curie temperature, and then the PMMA domains extends along the stacking direction of lamellar crystals. The fullerene derivative of [6,6]-phenyl C61 butyric acid methyl ester (PCBM) is observed to preferentially assemble into PMMA globular domains during solution casting. Due to the stress from deformed amorphous environment, the later induced crystal growth of PCBM is identified to be generally along the PMMA extension direction. The anisotropic deformation of PMMA amorphous domains is thus realized able to modify crystal growth within deformed domains. The involved phase interactions is expected to yield fruitful influences on the evolution of thin-film structures for desired physical properties. jrjeng Ruan 阮至正 2019 學位論文 ; thesis 64 zh-TW
collection NDLTD
language zh-TW
format Others
sources NDLTD
description 碩士 === 國立成功大學 === 材料科學及工程學系 === 107 === The unique polarity of P(VDF-TrFE) crystalline phase below curie transition temperature is attributed to the lattice packing of all-trans molecular segments, which allocates most of substituted fluorine atoms on one side of molecular segments and hydrogen atoms on the other side. In this study, the growth habits and stacking behavior of crystalline lamellae within thin films were explored. The coalescence of lamellar crystals has been identified to occur during the secondary crystallization above Curie temperature. It is viewed that, for the residue amorphous fractions in between lamellar crystals, the further crystallization above Curie temperature causes the assembly and coalescence of present lamellar crystal. With the presence of a limited fraction of amorphous poly(methyl methacrylate) (PMMA), the continuous coalescence and growth of lamellar crystals eventually result in regular stacking arrays. Furthermore, the shrinkage and deformation of the PMMA domains is observed as a result of continuous lamellae growth above the Curie temperature, and then the PMMA domains extends along the stacking direction of lamellar crystals. The fullerene derivative of [6,6]-phenyl C61 butyric acid methyl ester (PCBM) is observed to preferentially assemble into PMMA globular domains during solution casting. Due to the stress from deformed amorphous environment, the later induced crystal growth of PCBM is identified to be generally along the PMMA extension direction. The anisotropic deformation of PMMA amorphous domains is thus realized able to modify crystal growth within deformed domains. The involved phase interactions is expected to yield fruitful influences on the evolution of thin-film structures for desired physical properties.
author2 jrjeng Ruan
author_facet jrjeng Ruan
Chia-HungPan
潘嘉宏
author Chia-HungPan
潘嘉宏
spellingShingle Chia-HungPan
潘嘉宏
Study on the growth of functional crystals guided by coalescence and stacking behaviors of P(VDF-TrFE) ferroelectric lamellar crystals
author_sort Chia-HungPan
title Study on the growth of functional crystals guided by coalescence and stacking behaviors of P(VDF-TrFE) ferroelectric lamellar crystals
title_short Study on the growth of functional crystals guided by coalescence and stacking behaviors of P(VDF-TrFE) ferroelectric lamellar crystals
title_full Study on the growth of functional crystals guided by coalescence and stacking behaviors of P(VDF-TrFE) ferroelectric lamellar crystals
title_fullStr Study on the growth of functional crystals guided by coalescence and stacking behaviors of P(VDF-TrFE) ferroelectric lamellar crystals
title_full_unstemmed Study on the growth of functional crystals guided by coalescence and stacking behaviors of P(VDF-TrFE) ferroelectric lamellar crystals
title_sort study on the growth of functional crystals guided by coalescence and stacking behaviors of p(vdf-trfe) ferroelectric lamellar crystals
publishDate 2019
url http://ndltd.ncl.edu.tw/handle/ab7q2d
work_keys_str_mv AT chiahungpan studyonthegrowthoffunctionalcrystalsguidedbycoalescenceandstackingbehaviorsofpvdftrfeferroelectriclamellarcrystals
AT pānjiāhóng studyonthegrowthoffunctionalcrystalsguidedbycoalescenceandstackingbehaviorsofpvdftrfeferroelectriclamellarcrystals
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AT pānjiāhóng pvdftrfetiědiànxìngbǎnjīngderónghéjípáilièxíngwèiduìgōngnéngxìngjīngxiāngfēnbùdeyǐngxiǎng
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