Layer-by-layer assembly of polymeric complexes for electrochromic applications

Layer-by-Layer (LbL) self-assembly has been proven to be a very facile and versatile method for thin film fabrication with precise control of the film components and structures. This technique possesses great advantage on integrating materials with different functionalities into a film with designed...

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Main Author: Cui, Mengqi
Other Authors: Lee Pooi See
Format: Theses and Dissertations
Language:English
Published: 2017
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Online Access:http://hdl.handle.net/10356/69621
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Institution: Nanyang Technological University
Language: English
id sg-ntu-dr.10356-69621
record_format dspace
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic DRNTU::Engineering::Materials::Functional materials
spellingShingle DRNTU::Engineering::Materials::Functional materials
Cui, Mengqi
Layer-by-layer assembly of polymeric complexes for electrochromic applications
description Layer-by-Layer (LbL) self-assembly has been proven to be a very facile and versatile method for thin film fabrication with precise control of the film components and structures. This technique possesses great advantage on integrating materials with different functionalities into a film with designed structures. These features enable LbL self-assembly technique to be a suitable platform for electrochemical applications, which usually require integration of multiple functional components and regulation of interface properties. Conventional polymer LbL films adopt individual polymers as building blocks. However, these films suffer from slow deposition process with only limited amount of materials could be deposited onto the substrate within a deposition cycle. Moreover, LbL films fabricated from individual polymers usually demonstrate compact structure, which also hinders their application in fabricating thin films of which non-compact configuration is preferred. Due to the basic requirements of LbL technique that the adjacent layer should directly interact with each other, this method possesses inherent drawbacks where multi-interfaces are not favourable. Further exploration and modification of LbL technique is desired for better utilization of this prospected technique on electrochemical applications. In this thesis, we focus on developing polymeric complexes as building blocks for LbL self-assembly, in order to surmount the drawbacks and broaden the application field of LbL technique. Polymeric complexes (PCs) are supramolecular assemblies built up by nonstoichiometric combination of two components. Compared with free polymers, PCs have several advantages including rich varieties of compositions, relatively large dimensions and diverse structures. Thus introducing PCs into LbL enriches the diversity of LbL films, especially for fast deposition of LbL films with special structures and functionalities. However, there are limited reports on using PCs as building blocks for LbL deposition for electrochemical device applications. Aiming at exploiting the potential and merits of adopting PCs in LbL for electrochemical related studies and applications, this thesis is devoted to develop suitable PCs as building blocks to fabricate LbL films for three typical components in an electrochromic device: the electrochromic active layer, the solid polymer electrolyte (SPE) layer as well as the transparent conducting film (TCF). Based on the basic mechanism and requirements of these three functional layers, different types of PCs were developed to achieve superior performance. Polyelectrolyte-polyelectrolyte complexes (PECs) were chosen as building blocks for electrochromic active layer, contributing to a fast growth LbL film with porous structure due to the relative large dimensions and charge accumulation of PECs. The resultant electrochromic active films presented larger colouration modulation as well as fast kinetics compared to conventional LbL films. Polymer-alphaCD inclusion complexes via host-guest interaction were designed and adopted as building blocks for LbL SPE layer fabrication. Taking merits of the steric effect of polymer-alphaCD complexes, the resultant LbL films possessed lower glass transition temperature and higher ionic conductivity compared to LbL films made from uncomplexed polymers. Conductive PCs were selected to form capping layer on conducting Ag nanowire network. The LbL overcoated films lowered surface roughness of the metallic network without sacrificing the conductivity of the whole layer. The existence of LbL coating was demonstrated to protect Ag nanowire network from oxidation corrosion during the redox reaction. In conclusion, adopting PCs as building blocks was demonstrated to be a feasible and effective method to fabricate LbL films for electrochemical device applications, surmounting the drawbacks of conventional LbL technique and delivering superior performance.
author2 Lee Pooi See
author_facet Lee Pooi See
Cui, Mengqi
format Theses and Dissertations
author Cui, Mengqi
author_sort Cui, Mengqi
title Layer-by-layer assembly of polymeric complexes for electrochromic applications
title_short Layer-by-layer assembly of polymeric complexes for electrochromic applications
title_full Layer-by-layer assembly of polymeric complexes for electrochromic applications
title_fullStr Layer-by-layer assembly of polymeric complexes for electrochromic applications
title_full_unstemmed Layer-by-layer assembly of polymeric complexes for electrochromic applications
title_sort layer-by-layer assembly of polymeric complexes for electrochromic applications
publishDate 2017
url http://hdl.handle.net/10356/69621
_version_ 1759854645995372544
spelling sg-ntu-dr.10356-696212023-03-04T16:47:02Z Layer-by-layer assembly of polymeric complexes for electrochromic applications Cui, Mengqi Lee Pooi See School of Materials Science & Engineering DRNTU::Engineering::Materials::Functional materials Layer-by-Layer (LbL) self-assembly has been proven to be a very facile and versatile method for thin film fabrication with precise control of the film components and structures. This technique possesses great advantage on integrating materials with different functionalities into a film with designed structures. These features enable LbL self-assembly technique to be a suitable platform for electrochemical applications, which usually require integration of multiple functional components and regulation of interface properties. Conventional polymer LbL films adopt individual polymers as building blocks. However, these films suffer from slow deposition process with only limited amount of materials could be deposited onto the substrate within a deposition cycle. Moreover, LbL films fabricated from individual polymers usually demonstrate compact structure, which also hinders their application in fabricating thin films of which non-compact configuration is preferred. Due to the basic requirements of LbL technique that the adjacent layer should directly interact with each other, this method possesses inherent drawbacks where multi-interfaces are not favourable. Further exploration and modification of LbL technique is desired for better utilization of this prospected technique on electrochemical applications. In this thesis, we focus on developing polymeric complexes as building blocks for LbL self-assembly, in order to surmount the drawbacks and broaden the application field of LbL technique. Polymeric complexes (PCs) are supramolecular assemblies built up by nonstoichiometric combination of two components. Compared with free polymers, PCs have several advantages including rich varieties of compositions, relatively large dimensions and diverse structures. Thus introducing PCs into LbL enriches the diversity of LbL films, especially for fast deposition of LbL films with special structures and functionalities. However, there are limited reports on using PCs as building blocks for LbL deposition for electrochemical device applications. Aiming at exploiting the potential and merits of adopting PCs in LbL for electrochemical related studies and applications, this thesis is devoted to develop suitable PCs as building blocks to fabricate LbL films for three typical components in an electrochromic device: the electrochromic active layer, the solid polymer electrolyte (SPE) layer as well as the transparent conducting film (TCF). Based on the basic mechanism and requirements of these three functional layers, different types of PCs were developed to achieve superior performance. Polyelectrolyte-polyelectrolyte complexes (PECs) were chosen as building blocks for electrochromic active layer, contributing to a fast growth LbL film with porous structure due to the relative large dimensions and charge accumulation of PECs. The resultant electrochromic active films presented larger colouration modulation as well as fast kinetics compared to conventional LbL films. Polymer-alphaCD inclusion complexes via host-guest interaction were designed and adopted as building blocks for LbL SPE layer fabrication. Taking merits of the steric effect of polymer-alphaCD complexes, the resultant LbL films possessed lower glass transition temperature and higher ionic conductivity compared to LbL films made from uncomplexed polymers. Conductive PCs were selected to form capping layer on conducting Ag nanowire network. The LbL overcoated films lowered surface roughness of the metallic network without sacrificing the conductivity of the whole layer. The existence of LbL coating was demonstrated to protect Ag nanowire network from oxidation corrosion during the redox reaction. In conclusion, adopting PCs as building blocks was demonstrated to be a feasible and effective method to fabricate LbL films for electrochemical device applications, surmounting the drawbacks of conventional LbL technique and delivering superior performance. Doctor of Philosophy (MSE) 2017-03-09T01:57:16Z 2017-03-09T01:57:16Z 2017 Thesis Cui, M. (2017). Layer-by-layer assembly of polymeric complexes for electrochromic applications. Doctoral thesis, Nanyang Technological University, Singapore. http://hdl.handle.net/10356/69621 10.32657/10356/69621 en 173 p. application/pdf