Organic Synthesis and Characteristics of Thin Films

A special issue of Coatings (ISSN 2079-6412). This special issue belongs to the section "Thin Films".

Deadline for manuscript submissions: closed (31 August 2022) | Viewed by 6278

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Guest Editor
Department of Chemical Engineering and Materials Engineering, National Yunlin University of Science and Technology, Yunlin 64002, Taiwan
Interests: electrochromic polymers; light-emitting diodes; solar cell; fuel cell; functional polymers and materials for optoelectronic devices
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Special Issue Information

Dear Colleagues,

Organic synthesis includes many types of interesting reactions, and it is an excellent technology for the mass production of polymers with thin film formations. The synthesized polymers can be applied to various scientific fields, especially energy fields such as electrochromism, dye-sensitized solar cells, organic catalysis, supercapacitors, and polymers’ thin films. There are several methods of preparing thin films. The thickness of polymer films ranges from 10-10 m to 10-6 m. Many novel effective organic synthetic methods are still being studied and published. Therefore, topics of interest have focused on the preparation of many types of organic and polymeric derivatives with thin film formations in organic synthesis, for generating both new carbon–carbon (C-C) and carbon–heteroatom (C-X) bonds. The organic and polymeric derivatives will be used as precursors for highly functionalized materials.

The Special Issue “Organic Synthesis and Characteristics of Thin Films” aims to present the most recent achievements in the organic synthesis not only of organic and polymeric derivatives with thin film formation but also of their applications. In addition, feature articles and review papers about the progress of thin film materials in particular areas are also welcome.

In particular, topics of interest include but are not limited to the following:

  • Brushed, main-chain, and cross-linking types of polymers;
  • Optoelectronic functional thin films;
  • Properties and characteristics of thin films;
  • Thin film applications;
  • Polymer thin films.

Prof. Dr. Tzi-yi Wu
Guest Editor

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Published Papers (3 papers)

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Research

17 pages, 22488 KiB  
Article
Electrochromic Polymers Based on 1,4-Bis((9H-carbazol-9-yl)methyl)benzene and 3,4-Ethylenedioxythiophene Derivatives as Promising Electrodes for Flexible Electrochromic Devices
by Chung-Wen Kuo, Jui-Cheng Chang, Yu-Xuan Lin, Pei-Ying Lee, Tzi-Yi Wu and Tsung-Han Ho
Coatings 2022, 12(5), 646; https://doi.org/10.3390/coatings12050646 - 09 May 2022
Cited by 4 | Viewed by 1338
Abstract
A 1,4-bis((9H-carbazol-9-yl)methyl)benzene (DCB)-containing homopolymer (P(DCB)) and four DCB- and ED-derivative (3,4-ethylenedioxythiophene (EDOT) and 3,4-ethylenedioxythiophene-methanol (EDm))-containing copolymers (P(DCB-co-ED), P(2DCB-co-ED), P(DCB-co-EDm), and P(2DCB-co-EDm)) were electropolymerized on ITO-polyethylene terephthalate (PET) substrates and their electrochromic performances were studied. DCB [...] Read more.
A 1,4-bis((9H-carbazol-9-yl)methyl)benzene (DCB)-containing homopolymer (P(DCB)) and four DCB- and ED-derivative (3,4-ethylenedioxythiophene (EDOT) and 3,4-ethylenedioxythiophene-methanol (EDm))-containing copolymers (P(DCB-co-ED), P(2DCB-co-ED), P(DCB-co-EDm), and P(2DCB-co-EDm)) were electropolymerized on ITO-polyethylene terephthalate (PET) substrates and their electrochromic performances were studied. DCB displays a lower Eonset than that of EDOT and EDm, conjecturing that the biscarbazole-containing DCB group shows a stronger electron-donating property than that of the ED derivatives. The P(2DCB-co-ED) film presents slate grey, dark khaki, and dark olive green at 0.0, 1.0, and 1.2 V. Bleaching-to-coloring switching studies of polymers show that P(2DCB-co-EDm) shows a high ΔT (31.0% at 725 nm) in solutions. Five dual-layer flexible electrochromic devices (ECDs) based on P(DCB), P(DCB-co-ED), P(2DCB-co-ED), P(DCB-co-EDm), and P(2DCB-co-EDm) as the anodic materials and PEDOT-PSS as the cathodic material are constructed. The P(2DCB-co-ED)/PEDOT-PSS flexible ECD shows a high ΔT (40.3% at 690 nm) and long-term electrochemical cycling stability, while the P(DCB-co-EDm)/PEDOT-PSS ECD shows a high ΔT (39.1% at 640 nm) and short response time (≤1.5 s). These findings offer us a new structural insight for the valuable design of conjugated polymers in high-contrast, flexible ECDs. Full article
(This article belongs to the Special Issue Organic Synthesis and Characteristics of Thin Films)
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17 pages, 8765 KiB  
Article
4-(Trifluoromethoxy)phenyl-Containing Polymers as Promising Anodic Materials for Electrochromic Devices
by Wen-Hsin Wang, Jui-Cheng Chang, Pei-Ying Lee, Yuan-Chung Lin and Tzi-Yi Wu
Coatings 2020, 10(12), 1251; https://doi.org/10.3390/coatings10121251 - 18 Dec 2020
Cited by 4 | Viewed by 2090
Abstract
Three 4-(trifluoromethoxy)phenyl-based polydithienylpyrroles (PTTPP, P(TTPP-co-DTC), and P(TTPP-co-DTP)) were synthesized electrochemically and their electrochromic behaviors were characterized. The introduction of electron withdrawing trifluoromethoxy unit in the side chain of polydithienylpyrroles (PSNS) decreases the HOMO and LUMO energy levels of PSNS. [...] Read more.
Three 4-(trifluoromethoxy)phenyl-based polydithienylpyrroles (PTTPP, P(TTPP-co-DTC), and P(TTPP-co-DTP)) were synthesized electrochemically and their electrochromic behaviors were characterized. The introduction of electron withdrawing trifluoromethoxy unit in the side chain of polydithienylpyrroles (PSNS) decreases the HOMO and LUMO energy levels of PSNS. PTTPP film displays three various colors (grayish-yellow at 0 V, grayish-blue at 1.0 V, and bluish-violet at 1.4 V) from reduced to oxidized states. The optical contrast of PTTPP, P(TTPP-co-DTC), and P(TTPP-co-DTP) electrodes are 24.5% at 1050 nm, 49.0% at 916 nm, and 53.8% at 1302 nm, respectively. The highest η of the PTTPP electrode is 379.64 cm2 C−1 at 1050 nm. Three ECDs based on PTTPP, P(TTPP-co-DTC), or P(TTPP-co-DTP) as anodic film and PProDOT-Et2 as cathodic film were fabricated. PTTPP/PProDOT-Et2 ECD showed high transmittance change (35.7% at 588 nm) and high η (890.96 cm2·C−1 at 588 nm). P(TTPP-co-DTC)/PProDOT-Et2 and P(TTPP-co-DTP)/PProDOT-Et2 ECDs showed high transmittance change, rapid response time, adequate open circuit memory, and good electrochemical redox stability. Based on these findings, this work provides novel insights for appropriate design of high transmittance change and high efficient multi-colored electrochromic polymers. Full article
(This article belongs to the Special Issue Organic Synthesis and Characteristics of Thin Films)
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22 pages, 1658 KiB  
Article
Optical, Electrochemical, Thermal, and Structural Properties of Synthesized Fluorene/Dibenzosilole-Benzothiadiazole Dicarboxylic Imide Alternating Organic Copolymers for Photovoltaic Applications
by Ary R. Murad, A. Iraqi, Shujahadeen B. Aziz, Sozan N. Abdullah, Rebar T. Abdulwahid and Sarkawt A. Hussen
Coatings 2020, 10(12), 1147; https://doi.org/10.3390/coatings10121147 - 24 Nov 2020
Cited by 7 | Viewed by 2099
Abstract
In this work, four donor–acceptor copolymers, PFDTBTDI-DMO, PFDTBTDI-8, PDBSDTBTDI-DMO, and PDBSDTBTDI-8, based on alternating 2,7-fluorene or 2,7-dibenzosilole flanked by thienyl units, as electron-donor moieties and benzothiadiazole dicarboxylic imide (BTDI) as electron-accepting units, have been designed and synthesized for photovoltaic applications. All polymers were [...] Read more.
In this work, four donor–acceptor copolymers, PFDTBTDI-DMO, PFDTBTDI-8, PDBSDTBTDI-DMO, and PDBSDTBTDI-8, based on alternating 2,7-fluorene or 2,7-dibenzosilole flanked by thienyl units, as electron-donor moieties and benzothiadiazole dicarboxylic imide (BTDI) as electron-accepting units, have been designed and synthesized for photovoltaic applications. All polymers were synthesized in good yields via Suzuki polymerization. The impact of attaching two different alkyl chains (3,7-dimethyloctyl vs. n-octyl) to the BTDI units upon the solubilities, molecular weights, optical and electrochemical properties, and thermal and structural properties of the resulting polymers was investigated. PFDTBTDI-8 has the highest number average molecular weight (Mn = 24,900 g·mol−1) among all polymers prepared. Dibenzosilole-based polymers have slightly lower optical band gaps relative to their fluorene-based analogues. All polymers displayed deep-lying HOMO levels. Their HOMO energy levels are unaffected by the nature of either the alkyl substituents or the donor moieties. Similarly, the LUMO levels are almost identical for all polymers. All polymers exhibit excellent thermal stability with Td exceeding 350 °C. X-ray powder diffraction (XRD) studies have shown that all polymers have an amorphous nature in the solid state. Full article
(This article belongs to the Special Issue Organic Synthesis and Characteristics of Thin Films)
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