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1.
Preparation and performance of a transparent poly(3,4‐ethylene dioxythiophene)–poly(p‐styrene sulfonate‐co‐acrylic acid sodium) film with a high stability and water resistance
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Wanping Cai Xiangyan Ma Jiahong Guo Xing Peng Sai Zhang Zhoutong Qiu Jie Ying Jikui Wang 《应用聚合物科学杂志》2017,134(31)
Poly(p‐styrene sulfonate‐co‐acrylic acid sodium) (PSA) from the copolymerization of acrylic acid sodium and p‐styrene sulfonate monomers were used to dope poly(3,4‐ethylene dioxythiophene) (PEDOT) to generate PEDOT–PSA antistatic dispersions. Compared to those of the PEDOT–poly(p‐styrene sulfonate sodium) (PSS), the physical and electrical properties of the PEDOT–PSA conductive liquids were much better. The PEDOT–PSA films possessed a better water resistance without a decrease in the conductivity. The sheet resistance of the PEDOT–PSA–poly(ethylene terephthalate) (PET) films was about 1.5 × 104 Ω/sq with a 100 nm thickness, the same as the PEDOT–PSS–PET films. The transmittance of the PEDOT–PSA–PET films exceeded 88%. Furthermore, the environmental dispersity of the PEDOT–PSA antistatic dispersion was apparently improved by the dopant PSA so that the stability was extraordinarily promoted. Meanwhile, the water resistances of the PEDOT–PSA–PET and PEDOT–PSA films were also enhanced. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45163. 相似文献
2.
High cycling stability and well printability poly(3,4‐ethylenedioxythiophene):poly(styrene sulfonate)/multi‐walled carbon nanotube nanocomposites via in situ polymerization applied on electrochromic display
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A high cycling stability material and an additive manufacturing method are reported for the fabrication of solid electrochromic devices. The poly(3,4‐ethylenedioxythiophene):poly(styrene sulfonate)/multi‐walled carbon nanotube (PEDOT:PSS/MWCNT) nanocomposites were synthesized via in situ polymerization. A carboxymethyl cellulose gel was used as the ink vehicle for screen printing. The electrochromic (EC) performance of films patterned by screen printing was also examined. The results of characterization indicate that strong interfacial interactions occurred between PEDOT:PSS and the MWCNTs and the MWCNTs formed a network in these conducting polymers film, so the composite was more conductive than pure PEDOT:PSS. Devices containing PEDOT:PSS/MWCNTs were more stable after 1000 cycles, exhibited higher rate of ion exchange and faster increases in current. The composite containing 0.3 wt % MWCNTs also had a 23% higher color contrast (ΔE*) than pure PEDOT:PSS at 2.5 V applied voltages. The EC inks with well printability not only can be used to print large area films, but also can print fine lines and pixel‐type dots in displays. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45943. 相似文献
3.
Effect of microstructure on the dielectric properties of poly(vinyl alcohol)–poly(3,4‐ethylenedioxythiophene) doped with poly(styrenesulfonate) composite films
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Poly(3,4‐ethylenedioxythiophene) doped with poly(styrenesulfonate) (PEDOT–PSS) was blended with poly(vinyl alcohol) (PVA) to form 0, 10, 20, 30, 40, and 50 vol % PEDOT–PSS/PVA solutions, and their freestanding films were prepared with a simple and cost‐effective solution casting technique at 27 °C in the absence of additives. Field emission scanning electron microscopy images revealed changes in the cocontinuous network to a rodlike morphology in the composite films from 10 to 50 vol % PEDOT–PSS/PVA. The alternating‐current conductivity was found to obey Jonscher's power law. The obtained values of the dielectric constant at 27 °C were relatively high, and a maximum value of 6.7 × 104 at 100 Hz for 40 vol % PEDOT–PSS'/PVA was observed. The dielectric loss attained a maximum value of about 106 at 100 Hz for 40 vol % PEDOT–PSS/PVA. However, a decrease in the dielectric parameters was observed at 50 vol % PEDOT–PSS/PVA because of locally induced strain in the microstructure. The variations in polarization with respect to the applied electric field (P–E) were determined for 50, 100, and 500 Hz at 500 V for the freestanding composite films of lower concentrations up to 20 vol % PEDOT–PSS/PVA. In summary, the dielectric and P–E measurements confirmed that the electrical characteristics changed in accordance to the contribution from both resistive and capacitive sites in the PEDOT–PSS/PVA composites. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45079. 相似文献
4.
In this study, we prepared poly(3,4‐ethylenedioxythiophene) (PEDOT) via the chemical oxidation of the 3,4‐ethylenedioxythiophene monomer in a system consisting of miscible binary organic solvents, that is, acetonitrile (CH3CN) and chloroform (CHCl3). This successful technique was then used to synthesize a poly(3,4‐ethylenedioxythiophene) (PEDOT)/silver (Ag) nanocomposite as well. In this facile and efficient technique, a higher solubility of the oxidizing reagent, which originated from a relative enhancement in the polarity of the reaction medium, led to significant changes in the optical and thermal behaviors of the resulting products. To investigate the degree of validity of the technique applied, a pure sample of PEDOT (PEDOT I) was also synthesized with CHCl3 alone, and this was then compared with a sample prepared in CH3CN/CHCl3 binary solvents (PEDOT II). To prepare the PEDOT/Ag nanocomposite, first the PEDOT synthesized in binary solvents was thoroughly dissolved in a dimethyl sulfoxide solvent. Next, Ag nanopowder was uniformly dispersed in the previous solution of PEDOT with sonication. The PEDOT/Ag nanocomposite was then precipitated through the addition of a methanol nonsolvent. The approximate size of nano‐Ag within the polymer matrix was found to be about 40 nm. Scanning electron microscopy images of the pure PEDOT II and PEDOT/Ag nanocomposite exhibited an agglomerated sponge and nanospherical homogeneity, respectively. In comparison with PEDOT I, considerable redshifts in the ultraviolet–visible absorption spectra of the pure PEDOT II and PEDOT/Ag nanocomposite were observed. In addition, the thermostability order was found to be PEDOT/Ag > PEDOT II > PEDOT I at all temperatures above 300°C. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 2707–2712, 2013 相似文献
5.
Copolymers of 4‐vinylpyridine and styrene [P(4VP–St)s] with varied molar ratios were synthesized by means of radical mass polymerization with 2,2′‐azobisisobutyronitrile as an initiator. The insoluble (linear) pyridinium‐type polymers in the octyl‐pyridinium bromide form, which possess various macromolecular chain compositions, were prepared by the reaction of each P(4VP–St) with 1‐bromooctane. A series of membranes were prepared for use in electrochemistry. These membranes, prepared with quaternized poly(styrene‐co‐4‐vinylpyridine), were characterized by IRspectroscopy, X‐ray diffraction, differential scanning calorimetry, thermogravimetory, tensile strength measurements, scanning electron microscopy, and an electrochemistry workstation. Our emphasis was to select a membrane with appropriate properties for use in the electrochemistry field. A promising membrane was selected to use in the field of electrochemistry by these characterizations. This study could be the preparation for a study on the electrochemical properties of pyridinium‐type polymers. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 96: 2146–2153, 2005 相似文献
6.
Poly(3,4‐ethylenedioxythiophene) (PEDOT) doped with a series of anionic polysaccharides such as carboxymethyl cellulose, sodium hyaluronate, xanthan gum, pectin, gellan gum were prepared by electropolymerization in aqueous solutions. Some other dopants of potassium nitrate, potassium sulfate, sodium poly(styrenesulfonate), and sodium polyacrylate were used in comparison with the anionic polysaccharides. The electrochemical properties and stability of the obtained PEDOT films were also investigated. It was found that indium tin oxide (ITO) conductive glass could be used as the working electrode of the electropolymerization of EDOT and that the dopant had a great influence on polymerization potential and overoxidation potential. These charged biomolecules of anionic polysaccharides were found to facilitate electropolymerization of EDOT instead of common doping anions as counterion. The electroactive PEDOT films doped with anionic polysaccharides showed stable electrochemical properties, good texture, and adhesion properties to the ITO conductive glass. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012 相似文献
7.
Films of poly(3,4‐ethylenedioxythiophene) were prepared with single and multiple electropolymerization steps, where the numbers of polymerization steps (n's) were 3, 5, and 7, with identical experimental conditions and total polymerization times (τ's). The electroactivity of the films prepared with multiple steps remained almost unaltered when n increased, with the ability of the films to store charge with n > 3 being smaller than that of the films with similar thicknesses but derived from a single electrodeposition step. In contrast, the stability of the films produced with n polymerization steps was significantly higher than that of the films derived from a single step with the same τ, with the difference between the two systems increasing with n, that is, τ used to yield the films. On the other hand, although the morphological and topological characteristics of the surface and the electrical conductivity were affected by the procedure used to produce the films, the organization of the polymer molecules in the crystalline phase, the thermal stability, and the electronic properties (ionization potential, electron affinity, and lowest π–π* transition energy) were practically identical in both cases. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011 相似文献
8.
Acrylic acid is often used to make water‐soluble polymers while styrene is often modified to add special functions to polymers. However, when styrene and acrylic acid are copolymerized, the resulting polymer is much less water soluble. To regain water solubility, the effect of styrene sulfonic acid on solubility of poly(acrylic acid‐co‐styrene) copolymers was investigated. Even though acrylic acid polymers are known for their water solubility, the presence of styrene units within acrylic acid copolymers reduces the solubility of the copolymer substantially at the natural pH of the solutions. By adding styrene sulfonic acid as a termonomer, polymers that are water soluble at the natural pH of the polymerization could be obtained. The solubility of the polymer after removal of the solvent and by redissolving at different concentrations and pH levels is also reported. Solubility increases at higher pH especially with low styrene concentration in the copolymer. It was found that incorporation of as little as 5 mol % of styrene into poly(acrylic acid) reduced the aqueous solubility to less than 0.5 g dL?1 at pH 7. Upon adding 7 mol % styrene sulfonic acid as a termonomer, the water solubility increased to 5 g dL?1 at pH 7. At higher levels of styrene, more styrene sulfonic acid was needed, especially at low pH. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013 相似文献
9.
Long Zhang Yangping Wen Yuanyuan Yao Xuemin Duan Jingkun Xu Xiaoqiang Wang 《应用聚合物科学杂志》2013,130(4):2660-2670
Poly(2‐chloromethyl‐2,3‐dihydrothieno[3,4‐b][1,4]dioxine), a chloromethyl functionalized poly(3,4‐ethylenedioxythiophene) derivative (PEDOT‐MeCl), was synthesized electrochemically via the potentiostatic polymerization of its monomer in dichloromethane solution containing suitable tetrabutylammonium tetrafluoroborate, then it was used for the characterization of film properties and the fabrication of electrochemical sensor. The properties of the resulting PEDOT‐MeCl film were characterized by different methods such as cyclic voltammetry, electrochemical impedance spectroscopy, Fourier transform infrared and ultraviolet–visible techniques, scanning electron microscope, and thermogravimetric analysis. The PEDOT‐MeCl film displayed a good reversible redox activity, remarkable capacitance properties, good thermal stability, rough, and porous structure, especially fluorescent spectra indicated that PEDOT‐MeCl was a blue‐emitter with maximum emission centered at 396 and 398 nm. Finally, the PEDOT‐MeCl film was employed for the fabrication of the sensing electrode, and dopamine was chosen as a model analyte for the application of the electrochemical sensor. Results indicated that the PEDOT‐MeCl film as sensing interface was feasible, and studies of these film properties were very beneficial for studying properties and applications of other poly(3,4‐ethylenedioxythiophene) derivative films. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 2660–2670, 2013 相似文献
10.
The copolymerization of methylvinyldichlorosilane (MVDCS) and styrene was carried out with various monomer feed ratios under dechlorination conditions with sodium in toluene at 110°C. The copolymers were obtained in 84–95% yields. The copolymerization of MVDCS and styrene with monomer feed ratios of 1 : 0.25 and 1 : 0.5 mainly gave insoluble polymers. The copolymers synthesized with monomer feed ratios of 1 : 1, 1 : 3, and 1 : 7 contained soluble fractions of 3, 26, and 47%, respectively. The copolymers were characterized with infrared, 1H‐NMR, gel permeation chromatography, thermogravimetric analysis, pyrolysis/gas chromatography (PGC), X‐ray diffraction, and elemental analysis (silicon content). 1H‐NMR and PGC studies suggested that the soluble fractions were mainly polystyrene. PGC studies indicated that the copolymers obtained with monomer feed ratios of 1 : 0.25 and 1 : 0.5 did not have any significant amount of polystyryl blocks, whereas the copolymers obtained with higher styrene feed ratios contained appreciable amounts of polystyryl blocks. The composition of the insoluble fractions of the copolymers was obtained from PGC data and was in good agreement with the composition calculated from the silicon content of the copolymers.© 2004 Wiley Periodicals, Inc. J Appl Polym Sci 91:3774–3784, 2004 相似文献
11.
Enhanced thermoelectric performance by alcoholic solvents effects in highly conductive benzenesulfonate‐doped poly(3,4‐ethylenedioxythiophene)/graphene composites
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Benzenesulfonate‐doped poly(3,4‐ethylenedioxythiophene) (PEDOT‐Bzs)/graphene thermoelectric (TE) composites with various graphene filler contents were synthesized in five different kinds of solvents. Dodecylbenzenesulfonic acid (DBSA) was used to achieve good dispersion of graphene into the PEDOT matrix. Among the synthesized PEDOT materials, the one synthesized in methanol (PEDOT‐MeOH) had the highest electrical conductivity. X‐ray photoelectron spectroscopy (XPS) analysis showed almost the same charge carrier concentration for all PEDOT materials. However, the X‐ray diffraction (XRD) analysis highlighted the enhancement of PEDOT chain stacking by shorter‐chain alcoholic solvents, as a result of which the carrier mobility and electrical conductivity were increased. The electrical conductivity and the Seebeck coefficient of the PEDOT/graphene composites were significantly improved with increasing the graphene content, which strongly depended on increased carrier mobility. The thermal conductivity of the composites exhibited relatively small changes, attributed to phonon scattering effects. The maximum TE efficiency of the PEDOT‐MeOH/graphene composite with 75 wt % graphene showed a substantially improved value of 1.9 × 10?2, higher than that of the other PEDOT/graphene composites. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42107. 相似文献
12.
Mechanically enhanced electrically conductive films from polymerization of 3,4‐ethylenedioxythiophene with wood microfibers
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This study was aimed at enhancing the mechanical properties of poly(3,4‐ethylenedioxythiophene)/poly(styrene sulfonate) (PEDOT:PSS) using wood microfibers. Ultra fine friction grinding was conducted on wood particles to reduce their size to the micron scale and to induce fibrillation. Oxidative polymerization was performed on 3,4‐ethylenedioxythiophene (EDOT) monomer at seven dosages based on the content of microfibers in the formulation. The presence of PEDOT:PSS in the prepared films was verified by infrared spectroscopy and scanning electron microscopy. The composite films became stronger and stiffer as the fiber content increased. An EDOT:microfibers ratio of 33 wt % was considered the best among the seven tested levels, judging from their low sheet resistivity (340 Ω/sq.) and favorable tensile properties (38 MPa strength and 4.8 GPa stiffness). The selected films were also tested for their resistance to solvents to obtain information about their potential use in different environments. Among the tested solvents, sodium hydroxide greatly decreased the film conductivity. It also had the harshest effect on reducing the weight of the film. Findings from this study demonstrate the successful use of wood microfibers alternative to synthetic substrates and cellulose nanofiber as a supportive and reinforcing material for electrically conductive polymers. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45127. 相似文献
13.
The electrically conducting polyfuran/poly(2‐iodoaniline) (PFu/P2IAn) and P2IAn/PFu composites were prepared by chemical oxidative polymerization using polyfuran and poly(2‐iodoaniline) in HCl and CHCl3 media. The conductivities of composites were determined as a function of the amount of guest polymer. It was found out that the conductivities of P2IAn/PFu composites increased 100‐fold, whereas the conductivities of PFu/P2IAn composites did not show a specific increase. The composite compositions were altered by varying guest polymer feed ratios during preparation. Generally, the electrical conductivities of P2IAn/PFu composites increased with increasing the amount of PFu. Homopolymers and composites were further characterized thermally, employing thermogravimetry (TGA) and morphologically employing scanning electron microscopy (SEM). Further evidences concerning the polymer structures were obtained by FTIR and UV‐vis spectroscopies and magnetic susceptibility measurements. TGA results revealed that PFu/P2IAn among the homopolymers (PFu and P2IAn) and P2IAn/PFu composite have the highest thermal stability. The composites synthesized varying the host and the guest polymer order have different conductivities, morphological structures, and thermal properties. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 2823–2830, 2003 相似文献
14.
Synthesis and ferroelectric investigations of poly(vinylidene fluoride‐co‐hexafluoropropylene)‐Mg(NO3)2 films
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The free‐standing, flexible, and ferroelectric films of poly(vinylidenefluoride‐co‐hexafluoropropylene) [P(VDF‐HFP)] were prepared by spin coating method. The ferroelectric phase of the films was enhanced by adding magnesium nitrate Mg(NO3)2 in different wt % as the additive during the film fabrication. The effects on the structural, compositional, morphological, ferroelectric, dielectric, and leakage current behaviors of the films due to the addition of salt were analyzed. Based on the X‐ray diffraction (XRD) patterns and Fourier Transform Infrared (FTIR) spectra, it is confirmed that the addition of Mg(NO3)2 promotes the electroactive β phase that induces the ferroelectric property. The fiber‐like topography of the films exhibits a nodule‐like structure, and the roughness of the films increases by the addition of Mg(NO3)2. The ferroelectric studies show the higher polarization values for the composite films than that of the plain P(VDF‐HFP) film. The Piezo‐response force microscope images also confirm the domain switching behavior of the samples. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 44008. 相似文献
15.
Mechanical and thermal properties of poly(butylene succinate)/poly(3‐hydroxybutyrate‐co‐3‐hydroxyvalerate) biodegradable blends
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Biodegradable polymer blends of poly(butylene succinate) (PBS) and poly(3‐hydroxybutyrate‐co‐3‐hydroxyvalerate) (PHBV) were prepared with different compositions. The mechanical properties of the blends were studied through tensile testing and dynamic mechanical thermal analysis. The dependence of the elastic modulus and strength data on the blend composition was modeled on the basis of the equivalent box model. The fitting parameters indicated complete immiscibility between PBS and PHBV and a moderate adhesion level between them. The immiscibility of the parent phases was also evidenced by scanning electron observation of the prepared blends. The thermal properties of the blends were studied through differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). The DSC results showed an enhancement of the crystallization behavior of PBS after it was blended with PHBV, whereas the thermal stability of PBS was reduced in the blends, as shown by the TGA thermograms. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42815. 相似文献
16.
In this study, the effect of solvents on the morphology and conductivity of poly(3,4‐ethylenedioxythiophene):poly(styrenesulfonate)(PEDOT:PSS) nanofibers is investigated. Conductive PEDOT:PSS nanofibers are electrospun by dissolving a fiber‐forming polymer, polyvinyl alcohol, in an aqueous dispersion of PEDOT:PSS. The conductivity of PEDOT:PSS nanofibers is enhanced 15‐fold by addition of DMSO and almost 30‐fold by addition of ethylene glycol to the spinning dopes. This improvement is attributed to the change in the conformation of the PEDOT chains from the coiled benzoid to the extended coil quinoid structure as confirmed by Raman spectroscopy, X‐ray diffraction, and differential scanning calorimetry. Scanning electron microscopy images show that less beady and more uniform fiber morphology could be obtained by incorporation of ethylene glycol in the spinning dopes. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40305. 相似文献
17.
Poly(L ‐lactide‐co‐ε‐caprolactone)‐b‐poly(L ‐lactide) [P(LL‐co‐CL)‐b‐PLL] diblock copolyesters were synthesized in a two‐step process with 1‐dodecanol (DDC) and stannous octoate as the initiating system. In the first‐step reaction, a 50:50 mol % amorphous poly(L ‐lactide‐co‐ε‐caprolactone) [P(LL‐co‐CL)] copolyester was synthesized via the bulk copolymerization of L ‐lactide and ε‐caprolactone, which was followed by the polymerization of the PLL crystalline block at the end chain in the second‐step reaction. The yielded copolyesters were characterized with dilute‐solution viscometry, gel permeation chromatography, 1H‐ and 13C‐NMR, and differential scanning calorimetry methods. The molecular weights of the P(LL‐co‐CL) copolyesters from the first‐step reaction were controlled by the DDC concentrations, whereas in the second‐step reaction, the molecular weights of the P(LL‐co‐CL)‐b‐PLL diblock copolyesters depended on the starting P(LL‐co‐CL) copolyester molecular weights and L ‐lactide/prepolymer molar ratios. The starting P(LL‐co‐CL) copolyester molecular weights and PLL block lengths seemed to be the main factors affecting specific thermal properties, including the melting temperature (Tm), heat of melting (ΔHm), crystallizing temperature (Tc), and heat of crystallizing (ΔHc), of the final P(LL‐co‐CL)‐b‐PLL diblock copolyester products. Tm, ΔHm, Tc, and ΔHc increased when the PLL block lengths increased. However, these thermal properties of the diblock copolyesters also decreased when the P(LL‐co‐CL) block lengths increased. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007 相似文献
18.
Structural,optical, and conductive properties of a poly(styrene)‐b‐poly(thiophene) copolymer doped with fullerenes under different conditions
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Nikolaos Politakos Eftychia Grana Iñaki Zalakain Dimitrios Katsigiannopoulos Arantxa Eceiza Galder Kortaberria Apostolos Avgeropoulos 《应用聚合物科学杂志》2014,131(7)
19.
Veer Pal Singh Ramasubbu Ramani Ajit Shankar Singh Preeti Mishra Vijay Pal Amit Saraiya 《应用聚合物科学杂志》2016,133(41)
Herein, we present the dielectric and electrical conductivity properties of the partially miscible polymer blend prepared using pyrene functionalized polyaniline (pf‐PANI) and poly(vinylidene fluoride‐co‐hexafluoro propylene) (PVDF‐co‐HFP). The blend mostly retains the fluorescent nature of pf‐PANI as well as can be moldable and possesses good damping property. The dielectric properties have been investigated as a function of temperature at three different frequencies and the plausible origin of polarization responsible for dielectric behavior in this blend has been identified. The experimental results of dielectric measurements are compared with theoretical models and discussed. The surface morphology of the samples has been examined with a scanning electron microscope. The electrical conductivity has also been studied as a function of temperature and explained in terms of hopping of charge carriers/interconnected networks. The combined dielectric and conductivity results together with scanning electron microscope micrographs, reveal that there is hindrance to achieve percolation threshold even after pf‐PANI addition of 57 vol % and subsequent thermal treatment. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 44077. 相似文献
20.
Specroelectrochemical,switching kinetics,and chronoamperometric studies of dibenzyl derivative of poly(3,4‐propylenedioxythiophene) thin‐film‐based electrochromic device
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Raja Lakshmanan Palani Prabhu Raja Narayanapura Channegowda Shivaprakash Sindhu Sukumaran Nair 《应用聚合物科学杂志》2014,131(17)
The dibenzyl derivative of poly(3,4‐propylenedioxythiophene) (PProDOT‐Bz2) thin film is deposited onto ITO‐coated glass substrate by electropolymerization technique. The electropolymerization of ProDOT‐Bz2 is carried out by a three‐electrode electrochemical cell. The cyclic voltammogram shows the redox properties of electrochemically prepared films deposited at different scan rates. The thin films prepared were characterized for its morphological properties to study the homogeniety. Classic six‐layer structure of PProDOT‐Bz2 electrochromic device using this material was fabricated and reported for the first and its characterizations such as spectroelectrochemical, switching kinetics, and chronoamperometric studies are performed. The color contrast of the thin film and the device achieved are 64 and 40%, respectively, at λmax (628 nm). The switching time is recorded and the observed values are 5 s from the coloring state to the bleaching state and vice versa. The chronoamperometry shows that the device performed up to 400 cycles, and it is capable of working up to 35 cycles without any degradation. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40717. 相似文献