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1.
V. F. Ivanov A. A. Nekrasov K. V. Tcheberiako A. V. Vannikov A. S. Posed'ko S. I. Lishik Yu. V. Trofimov 《Journal of the Society for Information Display》2003,11(1):11-14
Abstract— An all solid‐state photoelectrochromic element (PECE) was developed on the basis of electrochromic layers of WO3 and polyaniline with a layer of polymer electrolyte placed on a base of polyamidosulfoacid, in which a thin‐film CdSxSe1?x photoresistor was used as an electronic key. The dependence of the sensitometric characteristics of the PECE on the applied voltage was studied. 相似文献
2.
热处理WO3电变色膜稳定性研究 总被引:1,自引:0,他引:1
采用电子束蒸发淀积WO3薄膜。根据已有的WO3薄膜脱水过程结论而选择适当温度对薄膜进行退火处理。在大量含水的和不含水的两类Li^+电解质中进行比较性着色和消色循环实验,表明在290℃以下热退火处理能明显增加WO3薄膜在含水 电解质中的循环寿命。 相似文献
3.
Rajiv Prakash 《应用聚合物科学杂志》2002,83(2):378-385
Polyaniline was electrochemically synthesized from an aqueous medium with various acid electrolytes via potentiodynamic and potentiostatic techniques. The electrochemical synthesis of polyaniline was studied over various substrates, including Pt, Ti, Ni, and SnO2 coated glass, and in various acid electrolytes. Cyclic voltammograms of electrochemically synthesized polyaniline were studied in HCl in a pH range of 1–4. Probable electrochemistry and chemical changes were deduced that occurred when polyaniline film was electrochemically oxidized and reduced between ?0.2 and 1.0 V versus a Ag/AgCl reference electrode in an acidic electrolyte at pH 1, and three corresponding oxidation and reduction peaks were described instead of two redox peaks (as observed by W. S. Huang, B. D. Humphrey, and A. G. MacDiarmid, J Chem Soc Faraday Trans 1 1986, 82, 2385). The electrochromic property was studied with changes in the chemical states of polyaniline during electrochemical oxidation and reduction. A new viscous electrolyte, aqueous AlCl3 (pH 2), saturated with AgCl was used for the construction of an electrochromic display device. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 83: 378–385, 2002 相似文献
4.
Semiconducting molybdenum trioxide thin films have been prepared by employing simple and inexpensive spray pyrolysis technique.
Films are found to be polycrystalline in nature with hexagonal phase. Optical band gap energy (direct) and room temperature
electrical resistivity are of the order of 2·9 eV and 108 ohm-cm, respectively. These films exhibit cathodic electrochromism. 相似文献
5.
Solid-state electrochromic display devices (ECDs) have been prepared using vacuum deposited tungstic oxide as the primary electrochromic material. Such devices form colour during irradiation from a fluorescent-tube as light source. Initial experiments incorporated (evaporated) CdS films and the proton-conducting poly(ethylene oxide)-phosphoric acid electrolyte (1:1) plasticised with acetonitrile. Successful photoelectrochromic devices were prepared in this way provided the electrolyte was anhydrous, since films of CdS are sensitive to water-attack. Another device to evince photoelectrochromism was one containing layers of WO3 and V2O5. This combination of oxides was the most promising, responding to a 1/20s flash of intense white light. As yet, the colour formed in this way cannot be electro-bleached. These displays may also be used as normal—electrolytically driven—devices in the absence of irradiation. 相似文献
6.
The complementary electrochromic device, where the optical transmittance changes upon the flow of cations back and forth between anodic and cathodic electrodes, operates in a rocking-chair fashion if it can inherently self-discharge. Herein, the first demonstration of a dual-mode electrochromic platform having self-coloring and self-bleaching characteristics is reported, which is realized by sandwiching zinc metal within a newly-designed Prussian blue (PB)-WO3 rocking-chair type electrochromic device. It is demonstrated that the redox potential differences between the zinc metal and the WO3/PB electrodes endow the self-color-switching of these electrodes. By employing a hybrid electrolyte of Zn2+/K+, it is further shown that the colored PB-WO3 rocking-chair device is capable of spontaneously bleaching when the anodic and cathodic electrodes are coupled. This dual-mode light-control strategy enables the electrochromic devices to exhibit four distinct optical states with the highest optical contrast of 72.6% and fast switching times (<5 s for the bleaching/coloration processes). Furthermore, the built-in voltage of the dual-mode electrochromic devices not only promotes energy efficiency, but also augments the bistability of the devices. It is envisioned that the broad implication of the present platform is in the development of self-powered smart windows, colorful displays, optoelectronic switches, and optical sensors. 相似文献
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A copolymer based on pyrrole and 3,4‐ethylenedioxythiophene (EDOT) was electrochemically synthesized on an indium tin oxide ITO/glass electrode in acetonitrile containing lithium perchlorate (LiClO4). The resultant copolymer is characterized via cyclic voltammetry, FTIR, SEM, XPS, and spectroelectrochemical analysis. The spectroelectrochemical analysis revealed the copolymer film has distinct electrochromic properties with respect to the homopolymers, and presented four colors (amaranth, brick red, dark grey, and light blue) under various applied potentials. For the copolymer in the neutral state, the calculated onset energy for the π–π* transition (Eg) is 1.69 eV, and the absorption peak (λmax) is located at 508 nm. The maximum transmittance contrast (ΔT%) is 39.2% at 946 nm between the fully oxidized and intermediate(?0.4 V) states. Successive cyclic voltammograms and electrochromic switching experiment indicate the good stability of the copolymer because of the incorporation of EDOT units into the polypyrrole. It retains 81% of the original electroactivity and 71.8% of contrast after 2000 cycles. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013 相似文献
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