New pyrrolo[3,4‐c]pyrrole‐1,4‐dione (DPP) derivatives carrying 3,4‐ethylenedioxy‐thiophenylphenyl (EDOT‐phenyl) substituent groups in the 3‐ and 6‐position, or in the 2‐ and 5‐position of the DPP chromophore were synthesised and electrochemically polymerised. The properties of the polymers were investigated using cyclic voltammetry and UV/Vis absorption spectroscopy. It was found that the optical and electronic properties differ greatly between the two polymers. Materials with EDOT‐phenyl groups in the 3‐ and 6‐positions represent conjugated polymers with a low oxidation potential and reversible electrochromic properties, whereas the polymer with EDOT‐phenyl groups in the 2‐ and 5‐positions is non‐conjugated and possesses a high oxidation potential and irreversible redox behaviour.
The complex of Fe(II) ions of general formula [Fe L 2](BF4)2 with triphenylamine-hydrazone ligand L has been synthesized and characterized. Oxidative electropolymerization of the complex proceeded smoothly on the working electrode producing a homogenous thin film of metallopolymer. The film thickness and morphology of the layer was investigated by microscopy techniques such as scanning electron microscopy and atomic force microscopy, and the composition of the film was confirmed by X-ray photoelectron spectroscopy analysis. It was found that fifty successive oxidation/reduction cycles resulted in a 120 nm thick film on the electrode surface. The metallopolymer was also characterized using cyclic voltammetry and spectroelectrochemical methods. The film was found to change its color from yellow to green-blue, exhibit high change in transmittance of 60 % at 770 nm, and possess good electrochemical stability during 375 cycles of switching of the potential between −0.1 V and +1.5 V, owing to the presence of metal ions that link two ligand molecules resulting in formation of highly cross-linked film. The switching times (coloration and bleaching) were calculated to be 34.2 s and 7.3 s, respectively. Coloration efficiency of the formed film of polymeric complex was found to be 144 cm2 C−1. 相似文献
This work examines the proton intercalation in vanadium pentoxide (V2O5) thin films and its optical properties in the near-infrared (near-IR) region. Samples were prepared via direct current magnetron sputter deposition and cyclic voltammetry was used to characterize the insertion and extraction behavior of protons in V2O5 in a trifluoroacetic acid containing electrolyte. With the same setup chronopotentiometry was done to intercalate a well-defined number of protons in the HxV2O5 system in the range of x=0 and x=1. These films were characterized with optical reflectometry in the near-IR region (between 700 and 1700 nm wavelength) and the refractive index n and extinction coefficient k were determined using Cauchy ’s dispersion model. The results show a clear correlation between proton concentration and n and k. 相似文献
Poly(3,4‐ethylenedioxythiophene) (PEDOT) films are deposited, using an electroless method, onto flexible plastic poly(ethylene terephthalate) (PET) substrates of approximately 20×6 cm2. The sheet resistance of a PEDOT–PET film is approximately 600 Ω per square, and the nanoscale conductivity is 0.103 S cm?1. A plastic electrochromic PEDOT–Prussian blue device is constructed. The device undergoes a color change of pale blue to deep violet–blue reversibly over 1000 cycles, thus demonstrating its use as a light‐modulating smart window. The PEDOT–PET film is also used in a quantum dot solar cell, and the resulting photoelectrochemical performance and work function indicate that it is also promising for photovoltaic cells. The high homogeneity of the PEDOT deposit on PET, the optimal balance between conductivity and optical transparency, and the demonstration of its use in an electro‐optical device and a solar cell, offer the opportunity to use this electrode material in a variety of low‐cost optoelectronic devices. 相似文献
Organic electrochromic materials change color rapidly under applied potential. A butterfly‐shaped compound, 5,5′,‐5″,‐5′″‐(thieno[3,2‐b]thiophene‐2,3,5,6‐tetrayl) tetrakis‐(2,3‐dihydrothieno[3,4‐b][1,4]dioxine) (t‐EDOT‐TT) is synthesized for the first time and polymerized at different potentials via electropolymerization technique. By applying different polymerization potentials, the optical and electrochromic properties of this newly synthesized polymer can be tuned. Owing to the dependence of functional group position in the polymer structure on the redox potential, this polymer can be utilized in very interesting organic optoelectronic applications.
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