Electrochromic devices (ECDs) are emerging as novel technology for various applications ranging from commercialized smart window glasses, goggles, and autodimming rear view mirrors to uncommon yet more sophisticated applications such as infrared camouflage in military and thermal control in space satellites. The development of low-power, lightweight, inexpensive, and flexible devices is the need of the hour. In this respect, utilizing PEDOT:PSS as transparent conducting electrode (TCE) to replace indium tin oxide (ITO) and metal based TCEs for ECDs is a promising solution for the aforementioned requirements. In this work we have demonstrated the performance of PEDOT:PSS films coated on flexible substrates, treated with PTSA-DMSO, as TCEs for ECD applications and their comparison with that of ITO based ECDs. The PEDOT:PSS based flexible TCEs used in this study have conductivity of 1400-1500 S·cm and figure of merit (FoM) of 70-77. The process of increasing the conductivity of PEDOT:PSS films also led to the broadening of the conducting potential window (CPW), which is important for electrochemical applications of PEDOT:PSS when used as a stand-alone electrode. More than achieving a comparable electrochromic contrast, switching time, and coloration efficiency with respect to the ITO based ECDs, PEDOT:PSS devices also had the added advantage of good mechanical flexibility. These devices demonstrated superior stability during electrochemical cycling and multiple mechanical bending tests, making them an inexpensive alternative to the costly ITO based ECD technology.
Conductivity enhancement of thin transparent films based on poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) (PEDOT-PSS) by a solution-processed route involving mixture of an organic acid and organic solvent is reported. The combined effect of p-toluenesulfonic acid and dimethyl sulfoxide on spin-coated films of PEDOT-PSS on glass substrates, prepared from its commercially available aqueous dispersion, was found to increase the conductivity of the PEDOT-PSS film to ∼3500 S·cm(-1) with a high transparency of at least 94%. Apart from conductivity and transparency measurements, the films were characterized by Raman, infrared, and X-ray photoelectron spectroscopy along with atomic force microscopy and secondary ion mass spectrometry. Combined results showed that the conductivity enhancement was due to doping, rearrangement of PEDOT particles owing to phase separation, and removal of PSS matrix throughout the depth of the film. The temperature dependence of the resistance for the treated films was found to be in accordance with one-dimensional variable range hopping, showing that treatment is effective in reducing energy barrier for interchain and interdomain charge hopping. Moreover, the treatment was found to be compatible with flexible poly(ethylene terephthalate) (PET) substrates as well. Apart from being potential candidates to replace inorganic transparent conducting oxide materials, the films exhibited stand-alone catalytic activity toward I(-)/I3(-) redox couple as well and successfully replaced platinum and fluorinated tin oxide as counter electrode in dye-sensitized solar cells.
In this communication, we report on a solvent free chemical oxidative polymerization route for the monomers based on 3,4-propylenedioxythiophenes wherein the process is applicable to both solid as well as liquid monomers and results in the bulk synthesis of ultra high molecular weight polymers.
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