The invention pertains to a process for the manufacture of a fluoropolymer film, to the fluoropolymer film obtainable therefrom and to use of said fluoropolymer film in electrochemical and photo-electrochemical devices.

Disclosed herein are new electrochromic materials, including small molecule, oligomeric, and polymeric electrochromic materials, and compositions comprising the electrochromic materials and a salt. Further disclosed are electrochromic devices prepared from the electrochromic materials and electrochromic material compositions. Also disclosed are melt processable polymeric electrochromic materials, melt processable compositions comprising the melt processable polymeric electrochromic material, and a salt; and devices prepared therefrom.

The present invention relates to an anodically-coloring electrochromic compound represented by the following Formula (I),

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With reference to Formula (I), R.sup.1 and R.sup.2 are each independently selected from linear or branched C.sub.3-C.sub.20 alkyl. The present invention also relates to electrochromic devices and compositions that include an anodically-coloring electrochromic compound represented by Formula (I).

The present invention is an electrochromic device which is provided with a first electrode; an electrochromic layer which is disposed on the first electrode, while containing an organic/metal hybrid polymer that contains at least an organic ligand and a metal ion to which the organic ligand is coordinated; an electrolyte layer which is disposed on the electrochromic layer; a counter electrode material layer which is disposed on the electrolyte layer and contains a conductive polymer; and a second electrode which is disposed on the counter electrode material layer. The conductive polymer may be at least one polymer that is selected from the group consisting of polypyrroles, polyanilines, polythiophenes, poly(p-phenylene)s, poly(3,4-ethylenedioxythiophene)-poly(styrene sulfonate)s (PEDOT:PSS), polyfluorenes, poly(p-phenylenevinylene)s, polythienylenevinylenes and organic/metal hybrid polymers.

An augmented display system with dynamic see-through transmittance control is disclosed. The augmented display system includes: an augmented display screen; a tandem electrochromic (EC) filter disposed over the augmented display screen. The tandem EC filter includes a first window having a dominant first transmittance characteristic and a second window having a dominant second transmittance characteristic; and an augmented display transmittance controller configured to individually control the activation of the first window and the second window of the tandem EC filter, wherein the augmented display transmittance controller is configured to: determine from an ambient light sensor output the transmittance required from the first window and the second window for a selected augmented display luminance; and apply appropriate drive voltage waveforms to the first window and the second window to achieve the determined transmittance.

An autonomous light management system for a window includes an electrochromic film stack comprising an electrochromic layer on a first transparent electrode, an ion storage layer on a second transparent electrode, and an electrolyte sandwiched between the ion storage and electrochromic layers. The electrochromic film stack exhibits a transmissive state or an absorptive state depending on charging or discharging of the electrochromic layer. The light management system further comprises an array of power units disposed on a front surface of the electrochromic film stack, where each power unit comprises at least one solar microcell. Collectively, the solar microcells cover an area no greater than about 6% of a total area of the front surface. The array of power units is configured to control the charging and discharging of the electrochromic layer, thereby manipulating light transmission through the electrochromic film stack.

It relates to a thermo-responsive dual band electrochromic device, which is capable of selectively controlling the amount of sunlight radiation transmitted in the visible and in the near-infrared regions by operating under four distinct optical regimes, namely: fully transparent, visible blocking, near-infrared blocking, and fully blocking. The device can be regulated either by an electric stimulus, namely by controlling the sign and the intensity of the applied bias voltage, or by a thermal stimulus. In the latter the attenuation of incoming thermal radiation results increased as temperature increases. The thermo-responsive dual band electrochromic device comprises a first electrode consisting of a first transparent conductive substrate topped by a first electro-optically active layer and a second electrode consisting of a second transparent conductive substrate topped by a second electro-optically active layer separated by a temperature-dependent ion conductive layer consisting of a thermo-responsive polymer gel, an ion conductor and a plasticizer.

The present invention concerns an electrochromic device, a method for depositing an organic electrochromic material and a method for producing an electrochromic device. The device is preferably an electrochromic display, preferably a full-color electrochromic display. The device preferably comprises an electrodeposited organic electrochromic material and/or a polymeric organic electrochromic material.

The present disclosure relates to a method for manufacturing a flexible electrochromic device, and more particularly, to a method for manufacturing a flexible electrochromic device that bonds an electrochromic part and a counter electrode part while solidifying a wet-coated electrolyte with ultraviolet rays, thereby being capable of eliminating the possibility of bubble generation in the electrolyte and improving transmittance characteristics and durability.

Composite assemblies are described that can be switched from a transparent state to a non transparent state, and in some examples even switched between different colors/reflectivities in the non transparent state. Switching between these states can be initiated by application of an electrical current to Ag carbon nanotube yarns in contact with an electrochromic electrolyte. The carbon nanotube yarns increase the efficiency with which electrons are provided to an electrolyte.