Showing papers on "Electrochromic devices published in 2020"

Fusing electrochromic technology with other advanced technologies: A new roadmap for future development

Abstract: Electrochromism is the phenomenon of certain materials reversibly changing their colours or optical properties through redox reactions under an applied electric field, which has found applications in smart windows, displays and so on. The past four decades have witnessed the rapid development of electrochromic technology; however, it remains severely developmentally challenged due to its limited practical applications. Predictably, as a colour control technology that gives visual information readable by the naked eye, electrochromism should have much wider applications by applying the visualization technique to various functional devices. Indeed, some recent research findings show that integrating electrochromic technology with other advanced technologies has imparted a new strong impetus for the further development of electrochromic technology. However, a systematic review of the literature on the fusing of electrochromic technology with other advanced technologies is still lacking, demonstrating the urgent need for further studies, although there are some review papers on electrochromic energy storage devices. In this review, we systematically discuss the recent advances in the fusing of electrochromic technology with other advanced technologies, including wearable technology, thermal control technology, energy storage technology, energy harvesting technology and sensing technology. The integration modes, design principles and performance optimization for different types of interdisciplinary electrochromic devices are highlighted. Finally, an outlook concerning future trends and issues in the research field is also provided.

Towards full-colour tunability of inorganic electrochromic devices using ultracompact fabry-perot nanocavities.

Abstract: Intercalation-based inorganic materials that change their colours upon ion insertion/extraction lay an important foundation for existing electrochromic technology. However, using only such inorganic electrochromic materials, it is very difficult to achieve the utmost goal of full-colour tunability for future electrochromic technology mainly due to the absence of structural flexibility. Herein, we demonstrate an ultracompact asymmetric Fabry-Perot (F-P) nanocavity-type electrochromic device formed by using partially reflective metal tungsten as the current collector and reflector layer simultaneously; this approach enables fairly close matching of the reflections at both interfaces of the WO3 thin layer in device form, inducing a strong interference. Such an interference-enhanced device that is optically manipulated at the nanoscale displays various structural colours before coloration and, further, can change to other colours including blue, red, and yellow by changing the optical indexes (n, k) of the tungsten oxide layer through ion insertion.

Transparent Zinc-Mesh Electrodes for Solar-Charging Electrochromic Windows

Abstract: Newly born zinc-anode-based electrochromic devices (ZECDs), incorporating electrochromic and energy storage functions in a single transparent platform, represent the most promising technology for next-generation transparent electronics. As the existing ZECDs are limited by opaque zinc anodes, the key focus should be on the development of transparent zinc anodes. Here, the first demonstration of a flexible transparent zinc-mesh electrode is reported for a ZECD window that yields a remarkable electrochromic performance in an 80 cm2 device, including rapid switching times (3.6 and 2.5 s for the coloration and bleaching processes, respectively), a high optical contrast (67.2%), and an excellent coloration efficiency (131.5 cm2 C-1 ). It is also demonstrated that such ZECDs are perfectly suited for solar-charging smart windows as they inherently address the solar intermittency issue. These windows can be colored via solar charging during the day, and they can be bleached during the night by supplying electrical energy to electronic devices. The ZECD smart window platform can be scaled to a large area while retaining its excellent electrochromic characteristics. These findings represent a new technology for solar-charging windows and open new opportunities for the development of next-generation transparent batteries.

Transparent inorganic multicolour displays enabled by zinc-based electrochromic devices

Abstract: Electrochromic displays have been the subject of extensive research as a promising colour display technology. The current state-of-the-art inorganic multicolour electrochromic displays utilize nanocavity structures that sacrifice transparency and thus limit their diverse applications. Herein, we demonstrate a transparent inorganic multicolour display platform based on Zn-based electrochromic devices. These devices enable independent operation of top and bottom electrochromic electrodes, thus providing additional configuration flexibility of the devices through the utilization of dual electrochromic layers under the same or different colour states. Zn–sodium vanadium oxide (Zn–SVO) electrochromic displays were assembled by sandwiching Zn between two SVO electrodes, and they could be reversibly switched between multiple colours (orange, amber, yellow, brown, chartreuse and green) while preserving a high optical transparency. These Zn–SVO electrochromic displays represent the most colourful transparent inorganic-based electrochromic displays to date. In addition, the Zn–SVO electrochromic displays possess an open-circuit potential (OCP) of 1.56 V, which enables a self-colouration behaviour and compelling energy retrieval functionality. This study presents a new concept integrating high transparency and high energy efficiency for inorganic multicolour displays. Transparent electrochromic displays with a richer colour palette are now possible. Electrochromic displays, which change their colour due to electrochemistry, are receiving interest due to their low power consumption but a lack of colours is problematic. Wu Zhang and coworkers from the University of Alberta in Canada and Louisiana State University in the USA fabricated multicolour displays using sodium ion stabilized vanadium oxide nanorods (Zn-SVO) as the electrochromic material. Two layers of this material, separated by a layer of zinc and a gel electrolyte were sandwiched between glass coated with indium tin oxide. Application of a small voltage causes the SVO film to exhibit a reversible switch between orange, yellow and green. The use of two independently-controlled films in the display provides a broader range of colours (orange, amber, yellow, brown, chartreuse and green).

Fabry-Perot Cavity-Type Electrochromic Supercapacitors with Exceptionally Versatile Color Tunability

Abstract: Electrochromic supercapacitors that can change their appearances according to their charged states are presently attracting significant interest from both academia and industry. Tungsten oxide is often used in electrochromic supercapacitors because it can serve as an active material for both benchmarking electrochromic devices and high-performance supercapacitor electrodes. Despite this, acceptable visual aesthetics in electrochromic supercapacitors have almost never been achieved using tungsten oxide, because, in its pure form, this compound only displays a 1-fold color modulation from transparent to blue. Herein, we defy this trend by reporting the first ever Fabry-Perot (F-P) cavity-type electrochromic supercapacitors based only on a tungsten oxide material. The devices were sensitively changeable according to their charge/discharge states and displayed a wide variety of fantastic patterns consisting of different, vivid colors, with both simple and complex designs being achieved. Our findings suggested a novel direction for the aesthetic design of intelligent, multifunctional electrochemical energy storage devices.

One-Dimensional π-d Conjugated Coordination Polymer for Electrochromic Energy Storage Device with Exceptionally High Performance.

Abstract: The rational design of previously unidentified materials that could realize excellent electrochemical-controlled optical and charge storage properties simultaneously, are especially desirable and useful for fabricating smart multifunctional devices. Here, a facile synthesis of a 1D π-d conjugated coordination polymer (Ni-BTA) is reported, consisting of metal (Ni)-containing nodes and organic linkers (1,2,4,5-benzenetetramine), which could be easily grown on various substrates via a scalable chemical bath deposition method. The resulting Ni-BTA film exhibits superior performances for both electrochromic and energy storage functions, such as large optical modulation (61.3%), high coloration efficiency (223.6 cm2 C-1), and high gravimetric capacity (168.1 mAh g-1). In particular, the Ni-BTA film can maintain its electrochemical recharge-ability and electrochromic properties even after 10 000 electrochemical cycles demonstrating excellent durability. Moreover, a smart energy storage indicator is demonstrated in which the energy storage states can be visually recognized in real time. The excellent electrochromic and charge storage performances of Ni-BTA films present a great promise for Ni-BTA nanowires to be used as practical electrode materials in various applications such as electrochromic devices, energy storage cells, and multifunctional smart windows.

Supramolecular G4 Eutectogels of Guanosine with Solvent‐Induced Chiral Inversion and Excellent Electrochromic Activity

Abstract: Supramolecular eutectogels, an emerging class of materials that have just developed very recently, offer a new opportunity for generating functional supramolecular gel materials in biocompatible anhydrous or low-water media. As the first example of supramolecular G4 eutectogels, complexes of natural guanosine and H3 BO3 exhibited excellent gelation capacity in choline chloride/alcohol deep eutectic solvents. The as-prepared supramolecular eutectogels displayed unexpected solvent-induced chiral inversion and significantly high ionic conductivity (up to 7.78 mS cm-1 ), as well as outstanding thixotropic/injectable properties, high thermal stability and excellent electrochromic activity. These features make these versatile supramolecular G4 eutectogels promising candidates for developing next-generation flexible electronics with low environmental impact.

Fast response of complementary electrochromic device based on WO 3 /NiO electrodes

Abstract: Nanoporous structures have proven as an effective way for enhanced electrochromic performance by providing a large surface area can get fast ion/electron transfer path, leading to larger optical modulation and fast response time. Herein, for the first time, application of vacuum cathodic arc plasma (CAP) deposition technology to the synthesis of WO3/NiO electrode films on ITO glass for use in fabricating complementary electrochromic devices (ECDs) with a ITO/WO3/LiClO4-Perchlorate solution/NiO/ITO structure. Our objective was to optimize electrochromic performance through the creation of electrodes with a nanoporous structure. We also examined the influence of WO3 film thickness on the electrochemical and optical characteristics in terms of surface charge capacity and diffusion coefficients. The resulting 200-nm-thick WO3 films achieved ion diffusion coefficients of (7.35 × 10−10 (oxidation) and 4.92 × 10−10 cm2/s (reduction)). The complementary charge capacity ratio of WO3 (200 nm thickness)/NiO (60 nm thickness) has impressive reversibility of 98%. A demonstration ECD device (3 × 4 cm2) achieved optical modulation (ΔT) of 46% and switching times of 3.1 sec (coloration) and 4.6 sec (bleaching) at a wavelength of 633 nm. In terms of durability, the proposed ECD achieved ΔT of 43% after 2500 cycles; i.e., 93% of the initial device.

Ultra-Low Power Electrochromic Heat Shutters Through Tailoring Diffusion-Controlled Behaviors.

Abstract: In this study, we propose low power consumption, all-in-one type electrochromic devices (ECDs) for effective heat shutters. Considering diffusion-controlled device operation, polymeric viologens (poly-viologens) are synthesized to lower the diffusivity of EC chromophores and to minimize self-bleaching. In comparison with devices based on mono-viologens corresponding to the monomer of poly-viologens, poly-viologen-containing ECDs exhibit advantages of lower coloration voltage (ca, -0.55 V) and higher coloration/bleaching cyclic stability (>1500 cycles). In particular, poly-viologen ECDs show remarkably reduced self-bleaching as designed, resulting in extremely low power consumption (∼8.3 μW/cm2) to maintain the colored state. Moreover, we successfully demonstrate solar heat shutters that suppress the increment of indoor temperature by taking the advantage of low-power operation and near-IR absorption of the colored poly-viologen-based ECDs. Overall, these results imply that the control of the diffusivity of EC chromophores is an effective methodology for achieving single-layered, low-power electrochemical heat shutters that can save indoor cooling energy when applied as smart windows for buildings or vehicles.

Simultaneously enabling dynamic transparency control and electrical energy storage via electrochromism

Abstract: Transparency-switchable electrochromic devices (ECDs) offer promising applications, including variable optical attenuators, optical shutters, optical filters, and smart windows for energy-efficient buildings. However, the operation of conventional ECDs requires external voltages to trigger coloration/de-coloration processes, which makes them far from being an optimal energy-efficient technology. Electrochromic batteries that incorporate electro-optical modulation and electrical energy storage functionalities in a single platform, are highly-promising in the realization of energy-efficient ECDs. Herein, we report a novel Zn-Prussian blue (PB) system for aqueous electrochromic batteries. By utilizing different dual-ion electrolytes with various cations (e.g. Zn2+-K+ and Zn2+-Al3+), the Zn-PB electrochromic batteries demonstrate excellent performance. We show that the K+-Zn2+ dual-ion electrolyte in the Zn-PB configuration endows a rapid self-bleaching time (2.8 s), a high optical contrast (83% at 632.8 nm), and fast switching times (8.4 s/3 s for the bleaching/coloration processes). Remarkably, the aqueous electrochromic battery exhibits a compelling energy retrieval of 35.7 mW h m-2, where only 47.5 mW h m-2 is consumed during the round-trip coloration-bleaching process. These findings may open a new direction for developing advanced net-zero energy-consumption ECDs.

Spectroelectrochemical Tracking of Nickel Hydroxide Reveals Its Irreversible Redox States upon Operation at High Current Density

Abstract: Transition-metal (oxy)hydroxides with an abundance of redox metal sites are important for the development of electrochromic devices, rechargeable metal–air batteries, pseudo-capacitors, and industr...

2D MoO 3 Nanosheets Synthesized by Exfoliationand Oxidation of MoS 2 for High Contrast and Fast ResponseTime Electrochromic Devices

Abstract: MoO3 has potential advantages in price and weight over more widely studied WO3 for electrochromic devices, but it typically suffers from inferior electrochromic performance. Here, it is demonstrate...

Electrodeposited Gold Nanostructures for the Enhancement of Electrochromic Properties of PANI-PEDOT Film Deposited on Transparent Electrode.

Abstract: Conjugated polymers (CPs) are attractive materials for use in different areas; nevertheless, the enhancement of electrochromic stability and switching time is still necessary to expand the commercialization of electrochromic devices. To our best knowledge, this is the first study demonstrating the employment of electrodeposited gold nanostructures (AuNS) for the enhancement of CPs’ electrochromic properties when a transparent electrode is used as a substrate. Polyaniline–poly(3,4-ethylenedioxythiophene) (PANI-PEDOT) films were electrodeposited on a transparent indium tin oxide glass electrode, which was pre-modified by two different methods. AuNS were electrodeposited at −0.2 V constant potential for 60 s using both the 1st method (synthesis solution consisted of 3 mM HAuCl4 and 0.1 M H2SO4) and 2nd method (15 mM HAuCl4 and 1 M KNO3) resulting in an improvement of optical contrast by 3% and 22%, respectively. Additionally, when using the 1st method, the coloration efficiency was improved by 50% while the switching time was reduced by 17%. Furthermore, in both cases, the employment of AuNS resulted in an enhancement of the electrochromic stability of the CPs layer. A further selection of AuNS pre-modification conditions with the aim to control their morphology and size can be a possible stepping stone for the further improvement of CPs electrochromic properties.

Electrically Activated UV-A Filters Based on Electrochromic MoO3- x

Abstract: Chromism-based optical filters is a niche field of research, due to there being only a handful of electrochromic materials. Typically, electrochromic transition metal oxides such as MoO3 and WO3 are utilized in applications such as smart windows and electrochromic devices (ECD). Herein, we report MoO3-x-based electrically activated ultraviolet (UV) filters. The MoO3-x grown on indium tin oxide (ITO) substrate is mechanically assembled onto an electrically activated proton exchange membrane. Reversible H+ injection/extraction in MoO3-x is employed to switch the optical transmittance, enabling an electrically activated optical filter. The devices exhibit broadband transmission modulation (325-800 nm), with a peak of ∼60% in the UV-A range (350-392 nm). Comparable switching times of 8 s and a coloration efficiency of up to 116 cm2 C-1 are achieved.

Electrochromic Niobium Oxide Nanorods

Abstract: Niobium oxide (Nb2O5) is an interesting active material for technologies ranging from catalysis and sensors to energy storage and electrochromic devices owing to its unique optical, electronic, and...

Tracking Dynamic Doping in a Solid-State Electrochromic Device: Raman Microscopy Validates the Switching Mechanism.

Abstract: Solid-state electrochromic devices often need appropriate characterization to establish the real working mechanism for optimization and diagnosis. Raman mapping has been used here to track “dynamic...

Toward Easy-to-Assemble, Large-Area Smart Windows: All-in-One Cross-Linked Electrochromic Material and Device

Abstract: Conventional electrochromic devices with a sandwich structure consist of multiple interfaces, which enhance electron trapping on the interfaces. Furthermore, crack generation in the electrochromic layer is inevitable due to repeated ion insertion and extraction during the service process. These problems increase the fabrication complexity and lead to poor performance and stability, which are severely limiting and prime concerns for the future development of the electrochromism field. Here, a strategy of synthesizing an all-in-one self-healing electrochromic material, TAFPy-MA, is presented, which has been utilized for the fabrication of a high-reliability, large-scale, and easy-assembly smart electrochromic window. The all-in-one self-healing electrochromic material can undergo in situ redox reactions with Li+ ions to reduce resistance transfer and avoid interface obstacles, and the reversible Diels-Alder cross-linking network structure can heal the cracks to improve the reliability of the electrochromic layer. High ion diffusivity (1.13 × 10-5 cm2 s-1), rapid color switching (3.9/3.7 s), high coloration efficiency (413 cm2 C-1), excellent stability (sustains 88.7% after 1000 cycles) and reliability (crack can be healed in 110 s), and large-scale smart windows (30 × 35 cm2) are achieved using the all-in-one electrochromic material, which exhibits fascinating and promising features for a wide range of applications in buildings, airplanes, etc.

Colorless-to-Black Electrochromism from Binary Electrochromes toward Multifunctional Displays.

Abstract: Cyclohexane-1,2,4,5-tetracarboxylic diimide with a nonconjugated core has been incorporated to bridge two conventional triphenylamine units. The obtained monomer has successfully hypsochromically shifted the maximum absorption wavelength by 10 nm in comparison to the one with a pyromellitic diimide bridge. Consequently, a colorless electrochromic (EC) polymer poly(bis(N,N-diphenyl-4-aminophenyl)cyclohexane-1,2,4,5-tetracarboxylic diimide) (PTPA-HDI) was electropolymerized on indium tin oxide (ITO)-coated glass. The morphology, absorption, and spectroelectrochemistry properties of polymer PTPA-HDI films electropolymerized by different scan cycles have been systematically investigated. It is found that comprehensive properties, such as color contrast and initial transparence, can be achieved for the polymer film electropolymerized by 15 scan cycles. Moreover, to realize colorless-to-black electrochromism, an asymmetric viologen derivative 1-(4-cyanophenyl)-1'-hexyl-4,4'-bipyridinium dihexafluorophosphate (HVCN) has been designed and straightforward synthesized. With the introduction of a cyanophenyl group and a hexyl chain on the two pyridinium units, colorless-to-green electrochromism can be realized for this processible viologen derivative. The absorption band at 495 nm of colorated PTPA-HDI compensates well for the valley in the absorption spectrum of colorated HVCN. Therefore, different types of colorless-to-black electrochromic devices (ECDs) are fabricated using polymer PTPA-HDI-deposited ITO electrode and HVCN-based gel electrolyte. Such a supporting electrolyte-free ECD with binary electrochromes exhibits fast coloration, high color contrast, and excellent reversibility. Furthermore, an encryption ECD is demonstrated by switching a black two-dimensional code. In addition, an autodigital display is integrated on a smart window and hence different functions can be realized in a single ECD. Overall, this study may facilitate the understanding of the EC behaviors of binary electrochromes and present a new path to design multifunctional displays.

Mechanical breathing in organic electrochromics

Abstract: The repetitive size change of the electrode over cycles, termed as mechanical breathing, is a crucial issue limiting the quality and lifetime of organic electrochromic devices. The mechanical deformation originates from the electron transport and ion intercalation in the redox active material. The dynamics of the state of charge induces drastic changes of the microstructure and properties of the host, and ultimately leads to structural disintegration at the interfaces. We quantify the breathing strain and the evolution of the mechanical properties of poly(3,4-propylenedioxythiophene) thin films in-situ using customized environmental nanoindentation. Upon oxidation, the film expands nearly 30% in volume, and the elastic modulus and hardness decrease by a factor of two. We perform theoretical modeling to understand thin film delamination from an indium tin oxide (ITO) current collector under cyclic load. We show that toughening the interface with roughened or silica-nanoparticle coated ITO surface significantly improves the cyclic performance. Though organic electrochromic devices are promising for various applications, their performance is limited by a cyclic change in volume of the material over time. Here, the authors study mechanical breathing in a model polymer and provide rules for the design of new mechanically-reliable materials.