Electrochromic Research Articles

An IoT-enabled monitoring and control system for electrochromic smart windows

Electrochromic (EC) smart windows are highly efficient in preventing solar irradiation. Nevertheless, an insufficient automated monitoring and control system for EC windows has been observed. This study outlined the framework for designing a control system that effectively regulated the voltage polarity of an EC smart window. Integrating Internet of Things (IoT) capabilities and environmental sensors enhanced the smart window control system. This integration allowed for automated monitoring and adjustment of light intensity (below and above 30,000 lx), temperature (below and above 32 °C), and UV index (below 3 and above 7) for the smart window. The magnitude of the current supplied from the output load of the operational circuit module was directly correlated with the switching time of the electrochromic window. Moreover, voltage fluctuation was observed during the evaluation testing of the control system, which was ascribed to the reliability of the breadboard platform. This study also provided a functional design analysis for a Wi-Fi-enabled control system, presented insights into manual and automatic control modes under diverse environmental conditions, and improved user interaction through real-time data visualization using the IoT Blynk platform. Overall, this study presented a range of cost-effective approaches for managing the dynamic EC window using Wi-Fi and sensor-enabled technology.

A Local‐Dissociation Solid‐State Polymer Electrolyte with Enhanced Li+ Transport for High‐Performance Dual‐Band Electrochromic Smart Windows

AbstractWindows through heat exchange play a vital role in energy saving for realizing a net‐zero carbon emission society. Dual‐band electrochromic (EC) smart windows by dynamically regulate visible (VIS) and near‐infrared (NIR) light are necessary for improving both building energy efficiency and habitant comfort. However, the rational design of high‐performance electrochromic devices (ECDs) suffers sluggish EC response due to the slow ion transport. In this work, a locally dissociated Li+ concept is proposed to construct a solid‐state polymer electrolyte (SPE) with ultrafast Li+ transport. The succinonitrile (SN) is employed to loosen the Li+‐anion pair and the crystallographic C─O chain in the poly(ethylene glycol) methyl ether methacrylate (PEGMA) electrolyte by its strong solvation capability. The as‐prepared SPE shows a high ionic conductivity of 6.48 mS cm−1 at 30 °C and a high transmittance of >90%. The SPE‐based EC smart windows exhibited a fast switching speed (3.0/3.2 s for coloration/bleaching), a high coloration efficiency (CE) of 373.8 cm2 C−1, and a high optical modulation in the full solar spectrum (85%, 70%, 43% at 673, 1200, and 1600 nm, respectively). Finally, the SPE‐based EC smart windows shows three working modes with a temperature regulation range of 19.1 °C, exhibiting great potential in practical application.

Electrochromic windows and flexible devices based on viologen-containing hydrogel electrolytes

Electrochromic devices (ECDs) with reversible optical modulation have great potential for smart window and flexible device applications. In this study, we propose low-power consumption, all-in-one-type ECDs based on LiCl-containing polyacrylamide (PAAm) hydrogel as a transparent and flexible gel electrolyte. Hydrophilic 1,1′-bis(3-hydroxypropyl) viologen dibromide (V-OHP) was served as the electrochromic (EC) material, hydroquinone (H2Q) was used as the anodic species, and H2Q/V-OHP/LiCl molar ratio was adjusted to obtain a balanced charge for the desired redox states of V-OHP. The basis for using V-OHP is derived from its hydroxyl groups, which enhance the hydrophilic characteristics of the radical cation (V-OHP*) and, as a result, the stability of the colored radical cations. This leads to enhanced stability, longer cycle life, and improved device dynamics. Investigations were also conducted into the EC behavior of viologen in solution. Following the utilization of various ECDs with various ratios of LiCl and H2Q, the most optimal sample was chosen and its efficiency in the application of EC windows and flexible devices was assessed. The created EC windows demonstrated distinct features including a significant contrast, outstanding stability, and a substantial cycle life (preserving over 94 % of the original transmittance after 800 cycles). Distinct device dynamics were also evident at a voltage of − 1.4 V with a time constant of about 10 s for coloring and 33 s for bleaching in open circuit condition.

Nanostructure of TiO\(_{2}\) and WO\(_{3}\) multilayer films deposited on ITO glass for electrochromic enhanced photocatalytic activity

The photocatalytic activity (PA) by electrochromic (EC) enhancement of single and multilayer films of TiO2, WO3, TiO2/WO3, and WO3/TiO2 was investigated. All films were deposited from metal on an ITO glass substrate using direct current (DC) magnetron sputtering via an oblique angle deposition (OAD) technique at 85°. Subsequently, a thermal oxidation (TO) process at 500℃ was applied for the samples to form metal oxide films. The morphology, elemental composition, crystal structure, and optical properties were studied by using field emission scanning electron microscopy (FE-SEM), energy-dispersive X-ray spectroscopy (EDS), X-ray diffractometry (XRD), and UV-vis spectroscopy, respectively. The photocatalytic properties were investigated by showing the degradation rate of methylene blue (MB) solution as an organic pollutant that was examined under ultraviolet irradiation of 300 µW∙cm‒2. The film samples were investigated by comparing the pre-color and colored states that were achieved through the EC process. The EC properties of WO3 led to increased charge insertion on the film surface. This observation was further supported by cyclic voltammetry (CV) testing, which revealed a higher current density for the thin film samples. The photodegradation results showed that the samples in the colored state exhibited a significantly higher degradation rate of MB compared to the pre-color state.

Revealing Enhanced Optical Modulation and Coloration Efficiency in Nanogranular WO3 Thin Films Through Precursor Concentration Modifications

Electrochromic (EC) materials allow for dynamic tuning of optical properties via an applied electric field, presenting great potential in energy-efficient technologies, such as smart windows for effective light and temperature regulation. The precise control of precursor concentration has proven to be a powerful approach in tailoring the physicochemical properties of semiconducting metal oxides. In this study, we employed a one-step electrodeposition technique to fabricate tungsten oxide (WO3) thin films, systematically exploring how varying precursor concentrations influence the material’s characteristics. X-ray diffraction analysis revealed significant changes in diffraction patterns, reflecting subtle structural modifications due to concentration variations. Additionally, scanning electron microscopy revealed significant changes in the microstructure, showing a progression from small nanogranules to larger agglomerations within the film matrix. The W-25 mM thin film delivered exceptional EC performance, efficiently accommodating lithium ions while showcasing superior EC properties. The optimized electrode, denoted as W-25 mM, showcased exceptional EC metrics, featuring the highest optical modulation at 82.66%, outstanding reversibility at 99%, and a notably high coloring efficiency of 83.01 cm2/C. These findings emphasize the importance of precursor concentration optimization in enhancing the EC properties of WO3 thin films, contributing to the advancement of high-performance, energy-efficient materials.

A Wide Color Gamut and Noniridescent Zinc-Anode Asymmetric Electrochromic Device for Self-Sustaining Color-Adaptive Bio-Camouflage System.

Inspired by camouflage-colored organisms, the development of bio-camouflage systems using electrochromic (EC) technology has gained significant interest. However, existing EC systems struggle with achieving a wide color gamut, noniridescent colors, and self-sustainability. Herein, a self-sustainable color-adaptive bio-camouflage system integrating EC and nanogenerator (NG) technologies, enabling environmental color adaptation, and thermal regulation without an external power source is proposed. The system is based on a zinc-anode EC device (ZECD) with an asymmetric structure, incorporating flexible tungsten oxide and vanadium oxide electrodes. During the EC process, tungsten oxide shifts between blue and transparent, allowing near-infrared thermal modulation, while the vanadium oxide transitions from yellow to transparent. This design enables reversible near-infrared modulation and noniridescent color conversion among black, blue, green, yellow, and transparent. For the self-sustainability of the system, an electromagnetic and triboelectric hybrid NG that collects biomechanical energy is developed. In a typical driven cycle, the integrated system transitions colors and achieves significant near-infrared spectral modulation, demonstrating environmental adaptability and thermal regulation. Experiments on human skin and simulated chameleon color changes further confirm the system's effectiveness. This work highlights the potential of integrating EC and NG technologies to advance color-adaptive camouflage systems, opening new an avenue for bio-camouflage design.

Carbazole-Based Dual-Band Electrochromic Polymers: The Effect of Linkage Sites on Electrochromic Performance.

Dual-band electrochromic (EC) materials are expected to be utilized as building materials for energy saving, but their cycle stability is still an obstacle. Here, two D-A conjugated polymers, PDPPCz36 and PDPPCz27, based on diketopyrrolopyrrole and carbazole linked with different sites, are synthesized. Both of them exhibit dual-band EC behaviors with a dark blue color in the neutral state and high absorption in the near-infrared (NIR) region when oxidized. However, PDPPCz36 exhibits better cycle stability and a shorter response time than PDPPCz27. In the visible (VIS) region, the PDPPCz36 film exhibits an initial light modulation range (ΔT) of 43.0% and that of the PDPPCz27 film is 41.3%. After 100 cycles of redox, the ΔT of the PDPPCz36 film declines by 32%, while that of PDPPCz27 attenuates by more than 50%. A similar tendency is evident in the NIR region. Moreover, PDPPCz36 shows subsecond colored switch times both in the VIS (0.4 s) and NIR (0.7 s) regions, while those of PDPPCz27 are 2.1 and 1.6 s, respectively. Further research suggests that 3,6-linked carbazoles in PDPPCz36 simultaneously inhibit the side reaction and film aggregation, which leads to better redox stability and shorter response time in both EC tests and devices.

Facilitating Charge Transfer via Ti-Knot Pathway in Electrochromic Three-Dimensional Metalated Covalent Organic Frameworks.

Due to the ordered one-dimensional channel as well as accessible redox sites, two-dimensional covalent organic frameworks (2D COFs) have garnered extensive attention in the field of electrochromism. However, organic 2D frameworks impose limitations on charge transfer and the weak interlayer interactions in 2D COFs, adversely affecting the stability during switching processes. Herein, we introduced Ti knots to construct three-dimensional metalated covalent organic frameworks (3D MCOFs), denoted as Ti-DHTA-Py. The Ti knots not only serve as templates for organizing organic units into unique 3D topological structures in a controlled manner but also establish charge transfer pathways conducive to electron delocalization and transmission within the framework. As a result, the 3D Ti-DHTA-Py MCOFs electrode exhibited a reduced band gap and remarkable electrochromic (EC) performances: electrochemical cyclic stability of 93.6% retention after 500 cycles, switching times (2.5 s/0.5 s), and a high coloration efficiency (423 cm2 C-1). This research underscores the potential of 3D MCOFs as promising candidates for advancing EC technologies, surmounting the limitations associated with traditional 2D COFs.

Optical and Structural Properties of V2O5 Electrochromic Thin Films

The increase in global temperature has led to a significant surge in energy consumption within the air conditioning industry, resulting in environmental deterioration. Electrochromic (EC) windows have emerged as a promising solution to address these challenges. Vanadium pentoxide (V2O5) stands out among all metal oxide materials due to its remarkable EC properties, including substantial Li+ ion insertion capacity and multicolor capabilities. Despite the potential of V2O5, there remains a lack of comprehensive research on the structural and optical properties of V2O5 films with varying thicknesses. Therefore, this study aims to investigate the structural and optical properties of V2O5 thin films with thicknesses ranging from 46 to 344 nm. By employing the sol-gel spin coating method, V2O5 thin films were fabricated and analyzed using X-ray diffraction (XRD) spectroscopy and ultraviolet-visible (UV-Vis) spectrophotometry. The fabricated V2O5 thin films with thicknesses of 46-274 nm demonstrated an average film transparency of 83 %. XRD analysis further revealed that the V2O5 thin films reached their peak crystallinity at a thickness of 344 nm. Moreover, CV analysis revealed that the V2O5 device, with a thickness of 274 nm, exhibited a cathodic peak current of -1.63 mA, indicating its excellent ability to facilitate Li+ ion diffusion. Additionally, CA measurements displayed a high optical modulation of 37.78 %. Ultimately, this research contributes to the development of energy-efficient solutions for sustainable environmental practices.

Synergistic design of processable Nb2O5-TiO2 bilayer nanoarchitectonics: enabling high coloration efficiency and superior stability in dual-band electrochromic energy storage

This paper introduces a proof of concept for a dual-band electrochromic (EC) device to modulate solar light transmission across visible and near-infrared regions selectively. EC materials based on ion insertion/extraction mechanisms also present the possibility for energy storage, widening its functionality to the supercapacitor platform. The bi-functional performance of dual-band radiation control and energy storage was achieved by exploiting two earth-abundant metal oxides that could absorb two different spectral regions when electrochemically charged. The bilayer structure was prepared using a one-step hydrothermal method, which produced Nb2O5-TiO2 bilayer on fluorine-doped tin oxide (FTO) conducting glass substrates. The nano-dimensions of the active materials endorse the development of high-transparency thin film under open circuit conditions. The variations in the TiO2 annealing temperature influence the crystallinity and surface morphology of the thin films, which influence the performance of dual-band EC energy storage. The well-optimized NT-500 sample facilitated exclusive electron-charge transport, producing excellent electrochemical performance in dual-band EC and energy storage. A large optical modulation of 80.4 % and 89.8 % at 600 nm and 800 nm (near-infrared) was achieved with an enhanced areal capacitance of 88.1 mF/cm2 and excellent cycling stability after continuous coloring/bleaching cycles for 18,000 s. This paper presents a prototype bi-functional device based on NT-500, which showed independent control and modulation of visible and near-infrared transmittance. Notably, the device retained excellent energy storage performance alongside its advanced optical functionalities. This bilayer nanostructure capitalizes on the inherent electrochemical properties of both materials and introduces novel features that can potentially revolutionize the platform of EC-energy storage.

Triphenylamine-Based Covalent Organic Framework Films for Dopamine-Responsive Electrofluorochromism.

Covalent organic framework (COF) film with electrofluorochromic (EFC) and electrochromic (EC) properties has been synthesized by using triphenylamine-based monomers. The film exhibited a high maximum fluorescence contrast of 151 when subjected to a drive voltage of 0.75 V vs the Ag/AgCl electrode, causing the fluorescence to be quenched, which resulted in the EFC process's "fluorescence off" state. The switching times for the fluorescence on and off states were 0.51 and 7.79 s, respectively. Over the same voltage range, the COF film also displayed EC properties, achieving a contrast of 50.23% and a coloration efficiency of 297.4 cm2 C-1 at 532 nm, with switching times of 18.6 s for coloration and 0.7 s for bleaching. Notably, the quenched fluorescence of the COF film could be restored by adding dopamine as a reductant. This phenomenon enabled the implementation of a NAND logic gate using the applied potential as a physical input and dopamine addition as a chemical input. This study demonstrates the successful development of COF films with bifunctional EFC and EC properties, showcasing their potential for use in constructing advanced optoelectronic devices.

Linker Conformation Controls Oxidation Potentials and Electrochromism in Highly Stable Zr-Based Metal-Organic Frameworks.

The development of tailor-made electrochromic (EC) materials requires a large variety of available substances with properties that precisely match the task. Since the inception of electrochromic metal-organic frameworks (MOFs), the field relies only on a limited set of building blocks, providing the desired electrochromic effect. Herein, we demonstrate for the first time the implementation of a Piccard-type system (N,N,N',N'-benzidinetetrabenzoate) into Zr-MOFs to obtain electrochromic materials. With fast switching rates, high contrast ratio, long-life stability, and exceptional chemical and physical stability, the novel material is on par with inorganic EC material. The new EC system exhibits an ultrahigh contrast from the bleaching state, with transmittance in the visible region >53%, to the colored state with a transmittance of ca. 3%. The 5 μm thick film attained up to 90% of the coloring in 12.5 s and exhibited high electrochemical reversibility. Moreover, the conformational lability of the electrochromic ligand chosen is locked via the topology design of the framework, which is not attainable in the solution. Locked conformations of the redox active linker in distinct polymorphous frameworks (DUT-65 and DUT-66) feature different redox characteristics and opens the door to the overarching control of the oxidation pathway in the Piccard-type systems.

Robust Dual-Color Electrochromism of Vanadium Oxide Nanorods Embedded on Reduced Graphene Oxide: Unraveling the Mechanism

Vanadium pentoxide (V2O5), associated with both cathodic and anodic coloration, is considered as one of the best electrochromic (EC) materials for energy-saving smart electronics. Here we present the fabrication and detailed mechanism analysis for improving the electrochromic properties of V2O5 incorporated in a reduced graphene oxide (rGO) matrix using a facile wet chemical method. The microstructural study disclosed the formation of prominent V2O5 nanorods embedded in the rGO matrix. The optimized electrochromic film resulted in coloration (tc) and bleaching time (tb) of ∼6.2 and ∼4.8 s, respectively, much faster than the color switching kinetics of the pristine V2O5 sample (tc ∼ 19.4 s, tb ∼ 15.3 s). The more dispersed structure also ensured an approximate 400% enhancement in the optical modulation of EC film and reflected a noticeable improvement in the coloration efficiency (∼347 cm2/C) of V2O5 film. Modification with rGO resulted in an outstanding improvement in the electrochemical redox stability of V2O5 up to 5000 CV cycles with minimum deterioration in the curve area. The formation of nanorod structure was the prime factor for better ion diffusion and thereby facilitating enhanced performance.

Construction of diverse adaptive camouflage nets based on soluble yellow-to-green switching electrochromic materials

The potential application of electrochromic (EC) materials and devices as adaptive camouflage in diverse environments requires further investigation. In this study, we aimed to enhance the camouflage effect of electrochromic devices (ECDs) by developing innovative EC camouflage nets. Three soluble EC materials (FTP, FEP and FBP) were synthesized by incorporating phenothiazine and ProDOT with different donors through direct(hetero) arylation polymerization. Due to the fine-tuning of the energy gap, the three materials exhibit yellow, yellowish-brown and reddish-brown colors in their neutral states, respectively. Particularly, FTP and FEP can switch between different yellow-to-green with superior EC performance. Furthermore, FTP-PEDOT and FEP-PEDOT ECDs were constructed. Notably, the FEP-PEDOT ECD demonstrated enhanced EC performance, characterized by a more noticeable yellow-to-green switch, faster switching times and improved cycle stability. To meet the adaptability for multi-environmental camouflage and wearable applications, we created diverse camouflage patterns using the mask-spray technique and developed three types (“stripe”/ “cross stripe”/ “block”) camouflage net ECDs. This study offers a comprehensive approach for developing adaptive camouflage nets tailored to diverse real combat settings.

Ionic conductivity and dielectric characteristics of a Li incorporated PVA electrolyte membrane and a study of a fully solid-state electrochromic device based on it

The construction and study of a fully solid state electrochromic (EC) device with cathodic coloration exhibiting very fast response times (< 1s) is reported using a WO3 EC layer and a poly (vinyl alcohol) (PVA)- Lithium acetate membrane electrolyte. Broadband dielectric studies on the polymer membranes with different Li concentrations show multiple relaxation mechanisms out of which a segmental relaxation prominent beyond a certain composition is strongly correlated with Li-ion conduction yielding better ionic conductivity and reversible coloration in the EC device. The relatively high Li conductivity in PVA has a direct correspondence with the lowering of the crystallinity of PVA and a decrease of the glass transition temperature, Tg with increasing Li addition. A simple model of the coloration process suggests that the short electrolyte diffusion length coupled with a high electric field and an interfacial emf that varies as ≈t−0.6 results in the swift current response of the film with an optimal performance at 20 wt.% Li in PVA, exceeding which irreversible coloration can occur on the surface. The transient current is crucial for the observed swift switching characteristics. Ageing studies for almost a month indicate potential stability of the EC device for over 150 cycles.

Ultralong Bistable, Electrolytic MnO2-Based, Electrochromic Battery Enabled by Porous, Low-Barrier, Hydroxylated TiO2 Interface.

Electrochromic (EC)battery technology shows great potential in future "zero-energy building" by controlling outdoor solar transmission to tune heat gain as well as storing the consumed energy to reuse across other building systems. However, challenges still exist in exploring an electrochemical system to satisfy requirements on both ultra-long optical memory (also called bistability) without continuous power supply and high energy density. Herein, an ECbattery is proposed to demonstrate ultra-long bistability (>760h) based on the reversible deposition and dissolution of manganese oxide (MnO2) without the addition of any mediators. A porous low-barrier hydroxylated titanium dioxide (TiO2) interface is incorporated to synergistically enrich Mn2+-affinity active sites for deposition and effectively reduce the electron transport barrier of MnO2 for dissolution, thereby significantly improving the reversibility, high optical modulation (60.2% at 400nm), and energy density (352mAhm-2). The modification strategy is also verified on the cathode-less button cells with a much higher average coulombic efficiency (99.9%) compared to the batteries without the porous hydroxylated TiO2 interface (74.6%). These achievements lay a foundation for advancements in both electrochromism and Zn-Mn aqueous batteries.

Unveiling dynamics evolution mechanism of electrochromic process in WO3-x film with thickness dependence

Response time (τ, defined as the time required for 90% change in the full transmittance modulation, including coloring time τc and bleaching time τb) is an important evaluation index for the performance of electrochromic (EC) materials, and it can directly reflect the microscopic rate of EC process. However, the research on the internal relationship between the response time and the process of electrochemical dynamics is rare. Herein, by controlling the thickness of the WO3-x EC film, a complete reversal of the response time (from τc > τb in the thinner film to τb > τc in the thicker film) is observed. Based on the detailed analysis of the characteristics presented in electrochemical impedance spectroscopy (EIS), especially focusing on the changing trend about the arc of different frequency ranges and the slope value of the linear part, it can be found that this reversal is due to the change of the main dynamics process from surface capacitive-controlled to bulk diffusion-controlled with the increase of WO3-x film thickness. Meanwhile, this change with obvious film thickness dependence requires a "trigger", which is reflected by the bleaching threshold potential. Besides, this study reveals the three stages of the EC coloring process from the perspective of dynamics, including the lithium-ions (Li-ions) adsorption charge layer, surface Faraday process, and bulk Faraday process, which also show significant film thickness dependence. The result of this work is beneficial to modulate the balance of response time and to improve the performance of EC films.

Design of a dynamically switchable metamaterial solar heating and daytime radiative cooling device based on reversible metal electrodeposition

Abstract The combination of daytime radiative cooling and solar heating can regulate the temperature of buildings in all seasons, which is vital to achieving energy savings. However, achieving a dynamic and efficient switch between radiative cooling and solar heating states is still challenging. The reversible metal electrodeposition is a promising electrochromic (EC) technology that can dynamically manipulate the visible and infrared spectrum by depositing a nanoscale metal layer. By combining it with a delicate nanostructure design, reconfigurable daytime radiative cooling and solar heating states can be achieved. In this work, a metamaterial EC device capable of efficiently switching between high solar reflectance (91.73%) and high solar absorptance (95.41%) via reversible silver layer electrodeposition has been developed. This device consists of a top layer, which is a visible transparent electrode of indium tin oxide covered with an ultrathin platinum film, an electrolyte in the middle, and a metamaterial absorber based on a metal/dielectric multilayered structure at the bottom. Afterward, we analyze the spectrum of each part of the device and carry out a parametric study on the practical performance with different ambient temperatures and convective heat transfer coefficients. The average solar reflectance of the device in the radiative cooling state is 93.41% within the range of 0.3–2.5 μm. In the solar heating mode, the average solar absorptance of the device reaches 95.46%. Numerical simulations show that the device in the cooling mode achieves a temperature drop of 5 °C–9.8 °C and an average cooling power of 140.8 W m − 2 . The device in heating mode achieves a maximum temperature rise of 45 °C and a maximum heating power of 700 W m − 2 . This work provides a feasible design for solar heating and daytime radiative cooling switching devices, which is promising in applications like energy-saving buildings, wearable devices, electric vehicles and other outdoors facilities.

Assessing the impact of glazing and window shade systems on view clarity

Windows provide access to daylight and outdoor views, influencing building design. Various glazing and window shade materials are used to mitigate glare, overheating and privacy issues, and they affect view clarity. Among them, we evaluated the effect of window films, electrochromic (EC) glass, and fabric shades on view clarity. We conducted an experiment with 50 participants using visual tests adapted from clinical vision tests (visual acuity, contrast sensitivity, color sensitivity) and images displayed on a computer monitor in a controlled laboratory. Window films and EC glass tints outperformed fabric shades in visual acuity, contrast sensitivity and view satisfaction with the exception of the darkest EC tint state and dark grey VLT 3% shade for color sensitivity and view satisfaction. The EC tints pose internal reflection issues and fabric shades are preferred for visual privacy. Window films and EC glass hinder participants’ blue–green color discrimination while fabric shades also decrease red–yellow color discrimination. Visual acuity predicts view satisfaction and contrast sensitivity is the strongest predictor for visual privacy. Generally, higher visible light transmittance and lower solar reflectance (darker color) enhance human visual performance. The proposed workflow provides an experimental procedure, identifies the primary variables and establishes a predictive framework for assessing view clarity of fenestration.

Utilization of Poly(Ethylene Terephthalate) Waste Bottle into Disodium Terephthalate: A Sustainable Electrolyte for Visible to Near‐Infrared Broadband Electrochromic Modulation

AbstractThe growing challenge of poly(ethylene terephthalate) (PET) plastic bottle waste underscores the urgent need for innovative solutions. This study introduces a pioneering approach to repurpose PET waste into valuable electrolytic material for electrochromic (EC) smart windows, presenting a novel strategy to address environmental concerns while advancing technology. Through alkaline depolymerization, disodium terephthalate (DST) electrolyte is derived from PET waste, offering an eco‐friendly and cost‐effective alternative. Integrated with chromogens such as 1‐hexyl‐[4,4′‐bipyridin]‐1‐ium iodide [MV(I)], or 1,1′‐dihexyl‐[4,4′‐bipyridine]‐1,1′‐diium iodide [DVH(I)], or 1,1′‐dihexyl‐[4,4′‐bipyridine]‐1,1′‐diium dihexafluorophosphate [DVH(PF6)], alongside hydroquinone [HQ] and poly(ethyene glycol) diacrylate [PEGDA]: water, novel EC gel‐based devices are fabricated. Notably, ED‐3 exhibits dual‐band absorption across the visible to near‐infrared spectrum, enabling seamless color transitions and exceptional optical contrast. With (ΔT) values of 88.03% at 550 nm and 73.7% at 900 nm, along with a coloration efficiency of 277 cm2C⁻¹ and cyclic stability exceeding 2000 cycles, this innovative approach marks a significant advancement in PET waste upcycling for EC applications. Furthermore, this research contributes to addressing the global challenges of plastic waste pollution and energy consumption, underscoring the transformative potential of sustainable material development.