Search Results (111)

Electrochromic (EC) devices are gaining increasing attention for next-generation smart windows and low-power displays due to their reversible color modulation, low operating voltage, and flexible form factors. Recently, electrochromic energy storage devices (EESDs) have emerged as a promising class of multifunctional systems, enabling simultaneous energy storage and real-time visual monitoring. In this study, we report a flexible dual-functional EESD constructed using polyaniline (PANI) films doped with anthraquinone-1-sulfonic acid sodium salt (AQS), coupled with a redox-active PVA-based gel electrolyte also incorporating AQS. The incorporation of AQS into both the polymer matrix and the gel electrolyte introduces synergistic redox activity, facilitating bidirectional Faradaic reactions at the film–electrolyte interface and within the bulk gel phase. The resulting vertically aligned PANI-AQS nanoneedle films provide high surface area and efficient ion pathways, while the AQS-doped gel electrolyte contributes to enhanced ionic conductivity and electrochemical stability. The device exhibits rapid and reversible color switching from light green to deep black (within 2 s), along with a high areal capacitance of 194.2 mF·cm⁻² at 1 mA·cm⁻² and 72.1% capacitance retention over 5000 cycles—representing a 31.5% improvement over undoped systems. These results highlight the critical role of redox-functionalized gel electrolytes in enhancing both the energy storage and optical performance of EESDs, offering a scalable strategy for multifunctional, gel-based electrochemical systems in wearable and smart electronics. Full article

Electrochromic supercapacitors (ECSCs), which visually indicate their operating status through color changes, have attracted considerable attention in the field of wearable electronics. The conductive polymer polyaniline (PANI) shows great potential for integrated intelligent devices by combining bi-functional electrochromic spectral modulation and energy storage capabilities. In this work, a microsphere-like structured PANI-based composite film was fabricated on a porous Au/nylon 66 electrode via a one-step electrochemical copolymerization process, using 1,3,6,8-pyrenetetrasulfonic acid tetrasodium salt (PTSA) as both the dopant and cross-linking agent for the PANI backbone, serving as the ECSC electrode. Compared to the pristine PANI electrode, the PANI-PTSA composite film exhibits lower intrinsic resistance and higher electrical conductivity, delivering a higher specific capacitance of 310.0 F g⁻¹@1 A g⁻¹ and an areal capacitance of 340.0 mF cm⁻²@1 mA cm⁻², respectively. The dopant facilitates enhanced electrochemical performance by promoting charge transport within the PANI polymer network. Meanwhile, as a counter anion to the PANI backbone, PTSA regulates the growth of PANI chains and acts as a morphological controller. Furthermore, a symmetric ECSC based on the PANI-PTSA_8:1 electrode was assembled, and its electrochemical properties were thoroughly investigated. The device demonstrated a high specific capacitance of 169.2 mF cm⁻² at 1 mA cm⁻², a notable energy density of 23.5 μWh cm⁻² at a power density of 0.5 mW cm⁻², and excellent cycling stability with 79% capacitance retention after 3000 cycles at a current density of 5 mA cm⁻², alongside remarkable mechanical flexibility. Additionally, the working status of the ECSCs can be directly monitored through reversible color changes from yellow-green to deep blue during charge–discharge processes. Full article

This research focuses on creating CuO/PANI nanocomposite films by electrodepositing copper oxide nanoparticles into a polyaniline matrix on ITO substrates. The CuO nanoparticle content was adjusted between 7% and 21%. These nanocomposites are promising for various applications, such as optoelectronic devices, gas sensors, electromagnetic interference shielding, and electrochromic devices. We utilized UV-Vis spectroscopy to examine the nanocomposites’ interaction with light, allowing us to ascertain their refractive indices and absorption coefficients. The Scherrer formula facilitated the determination of the average crystallite size, shedding light on the material’s internal structure. Tauc plots indicated a reduction in the energy-band gap from 3.36 eV to 3.12 eV as the concentration of CuO nanoparticles within the PANI matrix increased, accompanied by a rise in electrical conductivity. The incorporation of CuO nanoparticles into the polyaniline matrix appears to enhance the conjugation length of PANI chains, as evidenced by shifts in the quinoid and benzenoid ring vibrations in FTIR spectra. SEM analysis indicates that the nanocomposite films possess a relatively smooth and homogeneous surface. Additionally, FTIR and XRD analyses demonstrate an increasing degree of interaction between CuO nanoparticles and PANI chains with higher CuO concentrations. At lower concentrations, interactions were minimal. In contrast, at higher concentrations, more significant interactions were observed, which facilitated the stretching of polymer chains, improved molecular packing, and facilitated the formation of larger crystalline structures within the PANI matrix. The incorporation of CuO nanoparticles resulted in nanocomposites with electrical conductivities ranging from 1.2 to 17.0 S cm⁻¹, which are favorable for optimum performance in optoelectronic devices. These results confirm that the nanocomposite films combine pronounced crystallinity, markedly enhanced electrical conductivity, and tunable band-gap energies, positioning them as versatile candidates for next-generation optoelectronic devices. Full article

The electrochromic naphthalenediimide (NDI) based monomer containing styrene pedant groups, which are capable of polymerization, was prepared, and the formation of its polymer via a photopolymerization reaction was described. Both the monomer and polymer exhibited a color change in the visible range from transparent or slightly yellow, respectively, followed by brown-red to green. This was the result of a two-step reduction reaction of NDI core to radical anion and dianion, respectively. The device constructed using the polymer as an active material was found to exhibit good electrochromic stability over 500 redox cycles. The switching times were calculated to be 18 s and 6 s for the coloration and bleaching steps, respectively. The presented results showed the usability of the photopolymerization of styrene-based monomers in the generation of the stable electrochromic layers of polymers. Full article

Three new amide-preformed triphenylamine-diamine monomers, namely 4,4′-bis(p-aminobenzamido)triphenylamine (4), 4,4′-bis(p-aminobenzamido)-4″-methoxytriphenylamine (MeO-4), and 4,4′-bis(p-aminobenzamido)-4″-tert-butyltriphenylamine (t-Bu-4), were synthesized and subsequently used to produce three series of electroactive aromatic poly(amide-imide)s (PAIs) via two-step polycondensation reactions with commercially available tetracarboxylic dianhydrides. Strong and flexible PAI films could be obtained by solution casting of the poly(amic acid) films followed by thermal imidization or direct solution casting from the organosoluble PAI samples. The PAIs had high glass-transition temperatures of 296–355 °C and showed no significant decomposition below 500 °C. The PAIs based on diamines MeO-4 and t-Bu-4 showed high electrochemical redox stability and strong color changes upon oxidation. For the PAIs derived from diamine 4, the TPA radical cation formed in situ during the electro-oxidative process could dimerize to a tetraphenylbenzidine structure, resulting in an additional oxidation state and color change. These PAIs exhibited increased solubility, lowered oxidation potentials, and enhanced redox stability compared to their polyimide analogs. Full article

Aqueous zinc-ion batteries (AZIBs) have attracted interest for their low cost and environmental friendliness. Two bipolar organic materials with different degrees of conjugation, pPMQT and pNTQT, were rationally designed and synthesized as cathode candidates for AZIBs based on 4,4′-diaminotriphenylamine (TPA), 2,7-diaminoanthraquinone (AQ), and two anhydrides. This molecular design features an increased conjugation and electron cloud density, thereby improving charge transport kinetics, specific capacity, and cycling stability. In comparison with pPMQ and pNTQ (n-type), pPMQT and pNTQT demonstrate better electrochemical characteristics. In this work, pNTQT shows outstanding performance. It exhibits an initial capacity of 349.79 mAh g⁻¹ at 0.1 A g⁻¹ and retains a specific capacity of 190.25 mAh g⁻¹ (87.6%) after 5000 cycles at 5 A g⁻¹. In comparison, pNTQ demonstrates a specific capacity of only 207.55 mAh g⁻¹ at 0.1 A g⁻¹, and after 5000 cycles at 5 A g⁻¹, its capacity retention rate is only 81.2%. At the same time, both pPMQT and pNTQT polymer films demonstrate attractive electrochromic (EC) properties, displaying reversible color transitions from yellow to dark blue in the UV–visible spectrum. This work lays the foundation for the further development of triphenylamine-based polyimide materials for application in AZIBs and electrochromism. Full article

Flexible electrochromic devices (ECDs) represent a distinctive category in optoelectronics, leveraging advanced materials to achieve tunable coloration under applied electric voltage. This review delves into recent advancements in electrode materials for ECDs, with a focus on silver nanowires, metal meshes, conductive polymers, carbon nanotubes, and transparent conductive ceramics. Each material is evaluated based on its manufacturing methods and integration potential. The analysis highlights the prominent role of transparent conductive ceramics and conductive polymers due to their versatility and scalability, while also addressing challenges such as environmental stability and production costs. Use of other alternative materials, such as metal meshes, carbon materials, nanowires and others, are presented here as a comparison as well. Emerging hybrid systems and advanced coating techniques are identified as promising solutions to overcome limitations regarding flexibility and durability. This review underscores the critical importance of electrode innovation in enhancing the performance, sustainability, and application scope of flexible ECDs for next-generation technologies. Full article

An asymmetric two-arm polypyridine ligand 4′-{4-[4-(2,2′-dipyridyl)phenyl]}-2,2′:6′,2′-terpyridine (TPY-Ph-BPY) with double coordination units was synthesized using the one-step Suzuki reaction. The metallic supramolecular film was subsequently obtained by the Fe²⁺-induced self-assembly method at the CHCl₃-H₂O interface, which displayed a distinct flat and continuous morphology. The supramolecular film-coated ITO electrode demonstrated a reversible electrochemical redox behavior with pronounced color changes between purple and light green. Its solid-state electrochromic device had an optical contrast (ΔT%) of 26.2% at λ_max = 573 nm with balanced coloring (t_c = 2.4 s) and bleaching (t_b = 2.6 s) times and a high current efficiency of 507.8 cm²/C. Moreover, good cycling stability with a long-term reversible color change was observed beyond 900 cycles. These results suggested the promising potential of the TPY-Ph-BPY-Fe(II) supramolecular film for electrochromic applications. Full article

Synthesis of uniform and stable electrochromic films on a conductive layer is one of the effective ways to construct high-performance electrochromic devices. The development of more convenient and feasible polymer film preparation technology is important and necessary. Herein, we demonstrated the development of a continuous in situ polymerization method to prepare electrochromic film on ITO glass through Schiff base condensation of a tetraamine Fe-based complex and organic di-/tri-aldehyde precursors. The electrochromic film was successfully coated on the surface of the ITO conductive layer and exhibited uniform morphology and excellent stability. Film P1 exhibited two reversible redox processes allowing two steps of electrochromic processes, including the oxidation of Fe(II) to Fe(III) at 1.05 V and oxidation of triphenylamine moieties to cation radicals at 1.4 V, which induced three stable color states from initial yellow to orange red and blue. The utilization of the so-formed polymer film for the fabrication of electrochromic devices gave rise to excellent electrochromic performance of fast response time of 0.4−1.2 s and high coloration efficiencies of 241.5−352.9 cm²/C at 1.9 V (at 535 nm) and 2.5 V (at 755 nm). The present work provides a new feasible strategy for constructing polymer films for high-performance electrochromic devices. Full article

Electrochromic devices (ECDs) are devices that change their optical properties in response to a low applied voltage. These devices typically consist of an electrochromic layer, a transparent conducting substrate, and an electrolyte. The advancement in solid-state ECDs has been driven by the need for improved durability, optical performance, and energy efficiency. In this study, we investigate varying the temperature to the casting solution for polymethylmethacrylate (PMMA)-based electrolytes for solid-state ECDs with a structure of glass/ITO/WO₃/PMMA electrolyte/ITO/glass. The electrochromic layer, composed of WO₃, was deposited using the sol-gel method, while the electrolyte, comprising lithium perchlorate (LiClO₄) in propylene carbonate (PC) with PMMA, was prepared via solution casting. Various electrolyte samples were heated at different temperatures of 25, 40, 60, 80, and 100 °C to analyze the impact on the devices’ performance. Our findings indicate that the devices with electrolytes at 25 °C exhibited superior anodic and cathodic diffusion. An increase in heating temperature corresponded with an increase in switching time. Notably, the sample heated at higher temperatures (60, 80, and 100 °C) demonstrated exceptional cycle stability. Nevertheless, samples with higher temperatures displayed a decrease in optical modulation. Additionally, the 100 °C sample exhibited the highest coloration efficiency compared to other samples at lower temperatures. This research highlights the potential of varying the temperature of solution casting on PMMA-based electrolytes in optimizing the performance of solid-state ECDs, particularly regarding coloration efficiency and durability. Full article

Pyrene (Pr) was used to improve the electrochemical and electrochromic properties of polythiophene copolymerized with 3,4-ethylenedioxythiophene (EDOT). The corresponding product, poly(3,4-ethylenedioxythiophene-co-Pyrene) (P(EDOT-co-Pr)), was successfully synthesized by electrochemical polymerization with different monomer concentrations in propylene carbonate solution containing 0.1 M lithium perchlorate (LiClO₄/PC (0.1 M)). The homopolymer and copolymer films were analyzed by Fourier transform infrared spectroscopy (FT-IR), color-coordinate and colorimetric methods, cyclic voltammetry (CV), spectroelectrochemistry (SEC), and UV–visible spectroscopy (UV-Vis). Homopolymer poly(3,4-ethylenedioxythiophene) (PEDOT) and the P(EDOT-co-Pr) copolymer were investigated, which included examining their colorimetric, electrochemical, and electrochromic characteristics. The color shifts resulting from redox reactions of the polymers were also observed. The copolymers with different monomer concentrations achieved multicolor shifts, such as light purple, dark blue, dark red, green, and earthy yellow. Moreover, P(EDOT-co-Pr) had a small optical bandgap (1.74–1.83 eV), excellent optical contrast (31.68–45.96%), and high coloring efficiency (350–507 cm² C⁻¹). In particular, P(EDOT1-co-Pr3) exhibited outstanding cycling stability, retaining 91% of its initial optical contrast after cycling for 10,000 s, and it is expected to be a promising candidate copolymer for electrochromic applications. Full article

In this article, a series of novel conducting copolymers P(FuPy-co-EDOT) are prepared via cyclic voltammetry electropolymerization method by using N-furfuryl pyrrole (FuPy) and 3,4-ethylenedioxythiophene (EDOT) as comonomers. The molecular structure, surface morphology, electrochemical, and optical properties of the resulting copolymers are characterized in detail upon varying the feed ratios of FuPy/EDOT in the range of 1/1 to 1/9. The results demonstrate that the prepared P(FuPy-co-EDOT) copolymers with a higher proportion of EDOT units (FuPy/EDOT: 2/8~1/9) possess good redox activity, tunable optical absorption performances, and low band gaps (1.75~1.86 eV). Spectroelectrochemistry studies indicate that the resulting copolymers with increased EDOT units show strengthened electrochromic characteristics, exhibiting a red-to-green-to-blue multicolor reversible transition, especially for the P(FuPy₁-co-EDOT₉) copolymer films. They also show increased optical contrast (9~34%), fast response time (0.8~2.4 s), and good coloring efficiency (110~362 cm² C⁻¹). Additionally, the complementary bilayer P(FuPy-co-EDOT)/PEDOT electrochromic devices (ECDs) are also assembled and evaluated to hold excellent electrochromic switching performances with relatively high optical contrast (25%), rapid response time (0.9 s), and satisfactory coloring efficiency (416 cm² C⁻¹). Together with the superior open circuit memory and cycling stability, they can be used as a new type of electrochromic material and have considerable prospects as promising candidates for electrochromic devices. Full article

Phenoxazine, as an organic-small-molecule chromophore, has attracted much attention for its potential electrochromic applications recently. To develop appealing materials, phenoxazine chromophores were introduced at the N-position of carbazole–thiophene pigment, yielding two novel monomers (DTCP and DDCP), whose chemical structures were characterized by NMR, HRMS and FTIR. The results of the optical property study indicate that little influence could be observed in the presence of the phenoxazine chromophore. Corresponding polymer films on the surface of an ITO/glass electrode were obtained through electropolymerization. The electrochemical features displayed were various due to the introduction of the phenoxazine group. The spectroelectrochemical results demonstrate that the color of the polymer films could be changed. Compared with the PDDC films, the PDDCP films exhibited three different colors (tangerine, green and purple colors) in different redox states, which could be attributed to the synergistic effect between the carbazole–thiophene conjugate chain and the phenoxazine group. Moreover, fast switching time could be seen due to the presence of the phenoxazine chromophore. This study could provide a reference for obtaining high-performance electrochromic materials. Full article

Yellow-to-green electrochromic color switching plays a key role in the intelligent adaptive camouflage under the visible light environment in future military camouflage applications. Here, we designed and synthesized a soluble electrochromic conjugated pDPTD polymer, mainly based on perylo[1,12-bcd]thiophene and the novel ProDOT groups. The pDPTD polymer displayed a yellow-to-green electrochromism with large optical contrast and fast switching times. Based on the pDPTD polymer film, a yellow-to-green electrochromic device was achieved, showing an orange-yellow color at −0.4 V with L*a*b* color coordinates of 88.5, 18.5, and 34.2 and a pale green color at 0.7 V with L*a*b* color coordinates of 85.6, −4.8, and 11.5, together with a large optical contrast of 43.5% and fast switching times of 2.4/3.2 s. These results indicated that the pDPTD polymer could serve as a potential electrochromic material for yellow/green system camouflage applications. Full article

The electrochromic phenomenon of conducting polymer is mainly dominated by the π-π* band transition. The π conjugation is influenced by the coplanarity between polymer units, deviations from which can lead to an increased ionization potential and band gap values. In order to investigate the effect of plane distortion angle on electrochromic color in the main chain structure of polymerization, high-performance poly(3,3′-dimethyl-2,2′-bithiophene) (PDMeBTh) with a large plane distortion angle is successfully synthesized in boron trifluoride diethyl etherate (BFEE) by the electrochemical anodic oxidation method. The electrochemical and thermal properties of PDMeBTh prepared from BFEE and ACN/TBATFB are compared. The electrochromic properties of PDMeBTh are systematically investigated. The PDMeBTh shows a different color change (orange-yellow in the neutral state) compared to poly (3-methylthiophene) (light-red in the neutral state) due to the large torsion angle between thiophene rings of the main polymer chain. The optical contrast, response time, and coloring efficiency (CE) of the prepared PDMeBTh are also studied, which shows good electrochromic properties. For practical applications, an electrochromic device is fabricated by the PDMeBTh and PEDOT. The color of the device can be reversibly changed between orange-yellow and dark blue. The light contrast of the device is 27% at 433 nm and 61% at 634 nm. The CE value of the device is 403 cm² C⁻¹ at 433 nm and 577 cm² C⁻¹ at 634 nm. The constructed device also has good open circuit memory and electrochromic stability, showing good potential for practical applications. Full article