High Optical Contrast Research Articles

Organic Dye Molecule Intercalated Prussian Blue for Simultaneously Enhancing Coloration Efficiency and Energy Storage Capacity in Electrochromic Battery.

The dual-functional device combining electrochromic properties and energy storage has gained numerous attentions in the field of energy-saving smart electronics. However, achieving simultaneous optimization of coloration efficiency and energy storage capacity of materials poses a significant challenge. This study presents a novel approach by incorporating methyl orange into Prussian blue channels (PB-MO films) to adjust the internal electronic structure of Prussian blue. This modification allows the active layer to simultaneously improve the electrochromic and energy storage performance. The introduction of methyl orange not only alters the ratio of Fe3+/Fe2+ within the framework through the coordination reaction of Fe3+ with methyl orange, but also improves the reaction kinetics after intercalating organic dye molecules, including charge transfer resistance, diffusion capability of ions and capacitive contribution. The PB-MO films demonstrate remarkable properties: high optical contrast (81.4% at 670nm), excellent coloration efficiency (265 cm2C-1), and significant specific capacity (84 mAh m-2 at 0.05 A m-2), outperforming pure PB films. The PB-MO films are ideally suited for applications in displays and intelligent energy storage fields, boasting both high coloration efficiency and substantial energy storage capacity, thus advancing promote the development of dual-functional electrochromic devices.

Regulation of Br on molecular aggregation, film morphology and electrochromic performance of polythiophene derivatives

In this work, five polythiophene derivatives were synthesized through electrochemical copolymerization of 3,3-bis(bromomethyl)-3,4-dihydro-2H-thieno[3,4-b] (Deng et al., 2023; Li et al., 2020) [1,4]dioxepine (ProDOT-Br) and 3,3-dimethyl-3,4-dihydro-2H-thieno[3,4-b] (Deng et al., 2023; Li et al., 2020) [1,4]dioxepine (ProDOT-Me) at different mass ratios. DFT results prove that the layer spacing of conjugated blocks was increased from 5.94 Å for PProDOT-Me to 8.89 Å for PProDOT-Br due to the introduction of Br atom into side chain. And, the diverse film morphologies, such as fibre shape, cellular shape, flat shape, etc, were obtained by changing Br content in polymer. Additionally, through optimizing Br content, PBM(1,2) achieved enhanced electrochromic properties relative to two reference polymers [PProDOT-Br and PProDOT-Me], such as high optical contrast (ΔT = 76 %), fast response time (0.5 s), high transparency, and good stability. Finally, the flexible electrochromic device (8 cm × 4 cm) based on PBM(1,2) was constructed, which achieves rapid color change from purple to transparent blue. The results indicate that introducing various contents of Br atom into side chain is an effective strategy for regulating molecular microstructure and optimizing electrochromic properties of conjugated polymers.

Ti3C2Tx‐MXene‐Based Color‐Indicative All‐Organic Electrochromic Supercapacitors

An all‐organic multifunctional solid‐state electrochromic supercapacitor has been designed by utilizing 2D‐MXene and a combination of viologen and polythiophene. The 2D MXene is synthesized using selective etching method and properly characterized; afterward, it is doped in ethyl viologen (EV) and a solid‐state electrochromic supercapacitor device is prepared having poly‐3‐hexylthiophene (P3HT) as complementary electrode. The prepared device gives high optical contrast (OC) (≈85%) and coloration efficiency (CE) (≈340 cm2 C−1) with ≈1 s of switching time in the visible spectrum at 515 nm. A similar color modulation is observed in NIR region also. Along with high electrochromic properties, the device takes almost 23.1 s for discharging and 6.7 s for charging, giving high Columbic efficiency due to the pseudocapacitor‐type charge storage property providing necessary electrons for the redox reaction to occur. The current study proposes a new MXene‐based recipe for designing multifunctional electrochromic supercapacitors with a promise for practical use.

Photonic crystal topological interface state modulation for nonvolatile optical switching

Phase change materials (PCMs), characterized by high optical contrast (Δn>1), nonvolatility (zero static power consumption), and quick phase change speed (∼ns), provide new opportunities for building low-power and highly integrated photonic tunable devices. Optical integrated devices based on PCMs, such as optical switches and optical routers, have demonstrated significant advantages in terms of modulation energy consumption and integration. In this paper, we theoretically verify the solution for a highly integrated nonvolatile optical switch based on the modulation of the topological interface state (TIS) in the quasi-one-dimensional photonic crystal (quasi-1D PC). The TIS exciting wavelength changes with the crystalline level of the PCM. The extinction ratio (ER) of the topological optical switch is over 18 dB with a modulation length of 9 μm. Meanwhile, the insertion loss (IL) can be controlled within 2 dB. Furthermore, we have analyzed the impact of fabrication errors on the device’s performance. The obtained results show that, the topological optical switch, which changes its “on/off” state by modulating TIS, exhibits enhanced robustness to the fabrication process. We provide an interesting and highly integrated scheme for designing the on-chip nonvolatile optical switch. It offers great potential for designing highly integrated on-chip optical switch arrays and nonvolatile optical neural networks.

Reusing the Wasted Energy of Electrochromic Smart Window for Near-Zero Energy Building.

Electrochromic smart windows (ESWs) are an effective energy-saving technology for near-zero energy buildings. They consume electric energy unidirectionally during a round-trip coloring-bleaching process, with the energy involved in the bleaching process being wasted. It is highly desirable to reuse this wasted electric energy directly and/or transfer it into other energy storage equipment, further enhancing the overall efficiency of electric energy usage. Herein, a zinc anode-based ESW (ESW-PZ) is reported that not only has fascinating visible-near-infrared (VIS-NIR) dual-band electrochromic performance (a high optical contrast of 63%) but also showcases good energy storage characteristics (a wide voltage window of 2.6V and a high energy density of 127.5 µWh cm-2). The buildings utilizing ESW-PZ to modulate indoor environments demonstrated an average annual energy saving of 366MJ m-2 based on energy simulations, which is about 16% of the total energy consumption. Impressively, a high utilization efficiency of 90% (855 mWh m-2) of the wasted electric energy is realized through an ingenious circuit-switching strategy, which can be reused to power small household appliances.

Time Series Forecasting for Sparse Ring-shaped Array Photoacoustic Imaging Reconstruction

Abstract Photoacoustic computed tomography (PACT), which provides high optical absorption contrast and deep acoustic penetration, plays an important role in non-invasive biomedical imaging area. As the decrease of array elements, the reconstructed image suffers from severe artifacts. Recent studies utilize deep learning methods to improve the imaging quality of PACT based on image network design, but few were reported with raw data. To address this issue, this paper proposes a Wave to Wave Convolution Gate Recurrent-Net (WWCG-Net) to reconstruct photoacoustic image based on time series acoustic signal prediction. Simulation and experiment results show the superiority of our method compared with linear interpolation (LI) and eXtreme Gradient Boosting (XGBoost) in term of suppress artifact and improve resolution.

Electrochromic behaviors and applications of tetrasubstituted thienoviologen derivatives

Electrochromic materials have been widely used in various parts of life due to their advantages of energy conservation and rich colors. In this work, a series of novel viologen derivatives (tetrasubstituted thienoviologen derivatives, a–f) were designed and synthesized as electrochromic materials by decorating 4,4′,4″,4‴-(thiophene-2,3,4,5-tetrayl)tetrapyridine with different N-substituents (alkyl, benzyl and aryl). Electrochromic devices based on a–f exhibited a low working voltage of −1.4 V. The N-substituents markedly affected their electrochromic performance. The compounds with alkyl and benzyl substituents performed better than the compound with aryl substituent. Among them, compound c with benzyl substituent performed best with a high optical contrast (66 %), a high coloration efficiency (389 cm2/C), good cycling stability, and fast response time. Besides, compound c was also applicable to sodium carboxymethyl cellulose hydrogel ECD with good cycling stability and a broad absorption band (500–700 nm) in the visible region. The applications of compound c in electronic tags, functional displays and smart windows were explored, indicating it's a promising ECM with wide application prospects.

Triarylamine-based polyimide COFs for achieving high performance ambipolar multi-color electrochromic energy-storage films

Electrochromic energy storage materials that possess both electrochromic and electrochemical energy-storage properties have attracted significant attention for applications in visual energy-storage, energy-efficient windows, as well as displays. To fulfill their comprehensive applications, electrochromic energy-storage materials require specific characteristics, such as transparency, ambipolarity, multi-color capabilities, and high capacitance. Here, the polyimide covalent-organic framework based on triarylamine (PM-TPI and NT-TPI) COF films were grown successfully on FTO glass through solvothermal polycondensation, and exhibited crystallization, hierarchical porous structures, and ambipolar electrochemical redox activity. Notably, NT-TPI COF film displayed transparent bleached state, ambipolar electrochromism, multi-color (transparent, orange-red, cyan, gray), and high optical contrast. Due to their large specific surface area and efficient electron/ion transport ability, the NT-TPI COF film effectively controlled visible and near-infrared light, achieving optical contrasts of 49.8 % and 70.0 % at 420 and 850 nm, respectively. Moreover, the NT-TPI COF films showed promising electrochemical energy-storage properties and excellent charge–discharge rate performance, with a specific capacitance of 141.0 mAh/g. Additionally, NT-TPI COF/WO3-based ambipolar eclectrochromic energy-storage devices also exhibited high optical contrast from visible to near-infrared regions, and large capacitance. In summary, the NT-TPI COF film effectively combines the electrochromic and electrochemical energy-storage capabilities, making it a promising candidate for electrochromic energy-storage materials with transparency, ambipolarity, high optical contrast, multi-color functionality, and high specific capacitance.

Tunable optoelectronic performances of aminated benzothiadiazole-based D-A-D conjugated electrochromic polymers

Introducing heteroatom groups into benzothiadiazole (BT) unit has proven to be a very effective way to improve the optoelectronic properties of conjugate polymer due to its comprehensive advantages of lowering the HOMO or LUMO energy level, and increasing the interaction force on the polymer backbone. However, at present, little attention was paid to introducing amino groups into the BT unit. Herein, in this work, three D-A-D type aminated monomers (Th–NH2-BT, Th–2NH2-BT, and EDOT-2NH2-BT) with aminated benzothiadiazole as the acceptor unit and thiophene or 3,4-ethylenedioxythiophene (EDOT) as the donor unit were successfully synthesized by Stille coupling reaction, and their corresponding aminated polymers (P(Th–NH2-BT), P(Th–2NH2-BT), and P(EDOT-2NH2-BT)) were facilely achieved by electrochemical polymerization method. The optoelectronic properties of the aminated monomers and their D-A polymers were carefully analyzed, and the electrochemical and electrochromic properties of the resultant aminated polymers were further studied. The finally results show that the absorption and fluorescence spectra of Th–2NH2-BT and EDOT-2NH2-BT are both blue-shifted compared to Th–NH2-BT, and the corresponding optical bandgap are gradually increased (2.41 eV–2.65 eV). EDOT-2NH2-BT has a relatively lower oxidation potential (0.73 V) and P(EDOT-2NH2-BT) also has a wide potential window and better redox stability, which was very beneficial for improving its resultant D-A aminated polymers’ optoelectronic properties. As a result, as-formed P(EDOT-2NH2-BT) shown obvious color change from green in the neutral state to gray in the oxidized state with favorable electrochromic performances, with a high optical contrast (ΔT = 17.17 % at 860 nm) and high coloration efficiency (CE = 223 C−1 cm2 at 860 nm), so it is one of the promising materials that can be used in electrochromic devices.

3D-Printed Hydrogel-Based Flexible Electrochromic Device for Wearable Displays.

Flexible electrochromic devices (FECDs) are widely explored for diverse applications including wearable electronics, camouflage, and smart windows. However, the manufacturing process of patterned FECDs remains complex, costly, and non-customizable. To address this challenge, a strategy is proposed to prepare integrated FECDs via multi-material direct writing 3D printing. By designing novel viologen/polyvinyl alcohol (PVA) hydrogel inks and systematically evaluating the printability of various inks, seamless interface integration can be achieved, enabling streamlined manufacturing of patterned FECDs with continuous production capabilities. The resultant 3D-printed FECDs exhibit excellent electrochromic and mechanical properties, including high optical contrast (up to 54% at 360nm), nice cycling stability (less than 5% electroactivity reduction after 10000 s), and mechanical stability (less than 19% optimal contrast decrease after 5000 cycles of bending). The potential applications of these 3D-printed hydrogel-based FECDs are further demonstrated in wearable electronics, camouflage, and smart windows.

Polyacrylamide/sodium alginate double network hydrogel electrochromic devices based on 1,3,4-oxadiazole-extended viologen derivatives for energy-saving fields

In this paper, a novel electrochromic material of 1,3,4-oxadiazole-extended viologen derivative with good coplanarity and electron acceptor-electron donor-electron acceptor structure, BPYO-C6H13, was synthesized, and a polyacrylamide-sodium alginate dual network hydrogel (PAM-SA) with advantages of low cost, environmental protection, good biocompatibility, high optical transmittance (>85 %), good mechanical properties and good ionic conductivity (16.61 mS cm−1) was developed as the electrochromic hydrogel matrix for gel-state electrochromic devices based on BPYO-C6H13 (PAM-SA-ECD). BPYO-C6H13 showed good electrochromic properties in both solution-state electrochromic devices and gel-state electrochromic devices, and PAM-SA-ECD had a lower operating voltage (−1.4 V versus −1.7 V), a higher optical contrast (48.4 % versus 33.1 % and 22.1 %) as well as a higher coloration efficiency (348.7 cm2/C versus 234.8 and 120.7 cm2/C). Compared to PAM-SA gel-state electrochromic devices based on 1,1′-dihexyl-[4,4′-bipyridine]-1,1′-diium, BPYO-C6H13 with 1,3,4-oxadiazole π-extender showed a different colored state (green versus pink) and a higher coloration efficiency (348.7 cm2/C versus 275.9 cm2/C) due to different conjugated structure. PAM-SA-ECD was applied in smart windows and solar cell-powered displays, suggesting BPYO-C6H13 is promising in energy-saving fields.

Electrochromic windows with fast response and wide dynamic range for visible-light modulation without traditional electrodes

Electrochromic (EC) devices represent an emerging energy-saving technology, exhibiting the capability to dynamically modulate light and heat transmittance. Despite their promising potential, the commercialization of EC devices faces substantial impediments such as high cost, intricate fabrication process, and low optical contrast inherent in conventional EC materials relying on the ion insertion/extraction mechanism. In this study, we introduce an innovative “electrode-free” electrochromic (EC) device, termed the EECD, which lacks an EC-layer on the electrodes during device assembling and in the bleached state. This device features a simplified fabrication process and delivers superior optical modulation. It achieves a high optical contrast ranging from 68-85% across the visible spectrum and boasts a rapid response time, reaching 90% coloring in just 17 seconds. In addition, EECD exhibits stable cycling for over 10,000 cycles without noticeable degradation and maintains functionality across a broad temperature range (0 °C to 50 °C). Furthermore, the fabricated large-area devices (40 cm × 40 cm) demonstrate excellent tinting uniformity, suggesting excellent scalability of this approach. Our study establishes a paradigmatic breakthrough for EC smart windows.

High optical contrast, dual-responsive, wearable photochromic fibers for smart textile engineering

Smart textiles exhibiting responsiveness to external light stimuli show a great scope of applications in personalized decorations and intelligent wearable devices, among others. It's both rewarding and challenging to build wearable indicators based on fibers with high contrast and versatility to monitor the state of the external environment while maintaining good conformability and breathability for practical use. Here, we have integrated spiropyran photochromic compound (SP) into the spinning solution with polyvinyl alcohol (PVA) and aqueous polyurethane (WPU), and developed fibers by wet spinning featuring photochromic and photofluorescent dual outputs. Under UV and visible light illumination, the fibers demonstrate significant contrast optical signals, rapid color switching (4 s), long retention duration (7.5 h), as well as good cycling stability (20 times). The photochromic fibers can be used in the form of photochromic wristbands or embroidered on various textiles as flexible wearable UV indicators. Furthermore, the UV-induced fibers also produce pertinent color changes when subjected to acidic and alkaline vapors. We envision that the as-prepared fibers present promising applications in environmental acidity detection and multi-stimulus responsive materials.

Synthesis and Characterization of New Chiral Smectic Four-Ring Esters.

Orthoconic antiferroelectric liquid crystals (OAFLCs) represent unique self-organized materials with significant potential for applications in photonic devices due to their sub-microsecond switching times and high optical contrast in electro-optical effects. However, almost all known OALFCs suffer from low chemical stability and short helical pitch values. This paper presents the synthesis and study results of two chiral AFLCs, featuring a four-ring structure in the rigid core and high chemical stability. The mesomorphic properties of these compounds were investigated using polarizing optical microscopy and differential scanning calorimetry. Spectrometry and electro-optical studies were employed to estimate the helical pitch, tilt angle, and spontaneous polarization of the synthesized compounds and the prepared mixtures. All studied compounds exhibit enantiotropic chiral smectic mesophases including the SmA*, the SmC*, and a very broad temperature range of the SmCA* phase. Doping top-modern antiferroelectric mixture with synthesized compounds offers benefits such as increased helical pitch and tilt angle values without significantly influencing spontaneous polarization. This allows the prepared mixture to be regarded as an OAFLC with high optical contrast, characterized by an almost perfect dark state. These valuable physicochemical and optical properties suggest significant potential of studied materials for practical applications.

Photoacoustic imaging in brain disorders: Current progress and clinical applications

AbstractOver the past few decades, the number of patients with neurological diseases has increased significantly, posing huge challenges and opportunities for the development of brain imaging technology. As a hybrid imaging method combining optical excitation and acoustic detection techniques, photoacoustic tomography (PAT), has experienced rapid development, due to high optical contrast and spatial resolution at depth inside tissues. With the development of lasers, ultrasonic detectors, and data computations, PAT has been widely applied for the diagnosis of oncology, dermatosis, etc. However, the energy of light and ultrasound would be greatly attenuated while penetrating the skull, due to the reflection, absorption, and scattering effects, resulting in limited application of PAT in brain imaging. In this review, we summarized the achievements of PAT and its application in the detection of brain diseases including glioma, stroke, traumatic brain injury, Alzheimer's disease, epilepsy, and Parkinson's disease. Moreover, various PAT systems and multi‐modality photoacoustic imaging are introduced for potential clinical applications. Finally, the challenges and current limitations of PAT for further brain imaging are also discussed.

Electropolymerization of D-A-D type butterfly-shaped monomers based on triphenylamine-thiophene consisting of camphor substituted quinoxaline moiety for efficient electrochromism and supercapacitors

Two new butterfly-shaped monomers TTCQF and TTCQH consisting of camphor-substituted quinoxaline units as π-spacers were designed and synthesized, which were further electrochemical polymerized and deposited on ITO substrates for electrochromic energy storage devices. The present cross-linked polymer thin films PTTCQF and PTTCQH displayed prominent color changes with significant optical contrast in both the visible and near-infrared regions under external electrical stimuli. These two polymers showcased superior electrochromic performance, involving high optical contrast, fast switching speed, and good coloration efficiency. Additionally, both polymers demonstrated a high areal specific capacitance (12 mF/cm2 for PTTCQH and 9.97 mF/cm2 for PTTCQF) at a current density of 0.1 mA/cm2. Electrochromic energy storage devices based on these polymers were fabricated, and not only illuminated an LED bulb but also visually indicated the energy storage state, guaranteed their potential for applications in energy-saving smart windows. This work may provide valuable insights into the development of efficient cross-linked electrochromic energy storage polymers.

Redox-Stable and Multicolor Electrochromic Polyamides with Four Triarylamine Cores in the Repeating Unit.

Two new triarylamine-based diamine monomers, namely, N,N'-bis(4-methoxyphenyl)-N,N'-bis(4-(4-aminophenyl-4'-methoxyphenylamino)phenyl)-p-phenylenediamine (3) and N,N'-bis(4-methoxyphenyl)-N,N'-bis(4-((4-aminophenyl-1-naphthyl)amino)phenyl)-p-phenylenediamine (7), were successfully synthesized and led to two series of electroactive polyamides by polycondensation reactions with common aromatic dicarboxylic acids. The polymers demonstrated multicolored electrochromism, high optical contrast, and remarkable enhancements in redox and electrochromic stability. Compared to other triarylamine-based polymers, the studied polyamides exhibited enhanced electrochromic stability (only 3~6% decay of its coloration efficiency at 445 nm after 14,000 switching cycles) at the first oxidation stage. The polyamides also showed strong absorption in the near-infrared region upon oxidation. Polymers with multicolored electrochromism and high redox stability can be developed by incorporation of four triarylamine cores in each repeat unit and electron-donating methoxy groups on the active sites of the triphenylamine units.

Three-periodic 1D photonic crystals based on dielectric oxides SiO2, Al2O3, TiO2, ZrO2: an emerging class of structures with wide possibilities for applied photonics

One-dimensional three-periodic photonic-crystal (PC) structures based on dielectric nonmagnetic materials (SiO2, Al2O3, TiO2, ZrO2) that form [(ab)N(cd)M]K supercells including “internal” subcells of the (ab)N and (cd)M types are considered. The classification of this class of structures makes it possible to distinguish three large groups of subcells that differ in optical contrast values (low-, medium-, and high-contrast). Using the transfer matrix method, frequency-angle spectra and energy characteristics of the PC structures are studied and optimal combinations of layers (and contrast) are found, enabling obtaining controllable photonic band gaps (PBGs). A generalization of the obtained results shows that in the transparent region, the optical and energy properties of structures with high and medium optical contrast are of the greatest practical interest. It is found that the group of medium-contrast structures has a greater flexibility in the formation and rearrangement of the PBG due to a practically equivalent effect of the optical properties of both cells on the transmission spectrum. An analysis of the spatial-angular distribution of the transverse component of the Umov-Poynting vector and variation in the number of subcells (internal periods) shows that the structure of this group can provide a controlled radiation pattern (at a telecommunication wavelength of 1.55 μm) on the lateral surface of the PC. The findings may give a competitive advantage in the development of polarization-sensitive couplers, highly sensitive angle sensors for fiber-optic systems, and optical filters operating in the infrared range.

Transparent Electrochromic Polymers with High Optical Contrast and Contrast Ratio

Transparent Electrochromic Polymers with High Optical Contrast and Contrast Ratio

Electro‐Induced Self‐Reduction TiO2 in Viologen‐Based Ionogels for Multi‐Color Electrochromic Displays

AbstractReflective electrochromic (EC) technology is expected to e‐paper display field, and integrating optical reflective electrolyte as the optical reflective layer is a common strategy for constructing reflective EC devices. Compositing inorganic particles and electrolytes is one of the simplest and most efficient composite methods, but these composite electrolytes usually cannot perform well together in terms of both optical and electrochemical properties. Herein, the TiO2 nanoparticles are added to the ethyl viologen‐based ionogel (T‐EVG, one typical kind of EC/electrolyte) to have the highest visible light reflectivity and the best electrochemical performance compared with SiO2, Al2O3, and ZnO nanoparticles, which is attributed to the electro‐induced self‐reduction TiO2 produced in T‐EVG during EC cycling. Meanwhile, the corresponding EC devices can display red, green, and blue, and have high optical contrast (CIE Lab: ΔE>38), fast switching spend (<4 s, the fastest is 5 Hz), ultra‐low power density (<4.0 mW cm−2), and excellent cycling stability (>85% retained after 10 000 cycles). Finally, a simple 3×3 pixelated EC display array is prepared, and single‐ and multi‐point (including diagonal points) multi‐color display effects are realized through active‐matrix driving and high‐frequency refresh, demonstrating its application value in the high‐performance e‐paper display.