Color Tuning Research Articles

Differentiated Intra-Ligand Charge Transfer Boosting Multicolor Responsive MOF Heterostructures as Robust Anti-Counterfeiting Labels.

Metal-organic framework (MOF) heterostructures with hybrid architectures and abundant functional sites possess great potential applications in advanced information security, yet still suffer from the harsh stimuli mechanisms with restrained emission control. Herein, the differentiated design strategy on intra-ligand charge transfer is first reported to realize smart-responsive multicolor MOF heterostructures as robust anticounterfeiting labels. Designed similar MOF blocks with the differentiated intra-ligand charge transfer are integrated via time-dependent epitaxial growth to form multicolor MOF heterostructures. Different numbers of electron-donating groups in MOF blocks offer distinct space regulation on the torsion of charge transfer ligands, which trigger the diverse responsive emissions under the same mild stimuli, thus generating multiple tunable color patterns in heterostructures. These spatial-resolved MOF heterostructures with stable multicolor responsive modes permit the encoding of fingerprint information, which further functions as robust anti-counterfeiting labels with high-security convert states. These results offer a promising route for the function-oriented exploitation of smart-responsive MOF heterosystems for advanced information anticounterfeiting.

Electrochemically mutable soft metasurfaces.

Active optical metasurfaces, capable of dynamically manipulating light in ultrathin form factors, enable novel interfaces between humans and technology. In such interfaces, soft materials bring many advantages based on their flexibility, compliance and large stimulus-driven responses. Here, we create electrochemically mutable, soft metasurfaces that capitalize on the swelling of soft conducting polymers to alter the shape and associated resonant response of metasurface elements. Such geometric tuning overcomes the typical trade-off between achieving substantial tuning and low optical loss that is intrinsic to dynamic metasurfaces relying on index tuning of materials. Using the commercial polymer PEDOT:PSS, we demonstrate dynamic, high-resolution colour tuning and high-diffraction-efficiency (>19%) beam-steering devices that operate at CMOS-compatible voltages (~1.5 V). These results highlight how the deformability of soft materials can enable a class of high-performance metasurfaces that are suitable for body-worn technologies.

Activating Ultralong Room-Temperature Phosphorescence of Mono-Ring Arylboronic Acid by Hydrogen Bond for Tunable Afterglow Color and Stimulus Response.

Activating the ultralong room-temperature phosphorescence (RTP) of mono-ring arylboronic acid remains a great challenge, because the capacious free spaces shaped by a rubbery polymeric matrix allow the benzene ring skeleton to freely rotate. Herein, the ultralong RTP in mono-ring arylboronic acid derivatives embedded in a polyvinyl alcohol (PVA) matrix is activated, leveraging enhanced intermolecular and intramolecular hydrogen bonding and activating ultralong RTP. By incorporating diverse PBA derivatives into PVA via click chemistry, 3-aminophenylboronic acid (3A-PBA) doped PVA films showcase the most extended RTP lifetimes (2.24 s) and a high quantum yield (11.2%), alongside rapid and sensitive explosive vapor detection capabilities. These findings not only address the activation challenges of RTP in organic systems by highlighting the crucial role of hydrogen bonding and Förster resonance energy transfer in color tunability, but also mark a significant stride toward overcoming the limitations of current luminescent materials. This work heralds a new era in the development of organic phosphorescent materials, offering a promising strategy for broadening their practical applications and enhancing performance, particularly in environmental monitoring and security.

Self‐reduction triggered color tuning of Eu3+‐doped aluminosilicate glass for solid‐state white illumination

AbstractRare earth‐doped transparent glass, boasting high transmittance and excellent luminescent properties, holds great potential in the field of all‐inorganic solid‐state white illumination. Currently reported single‐structure solid‐state white lighting usually has the problems of low color rendering index (CRI) and high correlated color temperature (CCT) due to the lacking of red light emission. In this work, a novel single‐structure MgO–Al2O3–SiO2–Eu2O3 (MAS: Eu) glass with color tuning was prepared by the simple glass melting process. Interestingly, the prepared Eu3+‐doped aluminosilicate glass possessed a unique capability to achieve color emission under different excitation wavelengths. The reason for this was attributed to the good self‐reduction capability of the MAS glass, which effectively reduced Eu3+ to Eu2+ under an air atmosphere. Meanwhile, only by regulating the Eu3+ doping concentration, the MAS glass also achieved a tunable emission from blue to white to red light under 380 nm excitation. The acquisition of white light was realized through the multispectral emission of blue–green light emitted by Eu2+ and orange–red light emitted by Eu3+. Remarkably, the single‐structure MAS glass doped with 8 wt.% Eu3+ successfully achieved high‐quality white light and high thermal stability, exhibiting a high CRI of 86, a low CCT of 2761 K, good chromaticity parameters of (0.407 and 0.3192), and the emission intensity at 423 K remains above 86.35% that of room temperature. Meanwhile, the doped Eu3+ exceeded 12 wt.%, without any observable concentration quenching. Moreover, the MAS: Eu glass showed a high transmittance of 90 and a moderate thermal conductivity of 1.45 W/mK (epoxy resin ∼0.17 W/mK). These results would dramatically inspire the development of high‐quality solid‐state white lighting applications.

Solution Processed Bilayer Metal Halide White Light Emitting Diodes.

Metal halide perovskites and perovskite-related organic metal halide hybrids (OMHHs) have recently emerged as a new class of luminescent materials for light emitting diodes (LEDs), owing to their unique and remarkable properties, including near-unity photoluminescence quantum efficiencies, highly tunable emission colors, and low temperature solution processing. While substantial progress has been made in developing monochromatic LEDs with electroluminescence across blue, green, red, and near-infrared regions, achieving highly efficient and stable white electroluminescence from a single LED remains a challenging and under-explored area. Here, a facile approach to generating white electroluminescence is reported by combining narrow sky-blue emission from metal halide perovskites and broadband orange/red emission from zero-dimensional (0D) OMHHs. For the proof of concept, utilizing TPPcarz+ passivated two-dimensional (2D) CsPbBr3 nanoplatelets (NPLs) as sky blue emitter and 0D TPPcarzSbBr4 as orange/red emitter (TPPcarz+ = triphenyl (9-phenyl-9H-carbazol-3-yl) phosphonium), white LEDs (WLEDs) with a solution processed bilayer structure have been fabricated to exhibit a peak external quantum efficiency (EQE) of 4.8% and luminance of 1507 cd m-2 at the Commission Internationale de L'Eclairage (CIE) coordinate of (0.32, 0.35). This work opens a new pathway for creating highly efficient and stable WLEDs using metal halide perovskites and related materials.

Chromatic tuning of upconversion emission upon dual infrared wavelength co-excitation in Er3+ doped Ba3Lu4O9 phosphor

Emission color change of the upconversion luminescence materials is often required for applications in optical anti-counterfeiting, laser lighting, and 3D displays. In this work, we developed a new route for chromatic tuning of upconversion emission upon two wavelength co-excitation by changing excitation power density. The proposed route was used for Er3+ single-doped Ba3Lu4O9 phosphor which was derived from a traditional solid-state reaction. The crystal structure of the obtained Ba3Lu4O9:Er3+ phosphor was characterized by X-ray diffraction and Rietveld refinement modeling. Under individual excitation of 980 or 1550 nm, it was found that the luminescence intensity ratio of red to green changes slightly with respectively increasing excitation power density (working current of the laser) of 980 or 1550 nm laser. However, upon both 980 and 1550 nm co-excitation at the same time and by adjusting the excitation power density of one laser amongst the two lasers, the luminescence intensity ratio of red to green changes greatly with increasing excitation power density. The change of luminescence intensity ratio of red to green implies the upconversion emission color tuning. The mechanism for the color tuning was discovered. It was found that with changing excitation power density the ratio of red to green changed greatly when the phosphor was irradiated by 980 and 1550 together, but the ratio of red to green changed slightly when the phosphor was irradiated individually by 980 or 1550. It is proved that it is feasible to turn color by the method of two infrared wavelengths excitation.

Host dependent upconversion of Ho3+ activated system for extended luminescence color tunability and highly-sensitive optical thermometry

Host dependent upconversion of Ho3+ activated system for extended luminescence color tunability and highly-sensitive optical thermometry

Excitation wavelength and time dependent colour tunable room temperature phosphorescence from boron doped carbon nanodots.

Developing metal free room temperature phosphorescence (RTP) materials have received tremendous attention due its potential application in various fields such as sensing, optoelectronics and anticounterfeiting. Herein, we have synthesized an excitation wavelength and time dependent phosphorescent boron doped carbon nanodots (BCNDs) by thermal treatment of ethanolamine and boric acid at 240°C, where boric acid act as both doping and host agents. The obtained BCNDs display blue to orange fluorescence in both aqueous medium and solid state. In addition, the BCNDs display tunable orange-yellow-green phosphorescence in solid state under UV and visible light, lasting upto 10s, visible to naked eye. The boron and nitrogen doping regulates the band gap of the BCNDs, resulting the phosphorescence colour tunability. The average phosphorescence lifetime and quantum yield of BCNDs are found to be 1.27s and 8.61% respectively. Based on the optical properties, the BCNDs are applied as security ink in information encryption and security marking. Hence, this work can promote the development of metal free phosphorescent carbon based materials which may find application in various emerging fields.

Color tunability, concentration dependence, and temperature responsive afterglow of SrZn2(PO4)2: Eu2+, Mn2+ phosphors.

Long persistent luminescence (LPL) materials with color adjustable afterglow have a wide application prospect in display and information encryption, yet there are few reports on such materials. In this paper, SrZn2(PO4)2 phosphors with tunable and thermal stimuli-responsive afterglow emissions were synthesized by a solid-state method. After ultraviolet (UV) excitation, the prepared samples exhibited emission at 419 nm, 533 nm, and 633 nm due to Eu2+: 4f65d1 → 4f7 transitions, Mn2+: 4T2(4G) →6A1(6S) transitions, and Mn2+: 4T1(4G) → 6A1(6S) transitions, respectively. The Commission Internationale de I' Eclairage (CIE) coordinates of samples can be changed among blue, white, and yellow by varying the Mn2+ concentration. Additionally, due to the differing thermal stability of Eu2+ and Mn2+, the phosphor exhibited a temperature-responsive afterglow, and its colors can be adjusted between white and yellow over a temperature range from 293 K to 383 K. Given its distinctive temperature-responsive afterglow, the prepared phosphor is suitable for use as a temperature sensor. Moreover, the tunable afterglow colors of the phosphors are advantageous for application in anti-counterfeiting.

Modulation of Charge Transport Layer for Perovskite Light-Emitting Diodes.

Perovskite light-emitting diodes (Pero-LEDs) have garnered significant attention due to their exceptional emission characteristics, including narrow full width at half maximum, high color purity, and tunable emission colors. Recent efficiency and operational stability advancements have positioned Pero-LEDs as a promising next-generation display technology. Extensive research and review articles on the compositional engineering and defect passivation of perovskite layers have substantially contributed to the development of multi-color and high-efficiency Pero-LEDs. However, the crucial aspect of charge transport layer (CTL) modulation in Pero-LEDs remains relatively underexplored. CTL modulation not only impacts the charge carrier transport efficiency and injection balance but also plays a critical role in passivating the perovskite surface, blocking ion migration, enhancing perovskite crystallinity, and improving light extraction efficiency. Therefore, optimizing CTLs is pivotal for further enhancing Pero-LED performance. Herein, this review discusses the roles of CTLs in Pero-LEDs and categorizes both reported and potential CTL materials. Then, various CTL optimization strategies are presented, alongside an analysis of the selection criteria for CTLs in high-performance Pero-LEDs. Finally, a summary and outlook on the potential of CTL modulation to further advance Pero-LED performances are provided.

Color Tunable Three Terminal (3-T) Vertically Stacked Tandem Organic Electroluminescent Devices.

Traditional full-color displays typically use a pixel layout with three side-by-side subpixels emitting red (R), green (G), and blue (B) colors. However, this configuration limits the resolution especially in augmented reality (AR) and virtual reality (VR) applications. To address the issue of low pixel density in display technology, this study demonstrated vertically stacked three-terminal (3-T) bottom-emitting tandem OLEDs (sOLED). These OLEDs offer color tunability, facilitated by individually controlled colour units. This study demonstrates two combinations: G+B and R+G. Incorporating three generations of OLED's materials phosphorescent (R), thermally activated delayed fluorescence (TADF) (G), and hyperfluorescent (B). The OLEDs achieve maximum current efficiencies of approximately 11 cd/A, 52.4 cd/A, and 40.7 cd/A for R, G, and B, respectively, in their respective tandem configurations. A wide range of colors can be achieved by blending G+B and R+G color spectrum by adjusting the voltage of independent color unit. The optimal mix results in a fine cyan color with CIE coordinates (0.273,0.5) in G+B sOLED and a warm white with CIE coordinates (0.416,0.518)in R+G sOLED. This work demonstrate a better performing 3-T sOLED utilizing three different generations OLED materials, offering an individual control within a single pixel providing enhanced pixel density for display technology.

Cerium-infused tungstate nanocrystals: Illuminating the future of solid-state lighting

Rare earth based luminescent materials have emerged as a focal point of the scientific investigation owing to their remarkable optical behaviour and potential applications. An effort has been made to develop a series of Ce3+ doped CaWO4 nano-phosphors using an ethylene-glycol assisted reflux route. The detailed structural and morphological properties have been examined through various analytical techniques. The +3-oxidation state of the activator ion Ce has been verified through the XPS study. The change in optical band gap due to the substitution is well discussed using diffuse reflectance spectroscopy. In Photoluminescence study, a broad emission centred at 465 nm is observed due to the 5D3/2→2FJ transitions (J = 7/2 and 5/2) and a significant enhancement in the emission peak is obtained for the optimized phosphor. Concentration quenching phenomenon, observed after 3 mol% of Ce3+ is mainly mediated by the electric multipole-multipole type interaction. The CIE diagram indicates the tuning of emission colour from blue to white region and the emission near white region for the optimized phosphor is further authenticated by its low colour purity value (43 %). The effective tunability of photo-physical properties and colorimetric parameters suggest the applicability of the optimized nano-phosphor in solid state lighting especially for outdoor illumination.

Full‐Color Tunability Room Temperature Phosphorescence from Inorganic Crystal Frameworks

AbstractRoom temperature afterglow (RTA) materials have aroused prodigious research interests owing to their unique long‐life luminescent properties. However, it is rare for RTA materials to be reported with full‐color afterglow emission. Herein, a universal strategy is designed to activate full‐color tunability RTA based on phenylboronic acid derivatives (BOH) and boric acid (BA) via an ingenious solvent‐free solid‐phase heating. As the conjugation degrees of aromatic groups of the guest molecule expanded, the BOH/BA composites showed tunable afterglow colors ranging from blue to red after ultraviolet (UV) irradiation. This strategy is to firmly anchor the guest molecule in a rigid framework of the inorganic metaboric acid matrix by abundant hydrogen‐bonding interactions between the host and guest, suppressing molecular motion and promoting the intersystem crossing (ISC) rate between the singlet and triplet excited states for enhanced afterglow emission. In addition, through mixing in multiple guest molecules into BA simultaneously, the obtained composite can be modulated in a wide excitation range from blue to red. This fascinating study provides a simple and universal method to fabricate full‐color tunability RTA composites, making them a promising candidate for applications in advanced information security and multi‐level encryption.

Dynamic exciton-to-dopant energy transfer tuning of Mn2+-Doped perovskite nanocrystals by PBG effect

Cesium lead halide perovskite nanocrystals (CsPbX3 NCs) doped with Mn2+ brings attractive long-wavelength emission and flexible color tunability. However, modulating the exciton-to-Mn2+ energy transfer efficiency poses a challenge, particularly when relying on traditional methods such as changing halogen composition or incorporating external cations, which often complicate the process. In this work, a simple photonic bandgap (PBG)-modulation strategy is applied to modulate the exciton-to-Mn2+ energy transfer by constructing a sandwich “PC-Perovskite-PC” structure with two photonic crystal (PC) films and Mn2+ doped CsPb(ClBr)3 NPs. When the PBG and the host emission band change from deviation to coincidence, the lifetime of Mn2+ decreases from 0.54 ms to 0.36 ms owing to the enhancing energy transfer efficiency by PBG effect. Meanwhile, the ratios of orange and blue emissions (O/B) increase from 1.36 to 1.6. In addition, the back energy transfer also can be modulated. When the PBG matches well with the Mn2+ emission band, the lifetime of the host emission exhibits the largest value (1.25 ns) owing to back energy transfer from Mn2+ the host. Meanwhile, the O/B value shows the smallest value (0.52) attributed to the decreased spontaneous radiation of Mn2+ and the enhanced host emission. When PBG deviates from the Mn2+ emission band, the lifetime of the host emission decreases but O/B value increases gradually. This work provides new strategy for the modulation of energy transfer in Mn2+ doped CsPb(ClBr)3 NPs.

Direct Ink Writing of Cephalopod Skin‐Like Core‐Shell Fibers From Cholesteric Liquid Crystal Elastomers and Dyed Solutions

AbstractDirect ink writing (DIW) of core‐shell structures allows for patterning hollow or composite structures for shape morphing and color displays. Cholesteric liquid crystal elastomers (CLCEs) with liquid crystal mesogens assembled in a helix superstructure are attractive for generating tunable iridescent structural colors. Here, by fine‐tuning the rheology of the core and shell materials, respectively, this study creates droplets or a continuous filament in the core from the precursors of polydimethylsiloxane (PDMS) or poly(vinyl alcohol), whereas CLCE forms the outer shell. By introducing a dye in the droplets, the skin structures of cephalopods, consisting of chromatophores and iridocytes, are mimicked for enhanced color saturation, lightness, and camouflage. After removal of the core material, a CLCE hollow fiber is obtained, which can switch colors upon mechanical stretching and pneumatic actuation, much like papilla along with iridocytes. Further, liquid crystal mesogens assembled in the bulk of the fiber are in polydomain. Thus, the skin appears opalescent at room temperature, much like how leucophores enhance reflectins. Upon heating above the nematic to isotropic transition temperature, the skin becomes transparent. Lastly, a cephalopod model is constructed, where different parts of the model can change colors independently based on different mechanisms.

Advancements in Eco‐Friendly Colloidal Quantum Dots and their Application in Light Emitting Diodes: Achieving Bright and Color‐Pure Emission for Displays

AbstractSolution‐processable colloidal quantum dots (QDs) are regarded as promising light emitters for next‐generation displays owing to their high photoluminescence quantum yield (PLQY) and broad color tunability. Even though cadmium (Cd)‐based QDs and relevant electroluminescent light‐emitting diodes (LEDs) progressed rapidly, their commercial deployment remains prohibited due to potential environmental concerns. In this review, recent advances in synthesizing eco‐friendly, bright, and color‐pure emitting QDs including InP, ZnSeTe, and AgInGaS2 (AIGS) QDs toward high‐performing LEDs are presented. In particular, the synthetic strategies such as regulating the composition, core/shell structure, and surface ligands of QDs for enhancing the PLQY and reducing the spectral bandwidth are comprehensively discussed. Moreover, various techniques to obtain high‐performance QDs‐based LEDs (QLEDs) involving device architecture and interface engineering as well as modification in electron and hole transport layers are overviewed. Finally, the existing challenges and outlook regarding the optimization of QD's synthesis and optical properties for boosted QLEDs device performance are put forward to enable prospective advanced displays.

Facile nanofabrication and simultaneous color-and-Raman hybrid mechanism of economic SERS substrate with tunable structure color for high enhancement factor

The conventional SERS technique utilizing metal nanoparticles (MNPs) is a powerful optical sensing method, relying on the inelastic collision between incident light and the analyte. However, the development of traditional color-tunable MNP-SERS substrates remains limited to two separate components of the color supporter for generating structure color and followed by the MNPs coating to generate the localized surface plasmonic resonance for SERS sensing. Here, a novel color-tunable SERS substrate without MNPs based on the economic one-step anodic aluminum oxide (AAO) coated with nanoporous Pt films was proposed to generate the color-and-Raman hybrid effect for high enhancement factor. This novel SERS substrate employs an economic method, that is a facile and low-cost one-step anodization process to fabricate the AAO with tunable structure color, enabling adaptation to excitation of laser sources. The substrate with the lowest reflectance to laser light exhibits the highest enhancement factor due to the coupling between the laser and the substrate. The resultant SERS substrate demonstrates a high enhancement factor (EF) of 5.27x105 to methylene blue with a good uniformity of the relative standard deviation (RSD) of 6.35 %. In a practical application, one of preservative, benzoic acid, was detected with a low concentration of 1 ppm in the extraction solution of tapioca balls. This innovative approach promotes limitations associated with traditional color-tunable SERS substrates and offers a promising path for sensitive and versatile trace substance detection.

Size-Dependent Magnetic Responsiveness of a Photonic Crystal of Graphene Oxide Nanosheets.

A magnetically responsive photonic crystal of colloidal nanosheets can exhibit a controllable structural color, offering diverse potential applications. In this study, we systematically investigated how the lateral sizes of graphene oxide (GO) nanosheets affect their magnetic responsiveness in a photonic system. Contrary to the prediction that larger lateral sizes of nanosheets would be more responsive to an applied magnetic field based on the magnetic energy of anisotropic materials, we discovered that GO nanosheets with larger lateral sizes in the photonic system scarcely responded to a 12 T magnetic field. The lack of magnetic response may be due to the strongly restricted rotational motion of GO nanosheets by mutual electrostatic forces. In contrast, GO nanosheets with medium lateral sizes readily responded to the 12 T magnetic field, forming a uniaxially oriented structure that resulted in a vivid structural color. However, smaller GO nanosheets displayed a less vivid structural color, possibly because of less structural ordering of GO nanosheets. Finally, we found that the photonic crystal of GO nanosheets with optimized lateral sizes responded effectively to the 12 T magnetic field across various GO concentrations, resulting in a vivid and tunable structural color.

Tunable MXene/WO3 Fabry−Pérot Microcavity Architecture for Bioinspired Soft Electrochromic Actuators with Vivid Colors

AbstractInspired by stimuli‐responsive creatures in nature, developing devices with synergistic color change and deformation will be of great value for realizing the adaptive variants. Yet, integrating adaptive color variation and deformation into a single device remains elusive. Herein, an intriguing electrochromic actuator based on MXene/WO3 bilayer film is developed with Fabry−Pérot (F–P) microcavity, which successfully integrates both functions of reversible deformation and vivid color variations into the same device. Upon applying a small electric field, the ion intercalation/de‐intercalation can synchronously alter the stress distribution and optical absorption of MXene/WO3, resulting in the dual response of electrochromic phenomenon and ultra‐fast deformation with a maximum angle of 95° within 10 s. Moreover, the F–P microcavity architecture with the physical light interaction additionally endows the bilayer film with a bright color gamut and high color tunability (yellow–green, purple, pink, blue, etc.). Furthermore, an asymmetric soft actuator based on MXene/WO3 bilayer film is assembled, which displays robust grasping ability and excellent cycling stability up to 1000 cycles. These findings may open new opportunities for somatosensory soft robots and next‐generation intelligent robots.

Constructing Bionic Perovskite Smart Photovoltaic Windows with Switchable Colors and High Cycling Stability.

Smart photovoltaic windows (SPWs) provide a high-efficiency and energy-saving strategy owing to the dual capabilities of electricity generation and sunlight modulation achieved by tunable colors and transmittances. Due to the deterioration of chromic process on photovoltaic layers, SPWs usually suffer from poor cycling stability. Moreover, thermochromic SPWs with a multilayer structure usually change transmittance without reversible color transitions. To address these issues, inspired by chameleon skin, bionic SPWs are designed and constructed by integrating hydrogel, CsPbBr3 semitransparent perovskite solar cells (ST-PSCs), and transparent polymer film. The SPWs realize reversible transitions between transparent green (25°C) and opaque yellow (45°C) states in a short duration (2min) under natural conditions. By optimizing perovskite film and ultrathin-metal electrodes, CsPbBr3 ST-PSCs achieve a good trade-off between transmittance and efficiency, delivering the highest photovoltaic efficiency (8.35%) and a record light utilization efficiency (4.43). Ultimately, the multilayer SPWs maintain stable optical properties and more than 88% initial conversion efficiency after 100 transition cycles, presenting excellent cycling stability. This study proposes a novel approach and device structure for SPWs with high cycling stability, switchable colors, and switchable transmittances. It also paves the way for smart photovoltaic deployment in buildings and many other fields.