Color Tuning Research Articles

Omnidirectional color wavelength tuning of stretchable chiral liquid crystal elastomers

Wavelength-tunable structural colors using stimuli-responsive materials, such as chiral liquid crystals (CLCs), have attracted increasing attention owing to their high functionality in various tunable photonic applications. Ideally, on-demand omnidirectional wavelength control is highly desirable from the perspective of wavelength-tuning freedom. However, despite numerous previous research efforts on tunable CLC structural colors, only mono-directional wavelength tuning toward shorter wavelengths has been employed in most studies to date. In this study, we report the ideally desired omnidirectional wavelength control toward longer and shorter wavelengths with significantly improved tunability over a broadband wavelength range. By using areal expanding and contractive strain control of dielectric elastomer actuators (DEAs) with chiral liquid crystal elastomers (CLCEs), simultaneous and omnidirectional structural color-tuning control was achieved. This breakthrough in omnidirectional wavelength control enhances the achievable tuning freedom and versatility, making it applicable to a broad range of high-functional photonic applications.

Tunable emission color from lead-free zero-dimensional Mn2+-doped Cs3InCl6 single crystals

In recent years, the magneto-optical properties of zero-dimensional metal halides have attracted widespread interest. In this study, we employed a vacuum solid-state reaction method to synthesize zero-dimensional, lead-free, and all-inorganic Cs3InCl6 single crystals (SCs). In addition to the blue emission of self-trapped excitons (STEs) inherent to pristine Cs3InCl6, the strategic doping with Mn2+ ions not only facilitates multicolor emissions but also significantly boosts the photoluminescence quantum yield (PLQY) from a modest 1.21 % to an impressive 32.18 %. We carried out an exhaustive investigation into the fundamental mechanisms responsible for these multicolor emissions and the intricate compositional transitions that ensue. Furthermore, the pronounced correlation between temperature-dependent photoluminescence (PL) and magnetic characteristics unveiled the genesis of ferromagnetism within both the pristine and Cs3InCl6: xMn2+ samples. The doping-induced modifications in magnetic behavior furnish a coherent explanation for the anomalous inverse temperature dependence emission wavelength shift. Our research highlights the adjustable PL and magnetic attributes of Mn2+ doped Cs3InCl6, yielding invaluable insights that are poised to advance its application in the next wave of optoelectronic and magnetic technologies.

Strategies to Enhance the Electrochromic Properties of Conjugated Polymers Bearing Pyromellitic Diimide Acceptors.

A series of conjugated polymers bearing thiophene-based donors and pyromellitic diimide (PMDI) acceptor were prepared, and their electrochromic (EC) properties were studied via using fabricated thin-film EC devices. It was observed that structurally regular alternating polymers with fewer (1 and 2) thiophene donors do not exhibit any EC properties while increasing the number of donors eventually led to the emergence of orange-red-to-green colour switching. On this basis, two more random co-polymers containing higher donor-to-acceptor ratios were synthesized to further improve EC switching properties. The two polymers, which bear a PMDI-to-thiophene ratio of ca. 1 : 7 and 1 : 8, revealed orange red-to-blue colour switching and generally improved optical contrasts and switching speeds in both the visible and near infra-red (NIR) region. In addition, the subtle modulation of polymer colour and hue via variation of the number of thiophene donors was evident through colorimetric study. This work therefore demonstrates the potential and possibility of using the PMDI acceptor unit to construct EC-active conjugated polymers, and considerations for future tuning of colour and switching performances.

Fluorescence‐Enabled Colored Bilayer Subambient Radiative Cooling Coatings

AbstractPassive daytime radiative cooling has emerged as a promising green technology for the thermal management of buildings, vehicles, textiles, and electronics. Typically, both high solar reflectance and high thermal emissivity are prerequisites to achieve sufficient daytime cooling. However, colored radiative cooling materials are facing the dilemma of introducing visible light absorption, leading to challenges in balancing cooling and aesthetic demands. Here, three colored bilayer radiative cooling coatings, each comprised of a white base layer and a colored top layer with fluorescence enhancement are fabricated. Three phosphors (Sr2Si5N8:Eu2+, Y3Al5O12:Ce3+, and (Ba,Sr)SiO4:Eu2+) are employed with respective photoluminescence quantum yields (PLQYs) of 81%, 95.8%, and 91.0% as the colored pigment in the top layer. To mitigate the contradiction between coloration and solar reflectance, SiO2 microspheres are introduced into the top layer and utilize their Mie‐resonance‐based multiple scattering to increase the photoluminescent (PL) properties of the phosphors, which jointly boosts the effective solar reflectance (ESR) of the top layer. As a result, the three bilayer coatings exhibit soft colors while achieving subambient cooling with temperature drops of up to 1.5 °C. This fluorescence‐enhancement strategy may pave the way for preparing highly efficient radiative cooling coatings with tunable colors.

Brilliant thermochromic photonic liquid dominated by electrostatic repulsion

It is challenging for traditional methods to generate liquid photonic crystals (LPCs) with brilliant colors and clear self-assembly mechanisms, owing to the major limitations in solvent choice and undesired components. Here, novel LPCs with widely tunable solvents and desired components have been successfully fabricated by non-close-assembling silica particles from silica/ethanol solution into target solvents through alternative centrifugation and sonication. The as-fabricated LPCs exhibit 1) brilliant structural colors from high reflectance (maximal: 91 %) by using solvents with low refractive indexes, much higher than those (20–40 %) of traditional LPCs; 2) tunable color saturation with high precision, difficult for conventional LPCs; and 3) a clearer working mechanism: electrostatic repulsion rather than other interactions majorly dominating the non-close-packing of silica particles in solvents. Additionally, a new type of sensitive thermochromic display unit with thermo-switchable on-off structural colors has been prepared by constructing silica/bi-solvents LPCs. This work not only paves a new way for achieving thermal-responsive LPCs but also offers a new perspective for understanding colloidal assembly.

White-Emitting Gold Nanocluster Assembly with Dynamic Color Tuning.

We report that constructed Au nanoclusters (NCs) can afford amazing white emission synergistically dictated by the Au(0)-dominated core-state fluorescence and Au(I)-governed surface-state phosphorescence, with record-high absolute quantum yields of 42.1% and 53.6% in the aqueous solution and powder state, respectively. Moreover, the dynamic color tuning is achieved in a wide warm-to-cold white-light range (with the correlated color temperature varied from 3426 to 24 973 K) by elaborately manipulating the ratio of Au(0) to Au(I) species and thus the electron transfer rate from staple motif to metal kernel. This study not only exemplifies the successful integration of multiple luminescent centers into metal NCs to accomplish efficient white-light emission but also inspires a feasible pathway toward customizing the optical properties of metal NCs by regulating electron transfer kinetics.

A Tunable Hydrophilic-Hydrophobic, Stimulus Responsive, and Robust Iridescent Structural Color Bionic Film with Chiral Photonic Crystal Nanointerface.

Bio-inspired in nature, using nanomaterials to fabricate the vivid bionic structural color and intelligent stimulus responsive interface as smart skin or optical devices are widely concerned and remain a huge challenge. Here, the bionic flexible film is designed and fabricated with chiral nanointerface and tunable hydrophilic-hydrophobic by the ultrasonic energy perturbation strategy and crosslinking of the cellulose nanocrystals (CNC). An intelligent nanointerface with adjustable hydrophilic and hydrophobic properties is constructed by the supramolecular assembly using a smart ionic liquid molecule. The bionic flexible film possessed the variable hydrophilic-hydrophobic, stimulus responsive, and robust iridescent structural color. The reflective wavelength and the helical pitch of the film can be easily modulated through the ultrasonic energy perturbation strategy. The bionic flexible film by covalent cross-linking has excellent robustness, good elasticity and flexibility. The tunable brilliant structural color of the chiral nanointerface is attributed to the surface charge change of the CNC photonic crystal, which is disturbed by ultrasonic energy perturbation. The bionic flexible film with tunable structure color has intelligent hydrophilic and hydrophobic stimulus response properties. The chiral bionic materials have potential applications in smart skin, optical devices, bionic materials, robots, anti-counterfeiting, colorful displays, and stealth materials.

Modification of Local Site Preference for Achieving Tunable Color Emission from Blue to Near-White in Sr3(PO4)2:Dy3+ Phosphor

The color tunability of Sr3(PO4)2:1%Dy3+ phosphor from blue to near white is studied at various annealing conditions. Higher temperature annealing promotes agglomerated rhombohedral (α) phase formation. Experimental and theoretical analysis reveal dopant preference at the low-symmetry Sr(II) site, altering electric (4F9/2→6H13/2) and magnetic (4F9/2→6H15/2) dipole transitions, thereby affecting the yellow-to-blue (Y/B) ratio. The luminescence intensity variation and color tunability are explained based on the local site symmetry and occupation probability of the dopant in the host lattice. An increase in the luminescence intensity up to an annealing temperature of 1200 °C, followed by quenching is observed due to the oxygen vacancies. Commission Internationale d'Eclairage (CIE) color coordinates of (0.31, 0.38), Correlated Color Temperature (CCT) of 6341 K, and color purity of 22.57% confirm the potential of Sr3(PO4)2:1%Dy3+ phosphor annealed at (1200 °C, 6 hrs) for white light generation. A probable photoluminescence mechanism involving 4f→5d→4f transitions in Sr3(PO4)2:1%Dy3+ is proposed.

Pure Tunable Emissions from Cesium Manganese Bromide by Monitoring the Crystal Fields Through a Sustainable Approach

AbstractResearch on manganese (Mn) halide perovskite derivatives with tunable emissions and high color purity have gathered a significant amount of attention for display technology. Despite of mesmerizing optical properties, the synthesis of these all‐inorganic Mn halide compounds is followed by complex and toxic processes. Second, a precise control over the synthesis parameters is mandatory to achieve their pure emissions. Therefore, an ecologically sustainable water‐based solution approach is adapted here to tailor the phases and emissions of cesium manganese bromide (Cs‐Mn‐Br) perovskite derivatives. It is observed that a controlled injection of solution stabilizer plays a pivotal role in engineering the intrinsic properties of Mn halide perovskites. This solution stabilizer interacts with the Mn‐ions of those perovskite derivatives influencing their surrounding coordination environment and pure emission from then. A pure green emission with PLQY of 82% is achieved from as prepared Cs3MnBr5, whereas CsMnBr3 showed a red emission with PLQY of ≈20%. Encouraged by these properties phosphor‐driven light emitting diodes (LED) are designed that show a steady electroluminescence intensity. The CIE coordinates of the Cs3MnBr5 and CsMnBr3 LED prototypes are at (0.224, 0.659) and (0.688, 0.316). This study showcases simple, eco‐friendly tactics for developing green and red LED prototypes contributing toward sustainable device design.

Rational Design of Nitride Phosphor-In-Glass with Robust Stability and Photoluminescence Performance.

Phosphor-in-glass represents a promising avenue for merging the luminous efficiency of high-quality phosphor and the thermal stability of a glass matrix. Undoubtedly, the glass matrix system and its preparation are pivotal factors in achieving high stability and preserving the original performance of embedded phosphor particles. In contrast to the well-established commercial Y3Al5O12:Ce3+ oxide phosphor, red nitride phosphor, which plays a critical role in high-quality lighting, exhibits greater structural instability during the high-temperature synthesis of inorganic glasses. A telluride glass with a refractive index (RI = 2.15@615 nm) akin to that of nitride phosphor (∼2.19) has been devised, demonstrating high efficiency in photon utilization. The lower glass-transition temperature plays a crucial role in safeguarding phosphor particles against erosion resulting from exposure to high-temperature melts. Phosphor-in-glass retains 93% of the quantum efficiency observed for pure phosphor. The assembled white light-emitting diodes module has precise color tuning capabilities, achieving an optimal color rendering index of 93.7, a luminous efficacy of 80.4 lm/W, and a correlated color temperature of 5850 K. These outcomes hold potential for advancing the realm of inorganic package and high-quality white light illumination.

Colour tuning in Sm3+ activated and Sm3+/Eu3+ co-activated SrBi4Ti4O15 phosphors for w-LED applications

SrBi4Ti4O15 (SBT) phosphors activated by Sm3+ and co-activated by Eu3+ have been synthesized in the current research using a straightforward solid-state reaction technique. X-ray Diffraction (XRD) confirms the sample's crystallinity. Scanning electron microscopy (SEM), energy dispersive x-ray spectroscopy (EDX), and elemental mapping have been used to analyse the morphology and elemental composition of the synthesized phosphor. Fourier-transform infrared spectroscopy (FT-IR) analysis has confirmed the vibrational characteristics of the as prepared phosphor. Photoluminescence studies show increase in luminescence intensity in case of Sm3+/Eu3+ co-activated phosphors as compared with singly doped Eu3+ and Sm3+ activated SBTO phosphors. Colour tunability was also observed from reddish-orange to pure red region when Sm3+ activated phosphors were co-activated with Eu3+ ions. These outcomes demonstrate that SrBi4Ti4O15 phosphors activated or co-activated with Sm3+ and Eu3+ can be deployed in w-LEDs and other display devices applications.

Color tunability and temperature sensing capabilities in Dy3+/Sm3+ co-doped transparent oxyfluoride glass ceramics containing K3YF6 nanocrystals

This paper presents the preparation and characterization of transparent oxyfluoride glass ceramics (GCs) that contain nanocrystals of K3YF6 co-doped with Dy3+ and Sm3+. The study investigates the luminescence characteristics, the process of energy transfer (ET) and the behavior of the ratio-metric temperature sensing. The formation of well-defined nanocrystals of K3YF6 in the glass substrate was confirmed by X-ray diffraction (XRD) and transmission electron microscopy (TEM). By varying Sm3+ concentration, a tunable emission ranging from pale yellow to orange-red was observed. Energy transfer from Dy3+ to Sm3+ ions was confirmed through fluorescence spectra and decay curves. Sample K3YF6, containing 0.5 mol%Dy3+/1.2 mol%Sm3+, showed an absolute sensitivity (Sa) of 0.635 % K−1 and relative sensitivity (Sr) of 0.401 % K−1. These findings underscore the promising applications of K3YF6: Dy3+, Sm3+ GCs in multicolor displays and high-performance temperature sensing devices.

Versatile aggregation induced emissive molecular probes incorporating different donor/acceptor groups for tunable multiple color fluorescence

Excited state intramolecular proton transfer (ESIPT) and aggregation induced emission active multicolour fluorescent probes for bioimaging applications has grown popularly in recent years. Herein, we report a series of different donor/acceptor units (Cl, NO2 and O–CH3) bearing anthracene-salicylaldehyde based fluorescent probes and their antibacterial activity and fluorescence imaging of E. Coli bacteria and zebrafish embryos. All the compounds (ASA1, ASA2, ASA3 and ASA4) synthesized via facile one pot condensation reaction of anthracene hydrazide with Salicylaldehyde, 5-Chlorosalicylaldehyde, 5-Nitrosalicylaldehyde, 5-methoxysalicylaldehyde and characterized using all the possible spectroscopic techniques. The noteworthy tuneable emission wavelength shifts from 471 nm to 625 nm and ESIPT characteristics of the compounds were demonstrated through photophysical experiments and single crystal X-ray diffraction analysis. All the experimental results were completely analyzed theoretically on the ground as well as the excited state using density functional theory (DFT) and time dependent density functional theory (TD-DFT) calculations. Compounds ASA1-ASA4 showed fascinating different colour fluorescent (Green, Yellow and Orange) aggregation induced emission features in the THF-H2O mixture. AIE characteristics of ASA1, ASA2, ASA3 and ASA4 were recognized using absorption, emission, fluorescence quantum yield (Φ), DLS and SEM analysis. ASA1, ASA2, ASA3 and ASA4 showed excellent antibacterial activity and ROS generation against E. Coli bacteria. Further, owing to their multicolour fluorescent property all the compounds successfully applied for fluorescent imaging in E. Coli bacteria and live zebrafish embryos.

Role of Histidine 310 in Amydetes vivianii firefly luciferase pH and metal sensitivities and improvement of its color tuning properties.

Firefly luciferases emit yellow-green light and are pH-sensitive, changing the bioluminescence color to red in the presence of heavy metals, acidic pH and high temperatures. These pH and metal-sensitivities have been recently harnessed for intracellular pH indication and toxic metal biosensing. However, whereas the structure of the pH sensor and the metal binding site, which consists mainly of two salt bridges that close the active site (E311/R337 and H310/E354), has been identified, the specific role of residue H310 in pH and metal sensing is still under debate. The Amydetes vivianii firefly luciferase has one of the lowest pH sensitivities among the group of pH-sensitive firefly luciferases, displaying high bioluminescent activity and special spectral selectivity for cadmium and mercury, which makes it a promising analytical reagent. Using site-directed mutagenesis, we have investigated in detail the role of residue H310 on pH and metal sensitivity in this luciferase. Negatively charged residues at position 310 increase the pH sensitivity and metal sensitivity; H310G considerably increases the size of the cavity, severely impacting the activity, H310R closes the cavity, and H310F considerably decreases both pH and metal sensitivities. However, no substitution completely abolished pH and metal sensitivities. The results indicate that the presence of negatively charged and basic side chains at position 310 is important for pH sensitivity and metals coordination, but not essential, indicating that the remaining side chains of E311 and E354 may still coordinate some metals in this site. Furthermore, a metal binding site search predicted that H310 mutations decrease the affinity mainly for Zn, Ni and Hg but less for Cd, and revealed the possible existence of additional binding sites for Zn, Ni and Hg.

Near-unity quantum yield and long-term emission stability in halide perovskite nanocrystal glass composite

Metal halide perovskites are promising optoelectronic materials due to their outstanding luminescent properties. However, the instability of perovskites has long been the bottleneck to their practical applications. Here Cs4PbBr6 nanocrystals based glass composite (Cs4PbBr6 NCs@glass) are successfully prepared, which displays green emission color (520 nm), narrow bandwidth (23 nm) and a near-unity photoluminescence quantum yield (PLQY). The H2O molecules permeating in the lattice of Cs4PbBr6 were found to be a crucial role in the subband energy emission. The Cs4PbBr6 NCs@glass has excellent emission stability; maintains 93 % of initial PL intensity after ultraviolet light irradiation for over 5000 h. In addition, by adjusting the halogen content, we have achieved tunable emission color from blue (450 nm) to green (520 nm) and red (670 nm) on Cs4PbX6 NCs@glass (X = Cl, Br, I), which covers up to 127 % of the National Television Systems Board (NTSC) standard system. Our finding indicates the commercial applications of perovskite materials in lighting and display.

Three-dimensional core shell InGaN/GaN heterostructure for color tunable emitters on the aspect ratio controlled GaN nanorods

In the pursuit of developing red, green and blue emitters, comprehension of color tunability in relation to the nanostructure properties is imperative. Hence, we present a systematic study for the fabrication of color tunable emitters based on GaN nanorods (NRs) prepared via two-step etching technique. In the essence of tunable emission wavelength, aspect ratio controlled GaN NRs were employed for the growth of core shell heterostructure of InGaN/GaN multiple quantum wells (MQWs) using MOCVD and the impact of aspect ratio regulation on the emission wavelength modulation was studied. To analyze the role of the GaN NRs aspect ratio in facilitating the tunable emission wavelength, we employed metrological as well as optical characterizations. Photoluminescence spectra results established a direct relation of the aspect ratio to the emission profile of the GaN NRs. Furthermore, power-dependent photoluminescence (PL) and cathodoluminescence (CL) studies clarified the source of the emission, providing confirmation of the active region's exclusive growth on non-polar sidewalls and the absence of polarization-induced fields. Tunneling microscope measurements revealed a direct relation of the GaN NRs aspect ratio to the emission wavelength profile. In conclusion, we studied comprehensively the impact of aspect ratio regulation for the tunable emission wavelength.

Stimulus-responsive room-temperature phosphorescence with tunable color for time-resolved advanced dynamic anti-counterfeiting

Multi-stimuli responsive multicolored room-temperature phosphorescent (RTP) carbon quantum dots (CQDs) have recently attracted considerable attention, owing to their potential applications in advanced dynamic anti-counterfeiting. The design and development of carbon dots that exhibit both stimulus response characteristics and multicolor RTP emission remains a significant challenge in the field. In this work, we present a novel approach to control the dynamic phosphorescence color and stimulus response properties of CQDs coated on paper by fine-tuning the surface functional groups of the CQDs. Specifically, histidine and 2,4,6-triaminopyrimidine was separately used to prepare N, O co-doped CQDs (NOCQDs) and N-doped CQDs (NCQDs), respectively. These CQDs were further coated on filter paper substrates to achieve water and heating cascade stimulus–response RTP. These stimuli-responsive properties of NOCQDs can be modulated by deprotonating their surface oxygen-containing groups. Eventually, we achieved time-resolved multicolor dynamic anti-counterfeiting by exploiting the stimuli-response properties and lifetimes differences between NOCQDs and NCQDs, realizing the 5D information encryption in all five stimulus-, pattern-, time-, and color-dependent codes. These findings highlight the potential of NOCQDs as advanced anti-counterfeiting materials and lay a foundation for further exploration into the synthesis and properties of CQDs with tunable stimuli-response features and RTP emission.

Color-tunability and energy transfer of a highly thermal-stable BaZnB4O8:Tb3+/Eu3+ phosphor for single-component w-LEDs

A series of Tb3+ single-doped and Tb3+/Eu3+ co-doped BaZnB4O8 samples with color tuning were efficiently synthesized using the solid-state reaction method. The crystal structure, photoluminescence and the energy transfer process (ET) of the samples were systematically studied. The optimal BaZnB4O8:0.08Tb3+ sample shows efficient green emission, then tunable color was achieved by merely introducing a few of Eu3+ ions owing to the highly efficient ET process from Tb3+ to Eu3+ in the BaZnB4O8:0.08Tb3+/yEu3+ samples. The ET efficiency from Tb3+ to Eu3+ of the BaZnB4O8:0.08Tb3+, yEu3+ samples rose from 32.1 % to 51.6 %, simultaneously the luminescent quantum yield improved from 24.7 % to 36.8 %, as the Eu3+ doping concentration increased from 0.125 % to 2 %. Moreover, the Tb3+/Eu3+ co-doped samples exhibited great thermal stability, keeping about 90.2 % (@150 °C) of their original intensity at room temperature. Finally, white light was achieved by a warm w-LEDs fabricated by coating the BaZnB4O8:0.08Tb3+, 0.0025Eu3+ sample on a 365 nm chip. The w-LEDs showed outstanding performance characteristics, with a CCT of 3869 K and a CRI of 89.3. According to the results, Tb3+/Eu3+ co-doped BaZnB4O8 samples have the potential to serve as single-component multicolor-emitting or white-emitting phosphors upon excitation at near-UV wavelength.

Effect of lattice water on the photochromic property/photochromism of a Zn(II)-viologen coordination polymers

Electron transfer is crucial for the rapid response of viologen-based complexes and investigating the factors that affect electron transfer has always been a major challenge. Herein, a new viologen-based complex, formulated as {[Zn5(cbbbc)3(BTC)3(μ1,1-OH)(H2O)5]·22H2O}n, with a three-dimensional framework was successfully designed and synthesized by viologen ligand 1-(3-carboxybenzyl)-4,4′-bipyridinium chloride (Hcbbpy), trimesic acid (H3BTC) and Zn(NO3)2·6H2O. In particular, complex 1 does not exhibit photochromic properties. However, samples of complex 1 heated at 120 and 180 ℃ display tunable colors under UV light irradiation. The experimental results indicate that the compound's light response is less sensitive with higher water content in the lattice. The polarity and hydrogen bonding ability of lattice water in viologen-based complexes can interact with the donor of viologen, leading to a reduction in electron transfer. This study demonstrates the impact of lattice water on electron transfer in viologen-based complexes and offers insights for designing faster response complexes in the future.

Environmental friendly multifunctional orange pigment for cool coating applications

The present study illustrates the development of an environmentally benign intense orange inorganic pigment, by substituting Si4+ metal ion at the Bi3+ site of Bi4V2O11 via solid-state method. The partial replacement of Si4+, induced a strain in the crystal lattice of the compound, which resulted in a substantial improvement in the visible light reflectance. A reduction in oxygen deficiency in the lattice structure facilitated the colour tuning of the pigment series from brownish red to orange and then on to yellowish orange. The composition Bi3.8Si0.2V2O11+δ exhibited a bright orange hue with colour co-ordinates a* = 39, b* = 34 and L* = 52. Furthermore, NIR solar reflectance of the pigment was 86%, which is superior than the reported and commercial orange pigments. Compared to commercial pigment coatings, Bi3.8Si0.2V2O11+δ achieved a temperature reduction of 2 °C inside a foam model house. An exceptional corrosion resistance of 1.6 × 1010 Ωcm2, was registered by the pigment loaded epoxy coating with good stability. The corrosion inhibition mechanism of the pigment operates through the hand in hand working of passive Bi-O and Si-O, active FeOOH and vanadate moiety. On the whole, the new multifunctional orange pigment has the potential to be a viable replacement for the toxic commercial pigments in the market.