Vivid Colors Research Articles

Nanozyme microspheres with structural color-coding labels for synergistic therapy of psoriasis

Psoriasis is an immune system-mediated skin disease identified by the appearance of erythematous as a central symptom. As a recurrent and chronic inflammatory disease, psoriasis is influenced by both genetic and environmental factors and is known to be with no effective cure. Considering a multifaceted etiology of psoriasis, synergistic therapy exhibits great benefits over monotherapy, which becomes common for the treatment of various diseases. Herein, we present the nanozyme microspheres with structural color-coding labels for synergistic therapy of psoriasis. In particular, microsphere hydrogel is fabricated by the edible hydroxypropyl cellulose (HPC), which can generate a photonic liquid crystalline mesophase under lyotropic conditions in solution. Through adjustment of hydrogel components, microspheres endow with different functions, including moisturizing (paraffin), cfDNA scavenging (chitosan), and anti-inflammation (cerium oxide nanozyme). To improve patient convenience, hydrogel drops with different properties are tailored with different vivid structural colors by exploiting the lyotropic behavior of HPC. Of particular note, both in vitro and in vivo experiments have demonstrated the significant therapeutic effects of the encoded structural color microspheres. Green moisturizing microspheres facilitate to relieve dry, flaky skin patches; blue cfDNA scavenging and red anti-inflammatory microspheres significantly reduce skin inflammation. More importantly, combination therapy with encoded microspheres exerted the synergistic effects, including the increased body weight, thicker epidermal layer, and reduced immune activation. Overall, this synergistic treatment offers a promising platform for personalized management of psoriasis and various inflammatory skin diseases.

Highly sensitive colorimetric detection of ascorbic acid using molecularly imprinted photonic crystal hydrogel sensor

Molecular imprinted photonic crystal hydrogel (MICPH) sensors have gained recognition as an efficient platform for selectively detecting analyte molecules. In the present work, we report the development and implementation of a colorimetric sensor based on MIPCH for the selective detection of Ascorbic acid (AA). The fabrication process of the MIPCH sensor involves the photo-polymerization of a hydrogel precursor solution containing AA molecules, which is encapsulated in the interstitial spaces of photonic crystal (PC) opal film. Following the encapsulation, these molecules are selectively removed from the hydrogel network, forming an AA-MIPCH sensor. The sensor exhibits a vivid structural color that redshifts upon rebinding with different concentrations of AA molecules. This alteration in structural coloration serves as a straightforward and visually discernible indicator of the sensor response and enables the quantitative measurement of the target molecule. The sensor exhibits remarkable sensitivity, featuring a low limit of detection (LoD) of 0.011 µM with high selectivity, minimal response time, and promising long-term stability. In addition, the sensor demonstrates its capability to detect the AA even from the complex matrix. A CNN-based deep learning algorithm in MATLAB® was employed to quantitatively predict the concentration of the target molecule. The integration with the machine learning algorithm yields a highly efficient and accurate smart sensor system that is well-suited for real-time sensing of ascorbic acid.

Spontaneous Photonic Jammed Packing of Core-Shell Colloids in Conductive Aqueous Inks for Non-Iridescent Structural Coloration.

Integrating structural colors and conductivity into aqueous inks has the potential to revolutionize wearable electronics, providing flexibility, sustainability, and artistic appeal to electronic components. This study aims to introduce bioinspired color engineering to conductive aqueous inks. Our self-assembly approach involves mixing poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) with sulfonic acid-modified polystyrene (sPS) colloids to generate non-iridescent structural colors in the inks. This spontaneous structural coloration occurs because PEDOT:PSS and sPS colloids can self-assemble into core-shell structures and reversibly cluster into photonic aggregates of maximally random jammed packing within the aqueous environment, as demonstrated by small-angle X-ray scattering. Dissipative particle dynamics simulation confirms that the self-assembly aggregation of PEDOT:PSS chains and sPS colloids can be manipulated by the polymer-colloid interactions. Utilizing the finite-difference time-domain method, we demonstrate that the photonic aggregates of the core-shell colloids achieve close to maximum jammed packing, making them suitable for producing vivid structural colors. These versatile conductive inks offer adjustable color saturation and conductivity, with conductivity levels reaching 36 S cm-1 through the addition of polyethylene glycol oligomer, while enhanced water resistance and mechanical stability are achieved by doping with a cross-linker, poly(ethylene glycol) diglycidyl ether. With these unique features, the inks can create flexible, patterned circuits through processes like coating, writing, and dyeing on large areas, providing eco-friendly, visually appealing colors for customizable, stylish, comfortable, and wearable electronic devices.

Advancing Chlorophyll Photostability: Dual Physicochemical Protection via Ce-Doped Hydrotalcite Organic-Inorganic Hybrid Pigments.

In pursuit of enhancing the photostability of chlorophyll, a novel organic-inorganic hybrid pigment has been synthesized via a supramolecular intercalation assembly method, incorporating cerium-ion-doped hydrotalcite as the host matrix and chlorophyll as the intercalated guest molecule. This innovative pigment amalgamates the vivid coloration properties of organic dyes with the robust stability characteristic of inorganic substances. Determined from the detailed investigation of the structural evolution of chlorophyll during photodegradation, the dual physicochemical protection mechanism is critical to the advancement of chlorophyll photostability. It leverages the oxygen barrier attributes of the hydrotalcite's laminate structure and the ultraviolet light absorption and scattering capabilities of CeO2 nanoparticles formed in situ. Furthermore, Ce-doping introduces a redox cycle between Ce4+ and Ce3+ ions, which serves as a chemical defense by neutralizing reactive oxygen species that emerge during chlorophyll degradation. This multifaceted approach results in a substantial enhancement of photostability, with the hybrid pigment containing 0.3 Ce doped content, demonstrating a mere 5.90% alteration in reflectance at the 635 nm peak after 250 h of UV-accelerated aging. This breakthrough provides a dual physicochemical protective strategy that not only significantly prolongs the lifespan of chlorophyll pigments but also holds potential for broadening their application scope in various industries, including plastics and coatings, where color fastness and durability are paramount.

(Invited) Mie Resonant Silicon Nanosphere Nanoantenna for Fluorescence Enhancement

A nanoantenna is a device that manipulates light propagation and enhances light-matter interaction at the nanoscale. Integration of an emitter into a nanoantenna capable of increasing local density of photonic states at the emission wavelength results in the enhancement of the spontaneous emission rate (Purcell effect) and modifies the emission spectrum. A nanoantenna can also control the directionality and radiation pattern of an emitter. Traditionally, plasmonic nanoantennas made from gold or silver nanostructures supporting localized surface plasmon resonances had been the main stream of the nanoantenna research. Recently, high refractive index nanoparticles having low-order Mie resonances have been attracting attention as a new type of dielectric nanoantennas. Advantages of a dielectric nanoantenna compared to a plasmonic one are the smaller loss and the possession of magnetic type Mie resonances arising from light-induced displacement current. By properly controlling the overlap of the magnetic and electric multipole resonances, radiation patters of an emitter placed nearby can be tailored with high degree of freedom. Furthermore, magnetic-type Mie resonances can couple with higher-order optical transitions of an emitter such as a magnetic-dipole transition, and thus can enhance and control radiation from otherwise weak forbidden transitions.Recently, we have succeeded in producing perfectly spherical nanoparticles of crystalline silicon (Si) in 100-300 nm in diameters. These Si nanospheres exhibit the electric and magnetic multipole resonances at the optical frequency [1]. In this presentation, we first show scattering and absorption properties of the Mie resonant Si nanospheres. Especially, we show that solutions of size-purified Si nanospheres exhibit vivid structural color and the solutions can be used as structural color inks. We then show that the solutions can preserve helicity of incoming circularly-polarized light and can enhance local chiral fields around nanospheres [2, 3]. This property can be used to improve the sensitivity of enantiomer-selective chiral molecular sensing. We then show some examples of enhanced light-matter interaction by Si nanoparticles. These include enhancement of magnetic dipole transitions of an emitter by magnetic-type Mie resonances of Si nanospheres (magnetic Purcell effect) [4, 5], enhancement of excitation and emission processes of in-plane dipoles of monolayer transition metal dichalcogenides (TMDC) [6], and enhancement of a spin forbidden singlet-to-triplet absorption transition of a molecule by Si nanodisks [7, 8].

Chemically and geometrically programmable photoreactive polymers for transformational humidity-sensitive full-color devices

Humidity-sensitive structural color has emerged as a promising technology due to its numerous advantages that include fast response, intuitiveness, stand-alone capability, non-toxicity, as well as resistance to thermal and chemical stresses. Despite immense technological advancements, these structural colors lack the ability to present independent multiple images through transformation. Herein, we present an approach to address this constraint by introducing a chemically and geometrically programmable photoreactive polymer which allows preparation of transformational humidity-sensitive full-color devices. Utilizing azido-grafted carboxymethyl cellulose (CMC-N3) allows adjustments in swelling properties based on the grafting ratio (Γ) of azido groups upon UV-induced crosslinking. Also, the distinctive photo-curability of the polymer enables precise geometric control to achieve vivid colors in combination with disordered plasmonic cavities. Our work culminates in the development of an advanced anti-counterfeiting multiplexer capable of displaying different full-color images with variation in humidity levels. The showcased color displays signify pivotal breakthroughs in tunable optical technologies, illustrating how chemical modifications in hydrogels provides additional degrees of freedom in the design of advanced optical devices.

Photothermally Reconfigurable Biomimetic Photonic Structures Prepared via Crystallization of Polydopamine‐Incorporated Core–Shell Nanoparticles

AbstractSome creatures have periodic nanostructures and chromophores in their flexible organs that allow them to control the color and shape of their skin. Artificial photonic structures that can mimic the aforementioned ability of these natural structures are researched extensively. In this study, polydopamine‐incorporated core–interlayer–shell (CIS‐PDA) nanoparticles capable of shape reconfiguration and expressing vivid structural colors are designed. These nanoparticles can be readily assembled to produce colloidal photonic crystals (CPhCs) and can exhibit vivid structural colors by virtue of their light‐absorbing capability. Soft CPhC films prepared with these nanoparticles undergo stable elastic deformation at 15% strain and exhibit mechanochromic properties. Specifically, the PDA in the CIS nanoparticles can absorb broadband light and exhibit a photothermal effect resembling that of melanosomes in living organisms, which enables self‐healing between multiple CPhC films. Due to their favorable properties, the CPhC films prepared in this study represent promising photothermally reconfigurable photonic materials. Moreover, arbitrarily shaped 2D or 3D surfaces are conformally coated with the films via microimprinting or vacuum wrapping, courtesy of the reconfigurability of these films. These findings suggest that CPhC films prepared with CIS‐PDA nanoparticles can be used as form‐free mechanochromic strain sensors and nonfading optical films for industrial products.

A new genus and species of nudibranch-mimicking Syllidae (Annelida, Polychaeta)

Nudibranch mollusks, which are well-known for their vivid warning coloration and effective defenses, are mimicked by diverse invertebrates to deter predation through both Müllerian and Batesian strategies. Despite extensive documentation across different taxa, mimickers have not been detected among annelids, including polychaetes, until now. This study described a new genus and species of polychaete living on Dendronephthya octocorals in Vietnam and Japan. Belonging to Syllidae, it exhibits unique morphological adaptations such as a low number of body segments, simple chaetae concealed within the parapodia and large and fusiform antennae and cirri. Moreover, these appendages are vividly colored, featuring an internal dark red area with numerous terminal white spots and bright yellow tips, effectively contributing to mimicking the appearance of a nudibranch. This discovery not only documents the first known instance of such mimicry among annelids, but also expands our understanding of evolutionary adaptation and ecological strategies in marine invertebrates.

Topology Optimization Enables High-Q Metasurface for Color Selectivity.

Nonlocal metasurfaces, exemplified by resonant waveguide gratings (RWGs), spatially and angularly configure optical wavefronts through narrow-band resonant modes, unlike the broad-band and broad-angle responses of local metasurfaces. However, forward design techniques for RWGs remain constrained at lower efficiency. Here, we present a topology-optimized metasurface resonant waveguide grating (MRWG) composed of titanium dioxide on a glass substrate capable of operating simultaneously at red, yellow, green, and blue wavelengths. Through adjoint-based topology optimization, while considering nonlocal effects, we significantly enhance its diffraction efficiency, achieving numerical efficiencies up to 78% and Q-factors as high as 1362. Experimentally, we demonstrated efficiencies of up to 59% with a Q-factor of 93. Additionally, we applied our topology-optimized metasurface to color selectivity, producing vivid colors at 4 narrow-band wavelengths. Our investigation represents a significant advancement in metasurface technology, with potential applications in see-through optical combiners and augmented reality platforms.

Edible Flowers in Herbal Beverage Development

Herbal beverages with nutraceutical benefits are becoming more widely acknowledged as healthy dietary choices among mindful consumers. There are numerous types of herbal beverages prepared from different morphological plant elements. Edible flowers, with their unique flavors, distinct aromas, vivid colors, and nutraceutical properties, have gained predominance among all the other botanical ingredients utilized in the formulation of herbal beverages. This review elaborates on applications of edible flowers used in the preparation of herbal teas, infusions, and a few other novel developments in herbal beverages. Although several commercialized herbal beverages have been developed with edible flowers, many other edible flowers with medicinal properties remain unexplored. The review further elaborates on the pharmacotherapeutic properties of these flowers, emphasizing their potential to be used in herbal beverage formulations. Additionally, ensuring the food safety aspects of innovative herbal beverages derived from edible flowers by addressing their potential toxicity and microbiological quality is vitally important. Insights presented here pave the way for incorporating edible flowers in herbal beverages, encouraging nutritious and health-promoting beverage development and consumption.

Preparation and Electrochromic Properties of MnO2/PPy Composite Films with Coral-like Structures.

MnO2/polypyrrole (PPy) composite films were deposited on fluorine-doped tin oxide (FTO) conductive glasses by a two-step wet-chemical method, including electrochemical deposition and chemical bath deposition (CBD). The porous MnO2 films were first grown on FTO glasses by an electrodeposition method. Second, polypyrrole nanoparticles were polymerized by the oxidation-reduction reaction between MnO2 and pyrrole, using the presynthesized MnO2 as the skeleton. Then, MnO2/PPy composite films with coral-like structures were obtained. The electrochemical and electrochromic (EC) properties of the prepared films were investigated. The results show that, compared to the single MnO2 or PPy film, the MnO2/PPy composite film has a larger optical modulation (67.3% at a wavelength of 900 nm), faster response times (4 s for coloration and 3 s for bleaching), and a higher coloration efficiency (218.16 cm2·C-1). The high coloration efficiency attests to the exceptional performance of the composite film in converting electrical signals into vivid color changes. The electrochemical stability test results show that the composite film maintains a stable EC performance after 200 coloration/bleaching cycles. The coral-like structures of the composite film are responsible for the better EC properties.

Prussian blue pigment: Bridging the historical palette to modern innovations

This comprehensive review explores the multifaceted realm of Prussian Blue, a pigment with a rich history and varied applications tracing its origins, artistic applications, and chemical properties. Beginning with its origins as a laboratory creation, the paper traces its evolution into a revered pigment in the artistic world. The review explores the electronic transitions responsible for Prussian Blue's deep blue hue, shedding light on the intricate chemistry behind its vivid coloration. Additionally, the pivotal role of iron ions in determining the pigment's properties is examined in detail, highlighting the importance of precise composition in achieving desired color characteristics. Challenges in the reintegration of Prussian Blue into conservation and restoration projects are also explored, emphasizing the importance of careful preservation techniques to maintain the pigment's integrity and vibrancy. The review discusses the pigment's lightfastness and stability, addressing common issues such as fading and discoloration over time. A notable phenomenon of bronzing particularly associated with Chinese Blue has been characterized by the appearance of yellow or brown hues on the surface of the pigment, that has puzzled artists and conservators for centuries. The review delves into the underlying causes of bronzing, examining factors such as environmental conditions, pigment composition, and application techniques. The review explores the pigment's interactions with other blues and whites, offering insights into the spectrum of shades achievable through careful color mixing and layering techniques. The paper revisits the perennial debate surrounding the permanence of Prussian Blue. While some argue for its enduring stability and longevity, others point to instances of fading and discoloration observed in historical artworks. The manuscript navigates these conflicting perspectives, providing an understanding of Prussian Blue's permanence in different contexts. Prussian Blue stands as a testament to the symbiotic relationship between science and art, where its molecular structure and vibrant shades continue to inspire both chemists in laboratories and artists in studios. The Prussian Blue emerges as a captivating convergence of art and chemistry that has left an indelible mark on laboratory benches and artists' canvases. The unique interplay of ferric and ferrous ions, not only renders a deep blue color but also makes it sensitive to the variation of its environment. The interplay of its refractive index, bronzing tendencies, and tinting strength shapes its artistic applications, influencing the vibrant hues it contributes to diverse palettes. The permanence paradox surrounding Prussian Blue underscores the importance of precision in its preparation. As artists mix and blend, the pigment unveils its versatility, playing a pivotal role in color harmonies and shade variations. Beyond its role in art, Prussian Blue finds diverse applications in medicinal and industrial contexts. From its use as an antidote for heavy metal poisoning to its incorporation into high-performance materials such as batteries and sensors, Prussian Blue continues to demonstrate its versatility and utility in modern society. The review highlights these varied applications, showcasing Prussian Blue's enduring relevance and evolution beyond its historical roots.

Application of Integrated Geological and Geophysical Surveys on the Exploration of Chalcedony Deposits: A Case Study on Nanhong Agate in Liangshan, China

Nanhong agate, esteemed for its vivid color and natural shine, is experiencing a scarcity in supply despite its high demand. The primary deposits of agate, typically found near the surface, have not been extensively explored due to the predominance of traditional manual excavation methods. This research examined the Nanhong agate deposits in the Zhaojue–Meigu region of Liangshan, China, employing the integration of geological and geophysical surveys. Field geological surveys allowed us to outline the general areas where agate is found. Following this, using magnetic surveys, vertical electrical sounding, and controlled-source audio magnetotellurics, agate deposits were located within the conglomerate layer of the second member of the Feixianguan Formation from the Lower Triassic period at depths of less than 100 m. Our results identify mineralized layers, Xuanwei Formation mudstone, and the underlying bedrock, thus supporting the creation of a mineral prediction map. This research provides essential insights and guidance for agate exploration and the development of associated mineral resources.

Phase Separation Derived Anisotropic Adhesive Structural Color Hydrogel Films For Flexible Electronics

AbstractHydrogels hold great promise in the field of flexible electronics. Attempts in this area tend to the microstructure design of hydrogels, giving them specific adhesion and multi‐sensing functions. Here, a novel phase separation‐derived anisotropic adhesive structural color hydrogel film is presented for visually flexible electronics. The hydrogel film is generated by template replicating colloidal crystal by using phase separation emulsions of hydrophilic monomer (acrylic acid, AA), hydrophobic monomer (lauryl methacrylate, LMA), co‐monomer ([2‐(methacryloyloxy) ethyl] dimethyl‐(3‐sulfopropyl) ammonium hydroxide (SBMA)), surfactants (hexadecyl trimethyl ammonium bromide, CTAB) and initiator (ammonium persulphate (APS)). The appearance of phase separation results in asymmetric morphologies of hydrogel film, imparting them with anisotropic adhesive performance. Attributed to the formation of inverse opal scaffold structure, the hydrogel film is featured with vivid structural color, showing superior capability in self‐reporting mechanical behavior. Additionally, benefitting from the presence of abundant ions, the hydrogel film exhibits great conductivity. Thus, the resultant hydrogel film is demonstrated with stable dual‐signal sensing properties involving color‐changing and conductivity feedback ability to respond to human activities. These features make the proposed anisotropic adhesive structural color hydrogel film highly potential in the flexible electronic field.

Flower color modification in Torenia fournieri by genetic engineering of betacyanin pigments

BackgroundBetalains are reddish and yellow pigments that accumulate in a few plant species of the order Caryophyllales. These pigments have antioxidant and medicinal properties and can be used as functional foods. They also enhance resistance to stress or disease in crops. Several plant species belonging to other orders have been genetically engineered to express betalain pigments. Betalains can also be used for flower color modification in ornamental plants, as they confer vivid colors, like red and yellow. To date, betalain engineering to modify the color of Torenia fournieri—or wishbone flower—a popular ornamental plant, has not been attempted.ResultsWe report the production of purple-reddish-flowered torenia plants from the purple torenia cultivar “Crown Violet.” Three betalain-biosynthetic genes encoding CYP76AD1, dihydroxyphenylalanine (DOPA) 4,5-dioxygenase (DOD), and cyclo-DOPA 5-O-glucosyltransferase (5GT) were constitutively ectopically expressed under the cauliflower mosaic virus (CaMV) 35S promoter, and their expression was confirmed by quantitative real-time PCR (qRT-PCR) analysis. The color traits, measured by spectrophotometric colorimeter and spectral absorbance of fresh petal extracts, revealed a successful flower color modification from purple to reddish. Red pigmentation was also observed in whole plants. LC-DAD-MS and HPLC analyses confirmed that the additional accumulated pigments were betacyanins—mainly betanin (betanidin 5-O-glucoside) and, to a lesser extent, isobetanin (isobetanidin 5-O-glucoside). The five endogenous anthocyanins in torenia flower petals were also detected.ConclusionsThis study demonstrates the possibility of foreign betacyanin accumulation in addition to native pigments in torenia, a popular garden bedding plant. To our knowledge, this is the first report presenting engineered expression of betalain pigments in the family Linderniaceae. Genetic engineering of betalains would be valuable in increasing the flower color variation in future breeding programs for torenia.

The genomics of mimicry: Gene expression throughout development provides insights into convergent and divergent phenotypes in a Müllerian mimicry system.

A common goal in evolutionary biology is to discern the mechanisms that produce the astounding diversity of morphologies seen across the tree of life. Aposematic species, those with a conspicuous phenotype coupled with some form of defence, are excellent models to understand the link between vivid colour pattern variations, the natural selection shaping it, and the underlying genetic mechanisms underpinning this variation. Mimicry systems in which species share a conspicuous phenotype can provide an even better model for understanding the mechanisms of colour production in aposematic species, especially if comimics have divergent evolutionary histories. Here we investigate the genetic mechanisms by which mimicry is produced in poison frogs. We assembled a 6.02-Gbp genome with a contig N50 of 310 Kbp, a scaffold N50 of 390 Kbp and 85% of expected tetrapod genes. We leveraged this genome to conduct gene expression analyses throughout development of four colour morphs of Ranitomeya imitator and two colour morphs from both R. fantastica and R. variabilis which R. imitator mimics. We identified a large number of pigmentation and patterning genes differentially expressed throughout development, many of them related to melanophores/melanin, iridophore development and guanine synthesis. We also identify the pteridine synthesis pathway (including genes such as qdpr and xdh) as a key driver of the variation in colour between morphs of these species, and identify several plausible candidates for colouration in vertebrates (e.g. cd36, ep-cadherin and perlwapin). Finally, we hypothesise that keratin genes (e.g. krt8) are important for producing different structural colours within these frogs.

Widening the Gamut of Structural Colors of Gold via Insulator–Metal Bilayer Coatings

Tuning the color of Au has been a longstanding problem in the luxury industry. Conventional approaches, involving Au alloying, compromise purity and demand distinct alloy compositions for each hue. This study demonstrates a lithography‐free method for generating structural colors on a gold surface by adjusting the thickness of titanium dioxide, a high‐index dielectric. While color tuneability is limited if TiO2 is coated directly on the Au surface, a range of vivid colors can be generated if a 50−100 nm thick AuAl2 underlayer is used. AuAl2, an accepted alloy for purple gold, broadens the color gamut, providing a protective coating without diminishing gold purity. The reflectance dip of the bilayer structure exhibits a significant red shift with increasing thickness of the TiO2 layer, allowing diverse colors by TiO2 insulator tuning. Simulation studies corroborate experimental results, affirming that coating a TiO2 layer on the AuAl2 underlayer yields a wide range of colors. This method, based on thin‐film interference, shows promise for widespread use, offering a broad spectrum of structural colors in an industry striving for diverse Au color representation.

New Finding of Inversed Right‐Handed Helix in Dynamically Rotational Evaporation‐Induced Iridescent CNC Film

AbstractCellulose nanocrystal (CNC), as a typical natural photonic crystal material with outstanding advantages, has attracted increasing interests to develop stimulus‐responsive materials with vivid structural colors and circularly polarized light manipulators with high dissymmetry factors for widespread applications. However, limited by its spontaneous left‐handed cholesteric phase and absent right‐handed helical structure, current CNC‐based optical materials mainly achieve the selective reflection of left‐handed circularly polarized light (L‐CP) and the transmission of right‐handed circularly polarized light (R‐CP). Opposite to all reported intrinsic chirality in CNC assemblies, here first prominent twisted right‐handed helix in solid CNC film is found which is prepared through dynamically rotational self‐assembly. The dynamic rotation drives CNC particles to form a right‐handed helix with pitches of sub‐micron level regardless of rotary direction, realizing an ambidextrous reflection of both L‐CP and R‐CP for CNC film with maintained intrinsic structural color, and the first example of inversed right‐handed helix in CNC is further demonstrated. Moreover, the CNC films highly depend on the light propagation direction in term of apparent circular dichroism signals, presenting an exciting prospect for developing quantum transduction. This work is believed a breakthrough on chiral CNC photonic materials, providing new insights and application prospects for chiral CNC materials.

Development of a novel sensory material for rapid detection of mercury ions in various water sources: Solution and solid-state analysis

A xanthene propane nitrile-based sensor material was successfully prepared, and an attempt towards the preparation of polymer bead form was made for the sensitive or selective detection of mercury ions (Hg2+) in water. The sensor material in solution as well as in polymeric form showed amazing selectivity over other added metal ions with a naked eye color change, UV visible spectral and fluorescence spectral change, and a rapid and excellent color change from colorless to purple. The 1H NMR study exposed the probable binding site of the probe with the added mercury ion. In this study, the imine nitrogen and the C = O interact with the mercury ion, resulting in the ring opening of lactam with a vivid color change. The EDTA test was done to verify the reversible behavior of the probe and confirmed its reversibility by UV–visible and fluorescence spectral studies. The polymer bead made using this probe can be used as a tool for monitoring mercury ions in real time in different sources of water samples. The sensor molecule itself senses the mercury ion in its solid state by simple grinding and changes its color from pale yellow to deep purple. The sensor color change response is very rapid towards mercury detection, which is confirmed by the prepared test strip.

Multicolor Electrochromic Metamaterials Based on Mie Scatterer Nanospheres

AbstractElectrochromic materials (ECMs), the colors of which can be electrically modulated by small driving voltages with a unique open‐circuit memory effect, are in great demand in various application fields. However, traditional ECMs exhibit a narrow modulation range of color gamut under the electric stimulus, owing to the monotonous chemical coloration in an absorption manner. Multicolor ECMs with optical nanostructures can greatly extend the color gamut by incorporating complex optical interactions such as interference and diffraction. Mie scatterer nanospheres (MSNSs) are a kind of nanospheres with unique optical structures that can simply exhibit and change vivid structural colors by adjusting their diameters. Herein, this work reports multicolor ECMs based on MSNSs with polymer shells of poly‐3,4‐ethylenedioxythiophene (PEDOT) and poly‐pyrrole (PPY). They possess a superior optical modulation capability with a wide color gamut, a fast response rate, a visible‐angle‐independence, etc. Additionally, a nano‐dispersion strategy is used to prepare mixed electrochromic pigments with a nanoscale uniformity, further broadening the color gamut tunability. Simulations in wave optics and Mie scattering theory are conducted to unveil the multicolor modulation mechanism, demonstrating the interactions of MSNSs with incident lights. This work provides a feasible approach for fabricating multicolor ECMs with more application potential.