ABSTRACT
Cardiac reprogramming has emerged as a novel therapeutic approach to regenerating the damaged heart by directly converting endogenous cardiac fibroblasts (CFs) into induced cardiomyocytes (iCMs). Cardiac reprogramming requires the activation of the cardiogenic transcriptional program in concert with the repression of the fibroblastic transcriptional program. Lysine-specific demethylase 1 (LSD1) plays an instrumental role in many physiological processes such as cell growth, differentiation and metabolism. The epigenetic modifications of histones are essential for the accurate expression of genes in cardiomyocytes and the normal functioning of the heart. However, the effect of LSD1 in regulating the cardiogenic transcriptional program under myocardial ischemia/reperfusion (I/R) injury remains unclear. Thus, mice I/R injury was induced by 4 and 24 h reperfusion after 1-h occlusion of the left anterior descending coronary artery. The primary CFs and CMs were exposed under oxygen and glucose deprivation (OGD) to mimic I/R injury. The expression of LSD1 significantly decreased in I/R injured heart tissue and OGD-injured primary CFs and CM, and methylated histone presented a notable increase in OGD-injured primary CFs. Overexpression of LSD1 inhibited the injury of primary CFs induced by OGD, but showed limited inhibition on injured primary CMs. Under the OGD condition, LSD1 overexpression significantly increased cell viability, decreased cell apoptosis and reactive oxygen species (ROS) production of primary CFs. The expression of core cardiogenic transcription factors and cardiac genes were significantly decreased in OGD injured primary CFs, whereas LSD1 overexpression reversed the decrease of transcription factors and cardiac genes under the OGD condition. In conclusion, the overexpression of LSD1 has a protective role in I/R injury by inhibiting the histone methylation of primary CFs and regulates the expressions of core cardiogenic transcription factors and cardiac genes, which can prove to be a potential approach for direct cardiac reprogramming.
Subject(s)
Histone Demethylases , Myocardial Reperfusion Injury , Reperfusion Injury , Animals , Apoptosis , Fibroblasts/metabolism , Glucose/metabolism , Histone Demethylases/genetics , Histone Demethylases/metabolism , Histones , Mice , Myocardial Reperfusion Injury/genetics , Myocardial Reperfusion Injury/metabolism , Oxygen/metabolism , Reperfusion Injury/genetics , Reperfusion Injury/metabolism , Transcription Factors/metabolismABSTRACT
The trade-off problem between light absorption and charge collection under lower band-bending (bias) is extremely difficult to resolve in water splitting on photoelectrodes. Although the use of metallic back-reflectors, antireflection coatings, and textured substrates and light absorbers enable the improvement of light utilization efficiency, these methods still suffer from high cost and complex fabrication process, especially, incompetent separation of photogenerated carriers. Here taking the hematite (α-Fe2O3) photoanode as a model, we report that a noncontact photonic crystal (PC) film composed of silica nanoparticles and ethoxylated trimethylolpropane triacrylate (ETPTA) resin can significantly enhance the photoelectrochemical (PEC) activity of the photoelectrode. Specifically, more than 250 mV cathodic shift in the onset potential and 4 times larger photocurrent at 1.0 V versus a reversible hydrogen electrode (RHE) were achieved over the α-Fe2O3-PC photoanode hybrid system, compared with the pristine α-Fe2O3 photoanode. Our work showed that a PC film not only boosted light absorption of the α-Fe2O3 layer but also improved its charge transfer efficiency under light illumination. These new findings of the synergistic effect will open a new avenue to design high-performance solar energy conversion devices.
ABSTRACT
YOHCO3 colloidal particles with tunable size, composition, and optical properties were prepared, and they were used for the fabrication of amorphous photonic crystals? (APCs) patterns through direct hand painting. YOHCO3 colloids were synthesized by a seeding growth method, in which the colloid size could be controlled by altering the seed amounts and the composition and optical properties can be altered via the doping of Eu3+. APCs? films with bright, permanent, and tunable structural colors were prepared by the self-assembly of YOHCO3 colloids of different sizes. Multicolor patterns can be obtained quickly and efficiently by hand painting with the dispersion of YOHCO3 colloids as ink. An APCs? pattern assembled from YOHCO3:Eu colloids is also fabricated, and the pattern shows blue structural color under natural light and bright red colors under illumination of UV light. The facile synthesis procedure, simple assembly process, and unique optical properties of the APCs make it valuable for practical applications such as structural color-based printing and anticounterfeiting.
ABSTRACT
Resonance energy transfer (RET) describes the process that energy is transferred from an excited donor to an acceptor molecule, leading to a reduction in the fluorescence emission intensity of the donor and an increase in that of the acceptor. By this technique, measurements with the good sensitivity can be made about distance within 1 to 10 nm under physiological conditions. For this reason, the RET technique has been widely used in polymer science, biochemistry, and structural biology. Recently, a number of RET systems incorporated with nanoparticles, such as quantum dots, gold nanoparticles, and upconversion nanoparticles, have been developed. These nanocrystals retain their optical superiority and can act as either a donor or a quencher, thereby enhancing the performance of RET systems and providing more opportunities in excitation wavelength selection. Notably, lanthanide-doped upconversion nanophosphors (UCNPs) have attracted considerable attention due to their inherent advantages of large anti-Stoke shifts, long luminescence lifetimes, and absence of autofluorescence under low energy near-infrared (NIR) light excitation. These nanoparticles are promising for the biodetection of various types of analytes. Undoubtedly, the developments of those applications usually rely on resonance energy transfer, which could be regarded as a flexible technology to mediate energy transfer from upconversion phosphor to acceptor for the design of luminescent functional nanoplatforms. Currently, researchers have developed many RET-based upconversion nanosystems (RET-UCNP) that respond to specific changes in the biological environments. Specifically, small organic molecules, biological molecules, metal-organic complexes, or inorganic nanoparticles were carefully selected and bound to the surface of upconversion nanoparticles for the preparation of RET-UCNP nanosystems. Benefiting from the advantage and versatility offered by this technology, the research of RET-based upconversion nanomaterials should have significant implications for advanced biomedical applications. It should be noted that energy transfer in a UCNP based nanosystem is most often related to resonance energy transfer but that reabsorption (and maybe other energy transfer processes) may also play an important role and that more studies regarding the fundamental aspects for energy transfer with UCNPs is necessary. In this Account, we present an overview of recent advances in RET-based upconversion nanocomposites for biodetection with a particular focus on our own work. We have designed a series of upconversion nanoplatforms with remarkably high versatility for different applications. The experience gained from our strategic design and experimental investigations will allow for the construction of next-generation luminescent nanoplatform with marked improvements in their performance. The key aspects of this Account include fundamental principles, design and preparation strategies, biodetection in vitro and in vivo, future opportunities, and challenges of RET-UCNP nanosystems.
Subject(s)
Energy Transfer , Nanostructures , Infrared RaysABSTRACT
OBJECTIVE: Pulmonary arterial hypertension (PAH) is a fatal disease characterized by a persistent elevation of pulmonary artery pressure and ventricular hypertrophy. Tetrandrine is a bisbenzylisoquinoline alkaloid that can decrease blood pressure, inhibit the proliferation of vascular smooth muscle cells, and block cardiac hypertrophy, but whether it has a therapeutic effect on PAH remains poorly defined. This study was undertaken to investigate the efficacy of tetrandrine on PAH. METHODS: Forty-eight male Sprague-Dawley rats were randomly and equally divided into four groups. The control group was injected with normal saline; the others were injected with monocrotaline (MCT) to induce PAH, then treated with saline, tetrandrine, and vardenafil, respectively, from day 21 to day 42. On day 43, we measured the mean pulmonary artery pressure under general anesthesia, dissected the rat, and calculated the right ventricular hypertrophy index [right ventricle/(left ventricle plus septum)]. Later we observed the changes in the pulmonary vascular wall; measured the expression of cyclic guanosine monophosphate-dependent protein kinase type 1 and inducible nitric oxide synthase; measured the levels of superoxide dismutase, glutathione, malondialdehyde, and catalase; and then compared the results among groups. RESULTS: Compared with the MCT group, rats treated with tetrandrine had attenuated mean pulmonary artery pressure (20.48 ± 1.49 vs 30.07 ± 1.51; P < .01) and right ventricular hypertrophy index (49.19 ± 2.45 vs 68.50 ± 1.95; P < .01), inhibited proliferation of pulmonary artery smooth muscle cells, and improved endothelial function. Tetrandrine also upregulated the expression of protein kinase type 1 (90.86 ± 1.95 vs 67.34 ± 1.50; P < .01); downregulated the expression of inducible nitric oxide synthase (74.76 ± 1.48 vs 80.19 ± 0.28; P < .01); increased levels of superoxide dismutase (245.54 ± 12.98 vs 166.16 ± 21.42; P < .01), glutathione (0.699 ± 0.032 vs 0.514 ± 0.056; P < .01), and catalase (32.13 ± 2.33 vs 27.19 ± 2.72; P < .01); and decreased malondialdehyde (1.027 ± 0.039 vs 1.462 ± 0.055; P < .01). CONCLUSIONS: Tetrandrine alleviated MCT-induced PAH through regulation of nitric oxide signaling pathway and antioxidant and antiproliferation effects.
Subject(s)
Antihypertensive Agents/pharmacology , Arterial Pressure/drug effects , Benzylisoquinolines/pharmacology , Cyclic GMP-Dependent Protein Kinase Type I/metabolism , Hypertension, Pulmonary/prevention & control , Monocrotaline , Nitric Oxide Synthase Type II/metabolism , Pulmonary Artery/drug effects , Animals , Anti-Inflammatory Agents/pharmacology , Antioxidants/pharmacology , Catalase/metabolism , Cell Proliferation/drug effects , Disease Models, Animal , Glutathione/metabolism , Hypertension, Pulmonary/chemically induced , Hypertension, Pulmonary/enzymology , Hypertension, Pulmonary/physiopathology , Hypertrophy, Right Ventricular/chemically induced , Hypertrophy, Right Ventricular/enzymology , Hypertrophy, Right Ventricular/physiopathology , Hypertrophy, Right Ventricular/prevention & control , Male , Malondialdehyde/metabolism , Muscle, Smooth, Vascular/drug effects , Muscle, Smooth, Vascular/enzymology , Muscle, Smooth, Vascular/physiopathology , Myocytes, Smooth Muscle/drug effects , Myocytes, Smooth Muscle/enzymology , Oxidative Stress/drug effects , Pulmonary Artery/enzymology , Pulmonary Artery/physiopathology , Rats, Sprague-Dawley , Signal Transduction/drug effects , Superoxide Dismutase/metabolism , Time Factors , Vascular Remodeling/drug effects , Ventricular Remodeling/drug effectsABSTRACT
Mechanochromic photonic crystals are attractive due to their force-dependent structural colors; however, showing unrecordable color and unsatisfied performances, which significantly limits their development and expansion toward advanced applications. Here, a thermal-responsive mechanochromic photonic crystal with a multicolor recordability-erasability was fabricated by combining non-close-packing mechanochromic photonic crystals and phase-change materials. Multicolor recordability is realized by pressing thermal-responsive mechanochromic photonic crystals to obtain target colors over the phase-change temperature followed by fixing the target colors and deformed configuration at room temperature. The stable recorded color can be erased and reconfigured by simply heating and similar color-recording procedures respectively due to the thermoswitchable on-off mechanochromism of thermal-responsive mechanochromic photonic crystals along with solid-gel phase transition. These thermal-responsive mechanochromic photonic crystals are ideal rewritable papers for ink-freely achieving multicolor patterns with high resolution, difficult for conventional photonic papers. This work offers a perspective for designing color-recordable/erasable and other stimulus-switchable materials with advanced applications.
ABSTRACT
Pulmonary artery smooth muscle cell (PASMC) dysfunction is the central pathogenic mechanism in pulmonary hypertension (PH). This study explored the mechanism of action of RUNX1, a potential therapeutic target for PH, in PASMCs. A PH mouse model was used to investigate the impacts of RUNX1 knockdown on hemodynamics, right ventricular hypertrophy (RVH), and pulmonary artery remodeling (HE staining). Isolated PASMCs were transfected with RUNX1- or CBX5-related vectors and then subjected to cell function assays. Immunoprecipitation was used to detect molecular binding and ubiquitination. RUNX1 knockdown reduced right ventricular systolic pressure, RVH, and pulmonary artery remodeling in mice with PH. Knockdown of RUNX1 or CBX5 suppressed proliferation, invasion, and migration and stimulated apoptosis in PASMCs under hypoxia. RUNX1 enhanced USP15 promoter activity. USP15 bound to CBX5 and reduced CBX5 ubiquitination, thereby promoting CBX5 expression. CBX5 overexpression promoted the proliferation and movement of hypoxic PASMCs with reduced RUNX1 expression and decreased their apoptosis. In conclusion, RUNX1 knockdown alleviates PH in mice and reduces hypoxia-induced PASMC dysfunction by inhibiting USP15 transcription, thereby promoting the ubiquitination and degradation of CBX5.
ABSTRACT
Fluorescent photonic crystals (FPCs) are ideal candidates for regulating dyes' fluorescence through their unique photonic band gaps (PBGs). However, challenges, including the lack of dynamic regulation of fluorescence, dye release in solvents, and instability, dramatically limit their practical applications. Here, we report mechanochromic and solvomechanochromic rhodamine B (RhB)-based FPCs with dynamic regulation of photoluminescence (PL) by stretching and swelling, brilliant fluorescent and structural colors, and no release of the RhB in solvents. The FPCs with force/solvent-responsive nonclose-packing structures were fabricated by (1) preparing RhB-silica particles by combining click chemistry and cohydrolysis processes and (2) self-assembling these particles in poly(ethylene glycol) phenyl ether acrylate followed by a photopolymerization. Maximal PL inhibition (37%, stretching strain of 6.8%) and enhancement (150%, swelling time of 8 min) were gained when PBGs and their blue edges are precisely adjusted to the PL peak position, respectively. Compared with stretching, PL regulation is more efficient by swelling. These characteristics benefit from the rational design and combination of unique compositions, chemical bonds, nonclosely packed micro/nanostructures, and solvents for swelling. Moreover, these FPCs have been used to encrypt photonic patterns, which display background/strain/angle/UV-dependent color contrasts, showing their potential applications in multilevel anticounterfeiting, optical devices, wireless sensors, etc.
ABSTRACT
Smart colloidal photonic crystals (PCs) with stimuli-responsive periodic micro/nano-structures, photonic bandgaps, and structural colors have shown unique advantages (high sensitivity, visual readout, wireless characteristics, etc.) in sensing by outputting diverse structural colors and reflection signals. In this review, smart PC sensors are summarized according to their fabrications, structures, sensing mechanisms, and applications. The fabrications of colloidal PCs are mainly by self-assembling the well-defined nanoparticles into the periodical structure (supersaturation-, polymerization-, evaporation-, shear-, interaction-, and field-induced self-assembly process). Their structures can be divided into two groups: closely packed and non-closely packed nano-structures. The sensing mechanisms can be explained by Bragg's law, including the change in the effective refractive index, lattice constant, and the order degree. The sensing applications are detailly introduced according to the analytes of the target, including solvents, vapors, humidity, mechanical force, temperature, electrical field, magnetic field, pH, ions/molecules, and so on. Finally, the corresponding challenges and the future potential prospects of artificial smart colloidal PCs in the sensing field are discussed.
ABSTRACT
Photonic crystals (PCs) have attracted great interest and wide applications in displays, printing, anti-counterfeiting, etc. However, two main challenges significantly hinder their applications: 1) the tradeoff between high optical transparency across the whole visible range and brilliant colors requiring a large refractive index contrast (Δn), and 2) the way of regulating structural colors by altering tens of different sizes. To address these issues, a new type of metal-organic framework (MOF)-based transparent photonic crystal (TPC) has been fabricated through self-assembling MOF particles into three-dimensional ordered structures which were then infiltrated by polydimethylsiloxane (PDMS). Compared to conventional PCs, these TPCs exhibit 1) both brilliant forward iridescent structural colors and high transmittance (>75 %) across the whole visible spectra range, and 2) conveniently adjustable colors based on bidisperse particles. The unique color-generating mechanism of the light diffraction by each plane lattice and the small Δn between MOF particles and PDMS are the keys to TPCs' characteristics. Moreover, the prepared invisible anti-counterfeit labels can reversibly hide-reveal patterns with elaborate and exchangeable color contrast in a non-destructive way, showing potential applications in anti-counterfeiting, information encryption, and optical devices.
ABSTRACT
Solvent wrapped "metastable" crystalline colloidal arrays (CCAs) have been prepared by supersaturation induced precipitation and self-assembly of monodisperse particles in polar/nonpolar organic solvents. These metastable CCAs possess ordered structures but with less stability comparing with traditionally fixed colloidal crystal systems. They are stabilized by the balance between long-range attraction and electrostatic repulsion of neighboring like-charged particles. Monitoring the reflection intensity during evaporation suggests that these crystals can exist for several hours at 90 °C and even longer at room temperature. Based on the evolution of particle volume fraction in whole suspension (φ(SiO2)), crystal phase (φ(crystal)), and liquid phase (φ(liquid)), the formation of metastable CCAs can be understood as a microscopic phase separation process, where the homogeneous dispersion will separate into a "crystal phase" with orderly stacked particles and a "liquid phase" with randomly dispersed particles. Further calculation of the volume fraction of crystal phase (V(crystal)/V(total)) and the ratio of particles in crystal phase (f(crystal)) shows that with the increase of designed Φ(SiO2), more particles precipitate to form colloidal crystals with larger sizes but the lattice spacing of the microcrystals remains constant. Unlike fixed or traditional responsive CCAs, these metastable CCAs can reversibly assemble and disassemble with great ease, because little energy is involved or required in this transformation. Therefore, they can sense weak external disturbances, including subtle motion and slight friction or shearing forces.
ABSTRACT
Objectives: Epicardial adipose tissue (EpAT) is known for its role in supporting the cardiomyocytes. Lysine-specific demethylase 1 (LSD1), a typical lysine demethylase, is an essential regulator for the maintenance of beige adipocytes. However, the effect of LSD1 in the adipogenic differentiation of beige adipocytes in EpAT, and its function on oxygen and glucose deprivation (OGD)-injured cardiomyocytes remain unclear. Materials and Methods: Heart tissues from young mice and elder mice were collected for immunohistochemical staining. LSD1 in 3T3-L1 cells was knocked down by LSD1-shRNA lentivirus infection. The qRT-PCR, western blotting, and Oil Red O staining were employed to detect the adipogenic differentiation of 3T3-L1 cells and formation of beige adipocytes. The cardiomyocytes co-cultured with beige adipocytes were used for OGD treatment. Cell apoptosis was analyzed by flow cytometry. The lactate dehydrogenase (LDH) and superoxide dismutase (SOD) activity were analyzed using commercially available kits. Results: The decrease of LSD1 was related to the age-dependent loss of beige adipocytes in mice EpAT. LSD1 knockdown inhibited the adipogenic differentiation of 3T3-L1 cells and formation of beige adipocytes. The down-regulation of LSD1 in 3T3-L1 cells decreased the protective effect of mature adipocytes on OGD-injured cardiomyocytes. Conclusion: The decreased expression of LSD1 in mice EpAT was associated with age-dependent ablation of beige adipocytes. The protective effect of beige adipocytes on OGD-injured cardiomyocytes is reduced by knockdown of LSD1 in adipocytes. The present study provided exciting insights into establishing novel therapies against age-dependent cardiac diseases.
ABSTRACT
It is a great challenge to detect hydrofluoric acid (HF) with high precision, good selectivity, and visual readouts characteristics. Herein, a new photonic crystal (PC) hydrogel HF sensor based on the "selective etching-induced swelling" mechanism has been developed. This HF sensor consisting of silica/water/hydroxyethyl acrylate and non-closely packed structures was fabricated through simple non-close-assembling, photopolymerization, and water swelling processes. Silica slightly etched by HF induces the swelling of PC hydrogel, leading to the variation of reflection wavelength and structural colors, thereby realizing visually and spectrally sensing HF (0-10 mM). The unique structure and compositions of PC hydrogel are the keys to the high sensing precision, outstanding selectivity, and low detection limit (0.1 mM). Furthermore, the sensor possesses tailorable, portable, easy-to-operation, and low-cost (<0.01 $/sensor) advantages. This work provides an efficient and convenient tool for sensing and recognizing HF in the aqueous solution for practical applications and upgrades the basic understanding of the photonic sensing mechanism.
Subject(s)
Hydrofluoric Acid , Hydrogels , Hydrogels/chemistry , PhotonsABSTRACT
Retroreflective structural colors can usually be achieved based on interference combined with a total internal reflection mechanism or diffraction of a monolayer hexagonal two-dimensional (2D) colloidal array. Here, a novel retroreflective structural color was generated based on a hexagonal-parallelogram lattice transformation by stretching 3D photonic crystals with nonclosely packed long-range order. Compared to previous retroreflective colors, this new retroreflective color exhibits two unique off/on color switches: (1) a strain-dependent off/on color switch along the stretching direction and (2) a sample horizontal rotation angle-dependent off/on color switch under the fixed strain. These strain-responsive retroreflective colors are ideal candidates for visually sensing kinesio tapes' strain in practical applications and anticounterfeiting. This work reveals a new structural color regulation mechanism and will advance potential applications in anticounterfeiting, sensing, displays, etc.
ABSTRACT
Stimulus-responsive photonic crystals (PCs) possessing unconventional nonclosely packed structures have received growing attention due to their unique capability of mimicking the active structural colors of natural organisms (for example, chameleons' mechanochromic properties). However, there is rarely any systematic review regarding the progress of nonclose-packed photonic crystals (NPCs), involving their fabrication, working mechanisms, and applications. Herein, a comprehensive review of the fundamental principles and practical fabrication strategies of one/two/three-dimensional NPCs is summarized from the perspective of designing nonclose-packed structures. Subsequently, responsive NPCs with exciting functions and working mechanisms are sorted and delineated according to their diverse responses to physical (force, temperature, magnetic, and electric fields), chemical (ions, pH, vapors, and solvents), and biological (glucose, organophosphate, creatinine, and bacteria) stimuli. We then systematically introduced and discussed the applications of NPCs in sensors, printing, anticounterfeiting, display, optical devices, etc. Finally, the current challenges and development prospects for NPCs are presented. This review not only concludes the design principle for NPCs but also provides a significant basis for the exploration of next-generation NPCs.
ABSTRACT
Colloidal photonic crystals (PCs) feature face-centered cubic (FCC) lattices since spherical particles are usually used as building blocks; however, constructing structural colors originating from PCs with non-FCC lattices is still a big challenge due to the difficulty in preparing non-spherical particles with tunable morphologies, sizes, uniformity, and surface properties and assembling them into ordered structures. Here, uniform, positively charged, and hollow mesoporous cubic silica particles (hmc-SiO2) with tunable sizes and shell thicknesses prepared by a template approach are used to self-assemble into PCs with rhombohedral lattice. The reflection wavelengths and structural colors of the PCs can be controlled by altering the sizes or the shell thicknesses of the hmc-SiO2. Additionally, photoluminescent PCs have been fabricated by taking the advantage of the click chemistry between amino silane and isothiocyanate of a commercial dye. The PC pattern achieved by a hand-writing way with the solution of the photoluminescent hmc-SiO2 instantly and reversibly shows the structural color under visible light but a different photoluminescent color under UV illumination, which is useful for anticounterfeiting and information encryption. The non-FCC structured and photoluminescent PCs will upgrade the basic understanding of the structural colors and facilitate their applications in optical devices, anti-counterfeiting, and so forth.
ABSTRACT
Inspired by the brilliant and tunable structural colors based on the large refractive index contrast (Δn) and non-close-packing structures of chameleon skins, ZnS-silica photonic crystals (PCs) with highly saturated and adjustable colors are fabricated. Due to the large Δn and non-close-packing structure, ZnS-silica PCs show 1) intense reflectance (maximal: 90%), wide photonic bandgaps, and large peak areas, 2.6-7.6, 1.6, and 4.0 times higher than those of silica PCs, respectively; 2) tunable colors by simply adjusting the volume fraction of particles with the same size, more convenient than the conventional way of altering particle sizes; and 3) a relatively low threshold of PC's thickness (57 µm) possessing maximal reflectance compared to that (>200 µm) of the silica PCs. Benefiting from the core-shell structure of the particles, various derived photonic superstructures are fabricated by co-assembling ZnS-silica and silica particles into PCs or by selectively etching silica or ZnS of ZnS-silica/silica and ZnS-silica PCs. A new information encryption technique is developed based on the unique reversible "disorder-order" switch of water-responsive photonic superstructures. Additionally, ZnS-silica PCs are ideal candidates for enhancing fluorescence (approximately tenfold), approximately six times higher than that of silica PC.
ABSTRACT
Photonic crystal (PC) patterns have shown wide applications in optical devices, information encryption, anticounterfeiting, etc. Unfortunately, it is still a great challenge to reconfigure the PC patterns once fabricated. Herein, a new strategy is presented to reconfigure self-recordable PC patterns by printing local patterns into the chameleon-inspired PC papers using the phase change material (PCM) as ink and then erasing the patterns in ethanol. Multicolor and high-resolution (25 and 75 µm for dot and lines, respectively) patterns can be efficiently and repeatedly reconfigured. In addition, the photonic patterns based on the PC paper and PCM combinations are gifted with mechanochromic characteristics and can show programmable and reversible color change under pressure. The high melting point of the ink, nonclosely packed structures of the PC paper, and the similar solubility parameter of PC paper, PCM, and ethanol are the keys for all these characteristics. This work offers a simple, flexible, efficient way to reconfigure PC patterns with mechanochromic properties and could open up exciting applications for novel hand-operation-based anticounterfeiting and optical devices.
ABSTRACT
The skins of chameleons have attracted growing interest because they have sensitive mechano-chromic properties and bright colors due to the large surface-to-surface distances (Ds-s) between neighboring particles and contrast of the refractive index (Δn), respectively. Inspired by these, artificial mechano-chromic photonic skins (MPSs) mimicking those of chameleons were fabricated by the large Δn and Ds-s. The fabrication is considerably simple and efficient based on the self-assembly strategy using commercial chemicals and materials. The reflectance of MPSs depends on the value of Δn, which can be greatly increased to 70% with a Δn of 0.035, leading to their brilliant colors. Because of the large Ds-s, the MPSs possess outstanding mechano-chromic performances, including a large maximal (Δλ = 205 nm) and effective (Δλe = 184 nm) tuning range of the reflection wavelength, high sensitivity (368), fast responsiveness (2.2 nm/ms), good stabilities (>1 year), and reversibility (>100 times). Based on these advantages, MPSs have been used for self-reporting the strain of earthworms by outputting diverse colors during the peristaltic process, indicating the great potential of the MPSs as visual sensors and optical coatings.