Excitation Range Research Articles

Full‐Color Tunability Room Temperature Phosphorescence from Inorganic Crystal Frameworks

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

Facile synthesis of azines by carboxylic acid esters as catalyst and facilitation of intersystem crossing (ISC) in azines by azine chromophore

Development of new organic synthetic methods fascinating the researchers which facilitating the increasing demands of the modern society, environmental friendly with high efficiency and low cost. The introduction of chromophores in an organic molecules facilitating intersystem crossing (ISC) to harvest both singlet and triplet excitons is also currently demanding field. We report a facile synthesis of symmetrical azines from carbonyl compounds and hydrazine hydrate with carboxylic acid esters as catalyst in methanol. This reaction presents a condensation of primary amino groups in hydrazine hydrate and carbonyl compounds took place simultaneously in a very short refluxing time. The prepared azines 1–10 were structurally analysed by various analytical techniques such as LC-MS1, H NMR13, C NMR, UV-Vis, FTIR and single crystal X-ray diffraction. Photoluminescence properties of prepared azines were recorded in CCl4 at 1 × 10−3 M and excitation range from 329 to 362 nm. The photoluminescence analysis results revealed that compounds 1–10 (except 8) were showed delayed fluorescence and 8 was showed fluorescence property. The photophysical properties of compounds 1–10 such as electron density and band gap energies was calculated by density function theory. This results revealed that the intra-molecular charge transfer occurs within the azines. The azine function in the azines enabling intersystem crossing hence, it is showing phosphorescence.

On the rate-limiting dynamics of force development in muscle.

Skeletal muscles produce forces relatively slowly compared with the action potentials that excite them. The dynamics of force production are governed by multiple processes, such as calcium activation, cycling of cross-bridges between myofilaments, and contraction against elastic tissues and the body. These processes have been included piecemeal in some muscle models, but not integrated to reveal which are the most rate limiting. We therefore examined their integrative contributions to force development in two conventional types of muscle models: Hill-type and cross-bridge. We found that no combination of these processes can self-consistently reproduce classic data such as twitch and tetanus. Rather, additional dynamics are needed following calcium activation and facilitating cross-bridge cycling, such as for cooperative myofilament interaction and reconfiguration. We provisionally lump such processes into a simple first-order model of 'force facilitation dynamics' that integrate into a cross-bridge-type muscle model. The proposed model self-consistently reproduces force development for a range of excitations including twitch and tetanus and electromyography-to-force curves. The model's step response reveals relatively small timing contributions of calcium activation (3%), cross-bridge cycling (3%) and contraction (27%) to overall force development of human quadriceps, with the remainder (67%) explained by force facilitation. The same set of model parameters predicts the change in force magnitude (gain) and timing (phase delay) as a function of excitatory firing rate, or as a function of cyclic contraction frequency. Although experiments are necessary to reveal the dynamics of muscle, integrative models are useful for identifying the main rate-limiting processes.

A Novel Broadband Green Phosphor La2W2O9: Bi3+, and Its Application in High Color-Rendering Index pc-WLED

Broadband green phosphors have important applications in overcoming the blue-green (cyan) 470–510[Formula: see text]nm gap of phosphor-converted white LED (pc-WLED) and achieving high color rendering index (CRI) white lighting. In this work, a broadband green phosphor La2W2O9: [Formula: see text]Bi[Formula: see text] was synthesized by solid-state method. The phase, morphology and luminescence properties of the series of phosphors were systematically studied. The results showed the La2W2O9: [Formula: see text]Bi[Formula: see text] green phosphor exhibits a wide emission band in the range of 400–800[Formula: see text]nm with full width at half-maximum (FWHM) of 164[Formula: see text]nm, filling the cyan gap and reaching its peak at 550[Formula: see text]nm. The phosphor exhibits broadband excitation, and the excitation range covers the wavelength region of 200–500[Formula: see text]nm, and matches well with commercial ultraviolet LED. With the obtained broadband green phosphor, commercial CaAlSiN3:Eu[Formula: see text] red phosphor, commercial BaMgAl[Formula: see text]O17:Eu[Formula: see text] blue phosphor, and a 365[Formula: see text]nm commercial chip, a warm white pc-WLED device with a high color-rendering index (Ra[Formula: see text]97.4, R1–R15[Formula: see text]90) and low correlated color temperature (CCT[Formula: see text]3610[Formula: see text]K) was fabricated. The results demonstrate the wide range of applications for La2W2O9:Bi[Formula: see text] phosphor in the field of premium warm white LED lighting.

Broadband and robust vibration reduction in lattice-core sandwich beam with 3D-printed QZS resonators

The demand for lightweight lattice-core sandwich structures that exhibit superior mechanical and dynamic properties is widespread in many devices. This paper presents a lattice-core sandwich beam (LSB) with an embedded array of quasi-zero-stiffness (QZS) resonators, referred to as Q-LSB. This research distinguishes itself from existing studies on metamaterial structures with QZS resonators by investigating the nonlinear stiffness of QZS resonators and the damping of a soft three-dimensional (3D) printing material. The objective is to achieve efficient and robust vibration reduction beyond the band gap of its linear counterpart. We investigate the beam vibration using both experimental and numerical methods. The experimental results demonstrate that the resonators can entail significant vibration reduction in a wide frequency range, covering the first three eigenmodes of the host LSB. Furthermore, the reduction effect improves as the excitation level increases within the tested excitation range, highlighting the structure’s robustness against the excitation amplitude. A numerical model based on a dynamically equivalent homogenization method and the finite element method is established and experimentally validated. Subsequently, the numerical parametric results reveal that the broadband vibration reduction is due to the damping effect, while the robust vibration reduction effect is attributed to the nonlinear stiffness of the resonators.

Simultaneous Occurrence of Electromagnetic and Quasi‐Electrostatic Magnetosonic Waves

AbstractMagnetosonic (MS) waves usually manifest as electromagnetic fluctuations, while quasi‐electrostatic magnetosonic (QEMS) waves have been recently reported. Here we present an intriguing coexistence of low harmonic electromagnetic magnetosonic (EMMS) waves and QEMS waves within the same band. Ion Bernstein instabilities are calculated based on the observed proton distribution. Effective growth rates can occur in the first‐fourth harmonic bands with a broad wave number range when the wave normal angle is sufficiently large. In each harmonic band, the MS waves would transform from electromagnetic to electrostatic as the wave number increases. This study reveals that the simultaneous occurrence of EMMS and QEMS arises from the expansive excitation range of MS waves in ‐space, thereby implying the potential resonant interactions between MS and particles in a broad energy spectrum.

Controllable photoexfoliation of monolayer graphene quantum dots using temporally and spatially shaped femtosecond laser

Graphene quantum dots (GQDs) have displayed significant momentum in numerous fields due to their unique electronic properties. However, how to obtain uniformly monolayer quantum dots and explain the synthesis mechanism are still a key technical problem. Here, a rapid and controllable photoexfoliation rate of monolayer graphene quantum dots of up to 80 % was achieved by using temporally and spatially shaped femtosecond laser to ablate bulk highly oriented pyrolytic graphite targets in liquid. Theoretical calculations suggested that the temporally shaped laser can minimize the spatial range of electron excitation, maximize the Coulomb repulsion between the outer layers and Coulomb explosion within the topmost layer through multi-level electron excitation. The above multilevel photoexfoliations lead to the formation of monolayer GQDs. These findings demonstrate a perfect theoretical explanation of controllable and rapid preparation of monolayer quantum dots, accelerating its industrialization in energy storage devices.

Hydrolytic‐Resistance Long‐Persistent Luminescence SrAl2O4:Eu2+,Dy3+ Ceramics for Optical Information Storage

AbstractSrAl2O4:Eu2+, Dy3+ (SAED) is one of the most popular materials for information storage and night display applications because it has a wide excitation range and long afterglow duration. However improving the hydrolytic resistance of SAED remains a challenge. In this study, the SAED is presented to be the ceramic type by a solid‐state reaction in a vacuum ambiance. The achieved SAED ceramic has 8200 mcd m−2 initial luminescence intensity. It can also obtain long‐persistent luminescence after UV light irradiation even soaking in water for more than 30 days. This ceramic demonstrates sustained imaging capability irradiated under 365 nm UV light and X‐ray, as well as erasability and reproducibility of storage by lighting and heating. These results indicate the promising applications of SAED ceramics in optical information storage and night display in complex environments. The phase evolution in the SAED ceramic is identified directly in the micromorphology for the first time based on scanning electron microscopy coupled with a cathodoluminescence system.

Ratiometric Fluorescent pH Sensing with Carbon Dots: Fluorescence Mapping across pH Levels for Potential Underwater Applications.

Ocean acidification has become a major climate change concern requiring continuous observation. Additionally, in the industry, pH surveillance is of great importance. Consequently, there is a pressing demand to develop robust and inexpensive pH sensors. Ratiometric fluorescence pH sensing stands out as a promising concept. The application of carbon dots in fluorescent sensing presents a compelling avenue for the advancement of pH-sensing solutions. This potential is underpinned by the affordability of carbon dots, their straightforward manufacturing process, low toxicity, and minimal susceptibility to photobleaching. Thus, investigating novel carbon dots is essential to identify optimal pH-sensitive candidates. In this study, five carbon dots were synthesized through a simple solvothermal treatment, and their fluorescence was examined as a function of pH within the range of 5-9, across an excitation range of 200-550 nm and an emission range of 250-750 nm. The resulting optical features showed that all five carbon dots exhibited pH sensitivity in both the UV and visible regions. One type of carbon dot, synthesized from m-phenylenediamine, displayed ratiometric properties at four excitation wavelengths, with the best results observed when excited in the visible spectrum at 475 nm. Indeed, these carbon dots exhibited good linearity over pH values of 6-9 in aqueous Carmody buffer solution by calculating the ratio of the green emission band at 525 nm to the orange one at 630 nm (I525nm/I630nm), demonstrating highly suitable properties for ratiometric sensing.

On the glow of cremated remains: long-lived green photo-luminescence of heat-treated human bones.

The long-lived green luminescence of human bone (that has been heated to 600°C for a short duration) is attributed to a carbon quantum dot material (derived from collagen) encapsulated and protected by an inorganic matrix (derived from bone apatite) and is more intense in dense rigid and crystalline parts of (healthy) human bones. The strong collagen-apatite interaction results (upon decomposition) in a protective inorganic environment of the luminescent centers allowing long-lived triplet-based emission of a carbon (quantum) dot-like material at room temperature, as well as resilience against oxidation between 550 and 650°C. The graphitic black phase (obtained upon heating around 400°C) is a precursor to the luminescent carbon-based material, that is strongly interacting with the crystalline inorganic matrix. Human bone samples that have been heated to 600°C were subjected to steady-state and time-resolved spectroscopy. Excitation-emission matrix (EEM) luminescence spectroscopy revealed a broad range of excitation and emission wavelengths, indicating a heterogeneous system with a broad density of emissive states. The effect of low temperature on the heat-treated bone was studied with Cryogenic Steady State Luminescence Spectroscopy. Cooling the bone to 80K leads to a slight increase in total emission intensity as well as an intensity increase towards to red part of the spectrum, incompatible with a defect state model displaying luminescent charge recombination in the inorganic matrix. Time-resolved spectroscopy with an Optical Multichannel Analyzer (OMA) and Time Correlated Single Photon Counting (TCSPC) of these samples showed that the decay could be fitted with a multi-exponential decay model as well as with second-order decay kinetics. Confocal Microscopy revealed distinct (plywood type) structures in the bone and high intensity-fast decay areas as well as a spatially heterogeneous distribution of green and (fewer) red emissive species. The use of the ATTO 565 dye aided in bone-structure visualization by chemical adsorption. Conceptually our data interpretation corresponds to previous reports from the material science field on luminescent powders.

Non-degenerate two-photon imaging of deep rodent cortex using indocyanine green in the water absorption window.

We present a novel approach for deep vascular imaging in rodent cortex at excitation wavelengths susceptible to water absorption using two-photon microscopy with photons of dissimilar wavelengths. We demonstrate that non-degenerate two-photon excitation (ND-2PE) enables imaging in the water absorption window from 1400-1550 nm using two excitation sources with temporally overlapped pulses at 1300 nm and 1600 nm that straddle the absorption window. We explore the brightness spectra of indocyanine green (ICG) and assess its suitability for imaging in the water absorption window. Further, we demonstrate in vivo imaging of the rodent cortex vascular structure up to 1.2 mm using ND-2PE. Lastly, a comparative analysis of ND-2PE at 1435 nm and single-wavelength, two-photon imaging at 1300 nm and 1435 nm is presented. Our work extends the excitation range for fluorescent dyes to include water absorption regimes and underscores the feasibility of deep two-photon imaging at these wavelengths.

Remarkable broadband NIR emission of BaCa2MgSi2O8:Cr3+ phosphors and Eu2+ co-doping modulation

Developing high-performance broadband NIR (near-infrared) phosphors remains a crucial pursuit for the next-generation smart NIR light source. This study demonstrates the successful synthesis of BaCa2MgSi2O8:Cr3+ phosphors exhibiting exceptional broadband NIR emission via a high-temperature solid-state reaction. Notably, the 0.03Cr3+ doped composition, under 485 nm excitation, shines with a remarkable broadband emission spanning 700 nm–1100 nm and boasts a full width at half maximum (FWHM) of 134 nm. This work meticulously explores the intricate interplay between Cr3+ doping concentration, temperature, crystal field strength, and the Huang-Rhys parameter, shedding light on the underlying luminescence mechanisms. Moreover, the BaCa2MgSi2O8:0.03Cr3+ phosphor exhibits exceptional thermal stability, retaining approximately 70 % of its integrated emission intensity at 425 K compared to room temperature. To further expand the excitation range, Eu2+ was introduced as a co-dopant, successfully broadening the excitation spectrum to encompass nearly the entire ultraviolet–visible region (ranging from 250 nm to 750 nm). The presence of Eu2+→Cr3+ energy transfer was elucidated, and the impact of Eu2+ doping was thoroughly investigated. Moreover, the synthesized phosphor has been successfully integrated into a NIR phosphor-converted light-emitting diode (pc-LED), showcasing their potential application in the realms of night vision and NIR vascular imaging. These findings offer invaluable insights into Cr3+ luminescence behavior and pave the way for the development of novel NIR phosphors with enhanced functionalities, propelling us closer to the realization of next-generation smart lighting solutions.

Coupled axial and transverse currents method for finite element modelling of periodic superconductors

In this paper, we propose the Coupled Axial and Transverse currents (I) (CATI) method, as an efficient and accurate finite element approach for modelling the electric and magnetic behavior of periodic composite superconducting conductors. The method consists of a pair of two-dimensional models coupled via circuit equations to account for the conductor geometrical periodicity. This allows to capture three-dimensional effects with two-dimensional models and leads to a significant reduction in computational time compared to conventional three-dimensional models. After presenting the method in detail, we verify it by comparison with reference finite element models, focussing on its application to twisted multifilamentary superconducting strands. In particular, we show that the CATI method captures the transition from uncoupled to coupled filaments, with accurate calculation of the interfilament coupling time constant. We then illustrate the capabilities of the method by generating detailed loss maps and magnetization curves of given strand types for a range of external transverse magnetic field excitations, with and without transport current.

Effect of terminal substituents on intramolecular charge transfer in one- and two-photon absorption of zinc phthalocyanine derivatives

Zinc phthalocyanine derivatives have unique structure and photophysical properties, which make them a remarkable potential in the fields of optoelectronics as well as biomedicine. In order to reveal the effect of the terminal substituents on the electron transition mechanisms, one-photon absorption (OPA) and two-photon absorption (TPA) processes of three zinc phthalocyanines modified with different terminal substituents (PcZn-0, PcZn-1 and PcZn-2) have been analyzed by using density-functional theory (DFT) in combination with the sum-over-states (SOS) model, the visualization of the transition density matrix (TDM) as well as charge density difference (CDD) calculations. Red-shifted OPA absorption peaks with enhanced intensities, have been observed in molecules PcZn-1, PcZn-2 with long terminal substituents. However, for TPA process, a more effective charge transfer over almost the entire molecule has been observed in PcZn-1 molecule with 4-methoxybenonic acid as terminal substituents. When H-atoms in the hydroxyl groups of four terminal 4-Methoxybenzoic acid groups were substituted by dispersed red-one chains, a limited range of intramolecular charge transfer and localized excitation inside the dispersed red-one chain were observed, leading to a localized excitation absorption peak and expanding the wavelength region of TPA response. Furthermore, terminal substituents with conjugated branches exhibit a stronger cooperative effect between the terminal chains and shows larger TPA response. On the contrary, excessive dihedral angles between different groups can weaken the conjugation degree of molecules and affect intramolecular charge transfer as well as TPA response.

Theperception of emotion in music by people with hearing loss and people withcochlear implants.

Music is an important part of life for many people. It can evoke a wide range of emotions, including sadness, happiness, anger, tension, relief and excitement. People with hearing loss and people with cochlear implants have reduced abilities to discriminate some of the features of musical sounds that may be involved in evoking emotions. This paper reviews these changes in perceptual abilities and describes how they affect the perception of emotion in music. For people with acquired partial hearing loss, it appears that the perception of emotion in music is almost normal, whereas congenital partial hearing loss is associated with impaired perception of music emotion. For people with cochlear implants, the ability to discriminate changes in fundamental frequency (associated with perceived pitch) is much worse than normal and musical harmony is hardly perceived. As a result, people with cochlear implants appear to judge emotion in music primarily using tempo and rhythm cues, and this limits the range of emotions that can be judged. This article is part of the theme issue 'Sensing and feeling: an integrative approach to sensory processing and emotional experience'.

Dynamic characteristics of electromechanical coupling of body-suspended drive system for high-speed trains under wheel polygonal wear

Wheel polygonal wear can trigger intense wheel–rail interactions in railway vehicles, posing a significant threat to traffic safety. However, the mechanism and interaction of the influence of wheel polygonal wear on the electromechanical coupling characteristics of high-speed trains remain unclear. Therefore, this paper proposes a joint simulation modelling method that takes into account the integration of the electrical subsystem with the complete mechanical subsystem. A comprehensive analysis is conducted on the dynamic response of the high-speed train’s body-suspended drive system under a wide range of frequency excitations arising from harmonic torque, gear meshing, and wheel polygon wear. The results indicate that the electrical system generates a substantial amount of harmonic frequency components, resulting in a significant increase in the vibration of the train. The wheel polygon wear causes a broadening of the low-frequency resonance band, revealing a relatively prominent observation interval for the dynamic characteristics. Concurrently, it is discovered that the 23rd-order wheel polygon wear excites the system’s resonance frequency, and as the wavelength of the wheel polygon increases, the acceleration vibrations intensify progressively. Research reveals first the interaction of electrical system and mechanical system under wheel polygon wear, especially in the resonance gain characteristics under polygons and harmonic torques.

Down-shifting in Ce3+- Tb3+ co-doped phosphate glasses for solar cells application

The Down-Shifting (DS) of UV photons into the visible range has been attracting much attention for lighting appliances and solar cells. This work reported the DS luminescence in Ce3+-Tb3+ co-doped phosphate glasses. Photoluminescence and decay curves were measured and analysed. According to the emission spectra, it was noticed a decrease in emission of the Ce3+ peak intensity and an increase of the Tb3+ visible emission intensity when the Tb3+ concentration is enlarged, indicating an energy transfer process from Ce3+ to Tb3+. Moreover, it was observed that the blue emission of Tb3+ decreases, while the green emission enhances by gradually increasing Tb3+ concentration. According to the decay curves of Tb3+, this result can be explained by cross-relaxation between Tb3+ ions. The experimental temporal evolution of the green emission of Tb3+ ions obtained under excitation of the Ce3+ ions at 280 nm is well simulated using a proposed model. In this way, the dynamics of the processes involved is perfectly understood and can be applied for solar cell applications. Therefore, the samples were placed over a solar cell and excited with UV excitation. In this excitation range, the silicon solar cell is not efficient, but the Ce3+ ions absorb this energy and transfer to the Tb3+ ions, which produce an intense visible emission. This emission is detected by the solar cell and produces photocurrent. In summary, the use of co-doped phosphate glass could enhance the current in a solar cell in the UV region.

Enhanced red emission of MgAl2O4: Cr3+/Mn4+ phosphor co-doped with alkali metal ions

A series of MgAl2O4: Cr, Mn, M (M = Li, Na, K) red phosphors were prepared by solution combustion combined with subsequently annealing treatment. The influence of Cr3+ or Mn4+ single-doping, Cr3+ and Mn4+ double-doping and alkali metal ions co-doping on the luminescence performance of MgAl2O4 phosphors were systematically investigated. XRD and SEM were used to characterize the composition and morphology of the phosphors, and the optical absorption, photoluminescent excitation, photoluminescent emission, fluorescence lifetime and chromaticity coordinate were performed to characterize their luminescence properties. Compared with Cr3+ or Mn4+ single-doped MgAl2O4 phosphors, Cr3+ and Mn4+ double-doped ones can achieve red light emission under a wide range of excitation from ultraviolet to visible light. Co doping with alkali metal ion Li enhances the fluorescence intensity and lifetime of MgAl2O4: Cr, Mn phosphors.

Nonlinear liquid sloshing dynamics in upright circular cylindrical containers with FSI effects: Post-processing of conventional finite element solutions by digital filters

In this work we present a robust finite element procedure for modeling 3D nonlinear liquid sloshing phenomena using standard potential theory. A well known issue in simulating inviscid free-surface flows is an onset of spurious oscillations (“saw-tooth”) caused by numerical instabilities. Here we demonstrate that a novel post-processing procedure, based on the Savitzky–Golay filtering algorithm allows us to overcome this challenge. It is shown that unphysical numerical oscillations are smoothed out and nodal free-surface position along with velocity values are accurately recovered from conventional finite element analysis. Sloshing dynamics (limited to non-overlapping waves) is investigated for a partially filled vertical circular cylinder subjected to a broad range of harmonic and ElCentro seismic excitations. The results compare well with those obtained with finite volume OpenFOAM software. One-way coupling FSI analysis is also included to estimate stress and deflection experienced by cylindrical containers.

Lateral Confinement in 2D Nanoplatelets: A Strategy to Expand the Colloidal Quantum Engineering Toolbox

AbstractAmong colloidal nanocrystals, 2D nanoplatelets offer a unique set of properties with exceptionally narrow luminescence and low lasing thresholds. Furthermore, their anisotropic shape expands the playground for the complex design of heterostructures where spectra but also scattering rates can be engineered. A challenge that still remains is to combine shell growth which makes NPLs stable, with spectral tunability. Indeed, most reported shelled nanoplatelets end up being red emitters due to a loss of quantum confinement. Here, the combination of both lateral and in‐plane confinements within a single heterostructure is explored. A CdS/CdSe/CdS/CdZnS core–crown–crown shell structure that enables yellow emission is grown and that is responsive to a large range of excitation including visible photons, X‐ray photons, electron beams, and electrical excitations. k.p simulations predict that emission tunability of up to several 100 s of meV can be obtained in ideal structures. This material also displays stimulated emission resulting from bi‐exciton emission with a low threshold. Once integrated into an LED stack, this material is compatible with sub‐bandgap excitation and exhibits high luminance. Scaling of the electroluminescence properties by downsizing the pixel size is also investigated.