Light Emitters Research Articles

A novel halide hybrid white light emitter with remarkable structural and emission stability

Addressing the issues of self-absorption effect among different components in traditional white light-emitting diodes (WLEDs) and the high cost associated with rare earth elements, we propose the potential utility of zero-dimensional organic–inorganic metal halide hybrids (0D OIMHs) in white WLEDs fabrication. In this study, we synthesized a novel 0D OIMH, (C5N2H14)ZnCl4, characterized by broadband white light emission. The (C5N2H14)ZnCl4 crystal features a short ultraviolet cutoff situated at 190 nm and emits cold white light with a Color Rendering Index (CRI) of 73 under an excitation wavelength of 260 nm. Furthermore, (C5N2H14)ZnCl4 demonstrates exceptional structural and emission stability in an air atmosphere over a span of three months.

Multimodal Spectroscopy Assays for Advanced Nano-Optics Approaches by Tuning Nano-Tool Surface Chemistry and Metal-Enhanced Fluorescence

In this research work, different chemical modifications were applied to gold nanoparticles and their use in enhanced non-classical light emitters based on metal-enhanced fluorescence (MEF) was evaluated. In order to achieve this, gold core–shell nanoparticles with silica shells were modified via multilayered addition and the incorporation of a covalently linked laser dye to develop MEF. Their inter-nanoparticle interactions were evaluated by using additional silica shell multilayers and modified cyclodextrin macrocycles. In this manner, the sizes and chemical surface interactions on the multilayered nanoarchitectures were varied. These optical active nanoplatforms led to the development of different nanoassembly sizes and luminescence behaviors. Therefore, the interactions and nanoassembly properties were evaluated by using various spectroscopic and nanoimaging techniques. Highly dispersible gold core–shell nanoparticles with diameters of 50–60 nm showed improved colloidal dispersion that led to single ultraluminescent gold core–shell nanoparticles with MEF. Then, the addition of variable silica lengths produced increased interactions and consequent nanoaggregation. However, the silanized nanoparticles were easily dispersible after agitation or sonication. Thus, their sizes were proportional only to the diameter and the van de Waals interaction did not affect their sizes in bulk. Then, the covalent linking of different concentrations of modified cyclodextrins was applied to the chemical surfaces by incorporating additional hydroxyl groups from the glucose monomeric unities of cyclodextrins. In this manner, variable larger-sized and inter-branched grafted gold core–shell silica nanoparticles were generated. The ultraluminescent properties were conserved due to the non-optical activity of the cyclodextrins. However, they generated enhanced ultraluminescence phenomena. Laser fluorescence microscopy nanoimaging showed enhanced resolutions in comparison to non-grafted supramolecular gold core–shell nanoparticles. The differences in their interactions and the sizes of the nanoassemblies were explained by their single nanoparticle diameters and the interacting chemical groups on their nanosurfaces. While the varied luminescence emissions generated were tuned by plasmonics, enhanced plasmonic phenomena and light scattering properties were seen depending on the type of nanoassembly. Thus, optically active and non-optically active materials led to different optical properties in the bright field and enhanced the excited state within the electromagnetic near-field of the gold nanotemplates. In this manner, it was possible to achieve high sensitivity by varying the spacer lengths and optical properties. Therefore, further perspectives regarding the design of nano-tools composed of light for various applications were discussed.

Enhanced Photostability of Lead Halide Perovskite Nanocrystals with Mn3+ Incorporation.

Recently, lead halide perovskite nanocrystals (NCs) have shown great potential and have been widely studied in lighting and optoelectronic fields. However, the long-term stability of perovskite NCs under irradiation is an important challenge for their application in practice. Mn2+ dopants are mostly proposed as substitutes for the Pb site in perovskite NCs synthesized through the hot-injection method, with the aim of improving both photo- and thermal stability. In this work, we employed a facile ligand-assisted reprecipitate strategy to introduce Mn ions into perovskite lattice, and the results showed that Mn3+ instead of Mn2+, even with a very low level of incorporation of 0.18 mol % as interstitial dopant, can enhance the photostability of perovskite binder film under the ambient conditions without emission change, and the photoluminescent efficiency can retain 70% and be stable under intensive irradiation for 12 h. Besides, Mn3+ incorporation could prolong the photoluminescent decay time by passivating trap defects and modifying the distortion of the lattice, which underscores the significant potential for application as light emitters.

Design and simulation of light field patterns for angular color variation reduction in micro-LED and mini-LED RGB arrays.

We propose a methodology to mitigate angular color variation in full-color micron-scale LED arrays. By simulating light field distribution for red (AlGaAs) and green/blue (GaN) light across various RGB micro-LED sizes, we can select matching light field patterns for RGB chips, reducing angular color variation from 0.0201 to 0.0030. Applying this method to full-color mini-LED assemblies achieves a reduction from 0.0128 to 0.0032 by matching light field patterns with varying substrate thicknesses. This straightforward approach aligns with current mass transfer processes, offering practical implementation.

Chiral Viologen-Derived Water-Stable Small Band Gap Lead Halides: Synthesis, Characterization, and Optical Properties.

Chiral organic-inorganic metal halides (OIMHs) are attractive for their potential applications in chiral optoelectronics and spintronics, such as circular polarized light emitters, detectors, and chiral-induced spin selectivity. Here, we report three pairs of chiral OIMHs with great water stability constructed from chiral viologens. These OIMHs contain either 1D or 0D structures, however, with small band gaps around 2 eV. Circular dichroism (CD) spectroscopy on transparent thin films of two OIMH pairs showed a wide CD response covering most of the visible light range. Although the chiral center is not directly attached to the pyridinium in these chiral viologens, the chirality is still successfully transferred into both the band gap and the exciton absorption ranges. Liquid and solid CD studies of the chiral viologens further indicate that the chiral induction inside these OIMHs is possibly through chiral crystallization. This work demonstrated the design strategy of water-stable, small band gap chiral OIMHs through chiral viologens. These low-dimensional chiral materials may provide an interesting system to investigate chiral induction, and their broad CD response may enable their potential application as circular photodetectors with a wide detection range.

Unveiling heavy heterovalent doping-modulated microstructure and thermoelectric performance in bulk hybrid perovskite single crystals

Organic-inorganic hybrid metal halide perovskites have emerged as a promising candidate for low-temperature thermoelectric conversion. However, challenges remain in heavily doping bulk perovskite single crystals without phase segregation or self-doping compensation issues to increase the carrier concentration. Previous efforts to enhance their thermoelectric performance rely on photoexcitation or surface/interface doping, which is not suitable for bulk devices to work in dark. This study achieves high monovalent and trivalent doping concentrations of up to 5 % in bulk single crystals of MAPbI3 and MAPbBr3 without phase segregation or defect formation. For monovalent doping, K+ and Li+ are incorporated into the perovskite lattice as interstitials. The resulting lattice distortion/microstrain enhances the electrical conductivity by 10 ∼ 100 times of undoped samples at 420 K. Trivalent doping using SbCl3, BiBr3, and BiI3 significantly enhances the carrier concentration and electrical conductivity, up to 1012 cm−3 and 0.038 S m−1 for MAPbBr3 with 10 % BiI3 at 465 K, respectively, which is 105 times of the undoped samples and 10 times of the best reports on doped MAPbBr3. Interestingly, the Bi3+ dopant oxidizes the deep defect state Pb0, resulting in Bi+ and Pb2+ formation and contributing to the enhanced electrical conductivity. Enhanced thermoelectric figure of merit (ZT) is achieved in MAPbBr3 with 5 % BiI3 at 315 K, almost 100 times of the best reports on doped MAPbBr3. This study provides fundamental understanding of doping-modulated microstructural, charge carrier, and thermoelectric properties of hybrid halide perovskites, offering potential doping strategies to realize the theoretically predicted promising thermoelectric properties in their bulk single crystals for practical thermoelectric devices. The doping-modulated carrier transport will also guide the optimization of optoelectronic applications of halide perovskites for solar cells, light emitters, and photodetectors.

Henlea earthworm bioluminescence comprises violet-blue BRET from tryptophan 2-carboxylate to deazaflavin cofactor

We recently identified the deazaflavin cofactor as a light emitter in novel bioluminescence (BL) system from Siberian earthworms Henlea sp. (Petushkov et al., 2023, Org. Biomol. Chem. 21:415–427). In the present communication we compared in vitro BL spectra in the absence and in the presence of the cofactor and found a wavelength shift from 420 to 476 nm. This violet-blue BRET to deazaflavin cofactor (acceptor of photonless transfer) masks the actual oxyluciferin as an emitter (BRET donor) in the novel BL system. The best candidate for that masked chromophore is tryptophan 2-carboxylate (T2C) found previously as a building block in some natural products isolated from Henlea sp. (Dubinnyi et al., 2020, ChemSelect 5:13155–13159). We synthesized T2C and acetyl-T2C, verified their presence in earthworms by nanoflow-HRMS, explored spectral properties of excitation and emission spectra and found a chain of excitation/emission maxima with a perfect potential for BRET: 300 nm (excitation of T2C) - 420 nm (emission of T2C) - 420 nm (excitation of deazaflavin) - 476 nm (emission of deazaflavin, BL). An array of natural products with T2C chromophore are present in BL earthworms as candidates for novel oxyluciferin. We demonstrated for the Henlea BL that the energy of the excited state of the T2C chromophore is transferred by the Förster mechanism and then emitted by deazaflavin (BRET), similarly to known examples: aequorin-GFP in Aequorea victoria and antenna proteins in bacterial BL systems (lumazine from Photobacterium and yellow fluorescent protein from Vibrio fischeri strain Y1).

Progress, Prospects and Challenges of MXene Integrated Optoelectronics Devices

AbstractRecently, the emerging 2D materials MXene have gained a surge of attention to the production of optoelectronics devices such as solar cells, plasmonic, phototransistors, photodetectors, light‐emitting diodes, photothermal therapy, and so on. Its outstanding optical and electrical characteristics, unique structure, and large specific surface area make it suitable for future use in modern optoelectronics including ultrafast lasers, light emitters, modulators, and plasmonic generators. There is a lack of critical analysis on the prospects, challenges, overview of synthesis methods, mechanisms, and future research directions of MXene despite having some reviews have been published on the applications of MXene. Therefore, this study critically analyzed the existing challenges of MXene, such as poor stability in an oxygen environment, inadequate mechanical properties, ease of stacking, temperature barrier, and so on. In addition, the fundamentals, preparation techniques, properties, and applications of MXene have been summarized. The mechanism, limitations, and benefits of different preparation methods have been mentioned. A comprehensive analysis and guidelines have been provided to improve the existing synthesis methods. The ways to overcome these challenges, prospects, and future markets of the MXene‐based optoelectronic devices have been described.

Smart airbag vest with integrated light turn signaling and location tracking

Research on road safety is continuously developing with the applications of sensors and technologies. Another area that draws the attention of the developers for road safety are in the road accident response. As the number of riders and cyclists increase, so do the accidents particularly at night where visibility is limited. This study presents a method of integration of inflatable safety vests for riders with light emitting diode LED signaling strips embedded in its front and back, and sensors to send the location of the rider when an accident happens. The LED strips are controlled using a wireless remote switch to make the rider more visible other than that embedded in the motorcycle or bicycle. The airbag will activate once an accident occurs and or the rider is detached from the motorcycle. A force-sensitive resistor (FSR) is used as a triggering device attached to the vest when an accident happens where a global positioning system (GPS) module will send the location and a map to a specific mobile number for response. Three trials were conducted to test the functionality of the LED lights for signaling. The device functioned well, that both the left, right, and standby mode were activated. The functionality of the location tracker is also tested in three different locations. The FSR was triggered and it gave the exact location by sending the coordinates and a link to view it on google maps with an average transmit and receive time of 3 seconds. It is recommended that the prototype be developed using light-weight materials and batteries.

Optical Characterization of Ferric-Doped ZnO Thin Film Deposited By Chemical Bath Deposition Method

Fe-doped ZnO holds numerous potential uses in devices such as UV light emitters, piezoelectric transducers, transparent electronics in solar cells, and bright windows as an II-VI semiconductor material. This study looked into the band gap, surface characteristics, optical transmittance, and absorbance of ZnO thin films with Fe doping in different pH conditions such as 8, 9, and 10. The films were prepared using the chemical bath deposition (CBD) method at 350 °C on a glass substrate. The samples were characterized using UV-visible spectroscopy and scanning electron microscopy (SEM). The SEM images of the undoped samples exhibited a lack of cracks, but the doped samples displayed visible cracks due to the presence of Fe in the films. ZnO thin-film surface shape is altered by pH and Fe doping variations. There is a tendency for the films' visual transmission to decrease when the pH rises. The absorbance for all samples increases in the UV and declines in the visible. Fe doping causes the optical band gap Eg to drop. The band gap of both doped and undoped samples reduces when pH rises.

Segmented Acoustic Displays

For more than a century, segmented displays, such as the seven‐segment display, have been a popular and cost‐effective option. They can display various commonly used characters by controlling a few custom‐shaped binary light emitters. Herein, the acoustic equivalent of segmented displays, which uses heterogeneous sound modulators to generate a limited set of acoustic holographic images, is introduced. Designing segmented acoustic displays is more challenging than optical ones due to the complex relationship between emitted sound and generated holographic images. To address this challenge, a design methodology based on unsupervised learning techniques is proposed. The approach balances the cost of acoustic displays and the quality of the images they generate, resulting in segmented displays that outperform existing general‐purpose ones when generating a finite set of acoustic images. Using simulations and physical fabrication of metamaterial‐based acoustic displays, it is proven that the approach can create segmented acoustic displays that produce high‐quality images at a lower cost. Additionally, the methodology is applied to multifrequency acoustic displays and its scalability is assessed as the number of images increases. The cost reduction through segmentation presented herein is expected to democratize sound manipulators for acoustic displays and other applications like acoustic levitation and noise cancellation.

Stabilizing Single‐Source Evaporated Perovskites with Organic Interlayers for Amplified Spontaneous Emission

AbstractMetal halide perovskites are promising semiconductors with promising applications in optoelectronic and photonic technologies. When coherent emission applications are targeted, materials with lower lasing thresholds and increased stabilities must be developed to increase the performance under continuous wave optical pumping condition and finally allow the realization of the long sought‐after electrically pumped lasers. Perovskite multiple‐quantum‐wells (MQWs) can potentially ease the population inversion by confining photoexcitation within the heterostructure's wells, but their fabrication process and structural design still require a delicate optimization to make them valuable photonic platforms. Here, perovskite MQWs are fabricated based on organic semiconductors and CsPbBr3, using a facile and easily scalable sequential single‐source vacuum evaporation method. Perovskite with the organic interlayer shows radically enhanced phase stability, passivated defects, and improved radiative recombination properties. In this way, upon proper design of the heterostructure wells and barriers thicknesses, optically pumped amplified spontaneous emission can be achieved. This work reports an effective fabrication approach for perovskite MQWs, while providing a deeper understanding of their photophysical properties to foster their application as coherent light emitters.

Recent advances in bioluminescent probes for neurobiology.

Bioluminescence is a popular modality for imaging in living organisms. The platform relies on enzymatically (luciferase) generated light via the oxidation of small molecule luciferins. Since no external light is needed for photon production, there are no concerns with background autofluorescence or photobleaching over time-features that have historically limited other optical readouts. Bioluminescence is thus routinely used for longitudinal tracking across whole animals. Applications in the brain, though, have been more challenging due to a lack of sufficiently bioavailable, bright, and easily multiplexed probes. Recent years have seen the development of designer luciferase and luciferin pairs that address these issues, providing more sensitive and real-time readouts of biochemical features relevant to neurobiology. This review highlights many of the advances in bioluminescent probe design, with a focus on the small molecule light emitter, the luciferin. Specific efforts to improve luciferin pharmacokinetics and tissue-penetrant emission are covered, in addition to applications that such probes have enabled. The continued development of improved bioluminescent probes will aid in illuminating critical neurochemical processes in the brain.

The correlation between structural factors and Stokes shifts in zero-dimensional Antimony(III) halides

Zero-dimensional (0D) hybrid metal halides (HMHs) have recently garnered significant attention as promising light emitters due to their distinctively Stokes-shifted broadband emissions resulting from self-trapped excitons (STEs). However, the influence of crystalline structures on the Stokes shift remains inadequately understood. Herein, we design and synthesize a series of 0D (Ph4P)2SbCl5-xBrx (Ph4P = tetraphenylphosphonium, x = 0–5) compounds to elucidate the intrinsic relationship between structural factors and the Stokes shift in 0D Sb(III) halides. Our comprehensive investigations into their crystalline structures and photoluminescence (PL) properties unveil that the Stokes shift correlates with intra- and inter-pyramidal [SbCl5-xBrx]2- units. Specifically, a shorter vertical Sb–Cl bond within the square pyramid, coupled with a greater Sb⋯Sb distance between the pyramidal units, facilitates significant structural relaxation in excited states, resulting in a larger Stokes shift, and vice versa. Notably, this principle applies not only within identical space groups but also across different crystal systems. Furthermore, our findings are supported by analyses of the structures and PL properties of other reported 0D Sb(III) halides with square pyramidal coordination. This study elucidates the structure-dependent nature of the Stokes shift in 0D Sb(III) halides, offering a novel avenue for the design of functional 0D metal halide materials.

Built-in electric field and selenium vacancies synergistically enhance NiSe2@Co0.85Se high-performance supercapacitors

Sluggish kinetics and poor cycling stability are two major obstacles limiting large-scale energy storage in battery-type supercapacitors. Herein, a novel strategy has been proposed to address these issues, which is to use a simple two-step electrodeposition technology to prepare the NiSe2@Co0.85Se/NF(denoted as NS@CS/NF) core-shell heterostructure, generate built-in electric field, and subsequently introduced anionic vacancies to successfully construct unique Se vacancies-rich composites (denoted as Sev-NS@CS/NF). Systematic characterisation analysis and density functional theory (DFT) calculations confirm that Se vacancies and heterogeneous interfaces can modulate electronic structure and promote fast reaction kinetics to achieve excellent supercapacitor performance, with a specific capacitance of 1530 C g−1 at 1 A g−1, and a capacity retention of 86.35% even after undergoing 10,000 charge-discharge cycles. Furthermore, a hybrid supercapacitor (HSC) was constructed using Sev-NS@CS/NF as the cathode and activated carbon (AC) as the anode, exhibiting an energy density of 80 Wh kg−1 at 812 W kg−1 and maintained impressive performance metrics. Notably, when two HSC units were connected in series, they successfully illuminated an LED diode for a duration of 15 min, showcasing the considerable potential of this HSC device for various energy storage applications.

An All‐Colloidal and Eco‐Friendly Quantum‐Dot Laser

AbstractColloidal zinc‐chalcogenide quantum dots (QDs) are emerging as the promising heavy‐metal‐free light–emitters, however, the development of light amplification and lasing therein remains challenging. Here, corroborated by comprehensive in situ and transient spectroscopy, it is unraveled that the ultrafast photooxidization‐induced trapping process (≈2 ps) and the sub‐bandgap photoinduced absorption under intense excitation are the main hindrances to light amplification in ZnSeTe QDs. Upon tackling the hurdle by heterostructure engineering, this study demonstrates that the ZnSeTe QDs exhibit intrinsically superior gain performance, including the high gain cross‐section (5.6 × 10−16 cm2), long gain lifetime (615 ps), low pump threshold (≈25.9 µJ cm−2) and high fatigue resistance. On this basis, a microfluidic channel is designed to mass‐produce the micellar cavities whose surfaces are treated to combine with the ZnSeTe QDs. The active QD‐micelle hybrids show state‐of‐the‐art lasing performance and allow the fiber‐based micro‐manipulation toward the single‐mode lasers. These findings not only provide essential knowledge on the gain physics in ZnSeTe QDs, but also open a new avenue to develop high‐performance eco‐friendly lasers.

Innovation in higher education institutions towards sustainability using LED technology

Purpose There is a growing urgent concern in involving higher education institutions (HEIs) towards an international effort in implementing a more suitable role as conductors of sustainable development. This paper/study aims to present the application of light emiting diode (LED) technology in an HEI assuming technology innovation as part of a larger institutional innovation management strategy addressing multiple dimensions in sustainability. Design/methodology/approach Investments in LED technology are analyzed for their impact on consumption results and quantitative comparisons between 2008 and 2022 are impaired with detailed information on the types of luminaires and the amount of installed energy. Findings The collected data shows a clear economic advantage of using LED technology, and the results subsidize institutional planning, considering not only ongoing technological innovation, but also educational components and community involvement in the organization sustainability strategy. Research limitations/implications The study is limited to a specific HEI and further comparative research should be carried out. Practical implications A holistic approach on sustainability objectives encourages further investment in environmental-friendly technology, example to other HEIs. Social implications The strategic vision of innovation is confirmed with the involvement of the community, at various levels, such as the academic community, local community, scientific international community. Originality/value This study addresses the lack of examples in the literature of structural planning and management systems that see sustainability as a strategy built in HEIs. The elaboration of an environmental sustainability plan places environmental sustainability at the confluence of themes such as education, investigation, use of natural resources, waste separation. For each topic are listed measures, actions, environment improvements, institution improvements and their results.

Directing valley-polarized emission of 3 L WS2 by photonic crystal with directional circular dichroism.

The valley degree of freedom that results from broken inversion symmetry in two-dimensional (2D) transition-metal dichalcogenides (TMDCs) has sparked a lot of interest due to its huge potential in information processing. In this experimental work, to optically address the valley-polarized emission from three-layer (3 L) thick WS2 at room temperature, we employ a SiN photonic crystal slab that has two sets of holes in a square lattice that supports directional circular dichroism engendered by delocalized guided mode resonances. By perturbatively breaking the inversion symmetry of the photonic crystal slab, we can simultaneously manipulate s and p components of the radiating field so that these resonances correspond to circularly polarized emission. The emission of excitons from distinct valleys is coupled into different radiative channels and hence separated in the farfield. This directional exciton emission from selective valleys provides a potential route for valley-polarized light emitters, which lays the groundwork for future valleytronic devices.

Enhancement of light emission of a low-resistivity silicon nanocrystal thin film: A simulational and experimental study

A silicon nanocrystal (Si NC) white light-emitting (λ = ∼400–900 nm) thin film with a relatively low resistivity of 1.6 × 104 Ω m has been prepared as an active medium for electrically driven Si light sources. The average size of Si NC is 2.4 ± 0.4 nm. To enhance the light emission efficiency of this low-resistivity Si NC thin film, approach of hydrogen passivation suitable for the traditional high-resistivity (1.2 × 107 Ω m in this work for example) red light-emitting Si NC thin film has been tried and found unavailable unfortunately. Our first principles simulation shows that Si NCs bonded to −O, −NH2, −OH, and −H ligands are responsible for red, green, and blue (RGB) primary color emissions in this white light-emitting sample, respectively. Passivation of the sample in NH3 and H2O atmosphere is then conducted, aiming to increase the number of the RGB light emitters. The light emission is significantly enhanced, with photoluminescence intensity, photoluminescence quantum yield, electroluminescence intensity, and net optical gains increased by factors of 4.6, 4.2, 4.0, and ∼3.0, respectively, after 10-day passivation. Further enhancements are expected for longer passivation.

Size Dependence of Trion and Biexciton Binding Energies in Lead Halide Perovskite Nanocrystals.

Lead halide perovskite nanocrystals (NCs) have attracted much attention as light-source materials for light-emitting diodes, lasers, and quantum light emitters. The luminescence properties of perovskite NCs and the performance of NC-based light-source devices depend on trion and biexciton dynamics. Here, we examined the size dependence of trion and biexciton binding energies by conducting low-temperature single-dot spectroscopy on three different perovskite NCs: CsPbBr3, CsPbI3, and FAPbBr3. While the photoluminescence spectral widths of the all-inorganic CsPbBr3 and CsPbI3 NCs were narrow, compared with those of the organic-inorganic hybrid FAPbBr3 NCs, the binding energies of trions and biexcitons of all three samples showed similar size dependences, independent of the A-site cation and halogen. The effective-mass approximation calculations implied the importance of dynamical dielectric screening on the formation of trions and biexcitons.