Light Source Research Articles

Optimization of TiO2-based UV-LED Photocatalytic System for Mixed Dyes and Pharmaceutical Contaminants

To optimize the working efficiency of the novel UV-LED system based on TiO2 photocatalyst, the influence mechanism of LED lamp arrangement, light source wavelength and working voltage on photocatalytic efficiency was investigated. Acid red 26 (AR 26), acetaminophen (ACT) and diclofenac (DCF) were used as contaminant targets of the photocatalytic system. LED lamp arrangement had almost no effect on the degradation of AR26. However, the degradation efficiency of ACT and DCF was improved under a higher light uniformity. The ACT concentration and DCF concentration at 360 min decreased by 14% and 15%, respectively, with increasing light distribution from 45% to 66.5%. The main reason for this discrepancy in effect was whether the rate-determining step of the degradation mechanism was affected by the light uniformity. The short wavelength and high working voltage of LEDs were conducive to the photocatalytic degradation of contaminants to a different degree. When the wavelength was reduced from 405nm to 365nm, the conversion of AR26, ACT, and DCF increased by 77%, 227%, and 106%, respectively. The conversion rates of AR26, ACT, and DCF increased by 28%, 54%, and 32%, respectively, with voltage increasing from 3 V to 4 V. The data of this work will provide support for optimizing the working efficiency of UV-LED systems based on TiO2 photocatalysts. Copyright © 2024 by Authors, Published by BCREC Publishing Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).

Mirror-centered representation of a focusing hyperbolic mirror for X-ray beamlines.

Conic sections are commonly used in reflective X-ray optics. Hyperbolic mirrors can focus a converging light source and are frequently paired with elliptical or parabolic mirrors in Wolter type configurations. This paper derives the closed-form expression for a mirror-centered hyperbolic shape, with zero-slope at the origin. Combined with the slope and curvature, such an expression facilitates metrology, manufacturing and mirror-bending calculations. Previous works consider ellipses, parabolas, magnifying hyperbolas or employ lengthy approximations. Here, the exact shape function is given in terms of the mirror incidence angle and the source and image distances.

Electro-optically Modulated Nonlinear Metasurfaces.

Electrically reconfigurable nonlinear metasurfaces provide dynamic control over nonlinear phenomena such as second-harmonic generation (SHG), unlocking novel applications in signal processing, light switching, and sensing. Previous methods, like electric-field-induced SHG in plasmonic metasurfaces and Stark-tuned nonlinearities in quantum well metasurfaces, face limitations due to weak SHG responses from metals and mid-infrared constraints of quantum wells, respectively. Addressing the need for efficient SHG control in the visible and near-infrared ranges, we present a novel approach using the electro-optic (EO) effect to modulate SHG. By leveraging the exceptional EO and SHG properties of lithium niobate (LN), we integrate the EO effect with SHG within a metasurface framework for the first time. Our LN metasurface achieves an 11.3% modulation depth in SHG amplitude under a ±50 V alternating voltage. These results open new avenues for reconfigurable photonic applications. including tunable nonlinear light sources, quantum optics, and nonlinear information processing.

Correlative X-ray micro-nanotomography with scanning electron microscopy at the Advanced Light Source.

Geological samples are inherently multi-scale. Understanding their bulk physical and chemical properties requires characterization down to the nano-scale. A powerful technique to study the three-dimensional microstructure is X-ray tomography, but it lacks information about the chemistry of samples. To develop a methodology for measuring the multi-scale 3D microstructure of geological samples, correlative X-ray micro- and nanotomography were performed on two rocks followed by scanning electron microscopy with energy-dispersive spectroscopy (SEM-EDS) analysis. The study was performed in five steps: (i) micro X-ray tomography was performed on rock sample cores, (ii) samples for nanotomography were prepared using laser milling, (iii) nanotomography was performed on the milled sub-samples, (iv) samples were mounted and polished for SEM analysis and (v) SEM imaging and compositional mapping was performed on micro and nanotomography samples for complimentary information. Correlative study performed on samples of serpentine and basalt revealed multiscale 3D structures involving both solid mineral phases and pore networks. Significant differences in the volume fraction of pores and mineral phases were also observed dependent on the imaging spatial resolution employed. This highlights the necessity for the application of such a multiscale approach for the characterization of complex aggregates such as rocks. Information acquired from the chemical mapping of different phases was also helpful in segmentation of phases that did not exhibit significant contrast in X-ray imaging. Adoption of the protocol used in this study can be broadly applied to 3D imaging studies being performed at the Advanced Light Source and other user facilities.

Organic Two-Photon-Absorbing Photosensitizers Can Overcome Competing Light Absorption in Organic Photocatalysis.

Conventional organic photocatalysis typically relies on ultraviolet and short-wavelength visible photons as the energy source. However, this approach often suffers from competing light absorption by reactants, products, intermediates, and co-catalysts, leading to reduced quantum efficiency and side reactions. To address this issue, we developed novel organic two-photon-absorbing (TPA) photosensitizers capable of functioning under deep red and near-infrared light irradiation. Three model reactions including cyclization, Sonogashira Csp2-Csp cross-coupling, and Csp2-N cross-coupling reactions were selected to compare the performance of the new photosensitizers under both blue (427 nm) and deep red (660 nm) light irradiation. The obtained results unambiguously prove that for reactions involving blue light-absorbing reactants, products, and/or co-catalysts, deep red light source resulted in better performance than blue light when utilizing our TPA photosensitizers. This work highlights the potential of our metal-free TPA photosensitizers as a sustainable and effective solution to mitigate the competing light absorption issue in photocatalysis, not only expanding the scope of organic photocatalysts but also reducing reliance on expensive Ru/Ir/Os-based photosensitizers.

A general Bayesian algorithm for the autonomous alignment of beamlines.

Autonomous methods to align beamlines can decrease the amount of time spent on diagnostics, and also uncover better global optima leading to better beam quality. The alignment of these beamlines is a high-dimensional expensive-to-sample optimization problem involving the simultaneous treatment of many optical elements with correlated and nonlinear dynamics. Bayesian optimization is a strategy of efficient global optimization that has proved successful in similar regimes in a wide variety of beamline alignment applications, though it has typically been implemented for particular beamlines and optimization tasks. In this paper, we present a basic formulation of Bayesian inference and Gaussian process models as they relate to multi-objective Bayesian optimization, as well as the practical challenges presented by beamline alignment. We show that the same general implementation of Bayesian optimization with special consideration for beamline alignment can quickly learn the dynamics of particular beamlines in an online fashion through hyperparameter fitting with no prior information. We present the implementation of a concise software framework for beamline alignment and test it on four different optimization problems for experiments on X-ray beamlines at the National Synchrotron Light Source II and the Advanced Light Source, and an electron beam at the Accelerator Test Facility, along with benchmarking on a simulated digital twin. We discuss new applications of the framework, and the potential for a unified approach to beamline alignment at synchrotron facilities.

Scattering-Free and Fast Response Polymer Brush-Stabilized Liquid Crystals Beam Steering Using Surface-Initiated Polymerization Technique.

Nonmechanical fast response optical beam steering technology is increasingly essential for telecommunications, imaging systems, optical sensing, displays, and military applications. Polymer network liquid crystal (PNLC) beam steering can achieve submillisecond response times but faces limitations due to scattering issues arising from the refractive index mismatch between the polymer network and the liquid crystals (LCs). In this article, we demonstrate a scattering-free, fast-response LC beam steering by using polymer brushes to stabilize the gradient refractive index. First, the initiator is incorporated into the alignment layer and the monomer is mixed into the LC layer. Surface-initiated polymerization (SIP) is then employed to grow the polymer brushes exclusively on the substrate's surface, thus confining the polymer network's growth to the LC bulk and reducing interfacial scattering. For polymer brush stabilized liquid crystal (PBSLC) beam steering device with a period size of 225 μm and a cell gap of 7.2 μm, the average transmission rate reaches 88% in the visible light spectrum with a haze value of only 6.91. The steering angle is 0.16, and the diffraction efficiency is 80.3%. When a voltage of 35 Vrms is applied, the primary energy can be tuned to the zeroth order, with a response time close to 1 ms. By cascading two PBSLC beam steering devices with opposite steering directions, the primary energy of the beam can be adjusted between zeroth, +1, and -1 order. This method requires only a UV light source, a precision displacement stage, a power supply, and a mask, avoiding the need for expensive equipment and complex electrode fabrication. By adjustment of the phase change period, step width, and number of steps during fabrication, the steering angles and diffraction efficiency of the PBSLC beam steering device can be easily controlled, highlighting its significant potential for industrial production.

Identification of peripheral nerve functional fascicles in Sprague-Dawley rats by the carbon quantum dot-Annexin V antibody complex

To explore a method to identify the sensory and motor fascicles of the peripheral nerve to achieve accurate peripheral nerve functional fascicle suture. The peripheral nerve Sunderland V injury model, muscle branch of the femoral nerve and saphenous nerve were established in the bilateral femoral nerves of Sprague-Dawley (SD) rats. The specific samples were grouped as follows: the main trunk of the femoral nerve was exposed bilaterally and cut with microscopic scissors in the main trunk of the femoral nerve to prepare a model of Sunderland V injury in the mixed fascicle of peripheral nerves; the muscle branch of the femoral nerve was exposed bilaterally and cut in the middle section of the muscle branch of the femoral nerve to prepare a model of Sunderland V injury in the motor fascicle of peripheral nerves; the saphenous nerve was exposed bilaterally and cut at 1 cm below the patella to prepare a model of Sunderland V injury to the sensory fascicle of the peripheral nerves. A carbon quantum dot (CD)-annexin V antibody complex was prepared and applied to the distal and proximal nerve stumps of the peripheral nerve Sunderland V injury model groups of SD rats. Under the excitation light source of a 380 nm uv lamp, fluorescence color development was observed under a fluorescence microscope after 5, 10, 15, and 20 min. At 5 min, sections of the bilateral femoral nerve trunk, muscular branches of the femoral nerve, and Sunderland V lesion of the saphenous nerve in SD rats were only dark in color under the microscope, and there was no difference in fluorescence. The intensity of the staining increased significantly for 10–20 min. The sensory fascicles and saphenous nerves of the femoral nerve trunk showed blue fluorescence under the CD-Annexin V antibody complex staining, while the motor fascicles and muscle branches of the femoral nerve trunk showed no fluorescence. Fluorescence intensity gradually decreased after 20 min of staining. There was no significant difference in the staining intensity at 5, 10, 15, and 20 min in each group. Our results suggest that the CD-Annexin antibody complex can be used to identify functional fascicles of peripheral nerves in SD rats.

The role of BaTiO3 nanoparticles as photocatalysts in the synthesis and characterization of novel fruit dyes is investigated.

In the present work, the photocatalytic activity against the natural dye extracted from the novel fruits has been studied by the BaTiO3 nanoparticles (NPs) under a ultra-violet (UV) light source. The large concentrations of an essential phenolic agent present in this phytochemical extract superimposed with cloths fibers make strong stain and degrade into another form of toxic, which is excluded from the many textiles industries as the colorful waste waters without recycling and removal of that dye pigments have been investigated using both photodegradation and photoluminescence techniques. The entitled nanoparticles (NPs) were prepared using the soft chemical root-modified solvothermal synthesis combo method and exposure to heat treatment such that the annealing process has been done for different temperatures ranging from 100°C to 250°C. As for as concern the characterization, as a start, structural and morphology studies have been reported here that highly crystalline oriented peaks data using powder x-ray diffraction techniques (PXRD) as well as the surface morphology including the size, shape, and mass distribution using the field emission scanning electron microscopy (FESEM) techniques, which purely belong to rutile tetragonal structure of the crystal system and circular and noncircular flakes like rough surface morphology materials respectively. The lattice dissociation constant 'ε' value of the BaTiO3 NPs has determined to be ~2.71 × 10-3 using the Williamson-Hall (W-H plot) analysis of crystallographic data. In the UV visible spectroscopy findings, since the extreme quantum confinement of BaTiO3 nanoflakes/nanodisc, the optical energy bandgap has been estimated to be a range of 1.98 to 2.67 eV (~2.48 eV) found from the Tauc plot analysis, which contributes to the significantly owing to the enhanced photocatalytic efficiency with excellent performance along exciton formation, superoxide ions, and hydroxyl free radicals generations under UV-vis light irradiation resulting in efficient degradation of typical novel fruit organic dye. Photoluminescence spectra observed at room temperature and low temperature have been observed for the BaTiO3 nanoflakes, which exhibit the blue emission due to the crystalline defects such as the appearance of Ba vacancies leads to the conceivable beginning of p-type conductivity and the origination of free exciton emission reveals the direct bandgap transition nature of nanoflakes. RESEARCH HIGHLIGHTS: According to our findings, 89.71% of the natural syzygium cumin is degraded by photocatalysis reaction. As a plausible mechanism for the destruction of natural dyes under solar light, photocatalytic destruction has been proposed. The reaction between these reactive free radical species leads to high efficiency photodegradation with a short decay time. In addition to water treatment and environmental cleaning applications, the excellent performance of this photocatalyst makes it a promising candidate for other applications. Hence, the synthesized BaTiO3 nanoflakes showcase a highly significant advancement towards the development of a textiles dye recycling method.

Plasmonic Silver Nanoparticles Facilitate Electron Emission from Diamond upon Sun‐like Excitation

The development of a stable, non‐toxic material that emits electrons following absorption of visible light may have a major impact on the solar photocatalysis of difficult reactions such as CO$_2$ and N$_2$ reduction, as well as for targeted chemical transformations in general. Diamond is a good candidate, however it is a wide bandgap material requiring deep UV photons (λ < 227 nm) to promote electrons from the valence band into the conduction band. Embedding silver nanoparticles under the diamond surface allows the photoconductivity of the diamond in the spectral region of the surface plasmon resonance to be increased, while also leading to an enhancement of visible light photoemission. Considering the low intensity of the light sources used in this work and the spectral properties of the enhanced photoconductivity and photoemission a mechanism based on plasmonically enhanced photoconductivity which in turn allows surface states emptied by photoemission to be recharged thus leading to enhanced photoemission in the visible range is proposed.

Energy-Efficient and Smart Bicycle Lamps: A Comprehensive Review

In this review paper, information about bicycle lamp technical parameters is provided. The review is based on the searched Web of Science (WoS) and Scopus bibliographic databases and Transportation Research Information Services, which include references to books, technical reports, conference proceedings, and journal articles. This review showed that these papers about bicycle lighting legal rules in given countries are very easy to reach, but deep searching must be performed to find this research paper having the information about types of optical systems and light sources used in bicycle lamps. This research was conducted using PRISMA 2020 assumptions in the area of bicycle lighting technologies and innovations. The information about bicycle lamp technical parameters was obtained on the basis of the examination of technical documents and papers from high-impact journals. The author’s review shows that contemporary bicycle lamps are becoming increasingly smarter and more energy efficient, while also enhancing safety and comfort for cyclists on their routes in and beyond urban environments.

A Dynamic Hybrid Luminescent Display for Multilevel Anticounterfeiting

AbstractIncorporating specific motifs to provide tangible evidence of authenticity is a direct and effective measure against counterfeiting. However, achieving multi‐level anticounterfeiting through multiple motifs requires utilizing numerous stimulus sources to configure region‐specific emissions with customizable colors, which is complex, costly, and inaccessible. To address this challenge, a hybrid luminescent display is developed by integrating an internal down‐conversion layer with an organic light‐emitting diode (OLED). The internal down‐conversion layer can effectively extract the substrate and waveguide modes, resulting in a very rare outcome where the efficiency of a hybrid down‐conversion white OLED exceeds that of the pump light source. More importantly, by combining voltage‐modulated color‐tunable electroluminescence (EL) with EL‐induced down‐conversion luminescence, this unique design can precisely create dynamic and configurable multi‐color display patterns using only electrical stimulation. For anticounterfeiting purposes, the further amalgamation of the dynamic hybrid luminescent display device with the Internet of Things for digital authentication, and with fingerprint features for physical unclonable functions showcases unprecedented security. These results herald a new generation of multilevel luminescent anticounterfeiting technology.

Heralded Generation of Correlated Photon Pairs from CdS/CdSe/CdS Quantum Shells.

Quantum information processing demands efficient quantum light sources (QLS) capable of producing high-fidelity single photons or entangled photon pairs. Single epitaxial quantum dots (QDs) have long been proven to be efficient sources of deterministic single photons; however, their production via molecular-beam epitaxy presents scalability challenges. Conversely, colloidal semiconductor QDs offer scalable solution processing and tunable photoluminescence, but suffer from broader linewidths and unstable emissions. This leads to spectrally inseparable emission from exciton (X) and biexciton (XX) states, complicating the production of single photons and triggered photon pairs. Here, we demonstrate that colloidal semiconductor quantum shells (QSs) achieve significant spectral separation (∼75-80 meV) and long temporal stability of X and XX emissive states, enabling the observation of exciton-biexciton bunching in colloidal QDs. Our low-temperature single-particle measurements show cascaded XX-X emission of single photon pairs for over 200 s, with minimal overlap between X and XX features. The X-XX distinguishability allows for an in-depth theoretical characterization of cross-correlation strength, placing it in perspective with photon pairs of epitaxial counterparts. These findings highlight a strong potential of semiconductor quantum shells for applications in quantum information processing.

Highly Enhanced Light Recycling in Quantum Dot Displays by Sidewall Reflectors

AbstractQuantum dot (QD) color conversion‐based displays have emerged as one of the most promising next‐generation devices due to their superior emission properties in terms of color expression. To date, however, existing QD color conversion layer (QD‐CCL) technologies have suffered from low luminance and power efficiency, mainly due to significant light absorption by the bank structure. Here, the color conversion efficiency of QD‐CCL has been significantly enhanced by fabricating a highly reflective metal layer on the side surface of the bank structure. Using a high‐aspect‐ratio silver reflector fabricated through a secondary sputtering lithographic technique involving argon ion bombardment, the fabricated QD‐CCL is combined with a blue organic light‐emitting diode (OLED) serving as a light source. As a result, light recycling from the reflector significantly enhances color conversion efficiency and luminance by up to 4.60‐fold and 4.29‐fold, respectively. Optical simulation reveals that higher pixel resolution provides greater reflection probabilities during extraction. This photomask‐free approach is not only simple but also highly compatible with existing semiconductor fabrication processes, making it a viable commercial alternative for all color‐converting structures that utilize light‐emitting materials with omnidirectional emission characteristics.

Mini-LED Backlight: Advances and Future Perspectives

Miniaturized-light-emitting diode (mini-LED) backlights have emerged as the state-of-the-art technology for liquid crystal display (LCD), facilitating the improvement in a high dynamic range (HDR) and power saving. The local dimming technology divides the backlight into several dimming zones. Employing mini-LEDs, whose size ranges from 100 to 200 μm, as the light sources can enlarge the number of zones in the local dimming backlight, fulfilling the requirement for HDR. However, the halo effect still acts as one of the primary technological bottlenecks for mini-LED backlights. In this review, packaging technology of LEDs, color conversion, and the driving scheme of mini-LED backlights have been discussed. The strategies to reduce optical crosstalk in adjacent areas by various improved optical structures or to suppress the halo effect of LCDs by mini-LED backlights are summarized. The development trends of mini-LED backlights are also discussed.

Programmable C–N Bond Formation through Radical‐Mediated Chemistry in Plasma‐Microdroplet Fusion

Non‐thermal plasma discharge produced in the wake of charged microdroplets is found to facilitate catalyst‐free radical mediated hydrazine cross‐coupling reactions without the use of external light source, heat, precious metal complex, or trapping agents. A plasma‐microdroplet fusion platform is utilized for introduction of hydrazine reagent that undergoes homolytic cleavage forming radical intermediate species. The non‐thermal plasma discharge that causes the cleavage originates from a chemically etched silica capillary. The coupling of the radical intermediates gives various products. Plasma‐microdroplet fusion occurs online in a programmable reaction platform allowing direct process optimization and product validation via mass spectrometry. The platform is applied herein with a variety of hydrazine substrates, enabling i) self‐coupling to form secondary amines with identical N‐substitutions, ii) cross‐coupling to afford secondary amine with different N‐substituents, iii) cross‐coupling followed by in‐situ dehydrogenation to give the corresponding aryl‐aldimines with two unique N‐substitutions, and iv) cascade heterocyclic carbazole derivatives formation. These unique reactions were made possible in the charged microdroplet environment through our ability to program conditions such as reagent concentration (i.e., flowrate), microdroplet reactivity (i.e., presence or absence of plasma), and reaction timescale (i.e., operational mode source). The selected program is implemented in a co‐axial spray format.

Programmable C-N Bond Formation through Radical-Mediated Chemistry in Plasma-Microdroplet Fusion.

Non-thermal plasma discharge produced in the wake of charged microdroplets is found to facilitate catalyst-free radical mediated hydrazine cross-coupling reactions without the use of external light source, heat, precious metal complex, or trapping agents. A plasma-microdroplet fusion platform is utilized for introduction of hydrazine reagent that undergoes homolytic cleavage forming radical intermediate species. The non-thermal plasma discharge that causes the cleavage originates from a chemically etched silica capillary. The coupling of the radical intermediates gives various products. Plasma-microdroplet fusion occurs online in a programmable reaction platform allowing direct process optimization and product validation via mass spectrometry. The platform is applied herein with a variety of hydrazine substrates, enabling i) self-coupling to form secondary amines with identical N-substitutions, ii) cross-coupling to afford secondary amine with different N-substituents, iii) cross-coupling followed by in-situ dehydrogenation to give the corresponding aryl-aldimines with two unique N-substitutions, and iv) cascade heterocyclic carbazole derivatives formation. These unique reactions were made possible in the charged microdroplet environment through our ability to program conditions such as reagent concentration (i.e., flowrate), microdroplet reactivity (i.e., presence or absence of plasma), and reaction timescale (i.e., operational mode source). The selected program is implemented in a co-axial spray format.

Multiple Broadband Infrared Topological Photonic Crystal Valley States Based on Liquid Crystals

Spectral tunable technology has to meet the requirements of strong robustness and wide spectral range. We propose a method for the transmission and manipulation of infrared topological photonic crystal valley states based on tunable refractive index method that exhibits broad-spectrum and multi-band characteristics, along with a tunable emission angle. With this structure, different rotational directions of vortex light sources can independently excite the K valley and K′ valley within the frequency band ranging from 75.64 THz to 99.61 THz. At frequencies from 142.60 THz to 171.12 THz, it is possible to simultaneously excite both the K valley and K′ valley. The dual refractive index tunable design allows for the adjustment of the emission angle at a fixed frequency, enabling control over the independent excitation of either a single K valley or K′ valley, as well as their simultaneous excitation. This capability has significant implications for photonic computation and tunable filtering, offering enhanced operational flexibility and expanded functionality for future optical communications and integrated optical circuits.

Recent Advances in Thermally Activated Delayed Fluorescence-Based Organic Afterglow Materials.

Thermally activated delayed fluorescence (TADF)-based materials are attracting widespread attention for different applications owing to their ability of harvesting both singlet and triplet excitons without noble metals in their structures. As compared to the conventional fluorescence and room-temperature phosphorescence pathways, TADF originates from the reverse intersystem crossing process from the excited triplet state (T1) to the singlet state (S1). Therefore, TADF emitters enabling activated and long lifetime T1 excitons are potential candidates for generating long-lived afterglow emission, an effect that can still be observed for a while by the naked eye after the removal of the excitation light source. Recently, TADF-based organic afterglow materials featuring high photoluminescence quantum yields and long lifetimes above 100 ms under ambient conditions, have emerged for advanced information security, high-contrast biological imaging, optoelectronic devices, and intelligent sensors, whereas the related systematic review is still lacking. Herein, the recent progress in TADF-based organic afterglow materials is summarized and an overview of the photophysical mechanism, design strategies, and the performances for relevant applications is given. In addition, the challenge and perspective of this area are given at the end of the review.

Bottom Electrode Modification Enables Efficient and Bright Silicon-Based Top-Emission Perovskite Light-Emitting Diodes.

The integration of perovskites with mature silicon platform has emerged as a promising approach in the development of efficient on-chip light sources and high-brightness displays. However, the performance of Si-based green perovskite light-emitting diodes (PeLEDs) still falls significantly short compared to their red and near-infrared counterparts. In this study, it is revealed that the high work function Au, widely employed in Si-based top-emission PeLEDs as the reflective bottom electrode, exhibits considerably lower reflectivity in the green spectrum than in the longer wavelengths. Consequently, Ag electrode is introduced to replace Au to enhance the green light reflectivity, and the ultrathin MoO3 and self-assembled monolayers (SAMs) are sequentially deposited for surface modification. These results indicate that the MoO3 layer removes the energy barrier at Ag/polymer hole transport layer interface, enhancing the hole injection efficiency; while the SAMs firmly anchor onto the MoO3 layer, effectively preventing interfacial defect formation. Benefited from this organic/inorganic dual-layer modification strategy, Si-based green PeLEDs with an impressive peak external quantum efficiency of 18.2% and a maximum brightness of 81931 cd m-2 are successfully fabricated, on par with those of the red and near-infrared counterparts. This achievement marks an advancement in developing high-performance Si-based PeLEDs with full-spectrum output.