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Switchable Topologically Chiral [2]Catenane as Multiple Resonance Thermally Activated Delayed Fluorescence Emitter for Efficient Circularly Polarized Electroluminescence.

Aiming at the fabrication of circularly polarized organic light-emitting diodes (CP-OLEDs) with high dissymmetry factors (gEL) and color purity through the employment of novel chiral source, topologically chiral [2]catenanes were first utilized as the key chiral skeleton to construct novel multi-resonance thermally activated delayed fluorescence (MR-TADF) emitters. Impressively, the efficient chirality induction and unique switchable feature of topologically chiral [2]catenane not only lead to a high |gPL| value up to 1.6 × 10-2 but also facilitate in situ dynamic switching of the full-width at half-maximum (FWHM) and circularly polarized luminescence (CPL). Furthermore, the solution-processed CP-OLEDs based on the resultant topologically chiral emitters exhibit reveal narrow FWHM of 36 nm, maximum external quantum efficiency of 17.6%, and CPEL with |gEL| of 2.1 × 10-3. This study demonstrates the successful construction of the first CP-MR-TADF emitters based on topological chirality with the highest |gPL| among the reported CP-MR-TADF emitters and excellent device performance to the best of our knowledge. Moreover, it endowed the MR-TADF emitter with distinctive switchable CPL performances, thus providing a novel design strategy as well as a promising platform for developing intelligent CP-OLEDs.

Switchable Topologically Chiral [2]Catenane as Multiple Resonance Thermally Activated Delayed Fluorescence Emitter for Efficient Circularly Polarized Electroluminescence

Aiming at the fabrication of circularly polarized organic light‐emitting diodes (CP‐OLEDs) with high dissymmetry factors (gEL) and color purity through the employment of novel chiral source, topologically chiral [2]catenanes were first utilized as the key chiral skeleton to construct novel multi‐resonance thermally activated delayed fluorescence (MR‐TADF) emitters. Impressively, the efficient chirality induction and unique switchable feature of topologically chiral [2]catenane not only lead to a high |gPL| value up to 1.6 × 10‐2 but also facilitate in situ dynamic switching of the full‐width at half‐maximum (FWHM) and circularly polarized luminescence (CPL). Furthermore, the solution‐processed CP‐OLEDs based on the resultant topologically chiral emitters exhibit reveal narrow FWHM of 36 nm, maximum external quantum efficiency of 17.6%, and CPEL with |gEL| of 2.1 × 10‐3. This study demonstrates the successful construction of the first CP‐MR‐TADF emitters based on topological chirality with the highest |gPL| among the reported CP‐MR‐TADF emitters and excellent device performance to the best of our knowledge. Moreover, it endowed the MR‐TADF emitter with distinctive switchable CPL performances, thus providing a novel design strategy as well as a promising platform for developing intelligent CP‐OLEDs.

Efficient and spectrally stable pure blue light‐emitting diodes enabled by phosphonate passivated CsPbBr3 nanoplatelets with conjugated polyelectrolyte‐based energy transfer layer

AbstractLead halide perovskites exhibit a very wide color gamut due to their extremely narrow emission spectra, typically characterized by a full‐width at half‐maximum (FWHM) of less than 20 nm. Significant advancements have been made in developing highly efficient and stable green, red, and near‐infrared perovskite light‐emitting diodes (PeLEDs). However, achieving efficient and stable pure blue‐emitting PeLEDs remains a significant challenge. In this work, we successfully synthesized monoanionic octyl‐phosphonate capped CsPbBr3 nanoplatelets (OPA‐NPLs) using a combination of octyl‐phosphonic acid and oleylamine at room temperature, diverging from common approaches that necessitate complex high‐temperature methods, such as hot injection, to accommodate short‐chain ligands. The OPA‐NPLs exhibit pure blue photoluminescence at 462 nm with a FWHM of 14 nm. Compared with CsPbBr3 nanoplatelets synthesized using oleic acid, OPA‐NPLs demonstrate significantly improved thermal stability and higher photoluminescence quantum yield (PLQY) of 90%. Additionally, we introduced Poly[(9,9‐bis(3′‐((N,N‐dimethyl)‐N‐ethylammonium)‐propyl)‐2,7‐fluorene)‐alt‐2,7‐(9,9‐dioctylfluorene)]dibromide (PFN‐Br), a conjugated polyelectrolyte material, as a hole transport layer. This facilitated energy transfer between PFN‐Br and the CsPbBr3 nanoplatelets. The resulting device demonstrated an electroluminescence peak at 462 nm, an extremely narrow FWHM of 14 nm, and a maximum external quantum efficiency (EQE) of 4%. Notably, the device maintained pure blue emission without spectral peak shift even during degradation caused by excess joule heating.image

Performance improvement of red, green and blue InGaN micro-LEDs with distributed Bragg reflector

Abstract Red-green-blue (RGB) micro light-emitting diodes (micro-LEDs) without distributed Bragg reflector (DBR), with air-separating DBR, and with integrated DBR, were demonstrated. The effect of the DBRs as reflectors on the external quantum efficiency (EQE) and electroluminescence (EL) spectra enhancement of RGB micro-LEDs was systematically investigated for realizing higher-performance micro-LEDs for display applications. At 5 A/cm2, the EQEs of the RGB micro-LEDs with integrated DBR were improved by 38%, 33%, and 32%, respectively, with comparison to the RGB DBR free micro-LEDs. Further, the full width at half maximum (FWHM) of the red micro-LEDs was reduced by 4.3 nm at 50 A/cm2 with the integrated DBR due to the higher enhancement of the central wavelength spectrum. The green and blue micro-LEDs with integrated DBR had higher EQE and the red micro-LEDs with integrated DBR had narrower FWHM compared to those with air-separating DBR. However, the peak wavelength of the RGB micro-LEDs with integrated DBR shifted, resulting in a lower color gamut in CIE 1931. The above work provides guidance for future full-color micro-display applications based on RGB InGaN micro-LED technology.

Dual‐Core Engineering for Efficient Deep‐Blue Multiple Resonance Thermally Activated Delayed Fluorescent Materials

AbstractDeveloping narrowband blue multiple resonance (MR) organic emitters with Commission Internationale de L'Eclairage (CIE) y coordinates <0.1 is essential for advanced display technologies. This study proposes a deep‐blue thermally activated delayed fluorescence (TADF) emitter, named 2BNO, which integrates two independent MR cores. Unlike many TADF materials with single‐bonded dual emitting cores, 2BNO utilizes a steric hindrance‐assisted fluorene bridge to achieve an orthorhombic molecular structure. The dual‐core MR‐TADF emitter shows enhanced light absorption and a high photoluminescence quantum yield. Notably, the emission of 2BNO is not significantly redshifted compared to single‐core compounds and maintains a narrow full width at half‐maximum (FWHM) of 24 nm with CIE coordinates of (0.147, 0.041) in 2Me‐THF solution, nearing the BT.2020 blue standard. Organic light‐emitting diodes (OLEDs) incorporating 2BNO as the emitter exhibit deep‐blue emission at 460 nm with a narrow FWHM of 29 nm and CIE coordinates of (0.14, 0.09). The dual emitting core design significantly improves device efficiency, achieving a high external quantum efficiency (EQE) of 19.8%. The dual‐core molecular design strategy in this work is demonstrated to be effective in promoting the efficiency of the TADF emitters while preserving deep‐blue color purity.

Optimization of electrostatic seeding technique for wafer-scale diamond fabrication on β-Ga2O3

Integrating diamonds with β-Ga2O3 is a promising solution for addressing the problem of poor thermal conductivity and limited p-type dopability of β-Ga2O3. However, growing diamonds on β-Ga2O3 is challenging, especially without any interfacial layer, and achieving large-scale uniform diamond films is also tricky. This paper explores the vital role of an electrostatic seeding technique involving the use of Polydiallyldimethylammonium chloride (PDDAC) polymer with a positive zeta potential and diamond nano slurries with a negative zeta potential to facilitate the integration of diamond with β-Ga2O3. We conduct a detailed analysis of each step of this seeding technique, adjusting the spinning speed of the polymer coating, spinning period, baking period, and ultrasonication period to understand the underlying mechanisms preventing large-scale diamond growth and to identify strategies for achieving wafer-scale diamond fabrication on single crystal β-Ga2O3 film. This process facilitates the attainment of a uniform dispersion of diamond nanoparticles on β-Ga2O3 at a seeding density of ∼1.82 × 1011 cm−2. The optimized seeding technique has enabled the successful growth of wafer-scale diamond films on β-Ga2O3, as confirmed by scanning electron microscopy (SEM). Additionally, the high quality of the diamond film is affirmed by a quality factor of 96.75 % and a narrow full-width half maximum of 10.28 cm−1 in the T2g peak of the Raman spectra. The X-ray diffraction pattern reinforces the excellent quality of polycrystalline diamond films with minimum stress. In summary, this research provides valuable insights into the polymer-assisted electrostatic seeding technique, paving the way for the uniform growth of wafer-scale diamond films on β-Ga2O3, which is critical for realizing β-Ga2O3-based heterostructure devices.

Fusion of Selenium‐Embedded Multi‐Resonance Units Toward Narrowband Emission and Fast Triplet‐Singlet Exciton Conversion

AbstractDeveloping multi‐resonance thermally activated fluorescence (MR‐TADF) emitters with both fast reverse intersystem crossing (RISC) rate and narrow emission bandwidth still remains a formidable challenge. Herein, a design strategy of fused MR skeleton containing heavy chalcogen (sulfur or selenium) for high‐performance MR‐TADF molecules is developed. Impressively, Se‐embedded emitter (DSeBN) shows extremely narrow full width at half maximum (FWHM) value of 16 nm and ultrafast RISC rate constant up to 2.0 × 106 s−1. The organic light‐emitting diode (OLED) based on this emitter exhibits excellent performance parameters with extremely narrow FWHM of 17 nm and high external quantum efficiency (EQE) of 35.31%. Significantly, much suppressed efficiency roll‐off is achieved, in which the EQE still stayed at 32.47% and 25.05% at the luminance of 100 and 1000 cd m−2, respectively. These results represent the state‐of‐the‐art device performance in terms of efficiency and FWHM, shedding new light on the development of practical MR‐TADF emitters.

Quantum-Dot Light-Emitting Fiber Toward All-In-One Clothing-Type Health Monitoring.

In the Fourth Industrial Revolution, as the connection between objects and people becomes increasingly important, interest in wearable optoelectronic device-based medical diagnosis is on the rise. Pulse oximetry sensors based on a fiber platform, which is the smallest unit of clothing, could be considered an attractive candidate for this application. In this study, red and green quantum-dot light-emitting fibers (QDLEFs) based on a 250 μm-diameter 1-dimensional fiber were successfully implemented, achieving high current efficiencies of approximately 22.46 mW/sr/A and 23.6 mW/sr/A and narrow full-width at half-maximum (FWHM) of about 33 nm, respectively. In addition, its omnidirectional flexibility was confirmed through a vertical and lateral bending test with 0.92% strain. By employing a transparent and flexible elastomer, a wearable pulse oximeter incorporating QDLEFs was successfully demonstrated for oxygen saturation level (SpO2) monitoring on finger and wrist. It was demonstrated to be washable, and could be operated for up to about 18 h. Due to the elastomer and bottom emission, it exhibited excellent wear resistance characteristics in a 50 cycle reciprocating test conducted at about 2180.43 kPa with 220-grit abrasive paper sheet. A theoretical investigation based on modified photon diffusion analysis (MPDA) modeling also determined that using narrow FWHM light sources, such as QDLEFs, improves the resolution and accuracy of SpO2 monitoring. Accordingly, the proposed QDLEF showed distinguished potential as an all-in-one clothing type pulse oximetry.

Ultranarrow Deep-Blue Luminescence of Perovskite Nanocrystals by A-Site Cation Control.

Metal-halide perovskite nanocrystals (NCs) are one of the most promising emitters for the application of display and nanolight sources. The full width at half-maximum (FWHM) of photoluminescence (PL) emission is essential for color purity, which however remains a difficulty to further reduce the FWHM of the perovskite NCs at room temperature. Here, we show the quasi-sphere perovskite NCs with narrow PL emission at a deep-blue wavelength of ∼430 nm; its PL FWHM reaches ∼11 nm at room temperature, owing to the monodispersion in size distribution as well as the symmetric quasi-sphere morphology of NCs releasing the fine structure splitting-induced inhomogeneous broadening. Through regulating A cations with respect to the ratio of FA (or MA)-to-Cs and Cs-to-Pb, the PL emission of the NCs could be tuned from ∼505 to ∼430 nm combined with varied morphologies from large cube to small quasi-sphere. Such spectroscopic and morphological discrepancies are supposed to be attributed to the different crystalline kinetics that is strongly dependent on the synthetic condition. To be specific, in the case of increasing FA (or MA)-to-Cs, the growth rate of CsPbBr3 and FAPbBr3 (or MAPbBr3) perovskites is determined by the reactivity of transient species, while in the case of decreasing the Cs-to-Pb ratio, the growth rate of perovskites is slowed down by the serious reduction of Cs+ in the precursor. This study provides an effective strategy to adjust the emission across from green to deep-blue color and promotes the perovskite NCs with a narrow FWHM, and tunable PL emission facilitates in application of optoelectronic devices.

Robust Radicals Featuring B- and N-Embedded Dioxygen-Bridged Units: Synthesis, Structures, and Optical Properties.

Tris(2,4,6-trichlorophenyl)methyl (TTM) group has been widely used for constructing organic radicals, but the poor optical stabilities limit the application prospects of the TTM radicals. In this work, the rigid B- and N-embedded dioxygen-bridged (BO and NO) units were attached to the TTM skeleton as the strong electron-withdrawing and electron-donating groups, respectively. The rigidity and strong electronic effect of the BO and NO units contribute to the high chemical and optical stability of BO-TTM and NO-TTM radicals. Notably, NO-TTM exhibits near-infrared emission at 830 nm with a narrow full width at half maximum (FWHM) of 55 nm (100 meV), while BO-TTM shows blue-shifted luminescence at 635 nm and a narrower FWHM of merely 43 nm (130 meV). This study has developed a methodology to produce highly efficient and enduring luminescent radicals, which could tune emission properties such as wavelength and FWHM.

P‐198: Ideal Design of Platinum (II) Complex with Bulky Blocking Group for Narrow Emission and High Efficiency in Blue Organic Light‐Emitting Diodes

Platinum phosphorescent materials are emerging as promising candidates for efficient blue organic light‐emitting diodes. Especially, tetradentate ligands with a 5/6/6 configuration have the advantage of having twisted structure to minimize intermolecular interactions. However, the reported platinum complexes in the 5/6/6 configuration still exhibit relatively broad luminescence spectra and low efficiency at high doping concentration due to insufficient intermolecular interaction suppression. It is necessary to introduce the appropriate blocking group at the proper position on the ligand to ensure that intermolecular interactions are inhibited. In this work, we propose an ideal design introducing blocking group for platinum (II) complexes with small changes in efficiency and emission spectra at high doping concentration. The bulky blocking group, 2,6‐diisopropylphenyl, introduced at the 3‐position of the carbazole is distorted vertically due to steric hindrance, so the energy is still retained. However, the photophysical and device properties were improved by suppression of intermolecular interaction. As a result, Pt‐dipCz showed high efficiency of 25.0% with narrow full width at half maximum (FWHM) of 22 nm at 5 wt.% doping concentration. When doping concentration increased to 20 wt.%, high efficiency and narrow FWHM were maintained with small changes of only 4.8% reduction and 2 nm increase, respectively. These values indicate that 2,6‐diisopropylphenyl group introduced at carbazole is efficient for suppression of intermolecular interaction.

Stepwise Toward Pure Blue Organic Light-Emitting Diodes by Synergetically Locking and Shielding Carbonyl/Nitrogen-Based MR-TADF Emitters.

Deep-blue multi-resonance (MR) emitters with stable and narrow full-width-at-half-maximum (FWHM) are of great importance for widening the color gamut of organic light-emitting diodes (OLEDs). However, most planar MR emitters are vulnerable to intermolecular interactions from both the host and guest, causing spectral broadening and exciton quenching in thin films. Their emission in the solid state is environmentally sensitive, and the color purity is often inferior to that in solutions. Herein, a molecular design strategy is presented that simultaneously narrows the FWHM and suppresses intermolecular interactions by combining intramolecular locking and peripheral shielding within a carbonyl/nitrogen-based MR core. Intramolecularly locking carbonyl/nitrogen-based bears narrower emission of 2,10-dimethyl-12,12-diphenyl-4H-benzo[9,1]quinolizino[3,4,5,6,7-defg]acridine-4,8(12H)-dione in solution and further with peripheral-shielding groups, deep-blue emitter (12,12-diphenyl-2,10-bis(9-phenyl-9H-fluoren-9-yl)-4H-benzo[9,1]quinolizino[3,4,5,6,7-defg]acridine-4,8(12H)-dione, DPQAO-F) exhibits ultra-pure emission with narrow FWHM (c.a., 24nm) with minimal variations (∆FWHM ≤ 3nm) from solution to thin films over a wide doping range. An OLED based onDPQAO-F presents a maximum external quantum efficiency (EQEmax) of 19.9% and color index of (0.134, 0.118). Furthermore, the hyper-device of DPQAO-F exhibits a record-high EQEmax of 32.7% in the deep-blue region, representing the first example of carbonyl/nitrogen-based OLED that can concurrently achieve narrow bandwidth in the deep-blue region and a high electroluminescent efficiency surpassing 30%.

Sodium-based no-core fiber surface plasmon resonance sensor with high sensitivity and narrow FWHM

Since fiber-optic sensors using noble metal-excited surface plasmon resonance (SPR) effects have encountered bottlenecks in improving performance, we propose a fiber-optic sensor using sodium in combination with a no-core fiber (NCF) to measure both refractive index (RI) and temperature. We deposited sodium thin films on the surface of NCF optical fibers and protected them with polymethyl methacrylate (PMMA) or polydimethylsiloxane (PDMS) for RI sensing or temperature sensing. We performed computational simulations and performance analyses of the sensors using the finite element method, and the results show that the sodium-based SPR sensors have higher sensitivity, wider detection range, and narrower full width at half-maximum (FWHM) than the noble metal SPR sensors. SPR sensors with different sodium film thicknesses have different sensing characteristics, so we can get optical fiber sensors with more flexible transmission characteristics, which helps us arrange sensors more conveniently in practical applications. The simulation and numerical results show that when the sensor is used to measure RI, the average sensitivity of the sensor can reach 7977 nm RIU−1, the maximum sensitivity can reach 23100 nm RIU−1, the narrowest FWHM is 14.23 nm, and the maximum figure of merit (FOM) is 719.42 RIU−1 under different thicknesses of sodium film. The corresponding RI ranges from 1.32 to 1.41. When the temperature measurement range is 0 °C ∼ 100 °C, the average sensitivity can reach 7.86 nm °C−1, the maximum temperature sensitivity can reach 21.1 nm °C−1, and the narrowest FWHM is 17.84 nm. In summary, the proposed sodium-based SPR sensor has flexible and high-performance sensing characteristics, and our research work provides more powerful theoretical support for the application of sodium-based plasma devices.

Single crystal growth of complex layered oxychalcogenide by melt-solidification method

We have successfully grown single crystals of layered mixed-anion compound Sr2ZnCu2Se2O2 by a simple melt-growth method. Single crystals of the layered oxychalcogenides Sr2ZnCu2Se2O2 were grown by melt-solidification of stoichiometric raw materials. Plate-like single crystals were obtained, and the maximum size of crystals was 2.5 × 1.4 mm2. Thermal analysis result indicates simple melting-solidification-like behavior, and the size of crystals increases significantly above the melting point revealed by this measurement. X-ray rocking curve (XRC) measurement results of the single crystal showed no peak splitting, with a narrow full width half maximum of 30 and 97 arcsec in (105) and (0012) peaks, respectively. The electrical conductivity of single crystals on the a(b) plane was 4.34 × 10−1 S/cm at room temperature. Obtained single crystals were transparent, and the absorption edge was observed around 560 nm in the transmittance measurement. Although layered oxychalcogenide Sr2ZnCu2Se2O2 has a complex composition and structure, this compound exhibits congruent melting behavior in a sealed environment. This feature enables us to grow single crystals of mixed-anion compounds easily by the melt-growth method.

High-efficiency top-emitting organic light-emitting diodes based on metal/ITO composite electrodes

High-performance top-emitting organic light-emitting diodes (TEOLEDs) integrating the metal/ITO composite anodes were developed. The results revealed that covering the surface of Al anode with ITO layer could effectively improve the charge injection efficiency and balance the hole–electron charge. The effect of the thickness of ITO on the performance of TEOLEDs with Al/ITO anodes was further studied. The TEOLEDs with Al/ITO (5 nm) anode showed optimized performance, with the current efficiency (CE) and external quantum efficiency (EQE) enhanced by 40.0% and 34.5% compared to that of the OELD with pure Al anode, and increased by 93.1% and 33.5% compared to that of bottom-emitting OLEDs. In addition, the full width at half maximum (FWHM) was narrowed to 36 nm due to the micro-cavity effect of the top-emitting structure and the turn-on voltage decreased to as low as 2.3 V owing to the efficient charge injection and well-matched energy level. In addition, TEOLEDs using Ag/ITO as anode exhibited a slow roll-off of CE and EQE and a narrower FWHM of 30 nm, greatly improving the color purity. The strategy is simple and can significantly improve the efficiency of the TEOLEDs, which promotes the applications of OLEDs in the fields of ultra-high-definition displays and micro-displays.

Efficient narrowband yellow organic light-emitting diodes based on iridium(III) complexes with the rigid indolo[3,2,1-jk]carbazole unit.

Phosphorescent material with narrowband emission is crucial for advancing wide-color-gamut organic light-emitting diodes (OLEDs). In this work, two iridium(III) complexes, (PhthzICz)2Ir(tmd) and (thzICz)2Ir(tmd), using rigid 2-(benzothiazole-2-yl)indolo[3,2,1-jk]carbazole (PhthzICz) and 2-(thiazole-2-yl)indolo[3,2,1-jk]carbazole (thzICz) as cyclometalated ligands and 2,2,6,6-tetramethyl-3,5-heptanedione (tmd) as ancillary ligands, were synthesized. When these complexes were doped into the host material 3,3'-di(9H-carbazol-9-yl)-1,1'-biphenyl, the doped films exhibited yellow photoluminescence (PL) peaking at 537 and 531 nm, full width at half maximum (FWHM) bands of 35 and 60 nm, and PL quantum yields of 89.9% and 85.9%, respectively. OLEDs based on these two emitters display moderate performance characteristics with maximum external quantum efficiencies of 25.2% and 22.7%. Notably, the device based on (PhthzICz)2Ir(tmd) exhibits a narrow FWHM of 31 nm. Overall, the study highlights the practicality of incorporating rigid groups into the cyclometalated ligands of Ir(III) complexes as a viable strategy for achieving efficient Ir(III) complexes for OLEDs with narrow emission and high efficiency.

Interference filter based external-cavity diode laser with combined dual interference filters and largely adjustable feedback range

External-cavity diode lasers (ECDL) are widely used as light sources in laser spectroscopy, atomic physics, and quantum optics. This study demonstrated a home-made 852–nm ECDL with variable feedback, using the combined dual narrow-band interference filters (IFs) as the laser longitudinal mode selection element. The combination of narrow-band IFs, mainly for the current commercially available narrow-band IFs with the full width at half maximum (FWHM) of approximately 0.5 nm for 780-895 nm. We designed different narrow-band IFs combinations to achieve a narrower FWHM, and applied them in the ECDL. The combination of the dual narrow-band IFs further reduces the laser linewidth. We measured the laser linewidth using a high-finesse Fabry-Perot cavity with a linewidth of approximately 10 kHz. The laser linewidth is approximately 176 kHz for the Single-IF-ECDL and 96 kHz for the Dual-IF-ECDL with the same feedback. In addition, we have experimentally verified the results of narrower laser linewidth and larger tuning range with increase in the feedback. The developed Dual-IF-ECDL has the capability of narrow linewidth and wavelength tunability and can be applied to precision spectroscopy, cooling and trapping of neutral atoms.

Solid superacid catalysts promote high-performance carbon dots with narrow-band fluorescence emission for luminescence solar concentrators

Facile and efficient method for constructing carbon dots (CDs) with narrow full width at half maximum (FWHM) is a major challenge in the field, and researches on regulating the FWHM of CDs are also rare and scarce. In this work, we delved into the synthesis of CDs with narrow fluorescence emission FWHM (NFEF-CDs) in the m-phenylenediamine (m-PD)/ethanol system, utilizing solid superacid resin as catalyst with solvothermal method. The resulting NFEF-CDs exhibit a photoluminescent (PL) emission peak at 521 nm with a narrow FWHM of 41 nm, an absolute PL quantum yield (QY) of 80%, and display excitation-independent PL behavior. Through comprehensive characterization, we identified the protonation of edge amino on NFEF-CDs as the key factor in achieving the narrow FWHM. Subsequently, we validated the broad applicability of solid superacid resins as catalysts for synthesizing CDs with narrow FWHM in the m-PD/ethanol system. Finally, we utilized a self-leveling method to prepare NFEF-CDs film on the surface of poly(methyl methacrylate) (PMMA) substrate and investigated the solid-state fluorescence properties of NFEF-CDs as well as their performance as luminescence solar concentrator (LSC) for photovoltaic conversion. The results revealed that the as-prepared LSC exhibit an internal quantum efficiency (ηint) of 42.39% and an optical efficiency (ηopt) of 0.68%. These findings demonstrate the promising prospects of NFEF-CDs in the field of LSCs and provide a theoretical basis for their application in photovoltaic conversion.

Enhanced Near-Infrared Ultra-Narrow Absorber Based on a Dielectric Nano-Resonant Ring for Refractive Index Sensing.

In this paper, a plasmon resonance-enhanced narrow-band absorber based on the nano-resonant ring array of transparent conductive oxides (TCOs) is proposed and verified numerically. Due to the unique properties of TCOs, the structure achieves an ultra-narrowband perfect absorption by exhibiting a near-field enhancement effect. Consequently, we achieve a peak absorption rate of 99.94% at 792.2 nm. The simulation results indicate that the Full Width Half Maximum (FWHM) can be limited to within 8.8 nm. As a refractive index sensor, the device reaches a sensitivity S of 300 nm/RIU and a Figure of Merit (FOM) value of 34.1 1/RIU. By analyzing the distribution characteristics of the electromagnetic field at the 792.2 nm, we find high absorption with a narrow FWHM of the ITO nano-resonant ring (INRR) owing to plasmon resonance excited by the free carriers at the interface between the metal and the interior of the ITO. Additionally, the device exhibits polarization independence and maintains absorption rates above 90% even when the incident formed by the axis perpendicular to the film is greater than 13°. This study opens a new prospective channel for research into TCOs, which will increase the potential of compact photoelectric devices, such as optical sensing, narrowband filtering, non-radiative data transmission and biomolecular manipulation.

All-dielectric metasurface refractive index sensor with high figure of merit based on quasi-bound states in the continuum

All-Dielectric metasurfaces are widely used in the field of sense due to their small size, freedom of design, and low radiation loss. However, the optical sensor still has the problem of wide full width at half maximum (FWHM), which leads to a low figure of merit (FOM). In order to solve this problem, an all-dielectric metasurface based on quasi-bound states in the continuum (q-BIC) was proposed for refractive index sensing. The sensor structure consisted of a prism/metasurface/analyte, where the metasurface was composed of periodically arranged subwavelength asymmetric silicon gratings. The asymmetry of the structure led to the coupling of the tangential and radiative field components in the superficial layer at the resonance position, which formed a q-BIC resonance peak with a narrow FWHM in the reflection spectrum. We explained the causes of the q-BIC resonance peak generation by finite element analysis, and analyzed the factors affecting the FWHM, and also simulated the machining errors. The results showed that by reducing the asymmetry of the sensor, it could have a high FOM, with a FOM of 1.35 × 107 RIU−1. In addition, simulated machining errors within ±5 nm showed that small machining errors did not lead to the disappearance of q-BIC, which proved that the sensor had good robustness. These findings had provided ideas for the accurate detection of trace substances.