Enhancement mechanism of quantum yield in core/shell/shell quantum dots of ZnS-AgIn5S8/ZnIn2S4/ZnS.

To achieve a high quantum yield (QY) of nanomaterials suitable for optical applications, we improved the optical properties of AgIn5S8 (AIS) quantum dots (QDs) by employing an alloyed-core/inner-shell/outer-shell (ZAIS/ZIS/ZnS) structure. We also investigated the mechanism of optical transitions to clarify the improvement of QYs. In AIS, the low-energy absorption near the band edge region is attributed to the weakly allowed band gap transition, which gains oscillator strength through state intermixing and electron-phonon coupling. The main photoluminescence is also ascribed to the weakly allowed band gap transition with characteristics of self-trapped excitonic emission. With alloying/shelling processes, the weakly allowed transition is enhanced by the evolution of the electronic structures in the alloyed core, which improves the band gap emission. In shelled structures, the nonradiative process is reduced by the reconstructed lattice and passivated surface, ultimately leading to a high QY of 85% in ZAIS/ZIS/ZnS. These findings provide new insights into the optical transitions of AIS because they challenge previous conclusions. In addition, our work elucidates the mechanism behind the enhancement of QY accomplished through alloying/shelling processes, providing strategies to optimize nontoxic QDs for various applications using a green chemistry approach.

Development and Verification of a 480 nm Blue Light Enhanced/Reduced Human-Centric LED for Light-Induced Melatonin Concentration Control.

With the inherent sleep and wake cycle regulated by natural sunlight, the human body has evolved over millennia to be active during the day and to rest at night. However, maintaining an optimal 24 h cycle has become increasingly problematic in modern society as more people spend the majority of the day indoors. Many research groups have reported that inadequate artificial lighting interferes with melatonin production and disrupts the circadian rhythm. This study considered biological functions for light-emitting diodes (LEDs) of next-generation illumination, and LED packages and spectra suitable for both daytime and nighttime applications were designed. The prepared daytime human-centric (HC)-LEDs had a melanopic/photopic (M/P) ratio that was up to 26% higher than that of conventional (c)-LEDs, whereas the nighttime HC-LEDs exhibited up to a 26% lower M/P ratio compared to the c-LEDs. Nevertheless, because the HC-LED is designed to have almost the same color coordinates as the c-LED having the same correlated-color temperature (CCT), there is no change in the perceived color. To substantiate the biological effect, melatonin level data were obtained from 22 voluntary participants in c- and HC-LED lighting environments. In the HC-LED lighting environment, melatonin was suppressed by 21.9% after waking, and nocturnal melatonin secretion was increased by up to 12.2%. As human-centric lighting, our HC-LEDs are expected to become an essential element for modern life, where people spend most of their time indoors.

Molecular Mechanism of Selective Al2O3 Atomic Layer Deposition on Self-Assembled Monolayers.

Area-selective atomic layer deposition (AS-ALD) of insulating metallic oxide layers could be a useful nanopatterning technique for making increasingly complex semiconductor circuits. Although the alkanethiol self-assembled monolayer (SAM) has been considered promising as an ALD inhibitor, the low inhibition efficiency of the SAM during ALD processes makes its wide application difficult. We investigated the deposition mechanism of Al2O3 on alkanethiol-SAMs using temperature-dependent vibrational sum-frequency-generation spectroscopy. We found that the thermally induced formation of gauche defects in the SAMs is the main causative factor deteriorating the inhibition efficiency. Here, we demonstrate that a discontinuously temperature-controlled ALD technique involving self-healing and dissipation of thermally induced stress on the structure of SAM substantially enhances the SAM's inhibition efficiency and enables us to achieve 60 ALD cycles (6.6 nm). We anticipate that the present experimental results on the ALD mechanism on the SAM surface and the proposed ALD method will provide clues to improve the efficiency of AS-ALD, a promising nanoscale patterning and manufacturing technique.

Soft, adhesive and conductive composite for electroencephalogram signal quality improvement.

Since electroencephalogram (EEG) is a very small electrical signal from the brain, it is very vulnerable to external noise or motion artifact, making it difficult to measure. Therefore, despite the excellent convenience of dry electrodes, wet electrodes have been used. To solve this problem, self-adhesive and conductive composites using carbon nanotubes (CNTs) in adhesive polydimethylsiloxane (aPDMS), which can have the advantages of both dry and wet electrodes, have been developed by mixing them uniformly with methyl group-terminated PDMS. The CNT/aPDMS composite has a low Young's modulus, penetrates the skin well, has a high contact area, and excellent adhesion and conductivity, so the signal quality is enhanced. As a result of the EEG measurement test, although it was a dry electrode, results comparable to those of a wet electrode were obtained in terms of impedance and motion noise. It also shows excellent biocompatibility in a human fibroblast cell test and a week-long skin reaction test, so it can measure EEG with high signal quality for a long period of time.

Isolation of Bovine Milk Exosome Using Electrophoretic Oscillation Assisted Tangential Flow Filtration with Antifouling of Micro-ultrafiltration Membrane Filters.

Tangent flow-driven ultrafiltration (TF-UF) is an efficient isolation process of milk exosomes without morphological deformation. However, the TF-UF approach with micro-ultrafiltration SiNx membrane filters suffers from the clogging and fouling of micro-ultrafiltration membrane filter pores with large bioparticles. Thus, it is limited in the long term, continuous isolation of large quantities of exosomes. In this work, we introduced electrophoretic oscillation (EPO) in the TF-UF approach to remove pore clogging and fouling of with micro-ultrafiltration SiNx membrane filters by large bioparticles. As a result, the combined EPO-assisted TF (EPOTF) filtration can isolate large quantities of bovine milk exosomes without deformation. Furthermore, several morphological and biological analyses confirmed that the EPOTF filtration approach could isolate the milk exosomes in high concentrations with high purity and intact morphology. In addition, the uptake test of fluorescent-labeled exosomes by the keratinocyte cells visualized the biological function of purified exosomes. Hence, compared to the TF-UF process, the EPOTF filtration produced a higher yield of bovine milk exosomes without stopping the filtering process for over 200 h. Therefore, this isolation process enables scalable and continuous production of morphologically intact exosomes from bovine milk, suggesting that high-quality exosome purification is possible for future applications such as drug nanocarriers, diagnosis, and treatments.

Self-Repairable Silicon Anodes Using a Multifunctional Binder for High-Performance Lithium-Ion Batteries.

Despite of extremely high theoretical capacity of Si (3579 mAh g-1 ), Si anodes suffer from pulverization and delamination of the electrodes induced by large volume change during charge/discharge cycles. To address those issues, herein, self-healable and highly stretchable multifunctional binders, polydioxythiophene:polyacrylic acid:phytic acid (PEDOT:PAA: PA, PDPP) that provide Si anodes with self-healability and excellent structural integrity is designed. By utilizing the self-healing binder, Si anodes self-repair cracks and damages of Si anodes generated during cycling. For the first time, it is demonstrated that Si anodes autonomously self-heal artificially created cracks in electrolytes under practical battery operating conditions. Consequently, this self-healable Si anode can still deliver a reversible capacity of 2312 mAh g-1 after 100 cycles with remarkable initial Coulombic efficiency of 94%, which is superior to other reported Si anodes. Moreover, the self-healing binder possesses enhanced Li-ion diffusivity with additional electronic conductivity, providing excellent rate capability with a capacity of 2084 mAh g-1 at a very high C-rate of 5 C.

Passivation and Interlayer Effect of Zr(i-PrO)4 on Green CuGaS2/ZnS/Zr(i-PrO)4@Al2O3 and Red CuInS2/ZnS/Zr(i-PrO)4@Al2O3 QD Hybrid Powders.

Broadband emissive I-III-VI quantum dots (QDs) are synthesized as efficient and stable I-III-VI QDs to be used as eco-friendly luminescent materials in various applications. Here, we introduce the additional passivation of zirconium isopropoxide (Zr(i-PrO)4) to improve the optical properties and environmental stability of green-emitting CuGaS2/ZnS (G-CGS/ZnS) and red-emitting CuInS2/ZnS (R-CIS/ZnS) QDs. The photoluminescence quantum yield (PLQY) of both resultant Zr(i-PrO)4-coated G-CGS/ZnS and R-CIS/ZnS QDs reaches similar values of ~ 95%. In addition, the photostability and thermal-stability of G-CGS/ZnS/Zr(i-PrO)4 and R-CIS/ZnS/Zr(i-PrO)4 QDs are improved by reducing the ligand loss via encapsulation of the ligand-coated QD surface with Zr(i-PrO)4. It is also proved that the Zr(i-PrO)4-passivated interlayer mitigates the further degradation of I-III-V QDs from ligand loss even under harsh conditions during additional hydrolysis reaction of aluminum tri-sec-butoxide (Al(sec-BuO)3), forming easy-to-handle G-CGS/ZnS and R-CIS/ZnS QD-embedded Al2O3 powders. Therefore, the introduction of a Zr(i-PrO)4 complex layer potentially provides a strong interlayer to mitigate degradation of I-III-VI QD-embedded Al2O3 hybrid powders as well as passivation layer for protecting I-III-VI QD.

Synthesis of Cs3MnBr5 Green Phosphors Using an Eco-Friendly Evaporative Crystallization Process.

Green (G) and red (R) light-emitting materials, such as quantum dots, perovskite nanocrystals, and inorganic phosphor powders, owing to their excellent optical characteristics, have attracted researchers' attention as color-conversion materials for lighting and display applications. However, these materials contain environmentally harmful elements, such as Pb or Cd, and/or they are synthesized using environmentally harmful synthetic approaches and conditions, involving the use of organic solvents, high pressure, high temperature, harsh atmosphere, and long reaction time. In this study, as an eco-friendly synthetic approach to synthesize lead-free Cs3MnBr5 G powder phosphor, we suggest an evaporative crystallization process of aqueous reactant solution. This synthetic process does not use toxic elements or solvents and the crystallization process utilizes only low reaction temperature and short reaction time under air atmosphere conditions. We successfully synthesized Cs3MnBr5 green powder phosphor, with excellent optical properties, by evaporative heating of a 200 nm syringe-filtered solution at 150 °C for 2 h. The synthesized Cs3MnBr5 phosphors have a photoluminescence quantum yield of 66.3%, a peak wavelength of 520 nm, a narrow bandwidth of 38 nm, and a photoluminescence decay time of 0.34 ms under blue excitation. This phosphor is expected to be a useful alternative G-emitting material that can compete with commercial green quantum dots, perovskite nanocrystals, or inorganic phosphors.

Morphological-Electrical Property Relation in Cu(In,Ga)(S,Se)2 Solar Cells: Significance of Crystal Grain Growth and Band Grading by Potassium Treatment.

Solution-processed Cu(In,Ga)(S,Se)2  (CIGS) has a great potential for the production of large-area photovoltaic devices at low cost. However, CIGS solar cells processed from solution exhibit relatively lower performance compared to vacuum-processed devices because of a lack of proper composition distribution, which is mainly instigated by the limited Se uptake during chalcogenization. In this work, a unique potassium treatment method is utilized to improve the selenium uptake judiciously, enhancing grain sizes and forming a wider bandgap minimum region. Careful engineering of the bandgap grading structure also results in an enlarged space charge region, which is favorable for electron-hole separation and efficient charge carrier collection. Besides, this device processing approach has led to a linearly increasing electron diffusion length and carrier lifetime with increasing the grain size of the CIGS film, which is a critical achievement for enhancing photocurrent yield. Overall, 15% of power conversion efficiency is achieved in solar cells processed from environmentally benign solutions. This approach offers critical insights for precise device design and processing rules for solution-processed CIGS solar cells.

Diphylleia grayi-Inspired Intelligent Hydrochromic Adhesive Film.

Diphylleia grayi-inspired hydrochromic nano/microstructured films have received much attention for its promising smart hydrochromic applications owing to their simple and low-cost but energy-effective strategy. A new type of water-switchable glazing film patterned with various nano/micro air-hole inverse opal arrays is introduced by selectively removing nano/microsphere polystyrene arrays embedded in the surface of polydimethylsiloxane (PDMS) films. Using the significant contrast ratio of the bleaching and the scattering states, we have optimized the switching properties of Mie scattered patterns. As a result, we obtained a single inverse opal layer-embedded PDMS adhesive film with hexagonally close-packed 1 µm air-hole arrays as an optimum scattered film. The differences of diffusive transmittance and optical haze values between the dry and the wet states of the best scattered film reached 44.93% (ΔTD.T = 59.11-14.18%) and 54.88% (ΔH = 69.42-14.54%), respectively. In addition, using the best-optimized inverse opal layer-embedded PDMS film, we fabricated a perfectly imitated Diphylleia grayi structure for camouflage application and an intelligent hydrochromic window device. The dynamic water modulation of the scattered opaque and nonscattered transparent state of the inverse opal-patterned PDMS adhesive film can provide an advanced platform structure in the area of hydrochromic technology for smart windows, camouflage, and clear umbrellas for rainy days.

Narrow-Band SrMgAl10O17:Eu2+, Mn2+ Green Phosphors for Wide-Color-Gamut Backlight for LCD Displays.

The strength of the photoluminescence excitation (PLE) spectrum of SrMgAl10O17:Eu2+, Mn2+ (SAM:Eu2+, Mn2+) phosphor increased at deep blue (∼430 nm) and red-shifted from violet to deep blue with increasing concentrations of both Eu2+ ions Mn2+ ions. Eu2+-Mn2+ energy transfer between Eu2+ ions in Sr-O layer and Mn2+ ions at Al-O tetrahedral sites was maximized, and the photoluminescence (PL) intensity of the narrow-band Mn2+ emission was improved by optimizing the concentrations of Eu2+ and Mn2+ ions. The PL emission spectrum of the (Sr0.6Eu0.4)(Mg0.4Mn0.6)Al10O17 (SAM:Eu2+, Mn2+) phosphor peaks was optimized at 518 nm at a full width at half-maximum (FWHM) of 26 nm under light-emitting diode (LED) excitation at 432 nm LED. The color gamut area of a color-filtered RGB triangle of down-converted white LEDs (DC-WLEDs) incorporated with optimum SAM:Eu2+, Mn2+ green and K2SiF6:Mn4+ (KSF:Mn4+) red phosphors is enlarged by 114% relative to that of the NTSC standard system in the CIE 1931 color space. The luminous efficacy of our DC-WLED was measured and found to be ∼92 lm/W at 20 mA. Increased energy transfers between dual activators and red-shifted band-edge and enhanced intensity of PLE spectrum indicate the possibility of developing dual-activated narrow-band green phosphors for wide-color gamut in an LCD backlighting system.

Newly Developed Broadband Antireflective Nanostructures by Coating a Low-Index MgF2 Film onto a SiO2 Moth-Eye Nanopattern.

A newly developed nanopatterned broadband antireflective (AR) coating was fabricated on the front side of a glass/indium tin oxide/perovskite solar cell (PSC) by depositing a single interference layer onto a two-dimensional (2D)-patterned moth-eye-like nanostructure. The optimized developed AR nanostructure was simulated in a finite-difference time domain analysis. To realize the simulated developed AR nanostructure, we controlled the SiO2 moth-eye structure with various diameters and heights and a MgF2 single layer with varying thicknesses by sequentially performing nanosphere lithography, reactive ion etching, and electron-beam evaporation. Optimization of the developed AR nanostructure, which has a 100 nm-thick MgF2 film coated onto the SiO2 moth-eye-like nanostructure (diameter 165 nm and height 400 nm), minimizes the reflection loss throughout the visible range. As a result, the short-circuit current density (JSC) of the newly AR-coated PSC increases by 11.80%, while the open-circuit voltage (VOC) remains nearly constant. Therefore, the power conversion efficiency of the newly developed AR-decorated PSC increases by 12.50%, from 18.21% for a control sample to 20.48% for the optimum AR-coated sample. These results indicate that the newly developed MgF2/SiO2 AR nanostructure can provide an advanced platform technology that reduces the Fresnel loss and therefore increases the possibility of the commercialization of glass-based PSCs.

Stable and Colorful Perovskite Solar Cells Using a Nonperiodic SiO2/TiO2 Multi-Nanolayer Filter.

While research on building-integrated photovoltaics (BIPVs) has mainly focused on power-generating window applications, the utilization of other underutilized surface areas in buildings, including exteriors, facades, and rooftops, has still not been fully explored. The most important requirements for BIPVs are color, power conversion efficiency (PCE), and long-term stability. In this work, we achieved colorful (red, green, blue, RGB) perovskite solar cells (PSCs) with minimized PCE loss (<10%) and enhanced photostability by exploiting the optical properties of nonperiodic multi-nanolayer, narrow-bandwidth reflective filters (NBRFs). The NBRFs were fabricated by multilayering high-index TiO2/low-index SiO2 in a nonperiodic manner, which allowed devices to demonstrate various colors with effectively suppressed unwanted baseline ripple-shape reflectance. The PCEs of PSCs with nonperiodic RGB-NBRFs were 18.0%, 18.6%, and 18.9%, which represent reductions of only 10%, 7%, and 6% of PCE values, respectively, compared to a black control PSC (20.1%). Moreover, the photostability of the PSCs was substantially improved by using the NBRFs because of ultraviolet blocking in the TiO2 layers. The G-PSC retained 65% of the initial PCE after 60 h of continuous illumination (AM 1.5G one sun) at the maximum power point, whereas the black PSC retained only 30%. Aesthetic color value, low PCE loss, and enhanced photostability of PSCs were simultaneously achieved by employing our NBRFs, making this a promising strategy with potential applicability in power-generating building exteriors.

Dual wavelength lasing of InGaN/GaN axial-heterostructure nanorod lasers.

Optical confinement effects are investigated in InGaN/GaN axial-heterostructure nanolasers. Cylindrical nanorods with GaN/InGaN/GaN structures are prepared using combined processes of top-down and bottom-up approaches. The lasing of InGaN is observed at a low threshold (1 µJ cm-2), which is attributed to an efficient carrier transfer process from GaN to InGaN. The lasing of GaN is also found in the threshold range of 10-20 µJ cm-2 with a superlinear increase in emission intensity and high quality factors (Q = 1000), implying that dual wavelengths of lasing are tunable as a function of excitation intensity. The non-classical Fabry-Pérot modes suggest strong light-matter interactions in nanorods by optical confinement effects. The polarization of lasing indicates that the non-classical modes are in the identical transverse mode, which supports the formation of exciton-polaritons in nanorods. Polariton lasing in a single axial-heterostructure nanorod is observed for the first time, which proposes small-sized light sources with low threshold, polarized light, and tunable wavelengths in a single nanorod.

Stable and Efficient Green Perovskite Nanocrystal-Polysilazane Films for White LEDs Using an Electrospray Deposition Process.

We successfully fabricated a stable, efficient, and easy-to-use CsPbBr3 perovskite nanocrystal (PeNC)-embedded inorganic polymer film through an encapsulation step with a Si-N/Si-O-based polysilazane (PSZ) matrix via the electrospray (e-spray) deposition of a silazane (SZ) oligomer-decorated PeNC solution. To eliminate Pb2+ defect sites that are generated when the ligands are peeled from the PeNC surface, surface passivation of the Lewis acid/base adduct is possible by coupling the SZ oligomer (the donor of lone pairs) with Pb2+ sites (the acceptor of lone pairs). With the addition of the SZ oligomer, the photoluminescence quantum yield of photodegraded CsPbBr3 PeNC was recovered and increased by 2.35-fold whereas the stability was improved significantly from an untreated CsPbBr3 PeNC solution. During the e-spray deposition process, SZ-treated CsPbBr3 PeNC solution droplets can react with atmospheric moisture to polymerize and form a Si-N/Si-O network encapsulant via a sol-gel reaction. The resultant CsPbBr3-PSZ films showed improved stability levels under most environmental conditions, including air storage, blue light exposure, UV exposure, thermal exposure, and water immersion. The optimum CsPbBr3-PSZ film-covered blue light-emitting diode (LED) showed good performance capabilities, with a luminous efficacy (LE) of 85.9 lm/W and color-by-blue conversion efficiency (CE) of 60.1%. Furthermore, this easy-to-use CsPbBr3-PSZ film can be employed to realize a remote-type white-by-blue LED by combining it with red emissive K2SiF6:Mn4+/silicone film. The LE and CE rates of the white LED were 71.0 lm/W and 50.8%, respectively, at a correlated color temperature of 9334 K, with only an 8% drop in the LE for long-term operation of 100 h. This result indicates that e-spray deposition is a simple fabrication process by which to create stable and efficient PeNC films from an unstable PeNC solution using a rapid sol-gel reaction between droplets and moisture from the air.

RGB-Colored Cu(In,Ga)(S,Se)2 Thin-Film Solar Cells with Minimal Efficiency Loss Using Narrow-Bandwidth Stopband Nano-Multilayered Filters.

Colorful Cu(In,Ga)(S,Se)2 (CIGSSe) thin-film solar cells were achieved by integrating a narrow-bandwidth stopband filter (NBSF) on a CIGSSe cell. The full range of visible color of NBSF could be realized by depositing one-dimensional nano-multilayers of alternating high-index (Al2O3) and low-index (SiO2) films while controlling the thickness of each layer and the number of stacked layers. Particularly, high-purity red, green, and blue (RGB) colors were generated on black CIGSSe cells with minimal harvest efficiency drop, showing power conversion efficiency (PCE) losses for the red and green CIGSSe cells of 4.2 and 1.2%, respectively, with no reduction in the PCE of the blue CIGSSe cell. The minimal drop in the harvest efficiency was attributed to the antireflection effect of the NBSF and the low overlap between the reflectance spectrum of NBSFs with a narrow stopband and the absorption spectrum of CIGSSe. The esthetic value could be further enhanced through the color variation of the RGB NBSF with viewing angle, so-called pearl-like colors. The synergetic effect of minimal efficiency loss, full color realization, and the pearl-like color change of the newly developed NBSFs can make CIGSSe cells applicable to building-integrated photovoltaics.

Low-Yellowing Phosphor-in-Glass for High-Power Chip-on-board White LEDs by Optimizing a Low-Melting Sn-P-F-O Glass Matrix.

We introduce a low-melting-point (MP) Sn-P-F-O glass ceramic material into the phosphor-in-glass (PIG) material to realize an 'on-chip' chip-on-board (COB) type of phosphor-converted (pc) white light-emitting diode (WLED) with green (BaSr)2SiO4:Eu2+ and red (SrCa)AlSiN3:Eu2+ (SCASN) phosphors. The optimum Sn-P-F-O-based ceramic components can be sintered into the glass phase with a facile one-step heating process at 285 °C for 1 min. Specifically, these soft-fabrication conditions can be optimized to minimize the degradation of the luminescent properties of the red SCASN phosphor as well as the green silicate phosphor in PIG-based white COB-type pc-LEDs owing to the low thermal loss of the phosphors at low fabrication temperatures below 300 °C. Moreover, the constituents of the COB package, in this case the wire bonding and plastic exterior, can be preserved simultaneously from thermal damage. That is, the low sintering temperature of the glass ceramic encapsulant is a very important factor to realize excellent optical qualities of white COB LEDs. The optical performances of low-MP Sn-P-F-O-based PIG on-chip COB-type pc-WLEDs exhibit low yellowing phenomena, good luminous efficacy of 70.9-86.0 lm/W, excellent color rendering index of 94-97 with correlated color temperatures from 2700 to 10000 K, and good long-term stability.

Efficient and Stable CsPbBr3 Quantum-Dot Powders Passivated and Encapsulated with a Mixed Silicon Nitride and Silicon Oxide Inorganic Polymer Matrix.

Despite the excellent optical features of fully inorganic cesium lead halide (CsPbX3) perovskite quantum dots (PeQDs), their unstable nature has limited their use in various optoelectronic devices. To mitigate the instability issues of PeQDs, we demonstrate the roles of dual-silicon nitride and silicon oxide ligands of the polysilazane (PSZ) inorganic polymer to passivate the surface defects and form a barrier layer coated onto green CsPbBr3 QDs to maintain the high photoluminescence quantum yield (PLQY) and improve the environmental stability. The mixed SiN x/SiN xO y/SiO y passivated and encapsulated CsPbBr3/PSZ core/shell composite can be prepared by a simple hydrolysis reaction involving the addition of adding PSZ as a precursor and a slight amount of water into a colloidal CsPbBr3 QD solution. The degree of the moisture-induced hydrolysis reaction of PSZ can affect the compositional ratio of SiN x, SiN xO y, and SiO y liganded to the surfaces of the CsPbBr3 QDs to optimize the PLQY and the stability of CsPbBr3/PSZ core/shell composite, which shows a high PLQY (∼81.7%) with improved thermal, photo, air, and humidity stability as well under coarse conditions where the performance of CsPbBr3 QDs typically deteriorate. To evaluate the suitability of the application of the CsPbBr3/PSZ powder to down-converted white-light-emitting diodes (DC-WLEDs) as the backlight of a liquid crystal display (LCD), we fabricated an on-package type of tricolor-WLED by mixing the as-synthesized green CsPbBr3/PSZ composite powder with red K2SiF6:Mn4+ phosphor powder and a poly(methyl methacrylate)-encapsulating binder and coating this mixed paste onto a cup-type blue LED. The fabricated WLED show high luminous efficacy of 138.6 lm/W (EQE = 51.4%) and a wide color gamut of 128% and 111% without and with color filters, respectively, at a correlated color temperature of 6762 K.

Enhanced DC-Operated Electroluminescence of Forwardly Aligned   p/MQW/n InGaN Nanorod LEDs via DC Offset-AC Dielectrophoresis.

We introduce an orientation-controlled alignment process of p-GaN/InGaN multiquantum-well/n-GaN (p/MQW/n InGaN) nanorod light-emitting diodes (LEDs) by applying the direct current (DC) offset-alternating current (AC) or pulsed DC electric fields across interdigitated metal electrodes. The as-forwardly aligned p/MQW/n InGaN nanorod LEDs by a pulsed DC dielectrophoresis (DEP) assembly process improve the electroluminescence (EL) intensities by 1.8 times compared to the conventional AC DEP assembly process under DC electric field operation and exhibit an enhanced applied current and EL brightness in the current-voltage and EL intensity-voltage curves, which can be directly used as the fundamental data to construct DC-operated nanorod LED devices, such as LED areal surface lightings, scalable lightings (micrometers to inches) and formable surface lightings. The enhancement in the applied current, the improved EL intensity, and the increased number of forwardly aligned p/MQW/n InGaN nanorods in panchromatic cathodoluminescence images confirm the considerable enhancement of forwardly aligned one-dimensional nanorod LEDs between two opposite electrodes using DC offset-AC or a pulsed DC electric field DEP assembly process. These DC offset-AC or pulsed DC electric field DEP assembly processes suggest that designing for these types of interactions could yield new ways to control the orientation of asymmetric p/MQW/n InGaN diode-type LED nanorods with a relatively low aspect ratio.

Origin of highly efficient photoluminescence in AgIn5S8 nanoparticles.

The photoluminescence of AgIn5S8 nanoparticles was examined to clarify the emissive relaxation processes of defect states and to explain the highly efficient photoluminescence of defect states. The large Stokes shift of the defect emission was explained by strong electron-phonon coupling in the nanoparticles. Steady-state and time-resolved photoluminescence spectroscopy indicated two emissive defect states with characteristic emission energies and lifetimes. Change of the surface-to-volume ratio in the nanoparticles affected the relative contribution of the two states, implying that defect emission in higher energy was attributable to surface-related defects. The defect emission in lower energy was attributable to intrinsic defects, which were also present in bulk. The quantum yield of the surface defects was larger than that of the intrinsic defects, which accounted for the unusually high quantum yield of AgIn5S8 nanoparticles, although the origin of emission was the defect states, not the exciton recombination found in typical semiconductor nanoparticles.