ABSTRACT
PURPOSE: To evaluate the outcomes of wavefront-optimized (WFO) and topography-guided (TG) transepithelial photorefractive keratectomy (transPRK) in the treatment of myopia and myopic astigmatism. METHODS: Patients who underwent transPRK using the WaveLight EX500 excimer laser for the correction of myopia and myopic astigmatism between January 2022 and March 2023 were divided into groups of WFO transPRK (77 eyes of 36 patients) or TG transPRK (63 eyes of 31 patients) in this retrospective, observational cohort study. The preoperative and postoperative 3-month refractive and visual outcomes of the two groups were analyzed. RESULTS: In both groups, the uncorrected distance visual acuity was 0.0 logarithm of the minimum angle of resolution or better in 95% of eyes 3 months postoperatively, and the mean manifest refraction spherical equivalent was within ±1.0 diopter in 90% of eyes. No significant differences were observed between the groups in terms of the uncorrected distance visual acuity or astigmatism. A significant induction of higher order aberrations (HOAs) was observed in both groups. However, the induction of total corneal HOAs (p = 0.014) and spherical aberrations (p < 0.001) was significantly lower in the TG group than that in the WFO group. CONCLUSIONS: WFO and TG transPRK effectively improved the visual and refractive outcomes; however, the induction of total corneal HOAs and spherical aberration was lesser following the TG ablation.
Subject(s)
Corneal Topography , Lasers, Excimer , Myopia , Photorefractive Keratectomy , Refraction, Ocular , Visual Acuity , Humans , Retrospective Studies , Photorefractive Keratectomy/methods , Female , Male , Visual Acuity/physiology , Refraction, Ocular/physiology , Adult , Lasers, Excimer/therapeutic use , Myopia/surgery , Myopia/physiopathology , Treatment Outcome , Young Adult , Astigmatism/surgery , Astigmatism/physiopathology , Follow-Up Studies , Corneal Wavefront Aberration/physiopathology , Corneal Wavefront Aberration/diagnosis , Surgery, Computer-Assisted/methodsABSTRACT
Bowtie nano-apertures can confine light into deep subwavelength volumes with extreme field enhancement, making them a useful tool for various applications such as optical trapping, deep subwavelength imaging, nanolithography, and sensors. However, the correlation between the near- and far-field properties of bowtie nano-aperture arrays has yet to be fully explored. In this study, we experimentally investigated the polarization-dependent surface plasmon resonance in bowtie nano-aperture arrays using both optical transmission spectroscopy and photoemission electron microscopy. The experimental results reveal a nonlinear redshift in the transmission spectra as the gap size of the bowtie nanoaperture decreases for vertically polarized light, while the transmission spectra remain unchanged with different gap sizes for horizontally polarized light. To elucidate the underlying mechanisms, we present simulated charge and current distributions, revealing how the electrons respond to light and generate the plasmonic fields. These near-field distributions were verified by photoemission electron microscopy. This study provides a comprehensive understanding of the plasmonic properties of bowtie nano-aperture, enabling their further applications, one of which is the optical switching of the resonance wavelength in the widely used visible spectral region without changing the geometry of the nanostructure.
ABSTRACT
For stable lithium deposition without dendrites, three-dimensional (3D) porous structure has been intensively investigated. Here, we report the use of carbon-doped graphitic carbon nitride (C-doped g-C3N4) microspheres as a 3D host for lithium to suppress dendrite formation, which is crucial for stable lithium deposition. The C-doped g-C3N4microspheres have a high surface area and porosity, allowing for efficient lithium accommodation with high accessibility. The carbon-doping of the g-C3N4microspheres confers lithiophilic properties, which facilitate the regulation of Li+flux and dense filling of cavities with nucleated lithium, thereby preventing volume expansion and promoting dendrite-free Li deposition. The electrochemical performance was improved with cyclic stability and high Coulombic efficiency over 260 cycles at 1.0 mA cm-2for 1.0 mAh cm-2, and even over 70 cycles at 5.0 mA cm-2for 3.0 mAh cm-2. The use of C-doped g-C3N4microspheres as a 3D Li host shows promising results for stable lithium deposition without dendrite formation.
ABSTRACT
Sodium-ion batteries (SIBs) are emerging as power sources for large-scale storage owing to their abundant and inexpensive sodium (Na) source, but their limited energy density hinders their commercialization. High-capacity anode materials, such as antimony (Sb), which are potential energy boosters for SIBs, suffer from battery degradation owing to large-volume-changes and structural instability. The rational design of bulk Sb-based anodes to enhance the initial reversibility and electrode density inevitably requires atomic- and microscale-considered internal/external buffering or passivation layers. However, unsuitable buffer engineering causes electrode degradation and lowers energy density. Herein, the rationally designed intermetallic inner and outer oxide buffers for bulk Sb anodes are reported. The two chemistries in the synthesis process provide an atomic-scale aluminum (Al) buffer within the dense microparticles and an external mechanically stabilizing dual oxide layer. The prepared nonporous bulk Sb anode maintained excellent reversible capacity at a high current density and Na-ion full battery evaluations with Na3V2(PO4)3 (NVP) showing negligible capacity decay over 100 cycles. The demonstrated buffer designs for commercially favorable micro-sized Sb and intermetallic AlSb shed light on the stabilization of high-capacity or large-volume-change electrode materials for various metal-ion rechargeable batteries.
ABSTRACT
Efficient electrochemical hydrogen production and biomass refinery are crucial for the decarbonization of various sectors. However, their energy-intensive nature and low efficiency have hindered their practical application. In this study, earth-abundant and non-toxic photocatalysts that can produce hydrogen and reform biomass efficiently, utilizing unlimited solar energy, are presented. The approach involves using low-bandgap Si flakes (SiF) for efficient light-harvesting, followed by modification with Ni-coordinated N-doped graphene quantum dots (Ni-NGQDs) to enable efficient and stable light-driven biomass reforming and hydrogen production. When using kraft lignin as a model biomass, SiF/Ni-NQGDs facilitate record-high hydrogen productivity at 14.2 mmol gcat -1 h-1 and vanillin yield of 147.1 mg glignin -1 under simulated sunlight without any buffering agent and sacrificial electron donors. SiF/Ni-NQGDs can be readily recycled without any noticeable performance degradation owing to the prevention of deactivation of Si via oxidation. This strategy provides valuable insights into the efficient utilization of solar energy and practical applications of electro-synthesis and biomass refinement.
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Nanoscale optimization of late transition-metal oxides for fixing the reversible lithiation/delithiation mechanism with an in-depth mechanistic understanding of nanocrystal (NC) conversion chemistry is important for furthering next-generation Li-ion battery (LIB) technologies. Herein, 1 nm-thin Ni3CoOx (1 nm-NCO) nanosheets synthesized through isomorphic transformation of NiCo layered double hydroxides within a two-dimensional (2D)-SiO2 envelope are chosen. The interconversion of metal/metal-oxide NCs under redox-switching thermal treatment, while retaining reversibility, inspired the accomplishment of identical consequences under the harsh operational conditions of LIB redox cycles by application of the thin-NCO-defined 2D nanospace. During charge/discharge cycles, 1 nm-NCO covered with an in situ formed solid-electrolyte-interphase layer enables fully reversible interconversion between the reactive NC redox pairs, as evidenced by detailed morphological and electrochemical analyses, thus providing high-rate capability with a specific capacity of 61.2% at 5.0 C relative to 0.2 C, outstanding cycle stability delivering a reversible capacity of 1169 mAh g-1, and 913 mAh g-1 with high average Coulombic efficiency (>99.2%) at 3.0 and 5.0 C for 1000 cycles, respectively, which has not been achieved with other transition-metal oxides. Such a nanospace-confinement effect on sustainability of reactive NCs to follow-up a highly reversible conversion reaction at fast charging in LIBs is operative within a slit-like ultrathin 2D nanogap from 1 nm-NCO only, as a relatively thicker 7 nm-NCO anode, with accompanying larger space available, has evidenced poor reversibility of NCs and inadequate cyclic stability under potential high-power density LIB application.
ABSTRACT
Metal additive manufacturing (AM) is an innovative manufacturing technology that uses a high-power laser for the layer-by-layer production of metal components. Despite many achievements in the field of AM, few studies have focused on the nondestructive characterization of microstructures, such as grain size and porosity. In this study, various microstructures of additively manufactured metal components were characterized non-destructively using linear/nonlinear ultrasonic techniques. The contributions of this study are as follows: (1) presenting correlation analyses of various microstructures (grain size and texture, lack of fusion, and porosity) and ultrasonic properties (ultrasonic velocity, attenuation, and nonlinearity parameters), (2) development of nondestructive microstructural characterization techniques for additively manufactured components; and (3) exploring the potential for the online monitoring of AM processes owing to the nondestructive nature of the proposed technique. The performance of the proposed technique was validated using additively manufactured samples under varying laser beam speed conditions. The characteristics of the target microstructures characterized using the proposed technique were consistent with the results obtained using destructive optical microscopy and electron back-scattered diffraction methods.
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Solanum nigrum, known as black nightshade, is a medicinal plant that contains many beneficial metabolites in its fruit. The molecular mechanisms underlying the synthesis of these metabolites remain uninvestigated due to limited genetic information. Here, we identified 47,470 unigenes of S. nigrum from three different tissues by de novo transcriptome assembly, and 78.4% of these genes were functionally annotated. Moreover, gene ontology (GO) analysis using 18,860 differentially expressed genes (DEGs) revealed tissue-specific gene expression regulation. We compared gene expression patterns between S. nigrum and tomato (S. lycopersicum) in three tissue types. The expression patterns of carotenoid biosynthetic genes were different between the two species. Comparison of the expression patterns of flavonoid biosynthetic genes showed that 9 out of 14 enzyme-coding genes were highly upregulated in the fruit of S. nigrum. Using CRISPR-Cas9-mediated gene editing, we knocked out the R2R3-MYB transcription factor SnAN2 gene, an ortholog of S. lycopersicum ANTHOCYANIN 2. The mutants showed yellow/green fruits, suggesting that SnAN2 plays a major role in anthocyanin synthesis in S. nigrum. This study revealed the connection between gene expression regulation and corresponding phenotypic differences through comparative analysis between two closely related species and provided genetic resources for S. nigrum.
Subject(s)
Solanum lycopersicum , Solanum nigrum , Anthocyanins , Fruit/genetics , Fruit/metabolism , Gene Expression Profiling , Gene Expression Regulation, Plant , Solanum lycopersicum/genetics , Solanum lycopersicum/metabolism , Plant Proteins/genetics , Plant Proteins/metabolism , Solanum nigrum/metabolism , Transcription Factors/metabolism , TranscriptomeABSTRACT
The ability to realize a highly capacitive/conductive electrode is an essential factor in large-scale devices, requiring a high-power/energy density system. Germanium is a feasible candidate as an anode material of lithium-ion batteries to meet the demands. However, the application is constrained due to low charge conductivity and large volume change on cycles. Here, we design a hybrid conductive shell of multi-component titanium oxide on a germanium microstructure. The shell enables facile hybrid ionic/electronic conductivity for swift charge mobility in the germanium anode, revealed through computational calculation and consecutive measurement of electrochemical impedance spectroscopy. Furthermore, a well-constructed electrode features a high initial Coulombic efficiency (90.6%) and stable cycle life for 800 cycles (capacity retention of 90.4%) for a fast-charging system. The stress-resilient properties of dense microparticle facilitate to alleviate structural failure toward high volumetric (up to 1737 W h L-1) and power density (767 W h L-1 at 7280 W L-1) of full cells, paired with highly loaded NCM811 in practical application.
ABSTRACT
Despite its abundance, water is not widely used as a medium for organic reactions. However, under geothermal conditions, water exhibits unique physicochemical properties, such as viscosity and a dielectric constant, and the ionic product become similar to those of common organic solvents. We have synthesized highly crystalline polyimide-based covalent organic frameworks (PICs) under geomimetic hydrothermal conditions. By exploiting triphenylene-2,3,6,7,10,11-hexacarboxylic acid in combination with various aromatic diamines, PICs with various pore dimensions and crystallinities were synthesized. XRD, FT-IR, and DFT calculations revealed that the solubility of the oligomeric intermediates under hydrothermal conditions affected the stacking structures of the crystalline PICs. Furthermore, the synthesized PICs demonstrate promising potential as an anode material in lithium-ion batteries owing to its unique redox-active properties and high surface area.
ABSTRACT
Despite the extremely high energy density of the lithium metal, dendritic lithium growth caused by nonuniform lithium deposition can result in low Coulombic efficiency and safety hazards, thereby inhibiting its practical applications. Here, we report a new strategy for adopting a nanopatterned gold (Au) seed on a copper current collector for uniform lithium deposition. We find that Au nanopatterns enhance lithium metal battery performance, which is strongly affected by the feature dimensions of Au nanopatterns (diameter and height). Ex situ scanning electron microscopy images confirm that this can be attributed to the perfectly selective lithium nucleation and uniform growth resulting from the spatial confinement effect. The spatial arrangement of Au dot seeds homogenizes the Li+ flux and electric field, and the size-controlled Au seeds prevent both seed-/substrate-induced agglomeration and interseed-induced lithium growth, leading to uniform lithium deposition. This dendrite-free lithium deposition results in the improvement of electrochemical performance, and the system showed cyclic stability over 300 cycles at 0.5 mA cm-2 and 200 cycles at 1.0 mA cm-2 (1 mA h cm-2) and a high rate capability. This study provides in-depth insights into the more complicated and diverse seed geometry control of seed materials for the development of high-performance lithium metal batteries.
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A comparative study of doping aliovalent ions, Zr- or Al-, into Ni-rich Li(Ni,Co,Mn)O2 cathode materials is conducted in terms of the electrochemical properties and chemical analysis, especially on the surface region. The solubility and chemical composition for the given sol-gel treatment matches well with the computational results with which the infinitesimal Zr-coating is identified as exhibiting increased charge capacity with prolonged cycle life. Specifically, the whole process can be understood by the suppressed lithium-ion charge transfer resistance (RCT) during the cycles, which can be facilitated by the decreased NiO formation during the cyclic reactions.
ABSTRACT
The incident second harmonic wave is a problematic issue for the precise measurement of the acoustic nonlinearity parameter. This paper proposes a compensation method to remove the effect of the incident second harmonic component in the measurement of the absolute acoustic nonlinearity parameter using the calibration method. For this, the second harmonic component detected by the receiving transducer is considered as the sum of the component due to material nonlinearity and the component included in the incident signal and a numerical calculation model is developed as a function of the propagation distance. In the model, the factors related to the material nonlinear parameter and the magnitude of the incident second harmonic component are unknown and these are determined by finding a value that best matches the experimental data according to the change in the propagation distance; compensation for the incident second harmonic component is then achieved. The case where the phase of the second harmonic wave due to material nonlinearity is opposite to that of the fundamental wave is also considered. To verify the validity of the proposed method, fused silica and aluminum alloy Al6061-T6 specimens with different thicknesses corresponding to the propagation distance are tested. The experimental results show that the nonlinear parameters changed significantly according to the propagation distance before compensation but were very stable after compensation. Additionally, the average values of the nonlinear parameter are 11.04 in the fused silica, which is within the literature value range (10.1 to 12.4), and that for the Al6061-T6 is 6.59, which is close to the literature value range (4.5 to 6.12).
ABSTRACT
When a longitudinal wave passes through a contact interface, second harmonic components are generated due to contact acoustic nonlinearity (CAN). The magnitude of the generated second harmonic is related to the contact state of the interface, of which a model has been developed using linear and nonlinear interfacial stiffness. However, this model has not been sufficiently verified experimentally for the case where the interface has a rough surface. The present study verifies this model through experiments using rough interfaces. To do this, four sets of specimens with different interface roughness values (Ra = 0.179 to 4.524 µm) were tested; one set consists of two Al6061-T6 blocks facing each other. The second harmonic component of the transmitted signal was analyzed while pressing on both sides of the specimen set to change the contact state of the interface. The experimental results showed good agreement with the theoretical prediction on the rough interface. The magnitude of the second harmonic was maximized at a specific contact pressure. As the roughness of the contact surface increased, the second harmonic was maximized at a higher contact pressure. The location of this maximal point was consistent between experiments and theory. In this study, an FEM simulation was conducted in parallel and showed good agreement with the theoretical results. Thus, the developed FEM model allows parametric studies on various states of contact interfaces.
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The relationships between the microstructure and the dielectric properties of sol-gel prepared Y2O3 films with various Gd3+ doping were systematically investigated. Robust solution processed lanthanide films, (Y1-xGdx)2O3 (0 < x ≤ 0.5), are demonstrated as high-k gate insulators for low voltage-driven oxide thin film transistors and their optimized composition is presented. With the proper amount of Gd3+ doping, the corresponding thin film insulators exhibit low leakage current with increased dielectric constant. The resultant Zn-Sn-O/(Y, Gd)2O3 TFT exhibits enhanced performance, by a factor of 10.7 compared with TFTs using a SiO2 insulator, with a field-effect mobility of ~3.15 cm²V-1s-1 and an exceptionally low operating voltage <15 V.
ABSTRACT
The development of highly efficient catalysts in the cathodes of rechargeable Li-O2 batteries is a considerable challenge. Polyelemental catalysts consisting of two or more kinds of hybridized catalysts are particularly interesting because the combination of the electrochemical properties of each catalyst component can significantly facilitate oxygen evolution and oxygen reduction reactions. Despite the recent advances that have been made in this field, the number of elements in the catalysts has been largely limited to two metals. In this study, we demonstrate the electrochemical behavior of Li-O2 batteries containing a wide range of catalytic element combinations. Fourteen different combinations with single, binary, ternary, and quaternary combinations of Pt, Pd, Au, and Ru were prepared on carbon nanofibers (CNFs) via a joule heating route. Importantly, the Li-O2 battery performance could be significantly improved when using a polyelemental catalyst with four elements. The cathode containing quaternary nanoparticles (Pt-Pd-Au-Ru) exhibited a reduced overpotential (0.45 V) and a high discharge capacity based on total cathode weight at 9130 mAh g-1, which was â¼3 times higher than that of the pristine CNF electrode. This superior electrochemical performance is be attributed to an increased catalytic activity associated with an enhanced O2 adsorbability by the quaternary nanoparticles.
ABSTRACT
Solid-state lithium batteries have been intensively studied as part of research activities to develop energy storage systems with high safety and stability characteristics. Despite the advantages of solid-state lithium batteries, their application is currently limited by poor reversible capacity arising from their high resistance. In this study, we significantly improve the reversible capacity of solid-state lithium batteries by lowering the resistance through the introduction of a graphene and wrinkle structure on the surface of the copper (Cu) current collector. This is achieved through a process of chemical vapor deposition (CVD) facilitating graphene-growth synthesis. The modified graphene/wrinkled Cu current collector exhibits a periodic wrinkled pattern 420 nm in width and 22 nm in depth, and we apply it to a graphite composite electrode to obtain an improved areal loading average value of â¼2.5 mg cm-2. The surface-modified Cu current collector is associated with a significant increase in discharge capacity of 347 mAh g-1 at 0.2 C when used with a solid polymer electrolyte. Peel test results show that the observed enhancement is due to the improved strength of adhesion occurring between the graphite composite anode and the Cu current collector, which is attributed to mechanical interlocking. The surface-modified Cu current collector structure effectively reduces resistance by improving adhesion, which subsequently improves the performance of the solid-state lithium batteries. Our study can provide perspective and emphasize the importance of electrode design in achieving enhancements in battery performance.
ABSTRACT
Cesium copper halides (CCHs) show promise for optoelectronic applications, and their syntheses usually involve high-temperatures and hazard solvents. Herein, the synthesis of highly luminescent and phase-pure Cs3Cu2X5 (X = Cl, Br, and I) and CsCu2I3 via a solvent-free mechanochemical approach through manual grinding is demonstrated. This cost-effective approach can produce CCHs on a scale of tens to hundreds of grams. Rietveld refinement analysis of the X-ray diffraction patterns of the as-synthesized CCHs reveals their structural details. Notably, the emission characteristics of green-emitting, chloride-based CCHs remain stable even at elevated temperatures-maintaining 80% of initial PL efficiency at 150 °C. Lastly, a postsynthetic reversible transformation between zero- and one-dimensional CCH materials is demonstrated, indicating the labile nature of their crystal structure. The proposed study suggests that mechanochemistry can be an alternative and promising synthetic tool for fabricating high-quality lead-free metal halides.