Measuring Optokinetic Reflex and Vestibulo-Ocular Reflex in Unilateral Vestibular Organ Damage Model of Zebrafish.

One-sided vestibular disorders are common in clinical practice; however, their models have not been fully established. We investigated the effect of unilateral or bilateral deficits in the vestibular organs on the vestibulo-ocular reflex (VOR) and optokinetic reflex (OKR) of zebrafish using in-house equipment. For physical dislodgement of the otoliths in the utricles of zebrafish larvae, one or both utricles were separated from the surrounding tissue using glass capillaries. The video data from VOR and OKR tests with the larvae was collected and processed using digital signal processing techniques such as fast Fourier transform and low-pass filters. The results showed that unilateral and bilateral damage to the vestibular system significantly reduced VOR and OKR. In contrast, no significant difference was observed between unilateral and bilateral damage. This study confirmed that VOR and OKR were significantly reduced in zebrafish with unilateral and bilateral vestibular damage. Follow-up studies on unilateral vestibular disorders can be conducted using this tool.

Barocaloric Effects in Dialkylammonium Halide Salts.

Barocaloric effects─solid-state thermal changes induced by the application and removal of hydrostatic pressure─offer the potential for energy-efficient heating and cooling without relying on volatile refrigerants. Here, we report that dialkylammonium halides─organic salts featuring bilayers of alkyl chains templated through hydrogen bonds to halide anions─display large, reversible, and tunable barocaloric effects near ambient temperature. The conformational flexibility and soft nature of the weakly confined hydrocarbons give rise to order-disorder phase transitions in the solid state that are associated with substantial entropy changes (>200 J kg-1 K-1) and high sensitivity to pressure (>24 K kbar-1), the combination of which drives strong barocaloric effects at relatively low pressures. Through high-pressure calorimetry, X-ray diffraction, and Raman spectroscopy, we investigate the structural factors that influence pressure-induced phase transitions of select dialkylammonium halides and evaluate the magnitude and reversibility of their barocaloric effects. Furthermore, we characterize the cyclability of thin-film samples under aggressive conditions (heating rate of 3500 K s-1 and over 11,000 cycles) using nanocalorimetry. Taken together, these results establish dialkylammonium halides as a promising class of pressure-responsive thermal materials.

A Double Open-Shelled Au43 Nanocluster with Increased Catalytic Activity and Stability.

Atomically precise metal nanoclusters (NCs) are an intriguing class of crystalline solids with unique physicochemical properties derived from tunable structures and compositions. Most atomically precise NCs require closed-shells and coordinatively saturated surface metals in order to be stable. Herein, we report Au43(C≡CtBu)20 and Au42Ag1(C≡CtBu)20, which feature open electronic and geometric shells, leading to both paramagnetism (23 valence e-) and enhanced catalytic activity from a single coordinatively unsaturated surface metal. The Au-alkynyl surface motifs of these NCs form five helical stripes around the inner Au12 kernel, imparting chirality and high thermal stability. Density functional theory (DFT) calculations suggest that there are minimal energy differences between the open-shelled NCs and hypothetical closed-shell systems and that the open-shelled electronic configuration gives rise to the largest band gap, which is known to promote cluster stability. Furthermore, we highlight how coordinatively unsaturated surface metals create active sites for the catalytic oxidation of benzyl alcohol to benzaldehyde, leading to high selectivity and increased conversion. This work represents the first example of an atomically precise Au NC with a double open-shelled structure and provides a promising platform for investigating the magnetic and catalytic properties of noble metal nanoparticles.

Liquid and Glass Phases of an Alkylguanidinium Sulfonate Hydrogen-Bonded Organic Framework.

Glassy phases of framework materials feature unique and tunable properties that are advantageous for gas separation membranes, solid electrolytes, and phase-change memory applications. Here, we report a new guanidinium organosulfonate hydrogen-bonded organic framework (HOF) that melts and vitrifies below 100 °C. In this low-temperature regime, non-covalent interactions between guest molecules and the porous framework become a dominant contributor to the overall stability of the structure, resulting in guest-dependent melting, glass, and recrystallization transitions. Through simulations and X-ray scattering, we show that the local structures of the amorphous liquid and glass phases resemble those of the parent crystalline framework.

Silkworm Protein-Derived Nitrogen-Doped Carbon-Coated Li[Ni0.8Co0.15Al0.05]O2 for Lithium-Ion Batteries.

Li[Ni0.8Co0.15Al0.05]O2 (NCA) is a cathode material for lithium-ion batteries and has high power density and capacity. However, this material has disadvantages such as structural instability and short lifespan. To address these issues, herein, we explore the impact of N-doped carbon wrapping on NCA. Sericin, an easily obtained carbon- and nitrogen-rich component of silk cocoons, is utilized as the precursor material. The electrochemical performance evaluation of N-doped carbon-coated NCA shows that the capacity retention of 0.3 NC@NCA at 1C current density is 69.83% after 200 cycles, which is about 19% higher than the 50.65% capacity retention of bare NCA. The results reveal that the sericin-resultant N-doped carbon surface wrapping improves the cycling stability of NC@NCA.

Enhanced NaFe0.5Mn0.5O2/C Nanocomposite as a Cathode for Sodium-Ion Batteries.

Sodium-ion batteries (SIBs) have emerged as an alternative candidate in the field of energy storage applications. To achieve the commercial success of SIBs, the designing of active materials is highly important. O3-type layered-NaFe0.5Mn0.5O2 (NFM) materials provide higher specific capacity along with Earth-abundance and low cost. Nevertheless, the material possesses some disadvantages, such as a low rate capability and severe capacity fading during cycling. To overcome such drawbacks, composite O3-type layered NFM with carbon has been prepared for the cathode electrode of SIBs through a facile solution combustion method followed by calcination process. The introduction of carbon sources into NFM material provides excellent electrochemical performances; moreover, the practical limitations of NFM material such as low electrical conductivity, structural degradation, and cycle life are effectively controlled by introducing carbon sources into the host material. The NFM/C-2 material delivers the specific charge capacities of 171, 178, and 166 mA h g-1; and specific discharge capacities of 188, 169, and 162 mA h g-1, in the first 3 cycles, respectively.

Influence of R=Y, Gd, Sm on Crystallization and Sodium Ion Conductivity of Na5RSi4O12 Phase.

New sodium-based battery concepts require solid electrolytes as ion conducting separators. Besides NaSICON and ß-Al2O3 in the Na2O-R2O3-SiO2 system (R = rare earth), a rarely noticed glass-ceramic solid electrolyte with the composition Na5RSi4O12 (N5-type) exists. The present study addresses the investigation of the ionic conductivity of Na5RSi4O12 solid electrolytes sintered from pre-crystallized glass-ceramic powders. The sintering behavior (optical dilatometry), the microstructure (SEM/EDX), and phase composition (XRD), as well as electrochemical properties (impedance spectroscopy), were investigated. To evaluate the effect of the ionic radii, Y, Sm and Gd rare elements were chosen. All compositions were successfully synthesized to fully densified compacts having the corresponding conducting N5-type phase as the main component. The densification behavior was in agreement with the melting point, which decreased with increasing ionic radii and specific cell volume. Alternatively, the ionic conductivities of N5-phases decreased from Y to Gd and Sm containing samples. The highest ionic conductivity of 1.82 × 10-3 S cm-1 at 20 °C was obtained for Na5YSi4O12 composition. The impact of grain boundaries and bulk conductivity on measured values is discussed. A powder-based synthesis method of this glass-ceramic solid electrolyte using different rare earth elements opens possibilities for optimizing ionic conductivity and scalable technological processing by tape casting.

Thermally assisted conversion of biowaste into environment-friendly energy storage materials for lithium-ion batteries.

This study reports the thermally assisted solid-state synthesis of a cathode comprising a biowaste-derived nitrogen-doped carbon coating on LiFePO4 (LFP) for Li-ion batteries. The eggshell membrane (ESM), which mainly consists of collagen, is converted into nitrogen-doped carbon with good ionic and electrical conductivity during thermally driven decomposition. The ESM-coated LFP (ESM@LFP) containing pyrrolic nitrogen, pyridinic nitrogen, and oxidized pyridinic nitrogen has been motivated to improve its ionic and electrical conductivity, that promotes the movement of Li-ions and electrons on the LFP surface. ESM@LFP exhibits stable cyclability and ~16.3% of increased specific discharge capacity for 100 cycles at a current rate of 1C compared to bare LFP.

Surface modification of Ni-rich LiNi0.8Co0.1Mn0.1O2 with perovskite LaFeO3 for high voltage cathode materials.

Ni-rich LiNi0.8Co0.1Mn0.1O2 (NCM811) is regarded as a potential cathode material due to its higher capacity. However, the severe capacity fading which occurs above 4.2 V vs. Li/Li+ needs to be addressed to enhance the electrochemical performance. Herein, we report the surface modification of NCM811 cathodes with a perovskite material, i.e., lanthanum iron oxide (LaFeO3), which has drawn attention for various research areas due to its non-toxicity, electric conductivity, chemical stability, and low cost and systematically investigate the influence of the LaFeO3 coating on NCM811. The LaFeO3 coating layer significantly protects the cathode material from corrosion due to the HF formation and restrains the dissolution of other ions into liquid electrolyte during high voltage charge-discharge processes. Even after 80 cycles, 0.5 wt% LaFeO3-coated NCM811 cathode material shows about 13% higher cycling stability when compared to the bare NCM811 and other ratios of coated materials. Furthermore, the 0.5 wt% LaFeO3-coated NCM811 delivers excellent rate capability and demonstrates improved structural stability at 4.6 V vs. Li/Li+ under high voltage conditions with Ni-rich cathode active materials.

Vehicular Localization Enhancement via Consensus.

This paper presents a strategy to cooperatively enhance the vehicular localization in vehicle-to-everything (V2X) networks by exchanges and updates of local data in a consensus-based manner. Where each vehicle in the network can obtain its location estimate despite its possible inaccuracy, the proposed strategy takes advantage of the abundance of the local estimates to improve the overall accuracy. During the execution of the strategy, vehicles exchange each other's inter-vehicular relationship pertaining to measured distances and angles in order to update their own estimates. The iteration of the update rules leads to averaging out the measurement errors within the network, resulting in all vehicles' localization error to retain similar magnitudes and orientations with respect to the ground truth locations. Furthermore, the estimate error of the anchor-the vehicle with the most reliable localization performance-is temporarily aggravated through the iteration. Such circumstances are exploited to simultaneously counteract the estimate errors and effectively improve the localization performance. Simulated experiments are conducted in order to observe the nature and its effects of the operations. The outcomes of the experiments and analysis of the protocol suggest that the presented technique successfully enhances the localization performances, while making additional insights regarding performance according to environmental changes and different implementation techniques.

Juglone Suppresses LPS-induced Inflammatory Responses and NLRP3 Activation in Macrophages.

The NLRP3 (NACHT, LRR and PYD domains-containing protein 3) inflammasome has been implicated in a variety of diseases, including atherosclerosis, neurodegenerative diseases, and infectious diseases. Thus, inhibitors of NLRP3 inflammasome have emerged as promising approaches to treat inflammation-related diseases. The aim of this study was to explore the effects of juglone (5-hydroxyl-1,4-naphthoquinone) on NLRP3 inflammasome activation. The inhibitory effects of juglone on nitric oxide (NO) production were assessed in lipopolysaccharide (LPS)-stimulated J774.1 cells by Griess assay, while its effects on reactive oxygen species (ROS) and NLRP3 ATPase activity were assessed. The expression levels of NLRP3, caspase-1, and pro-inflammatory cytokines (IL-1ß, IL-18) and cytotoxicity of juglone in J774.1 cells were also determined. Juglone was non-toxic in J774.1 cells when used at 10 µM (p < 0.01). Juglone treatment inhibited the production of ROS and NO. The levels of NLRP3 and cleaved caspase-1, as well as the secretion of IL-1ß and IL-18, were decreased by treatment with juglone in a concentration-dependent manner. Juglone also inhibited the ATPase activities of NLRP3 in LPS/ATP-stimulated J774.1 macrophages. Our results suggested that juglone could inhibit inflammatory cytokine production and NLRP3 inflammasome activation in macrophages, and should be considered as a therapeutic strategy for inflammation-related diseases.

Relation between work function and structural properties of triangular defects in 4H-SiC epitaxial layer: Kelvin probe force microscopic and spectroscopic analyses.

To understand the relationship between the work function and structural properties of sufficiently expanded triangular defects (size: ∼250 µm) in the 4H-SiC epitaxial layer, Kelvin probe force microscopy (KPFM) and spectroscopic [micro-Raman spectroscopy and photoluminescence (PL)] analyses were performed. Spectroscopic analysis demonstrated that the triangular defects mostly comprise the 3C polytypes and that it experiences internal stress, defects, and defect-induced carrier generation. The distinguishable areas in the triangular defects had surface potential values different from those of the 4H-SiC matrix; this could be explained by the work function difference, which arises from variations in the electron affinity of the 3C polytype as well as the positional variations of the Fermi energy level in terms of electron concentration. In addition, tensile-stress-induced surface disorder leading to variations in electron affinity was discussed. The mechanical properties of the triangular defects measured by a nanoindenter were significantly deteriorated because of many dislocation arrays and stacking faults with many broken and/or strained bonds.

A Distributed Cooperative Localization Strategy in Vehicular-to-Vehicular Networks.

This work develops a distributed message-passing approach to cooperative localization for autonomous mobile vehicles that communicate via mm-wave wireless connection in vehicle-to-vehicle networks. Vehicles in the network obtain the measurement information about the relative distance and the angle of arrival from the mm-wave connections made with each other. Some vehicles may obtain knowledge about their absolute position information of different quality, for example, via additional localization feature. The main objective is to estimate the locations of all vehicles using reciprocal exchanges of simple information called a message in a distributed and autonomous way. A simulation is developed to examine the performance of the localization and navigation of vehicles under various network configurations. The results show that it does provide better positioning results in most cases and there are also several cases where the use of the cooperative technique adapts to design parameters such as accuracies of measurement equipment, and initial position estimates, that can affect the localization performance.

Extratympanic Observation of Middle and Inner Ear Structures in Rodents Using Optical Coherence Tomography.

OBJECTIVES: This study aimed to investigate whether optical coherence tomography (OCT) provides useful information about the microstructures of the middle and inner ear via extratympanic approach and thereby could be utilized as an alternative diagnostic technology in ear imaging. METHODS: Five rats and mice were included, and the swept-source OCT system was applied to confirm the extent of visibility of the middle and inner ear and measure the length or thickness of the microstructures in the ear. The cochlea was subsequently dissected following OCT and histologically evaluated to compare with the OCT images. RESULTS: The middle ear microstructures such as ossicles, stapedial artery and oval window through the tympanic membrane with the OCT could be confirmed in both rats and mice. It was also possible to obtain the inner ear images such as each compartment of the cochlea in the mice, but the bone covering bulla needed to be removed to visualize the inner ear structures in the rats which had thicker bulla. The bony thickness covering the cochlea could be measured, which showed no significant differences between OCT and histologic image at all turns of cochlea. CONCLUSION: OCT has been shown a promising technology to assess real-time middle and inner ear microstructures noninvasively with a high-resolution in the animal model. Therefore, OCT could be utilized to provide additional diagnostic information about the diseases of the middle and inner ear.

The Mechanism of Copper-Catalyzed Trifunctionalization of Terminal Allenes.

A highly selective copper-catalyzed trifunctionalization of allenes has been established based on diborylation/cyanation with bis(pinacolato)diboron (B2 pin2 ) and N-cyano-N-phenyl-p-toluenesulfonamide (NCTS). The Cu-catalyzed trifunctionalization of terminal allenes is composed of three catalytic reactions (first borocupration, electrophilic cyanation, and second borocupration) that provide a densely functionalized product with regio-, chemo- and diastereoselectivity. Allene substrates have multiple reaction-sites, and the selectivities are determined by the suitable interactions (e.g., electronic and steric demands) between the catalyst and substrates. We employed DFT calculations to understand the cascade copper-catalyzed trifunctionalization of terminal allenes, providing densely-functionalized organic molecules with outstanding regio-, chemo- and diastereoselectivity in high yields. The selectivity challenges presented by cumulated π-systems are addressed by systematic computational studies; these give insight to the catalytic multiple-functionalization strategies and explain the high selectivities that we see for these reactions.

A pilot study using machine learning methods about factors influencing prognosis of dental implants.

PURPOSE: This study tried to find the most significant factors predicting implant prognosis using machine learning methods. MATERIALS AND METHODS: The data used in this study was based on a systematic search of chart files at Seoul National University Bundang Hospital for one year. In this period, oral and maxillofacial surgeons inserted 667 implants in 198 patients after consultation with a prosthodontist. The traditional statistical methods were inappropriate in this study, which analyzed the data of a small sample size to find a factor affecting the prognosis. The machine learning methods were used in this study, since these methods have analyzing power for a small sample size and are able to find a new factor that has been unknown to have an effect on the result. A decision tree model and a support vector machine were used for the analysis. RESULTS: The results identified mesio-distal position of the inserted implant as the most significant factor determining its prognosis. Both of the machine learning methods, the decision tree model and support vector machine, yielded the similar results. CONCLUSION: Dental clinicians should be careful in locating implants in the patient's mouths, especially mesio-distally, to minimize the negative complications against implant survival.

Activation of the Basal Plane in Two Dimensional Transition Metal Chalcogenide Nanostructures.

Achieving a molecular level understanding of chemical reactions on the surface of solid-state nanomaterials is important, but challenging. For example, the fully saturated basal plane is believed to be practically inert and its surface chemistry has been poorly explored, while two-dimensional (2D) layered transition-metal chalcogenides (TMCs) display unique reactivities due to their unusual anisotropic nature, where the edges consisting of unsaturated metals and chalcogens are sites for key chemical reactions. Herein, we report the use of Lewis acids/bases to elucidate the chemical reactivity of the basal plane in 2D layered TMCs. Electrophilic addition by Lewis acids (i.e., AlCl3) selectively onto sulfides in the basal plane followed by transmetalation and subsequent etching affords nanopores where such chemical activations are initiated and propagated from the localized positions of the basal plane. This new method of surface modification is generally applicable not only to various chemical compositions of TMCs, but also in crystal geometries such as 1T and 2H. Nanoporous NbS2 obtained by this method was found to have an enhanced electrochemical energy storage capacity, offering this chemical strategy to obtain functional 2D layered nanostructures.

Preparation of Ultrasensitive Humidity-Sensing Films by Aerosol Deposition.

Aerosol deposition (AD) is a novel ceramic film preparation technique exhibiting the advantages of room-temperature operation and highly efficient film growth. Despite these advantages, AD has not been used for preparing humidity-sensing films. Herein, room-temperature AD was utilized to deposit BaTiO3 films on a glass substrate with a Pt interdigital capacitor, and their humidity-sensing performances were evaluated in detail, with further optimization performed by postannealing at temperatures of 100, 200, ..., 600 °C. Sensor responses (i.e., capacitance variations) were measured in a humidity chamber for relative humidities (RHs) of 20-90%, with the best sensitivity (461.02) and a balanced performance at both low and high RHs observed for the chip annealed at 500 °C. In addition, its response and recovery were extremely fast, respectively, at 3 and 6 s and it kept a stable recording with the maximum error rate of 0.1% over a 120 h aging test. Compared with other BaTiO3-based humidity sensors, the above chip required less thermal energy for its preparation but featured a more than 2-fold higher sensitivity and a superior detection balance at RHs of 20-90%. Cross-sectional transmission electron microscopy imaging revealed that the prepared film featured a transitional variable-density structure, with moisture absorption and desorption being promoted by a specific capillary structure. Finally, a bilayer physical model was developed to explain the mechanism of enhanced humidity sensitivity by the prepared BaTiO3 film.

3,5-Diarylimidazo[1,2-a]pyridines as Color-Tunable Fluorophores.

A new protocol for the synthesis of color-tunable fluorescent 3,5-diarylimidazo[1,2-a]pyridines has been achieved via palladium-catalyzed C-H amination of pyridinium zwitterions. Based on experimental results and computational analysis, we extracted a high correlation of photophysical properties with the theoretical concept and predicted emission wavelengths of 3,5-diarylimidazo[1,2-a]pyridines. The emission wavelengths of imidazo[1,2-a]pyridines increase as a function of the electron-withdrawing nature of the substituent on the C5-aryl group of imidazo[1,2-a]pyridine as a result of inductive effects on the LUMO levels. Varying the substituent on the C3-aryl group imidazo[1,2-a]pyridine changes the HOMO levels. Combining these two sites, the HOMO and LUMO levels can be tuned fairly decoupled from each other. This conceptual trend is demonstrated across a series where the C3 and C5 positions were functionalized independently and then utilizes a combination strategy where both sites are used to prepare fluorophores with a large window of emission wavelengths. In view of the biological properties of imidazo[1,2-a]pyridines, the developed method provides an efficient approach for understanding and preparing strongly fluorescent bioprobes.

Posterior Trans-Dural Repair of Iatrogenic Spinal Cord Herniation after Resection of Ossification of Posterior Longitudinal Ligament.

Iatrogenic spinal cord herniation is a rare complication following spinal surgery. We introduce a posterior trans-dural repair technique used in a case of thoracic spinal cord herniation through a ventral dural defect following resection of ossification of the posterior longitudinal ligament (OPLL) in the cervicothoracic spine. A 51-year-old female was suffering from paraplegia after laminectomy alone for cervicothoracic OPLL. Magnetic resonance imaging revealed a severely compressed spinal cord with pseudomeningocele identified postoperatively. Cerebrospinal fluid leak and iatrogenic spinal cord herniation persisted despite several operations with duroplasty and sealing agent. Finally, the problems were treated by repair of the ventral dural defect with posterior trans-dural duroplasty. Several months after surgery, the patient could walk independently. This surgical technique can be applied to treat ventral dural defect and spinal cord herniation.