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Antimony (Sb) is considered a promising anode material for sodium-ion batteries due to its high specific capacity and moderate working potential. However, the non-negligible volume variation leads to the rapid decay of capacity, which hinders the practical application of Sb anode materials. Here, an economical and scalable route with high yield is proposed to obtain Sb ultrafine nanocrystals embedded in a porous carbon skeleton. Notably, the synergetic effect of the heterogeneous structure is maximized by inducing the interfacial coupling SbOC and creating buffering space for the volume effect of Sb. The high-entropy phase interface creates the doping site breaking the periodicity of atoms and alters the electronic structure, also bridging the slip of intergranular defects. Thus, the electronic conductivity and phase interface structural stability are reinforced. PIN1 inhibitor API-1 purchase The mechanism of accelerating electron migration at the heterogeneous phase interface is visualized through the density functional theory method, and the mass/charge-transfer kinetics is analyzed via the calculation of surface-induced capacitive contribution.Mechanical deformation-induced strain gradients and coupled spontaneous electric polarization field in centrosymmetric materials, known as the flexoelectric effect, can generate ubiquitous mechanoelectrical functionalities, like the flexo-photovoltaic effect. Concurrently, nano/micrometer-scale inhomogeneous strain reengineers the electronic arrangements and in turn, could alter the fundamental limits of optoelectronic performance. Here, the flexoelectric effect-driven self-powered giant short-wavelength infrared (λ ≤ 1800 nm) photoresponse from centrosymmetric bulk silicon, indeed far beyond the fundamental bandgap (λ = 1100 nm) is demonstrated. Particularly, large on/off ratio (≈105 ), extremely high sensitivity (2.5 × 108 %), good responsivity of 96 mA W-1 , decent specific detectivity of ≈1.54 × 1014 Jones, and a rapid response speed of ≈100 µs, even at nanoscale ( less then 30 nm), are measured at λ = 1620 nm. The infrared response sensitivity is tuned in a wide range (up to 1.4 × 108 %) by controlling the applied pointed force from 1 to 10 µN. These results confirm that emerging mechanoelectrical coupling not only sheds to achieve tunable optoelectronic performance beyond the fundamental limit, but also offers innovative numerous applications like mechanoptical switch, photovoltaic, sensors, and self-driving vehicles.The edge sites of MoS2 are catalytically active for hydrogen evolution reactions (HER). However, pristine edge sites usually contain only intrinsic atoms or defects, limiting the tuning of on-site hydrogen species adsorption and desorption, the critical steps for HER. In addition, the number of atoms on pristine edges is small compared to that of electrochemically inert atoms in bulk. Thus, it is desirable to develop a scalable technique of creating a large number of highly HER-active edge sites. Here, a plasma etching strategy is developed for creating MoS2 edge electrodes with a controllable number of active sites that enable the quantitative characterization of their HER activity using a local probe method. Fluorine atoms with large electronegativity are doped on the MoS2 edge sites that lead to a fivefold activity enhancement compared to that from pristine edges and is attributed to the more moderate binding energy for hydrogen species. The scalability of such a method is further demonstrated by activating MoS2 catalyst in macroscopic quantities with enhanced HER performance and stability. The work provides two-dimensional materials as a platform for understanding the doping effect on the edge sites at atomic-level, and offers a novel route for the design of efficient catalysts.The past year has established the link between the COVID-19 pandemic and the global spread of severe fungal infections; thus, underscoring the critical need for rapid and realizable fungal disease diagnostics. While in recent years, health authorities, such as the Centers for Disease Control and Prevention, have reported the alarming emergence and spread of drug-resistant pathogenic fungi and warned against the devastating consequences, progress in the diagnosis and treatment of fungal infections is limited. Early diagnosis and patient-tailored therapy are established to be key in reducing morbidity and mortality associated with fungal (and cofungal) infections. As such, antifungal susceptibility testing (AFST) is crucial in revealing susceptibility or resistance of these pathogens and initiating correct antifungal therapy. Today, gold standard AFST methods require several days for completion, and thus this much delayed time for answer limits their clinical application. This review focuses on the advancements made in developing novel AFST techniques and discusses their implications in the context of the practiced clinical workflow. The aim of this work is to highlight the advantages and drawbacks of currently available methods and identify the main gaps hindering their progress toward clinical application.The rational design and construction of cost-effective nickel-based phosphide or sulfide (photo)electrocatalysts for hydrogen production from water splitting has sparked a huge investigation surge in recent years. Whereas, nickel phosphides (Nix Py ) possess more than ten stoichiometric compositions with different crystalline. Constructing Nix Py with well crystalline and revealing their intrinsic catalytic mechanism at atomic/molecular levels remains a great challenge. Herein, an easy-to-follow phase-controllable phosphating strategy is first proposed to prepare well crystalline Nix Py (Ni3 P and Ni12 P5 ) modified CdS@Ni3 S2 heterojunction electrocatalysts. It is found that Ni3 P modified CdS@Ni3 S2 (CdS@Ni3 S2 /Ni3 P) exhibits remarkable stability and bifunctional electrocatalytic activities in both hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). Density functional theory results suggest that P-Ni sites and P sites in CdS@Ni3 S2 /Ni3 P, respectively, serve as OER and HER active sites during electrocatalytic water splitting processes. Moreover, benefiting from the advantageous photocatalyst@electrocatalyst core@shell structure, CdS@Ni3 S2 /Ni3 P delivers an advantaged photoassisted electrocatalytic water splitting property. The champion electrical to hydrogen and solar to hydrogen energy conversion efficiencies of CdS@Ni3 S2 /Ni3 P, respectively, reach 93.35% and 4.65%. This work will provide a general guidance for synergistically using solar energy and electric energy for large-scale H2 production from water splitting.2D transition metal dichalcogenides (TMDs) exhibit intriguing properties for applications in optoelectronics and electronics, among which memtransistors received extensive attention as multifunctional devices. For practical applications of 2D TMDs, large-area fabrication of the materials via reliable processes, which is in trade-off with their quality, has been a long-standing issue. Here, a simple and effective way is proposed to fabricate large-area and high-quality molybdenum disulfide thin films using MoS2 colloidal ink through a spray coating, followed by a postsulfurization process. High-quality MoS2 thin films exhibit excellent optical and electrical properties that can be utilized in field-effect transistors (FETs) and memtransistor arrays. The MoS2 FETs show an average on/off ratio of 5 × 106 and a high electron mobility of 10.34 cm2 V-1 s-1 , which can be understood by the healing of sulfur vacancies, recrystallization, and the removal of the carbon contamination of the MoS2 . These MoS2 -based memtransistors present stable operations with a high switching ratio tuned by back gate and light illumination, which is promising for multiple-levels memory and complex neuromorphic computing. This study demonstrates a new strategy to fabricate 2D TMDs with large-area and high quality for integrated optoelectronic and memory device applications.Uncontrollable growth of sodium dendrites during the sodium deposition and stripping processes remains a huge challenge for achieving high-performance sodium metal batteries (SMBs), which results in ineffective utilization of metallic Na, low Coulombic efficiency, and inferior cycling life. Here, a single Co atom uniformly decorated porous nitrogen-doped carbon polyhedron (CoSA @NC) matrix has been fabricated and introduced to control the Na growth and achieve uniform Na nucleation/deposition. Cryo-electron microscopy and in situ optical microscopy techniques have been utilized to analyze the morphology change of metallic Na during plating/stripping processes. The single Co atoms evenly embedded in NC electrodes can provide stable Na-philic sites for Na ions adsorption, which is helpful to guide the uniform sodium deposition and prevent Na dendrites growth. This work thus provides an effective solution to inhibit Na dendrite growth and control Na nucleation behavior from the perspective of atomic level, towards the fabrication of high-safety and long-cycling SMBs.Electrolyzers coupling electrocatalytic hydrogen evolution with oxidation reactions of small organic molecules have the merits of reducing cell voltage and generating high-value products. Herein, an electrolyzer is designed and optimized that can simultaneously achieve efficient hydrogen generation at the cathode, CO2 absorption by the catholyte, and methanol upgrading to formate at the anode. For these purposes, transition metal phosphides are used as the low-cost catalysts. The unique electrolyzer exhibits a low working voltage of 1.1 V at 10 mA cm-2 . Under optimal conditions, the Faraday efficiencies of hydrogen evolution and formic acid conversion reactions, which are the reaction products at the cathode and anode, respectively, are nearly 100% at various current densities from 10 to 400 mA cm-2 . Meanwhile, the CO2 absorption rate is about twice that of the hydrogen generation rate, which is close to the theoretical value. An innovative and energy-efficient strategy is presented in this work to realize simultaneous hydrogen production and CO2 capture based on low-cost catalyst materials.Lignin, one of the renewable constituents in natural plant biomasses, holds great potential as a sustainable source of functional carbon materials. Tremendous research efforts have been made on lignin-derived carbon electrodes for rechargeable batteries. However, lignin is considered as one of the most promising carbon precursors for the development of high-performance, low-cost porous carbon electrode materials for supercapacitor applications. Yet, these efforts have not been reviewed in detail in the current literature. This review, therefore, offers a basis for the utilization of lignin as a pivotal precursor for the synthesis of porous carbons for use in supercapacitor electrode applications. Lignin chemistry, the synthesis process of lignin-derived porous carbons, and future directions for developing better porous carbon electrode materials from lignin are systematically reviewed. Technological hurdles and approaches that should be prioritized in future research are presented.The production of hydrogen via electrochemical water splitting has the potential to enable the utilization of hydrogen-powered fuel cells on a large scale. However, to realize this technology, inexpensive, noble metal-free electrocatalysts possessing high performances for the hydrogen evolution reaction (HER) are needed. Mo2 C nanoparticles recently receive much attention as alternative noble metal-free electrocatalysts because their electronic structures are akin to that of Pt. However, the synthesis of Mo2 C at nanoscale with high catalytic activity for HER remains a great challenge. Moreover, although efforts have been made to prevent their aggregation, the particles coalesce during high temperature carbonization, which is typically used to produce such transition metal carbides. Here, the synthesis of Mo2 C nanodots that are well-dispersed within 3D cage-like carbon microparticles using rationally designed Mo-based xerogels, which are prepared via the sol-gel process as precursors, is reported. During their pyrolysis, the xerogels maintain their structures while the Mo species in them transform into well-dispersed Mo2 C nanodots in situ.