Laser-Induced Synthesis of Tin Sulfides.

Various polytypes of van der Waals (vdW) materials can be formed by sulfur and tin, which exhibit distinctive and complementary electronic properties. Hence, these materials are attractive candidates for the design of multifunctional devices. This work demonstrates direct selective growth of tin sulfides by laser irradiation. A 532 nm continuous wave laser is used to synthesize centimeter-scale tin sulfide tracks from single source precursor tin(II) o-ethylxanthate under ambient conditions. Modulation of laser irradiation conditions enables tuning of the dominant phase of tin sulfide as well as SnS2/SnS heterostructures formation. An in-depth investigation of the morphological, structural, and compositional characteristics of the laser-synthesized tin sulfide microstructures is reported. Furthermore, laser-synthesized tin sulfides photodetectors show broad spectral response with relatively high photoresponsivity up to 4 AW-1 and fast switching time (τ rise = 1.8 ms and τ fall = 16 ms). This approach is versatile and can be exploited in various fields such as energy conversion and storage, catalysis, chemical sensors, and optoelectronics.

A Complex Investigation of LATP Ceramic Stability and LATP+PVDF Composite Membrane Performance: The Effect of Solvent in Tape-Casting Fabrication.

Redox flow batteries (RFBs) are a prospective energy storage platform to mitigate the discrepancy between barely adjustable energy production and fluctuating demand. The energy density and affordability of RFBs can be improved significantly through the transition from aqueous systems to non-aqueous (NAq) due to their wider electrochemical stability window and better solubility of active species. However, the NAqRFBs suffer from a lack of effective membranes with high ionic conductivity (IC), selectivity (low permeability), and stability. Here, we for the first time thoroughly analyse the impact of tape-casting solvents (dimethylformamide-DMF; dimethylsulfoxide-DMSO; N-methyl-2-pyrrolidone-NMP) on the properties of the composite Li-conductive membrane (Li1.3Al0.3Ti1.7(PO4)3 filler within poly(vinylidene fluoride) binder-LATP+PVDF). We show that the prolonged exposure of LATP to the studied solvents causes slight morphological, elemental, and intrastructural changes, dropping ceramic's IC from 3.1 to 1.6-1.9 ∙ 10-4 S cm-1. Depending on the solvent, the final composite membranes exhibit IC of 1.1-1.7 ∙ 10-4 S cm-1 (comparable with solvent-treated ceramics) along with correlating permeability coefficients of 2.7-3.1 ∙ 10-7 cm2 min-1. We expect this study to complement the understanding of how the processes underlying the membrane fabrication impact its functional features and to stimulate further in-depth research of NAqRFB membranes.

Thermodynamics as a Driving Factor of LiCoO2 Grain Growth on Nanocrystalline Ta-LLZO Thin Films for All-Solid-State Batteries.

All-solid-state batteries primarily focus on macrocrystalline solid electrolyte/cathode interfaces, and little is explored on the growth and stability of nanograined Li-garnet and cathode ones. In this work, a thin (∼500 nm) film of LiCoO2 (LCO) has been grown on top of the polycrystalline layer of Ta-doped Li7La3Zr2O12 (Ta-LLZO) solid electrolyte using the pulsed laser deposition (PLD) technique. Scanning transmission electron microscopy, electron diffraction, and electron tomography demonstrated that the LCO film is formed by columnar elements with the shape of inverted cones. The film appears to be highly textured, with the (003) LCO crystal planes parallel to the LCO/Ta-LLZO interface and with internal pores shaped by the {104} and {102} planes. According to density functional theory (DFT) calculations, this specific microstructure is governed by a competition between free energies of the corresponding crystal planes, which in turn depends on the oxygen and lithium chemical potentials during the deposition, indicating that thermodynamics plays an important role in the resulting LCO microstructure even under nonequilibrium PLD conditions. Based on the thermodynamic estimates, the experimental conditions within the LCO stability domain are proposed for the preferential {104} LCO orientation, which is considered favorable for enhanced Li diffusion in the positive electrode layers of all-solid-state batteries.

Effect of Graphene Oxide and Nanosilica Modifications on Electrospun Core-Shell PVA-PEG-SiO2@PVA-GO Fiber Mats.

Electrospinning is a well-established method for the fabrication of polymer biomaterials, including those with core-shell nanofibers. The variability of structures presents a great range of opportunities in tissue engineering and drug delivery by incorporating biologically active molecules such as drugs, proteins, and growth factors and subsequent control of their release into the target microenvironment to achieve therapeutic effect. The object of study is non-woven core-shell PVA-PEG-SiO2@PVA-GO fiber mats assembled by the technology of coaxial electrospinning. The task of the core-shell fiber development was set to regulate the degradation process under external factors. The dual structure was modified with silica nanoparticles and graphene oxide to ensure the fiber integrity and stability. The influence of the nano additives and crosslinking conditions for the composite was investigated as a function of fiber diameter, hydrolysis, and mechanical properties. Tensile mechanical tests and water degradation tests were used to reveal the fracture and dissolution behavior of the fiber mats and bundles. The obtained fibers were visualized by confocal fluorescence microscopy to confirm the continuous core-shell structure and encapsulation feasibility for biologically active components, selectively in the fiber core and shell. The results provide a firm basis to draw the conclusion that electrospun core-shell fiber mats have tremendous potential for biomedical applications as drug carriers, photocatalysts, and wound dressings.

Solid-electrolyte interphase nucleation and growth on carbonaceous negative electrodes for Li-ion batteries visualized with in situ atomic force microscopy.

Li-ion battery performance and life cycle strongly depend on a passivation layer called solid-electrolyte interphase (SEI). Its structure and composition are studied in great details, while its formation process remains elusive due to difficulty of in situ measurements of battery electrodes. Here we provide a facile methodology for in situ atomic force microscopy (AFM) measurements of SEI formation on cross-sectioned composite battery electrodes allowing for direct observations of SEI formation on various types of carbonaceous negative electrode materials for Li-ion batteries. Using this approach, we observed SEI nucleation and growth on highly oriented pyrolytic graphite (HOPG), MesoCarbon MicroBeads (MCMB) graphite, and non-graphitizable amorphous carbon (hard carbon). Besides the details of the formation mechanism, the electrical and mechanical properties of the SEI layers were assessed. The comparative observations revealed that the electrode potentials for SEI formation differ depending on the nature of the electrode material, whereas the adhesion of SEI to the electrode surface clearly correlates with the surface roughness of the electrode. Finally, the same approach applied to a positive LiNi1/3Mn1/3Co1/3O2 electrode did not reveal any signature of cathodic SEI thus demonstrating fundamental differences in the stabilization mechanisms of the negative and positive electrodes in Li-ion batteries.

In Situ Formation of Nanoporous Silicon on a Silicon Wafer via the Magnesiothermic Reduction Reaction (MRR) of Diatomaceous Earth.

Successful direct route production of silicon nanostructures from diatomaceous earth (DE) on a single crystalline silicon wafer via the magnesiothermic reduction reaction is reported. The formed porous coating of 6 µm overall thickness contains silicon as the majority phase along with minor traces of Mg, as evident from SEM-EDS and the Focused Ion Beam (FIB) analysis. Raman peaks of silicon at 519 cm-1 and 925 cm-1 were found in both the film and wafer substrate, and significant intensity variation was observed, consistent with the SEM observation of the directly formed silicon nanoflake layer. Microstructural analysis of the flakes reveals the presence of pores and cavities partially retained from the precursor diatomite powder. A considerable reduction in surface reflectivity was observed for the silicon nanoflakes, from 45% for silicon wafer to below 15%. The results open possibilities for producing nanostructured silicon with a vast range of functionalities.