Firmly interlocked Janus-type metallic Ni3Sn2S2-carbon nanotube heterostructure suppresses polysulfide dissolution and Sn aggregation.

Ternary transition-metal tin chalcogenides, with their diverse compositions, abundant constituents, high theoretical capacities, acceptable working potentials, excellent conductivities, and synergistic active/inactive multi-components, hold promise as anode materials for metal-ion batteries. However, abnormal aggregation of Sn nanocrystals and the shuttling of intermediate polysulfides during electrochemical tests detrimentally affect the reversibility of redox reactions and lead to rapid capacity fading within a limited number of cycles. In this study, we present the development of a robust Janus-type metallic Ni3Sn2S2-carbon nanotube (NSSC) heterostructured anode for Li-ion batteries (LIBs). The synergistic effects of Ni3Sn2S2 nanoparticles and a carbon network successfully generate abundant heterointerfaces with steady chemical bridges, thereby enhancing ion and electron transport, preventing the aggregation of Ni and Sn nanoparticles, mitigating the oxidation and shuttling of polysulfides, facilitating the reforming of Ni3Sn2S2 nanocrystals during delithiation, creating a uniform solid-electrolyte interphase (SEI) layer, protecting the mechanical integrity of electrode materials, and ultimately enabling highly reversible lithium storage. Consequently, the NSSC hybrid exhibits an excellent initial Coulombic efficiency (ICE > 83 %) and superb cyclic performance (1218 mAh/g after 500 cycles at 0.2 A/g and 752 mAh/g after 1050 cycles at 1 A/g). This research provides practical solutions for the intrinsic challenges associated with multi-component alloying and conversion-type electrode materials in next-generation metal-ion batteries.

In vitro study of a novel multi-substituted hydroxyapatite nanopowder synthesized by an ultra-fast, efficient and green microwave-assisted method.

In order to improve the biological activity of hydroxyapatite (HA), a multi-substituted HA (SHA) nanopowder with the chemical composition of Ca9.5Mg0.25Sr0.25(PO4)5.5(SiO4)0.5(OH)1.2F0.8 was synthesized using the microwave-assisted method. X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), and transmission electron microscopy (TEM) revealed that all ions were substituted in the HA crystal lattice. The HA and SHA nanoparticles had a semi-spherical morphology with the average size of 90 and 80 nm, respectively. In-vitro bioactivity assessments showed that after the 28-day immersion of the samples in the simulated body fluid, the morphology of the precipitated apatites on the surface of the HA sample still consisted of spherical particles with a cauliflower-like structure. However, in the SHA sample, the morphology of the precipitated apatites was changed to a nanorod-like one similar to the bone-like apatite, which may be attributed the presence of Sr in the precipitated apatites. The results showed that the release of the substituted ions not only had no adverse effect on the cell viability and cell attachment, but also enhanced the alkaline phosphatase activity of MG63 osteoblast like cells in the SHA group, as compared to the HA and control groups. The results indicated that the simultaneous substitution of Si, Mg, Sr, and F in HA nanoparticles could effectively promote bioactivity, cell proliferation and differentiation. This novel HA composition could be, therefore, well used for implant coating, bone tissue engineering and other orthopedic applications.

Exceptionally Reversible Li-/Na-Ion Storage and Ultrastable Solid-Electrolyte Interphase in Layered GeP5 Anode.

In this study, we synthesize two layered and amorphous structures of germanium phosphide (GeP5) and compare their electrochemical performances to better understand the role of layered, crystalline structures and their ability to control large volume expansions. We compare the results obtained with those of previous, conventional viewpoints addressing the effectiveness of amorphous phases in traditional anodes (Si, Ge, and Sn) to hinder electrode pulverization. By means of both comprehensive experimental characterizations and density functional theory calculations, we demonstrate that layered, crystalline GeP5 in a hybrid structure with multiwalled carbon nanotubes exhibits exceptionally good transport of electrons and electrolyte ions and tolerance to extensive volume changes and provides abundant reaction sites relative to an amorphous structure, resulting in a superior solid-electrolyte interphase layer and unprecedented initial Coulombic efficiencies in both Li-ion and Na-ion batteries. Moreover, the hybrid delivers excellent rate-capability (symmetric and asymmetric) performance and remarkable reversible discharge capacities, even at high current rates, realizing ultradurable cycles in both applications. The findings of this investigation are expected to offer insights into the design and application of layered materials in various devices.

Ultra-fast, highly efficient and green synthesis of bioactive forsterite nanopowder via microwave irradiation.

Forsterite (Mg2SiO4) has recently attracted considerable attention in different fields because of its wide range of applications. In this paper, pure forsterite nanopowders were synthesized by an ultra-fast, highly efficient and green method for the first time. Microwave irradiation was used to synthesize forsterite nanopowder. The formation of highly crystalline forsterite nanopowder was confirmed by X-ray diffraction (XRD) and energy dispersive X-ray spectrometer (EDS) analyses. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) analyses showed that the agglomerated powder composed of nanocrystalline particles with the mean particle size of ~100 nm. Microwave irradiation significantly accelerated the rate of the reactions and dramatically decreased reaction times from hours to minutes and seconds. In vitro bioactivity evaluation was performed by soaking the forsterite samples in simulated body fluid (SBF). Results indicated that synthesized forsterite nanopowder via microwave irradiation method possessed excellent apatite-forming ability in SBF. Cell viability results showed that synthesized forsterite nanopowder not only showed no cytotoxicity but also improved cell proliferation. Alkaline phosphatase (ALP) activity assay indicated that the fabricated forsterite nanopowder could facilitate the MG63 osteoblast-like cells to proliferate and differentiate. Therefore, microwave-assisted synthesis technique could be considered as a novel, safe and high efficient method in saving time and energy for bioactive forsterite nanopowder production.

EBSD investigation of Al/(Al13 Fe4 +Al2 O3 ) nanocomposites fabricated by mechanical milling and friction stir processing.

The application of ball-milling for reactant powders (Fe2 O3 +Al) to form in situ nanosized reaction products in the stir zone of 1050 aluminium alloy was examined and the evolution of microstructure, grain boundaries and microtexture of the fabricated Al/(Al13 Fe4 +Al2 O3 ) nanocomposite was investigated. The mean matrix grain size of the fabricated nanocomposites by the combination of ball milling and friction stir processing were found to be ∼3.2, 3.1 and 2.1 µm for 1, 2 and 3 h milled powder mixtures, respectively. The fraction of high-angle grain boundaries increased markedly in the stir zone indicating the occurrence of dynamic restoration of the aluminium matrix. This was also associated with increasing of the fraction of low ∑CSL boundaries. In addition, the fraction of high-angle grain boundaries increased as the reaction product increased. The developed textures were compared with the most important deformation and recrystallisation texture components of cubic close packed structure. Some of the main texture components formed due to the restoration of aluminium in the stir zone of the material with no powder addition were CubeND {001}<310>, BR {236}<385> and R (or retained S{123} <634>); these are usually found in the rolled materials. However, the presence of nanosized reaction products in the fabricated nanocomposite changed the texture components to the dominant Goss {011}<100>, P {011}<122> and R{124}<211> textures.

Nanostructured ß-type titanium alloy fabricated by ultrasonic nanocrystal surface modification.

The surface of ß-type Ti-Nb-Ta-Zr (TNTZ) alloy, which is a promising material for biomedical applications, was treated with the ultrasonic nanocrystal surface modification (UNSM) technique to enhance its hardness. As a result, a gradient nanostructured (GNS) layer was generated in the surface; the microstructure of the top surface layer consisted of nanoscale lamellae with a width of about 60-200nm. In addition, there were lamellar grains consisting of nanostructured subgrains having unclear and wavy boundaries. The treated surface exhibited a hardness value of ∼385HV compared to 190HV for the untreated alloy. It was further determined that highly dense deformation twins were generated at a depth of ∼40-150µm below the UNSM-treated surface. These deformation twins led to a significant work hardening effect which aided in enhancing the mechanical properties. It was also found that UNSM treatment resulted in the formation of micropatterns on the surface, which would be beneficial for high bioactivity and bone regeneration performance of TNTZ implants.