Tailoring epitaxial growth and magnetism in La1-xSrxMnO3 / SrTiO3 heterostructures via temperature-driven defect engineering

Among the class of strongly-correlated oxides, La1-xSrxMnO3 $-$ a half metallic ferromagnet with a Curie temperature above room temperature $-$ has sparked a huge interest as a functional building block for memory storage and spintronic applications. In this respect, defect engineering has been in the focus of a long-standing quest for fabricating LSMO thin films with highest quality in terms of both structural and magnetic properties. Here, we discuss the correlation between structural defects, such as oxygen vacancies and impurity islands, and magnetism in La0.74Sr0.26MnO3/SrTiO3 (LSMO/STO) epitaxial heterostructures by systematic control of the growth temperature and post-deposition annealing conditions. Upon increasing the growth temperature within the 500 $-$ 700 $^{\circ}$C range, the epitaxial LSMO films experience a progressive improvement in oxygen stoichiometry, leading to enhanced magnetic characteristics. Concurrently, however, the use of a high growth temperature triggers the diffusion of impurities from the bulk of STO, which cause the creation of off-stoichiometric, dendritic-like SrMoOx islands at the film/substrate interface. As a valuable workaround, post-deposition annealing of the LSMO films grown at a relatively-low temperature of about 500 $^{\circ}$C permits to obtain high-quality epitaxy, atomically-flat surface as well as a sharp magnetic transition above room temperature and robust ferromagnetism. Furthermore, under such optimized fabrication conditions possible scenarios for the formation of the magnetic dead layer as a function of LSMO film thickness are discussed. Our findings offer effective routes to finely tailor the complex interplay between structural and magnetic properties of LSMO thin films via temperature-controlled defect engineering

Nanoarchitectonics of triboelectric nanogenerator for conversion of abundant mechanical energy to green hydrogen

In the present world, the high energy demand rapidly depletes existing fossil fuel reserves, urging the necessity to harvest energy from clean and renewable resources. In this study, the use of a triboelectric nanogenerator (TENG) is shown beyond the conventional practice of use in self-powered electronics, to the production of green hydrogen from renewable mechanical energy. For the first time the use of a magnetic covalent organic framework composite as positive triboelectric material for a contact-separation mode TENG (CS-TENG) in which MXene incorporated polydimethylsiloxane (PDMS) film serves as negative triboelectric material, is demonstrated. A facile way of incorporating micropatterns on the surface of PDMS/MXene film is shown utilizing the advantages of 3D printing technology. The CS-TENG harvests energy from simple mechanical actions such as human handclapping and toe-tapping. The energy from such low-scale mechanical actions is applied for water electrolysis. Scanning electrochemical microscopy is employed to confirm the evolution of hydrogen and oxygen by the harvested electrical energy from mechanical actions. This research is expected to pave the way for producing green hydrogen anywhere, by utilizing the mechanical energy from nature such as raindrops, wind, and the movement of vehicles.Web of Science131

Biosynthesis of ternary NiCoFe2_2O4_4 nanoflowers: investigating their 3D structure and potential use in gene delivery

Multicomponent nanoparticle systems are known for their varied properties and functions, and have shown potential as gene nanocarriers. This study aims to synthesize and characterize ternary nickel–cobalt-ferrite (NiCoFe$_2$O$_4$) nanoparticles with the potential to serve as gene nanocarriers for cancer/gene therapy. The biogenic nanocarriers were prepared using a simple and eco-friendly method following green chemistry principles. The physicochemical properties of the nanoparticles were analyzed by X-ray diffraction, vibrating sample magnetometer, X-ray photoelectron spectroscopy, and Brunauer–Emmett–Teller. To evaluate the morphology of the nanoparticles, the field emission scanning electron microscopy with energy dispersive X-Ray spectroscopy, high-resolution transmission electron microscopy imaging, and electron tomography were conducted. Results indicate the nanoparticles have a nanoflower morphology with a mesoporous nature and a cubic spinel structure, where the rod and spherical nanoparticles became rose-like with a specific orientation. These nanoparticles were found to have minimal toxicity in human embryonic kidney 293 (HEK-293 T) cells at concentrations of 1 to 250 µg·mL–1. We also demonstrated that the nanoparticles could be used as gene nanocarriers for delivering genes to HEK-293 T cells using an external magnetic field, with optimal transfection efficiency achieved at an N/P ratio of 2.5. The study suggests that biogenic multicomponent nanocarriers show potential for safe and efficient gene delivery in cancer/gene therapy

Fracture Resistance of 14Cr ODS Steel Exposed to a High Temperature Gas

This paper studies the impact fracture behavior of the 14%Cr Oxide Dispersion Strengthened (ODS) steel (ODM401) after high temperature exposures in helium and air in comparison to the as-received state. A steel bar was produced by mechanical alloying and hot-extrusion at 1150 °C. Further, it was cut into small specimens, which were consequently exposed to air or 99.9% helium in a furnace at 720 °C for 500 h. Impact energy transition curves are shifted towards higher temperatures after the gas exposures. The transition temperatures of the exposed states significantly increase in comparison to the as-received steel by about 40 °C in He and 60 °C in the air. Differences are discussed in terms of microstructure, surface and subsurface Scanning Electron Microscope (SEM) and Transmission Electron Microscope (TEM) observations. The embrittlement was explained as temperature and environmental effects resulting in a decrease of dislocation level, slight change of the particle composition and interface/grain boundary segregations, which consequently affected the nucleation of voids leading to the ductile fracture

Bismuth Oxychloride Nanoplatelets by Breakdown Anodization

Herein, the synthesis of BiOCl nanoplatelets of various dimensions is demonstrated. These materials were prepared by anodic oxidation of Bi ingots in diluted HCl under dielectric breakdown conditions, triggered by a sufficiently high anodic field. Additionally, it is shown that the use of several other common diluted acids (HNO3, H2SO4, lactic acid) resulted in the formation of various different nanostructures. The addition of NH4F to the acidic electrolytes accelerated the growth rate resulting in bismuth based nanostructures with comparably smaller dimensions and an enormous volume expansion observed during the growth. On the other hand, the addition of lactic acid to the acidic electrolytes decelerated the oxide growth rate. The resulting nanostructures were characterized using SEM, XRD and TEM. BiOCl nanoplatelets received by anodization in 1 M HCl were successfully employed for the photocatalytic decomposition of methylene blue dye and showed a superior performance compared to commercially available BiOCl powder with a similar crystalline structure, confirming its potential as a visible light photocatalyst

2D Germanane-MXene Heterostructures for Cations Intercalation in Energy Storage Applications

Heterostructures offer an exceptional possibility of combining individual 2D materials into a new material having altered properties compared to the parent materials. Germanane (GeH) is a 2D material with many favorable properties for energy storage and catalysis, however, its performance is hindered by its low electrical conductivity. To address the low electrochemical performance of GeH, a heterostructure of GeH and Ti3C2Tx is fabricated. The Ti3C2TX is a layered material belonging to the family of MXenes. The resulting heterostructure (GeMXene) at a defined mass ratio of GeH and Ti3C2Tx shows superior capacitive performance that surpasses that of both pristine materials. The effect of the size of cations and anions for intercalation into GeMXene in different aqueous salt solutions is studied. GeMXene allows only cation intercalation, which is evidenced by the gravimetric electrochemical quartz crystal microbalance (EQCM) technique. The capacitive performance of the GeMXene is compared in neutral, acidic, and alkaline electrolytes to determine the best electrochemical performance. This unleashes the potential use of GeMXene heterostructure in different electrolytes for supercapacitors and batteries. This work will pave the way to explore the heterostructures of other 2D materials such as novel MXenes and functionalized germanane for highly energy-storage efficient systems, and beyond.Web of Science34

ALD growth of MoS2 nanosheets on TiO2 nanotube supports

Two-dimensional MoS2 nanostructures are highly interesting and effective in a number of energy-related applications. In this work, the synthesis of ultra-thin MoS2 nanosheets produced by the thermal Atomic Layer Deposition (ALD) process is reported for the first time using a previously unpublished set of precursors, namely bis(t-butylimido)bis(dimethylamino)molybdenum and hydrogen sulfide. These nanosheets are homogenously deposited within one-dimensional anodic TiO2 nanotube layers that act as a high surface area conductive support for the MoS2 nanosheets. The decoration of high aspect ratio TiO2 nanotube layers with MoS2 nanosheets over the entire nanotube layer thickness is shown for the first time. The homogeneous distribution of the MoS2 nanosheets is proved by STEM/EDX. This resulting new composite is employed as anode for Li-ion microbatteries. The MoS2-decorated TiO2 nanotube layers show a superior performance compared to their counterparts without MoS2. Compared to electrochemical performance of pristine TiO2 nanotube, a more than 50% higher areal capacity and a coulombic efficiency of 98% are obtained on the MoS2 decorated TiO2 nanotube layers, demonstrating clear synergic benefits of the new composite structure

Behavior of W-based materials in hot helium gas

Materials for the plasma facing components of future fusion reactors will be subjected to complex loading and various forms of interaction with low Z species (hydrogen isotopes and helium). The divertor components will be among the most intensely loaded, as they will have to transfer heat loads up to 10–20 MW/m2. Besides the plasma facing surface being irradiated by highly energetic deuterium, tritium and helium particles from the burning plasma, the opposite surface will be exposed to a cooling medium at elevated temperature. Helium- and water-based cooling systems are currently being considered. While tungsten is the prime candidate material for the plasma facing components, in the helium-cooled divertor designs, it is also foreseen as a structural material, together with ferritic–martensitic steels. The behavior of these materials in He atmosphere at elevated temperatures has been little studied thus far, and therefore is the subject of the current work. A number of W-based materials (pure tungsten and some of its alloys) prepared by powder metallurgy techniques was exposed to He atmosphere at 720 C and 500 kPa for 500 h. Morphological surface changes were observed by SEM, chemical and phase composition was analyzed by EDS and XRD, respectively. The internal microstructure was observed by a combination of SEM, FIB and TEM techniques. Mechanical properties were determined by instrumented indentation. Some alloys developed a thin oxide layer, in some cases new morphological features were observed, while some samples remained mostly intact. The observed changes are correlated with specific compositions and microstructures

Atomically sharp domain walls in an antiferromagnet

The interest in understanding scaling limits of magnetic textures such as domain walls spans the entire field of magnetism from its relativistic quantum fundamentals to applications in information technologies. The traditional focus of the field on ferromagnets has recently started to shift towards antiferromagnets which offer a rich materials landscape and utility in ultra-fast and neuromorphic devices insensitive to magnetic field perturbations. Here we report the observation that domain walls in an epitaxial crystal of antiferromagnetic CuMnAs can be atomically sharp. We reveal this ultimate domain wall scaling limit using differential phase contrast imaging within aberrationcorrected scanning transmission electron microscopy, which we complement by X-ray magnetic dichroism microscopy and ab initio calculations. We highlight that the atomically sharp domain walls are outside the remits of established spin-Hamiltonian theories and can offer device functionalities unparalleled in ferromagnets.Comment: 8 pages, 4 figures, Supplementary informatio