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Solution-processed metal oxide (MO) thin films have been extensively studied for use in thin-film transistors (TFTs) due to their high optical transparency, simplicity of fabrication methods, and high electron mobility. Here, we report, for the first time, the improvement of the electronic properties of solution-processed indium oxide (InOx) films by the subsequent addition of an organic p-type semiconductor material, here 6,13-bis(triisopropylsilylethynyl)pentacene (TIPS-pentacene), yielding organic-inorganic hybrid TFTs. The addition of TIPS-pentacene not only improves the electron mobility by enhancing the charge carrier percolation pathways but also improves the electronic and temporal stability of the IDS(VG) characteristics as well as reduces the number of required spin-coating steps of the InOx precursor solution. Very interestingly, the introduction of 10 nm TIPS-pentacene films on top of 15 nm InOx layers allows the fabrication of either enhancement- or depletion-mode devices with only minimal changes to the fabrication process. Specifically, we find that when the TIPS-pentacene layer is added on top of the source/drain electrodes, resulting in devices with embedded source/drain electrodes [embedded electrode TFTs (EETFTs)], the devices exhibit an enhancement-mode behavior with an average mobility (μ) of 6.4 cm2 V-1 s-1, a source-drain current ratio (Ion/Ioff) of around 105, and a near-zero threshold voltage (VTH). When on the other hand the TIPS-pentacene layer is added before the source-drain electrodes, i.e., in top-contact electrode TFTs (TCETFTs), a very clear depletion mode behavior is observed with an average μ of 6.3 cm2 V-1 s-1, an Ion/Ioff ratio of over 105, and a VTH of -80.3 V. Furthermore, a logic inverter is fabricated combining the enhancement (EETFTs)- and depletion (TCETFTs)-mode transistors, which shows a potential for the construction of organic-inorganic hybrid electronics and circuits.

We demonstrate the selective detection of hydrogen sulfide at breath concentration levels under humid airflow, using a self-validating 64-channel sensor array based on semiconducting single-walled carbon nanotubes (sc-SWCNTs). The reproducible sensor fabrication process is based on a multiplexed and controlled dielectrophoretic deposition of sc-SWCNTs. The sensing area is functionalized with gold nanoparticles to address the detection at room temperature by exploiting the affinity between gold and sulfur atoms of the gas. Sensing devices functionalized with an optimized distribution of nanoparticles show a sensitivity of 0.122%/part per billion (ppb) and a calculated limit of detection (LOD) of 3 ppb. Beyond the self-validation, our sensors show increased stability and higher response levels compared to some commercially available electrochemical sensors. The cross-sensitivity to breath gases NH3 and NO is addressed demonstrating the high selectivity to H2S. Finally, mathematical models of sensors’ electrical characteristics and sensing responses are developed to enhance the differentiation capabilities of the platform to be used in breath analysis applications. Electronic Supplementary Material Supplementary material (details on the dielectrophoretic deposition, AuNP functionalization optimization, full range of experimental and model H2S sensing response up to 820 ppb, and sensing response to NO gas) is available in the online version of this article at 10.1007/s12274-021-3771-7.

Low-dimensional Ge is perceived as a promising building block for emerging optoelectronic devices. Here, we present a wafer-scale platform technology enabling monolithic Al-Ge-Al nanostructures fabricated by a thermally induced Al-Ge exchange reaction. Transmission electron microscopy confirmed the purity and crystallinity of the formed Al segments with an abrupt interface to the remaining Ge segment. In good agreement with the theoretical value of bulk Al-Ge Schottky junctions, a barrier height of 200 ± 20 meV was determined. Photoluminescence and μ-Raman measurements proved the optical quality of the Ge channel embedded in the monolithic Al-Ge-Al heterostructure. Together with the wafer-scale accessibility, the proposed fabrication scheme may give rise to the development of key components of a broad spectrum of emerging Ge-based devices requiring monolithic metal-semiconductor-metal heterostructures with high-quality interfaces.

The isolation of 2D nanosheets of layered metal–organic frameworks (MOFs) has become an active research field due to the various advantages resulting from shape anisotropy. The most sophisticated method to obtain the nanostructures of interest is the top-down approach using an external physical energy input, such as ultrasound. In the present work, we rationalize the choice of solvent most suitable for the delamination of the bulk crystals of paddle wheel-based layered MOF [Cu2(dttc)2]n (DUT-134(Cu); dttc: dithieno[3,2-b:2′,3′-d]thiophene-2,6-dicarboxylate) as a model system, containing a bent organic linker. The ideal delamination solvent can tear the layers apart and prevent the agglomeration of nanosheets in suspension. The impact of different guest molecules, such as alcohols and ketones on the MOF structure, was studied by analyzing the single-crystal structures of the respective compounds and the behavior of desolvated MOF upon the physisorption of corresponding guests. In situ experiments facilitated the understanding of the adsorption process and structural transition in this layered structure. The most suitable solvents to delaminate DUT-134(Cu) turned out to be ketones, particularly acetone and butanone, giving a stable suspension of ∼10 nm-thick nanosheets.

Transition metal chalcogenides such as CoS

The present work focuses on energy neutral, bias free, scalable galvanic synthesis of highly crystalline thin films of BiOI on a fluorine doped tin oxide (FTO) electrode (BiOI/FTO). Electrodes as d...

Thermal evaporation is a well-established and versatile method for the deposition of large-area, uniform, high-quality semiconducting layers in a broad range of optoelectronic applications. Despite extensive investigation of deposition by thermal evaporation in the field of perovskite solar cells, solution-processed perovskite devices still significantly outperform those fabricated by thermal evaporation, particularly in the case of methylammonium-free perovskite compositions. Herein, we fabricate and investigate thermally evaporated Cs0.1FAxPbI2+xBr0.1 perovskite solar cells and explore the effects of FAI deficiency or excess and that of post-annealing on the perovskite layer properties and device performance. We find that annealing can significantly improve the optical and structural properties of FAI-poor perovskite layers, resulting in a stark enhancement of their photovoltaic performance. While stoichiometric devices are also improved, albeit to a lesser degree, by post-annealing, this process is found to be detrimental for the FAI-rich devices, resulting in a drastic loss of performance. We show that annealed stoichiometric devices with an optimised active layer thickness result in power conversion efficiencies of up to 16.6%, approaching the performance of solution-processed devices of similar composition.

The topological Hall effect (THE), induced by the Berry curvature that originates from non-zero scalar spin chirality, is an important feature for mesoscopic topological structures, such as skyrmions. However, the THE might also arise from other microscopic non-coplanar spin structures in the lattice. Thus, the origin of the THE inevitably needs to be determined to fully understand skyrmions and find new host materials. Here, we examine the Hall effect in both, bulk- and micron-sized lamellar samples of MnBi. The sample size affects the temperature and field range in which the THE is detectable. Although a bulk sample exhibits the THE only upon exposure to weak fields in the easy-cone state, in micron-sized lamella the THE exists across a wide temperature range and occurs at fields near saturation. Our results show that both the non-coplanar spin structure in the lattice and topologically non-trivial skyrmion bubbles are responsible for the THE, and that the dominant mechanism depends on the sample size. Hence, the magnetic phase diagram for MnBi is size-dependent. Our study provides an example in which the THE is simultaneously induced by two mechanisms, and builds a bridge between mesoscopic and microscopic magnetic structures. © 2022. This work was financially supported by an Advanced Grant from the European Research Council (No. 742068 ) “TOPMAT,” the European Union's Horizon 2020 research and innovation programme (No. 824123 ) “SKYTOP,” the European Union's Horizon 2020 research and innovation programme (No. 766566 ) “ASPIN,” the Deutsche Forschungsgemeinschaft (Project-ID 258499086) “SFB 1143,” the Deutsche Forschungsgemeinschaft (Project-IDs FE 633/30-1, RE 1164/6-1 and LU 2261/2-1) “SPP Skyrmionics,” the DFG through the Würzburg-Dresden Cluster of Excellence on Complexity and Topology in Quantum Matter ct.qmat (EXC 2147, Project-ID 39085490). I.S. is grateful to Deutsche Forschungsgemeinschaft for supporting this work through project SO 1623/2-1. D.W. has received funding from the European Research Council (ERC) under the Horizon 2020 research and innovation program of the European Union (grant agreement number 715620 ).

The perovskite solar era has demonstrated 25.5% efficiency in only 10 years of research, reaching the performance levels of other photovoltaics technologies such as Si and GaAs, showing potentially low-cost manufacturing and process versatility. However, these results are achieved only on small area cells, with an active area equal or lower to 0.1 cm(2). The upscaling development of perovskite solar technology requires the use of additional processes to reduce losses encountered for large areas; for this reason, laser processing becomes necessary to design connected cells into modules. In this work, cell-to-module losses in perovskite solar modules are reduced by optimizing the laser design, establishing a relationship between geometrical fill factor, cell area width, and P1-P2-P3 laser parameters. Upscaling the process from 2.5 x 2.5 to 10 x 10 cm(2) an efficiency of 18.71% and 17.79% is achieved on active area of 2.25 and 48 cm(2) respectively, with only 5% relative losses when scaling from to minimodule to module size. A minipanel is fabricated on 20 x 20 cm(2), showing 11.9% stabilized efficiency and 2.3 W on an active area of 192 cm(2), among the highest reported in literature so far at this size.

The surface spin flop, observed in synthetic antiferromagnets (SAFs) with uniaxial anisotropy and strong antiferromagnetic (AF) interlayer exchange coupling, can be considered as a laterally homogeneous, vertical AF domain wall pushed into the SAF from either the top or the bottom in the presence of a strong external vertical magnetic field. As a result, the AF domain wall can be described as a one-dimensional entity. In this work, we present a concept to stabilize laterally homogeneous vertical AF domain walls by local variation of the perpendicular magnetic anisotropy in $\mathrm{Co}/\mathrm{Pt}$-based SAFs. Our approach not only allows the stabilization of the vertical AF domain wall in the absence of any external magnetic field, but furthermore enables a deterministic selection among four different remanent states, each one stable within a broad external magnetic field range of almost one tesla. We also demonstrate an extension to our concept by stabilizing two coexisting vertical AF domain walls, thus yielding a system with a total of six different selectable (and reprogrammable) remanent states. The controlled stabilization of noncollinear AF textures in the form of vertical AF domain walls at remanence could be used as an infrastructure for propagating spin waves within the AF domain wall itself, as well as for tuning the dynamic behavior of perpendicular standing spin wave modes existing vertically across the SAF.

The spin Hall effect in a heavy metal thin film allows to probe the magnetic properties of an adjacent magnetic insulator via magnetotransport measurements. Here, we investigate the magnetoresistive response of yttrium iron garnet/platinum heterostructures from room temperature to beyond the Curie temperature $T_\mathrm{C, YIG} \approx 560\,\mathrm{K}$ of the ferrimagnetic insulator. We find that the amplitude of the (local) spin Hall magnetoresistance decreases monotonically from $300\,\mathrm{K}$ towards $T_\mathrm{C}$, mimicking the evolution of the saturation magnetization of yttrium iron garnet. Interestingly, the spin Hall magnetoresistance vanishes around $500\,\mathrm{K}$, well below $T_\mathrm{C}$, which we attribute to the formation of a parasitic interface layer by interdiffusion. Around room temperature the non-local magnon-mediated magnetoresistance exhibits a power law scaling $T^{\alpha}$ with $\alpha = 3/2$, as already reported. The exponent decreases gradually to $\alpha \sim 1/2$ at around $420\,\mathrm{K}$, before the non-local magnetoresistance vanishes rapidly at a similar temperature as the spin Hall magnetoresistance. We attribute the reduced $\alpha$ at high temperatures to the increasing thermal magnon population which leads to enhanced scattering of the non-equilibrium magnon population and a reduced magnon diffusion length. Finally, we find a magnetic field independent offset voltage in the non-local signal for $T > 470\,\mathrm{K}$ which we associate with electronic leakage currents through the normally insulating yttrium iron garnet film. Indeed, this non-local offset voltage is thermally activated with an energy close to the band gap., Comment: 7 pages, 4 figures

Fine-tuning chemistry by doping with transition metals enables new perspectives for exploring Kitaev physics on a two-dimensional (2D) honeycomb lattice of α-RuCl3, which is promising in the field of quantum information protection and quantum computation. The key parameters to vary by doping are both Heisenberg and Kitaev components of the nearest-neighbor exchange interaction between the Jeff = 1/2 Ru3+ spins, depending strongly on the peculiarities of the crystal structure. Here, we present crystal growth by chemical vapor transport and structure elucidation of a solid solution series Ru1- xCr xCl3 (0 ≤ x ≤ 1), with Cr3+ ions coupled to the Ru3+ Kitaev host. The Cr3+ substitution preserves the honeycomb type lattice of α-RuCl3 and creates mixed occupancy of Ru/Cr sites without cationic order within the layers as confirmed by single-crystal X-ray diffraction and transmission electron microscopy investigations. In contrast to high-quality single crystals of α-RuCl3 with ABAB-stacked layers, the ternary compounds demonstrate a significant stacking disorder along the c-axis direction as evidenced by X-ray diffraction and high resolution scanning transmission electron microscopy (HR-STEM). Raman spectra of substituted samples are in line with the symmetry conservation of the parent lattice upon chromium doping. At the same time, our magnetic susceptibility data indicate that the Kitaev physics of α-RuCl3 is increasingly suppressed by the dominant spin-only driven magnetism of Cr3+ ( S = 3/2) in Ru1- xCr xCl3.

The efficiency of PbS quantum dot (QD) solar cells has significantly increased in recent years, strengthening their potential for industrial applications. The vast majority of state-of-the-art devices utilize 1,2-ethanedithiol (EDT)-coated PbS QD hole extraction layers, which lead to high initial performance, but result in poor device stability. While excellent performance has also been demonstrated with organic extraction layers, these devices include a molybdenum trioxide (MoO

Magnetic skyrmions are stable topological solitons with complex non-coplanar spin structures. Their nanoscopic size and the low electric currents required to control their motion has opened a new field of research, skyrmionics, that aims for the usage of skyrmions as information carriers. Further advances in skyrmionics call for a thorough understanding of their three-dimensional (3D) spin texture, skyrmion–skyrmion interactions and the coupling to surfaces and interfaces, which crucially affect skyrmion stability and mobility. Here, we quantitatively reconstruct the 3D magnetic texture of Bloch skyrmions with sub-10-nanometre resolution using holographic vector-field electron tomography. The reconstructed textures reveal local deviations from a homogeneous Bloch character within the skyrmion tubes, details of the collapse of the skyrmion texture at surfaces and a correlated modulation of the skyrmion tubes in FeGe along their tube axes. Additionally, we confirm the fundamental principles of skyrmion formation through an evaluation of the 3D magnetic energy density across these magnetic solitons.

We report on the controlled switching of domain-wall (DW) magnetization in aligned stripe-domain structures, stabilized in [$\mathrm{Co}$(0.44 nm)/$\mathrm{Pt}$(0.7 nm)]${}_{X}$($X=48$, 100, 150) multilayers with perpendicular magnetic anisotropy. The switching process, induced by an external magnetic field, is monitored by measuring the evolution of the in-plane magnetization. We show that the remanent in-plane magnetization originates from the polarization of the Bloch-type DWs. With micromagnetic simulations, we reveal that the reversal of the DW polarization is the result of the emergence and collapse of horizontal Bloch lines within the DWs at particular strengths of the external magnetic field, applied opposite to the DW polarization. Our findings are relevant for DW-based magnonics and bubble-skyrmion applications in magnetic multilayers.

Significance Using hybrid silica/protein templates, nature has mastered the fabrication of extremely complex macroscopic glass assemblies. Highly symmetric skeletal elements in demosponges are formed following a unique biomineralization mechanism in which polycondensation of an inherently disordered amorphous silica is guided by highly ordered proteinaceous filaments. Here we provide a comprehensive three-dimensional atomistic view of this hybrid assembly. The structure, occurring in the crystalline form in vivo, was measured in situ using the serial crystallography method. Together with a high-resolution transmission electron microscopy and energy-dispersive X-ray spectroscopy study, we provide structural, chemical, and functional information on a naturally forming hybrid mineral/organic crystal., Formation of highly symmetric skeletal elements in demosponges, called spicules, follows a unique biomineralization mechanism in which polycondensation of an inherently disordered amorphous silica is guided by a highly ordered proteinaceous scaffold, the axial filament. The enzymatically active proteins, silicateins, are assembled into a slender hybrid silica/protein crystalline superstructure that directs the morphogenesis of the spicules. Furthermore, silicateins are known to catalyze the formation of a large variety of other technologically relevant organic and inorganic materials. However, despite the biological and biotechnological importance of this macromolecule, its tertiary structure was never determined. Here we report the atomic structure of silicatein and the entire mineral/organic hybrid assembly with a resolution of 2.4 Å. In this work, the serial X-ray crystallography method was successfully adopted to probe the 2-µm-thick filaments in situ, being embedded inside the skeletal elements. In combination with imaging and chemical analysis using high-resolution transmission electron microscopy, we provide detailed information on the enzymatic activity of silicatein, its crystallization, and the emergence of a functional three-dimensional silica/protein superstructure in vivo. Ultimately, we describe a naturally occurring mineral/protein crystalline assembly at atomic resolution.

Diatoms are single-celled microalgae that produce silica-based cell walls with intricate nano- and micropatterns. Biogenesis of diatom biosilica is a bottom-up process that occurs in large intracellular compartments termed silica deposition vesicles (SDVs). Investigating the mechanism of silica morphogenesis has so far been severely limited by the lack of methods for imaging the entire volume of an SDV with high spatial resolution during all stages of development. Here we have developed a method that allows for rapid identification and electron microscopy imaging of many different, full sized SDVs that are in the process of producing biosilica valves. This enabled visualizing the development of characteristic morphological biosilica features with unprecedented spatio-temporal resolution. During early to mid-term development, valve SDVs contained ~20 nm sized particles that were primarily associated with the radially expanding rib-like biosilica structures. The results from electron dispersive X-ray analysis suggests that the immature biosilica patterns are silica-organic composites. This supports the hypothesis that silica morphogenesis is dependent on organic biomolecules inside the SDV lumen.

Diatoms are single-celled microalgae that produce silica-based cell walls with intricate nano- and micropatterns. Biogenesis of diatom biosilica is a bottom-up process that occurs in large intracellular compartments termed silica deposition vesicles (SDVs). Investigating the mechanism of silica morphogenesis has so far been severely limited by the lack of methods for imaging the entire volume of an SDV with high spatial resolution during all stages of development. Here we have developed a method that allows for rapid identification and electron microscopy imaging of many different, full sized SDVs that are in the process of producing biosilica valves. This enabled visualizing the development of characteristic morphological biosilica features with unprecedented spatio-temporal resolution. During early to mid-term development, valve SDVs contained ~ 20 nm sized particles that were primarily associated with the radially expanding rib-like biosilica structures. The results from electron dispersive X-ray analysis suggests that the immature biosilica patterns are silica-organic composites. This supports the hypothesis that silica morphogenesis is dependent on organic biomolecules inside the SDV lumen.

Angewandte Chemie / International edition International edition 59(15), 6028 - 6036 (2020). doi:10.1002/anie.201915217, Single‐layer and multi‐layer 2D polyimine films have been achieved through interfacial synthesis methods. However, it remains a great challenge to achieve the maximum degree of crystallinity in the 2D polyimines, which largely limits the long‐range transport properties. Here we employ a surfactant‐monolayer‐assisted interfacial synthesis (SMAIS) method for the successful preparation of porphyrin and triazine containing polyimine‐based 2D polymer (PI‐2DP) films with square and hexagonal lattices, respectively. The synthetic PI‐2DP films are featured with polycrystalline multilayers with tunable thickness from 6 to 200 nm and large crystalline domains (100–150 nm in size). Intrigued by high crystallinity and the presence of electroactive porphyrin moieties, the optoelectronic properties of PI‐2DP are investigated by time‐resolved terahertz spectroscopy. Typically, the porphyrin‐based PI‐2DP 1 film exhibits a p‐type semiconductor behavior with a band gap of 1.38 eV and hole mobility as high as 0.01 cm2 V−1 s−1, superior to the previously reported polyimine based materials., Published by Wiley-VCH, Weinheim

Here we present a novel solvothermal synthesis approach for the accurate control over the structural features of nickel/reduced graphene oxide (Ni/rGO) nanocomposites for tuneable electrical properties. We discovered that the dynamic chemical structure of GO during reaction, acts as an active template for the controlled nanostructured growth of nickel nanoparticles (Ni NPs). Therefore, the precise control of reaction time offered the possibility to modulate nucleation and coalescence phenomena of Ni NPs, allowing in this way to precisely adjust their size, density and NiO@Ni structure on the final Ni/rGO nanocomposites. The electrophysical properties (work function and conductivity) of different Ni/rGO nanocomposites were determined and found to be directly dependent on the Ni NPs radius and also on the NiO buffer layer width. We confirmed a crucial role of the NiO buffer layer thickness at the Pt-NiO-Ni-NiO-rGO interface changing the conductivity from metallic to those specific to a Schottky contact or to a p-n heterojunction. These new findings reveal a relevant potential for using Ni/rGO nanocomposites as a versatile and promising material for micro-, nano- and optoelectronics as well as for energy storage technologies.

Single atoms are the ultimate minimum size limit for catalysts. Graphene, as an exciting, ultimately thin (one atom thick) material can be imaged in a transmission electron microscope with relatively few imaging artefacts. Here, we directly observe the behavior of single Cr atoms in graphene mono- and di-vacancies and, more importantly, at graphene edges. Similar studies at graphene edges with other elemental atoms, with the exception of Fe, show catalytic etching of graphene. Fe atoms have been shown to both etch and grow graphene. In contrast, Cr atoms are only observed to induce graphene growth. Complementary theoretical calculations illuminate the differences between Fe and Cr, and confirm single Cr atoms as superior catalysts for sp2 carbon growth.

In the present work, we demonstrate different synthesis procedures for filling carbon nanotubes (CNTs) with equimolar binary nanoparticles of the type Fe–Co. The CNTs act as templates for the encapsulation of magnetic nanoparticles and provide a protective shield against oxidation as well as prevent nanoparticle agglomeration. By variation of the reaction parameters, we were able to tailor the sample purity, degree of filling, the composition and size of the filling particles, and therefore, the magnetic properties. The samples were analyzed by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), superconducting quantum interference device (SQUID) and thermogravimetric analysis (TGA). The Fe–Co-filled CNTs show significant enhancement in the coercive field as compared to the corresponding bulk material, which make them excellent candidates for several applications such as magnetic storage devices.

The development of core-shell structures remains a fundamental challenge for pure metallic aerogels. Here we report the synthesis of Pdx Au-Pt core-shell aerogels composed of an ultrathin Pt shell and a composition-tunable Pdx Au alloy core. The universality of this strategy ensures the extension of core compositions to Pd transition-metal alloys. The core-shell aerogels exhibited largely improved Pt utilization efficiencies for the oxygen reduction reaction and their activities show a volcano-type relationship as a function of the lattice parameter of the core substrate. The maximum mass and specific activities are 5.25 A mgPt-1 and 2.53 mA cm-2 , which are 18.7 and 4.1 times higher than those of Pt/C, respectively, demonstrating the superiority of the core-shell metallic aerogels. The proposed core-based activity descriptor provides a new possible strategy for the design of future core-shell electrocatalysts.

Here we report on structural properties and the photo-electrochemical response of annealed TiO2 nanotube layers, grown on four different Ti substrates by an identical anodization process. TiO2 nanotube layers were grown on Ti substrates by anodization in glycerol containing NH4F and water. The layers were then annealed at 400 °C for 1 h in air. Photocurrent densities of annealed nanotubes were recorded upon irradiation with ultraviolet (UV) light at a constant potential of 0.4 V, in a 0.1 M Na2SO4 aqueous solution. Approximately, a 280% difference in the photocurrent densities was recorded from TiO2 nanotubes fabricated from different Ti substrates. To elucidate the origin of this difference, the nanotube layers were scrutinized by Mott-Schottky measurements, X-ray diffraction (XRD) and Electron Energy Loss Spectroscopy (EELS). Inspection of the XRD patterns revealed preferential crystallographic orientations in various Ti substrates from which TiO2 nanotube layers were produced. Subsequent EELS analyses of the annealed nanotube layers disclosed significant differences in the Ti:O stoichiometry, in accordance with XRD evaluation of preferential orientation differences among used Ti substrates.

To establish high-bandwidth chip-to-chip interconnects in optoelectronic integrated circuits, requires high-performance photon emitters and signal receiving components. Regarding the photodetector, fast device concepts like Schottky junction devices, large carrier mobility materials and shrinking the channel length will enable higher operation speed. However, integrating photodetectors in highly scaled ICs technologies is challenging due to the efficiency-speed trade-off. Here, we report a scalable and CMOS-compatible approach for an ultra-scaled germanium (Ge) based photodetector with tunable polarity. The photodetector is composed of a Ge Schottky barrier field effect transistor with monolithic aluminum (Al) source/drain contacts, offering plasmon assisted and polarization-resolved photodetection. The ultra-scaled Ge photodetector with a channel length of only 200 nm shows high responsivity of aboutR = 424 A W-1and a maximum polarization sensitivity ratio of TM/TE = 11.

The integration of new materials such as high-k dielectrics or metals into advanced CMOS gate stacks has led to major developments in plasma etching. The authors present a study which is dedicated to the etching of amorphous hafnium zirconium oxide (HZO) and titanium nitride (TiN) layers with Ar/Cl2 chemistry in one single step. By adjusting the gas ratio and the inductively coupled plasma power, the etching process is shown to have a slow and well controllable etch rate for HZO and TiN. Additionally, a high selectivity between both materials and SiO2 can be achieved. Gate stack etching was successfully demonstrated and transmission electron microscopy-images revealed good anisotropic etching for HZO and TiN with an etch stop in SiO2 without damaging the silicon underneath. The process is further applied for the fabrication of metal-ferroelectric-metal capacitors, here TiN-HZO-TiN, and the feasibility of the chosen material combination is proven by electrical characterization. The strategy of using low temperature plasma-enhanced atomic layer deposition for TiN-deposition and forming gas anneal after structuring leads to high remanent polarization-values.

The phase shift of the electron wave is a useful measure for the projected magnetic flux density of magnetic objects at the nanometer scale. More important for materials science, however, is the knowledge about the magnetization in a magnetic nano-structure. As demonstrated here, a dominating presence of stray fields prohibits a direct interpretation of the phase in terms of magnetization modulus and direction. We therefore present a model-based approach for retrieving the magnetization by considering the projected shape of the nano-structure and assuming a homogeneous magnetization therein. We apply this method to FePt nano-islands epitaxially grown on a SrTiO3 substrate, which indicates an inclination of their magnetization direction relative to the structural easy magnetic [001] axis. By means of this real-world example, we discuss prospects and limits of this approach.

Electron energy-loss magnetic chiral dichroism (EMCD) allows for the quantification of magnetic properties of materials at the nanometer scale. It is shown that with the support of simulations that help to identify the optimal conditions for a successful experiment and upon implementing measurement routines that effectively reduce the noise floor, EMCD measurements can be pushed towards quantitative magnetic measurements even on individual nanoparticles. With this approach, the ratio of orbital to spin magnetic moments for the Fe atoms in a single L10 ordered FePt nanoparticle is determined to be ml/ms=0.08±0.02. This finding is in good quantitative agreement with the results of XMCD ensemble measurements.

Fine-tuning chemistry by doping with transition metals enables new perspectives for exploring Kitaev physics on a two-dimensional (2D) honeycomb lattice of α-RuCl

Antiferromagnetic (AF) domain walls have recently attracted revived attention, not only in the emerging field of AF spintronics, but also more specifically for offering fast domain wall velocities and dynamic excitations up to the terahertz frequency regime. Here we introduce an approach to nucleate and stabilize an AF domain wall in a synthetic antiferromagnet (SAF). We present experimental and micromagnetic studies of the magnetization reversal in [(Co/Pt)$_{X-1}$/Co/Ir]$_{N-1}$(Co/Pt)$_X$ SAFs, where interface induced perpendicular magnetic anisotropy (PMA) and AF interlayer exchange coupling (IEC) are completely controlled via the individual layer thicknesses within the multilayer stack. By combining strong PMA with even stronger AF IEC, the SAF reveals a collective response to an external magnetic field applied normal to the surface, and we stabilize the characteristic surface spin flop (SSF) state for an even number N of AF-coupled (Co/Pt)$_{X-1}$/Co multilayer blocks. In the SSF state our system provides a well-controlled and fully tunable vertical AF domain wall, easy to integrate as no single crystal substrates are required and with uniform 2D-magnetization in the film plane for further functionalization options, such as for example lateral patterning via lithography., 15 pages, 3 figures

Large-scale-applicable thermoelectric materials should be both self-sustaining, in order to survive long-term duty cycles, and nonpolluting. Among all classes of known thermoelectric materials, these criteria reduce the available candidate pool, leaving silicon as one of the remaining options. Here we first review the thermoelectric properties of various silicon-related materials with respect to their morphologies and microstructures. We then report the thermoelectric properties of silicon sawing wastes recycled from silicon wafer manufacturing. We obtain a high power factor of ∼32 μW cm−1 K−2 at 1273 K with 6% phosphorus substitution in the Si crystal, a value comparable to that of phosphorus-doped silicon-germanium alloys. Our work suggests the large-scale thermoelectric applicability of recycled silicon that would otherwise contribute to the millions of tons of industrial waste produced by the semiconductor industry. Keywords: Silicon, Thermoelectric, Nanostructure, Power factor, Sawing waste

Chains of metallic nanoparticles sustain strongly confined surface plasmons with relatively low dielectric losses. To exploit these properties in applications, such as waveguides, the fabrication of long chains of low disorder and a thorough understanding of the plasmon-mode properties, such as dispersion relations, are indispensable. Here, we use a wrinkled template for directed self-assembly to assemble chains of gold nanoparticles. With this up-scalable method, chain lengths from two particles (140 nm) to 20 particles (1500 nm) and beyond can be fabricated. Electron energy-loss spectroscopy supported by boundary element simulations, finite-difference time-domain, and a simplified dipole coupling model reveal the evolution of a band of plasmonic waveguide modes from degenerated single-particle modes in detail. In striking difference from plasmonic rod-like structures, the plasmon band is confined in excitation energy, which allows light manipulations below the diffraction limit. The non-degenerated surface plasmon modes show suppressed radiative losses for efficient energy propagation over a distance of 1500 nm. �� 2019 American Chemical Society.

Chemistry of materials 31(8), 2795 - 2806 (2019). doi:10.1021/acs.chemmater.8b05017, High-quality single crystals of MnBi2Te4 are grown for the first time by slow cooling within a narrow range between the melting points of Bi$_2$Te$_3$ (586 °C) and MnBi$_2$Te$_4$ (600 °C). Single-crystal X-ray diffraction and electron microscopy reveal ubiquitous antisite defects in both cation sites and, possibly, Mn vacancies (Mn$_{0.85(3)}$Bi$_{2.10(3)}$Te$_4$). Thermochemical studies complemented with high-temperature X-ray diffraction establish a limited high-temperature range of phase stability and metastability at room temperature. Nevertheless, the synthesis of MnBi$_2$Te$_4$ can be scaled-up as powders can be obtained at subsolidus temperatures and quenched at room temperature. Bulk samples exhibit long-range antiferromagnetic ordering below 24 K. The Mn(II) out-of-plane magnetic state is confirmed by the magnetization, X-ray photoemission, X-ray absorption, and linear dichroism measurements. The compound shows a metallic type of resistivity in the range 4.5–300 K and is an n-type conductor that reaches a thermoelectric figure of merit up to ZT = 0.17. Angle-resolved photoemission experiments show a surface state forming a gapped Dirac cone, thus strengthening MnBi$_2$Te$_4$ as a promising candidate for the intrinsic magnetic topological insulator, in accordance with theoretical predictions. The developed synthetic protocols enable further experimental studies of a crossover between magnetic ordering and nontrivial topology in bulk MnBi$_2$Te$_4$., Published by American Chemical Society, Washington, DC

Herein, we present the effect of the nanoconfinement of LiBH 4 within porous aerogel-like carbon on its hydrogen storage properties. The carbon scaffold is prepared by salt templating – a facile and sustainable technique for the production of micro- and mesoporous carbon-based materials. A loading of up to 40 wt. % of LiBH 4 is achieved by melt infiltration, and the hydride remains amorphous as shown by differential scanning calorimetry (DSC), X-ray diffractometry (XRD) and scanning transmission electron microscopy (STEM). Simultaneous thermogravimetry and mass spectroscopy (TG-MS) reveal that the nanoconfined LiBH 4 starts to desorb hydrogen already at 200 °C with the main release at 310 °C. A partial rehydrogenation at moderate conditions (100 bar and 300 °C) is demonstrated. In contrast to recent reports, in-situ heating in the transmission electron microscope (STEM) and electron energy loss spectroscopy (EELS) indicate that both decomposition products (B and LiH) remain within the carbon pores. Nuclear magnetic resonance (NMR) measurements reveal the presence of amorphous and partially oxidized boron in the dehydrogenated sample that may impede the reversibility of the (de)hydrogenation process.

Improved properties arise in transition metal dichalcogenide (TMDC) materials when they are stacked onto insulating hexagonal boron nitride (h-BN). Therefore, the scalable fabrication of TMDCs/h-BN heterostructures by direct chemical vapor deposition (CVD) growth is highly desirable. Unfortunately, to achieve this experimentally is challenging. Ideal substrates for h-BN growth, such as Ni, become sulfides during the synthesis process. This leads to the decomposition of the pregrown h-BN film, and thus no TMDCs/h-BN heterostructure forms. Here, we report a thoroughly direct CVD approach to obtain TMDCs/h-BN vertical heterostructures without any intermediate transfer steps. This is attributed to the use of a nickel-based alloy with excellent sulfide-resistant properties and a high catalytic activity for h-BN growth. The strategy enables the direct growth of single-crystal MoS2 grains of up to 200 μm2 on h-BN, which is approximately 1 order of magnitude larger than that in previous reports. The direct band g...

Electron magnetic circular dichroism (EMCD), the electron wave analog of x-ray magnetic circular dichroism (XMCD), allows for the element specific measurement of the spin and orbital magnetic moments with up to nanometer resolution. However, due to dynamical diffraction effects, the signal-to-noise ratios of EMCD spectra are often very low. We describe a simple set of rules, how to set up a geometry for a classical EMCD experiment on an arbitrary crystal structure to get a maximum dichroic signal. The procedure is based on an evaluation of the structure factor and extinction distances. Proof-of-concept simulations and experiments on a FeGe crystal present a successful test of these guidelines.

Envisaged applications of Skyrmions in magnetic memory and logic devices crucially depend on the stability and mobility of these topologically nontrivial magnetic textures in thin films. We present for the first time quantitative maps of the magnetic induction that provide evidence for a 3D modulation of the Skyrmionic spin texture. The projected in-plane magnetic induction maps as determined from in-line and off-axis electron holography carry the clear signature of Bloch Skyrmions. However, the magnitude of this induction is much smaller than the values expected for homogeneous Bloch Skyrmions that extend throughout the thickness of the film. This finding can only be understood if the underlying spin textures are modulated along the out-of-plane $z$ direction. The projection of (the in-plane magnetic induction of) helices is further found to exhibit thickness-dependent lateral shifts, which show that this $z$ modulation is accompanied by an (in-plane) modulation along the $x$ and $y$ directions.