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Transport in multilayered nanostructures : the dynamical mean-field theory approach
\"Over the last 25 years, dynamical mean-field theory (DMFT) has emerged as one of the most powerful new developments in many-body physics. Written by one of the key researchers in the field, this book presents the first comprehensive treatment of this ever-developing topic. Transport in Mutlilayered Nanostructures is varied and modern in its scope, and: Develops the formalism of many-body Green's functions using the equation-of-motion approach Applies DMFT to study transport in multilayered nanostructures, which is likely to be one of the most prominent applications of nanotechnology in the coming years Develops formalism first for the bulk and then for the inhomogeneous multilayered systems Describes in great detail the science behind the metal-insulator transition, electronic charge reconstruction, strongly correlated contributions to capacitance, and superconductivity Includes complete derivations and emphasizes how to carry out numerical calculations, including discussions of parallel programming algorithms Provides descriptions of the crossover from tunneling to thermally activated transport, of the properties of Josephson junctions with barriers tuned near the metal-insulator transition of thermoelectric coolers and power generators and of nonequilibrium extensions to determine current-voltage characteristics as applications of the theory A series of over 40 problems help develop the skills to allow readers to reach the level of being able to contribute to research. This book is suitable for an advanced graduate course in DMFT, and for individualized study by graduate students, postdoctoral fellows and advanced researchers wishing to enter the field\"-- Provided by publisher.
Book
Transport in multilayered nanostructures
This novel book is the first comprehensive text on dynamical mean-field theory (DMFT), which has emerged over the past two decades as one of the most powerful new developments in many-body physics. Written by one of the key researchers in the field, the volume develops the formalism of many-body Green's functions using the equation of motion approach, which requires an undergraduate solid state physics course and a graduate quantum mechanics course as prerequisites. The DMFT is applied to study transport in multilayered nanostructures, which is likely to be one of the most prominent applications of nanotechnology in the coming years. The text is modern in scope focusing on exact numerical methods rather than the perturbation theory. Formalism is developed first for the bulk and then for the inhomogeneous multilayered systems. The science behind the metal-insulator transition, electronic charge reconstruction, and superconductivity are thoroughly described. The book covers complete derivations and emphasizes how to carry out numerical calculations, including discussions of parallel programing algorithms. Detailed descriptions of the crossover from tunneling to thermally activated transport, of the properties of Josephson junctions with barriers tuned near the metal-insulator transition, and of thermoelectric coolers and power generators are provided as applications of the theory.
eBook
Unveiling the Assembly of Neutral Marine Polysaccharides into Electrostatic-Driven Layer-by-Layer Bioassemblies by Chemical Functionalization
Marine-origin polysaccharides, in particular cationic and anionic ones, have been widely explored as building blocks in fully natural or hybrid electrostatic-driven Layer-by-Layer (LbL) assemblies for bioapplications. However, the low chemical versatility imparted by neutral polysaccharides has been limiting their assembly into LbL biodevices, despite their wide availability in sources such as the marine environment, easy functionality, and very appealing features for addressing multiple biomedical and biotechnological applications. In this work, we report the chemical functionalization of laminarin (LAM) and pullulan (PUL) marine polysaccharides with peptides bearing either six lysine (K6) or aspartic acid (D6) amino acids via Cu(I)-catalyzed azide-alkyne cycloaddition to synthesize positively and negatively charged polysaccharide-peptide conjugates. The successful conjugation of the peptides into the polysaccharide’s backbone was confirmed by proton nuclear magnetic resonance and attenuated total reflectance Fourier-transform infrared spectroscopy, and the positive and negative charges of the LAM-K6/PUL-K6 and LAM-D6/PUL-D6 conjugates, respectively, were assessed by zeta-potential measurements. The electrostatic-driven LbL build-up of either the LAM-D6/LAM-K6 or PUL-D6/PUL-K6 multilayered thin film was monitored in situ by quartz crystal microbalance with dissipation monitoring, revealing the successful multilayered film growth and the enhanced stability of the PUL-based film. The construction of the PUL-peptide multilayered thin film was also assessed by scanning electron microscopy and its biocompatibility was demonstrated in vitro towards L929 mouse fibroblasts. The herein proposed approach could enable the inclusion of virtually any kind of small molecules in the multilayered assemblies, including bioactive moieties, and be translated into more convoluted structures of any size and geometry, thus extending the usefulness of neutral polysaccharides and opening new avenues in the biomedical field, including in controlled drug/therapeutics delivery, tissue engineering, and regenerative medicine strategies.
Journal Article
Fuzzy Nanoassemblies: Toward Layered Polymeric Multicomposites
Multilayer films of organic compounds on solid surfaces have been studied for more than 60 years because they allow fabrication of multicomposite molecular assemblies of tailored architecture. However, both the Langmuir-Blodgett technique and chemisorption from solution can be used only with certain classes of molecules. An alternative approach-fabrication of multilayers by consecutive adsorption of polyanions and polycations-is far more general and has been extended to other materials such as proteins or colloids. Because polymers are typically flexible molecules, the resulting superlattice architectures are somewhat fuzzy structures, but the absence of crystallinity in these films is expected to be beneficial for many potential applications.
Journal Article
Perovskite solar cells with atomically coherent interlayers on SnO2 electrodes
In perovskite solar cells, the interfaces between the perovskite and charge-transporting layers contain high concentrations of defects (about 100 times that within the perovskite layer), specifically, deep-level defects, which substantially reduce the power conversion efficiency of the devices
1
–
3
. Recent efforts to reduce these interfacial defects have focused mainly on surface passivation
4
–
6
. However, passivating the perovskite surface that interfaces with the electron-transporting layer is difficult, because the surface-treatment agents on the electron-transporting layer may dissolve while coating the perovskite thin film. Alternatively, interfacial defects may not be a concern if a coherent interface could be formed between the electron-transporting and perovskite layers. Here we report the formation of an interlayer between a SnO
2
electron-transporting layer and a halide perovskite light-absorbing layer, achieved by coupling Cl-bonded SnO
2
with a Cl-containing perovskite precursor. This interlayer has atomically coherent features, which enhance charge extraction and transport from the perovskite layer, and fewer interfacial defects. The existence of such a coherent interlayer allowed us to fabricate perovskite solar cells with a power conversion efficiency of 25.8 per cent (certified 25.5 per cent)under standard illumination. Furthermore, unencapsulated devices maintained about 90 per cent of their initial efficiency even after continuous light exposure for 500 hours. Our findings provide guidelines for designing defect-minimizing interfaces between metal halide perovskites and electron-transporting layers.
An atomically coherent interlayer between the electron-transporting and perovskite layers in perovskite solar cells enhances charge extraction and transport from the perovskite, enabling high power conversion efficiency.
Journal Article
Biomimetic Pathways for Assembling Inorganic Thin Films
Living organisms construct various forms of laminated nanocomposites through directed nucleation and growth of inorganics at self-assembled organic templates at temperatures below 100°C and in aqueous solutions. Recent research has focused on the use of functionalized organic surfaces to form continuous thin films of single-phase ceramics. Continuous thin films of mesostructured silicates have also been formed on hydrophobic and hydrophilic surfaces through a two-step mechanism. First, under acidic conditions, surfactant micellar structures are self-assembled at the solid/liquid interface, and second, inorganic precursors condense to form an inorganic-organic nanocomposite. Epitaxial coordination of adsorbed surfactant tubules is observed on mica and graphite substrates, whereas a random arrangement is observed on amorphous silica. The ability to process ceramic-organic nanocomposite films by these methods provides new technological opportunities.
Journal Article
Synthesis of Novel Thin-Film Materials by Pulsed Laser Deposition
Pulsed laser deposition (PLD) is a conceptually and experimentally simple yet highly versatile tool for thin-film and multilayer research. Its advantages for the film growth of oxides and other chemically complex materials include stoichiometric transfer, growth from an energetic beam, reactive deposition, and inherent simplicity for the growth of multilayered structures. With the use of PLD, artificially layered materials and metastable phases have been created and their properties varied by control of the layer thicknesses. In situ monitoring techniques have provided information about the role of energetic species in the formation of ultrahard phases and in the doping of semiconductors. Cluster-assembled nanocrystalline and composite films offer opportunities to control and produce new combinations of properties with PLD.
Journal Article
Electrical detection of single magnetic skyrmions in metallic multilayers at room temperature
Magnetic skyrmions are topologically protected whirling spin textures that can be stabilized in magnetic materials by an asymmetric exchange interaction between neighbouring spins that imposes a fixed chirality. Their small size, together with the robustness against external perturbations, make magnetic skyrmions potential storage bits in a novel generation of memory and logic devices. To this aim, their contribution to the electrical transport properties of a device must be characterized—however, the existing demonstrations are limited to low temperatures and mainly in magnetic materials with a B20 crystal structure. Here we combine concomitant magnetic force microscopy and Hall resistivity measurements to demonstrate the electrical detection of sub-100 nm skyrmions in a multilayered thin film at room temperature. Furthermore, we detect and analyse the Hall signal of a single skyrmion, which indicates that it arises from the anomalous Hall effect with a negligible contribution from the topological Hall effect.
Journal Article
Enhanced Perpendicular Exchange Bias in Co/Pd Antidot Arrays
Magnetic nanostructures revealing the exchange bias (EB) effect have attracted much interest in recent years due to their promising applications in spintronics, magnetic sensing and recording devices with various functionalities. In this paper, we report on the perpendicular exchange bias effect in a multilayered thin film composed of [Co/Pd] ferromagnetic multilayers exchange-coupled to an antiferromagnetic IrMn. The film was deposited on a porous anodized titania template. Influences of the films’ surface morphology as well as the order of layers deposited on the EB effect were studied. The enhancements of the EB field HEB (up to 30%) and the coercive field HC (two times) were achieved in the nanoporous films relative to their continuous film counterparts, which could be attributed to the specific morphology of the porous surfaces.
Journal Article
Stepwise Formation of Multilayered Nanostructural Films from Macromolecular Precursors
Sequential adsorption of a cationic polyelectrolyte and individual sheets of the silicate mineral hectorite has allowed controlled, stepwise formation of multilayered films on silicon wafers. Each component adsorbs rapidly by an ion-exchange mechanism, and x-ray diffractometry indicates structural order even in films with thicknesses greater than 0.2 micrometer. The large lateral extent of the silicate sheets (about 25 to 35 nanometers) allows each layer to cover any packing defects in the underlying layer, thus preserving structural order in the growing film. With careful choice of component materials, this method should allow for the preparation of multilayered films with a variety of technologically important properties.
Journal Article