This article reviews the basic theoretical aspects of graphene, a one-atom-thick allotrope of carbon, with unusual two-dimensional Dirac-like electronic excitations. The Dirac electrons can be controlled by application of external electric and magnetic fields, or by altering sample geometry and/or topology. The Dirac electrons behave in unusual ways in tunneling, confinement, and the integer quantum Hall effect. The electronic properties of graphene stacks are discussed and vary with stacking order and number of layers. Edge (surface) states in graphene depend on the edge termination (zigzag or armchair) and affect the physical properties of nanoribbons. Different types of disorder modify the Dirac equation leading to unusual spectroscopic and transport properties. The effects of electron-electron and electron-phonon interactions in single layer and multilayer graphene are also presented.

/pdf/the-electronic-properties-of-graphene-2siyzsnf5w.pdf

The electronic properties of graphene

Deposits of clastic carbonate-dominated (calciclastic) sedimentary slope systems in the rock record have been identified mostly as linearly-consistent carbonate apron deposits, even though most ancient clastic carbonate slope deposits fit the submarine fan systems better. Calciclastic submarine fans are consequently rarely described and are poorly understood. Subsequently, very little is known especially in mud-dominated calciclastic submarine fan systems. Presented in this study are a sedimentological core and petrographic characterisation of samples from eleven boreholes from the Lower Carboniferous of Bowland Basin (Northwest England) that reveals a >250 m thick calciturbidite complex deposited in a calciclastic submarine fan setting. Seven facies are recognised from core and thin section characterisation and are grouped into three carbonate turbidite sequences. They include: 1) Calciturbidites, comprising mostly of highto low-density, wavy-laminated bioclast-rich facies; 2) low-density densite mudstones which are characterised by planar laminated and unlaminated muddominated facies; and 3) Calcidebrites which are muddy or hyper-concentrated debrisflow deposits occurring as poorly-sorted, chaotic, mud-supported floatstones. These

Phd by thesis

It is possible to say that zeolites are the most widely used catalysts in industry They are crystalline microporous materials which have become extremely successful as catalysts for oil refining, petrochemistry, and organic synthesis in the production of fine and speciality chemicals, particularly when dealing with molecules having kinetic diameters below 10 A The reason for their success in catalysis is related to the following specific features of these materials:1 (1) They have very high surface area and adsorption capacity (2) The adsorption properties of the zeolites can be controlled, and they can be varied from hydrophobic to hydrophilic type materials (3) Active sites, such as acid sites for instance, can be generated in the framework and their strength and concentration can be tailored for a particular application (4) The sizes of their channels and cavities are in the range typical for many molecules of interest (5-12 A), and the strong electric fields2 existing in those micropores together with an electronic confinement of the guest molecules3 are responsible for a preactivation of the reactants (5) Their intricate channel structure allows the zeolites to present different types of shape selectivity, ie, product, reactant, and transition state, which can be used to direct a given catalytic reaction toward the desired product avoiding undesired side reactions (6) All of these properties of zeolites, which are of paramount importance in catalysis and make them attractive choices for the types of processes listed above, are ultimately dependent on the thermal and hydrothermal stability of these materials In the case of zeolites, they can be activated to produce very stable materials not just resistant to heat and steam but also to chemical attacks Avelino Corma Canos was born in Moncofar, Spain, in 1951 He studied chemistry at the Universidad de Valencia (1967−1973) and received his PhD at the Universidad Complutense de Madrid in 1976 He became director of the Instituto de Tecnologia Quimica (UPV-CSIC) at the Universidad Politecnica de Valencia in 1990 His current research field is zeolites as catalysts, covering aspects of synthesis, characterization and reactivity in acid−base and redox catalysis A Corma has written about 250 articles on these subjects in international journals, three books, and a number of reviews and book chapters He is a member of the Editorial Board of Zeolites, Catalysis Review Science and Engineering, Catalysis Letters, Applied Catalysis, Journal of Molecular Catalysis, Research Trends, CaTTech, and Journal of the Chemical Society, Chemical Communications A Corma is coauthor of 20 patents, five of them being for commercial applications He has been awarded with the Dupont Award on new materials (1995), and the Spanish National Award “Leonardo Torres Quevedo” on Technology Research (1996) 2373 Chem Rev 1997, 97, 2373−2419

From Microporous to Mesoporous Molecular-Sieve Materials and Their Use in Catalysis

Graphene — a recently isolated one-atom-thick layered form of graphite — is a hot topic in the materials science and condensed matter physics communities, where it is proving to be a popular model system for investigation. An experiment involving individual graphene sheets suspended over a microscale scaffold has allowed structure determination using transmission electron microscopy and diffraction, perhaps paving the way towards an answer to the question of why graphene can exist at all. The 'two-dimensional' sheets, it seems, are not flat, but wavy. The undulations are less pronounced in a two-layer system, and disappear in multilayer samples. Learning more about this 'waviness' may reveal what makes these extremely thin carbon membranes so stable. Investigations of individual graphene sheets freely suspended on a microfabricated scaffold in vacuum or in air reveal that the membranes are not perfectly flat, but exhibit an intrinsic waviness, such that the surface normal varies by several degrees, and out-of-plane deformations reach 1 nm. The recent discovery of graphene has sparked much interest, thus far focused on the peculiar electronic structure of this material, in which charge carriers mimic massless relativistic particles1,2,3. However, the physical structure of graphene—a single layer of carbon atoms densely packed in a honeycomb crystal lattice—is also puzzling. On the one hand, graphene appears to be a strictly two-dimensional material, exhibiting such a high crystal quality that electrons can travel submicrometre distances without scattering. On the other hand, perfect two-dimensional crystals cannot exist in the free state, according to both theory and experiment4,5,6,7,8,9. This incompatibility can be avoided by arguing that all the graphene structures studied so far were an integral part of larger three-dimensional structures, either supported by a bulk substrate or embedded in a three-dimensional matrix1,2,3,9,10,11,12. Here we report on individual graphene sheets freely suspended on a microfabricated scaffold in vacuum or air. These membranes are only one atom thick, yet they still display long-range crystalline order. However, our studies by transmission electron microscopy also reveal that these suspended graphene sheets are not perfectly flat: they exhibit intrinsic microscopic roughening such that the surface normal varies by several degrees and out-of-plane deformations reach 1 nm. The atomically thin single-crystal membranes offer ample scope for fundamental research and new technologies, whereas the observed corrugations in the third dimension may provide subtle reasons for the stability of two-dimensional crystals13,14,15.

/pdf/the-structure-of-suspended-graphene-sheets-1hs19mwg5z.pdf

The structure of suspended graphene sheets

N G van Kampen 1981 Amsterdam: North-Holland xiv + 419 pp price Dfl 180 This is a book which, at a lower price, could be expected to become an essential part of the library of every physical scientist concerned with problems involving fluctuations and stochastic processes, as well as those who just enjoy a beautifully written book. It provides an extensive graduate-level introduction which is clear, cautious, interesting and readable.

https://iopscience.iop.org/article/10.1088/0031-9112/34/4/040/pdf

Stochastic Processes in Physics and Chemistry

We give a pedagogical introduction into the functional renormalization group treatment of disordered systems. After a review of its phenomenology, we show why in the context of disordered systems a functional renormalization group treatment is necessary, contrary to pure systems, where renormalization of a single coupling constant is sufficient. This leads to a disorder distribution, which after a finite renormalization becomes non-analytic, thus overcoming the predictions of the seemingly exact dimensional reduction. We discuss, how the non-analyticity can be measured in a simulation or experiment. We then construct a renormalizable field theory beyond leading order. We discuss an elastic manifold embedded in N dimensions, and give the exact solution for N to infinity. This is compared to predictions of the Gaussian replica variational ansatz, using replica symmetry breaking. We further consider random field magnets, and supersymmetry. We finally discuss depinning, both isotropic and anisotropic, and universal scaling function.

/pdf/functional-renormalization-for-disordered-systems-basic-5f8wehiwca.pdf

Functional Renormalization for Disordered Systems. Basic Recipes and Gourmet Dishes

We reveal a phase transition with decreasing viscosity $\nu$ at \nu=\nu_c>0 in one-dimensional decaying Burgers turbulence with a power-law correlated random profile of Gaussian-distributed initial velocities \sim|x-x'|^{-2}. The low-viscosity phase exhibits non-Gaussian one-point probability density of velocities, continuously dependent on \nu, reflecting a spontaneous one step replica symmetry breaking (RSB) in the associated statistical mechanics problem. We obtain the low orders cumulants analytically. Our results, which are checked numerically, are based on combining insights in the mechanism of the freezing transition in random logarithmic potentials with an extension of duality relations discovered recently in Random Matrix Theory. They are essentially non mean-field in nature as also demonstrated by the shock size distribution computed numerically and different from the short range correlated Kida model, itself well described by a mean field one step RSB ansatz. We also provide some insights for the finite viscosity behaviour of velocities in the latter model.

Freezing Transition in Decaying Burgers Turbulence and Random Matrix Dualities

In a recent work Povolotsky provided a three-parameter family of stochastic particle systems with zero-range interactions in one dimension which are integrable by coordinate Bethe ansatz. Using these results we obtain the corresponding condition for integrability of a class of directed polymer models with random weights on the square lattice. Analyzing the solutions we find, besides known cases, a new two-parameter family of integrable DP model, which we call the Inverse-Beta polymer, and provide its Bethe ansatz solution.

On integrable directed polymer models on the square lattice

We show that the stochastic field theory for directed percolation in the presence of an additional conservation law [the conserved directed-percolation (C-DP) class] can be mapped exactly to the continuum theory for the depinning of an elastic interface in short-range correlated quenched disorder. Along one line of the parameters commonly studied, this mapping leads to the simplest overdamped dynamics. Away from this line, an additional memory term arises in the interface dynamics; we argue that this does not change the universality class. Since C-DP is believed to describe the Manna class of self-organized criticality, this shows that Manna stochastic sandpiles and disordered elastic interfaces (i.e., the quenched Edwards-Wilkinson model) share the same universal large-scale behavior.

Exact mapping of the stochastic field theory for Manna sandpiles to interfaces in random media.

all cumulants of the magnetization. We find that ρ(�M ) ∼ �M −τ with an avalanche exponent τ = 1f or the SK model, originating from the marginal stability (criticality) of the model. It holds for jumps of size 1 � �M < N 1/2 , being provoked by changes of the external field by δH = O(N −1/2 )w hereN is the total number of spins. Our general formula also suggests that the density of overlap q between initial and final states in an avalanche is ρ(q) ∼ 1/(1 − q). These results show interesting similarities with numerical simulations for the out-of-equilibrium dynamics of the SK model. For finite-range models, using droplet arguments, we obtain the prediction τ = (df + θ )/dm where df ,d m ,a ndθ are the fractal dimension, magnetization exponent, and energy exponent of a droplet, respectively. This formula is expected to apply to other glassy disordered systems, such as the random-field model and pinned interfaces. We make suggestions for further numerical investigations, as well as experimental studies of the Barkhausen noise in spin glasses.

/pdf/equilibrium-avalanches-in-spin-glasses-4cv9ii75qq.pdf

Pierre Le Doussal

Papers

Functional Renormalization for Disordered Systems. Basic Recipes and Gourmet Dishes

Freezing Transition in Decaying Burgers Turbulence and Random Matrix Dualities

On integrable directed polymer models on the square lattice

Exact mapping of the stochastic field theory for Manna sandpiles to interfaces in random media.

Equilibrium avalanches in spin glasses