Exactly quantized dynamics of classical incommensurate sliders

We report peculiar velocity quantization phenomena in the classical motion of an idealized 1D solid lubricant, consisting of a harmonic chain interposed between two periodic sliders. The ratio v_cm/v_ext of the chain center-of-mass velocity to the externally imposed relative velocity of the sliders stays pinned to exact "plateau" values for wide ranges of parameters, such as sliders corrugation amplitudes, external velocity, chain stiffness and dissipation, and is strictly determined by the commensurability ratios alone. The phenomenon is explained by one slider rigidly dragging the kinks that the chain forms with the other slider. Possible consequences of these results for some real systems are discussed.Comment: 5 pags 4 fig

Fully inkjet-printed two-dimensional material field-effect heterojunctions for wearable and textile electronics.

Fully printed wearable electronics based on two-dimensional (2D) material heterojunction structures also known as heterostructures, such as field-effect transistors, require robust and reproducible printed multi-layer stacks consisting of active channel, dielectric and conductive contact layers. Solution processing of graphite and other layered materials provides low-cost inks enabling printed electronic devices, for example by inkjet printing. However, the limited quality of the 2D-material inks, the complexity of the layered arrangement, and the lack of a dielectric 2D-material ink able to operate at room temperature, under strain and after several washing cycles has impeded the fabrication of electronic devices on textile with fully printed 2D heterostructures. Here we demonstrate fully inkjet-printed 2D-material active heterostructures with graphene and hexagonal-boron nitride (h-BN) inks, and use them to fabricate all inkjet-printed flexible and washable field-effect transistors on textile, reaching a field-effect mobility of ~91 cm2 V-1 s-1, at low voltage (<5 V). This enables fully inkjet-printed electronic circuits, such as reprogrammable volatile memory cells, complementary inverters and OR logic gates

Quasi-1D hyperbranched WO<inf>3</inf> nanostructures for low-voltage photoelectrochemical water splitting

Arrays of hyperbranched mesostructures self-assembled from the gas phase display a decreased overpotential for the water oxidation reaction.M.B. and A.M. and F.D.F acknowledge financial support from European Union through projects PHOCS, ENERGY 2012- 10.2.1, Future Emerging Technologies Collaborative Project, grant N. 309223. G.D. and C.D. acknowledge funding from the ERC under grant number 259619 PHOTO EM.This is the accepted manuscript. The final version is available at http://pubs.rsc.org/en/Content/ArticleLanding/2015/TA/c4ta06786j#!divAbstract

Hyperbranched Quasi-1D TiO2 Nanostructure for Hybrid Organic-Inorganic Solar Cells

The performance of hybrid solar cells is strongly affected by the device morphology. In this work we demonstrate a Poly(3-hexylthiophene-2,5-diyl)/TiO2 hybrid solar cell where the TiO2 photoanode comprises an array of tree-like hyperbranched quasi-1D nanostructures self-assembled from the gas phase. This advanced architecture enables us to increase the power conversion efficiency to over 1%, doubling the efficiency with respect to state of the art devices employing standard mesoporous titania photoanodes. This improvement is attributed to several peculiar features of this array of nanostructures: high interfacial area; increased optical density thanks to the enhanced light scattering; and enhanced crystallization of Poly(3-hexylthiophene-2,5-diyl) inside the quasi-1D nanostructure

Structural properties of thin-film ferromagnetic topological insulators

We present a comprehensive study of the crystal structure of the thin-film, ferromagnetic topological insulator (Bi, Sb)2 xVxTe3 .The dissipationless quantum anomalous Hall edge states it manifests are of particular interest for spintronics, as a natural spin filter or pure spin source, and as qubits for topological quantum computing. For ranges typically used in experiments, we investigate the effect of doping, substrate choice and film thickness on the (Bi, Sb)2Te3 unit cell using high-resolution X-ray diffractometry. Scanning transmission electron microscopy and energy-dispersive X-ray spectroscopy measurements provide local structural and interfacial information. We find that the unit cell is unaffected in-plane by vanadium doping changes, and remains unchanged over a thickness range of 4–10 quintuple layers (1 QL 1 nm). The in-plane lattice parameter (a) also remains the same in films grown on different substrate materials. However, out-of-plane the c-axis increases with the doping level and thicknesses >10 QL, and is potentially reduced in films grown on Si (1 1 1).This work was financially supported by the Leverhulme Trust (RPG-2013-337), the European Commission through a Marie Curie Grant (MSCA-IFEF-ST No. 656485-Spin3), the Royal Society, and the Engineering and Physical Sciences Research Council (EP/P026311/1).C.-Z.C. and J.S.M. acknowledge support from from the NSF (DMR-1207469, DMR-1700137), ONR (N00014-13-1-0301, N00014-16-1-2657), and the STC Center for Integrated Quantum Materials under NSF grant DMR-1231319

All-Optical Detection of Neuronal Membrane Depolarization in Live Cells Using Colloidal Quantum Dots

Luminescent semiconductor quantum dots (QDs) have recently been suggested as novel probes for imaging and sensing cell membrane voltages. However, a key bottleneck for their development is a lack of techniques to assess QD responses to voltages generated in the aqueous electrolytic environments typical of biological systems. Even more generally, there have been relatively few efforts to assess the response of QDs to voltage changes in live cells. Here, we develop a platform for monitoring the photoluminescence (PL) response of QDs under AC and DC voltage changes within aqueous ionic environments. We evaluate both traditional CdSe/CdS and more biologically compatible InP/ZnS QDs at a range of ion concentrations to establish their PL/voltage characteristics on chip. Wide-field, few-particle PL measurements with neuronal cells show the QDs can be used to track local voltage changes with greater sensitivity (ΔPL up to twice as large) than state-of-the-art calcium imaging dyes, making them particularly appealing for tracking subthreshold events. Additional physiological observation studies showed that while CdSe/CdS dots have greater PL responses on membrane depolarization, their lower cytotoxicity makes InP/ZnS far more suitable for voltage sensing in living systems. Our results provide a methodology for the rational development of QD voltage sensors and highlight their potential for imaging changes in cell membrane voltage

Left-handedness and risk of breast cancer

Left-handedness may be an indicator of intrauterine exposure to oestrogens, which may increase the risk of breast cancer. Women (n=1786) from a 1981 health survey in Busselton were followed up using death and cancer registries. Left-handers had higher risk of breast cancer than right-handers and the effect was greater for post-menopausal breast cancer (hazard ratio=2.59, 95% confidence interval 1.11–6.03)

Copper Single Atoms Chelated on Ligand-Modified Carbon for Ullmann-type C−O Coupling

Cross-coupling reactions are of great importance in chemistry due to their ability to facilitate the construction of complex organic molecules. Among these reactions, the Ullmann-type C−O coupling between phenols and aryl halides is particularly noteworthy and useful for preparing diarylethers. However, this reaction typically relies on homogeneous catalysts that rapidly deactivate under harsh reaction conditions. In this study, we introduce a novel heterogeneous catalyst for the Ullmann-type C−O coupling reaction, comprised of isolated Cu atoms chelated to a tetraethylenepentamine-pyrrole ligand that is immobilized on graphite nanoplatelets. The catalytic study reveals the recyclability of the material, and demonstrates the crucial role of the pyrrole linker in stabilizing the Cu sites. The work expands the potential of single-atom catalyst nanoarchitectures and underscores the significance of ligands in stabilizing metals in cationic forms, providing a novel, tailored catalyst for cross-coupling chemistries

A Language for the Specification of Administrative Workflow Processes with Emphasis on Actors’ Views

International audienceAdministrative workflows refer to variable business processes in which all cases are known; tasks are predictable and their sequencing rules are simple and clearly defined. When such processes are collaboratively executed by several actors, it may be desirable, for security reasons (confidentiality), that each of them has at all times, only a partial perception (this is what we call "actor's view") of the current process state. This concern seems sufficiently important to be considered when specifying such workflows. However, traditional workflow specification languages (BPMN, BPEL, YAWL) only partially address it. This is why we present in this paper, a new language for specifying administrative workflows that allows us not only to simply model all of the processes tasks and their sequence, but also and especially to explicitly express the rights of the various actors with respect to each of them, in order to guarantee a certain degree of security. The proposed model is an executable grammatical specification that allows to express using decorated productions, the different types of basic flows (sequential, parallel, alternative and iterative) that are found in workflow specification languages; moreover, it also allows to specify the rights of each actor in each process and on its data in a formalism similar to that used in UNIX-like operating systems

Unveiling the Chemical Composition of Halide Perovskite Films Using Multivariate Statistical Analyses

The local chemical composition of halide perovskites is a crucial factor in determining their macroscopic properties and their stability. While the combination of scanning transmission electron microscopy (STEM) and energy-dispersive X-ray spectroscopy (EDX) is a powerful and widely used tool for accessing such information, electron-beam-induced damage and complex formulation of the films make this investigation challenging. Here we demonstrate how multivariate analysis, including statistical routines derived from “big data” research, such as principal component analysis (PCA), can be used to dramatically improve the signal recovery from fragile materials. We also show how a similar decomposition algorithm (non-negative matrix factorisation (NMF)) can unravel elemental composition at the nanoscale in perovskite films, highlighting the presence of segregated species and identifying the local stoichiometry at the nanoscale.S.C., C.D. and G.D. acknowledge funding from ERC under grant number 25961976 PHOTO EM and financial support from the EU under grant number 77 312483 ESTEEM2. S.C., C.D. and G.D. also thank Dr. Francisco de la Peña and Dr. Pierre Burdet for very helpful discussions regarding Hyperspy and MVA. The CHOSE team gratefully acknowledges the European Union's Horizon 2020 Framework Program for funding Research and Innovation under Grant agreement no. 653296 (CHEOPS). M.A.-J. thanks Nava Technology Limited, Cambridge Materials Limited and EPSRC (grant number: EP/M005143/1) for their funding and technical support. S.D.S. acknowledges support from the Royal Society and Tata Group (UF150033) and the European Research Council (ERC) under the European Union’s Horizon 2020 research and innovation programme (grant agreement number 756962)