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The mechanical response of naturally abundant amorphous solids such as gels, jammed grains, and biological tissues are not described by the conventional paradigm of broken symmetry that defines crystalline elasticity. In contrast, the response of such athermal solids are governed by local conditions of mechanical equilibrium, i.e., force and torque balance of its constituents. Here we show that these constraints have the mathematical structure of a generalized electromagnetism, where the electrostatic limit successfully captures the anisotropic elasticity of amorphous solids. The emergence of elasticity from local mechanical constraints offers a new paradigm for systems with no broken symmetry, analogous to emergent gauge theories of quantum spin liquids. Specifically, our U(1) rank-2 symmetric tensor gauge theory of elasticity translates to the electromagnetism of fractonic phases of matter with the stress mapped to electric displacement and forces to vector charges. We corroborate our theoretical results with numerical simulations of soft frictionless disks in both two and three dimensions, and experiments on frictional disks in two dimensions. We also present experimental evidence indicating that force chains in granular media are subdimensional excitations of amorphous elasticity similar to fractons.We study the unconventional superconducting correlations caused by a single isolated magnetic impurity in a conventional s-wave superconductor. Because of the local breaking of time-reversal symmetry, the impurity induces unconventional superconductivity, which is even in both space and spin variables but odd under time inversion. We derive an exact proportionality relation between the even-frequency component of the local electron density of states and the imaginary part of the odd-frequency local pairing function. #link# By applying this relation to scanning tunneling microscopy spectra taken on top of magnetic impurities immersed in a Pb/Si(111) monolayer, we show experimental evidence of the occurrence of the odd-frequency pairing in these systems and explicitly extract its superconducting function from the data.Quantum networks play a major role in long-distance communication, quantum cryptography, clock synchronization, and distributed quantum computing. Generally, these protocols involve many independent sources sharing entanglement among distant parties that, upon measuring their systems, generate correlations across the network. The question of which correlations a given quantum network can give rise to remains almost uncharted. Here we show that constraints on the observable covariances, previously derived for the classical case, also hold for quantum networks. The network topology yields tests that can be cast as semidefinite programs, thus allowing for the efficient characterization of the correlations in a wide class of quantum networks, as well as systematic derivations of device-independent and experimentally testable witnesses. We obtain such semidefinite tests for fixed measurement settings, as well as parties that independently choose among collections of measurement settings. The applicability of the method is demonstrated for various networks, and compared with previous approaches.Modern experimental platforms such as superconducting circuit arrays call for the exploration of bosonic tight-binding models in unconventional situations with no counterpart in real materials. Here we investigate one such situation in which excitations are driven and damped by pairs, leading to pattern formation and exotic bosonic states emerging from a nonequilibrium quantum many-body system. Focusing on a two-dimensional driven-dissipative Bose-Hubbard model, we find that its steady states are characterized by the condensation of bosons around momenta lying on a "Bose surface," a bosonic analog of the Fermi surface in solid-state systems. The interplay between instabilities generated by the driving, the nonlinear dissipative mode coupling, and the underlying lattice effect allows the system to equilibrate into an exotic superfluid state of bosons condensed on a closed ring in momentum space instead of discrete points. Such an unconventional state with a spatially uniform density distribution goes beyond the traditional scope of pattern formation and thus has no counterpart in the classical literature. In addition, it is a state connected to several open problems in modern condensed-matter physics. Here we provide the means to stabilize it, opening the way to its experimental study. Moreover, we also provide a concrete experimental implementation of our model in currently available superconducting circuit arrays. We also investigate the relaxation spectrum around the condensate, which shows a characteristic purely diffusive behavior.The exciton-phonon coupling in highly oriented pyrolytic graphite is studied using resonant inelastic x-ray scattering (RIXS) spectroscopy. With ∼70  meV energy resolution, multiple low energy excitations associated with coupling to phonons can be clearly resolved in the RIXS spectra. link2 Using resonance dependence and the closed form for RIXS cross section without considering the intermediate state mixing of phonon modes, the dimensionless coupling constant g is determined to be 5 and 0.35, corresponding to the coupling strength of 0.42  eV+/-20  meV and 0.20  eV+/-20  meV, for zone center and boundary phonons, respectively. The reduced g value for the zone-boundary phonon may be related to its double resonance nature.Small sugars are known to stabilize biological membranes under extreme conditions of freezing and desiccation. The proposed mechanisms of stabilization suggest membrane-sugar interactions to be either attractive or repulsive. To obtain new insight into the problem, we use a recently developed low-frequency Raman scattering approach which allows detecting membrane mechanical vibrations. For selleck products of palmitoyl-oleoyl-glycero-phosphocholine (POPC) hydrated in aqueous sucrose and trehalose solutions, we studied the Raman peak between 12 and 15 cm-1 that is attributed to an eigenmode of the normal mechanical vibrations of a lipid monolayer. link3 For both sugars, similar results were obtained. With an increase in sugar concentration in solution, the frequency position of the peak was found to decrease by ∼13% which was interpreted as a consequence of the membrane thickening due sugar monolayer adsorption on the membrane surface. The concentration dependence of the peak frequency position was satisfactorily described by a Langmuir monolayer adsorption model. It is concluded that, at small sugar concentrations (less than 0.2 M), the membrane-sugar interactions are attractive, while at higher concentrations (more than 0.4 M) the attraction disappears. The data obtained show that one sugar molecule on the surface interacts with approximately 3-4 polar lipid heads.We report measurements of current-induced thermoelectric and spin-orbit torque effects within devices in which multilayers of the semiconducting two-dimensional van der Waals magnet Cr2Ge2Te6 (CGT) are integrated with Pt and Ta metal overlayers. We show that the magnetic orientation of the CGT can be detected accurately either electrically (using an anomalous Hall effect) or optically (using magnetic circular dichroism) with good consistency. The samples exhibit large thermoelectric effects, but nevertheless, the spin-orbit torque can be measured quantitatively using the angle-dependent second harmonic Hall technique. For CGT/Pt, we measure the spin-orbit torque efficiency to be similar to conventional metallic-ferromagnet/Pt devices with the same Pt resistivity. The interfacial transparency for spin currents is therefore similar in both classes of devices. Our results demonstrate the promise of incorporating semiconducting 2D magnets within spin-orbitronic and magneto-thermal devices.The exploration of Pickering emulsions is very significant owing to their versatile and important applications in many scopes. In this study, synthesis of a novel kind of single-chain polymer nanoparticle (SCPN) and its stabilized Pickering emulsions were demonstrated. To this end, linear-dendritic diblock copolymers consisting of poly((2-dimethylamino) ethyl methacrylate) (PDMAEMA) blocks and four-generation dendritic aliphatic polyester blocks (G4) have been first synthesized by the combination of click chemistry and reversible addition-fragmentation chain transfer (RAFT) polymerization reaction. The subsequent intramolecular cross-linking of the PDMAEMA block of PDMAEMA-b-G4 copolymers in DMF using 1,4-diiodobutane as cross-linkers afforded Janus-like SCPNs that exhibited a cross-linked PDMAEMA head tethered by a short dendritic tail. The molecular weight and distribution together with the structure of polymers were carefully characterized by GPC and NMR spectroscopy. By the employment of the as-synthesized Janus-like SCPNs as Pickering emulsifiers, aqueous and nonaqueous Pickering emulsions including water-in-oil and oil-in-oil as well as ionic liquid-in-oil were generated. Under the same conditions, it was found that the long-term stabilities of Pickering emulsions stabilized by Janus-like SCPNs were superior to those of Pickering emulsions stabilized by their linear quaternized PDMAEMA-b-G4 by CH3I analogous.Activating mutations in FLT3 receptor tyrosine kinase are found in a third of acute myeloid leukemia (AML) patients and are associated with disease relapse and a poor prognosis. The majority of these mutations are internal tandem duplications (ITDs) in the juxtamembrane domain of FLT3, which have been validated as a therapeutic target. The clinical success of selective inhibitors targeting oncogenic FLT3, however, has been limited due to the acquisition of drug resistance. Herein the identification of a dual FLT3/microtubule polymerization inhibitor, chalcone 4 (2'-allyloxy-4,4'-dimethoxychalcone), is reported through screening of 15 related chalcones for differential antiproliferative activity in leukemia cell lines dependent on FLT3-ITD (MV-4-11) or BCR-ABL (K562) oncogenes and by subsequent screening for mitotic inducers in the HCT116 cell line. Three natural chalcones (1-3) were found to be differentially more potent toward the MV-4-11 (FLT3-ITD) cell line compared to the K562 (BCR-ABL) cell line. Notably, the new semisynthetic chalcone 4, which is a 2'-O-allyl analogue of the natural chalcone 3, was found to be more potent toward the FLT3-ITD+ cell line and inhibited FLT3 signaling in FLT3-dependent cells. An in vitro kinase assay confirmed that chalcone 4 directly inhibited FLT3. Moreover, chalcone 4 induced mitotic arrest in these cells and inhibited tubulin polymerization in both cellular and biochemical assays. Treatment of MV-4-11 cells with this inhibitor for 24 and 48 h resulted in apoptotic cell death. Finally, chalcone 4 was able to overcome TKD mutation-mediated acquired resistance to FLT3 inhibitors in a MOLM-13 cell line expressing FLT3-ITD with the D835Y mutation. Chalcone 4 is, therefore, a promising lead for the discovery of dual-target FLT3 inhibitors.Electrospray ionization mass spectrometry supported by mobility classification (ESI-DMA-MS) is a strong technique for a comprehensive analysis of organic and inorganic clusters and small nanoparticles. In-depth understanding and optimization of the electrospray process are key for unlocking new fields of application and for extension of the accessible range of data. We show that the combination of mobility-classified mass spectrometry (DMA-MS) with an electrospray operated in a well-defined cone-jet mode is capable of providing a full picture of the outcome of the electrospray process including the evaporation residues of the parent droplets. Based on ESI-DMA-MS measurements of lysozyme, we find that clusters up to almost 1 MDa (around 60 lysozyme molecules per cluster) formed as evaporation residues of the parent droplets can be detected. The escape probability of lysozyme molecules from the parent droplets is polarity-dependent. A quantitative analysis of clusters is possible at analyte concentrations where the likeliness of finding more than a single molecule in the generated droplet is low.

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