In this Letter, we introduce a novel scheme for extrapolating the equation of state of QCD to finite chemical potential that features considerably improved convergence properties and allows us to extend its reach to unprecedentedly high baryonic chemical potentials. see more We present continuum extrapolated lattice results for the new expansion coefficients and show the thermodynamic observables up to μ_B/T≤3.5. This novel expansion does not suffer from the shortcomings that characterize the traditional Taylor expansion method, such as difficulties inherent in performing such an expansion with a limited number of coefficients and the poor signal-to-noise ratio that affects Taylor coefficients determined from lattice calculations.While the drop impact dynamics on stationary surfaces has been widely studied, the way a drop impacts a moving solid is by far less known. Here, we report the physical mechanisms of water drops impacting on superhydrophobic surfaces with horizontal motions. We find that a viscous force is created due to the entrainment of a thin air layer between the liquid and solid interfaces, which competes with the capillary and inertia forces, leading to an asymmetric elongation of the drop and an unexpected contact time reduction. Our experimental and theoretical results uncover consolidated scaling relations the maximum spreading diameter is controlled by both the Weber and capillary numbers D_max/D_0∼We^1/4Ca^1/6, while the dimensionless contact time depends on the capillary number τ/τ_0∼Ca^-1/6. These findings strengthen our fundamental understandings of interactions between drops and moving solids and open up new opportunities for controlling the preferred water repellency through largely unexplored active approaches.Long-distance quantum communication requires quantum repeaters to overcome photon loss in optical fibers. Here we demonstrate a repeater node with two memory atoms in an optical cavity. Both atoms are individually and repeatedly entangled with photons that are distributed until each communication partner has independently received one of them. An atomic Bell-state measurement followed by classical communication serves to establish a key. We demonstrate scaling advantage of the key rate, increase the effective attenuation length by a factor of 2, and beat the error-rate threshold of 11% for unconditionally secure communication, the corner stones for repeater-based quantum networks.In this Letter, we propose a mechanism for driving bioinspired fish swimming locomotion based on proprioceptive sensing. Proprioception provides information about and representation of a body’s position, motion, and acceleration in addition to the usual five senses. We hypothesize that a feedback loop based on this “sixth” sense results in an instability, driving the locomotion. In order to test our assumptions, we use a biomimetic robot and compare the experimental results to a simple yet generic model with excellent agreement.Free electrons provide a powerful tool for probing material properties at atomic resolution. Recent advances in ultrafast electron microscopy enable the manipulation of free-electron wave functions using laser pulses. It would be of great importance if one could combine the spatial resolution of electron microscopes with the ability of laser pulses to probe coherent phenomena in quantum systems. To this end, we propose a novel concept that leverages free electrons that are coherently shaped by laser pulses to measure quantum coherence in materials. We develop the quantum theory of interactions between shaped electrons and arbitrary qubit states in materials, and show how the postinteraction electron energy spectrum enables measuring the qubit state (on the Bloch sphere) and the decoherence or relaxation times (T_2/T_1). Finally, we describe how such electrons can detect and quantify superradiance from multiple qubits. Our scheme can be implemented in ultrafast transmission electron microscopes (UTEM), opening the way toward the full characterization of the state of quantum systems at atomic resolution.Symmetry-protected topological edge modes are one of the most remarkable phenomena in topological physics. Here, we formulate and quantitatively examine the effect of a quantum bath on these topological edge modes. Using the density matrix renormalization group method, we study the ground state of a composite system of spin-1 quantum chain, where the system and the bath degrees of freedom are treated on the same footing. We focus on the dependence of these edge modes on the global and partial symmetries of system-bath coupling and on the features of the quantum bath. It is shown that the time-reversal symmetry (TRS) plays a special role for an open quantum system, where an emergent partial TRS breaking will result in a TRS-protected topological mode diffusing from the system edge into the bath, thus make it useless for quantum computation.Spin-charge conversion via spin-orbit interaction is one of the core concepts in the current spintronics research. The efficiency of the interconversion between charge and spin current is estimated based on Berry curvature of Bloch wave function in the linear-response regime. Beyond the linear regime, nonlinear spin-charge conversion in the higher-order electric field terms has recently been demonstrated in noncentrosymmetric materials with nontrivial spin texture in the momentum space. Here, we report the observation of the nonlinear charge-spin conversion in a nominally centrosymmetric oxide material SrIrO_3 by breaking inversion symmetry at the interface. A large second-order magnetoelectric coefficient is observed at room temperature because of the antisymmetric spin-orbit interaction at the interface of Dirac semimetallic bands, which is subject to the symmetry constraint of the substrates. Our study suggests that nonlinear spin-charge conversion can be induced in many materials with strong spin-orbit interaction at the interface by breaking the local inversion symmetry to give rise to spin splitting in otherwise spin degenerate systems.Measured angular distributions of photoelectrons from size-selected copper and sodium cluster anions are demonstrated to exhibit a universal behavior independent of the initial electron state, cluster size, or material, which can be traced back to momentum conservation upon photoemission. Quantum simulations reproduce the universality under the assumption that multielectron dynamics localizes the emission on the cluster surface and renders the cluster opaque to photoelectrons, thereby quenching interference effects that would otherwise obscure this almost classical behavior.