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Direct proton-knockout reactions of ^{55}Sc at ∼220 MeV/nucleon were studied at the RIKEN Radioactive Isotope Beam Factory. Populated states of ^{54}Ca were investigated through γ-ray and invariant-mass spectroscopy. Level energies were calculated from the nuclear shell model employing a phenomenological internucleon interaction. Theoretical cross sections to states were calculated from distorted-wave impulse approximation estimates multiplied by the shell model spectroscopic factors, which describe the wave function overlap of the ^{55}Sc ground state with states in ^{54}Ca. Despite the calculations showing a significant amplitude of excited neutron configurations in the ground-state of ^{55}Sc, valence proton removals populated predominantly the ground state of ^{54}Ca. This counterintuitive result is attributed to pairing effects leading to a dominance of the ground-state spectroscopic factor. Owing to the ubiquity of the pairing interaction, this argument should be generally applicable to direct knockout reactions from odd-even to even-even nuclei.

We derive fundamental per-channel bounds on angle-integrated absorption and thermal radiation for arbitrary bodies---for any given material susceptibility and bounding region---that simultaneously encode both the per-volume limit on polarization set by passivity and geometric constraints on radiative efficiencies set by finite object sizes through the scattering $\mathbb{T}$-operator. We then analyze these bounds in two practical settings, comparing against prior limits as well as near optimal structures discovered through topology optimization. Principally, we show that the bounds properly capture the physically observed transition from the volume scaling of absorptivity seen in deeply subwavelength objects (nanoparticle radius or thin film thickness) to the area scaling of absorptivity seen in ray optics (blackbody limits)., Comment: 9 pages including appendices, 2 figures, 1 table

Exclusive cross sections and momentum distributions have been measured for quasifree one-neutron knockout reactions from a ^{54}Ca beam striking on a liquid hydrogen target at ∼200 MeV/u. A significantly larger cross section to the p_{3/2} state compared to the f_{5/2} state observed in the excitation of ^{53}Ca provides direct evidence for the nature of the N=34 shell closure. This finding corroborates the arising of a new shell closure in neutron-rich calcium isotopes. The distorted-wave impulse approximation reaction formalism with shell model calculations using the effective GXPF1Bs interaction and ab initio calculations concur our experimental findings. Obtained transverse and parallel momentum distributions demonstrate the sensitivity of quasifree one-neutron knockout in inverse kinematics on a thick liquid hydrogen target with the reaction vertex reconstructed to final state spin-parity assignments.

In a previous Letter, we derived fundamental limits to radiative heat transfer applicable in near- through far-field regimes, based on the choice of material susceptibilities and bounding surfaces enclosing arbitrarily shaped objects; the limits exploit algebraic properties of Maxwell's equations and fundamental principles such as electromagnetic reciprocity and passivity. In this Letter, we apply these bounds to two different geometric configurations of interest, namely dipolar particles or extended structures of infinite area in the near field of one another. We find that while near-field radiative heat transfer between dipolar particles can saturate purely geometric ``Landauer'' limits, bounds on extended structures cannot, instead growing very slowly with respect to a material response figure of merit (an ``inverse resistivity'' for metals) due to the deleterious effects of multiple scattering between bodies. While nanostructuring can produce infrared resonances, it is generally unable to further enhance the resonant energy transfer spectrum beyond what is practically achieved by planar media at the surface polariton condition.

The first γ-ray spectroscopy of ^{52}Ar, with the neutron number N=34, was measured using the ^{53}K(p,2p) one-proton removal reaction at ∼210 MeV/u at the RIBF facility. The 2_{1}^{+} excitation energy is found at 1656(18) keV, the highest among the Ar isotopes with N>20. This result is the first experimental signature of the persistence of the N=34 subshell closure beyond ^{54}Ca, i.e., below the magic proton number Z=20. Shell-model calculations with phenomenological and chiral-effective-field-theory interactions both reproduce the measured 2_{1}^{+} systematics of neutron-rich Ar isotopes, and support a N=34 subshell closure in ^{52}Ar.

We formulate and exploit a computational inverse-design method based on topology optimization to demonstrate photonic crystal structures supporting complex spectral degeneracies. In particular, we discover photonic crystals exhibiting third-order Dirac points formed by the accidental degeneracy of monopolar, dipolar, and quadrupolar modes. We show that, under suitable conditions, these modes can coalesce and form a third-order exceptional point, leading to strong modifications in the spontaneous emission (SE) of emitters, related to the local density of states. We find that SE can be enhanced by a factor of 8 in passive structures, with larger enhancements ∼sqrt[n^{3}] possible at exceptional points of higher order n.

We show that the near-field functionality of hyperbolic metamaterials (HMM), typically proposed for increasing the photonic local density of states (LDOS), can be achieved with thin metal films. Although HMMs have an infinite density of internally-propagating plane-wave states, the external coupling to nearby emitters is severely restricted. We show analytically that properly designed thin films, of thicknesses comparable to the metal size of a hyperbolic metamaterial, yield a LDOS as high as (if not higher than) that of HMMs. We illustrate these ideas by performing exact numerical computations of the LDOS of multilayer HMMs, along with their application to the problem of maximizing near-field heat transfer, to show that thin films are suitable replacements in both cases., Comment: 5 pages, 3 figures

We predict that a low-permittivity oblate body (disk-shaped object) above a thin metal substrate (plate with a hole) immersed in a fluidof intermediate permittivity will experience a meta-stable equilibrium (restoring force) near the center of the hole. Stability is the result of a geometry-induced transition in the sign of the force, from repulsive to attractive, that occurs as the disk approaches the hole---in planar or nearly-planar geometries, the same material combination yields a repulsive force at all separations in accordance with the Dzyaloshinskii--Lifshitz--Pitaevskii condition of fluid-induced repulsion between planar bodies. We explore the stability of the system with respect to rotations and lateral translations of the disks, and demonstrate interesting transitions (bifurcations) in the rotational stability of the disks as a function of their size. Finally, we consider the reciprocal situation in which the disk--plate materials are interchanged, and find that in this case the system also exhibits meta-stability. The forces in the system are sufficiently large to be observed in experiments and should enable measurements based on the diffusion dynamics of the suspended bodies.

We predict that the near-field radiative heat-transfer rate between a cylinder and a perforated surface depends nonmonotonically on their separation. This anomalous behavior, which arises due to evanescent-wave effects, is explained using a heuristic model based on the interaction of a dipole with a plate. We show that nonmonotonicity depends not only on geometry and temperature but also on material dispersion---for micron and submicron objects, nonmonotonicity is present in polar dielectrics but absent in metals with small skin depths.

The fastest self-sustained chemical reactions in nature occur during detonation of energetic materials where reactions are thought to occur on nanosecond or longer time scales in carbon-containing materials. Here we perform the first atomistic simulation of an azide energetic material, ${\mathrm{HN}}_{3}$, from the beginning to the end of the chemical evolution and find that the time scale for complete decomposition is a mere 10 ps, orders of magnitude shorter than that of secondary explosives and approaching the fundamental limiting time scale for chemistry; i.e., vibrational time scale. We study several consequences of the short time scale including a state of vibrational disequilibrium induced by the fast transformations.

We demonstrate the possibility of achieving enhanced frequency-selective near-field radiative heat transfer between patterned (photonic-crystal) slabs at designable frequencies and separations, exploiting a general numerical approach for computing heat transfer in arbitrary geometries and materials based on the finite-difference time-domain method. Our simulations reveal a tradeoff between selectivity and near-field enhancement as the slab-slab separation decreases, with the patterned heat transfer eventually reducing to the unpatterned result multiplied by a fill factor (described by a standard proximity approximation). We also find that heat transfer can be further enhanced at selective frequencies when the slabs are brought into a glide-symmetric configuration, a consequence of the degeneracies associated with the nonsymmorphic symmetry group.

We propose a method of achieving large temperature sensitivity in the Casimir force that involves measuring the stable separation between dielectric objects immersed in fluid. We study the Casimir force between slabs and spheres using realistic material models, and find large > 2nm/K variations in their stable separations (hundreds of nanometers) near room temperature. In addition, we analyze the effects of Brownian motion on suspended objects, and show that the average separation is also sensitive to changes in temperature . Finally, this approach also leads to rich qualitative phenomena, such as irreversible transitions, from suspension to stiction, as the temperature is varied.

We present a scheme for obtaining stable Casimir suspension of dielectric nontouching objects immersed in a fluid, validated here in various geometries consisting of ethanol-separated dielectric spheres and semi-infinite slabs. Stability is induced by the dispersion properties of real dielectric (monolithic) materials. A consequence of this effect is the possibility of stable configurations (clusters) of compact objects, which we illustrate via a "molecular" two-sphere dicluster geometry consiting of two bound spheres levitated above a gold slab. Our calculations also reveal a strong interplay between material and geometric dispersion, and this is exemplified by the qualitatively different stability behavior observed in planar versus spherical geometries.

We introduce an efficient technique for computing Casimir energies and forces between objects of arbitrarily complex 3D geometries. In contrast to other recently developed methods, our technique easily handles non-spheroidal, non-axisymmetric objects and objects with sharp corners. Using our new technique, we obtain the first predictions of Casimir interactions in a number of experimentally relevant geometries, including crossed cylinders and tetrahedral nanoparticles., Comment: 4 pages, 4 figures