Magnetic Exciton-Polariton with Strongly Coupled Atomic and Photonic Anisotropies

Anisotropy plays a key role in science and engineering. However, the interplay between the material and engineered photonic anisotropies has hardly been explored due to the vastly different length scales. Here we demonstrate a matter-light hybrid system, exciton-polaritons in a 2D antiferromagnet, CrSBr, coupled with an anisotropic photonic crystal (PC) cavity, where the spin, atomic lattice, and photonic lattices anisotropies are strongly correlated, giving rise to unusual properties of the hybrid system and new possibilities of tuning. We show exceptionally strong coupling between engineered anisotropic optical modes and anisotropic excitons in CrSBr, which is stable against excitation densities a few orders of magnitude higher than polaritons in isotropic materials. Moreover, the polaritons feature a highly anisotropic polarization tunable by tens of degrees by controlling the matter-light coupling via, for instance, spatial alignment between the material and photonic lattices, magnetic field, temperature, cavity detuning and cavity quality-factors. The demonstrated system provides a prototype where atomic- and photonic-scale orders strongly couple, opening opportunities of photonic engineering of quantum materials and novel photonic devices, such as compact, on-chip polarized light source and polariton laser

2D Semiconductor Nonlinear Plasmonic Modulators

A plasmonic modulator is a device that controls the amplitude or phase of propagating plasmons. In a pure plasmonic modulator, the presence or absence of a pump plasmonic wave controls the amplitude of a probe plasmonic wave through a channel. This control has to be mediated by an interaction between disparate plasmonic waves, typically requiring the integration of a nonlinear material. In this work, we demonstrate the first 2D semiconductor nonlinear plasmonic modulator based on a WSe2 monolayer integrated on top of a lithographically defined metallic waveguide. We utilize the strong coupling between the surface plasmon polaritons, SPPs, and excitons in the WSe2 to give a 73 percent change in transmission through the device. We demonstrate control of the propagating SPPs using both optical and SPP pumps, realizing the first demonstration of a 2D semiconductor nonlinear plasmonic modulator, with a modulation depth of 4.1 percent, and an ultralow switching energy estimated to be 40 aJ

Problems in the assessment of magnesium depletion in the rat by in vivo 31P NMR

Prior in vitro studies, utilizing 31Pn uclear magnetic resonance (31PN MR) to measure the chemical shift (CT) of 0-ATP and lengthening of the phosphocreatine spin-spin (7"') relaxation time, suggested an assessment of their efficacy in measuring magnesium depletion in vivo. Dietary magnesium depletion (Me$) produced markedly lower magnesium in plasma (0.44 vs 1. I3 mmol/liter) and bone (1 30 vs 190 pmol/g) but much smaller changes in muscle (41 vs 45 pmol/g, P < 0.01), heart (42.5 vs 44.6 prnol/g), and brain (30 vs 32 pmollg). NMR experiments in anesthetized rats in a Bruker 7-T vertical bore magnet showed that in M e$ rats there was a significant change in brain j3-ATP shift (16.15 vs 16.03 ppm, P < 0.05). These chemical shifts gave a calculated free [Mg"] of 0.71 mM (control) and 0.48 mM (MgZ+$). In muscle the change in j3-ATP shift was not significant (Me$ 15.99 ppm, controls 15.96 ppm), corresponding to a calculated free M P of 0.83 and 0.95 mM, respectively. Phosphccreatine Tz (Carr-Purcell, spin-echo pulse sequence) was no different with M e $in muscle in vivo (surface coil) (M$+$136, control 142 ms) or in isolated perfused hearts (Helmholtz coil) (control 83, M e$ 92 ms). 3'P NMR is severely limited in its ability to detect dietary magnesium depletion in vivo. Measurement of j3-ATP shift in brain may allow studies of the effects of interaction in group studies but does not allow prediction of an individual magnesium status

Macroscopic transition metal dichalcogenides monolayers with uniformly high optical quality

The optical quality of large-area transition metal dichalcogenide (TMD) monolayers is usually limited by surface defects and inhomogeneities. Here, the authors report a method based on 1-dodecanol encapsulation to improve the optical properties of TMD monolayers over mm-scale, enabling the fabrication of an array of polariton photonic crystal cavities

Toward the accurate modeling of amorphous nonlinear materialspolymer stress relaxation (I)

We expand our analytical modeling strategy for polymer non-linear stress relaxation (A) to specify the remaining steps to accurately deal with the nonaffine nature of the materials' local strains and stresses relative to their average overall values, and (B) to make it consistent with a new cooperative theory of amorphous materials dynamics, providing a model of tunable fragility that sheds light to most aspects of the behavior, including the glass transition. The stress relaxation models (1) describe a nonlinear (strain-dependent) behavior that becomes linear at very low strains, (2) quantify the effect of temperature, (3) may quantify the effects of changes in free volume, and (4) ensure very fast computations of the materials' response irrespective of the experimental time scale. The models are sensitive to the influence of different initial states of the material, as may result from varying degrees of molecular orientation and aging levels, and are able to predict from experimental stress relaxation moduli (for a poly (methylmethacrylate)PMMA and a bis-phenol-A polycarbonatePC) the values of the crossover frequency, (c), crossover temperature, T-c, and the minimum activation energy, in addition to the initial and long-time plateau moduli, in agreement with independently measured values. POLYM. ENG. SCI., 56:348-360, 2016. (c) 2016 Society of Plastics Engineer