Stronger quantum correlations with loophole-free postselection

One of the most striking nonclassical features of quantum mechanics is in the correlations it predicts between spatially separated measurements. In local hidden variable theories, correlations are constrained by Bell inequalities, but quantum correlations violate these. However, experimental imperfections lead to loopholes whereby LHV correlations are no longer constrained by Bell inequalities, and violations can be described by LHV theories. For example, loopholes can emerge through selective detection of events. In this Letter, we introduce a clean, operational picture of multiparty Bell tests, and show that there exists a nontrivial form of loophole-free postselection. Surprisingly, the same postselection can enhance quantum correlations, and unlock a connection between nonclassical correlations and nonclassical computation.     

Arrangements on Parametric Surfaces II: Concretizations and Applications

We describe the algorithms and implementation details involved in the concretizations of a generic framework that enables exact construction, maintenance, and manipulation of arrangements embedded on certain two-dimensional orientable parametric surfaces in three-dimensional space. The fundamentals of the framework are described in a companion paper. Our work covers arrangements embedded on elliptic quadrics and cyclides induced by intersections with other algebraic surfaces, and a specialized case of arrangements induced by arcs of great circles embedded on the sphere. We also demonstrate how such arrangements can be used to accomplish various geometric tasks efficiently, such as computing the Minkowski sums of polytopes, the envelope of surfaces, and Voronoi diagrams embedded on parametric surfaces. We do not assume general position. Namely, we handle degenerate input, and produce exact results in all cases. Our implementation is realized using Cgal and, in particular, the package that provides the underlying framework. We have conducted experiments on various data sets, and documented the practical efficiency of our approach.     

On the effects of gating in diffusion imaging of the brain using single shot EPI.

To reduce image artifacts in diffusion tensor imaging using single shot EPI, cardiac gating may be performed to prevent brain motion induced signal void in the DWI data. In this work the necessity of performing cardiac gating with single shot echo planar imaging has been explored using F statistics of the variance in DWI data. Peripheral measurement of the cardiac cycle has been employed because of its greater convenience, and hence use, compared to ECG gating. Four volunteers have been studied. Six different trigger delays have been evaluated in the range 18-500 ms relative the peripheral pulse wave. Brain motion was found significant in and inferior to the corpus callosum area. A trigger delay of 500 ms was found to be optimal. However, a long delay allows only for one slice per R-R interval. Therefore, a minimum trigger delay may be the best choice in terms of SNR per unit of experiment time.     

Fuzzy subobjects in a category and the theory of C-sets

In this paper we shall define the concept of a fuzzy subobject of an object in arbitrary categories. This concept is generated by the representation theorem of fuzzy sets. By using fuzzy subobjects one can include most of the fuzzy concepts defined in the literature, such as: fuzzy groups, fuzzy relations and fuzzy convex sets. In the second part of the paper we shall define a new concept; that of a $\text{C}$-set. This concept will generalize that of a fuzzy set and we shall also prove that $\text{C}$-sets can be represented by some sets of functors. More precisely, $\text{C}$-sets form a category which can be represented by a category of functors. The utility of $\text{C}$-sets resides in the fact that one can replace “ordering” by the more general concept of a morphism in category. The new representation of $\text{C}$-sets is weaker than that of fuzzy sets.     

High sensitivity gas spectroscopy of porous, highly scattering solids

We present minimalistic and cost-efficient instrumentation employing tunable diode laser gas spectroscopy for the characterization of porous and highly scattering solids. The sensitivity reaches 3 x 10(-6) (absorption fraction), and the improvement with respect to previous work in this field is a factor of 10. We also provide the first characterization of the interference phenomenon encountered in high-resolution spectroscopy of turbid samples. Revealing that severe optical interference originates from the samples, we discuss important implications for system design. In addition, we introduce tracking coils and sample rotation as new and efficient tools for interference suppression. The great value of the approach is illustrated in an application addressing structural properties of pharmaceutical materials.     

Neutron powder diffraction of metal-organic frameworks for hydrogen storage

We review recent structural studies that we have undertaken aimed at elucidating the fundamental properties of metal-organic framework materials and their interactions with hydrogen. We have shown that exposing coordinatively unsaturated metal centers can greatly enhance the hydrogen binding energy and that they result in a significant increase of the surface packing density of adsorbed hydrogen molecules on materials’ surface. We will review some of the structural aspects of these materials, especially the adsorbed hydrogen molecule surface packing density in one type of metal-organic framework, MOF-74, which can be packed even denser than that in solid hydrogen.      

Vertically aligned γ-AlOOH nanosheets on Al foils as flexible and reusable substrates for NH<Subscript>3</Subscript> adsorption

Vertically aligned γ-AlOOH nanosheets (NSs) have been successfully fabricated on flexible Al foils via a solvothermal route without morphology-directing agents. Three different reaction temperature (25, 80, and 120 ?C) and time (30 min, 45 min, and 24 h) are discussed for the growth period, which efficiently tune the density and size of the γ-AlOOH NSs. Meanwhile, the growth speed of the nanosheets confirms that dominant growth stage is seen in the initial 45 min. Furthermore, the interlayer of the γ-AlOOH NSs displays an average height of 140 nm and superhydrophilicity. By dynamic adsorption, the assynthesized γ-AlOOH NSs exhibit an outstanding NH₃ adsorption capacity of up to 146 mg/g and stably excellent regeneration for 5 cycles. The mechanism of NH₃ adsorption on the in-plane of the γ-AlOOH NSs is explained by the Lewis acid/base theory. The H-bond interactions among the NH₃ molecules and the edge groups (-OH) further improve the capture ability of the nanosheets.     

Improving the gas barrier,mechanical and thermal properties of poly(vinyl alcohol) with molybdenum disulfide nanosheets

New multifunctional materials with both high structural and gas barrier performances are important for a range of applications. Herein we present a one‐step mechanochemical process to prepare molybdenum disulfide (MoS₂) nanosheets with hydroxy functional groups that can simultaneously improve mechanical strength, thermal conductivity, and gas permittivity of a polymer composite. By homogeneously incorporating these functionalized MoS₂ nanosheets at low loading of less than 1 vol %, a poly(vinyl alcohol) (PVA) polymer exhibits elongation at break of 154%, toughness of 82 MJ/m³, and in‐plane thermal conductivity of 2.31 W/m K. Furthermore, this composite exhibits significant gas barrier performance, reducing the permeability of helium by 95%. Under fire condition, the MoS₂ nanosheets form thermally stable char, thus enhancing the material's resistance to fire. Hydrogen bonding has been identified as the main interaction mechanism between the nanofillers and the polymer matrix. The present results suggest that the PVA composite reinforced with 2D layered nanomaterial offers great potentials in packaging and fire retardant applications. © 2019 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2019 , 57, 406–414     

Absolute control of helicity at the C-termini in quinoline oligoamide foldamers by chiral oxazolylaniline moieties

Absolute one-handed chiral quinoline tetramers andoctamers containing different oxazolylanilines at the C-terminus have been synthesized.The absolute one-handed sense and diastereomeric excess values were valued by^1H NMR.X-ray crystal diffractionand CD studies reveal that the S-oxazolylaniline always induces a P-handed helicity and the absolute helicity is driven by the stable three-center hydrogen bonding between protons in the amide and N atoms in oxazolylaniline and adjacent quinoline ring.CPL investigations demonstrated that S-CQn-a-d are CPL active and its g(lum)values are dependent on its length.Interestingly,the sizes of the substituents in the chiral centers are different,howeve r,they exert no effect on the dissymmetric factors g(abs)and g(lum)of quinoline oligoamide foldamers.