640 Gbits/s photonic logic gates

We demonstrate 640 Gbits/s all-optical A AND B, and ā AND B logic functions using pump depletion in a periodically poled lithium niobate waveguide. Bit-error-rate measurements show the effectiveness of the scheme, with a penalty of <2 dB.     

Near-surface turbulence in the atmospheric boundary layer

Measurements of the near-surface turbulence in the atmospheric boundary layer have been made using hot-wire probes above the salt flats of northwestern Utah, where the momentum thickness Reynolds number, R_θ, is O(10⁶), and the surface is smooth and nearly devoid of flow obstructions. The measurements were made with arrays of up to 24 parallel straight sensors and with a modular 12-sensor probe capable of measuring all of the components of the instantaneous velocity vector and velocity gradient tensor. Measurements were also made in a laboratory wind tunnel at R_θ=1730 using 22 straight sensors. The data analysis focuses on the effects of the Reynolds number on turbulence properties and on the physics of the dissipation rate of turbulent kinetic energy.Some properties are found to be dependent on the Reynolds number when normalized with inner variables, while others are not. Among those that show the significant Reynolds number dependence are the rms and the skewness factor of the streamwise velocity fluctuations.Significant differences in flow structure, particularly those related to high rates of dissipation, are implied by the data. The joint PDF and covariance integrand of streamwise and wall normal vorticity fluctuations show less preferred orientation of the vorticity vector in the buffer layer at R_θ of O(10⁶) than at R_θ=1070. The largest contribution to the dissipation rate, at O(10⁶) is by the ∂w/∂z velocity gradient, while this term makes a quite small contribution to the dissipation rate at low R_θ. Here w and z are the spanwise velocity fluctuations and direction, respectively. Conditional analysis in the streamwise-wall normal (x−y) plane based on high instantaneous dissipation rate shows that the typical high dissipation rate events are generally similar at high and low Reynolds numbers, but display some significant differences.     

Extended Antipodal Theorems

In infinite-dimensional Hilbert spaces, we prove that the iterative sequence generated by the extragradient method for solving pseudo-monotone variational inequalities converges weakly to a solution. A class of pseudo-monotone variational inequalities is considered to illustrate the convergent behavior. The result obtained in this note extends some recent results in the literature; especially, it gives a positive answer to a question raised in Khanh (Acta Math Vietnam 41:251–263, 2016).     

Real-variables characterization of generalized Stieltjes functions

We obtain a characterization of generalized Stieltjes functions of any order λ>0$\lambda >0$ in terms of inequalities for their derivatives on (0,∞)$(0,\infty )$. When λ=1$\lambda =1$, this provides a new and simple proof of a characterization of Stieltjes functions first obtained by Widder in 1938.     

Liquid structure of the ionic liquid 1,3-dimethylimidazolium bis[(trifluoromethyl)sulfonyl]amide

Neutron diffraction has been used to determine the liquid structure of 1,3-dimethylimidazolium bis[(trifluoromethyl)sulfonyl]amide ([dmim][NTf2]). Significantly smaller charge ordering is found in this liquid compared with analogous chloride and hexafluorophosphate salts due to the diffuse charge density and size of the [NTf2]- anion. This is manifested in a much larger cation-cation and cation-anion separation and an overlap of the cation-cation and cation-anion shells. Comparison of the liquid structure with the crystal structure reported by Holbrey et al. (Dalton Trans. 2004, 2267) indicates little correlation, for example, the [NTf2]- anion adopts a trans orientation predominantly in the liquid whereas a cis orientation is found in the solid phase.     

Synthesis and characterization of long perylenediimide polymer fibers: from bulk to the single-molecule level

The synthesis and characterization of perylenediimide polyisocyanides is reported. In addition to short oligomers, our synthetic approach results in the formation of extremely long, well-defined, and rigid perylenediimide polymers. Ordering and close-packing of the chromophores in these long polymers is guaranteed by attachment to a polyisocyanide backbone with amino acid side chains. Hydrogen bonding interactions between those groups stabilize and rigidify the helical polymer structure. The rodlike nature of the synthesized long perylenediimide pendant polyisocyanides as well as the helical arrangement of the chromophores is demonstrated by means of atomic force microscopy. Remarkably, polymer fibers up to 1 mum in length have been visualized, containing several thousands of perylenediimide molecules. Circular dichroism spectroscopy reveals the chiral organization of the chromophore units in the polymer, whereas absorption and emission measurements prove the occurrence of excited-state interactions between those moieties due to the close packing of the chromophore groups. However, an intricate optical behavior is encountered in bulk as a result of the coexistence of short oligomers and long polymers of perylenediimide, a situation subsequently uncovered by means of single-molecule experiments. Individual long helical perylenediimide polyisocyanides exhibit a typical red-shifted fluorescence spectrum, which, together with depolarized emission continuously decreasing in time, demonstrate that fluorescence arises from multiple excimer-like species in the polymer. Upon continuous irradiation of these long polymers, a fast decay in fluorescence lifetime is observed, a situation explained by photoinduced creation of quenching sites. Radical/ion formation by intramolecular electron transfer between close-by perylenediimide moieties is the most probable mechanism for this process. Appropriate control of the electron-transfer process might open the possibility of applying these polymers as perylenediimide-based supramolecular nanowires.     

Probing electron transfer dynamics at MgO surfaces by Mg-atom desorption

Ultraviolet excitation of high surface area MgO films using 4.7 eV femtosecond pulses results in neutral Mg-atom desorption with hyperthermal kinetic energies in the range 0.1-0.4 eV. The Mg-atom hyperthermal energies and power dependences are similar to those previously observed using nanosecond pulsed excitation. Femtosecond two-pulse correlation measurements reveal the existence of different dynamical paths for Mg-atom desorption. One mechanism displays a sub-150 fs time scale and involves the simultaneous or near-simultaneous transition of two electrons to a 3-coordinated Mg(2+) site. Other paths display picosecond time scales that we associate with dynamics following electron trapping at 3-coordinated Mg(2+) surface sites.     

Experimental charge density study of estrogens: 17beta-estradiol.urea

To relate the molecular electrostatic potential to the biological activities of estrogens, a comparative charge density study of different derivatives has been initiated. The second completed charge density analysis of this series for 17beta-estradiol*urea is presented here. This is a large organic system with 52 atoms in a noncentrosymmetric space group, therefore special tools such as an optimal coordinate system and slow, initially constrained refinement have been used to accomplish this study. Our results for the urea molecule reasonably agree with previous experimental and theoretical results. In the 17beta-estradiol molecule, the oxygen atoms appear to be close to sp3 in shape, exhibiting two consistent, distinct lone pairs despite different chemical environments. No significant interaction of the hydroxyl group oxygen with the orbitals of the aromatic ring is observed. Analysis of the electrostatic potential revealed that the negative potential in the lone pair region of the two oxygen atoms is quite different. The topological analysis of the electron density has been performed, and the atomic charges have been estimated.