Implementing a Two-Photon Three-Degrees-of-Freedom Hyper-Parallel Controlled Phase Flip Gate Through Cavity-Assisted Interactions

Hyper-parallel quantum information processing is a promising and beneficial research field. Herein, a method to implement a hyper-parallel controlled-phase-flip (hyper-CPF) gate for frequency-, spatial-, and time-bin-encoded qubits by coupling flying photons to trapped nitrogen vacancy (NV) defect centers is presented. The scheme, which differs from their conventional parallel counterparts, is specifically advantageous in decreasing against the dissipate noise, increasing the quantum channel capacity, and reducing the quantum resource overhead. The gate qubits with frequency, spatial, and time-bin degrees of freedom (DOF) are immune to quantum decoherence in optical fibers, whereas the polarization photons are easily disturbed by the ambient noise.     

First-principles study on the origin of optical transitions to be associated with F colour centers for PbWO4 crystals

The electronic structures of PbWO₄ crystals containing F type color centers with the lattice structure optimized are studied within the framework of the fully relativistic self-consistent Direc–Slater theory, using a numerically discrete variational (DV-Xα) method. The calculated results show that F and F⁺ centers have donor energy level in forbidden band. Their optical transition energy are 1.84 eV, 2.21 eV, respectively, which corresponds to the 680 nm, 550 nm absorption bands. It predicts that the 680 nm, 550 nm absorption bands originate form the F and F⁺ centers in PbWO₄ crystals.     

Effect of External Acidity of Mordenite-Supported Catalysts on the 2,2-Dimethylbutane Content in Hydroisomerization Products of n-Hexane

We have used potentiometric titration with tetrabutylammonium hydroxide to determine the acid center content on the outer surface of dealuminated natural and synthetic mordenites. We have established a symbatic relationship between the 2,2-dimethylbutane content in the hydroisomerization products of n-hexane on dealuminated palladium-containing mordenites and the number of their external acid centers. We have studied the possibility of partial deactivation of such centers during ion-exchange deposition of palladium on the catalysts, using a tetraammine palladium solution.     

高功率可调谐连续NaCl：（F2^＋）H色心激光器

报道了掺硫和掺氧ＮａＣｌ：（Ｆ２＾＋）Ｈ色心激光器最新实验结果。最高输出功率分别达３Ｗ和４．８Ｗ。实验比较了掺硫及掺氧（Ｆ２＾＋）Ｈ心的热光稳定性。     

Histidine in enzyme active centers.

The presence of histidine in the active center of an enzyme can be demonstrated by kinetic measurements, chemical modification, NMR spectroscopy or X-ray structure analysis. Histidine is the only naturally occurring amino acid to contain an imidazole residue as a side chain. The role of histidine in enzyme catalysis depends, inter alia, upon the special features of the imidazole residue: it thus tends to form hydrogen bonds, combines donor and acceptor properties and can take part in either nucleophilic or base catalysis. In some of these enzymes the position of each atom is known; however, the theories as to how the catalysis proceeds at a molecular level are controversial.     

手性5-(R)-(1′R,2′S,5′R)-孟氧基丁内酯并[3,4-b]-2(S)-6(R)-1-N-环己基氮杂环丙烷的合成及晶体结构

环己胺与手性元5-(R)-(1′R,2′S,5′R)-孟氧基-3-溴-2(5H)-呋喃酮的不对称M ichael加成/分子内亲核取代反应,得到含有两个新手性中心的氮杂环丙烷/稠合丁内酯标题化合物。对其进行了谱学表征和X-射线单晶衍射测定。标题化合物分子式为C20H33NO3,M r=335.47,三斜晶系,P1空间群,晶胞参数:a=5.438(11)。A,b=8.117(2)。A,c=11.572(2)。A,α=96.84(3)°,β=94.48(3)°,γ=101.86(3),°V=493.5(2)。A3,Z=1,D c=1.129g/cm3,R=0.0867,wR=0.2344。     

Estimating the complexity of a class of path-following methods for solving linear programs by curvature integrals

In this paper we study a particular class of primal-dual path-following methods which try to follow a trajectory of interior feasible solutions in primal-dual space toward an optimal solution to the primal and dual problem. The methods investigated are so-called first-order methods: each iteration consists of a long step along the tangent of the trajectory, followed by explicit recentering steps to get close to the trajectory again. It is shown that the complexity of these methods, which can be measured by the number of points close to the trajectory which have to be computed in order to achieve a desired gain in accuracy, is bounded by an integral along the trajectory. The integrand is a suitably weighted measure of the second derivative of the trajectory with respect to a distinguished path parameter, so the integral may be loosely called a curvature integral.     

A global Newton method II: Analytic centers

This paper modifies the convergence conditions of a back-tracking global Newton method announced in Goldstein (1991), making them sharper and easier to apply. A new version of the Kantorovich inequalities is presented that is simple to state and prove. An application is made to the centering problem for polytopes. Based on an idea of Ye (1989), an algorithm is given for the feasibility problem of linear inequalities.This paper is dedicated to Phil Wolfe on the occasion of his 65th birthday.     

Interaction of Water and Methanol Molecules with the Surface of Carbonaceous Materials According to Gas Chromatographic Data

We have used gas chromatography to study the interaction of water and methanol molecules with active hydrophilic centers on the surface of thermally expanded graphite and graphitized thermal carbon black. We have determined the concentration of carboxyl and phenol hydroxyl groups on the surface of the sorbents and the heats of adsorption for adsorption of the studied substances on these groups. We have shown that water molecules are adsorbed as clusters on the hydrophilic centers of the studied sorbents at very low relative pressures, with n = 2 molecules in the cluster.     

Surface and Subsurface Oxygen on Platinum in a Copper Perchlorate Solution

The formation of an adatom layer on polycrystalline platinum and the three-dimensional nucleation of copper in a copper perchlorate solution are studied by cyclic voltammetry at 0.1 V s^–1 while varying potential ranges and by recording potentiostatic current transients. About 0.6 monolayers of copper adatoms are deposited when cycling with anodic limit E _a = 1.35 V, the process is slower than that in an acid sulfate solution. Decreasing E _a accelerates the process (nearly one monolayer forms for E _a = 0.80–0.95 V in a cathodic scan) due to an increased number of active centers (metastable copper oxides) and, probably, to a change in the platinum surface microstructure. Oxygen for copper oxides is presumably supplied by water molecules adsorbed on a monolayer of copper adsorbed atoms and by subsurface oxygen (O_ss), which appears on the platinum surface after the destruction of complexes O_ss–Pt _n –ClO₄. Both the copper nucleation and the deposit growth accelerate at higher concentrations of copper oxides, which form at low E _a. High cathodic overvoltages decrease the number of active crystallization centers due to reduction or removal of copper oxides.