Harmonic and attosecond pulse enhancement in the presence of noise

In this paper, we theoretically investigate the effect of noise on the photoionization, the generation of the high-order harmonic and the attosecond pulse irradiated from a model He＋ ion. It shows that by properly adding noise fields, such as Gaussian white noise, random light or colored noise, both the ionization probabilities （IPs） and the harmonic yields can be enhanced by several orders of magnitude. Further, by tuning the noise intensity, a stochastic resonance-like curve is observed, showing the existence of an optimal noise in the ionization enhancement process. Finally, by superposing a properly selected harmonic, an intense attosecond pulse with a duration of 67 as is directly generated.

Absorption Ability of Different M/G Values of Alginate Fiber

不同的钠 alginate 的 M/G 价值借助于 1H-NMR 被学习。alginate 纤维经由湿旋转的技术被准备。M/G， sodium-alginate 的集中，凝结洗澡的集中和 alginate 纤维的吸收性的能力上的凝结的时间的效果被讨论。结果证明不同物质的吸收性的能力在如此的顺序变化：生理盐 > 血 > 自来水 > 提取的水。alginate 纤维的吸收性的能力随 M/G 价值的增加和 sodium-aiginate 的集中增加。逐渐地增加凝结洗澡的 conceatration，它增加直到集中直到 5% 。然而，它与持续减少使时间凝结。

Mechanism of Excited State Double Proton Transfer in 2-Amino-3-Methoxypyridine and Acetic Acid Complex

The excited-state double-proton transfer （ESDPT） mechanism of 2-amino-3-methoxypyridine and acetic acid com- plex is studied by the density functional theory （DFT） and time-dependent DFT with CAM-B3LYP functional. The complex is connected through two different types of inter-molecular hydrogen bonds. After photo-excitation, both hydrogen bonds get strengthened, which can facilitate the ESDPT reaction. The scanned potential energy curve along the proton transfer coordinate indicates that the ESDPT reaction proceeds in a stepwise pattern.

The stereodynamic properties of the F+HO(v,j) → HF+O reaction on^1 A' and ~3A' potential energy surfaces by quasi-classical trajectory calculations:Initial excitation effect(v=1-3, j=0 and v= 0, j=1-3)

The stereodynamic properties of the F ＋ HO （v, j） reaction are explored by quasi-classical trajectory （QCT） calculations performed on the 1At and 3At potential energy surfaces （PESs）. Based on the polarization-dependent differential cross sections （PDDCSs） and the angular distributions of the product angular momentum with the reactant at different values of initial v or j, the results show that the product scattering and product polarization have strong links with initial vibrationalrotational numbers of v and j. The significant manifestation of the normal DCSs is that the forward scattering gradually becomes predominant with the initial vibrational excitation increasing, and the scattering angle of the HF product taking place on the 3At potential energy surface is found to be more sensitive to the initial value of v. The product orientation and alignment are strongly dependent on the initial rovibrational excitation effect. With enhancement in the initial rovibrational excitation effect, there is an overall decrease in the product orientation as well as in the product alignment either perpendicular to the reagent relative velocity vector k or along the direction of the y axis, for which the initial rotational excitation effect is much more noticeable than the vibrational excitation effect. Moreover, the initial rovibrational excitation effect on the product polarization is more pronounced for the 3At potential energy surface than for the 1At potential energy surface.

Influence of Isotope Effects on Product Polarizations of N(~2D)+D_2, N(~2D)+H_2 and N(~2D)+HD Reactive Systems

To figure out the influence of isotope effect on product polarizations of the N（2D）＋D2 reactive system and its isotope variants, quasi-classical trajectory（QCT） calculation was performed on Ho＇s potential energy surface（PES） of 2A″ state. Product polarizations such as product distributions of P（θr）, P（φr） and P（θr,φr）, as well as the generalized polarization-dependent differential cross sections（PDDCSs） were discussed and compared in detail among the four product channels of the title reactions. Both the intermolecular and intramolecular isotope effects were proved to be influential on product polarizations.

Low-energy structure in the ionization of argon:Comparison of experiment with theory

The above-threshold ionization of argon in an intense 70-fs,400-nm linearly polarized laser pulse has been investigated by the velocity map imaging techniques,combined with an attosecond-resolution quantum wave packet dynamics method.There is a quantitative agreement in all dominant features between the experiment and the theory.Moreover,a peak-splitting phenomenon in the first energy peak has been observed at high pulse intensity.Further,through the theoretical analysis,an ac Stark splitting with evident resonant and nonresonant ionization pathways has been found to be the physical reason for the experimental observations.

Numerical Estimation of the Thermal Response of Thermal Protective Clothing-Air Gap-Human Skin Micro-system

Thermal protective clothing has been recognized as the primary shielding against emergency fire hazard and inflammable gas leakage. Therefore,the thermal response of human covered with thermal protective clothing under high temperature is the key work to investigate the thermal insulation of thermal protective clothing. A coupling model composed of thermal protective clothing,air gap and human skin is established and the temperature of the micro-system is numerically solved via the finite element method( FEM).Especially,the heat transfer of air gap located between clothing and human skin considering conduction and radiation is established while the human skin layers involve the effect of blood perfusion. Then the effect of thermophysical properties( thermal conductivity and volumetric capacity) of fabric and thickness of fabric and air on the thermal response of the micro-system is elucidated and compared.The results indicate that the volumetric heat capacity of fabric is the key parameter to affect the thermal shielding performance of thermal protective clothing,and the thicker fabric thickness and air gap thickness can improve the thermal protective properties of the micro-system.

One-Pot Synthesis of Dimethyl Carbonate over Basic Zeolite Catalysts

One-pot synthesis of dimethyl carbonate (DMC) from methanol, propylene oxide (PO) and carbon dioxide has been investigated using the basic zeolites as catalysts. Among the zeolites studied, Beta showed the best catalytic performance for DMC production. That the desilication of zeolite structure resulted in a hierarchical porosity of Beta, leading to more amount of KOH can be loaded on the surface of zeolite and therefore enhancing the base strength of the catalyst was proposed to be the reason for improved catalytic performance.

Stereoselectivities in α- and β-Amino Acids Catalyzed Mannich Reactions Involving Cyclohexanone

The effects of two different amino acid catalysts on the stereoselectivities in the direct Mannich reactions of cyclohexanone,p-anisidine and p-nitrobenzaldehyde were studied with the aid of density functional theory.Transition states of the stereo-determining C ＂C bond-forming step with the addition of enamine intermediate to the imine for the L-proline（·-amino acid） and （R）-3-pyrrolidinecarboxylic acid（·-amino acid）-catalyzed processes were reported.B3LYP/6-31G calculations provide a good explanation for the opposite syn vs.anti diastereoselectivities of these two different kinds of catalysts（syn-selectivity for the ·-amino acid catalysts,anti-selectivity for the ·-amino acid catalysts）.Calculated and observed diastereomeric ratio and enantiomeric excess values are in reasonable agreement.

Influence of Isotope Effects on the Stereodynamics of the N(^(4)S)+H_(2)→NH+H Reactive System:a QCT Study

To investigate the isotopic effects and their influence on the stereodynamical properties of the N(^(4)S)+H_(2) reaction system,quasi−classical trajectory(QCT)calculations are carried out on the 4A"double many−body expansion(DMBE)potential energy surface(PES)[Phys.Chem.Chem.Phys.7(2005)2867]at a collision energy of 40 kcal/mol.The generalized polarization-dependent differential cross sections(PDDCSs)and the three angular distributions of P(θr),P(φr)and P(θr,φr)are presented and discussed for the title reaction and its isotope variants.It is revealed that both intermolecular and intramolecular isotope effects can exert a substantial influence on the product polarizations.

Templated synthesis of patterned gold nanoparticle assemblies for highly sensitive and reliable SERS substrates

Formation of plasmonic structure in closely packed assemblies of metallic nanoparticles(NPs)is essential for various applications in sensing,renewable energy,authentication,catalysis,and metamaterials.Herein,a surface-enhanced Raman scattering(SERS)substrate is fabricated for trace detection with ultrahigh sensitivity and stability.The SERS substrate is constructed from a simple yet robust strategy through in situ growth patterned assemblies of Au NPs based on a polymer brush templated synthesis strategy.Benefiting from the dense and uniform distribution of Au NPs,the resulting Au plasmonic nanostructure demonstrates a very strong SERS effect,while the outer polymer brush could restrict the excessive growth of Au NPs and the patterned design could achieve uniform distribution of Au NPs.As results,an ultra-low limit of detection(LOD)of 10^(−15)M,which has never been successfully detected in other work,is determined for 4-acetamidothiophenol(4-AMTP)molecules and the Raman signals in the random region show good signal homogeneity with a low relative standard deviation(RSD)of 7.2%,indicating great sensitivity and reliability as a SERS substrate.The LOD values of such Au plasmonic nanostructures for methylene blue,thiram,and R6G molecules can also reach as low as 10^(−10)M,further indicating that the substrate has a wide range of applicability for SERS detection.With the help of finite difference time domain simulations(FDTD)calculation,the electric field distribution of the Au plasmonic nanostructures is simulated,which quantitatively matches the experimental observations.Moreover,the Au plasmonic nanostructures show good shelf stability for at least 10 months of storage in an ambient environment,indicating potentials for practical applications.