Calculation of Total Cross Section for γγ→γZ Scattering at High Energy

The total cross sections of γγ→γZ process for γγ c.m.s. energy 91.2—2000GeV are presented. W loop contribution is dominating when γγ c.m.s. energy is larger than 140GeV. The total cross section has a maximum, 220 fb(|cosθ|33cm^－2·s^－1 in which case more than 6000 events for γγ→γZ would be observable. In principle this process provides a test of the non-abelian nature of the standard model, especially the anomalous triple and quartic W-boson vertices.     

γγ→γZ过程高能总截面的数值计算

给出了γγ→γZ过程,质心系总能量在91.2—2000GeV的总截面.结果表明在总能量大于140GeV时,W玻色子图的贡献比起费米子图的贡献要大,当总能量在750GeV左右,截面达到极大值220fb(|cosθ|33cm^－2·sec^－1,每年在总能量750GeV处可观察到6000多个γγ→γZ事例,用它可以进一步验证标准模型,特别是其中规范粒子的三顶角和四顶角相互作用.     

局域模(实的及虚的)的一种新表述

本文给出了一种新的表述局域模(实的及虚的)的方法。我们引入了变形豫解式的迹P(z).它仅在z平面的实轴上有奇异性,孤立极点对应于实局域模。将P(E+iη)向下解析延拓至第二黎曼面,则其复极点对应于虚的(或不稳定的)局域模。复极点的实部是不稳定局域模的能量,虚部是它寿命的倒数,自然地得到了寿命为正的限制。此能量与寿命符合于相应共振散射的能量与宽度。本文还讨论了实局域模与虚局域模之间的关系。最后,比较了P(z)的奇异性与态密度的变化,并进一步阐明了寿命为正的及负的解之间的差别。指出,一般说来,只有寿命为正的解当作用强度增加时会变成实的局域模,负寿命的解是不会的。     

Third User Workshop on High-Power Lasers at the Linac Coherent Light Source

On October 5–6, 2015, the third international user workshop focusing on high-power lasers at the Linac Coherent Light Source (LCLS) was held in Menlo Park, CA, USA [1 R. Falcone, S. Glenzer, and S. Hau-Riege, Synchrotron Radiation News 27(2), 56–58 (2014).[Taylor &; Francis Online] , [Google Scholar], 2 P. Heimann and S. Glenzer, Synchrotron Radiation News 28(3), 54–56 (2015).[Taylor &; Francis Online] , [Google Scholar]]. The workshop was co-organized by Los Alamos National Laboratory and SLAC National Accelerator Laboratory. More than 110 scientists attended from North America, Europe, and Asia to discuss high-energy-density (HED) science that is enabled by the unique combination of high-power lasers with the LCLS X-rays at the LCLS-Matter in Extreme Conditions (MEC) endstation.     

Ultrafast dynamic ellipsometry measurements of early time laser ablation of titanium thin films

The dynamics of laser ablated titanium thin films are investigated using a recently developed technique that measures time-resolved and one-dimensional spatially-resolved ablation dynamics in a single shot. Ultrafast dynamic ellipsometry, a technique based on space-shifted spectral interferometry, uses the time-dependent frequency of a chirped laser pulse to provide time encoding, allowing the picosecond probing of material dynamics in a single shot. With this technique, the sample is probed at two different incident angles with both s- and p-polarized light, which measures the motion of the material and any change in its complex refractive index. Ultrafast dynamic ellipsometry is applied to study the mechanism of initiation by laser-based optical detonators that employ the ablation of titanium thin films. The resulting data indicate that the titanium is ablated as a fragmented flyer and not as an expanding plasma.     

Femtosecond stimulated Raman scattering picosecond molecular thermometry in condensed phases

We demonstrate the capability of femtosecond stimulated Raman scattering (FSRS) data to measure the temperature of condensed matter at the molecular vibrational level. We report the temperature dependence of Raman loss to Raman gain ratios for low frequency modes (<300 cm(-1)) in a CaCO3 single crystal from cryogenic to room temperature, which is shown to be in agreement with theoretical predictions. We also report the measurements of nonequilibrium time evolution of mode specific vibrational temperatures in the CaCO3 single crystal to demonstrate that FSRS can measure temperature on picosecond time scales. Finally, we point out the unique origin of this temperature dependent anti-Stokes to Stokes ratio in stimulated Raman, which is not present in other coherent Raman spectroscopies. These measurements require no material dependent parameters or prior calibration.     

Temperature measurements in condensed phases using non‐resonant femtosecond stimulated Raman scattering

We have previously demonstrated the capability of femtosecond stimulated Raman scattering (FSRS) data to measure the temperature (T) of condensed matter at the molecular vibrational level. [Phys. Rev. Lett. 2011, 107, 43001] In this paper, we expand the theory for the FSRS temperature dependence by considering the effects of an isolated change of T as well as a coupled change of T and chemical concentration. We point out that the origin of the temperature sensitivity of the Stokes to anti‐Stokes ratio of FSRS lies in the exponential nonlinearity of the gain and loss. We establish that FSRS of two Raman modes can be used to simultaneously determine the vibrational temperature and the change in concentration of the species contributing to those two modes. Single‐shot experimental results using FSRS are presented to demonstrate over four orders of magnitude higher efficiency than spontaneous Raman in small volume samples with picosecond resolution. Copyright © 2012 John Wiley & Sons, Ltd.