On the contribution of twist-3 multi-gluon correlation functions to single transverse-spin asymmetry in SIDIS

We study the single spin asymmetry (SSA) induced by purely gluonic correlation inside a nucleon, in particular, by the three-gluon correlation functions in the transversely polarized nucleon, $p^\uparrow$. This contribution is embodied as a twist-3 mechanism in the collinear factorization framework and controls the SSA to be observed in the $D$-meson production with large transverse-momentum in semi-inclusive DIS (SIDIS), $ep^\uparrow \rightarrow eDX$. We define the relevant three-gluon correlation functions in the nucleon, and determine their complete set at the twsit-3 level taking into account symmetry constraints in QCD. We derive the single-spin-dependent cross section for the $D$-meson production in SIDIS, taking into account all the relevant contributions at the twist-3 level. The result is obtained in a manifestly gauge-invariant form as the factorization formula in terms of the three-gluon correlation functions and reveals the five independent structures with respect to the dependence on the azimuthal angle for the produced $D$ meson. We also demonstrate the remarkable relation between the twist-3 single-spin-dependent cross section and twist-2 cross sections for the $D$-meson production, as a manifestation of universal structure behind the SSA in a variety of hard processes.Comment: 8 pages, 2 figures. To appear in the proceedings of the 19th International Spin Physics Symposium (SPIN2010), Juelich, Germany, Sept.27 - Oct.2, 201

Three-gluon contribution to the single spin asymmetry in Drell-Yan and direct-photon processes

We derive the single-spin-dependent cross section for the Drell-Yan lepton-pair production and the direct-photon production in the $pp$-collision induced by the twist-3 three-gluon correlation functions in the transversely polarized nucleon in the leading order with respect to the QCD coupling constant. Combined with the contribution from the twist-3 quark-gluon correlation functions in the literature, this completes the twist-3 cross section for these processes. We also present a model calculation of the asymmetry for the direct photon production at the RHIC energy, demonstrating the sensitivity of the asymmetry to the form of the three-gluon correlation functions. In particular, we show that the asymmetry in the backward direction of the polarized nucleon is determined by the small-$x$ behavior of the correlation functions.Comment: 15 pages, 3 figure

Probing the twist-3 multi-gluon correlation functions by pp \to DX

We study the single spin asymmetry (SSA) for the D-meson production $A_N^D$ in the $pp$ collision, $p^\uparrow p\to DX$, in the framework of the collinear factorization. Since the charm quark is mainly produced through the $c\bar{c}$-pair creation from the gluon-fusion process, this is an ideal process to probe the twist-3 triple-gluon correlation functions in the polarized nucleon. We derive the corresponding cross section formula for the contribution of the triple-gluon correlation function to $A_N^D$ in $p^\uparrow p\to DX$, applying the method developed for $ep^\uparrow\to eDX$ in our previous study. As in the case of $ep^\uparrow\to eDX$, our result differs from a previous study in the literature. We will also present a simple estimate of the triple-gluon correlation functions based on the preliminary data on $A_N^D$ by RHIC.Comment: to appear in the proceedings of the 19th International Spin Physics Symposium (Spin2010), Sept.27 - Oct.2, 2010, Juelich, Germany, 5 pages, 2 figure

New phenomena in interaction of intense ultrashort light pulses with transparent materials: from 3D self-assembled nanostructures to quill writing and nonreciprocal photosensitivity

Interaction of intense ulrashort light pulses with transparent materials reveal new ultrafast phenomena. Recent demonstrations of 3D nanoripple formation, ultrafast laser calligraphy and nonreciprocal photosensitivity are reviewed

Recent advances in ultrafast laser processing of transparent materials

Interaction of intense ulrashort light pulses with transparent materials reveal new interesting properties and phenomena. Recent demonstrations of 3D nanoripple formation, self-assembled form birefringency and ultrafast laser calligraphy are reviewed

Material processing using ultrashort light pulses with tilted front

Femtosecond laser writing in glass is controlled by the polarization plane azimuth and intensity front tilt of light pulse. Polarization dependent distribution of extraordinary modifications along the light propagation direction is observed

Scalar Perturbations Through Cycles

We analytically and numerically investigate the evolutions of the scalar perturbations through the cycles with nonsingular bounce. It is found that the amplitude of the curvature perturbation on large scale will be amplified cycle by cycle, and the isocurvature perturbations also obtain an amplification, but the rate of its amplification is slower than that of curvature perturbation, unless its coupling to the metric perturbation is not negligible.Comment: 7 pages, 10 figure

Transient Absorption and Raman Spectroscopies in Organic Electronics

Raman spectroscopy has proved to be a very valuable tool for characterization in a large number of research fields, both biological, chemical and material sciences.[1] In the last decades, organic electronics has broken out as a real alternative to conventional electronics, based on inorganic materials. However, in order to advance significantly in this field of research is paramount the full characterization of electronic devices, going from the individual molecule to the system as a whole. Moreover, the study of photophysical and photochemical processes crosses the interest of many fields of research in physics, chemistry and biology. Among the experimental approaches developed for this purpose, the advent of ultrafast transient absorption spectroscopy has become a powerful and widely used method.[2,3] This pump-probe technique is a popular means of studying photophysics, because of its versatile time resolution and its ease of comparison with ground-state absorption spectra. In this communication, I will present the basic principles of transient absorption spectroscopy, along with some examples where its combination with Raman spectroscopy allows the great characterization of organic molecules with potential applications in organic electronics.[4,5] References [1] H. Schulz, M. Baranska, R. Baranski. Biopolymers 2005, 77, 212 - 221. [2] U. Megerle, I. Pugliesi, C. Schriever, C.F. Sailer, E. Riedle. Appl. Phys. B, 2009, 96, 215 - 231. [3] R. Berera, R. van Grondelle, J.T.M. Kennis. Photosynth. Res. 2009, 101, 105 - 118. [4] E. Anaya-Plaza, M. Moreno Oliva, A. Kunzmann, C. Romero-Nieto, R.D. Costa, A. de la Escosura, D.M. Guldi, T. Torres. Adv. Funct. Mater. 2015, 25, 7418 - 7427. [5] F. Liu, G.L. Espejo, S. Qiu, M. Moreno Oliva, J. Pina, J.S. Seixas de Melo, J. Casado, X. Zhu. J. Am. Chem. Soc. 2015, 137, 10357 - 10366.Universidad de Málaga. Campus de Excelencia Internacional Andalucía Tech