Nonthermal fixed points: effective weak coupling for strongly correlated systems far from equilibrium

Strongly correlated systems far from equilibrium can exhibit scaling solutions with a dynamically generated weak coupling. We show this by investigating isolated systems described by relativistic quantum field theories for initial conditions leading to nonequilibrium instabilities, such as parametric resonance or spinodal decomposition. The nonthermal fixed points prevent fast thermalization if classical-statistical fluctuations dominate over quantum fluctuations. We comment on the possible significance of these results for the heating of the early Universe after inflation and the question of fast thermalization in heavy-ion collision experiments.     

Screened radiative corrections from hyperfine-split dielectronic resonances in lithiumlike scandium

Term energies for dielectronic-recombination Rydberg resonances below 0.07 eV are determined for Sc18+ with absolute accuracies below 0.0002 eV by electron collision spectroscopy in an ion storage ring, using the twin-electron-beam technique and a cryogenic photocathode. The lithiumlike 2s_{1/2}-2p_{3/2} transition energy for Z=21 is determined to 4.6 ppm, less than 1% of the few-body effects on radiative corrections. Features from the hyperfine structure of the 2s state could be resolved in the dielectronic-recombination spectrum.     

Powder diffraction from a continuous microjet of submicrometer protein crystals

Atomic‐resolution structures from small proteins have recently been determined from high‐quality powder diffraction patterns using a combination of stereochemical restraints and Rietveld refinement [Von Dreele (2007), J. Appl. Cryst. 40 , 133–143; Margiolaki et al. (2007), J. Am. Chem. Soc. 129 , 11865–11871]. While powder diffraction data have been obtained from batch samples of small crystal‐suspensions, which are exposed to X‐rays for long periods of time and undergo significant radiation damage, the proof‐of‐concept that protein powder diffraction data from nanocrystals of a membrane protein can be obtained using a continuous microjet is shown. This flow‐focusing aerojet has been developed to deliver a solution of hydrated protein nanocrystals to an X‐ray beam for diffraction analysis. This method requires neither the crushing of larger polycrystalline samples nor any techniques to avoid radiation damage such as cryocooling. Apparatus to record protein powder diffraction in this manner has been commissioned, and in this paper the first powder diffraction patterns from a membrane protein, photosystem I, with crystallite sizes of less than 500 nm are presented. These preliminary patterns show the lowest‐order reflections, which agree quantitatively with theoretical calculations of the powder profile. The results also serve to test our aerojet injector system, with future application to femtosecond diffraction in free‐electron X‐ray laser schemes, and for serial crystallography using a single‐file beam of aligned hydrated molecules.     

57 W, 27 fs pulses from a fiber laser system using nonlinear compression

We report on the generation of 27 fs pulses with an average output power of 57 W and a repetition rate of 78 MHz. The pulses are generated by combining a high average power fiber chirped pulse amplification (FCPA) system with a microstructured large-mode-area fiber for nonlinear compression. The FCPA system delivers 270 fs pulses in a linearly polarized beam with diffraction-limited quality. Nonlinear compression is achieved by launching the pulses into a short (few cm) piece of microstructured fiber and subsequent compression by a pair of chirped mirrors. PACS  42.55.Wd; 42.55.Xi, 42.65.Re     

Azobenzene-functionalized alkanethiols in self-assembled monolayers on gold

Self-assembled monolayers (SAMs) of 4-trifluoromethyl-azobenzene-4′-methyleneoxy-alkanethiols (CF₃– C₆H₄–N=N–C₆H₄–O–(CH₂) _n –SH on (111)-oriented poly-crystalline gold films on mica were examined by X-ray photoelectron spectroscopy (XPS) and X-ray absorption spectroscopy (XAS). The spectra are analyzed with the help of density-functional-theory calculations of the isolated molecule. Only one doublet is detected in the sulphur 2p spectra of the investigated SAMs, consistent with a thiolate bond of the molecule to the gold surface. The C 1s XP spectra and the corresponding XAS π ^* resonance exhibit a rich structure which is assigned to the carbon atoms in the different chemical surroundings. Comparing XPS binding energies of the azobenzene moiety and calculated initial-state shifts reveals comparable screening of all C 1s core holes. While the carbon 1s XPS binding energy lies below the π ^*-resonance excitation-energy, the reversed order is found comparing core ionization and neutral core excitation of the nitrogen 1s core-hole of the azo group. This surprising difference in core-hole binding energies is interpreted as site-dependent polarization screening and charge transfer among the densely packed aromatic moieties. We propose that a quenching of the optical excitation within the molecular layer is thus one major reason for the low trans to cis photo-isomerization rate of azobenzene in aromatic-aliphatic SAMs.     

An anchoring strategy for photoswitchable biosensor technology: azobenzene-modified SAMs on Si(111)

A mild and efficient procedure has been developed to obtain covalently attached self-assembled monolayers (SAMs) on Si(111) with photochromic azobenzene head-groups. Starting from neat or diluted carboxylic acid functionalized monolayers on-chip coupling reactions were applied to attach hydroxyl-functionalized azobenzene units to the SAMs by ester bond formation. The modified surfaces were characterized by high-resolution X-ray photoelectron spectroscopy (XPS), transmission Fourier transform infrared spectroscopy (FT-IR), and contact angle measurements. Reversible cis ↔ trans isomerizations of photoswitchable SAMs were monitored by wettability measurements. Electronic Supplementary Material  The online version of this article () contains supplementary material, which is available to authorized users. Dedicated with respect and compliments to Professor Helmut Schwarz on the occasion of his 65th birthday.     

Sr3P3N7: Complementary Approach by Ammonothermal and High-Pressure Syntheses

Nitridophosphates exhibit an intriguing structural diversity with different structural motifs, for example, chains, layers or frameworks. In this contribution the novel nitridophosphate Sr₃P₃N₇ with unprecedented dreier double chains is presented. Crystalline powders were synthesized using the ammonothermal method, while single crystals were obtained by a high-pressure multianvil technique. The crystal structure of Sr₃P₃N₇ was solved and refined from single-crystal X-ray diffraction and confirmed by powder X-ray methods. Sr₃P₃N₇ crystallizes in monoclinic space group P2/c. Energy-dispersive X-ray and Fourier-transformed infrared spectroscopy were conducted to confirm the chemical composition, as well as the absence of NH_x functionality. The optical band gap was estimated to be 4.4 eV using diffuse reflectance UV/Vis spectroscopy. Upon doping with Eu²⁺, Sr₃P₃N₇ shows a broad deep-red to infrared emission (λ_em=681 nm, fwhm≈3402 cm⁻¹) with an internal quantum efficiency of 42 %.