Development of diamond-based X-ray detection for high-flux beamline diagnostics

High‐quality single‐crystal and polycrystalline chemical‐vapor‐deposition diamond detectors with platinum contacts have been tested at the white‐beam X28C beamline at the National Synchrotron Light Source under high‐flux conditions. The voltage dependence of these devices has been measured under both DC and pulsed‐bias conditions, establishing the presence or absence of photoconductive gain in each device. Linear response consistent with the theoretically determined ionization energy has been achieved over eleven orders of magnitude when combined with previous low‐flux studies. Temporal measurements with single‐crystal diamond detectors have resolved the nanosecond‐scale pulse structures of both the NSLS and the APS. Prototype single‐crystal quadrant detectors have provided the ability to simultaneously resolve the X‐ray beam position and obtain a quantitative measurement of the flux.     

Micro‐Raman spectroscopy and VP‐SEM/EDS applied to the identification of mineral particles and fibres in histological sections

Histological sections of a patient affected by an important respiratory disease were analysed firstly by optical microscope(OM)—crossed polarisers—to identify the presence of incorporated inorganic particles, with particular attention to the fibrous ones. Then, the particles/fibres that were found were studied both with micro‐Raman spectroscopy and variable‐pressure scanning electron microscopy with energy‐dispersive spectroscopy (VP‐SEM/EDS). The two techniques allowed the in situ characterisation of the inorganic phases without disintegration of the organic matter. Micro‐Raman spectroscopy was able to identify the vibrating chemical groups of the mineral phase associated with the inorganic grain while the crystalline structure was preserved by the biological system. The VP‐SEM/EDS characterisation, defining the elemental chemical composition of the analysed particle/fibre, allowed confirmation of the mineral phase deducible from spectroscopic data or its identification with certainty when the spectroscopic data were not exhaustive. Copyright © 2009 John Wiley & Sons, Ltd.     

Raman spectroscopic studies of vibrational relaxation and non‐coincidence effect in substituted benzaldehyde binary mixtures

The molecular interaction in the binary mixture of 3‐phenoxybenzaldhyde (3Phbz) and 4‐ethoxybenzaldehyde (4Etob) was analysed in four different solvents. The concentration dependence of vibrational relaxation of the CO stretching band of 3Phbz in different solvents was investigated by varying the concentration of the solute molecule in the solvents by performing Raman spectroscopic measurements. The self‐associated nature and the formation of hydrogen‐bonded complexes in the solute molecule, 4Etob, were considered to analyse the wavenumber separation between the peaks of hydrogen‐bonded and free carbonyl groups. Copyright © 2009 John Wiley & Sons, Ltd.     

Della Robbia blue glaze: micro‐Raman temperature study and X‐ray fluorescence spectroscopy characterization

Micro‐Raman temperature study and X‐ray fluorescence (XRF) spectroscopy were used for characterization of the blue glaze on Saint John the Baptist—majolica terracotta relief attributed to Andrea Della Robbia and Saint John the Baptist with Cross—majolica terracotta statue attributed to Giovanni Della Robbia. Both objects are on permanent exhibition in the John and Mable Ringling Museum of Art in Sarasota, FL. This study proves that the detection of the 548 cm⁻¹ Raman band alone cannot serve as evidence for presence of lazurite crystallites in the pigment in the glaze. It was established that the famous Della Robbia blue is due to the combined effect of Co Ni Cu Zn atoms and S₃⁻ ions embedded in a lead silicate matrix. It is proposed that the Della Robbia family used Co‐containing sulfide ores as a source for manufacturing their blue pigments. Copyright © 2009 John Wiley & Sons, Ltd.     

Ultrathin silver‐coated gold nanoparticles as suitable substrate for surface‐enhanced Raman scattering

Surface‐enhanced Raman scattering (SERS) is an extremely powerful tool for the analysis of the composition of bimetallic nanoparticle (BNP) surfaces because of the different adsorption schemes adopted by several molecules on different metals, such as Au and Ag. The preparation of BNPs normally implies a change in the plasmonic properties of the core metal. However, for technological applications it could be interesting to synthesize core–shell structures preserving these original plasmonic properties. In this work, we present a facile method for coating colloidal gold nanoparticles (NPs) in solution with a very thin shell of silver. The resulting bimetallic Au@Ag system maintains the optical properties of gold but shows the chemical surface affinity of silver. The effectiveness of the coating method, as well as the progressive silver enrichment of the outermost part of the Au NPs, has been monitored through the SERS spectra of several species (chloride, luteolin, thiophenol and lucigenin), which show different behaviors on gold and silver surfaces. A growth mechanism of the Ag shell is proposed on the basis of the spectroscopic and microscopic data consisting in the formation and deposit of Ag clusters on the Au NP surface. Copyright © 2009 John Wiley & Sons, Ltd.     

Interaction between rhodanine and silver species on a nanocolloidal surface and in the solid state

This paper discusses and compares molecular interactions of rhodanine (Rd), the heterocyclic compound containing N, S, and O atoms, with two forms of silver species, i.e. Ag(I) ions and silver nanocolloidal particles. Vibrational spectroscopic and powder crystallography studies on coordination of Ag(I) ions in the solid state, supported by density functional theory, clearly indicate complexation through the nitrogen (the deprotonated imino group) and exocyclic sulfur atoms. Molecules of the complex are arranged in a one‐dimensional infinite polymeric chain structure that intertwines to give a helix motif. On the other hand, adsorption geometry of Rd on the silver surface was determined by using surface‐enhancement Raman scattering (SERS) spectroscopy. Observed differences between the SERS and the normal Raman spectra of Rd suggest that Rd adsorbs on the silver species after the rearrangement of the keto‐thione form into the enol‐thiol tautomer in acidic and neutral solutions. This leads to adsorption on this silver species through the thiolate ion. On the other hand, the alkaline pH forces first N‐deprotonation of Rd, and, in consequence, the obtained anion of the keto‐thione form interacts with the silver surface as a result of the presence of lone pairs of nitrogen and sulfur atoms, similar to the case discussed for the solid state. Copyright © 2009 John Wiley & Sons, Ltd.     

Heterodyne interferometric polarization coherent anti‐Stokes Raman scattering (HIP‐CARS) spectroscopy

We demonstrate a new technique that combines polarization sensitivity of the coherent anti‐Stokes Raman scattering (CARS) response with heterodyne amplification for background‐free detection of CARS signals. In this heterodyne interferometric polarization CARS (HIP‐CARS), the major drawbacks of polarization and heterodyne CARS are rectified. Using a home‐built picosecond optical parametric oscillator, we are able to address vibrational stretches between 600 and 1650 cm⁻¹ and record continuous high‐resolution Raman equivalent HIP‐CARS spectra. Copyright © 2010 John Wiley & Sons, Ltd.     

Attosecond‐precision ultrafast photonics

We review our recent progress toward attosecond‐precision ultrafast photonics based on ultra‐low timing jitter optical pulse trains from mode‐locked lasers. In femtosecond mode‐locked lasers, the concentration of a large number of photons in an extremely short pulse duration enables the scaling of timing jitter into the attosecond regime. To characterize such jitter levels, we developed new attosecond‐resolution measurement techniques and show that standard fiber lasers can achieve sub‐fs high‐frequency jitter. By leveraging the ultra‐low jitter of free‐running mode‐locked lasers, we pursued high‐precision optical‐optical and optical‐microwave synchronization techniques. Optical signals spanning 1.5 octaves were synthesized by attosecond‐precision timing and phase synchronization of two independent mode‐locked lasers. High‐stability microwave signals were also synthesized from mode‐locked lasers with drift‐free sub‐10‐fs precision. We further demonstrated the attosecond‐precision distribution of optical pulse trains to remote locations via timing‐stabilized fiber links. Finally, the application of optical pulse trains for high‐resolution sampling and analog‐to‐digital conversion is discussed.     

Slow and fast light: basic concepts and recent advancements based on nonlinear wave‐mixing processes

After a review of the basic concepts of slow and fast light, recent advancements based on nonlinear wave‐mixing processes are described. As a nonlinear medium, the authors focus on a liquid crystal light valve showing that it allows obtaining a large control of the group delay, with a maximum fractional delay of 1, and a deceleration of light pulses down to group velocities as small as 0.2 mm/s. A theoretical model accompanies the observations and accounts for them in the general framework of two‐wave mixing in the light valve. At the end, a high‐sensitivity interferometer is presented as an example of slow light applications.     

整体毛细管X光透镜在大气颗粒物单颗粒分析中的应用

对大气颗粒物进行单颗粒X射线荧光(XRF)分析,是一种识别大气颗粒物来源的有力手段.为了利用实验室X射线光源对大气颗粒物进行单颗粒XRF分析,建立了基于整体毛细管X光透镜和实验室X射线光源的微束X射线谱仪.透镜焦斑处的功率密度增益在103数量级,焦斑直径为30 μm左右.该微束X射线谱仪对Fe-Kα线的最小探测极限为0.7 Pg.在Mo靶光源电压和电流分别为30 kV和50 mA的条件下,利用该谱仪对直径为9 μm的大气颗粒物单颗粒进行XRF分析时,测谱时间在180 s左右.实验表明,基于毛细管X光透镜和实验室X射线光源的微束X射线分析技术在大气颗粒物单颗粒分析中有着潜在的应用价值.