Polarization observablesΣ,P y,T 1 in the reaction\vec \gamma d \to \vec pn at photon energies between 200 and 600 MeV and dibaryon resonances

The polarization observables Σ,P _y ,T ₁,P _y ^⊥ ,P _y ^∥ are derived in proton polarization measurements of the \(\vec \gamma d \to \vec pn\) reaction, using a linearly polarized photon beam of energies between 300 and 600 MeV for c.m.s. proton emission angles of 90° and 120°. A multipole analysis is performed in the framework of the gauge-invariant pole model considering theγN→πN amplitudes and the deuteron structure without dibaryon resonances and with different sets of isovector and isoscalar dibaryon resonances. It is shown that the inclusion of dibaryon resonances substantially improves agreement with experimental data.     

Pion pair production in photon-photon collisions

The process γγ→π⁺π^? was measured using the detector MD-1 at VEPP-4. The two-photon reactionse ⁺ e ^?, μ⁺ μ^? and π⁺ π^? pair production were separated using scintillation counters, Cherenkov counters and shower-range chambers. A radiation widthГ _γγ(f ₂(1270))=3.1±0.35±0.35 keV was obtained.     

Dielectric properties of the nanoporous MCM-41 matrix filled with the (NH4)2SO4 ferroelectric

Variations with temperature of the linear dielectric permittivity and amplitude of the third harmonic were studied for nanoporous MCM-41 matrices with 4.0-nm channel pores filled with the (NH₄)₂SO₄ ferroelectric, in comparison with bulk ammonium sulfate. The measurements were performed upon heating and cooling in the temperature range from 100 K to room temperature. A noticeable shift to low temperatures (by approximately 25 K) for the ferroelectric phase transition in the MCM-41/(NH₄)₂SO₄ nanocomposite as compared to bulk (NH₄)₂SO₄ was revealed. The temperature hysteresis observed at the phase transition in the nanocomposite was approximately 2 K which is close to that in bulk ammonium sulfate. The significant decrease of the transition temperature in nanostructured ammonium sulfate agrees with the theoretical predictions based on the Landau and Ising models of the size effect on the ferroelectric phase transition in isolated small particles.     

油酸和亚油酸的激光拉曼光谱

不同的不饱和脂肪酸各自具有其不同的生理功能,但常见的不饱和脂肪酸产品大部分为几种脂肪酸的混合物,故在应用前对不纯的脂肪酸产品进行组成分析是必须的。测量了不饱和脂肪酸产品组分中最常见的油酸和亚油酸的拉曼光谱,确定了各拉曼谱线的振动模归属,分析了其分子的构象特征。该结果为研究长链不饱和脂肪酸的振动能级结构及能级间跃迁等做了基础工作,丰富了有机物分子的价键数据和性质。同时详细分析比较了油酸和亚油酸拉曼光谱的差异,为定性鉴别脂肪酸产品的成分提供了一种简便有效的方法,对拉曼光谱在地沟油检测方面的应用具有重要的指导意义。     

Point defect interaction in alkali halide crystals

Abstract

Molecular statics method is used to determine the energy and configuration peculiarities of vacancy-bivacancy interaction in alkali halide crystals. It is shown that high level of local vacancy supersaturation defines the possibility of cluster formation. The study of carrier traps by luminescence methods is used to reveal vacancy clusters.     

Trace analysis of polycyclic aromatic hydrocarbons using calixarene layered gold colloid film as substrates for surface‐enhanced Raman scattering

A surface‐enhanced Raman scattering (SERS) active substrate for the detection of polycyclic aromatic hydrocarbons (PAHs) was developed, which used 25, 27‐dimercaptoacetic acid‐26, 28‐dihydroxy‐4‐terbutyl calix[4]arene (DMCX) to functionalize a gold colloid film. This SERS‐active substrate prepared by self‐assembly method exhibits a high sensitivity, especially for the detection of PAHs. With the use of this SERS‐active substrate and with the application of the shifted excitation Raman difference spectroscopy (SERDS) technique, Raman signals of pyrene and anthracene in aqueous solutions at low concentration level (500 pM) can be obtained. Moreover, because PAHs are blocked from being directly adsorbed on gold colloid by DMCX and the photochemical reactions of adsorbates are avoided, the Raman bands of PAHs adsorbed on DMCX‐fuctionalized gold colloid film can be one‐to‐one correspondence with those of solid PAHs, and additionally, this SERS‐active substrate can be easily cleaned and reused. The obtained results demonstrate that the DMCX‐functionalized gold colloid films prepared by self‐assembly method have great potential to be developed to an in situ PAHs detection substrate. Copyright © 2012 John Wiley & Sons, Ltd.     

Quadruplex CARS micro‐spectroscopy

We demonstrate a technique for simultaneous detection of coherent anti‐Stokes Raman scattering (CARS) at four vibrational frequencies, using simple passive optical elements and without spectrally resolved detection. The technique is based on pump and Stokes femtosecond pulses selectively exciting vibrational resonances through spectral focusing. By replicating the pump and Stokes pair into four pairs, each traveling through appropriate glass elements, we simultaneously excite four different vibrational frequencies. The resulting CARS is a periodic train of intensities detected by a single photomultiplier and frequency analyzed to retrieve its Fourier coefficients. We demonstrate detection of methanol and ethanol mixtures in water and quantitative determination of their concentration owing to the improved chemical selectivity of this quadruplex CARS scheme. Copyright © 2012 John Wiley & Sons, Ltd.     

SERS signal response and SERS/SERDS spectra of fluoranthene in water on naturally grown Ag nanoparticle ensembles

We present experimental results of the time‐dependent Raman signal response of fluoranthene adsorbed on a naturally grown Ag nanoparticle ensemble, which serves as surface enhanced Raman scattering (SERS) substrate. In addition, SERS characteristics such as the concentration‐dependent calibration curves and the limit of detection (LOD) for fluoranthene in distilled water will be shown. The SERS substrate was prepared by Volmer–Weber growth under ultrahigh vacuum condition and exhibits a plasmon resonance wavelength at 491 nm. For the measurement of SERS signal response and SERS/shifted excitation Raman difference spectroscopy spectra of fluoranthene in water, experimental Raman setup containing a microsystem light source with two emission wavelengths (487.61 nm and 487.91 nm) was used. We experimentally demonstrate that the maximum SERS intensity is achieved 9 min after changing the analyte concentration from 0 nmol/l to 600 nmol/l. This response time is explained by a time‐dependent adsorption of the probe molecules onto the nanoparticles. The LOD for fluoranthene in water was evaluated applying shifted excitation Raman difference spectroscopy (SERDS) at different molecule concentrations. For SERDS, two emission wavelengths of a prototype microsystem light source have been used for Raman excitation. The experimental results reveal that the LOD for the probe molecules is very low. Experimentally, we have detected a fluoranthene concentration of only 4 nmol/l, which is very close to our estimated LOD of 2 nmol/l. Thus, the presented Raman setup, with a SERS substrate, whose plasmon resonance coincides with the excitation wavelength for SERS measurements, is well suited for in‐situ trace detection of pollutant chemicals in water. Copyright © 2013 John Wiley & Sons, Ltd.     

pH‐sensing nanostar probe using surface‐enhanced Raman scattering (SERS): theoretical and experimental studies

Local pH environment has been considered to be a potential biomarker for tumor diagnosis because solid tumors contain highly acidic environments. A pH‐sensing nanoprobe based on surface‐enhanced Raman scattering (SERS) using nanostars under near‐infrared excitation has been developed for potential biomedical applications. To theoretically investigate the effect of protonation state on SERS spectra of p‐mercaptobenzoic acid (pMBA), we used the density functional theory (DFT) with the B3LYP functional to calculate Raman vibrational spectra of pMBA‐Au/Ag complex in both protonated and deprotonated states. Vibrational spectral bands were assigned with DFT calculation and used to investigate SERS spectral changes observed from experiment when varying pH value between five and nine. The SERS peak position of pMBA at ~1580 cm⁻¹ was identified to be a novel pH‐sensing index, which has small but noticeable downshift with pH increase. This phenomenon is confirmed and well‐explained with theoretical simulation. The study demonstrates that SERS is a sensitive tool to monitor minor structural changes due to local pH environment, and DFT calculations can be used to investigate Raman spectra changes associated with minor differences in molecular structure. Copyright © 2013 John Wiley & Sons, Ltd.     

High‐power HgGa2S4 optical parametric oscillator pumped at 1064 nm and operating at 100 Hz

The defect chalcopyrite crystal HgGa₂S₄ has been employed in a 1064‐nm pumped optical parametric oscillator operating at 100 Hz, to generate ∼5 ns long idler pulses near 4 µm with energies as high as 6.1 mJ and average power of 610 mW. At crystal dimensions comparable to those available for the commercial AgGaS₂ crystal, operation of the 1064‐nm pumped HgGa₂S₄ OPO is characterized by much lower pump threshold and higher conversion efficiency, with the most important consequence that such a device might become practical at pump levels sufficiently lower than the optical damage threshold.