Abstract:We theoretically and experimentally investigate the spectral tunability and purity of photon pairs generated from spontaneous parametric down conversion in periodically poled KTiOPO 4 crystal with group-velocity matching condition. The numerical simulation predicts that the purity of joint spectral intensity (P JSI ) and the purity of joint spectral amplitude (P JSA ) can be kept higher than 0.98 and 0.81, respectively, when the wavelength is tuned from 1460 nm to 1675 nm, which covers the S-, C-, L-, and U-band in telecommunication wavelengths. We also directly measured the joint spectral intensity at 1565 nm, 1584 nm and 1565 nm, yielding P JSI of 0.989, 0.983 and 0.958, respectively. Such a photon source is useful for quantum information and communication systems.

Levels and particle-size distributions of environmentally persistent free radicals (EPFRs) in haze-associated atmospheric particulate matter (PM) have not been highlighted, even though they may enter the human body along with PM and adversely affect human health. This study quantified the levels of EPFRs in airborne PM with different aerodynamic diameters (d) using electron paramagnetic resonance (EPR) spectroscopy. EPR spectra showed a single, unstructured signal from persistent semiquinone radicals. The average concentration of EPFRs in the airborne PM during haze events was 2.18 × 12 spins/g (range: 3.06 × 10-6.23 × 10 spins/g), approximately 2 orders of magnitude higher than that reported previously in the US atmosphere. Particle-size distributions of EPFRs in four different PM fractions (d > 10 μm, 10 μm < d < 2.5 μm, 2.5 μm

Environmentally persistent free radicals (EPFRs) are emerging pollutants that can adversely affect human health. Although the pivotal roles of metal oxides in EPFR formation have been identified, few studies have investigated the influence of the metal oxide species, size, or concentration on the formation of EPFRs. In this study, EPFR formation from a polyaromatic hydrocarbon with chlorine and hydroxyl substituents (2,4-dichloro-1-naphthol) was investigated using electron paramagnetic resonance spectroscopy. The effect of the metal oxide on the EPFR species and its lifetime and yield were evaluated. The spectra obtained with catalysis by CuO, Al 2 O 3 , ZnO, and NiO were obviously different, indicating that different EPFRs formed. The abilities of the metal oxides to promote EPFR formation were in the order Al 2 O 3 > ZnO > CuO > NiO, which were in accordance with the oxidizing strengths of the metal cations. A decay study showed that the generated radicals were persistent, with a maximum 1/e lifetime of 108 days on the surface of Al 2 O 3 . The radical yields were dependent on the concentration and particle size of the metal oxide. Metal oxide nanoparticles increased the EPFR concentrations more than micrometer-sized particles.

We demonstrate pulsed polarization-entangled photons generated from a periodically poled KTiOPO(4) (PPKTP) crystal in a Sagnac interferometer configuration at telecom wavelength. Since the group-velocity-matching (GVM) condition is satisfied, the intrinsic spectral purity of the photons is much higher than in the previous scheme at around 800 nm wavelength. The combination of a Sagnac interferometer and the GVM-PPKTP crystal makes our entangled source compact, stable, highly entangled, spectrally pure and ultra-bright. The photons were detected by two superconducting nanowire single photon detectors (SNSPDs) with detection efficiencies of 70% and 68% at dark counts of less than 1 kcps. We achieved fidelities of 0.981 ± 0.0002 for |ψ(-)〉 and 0.980 ± 0.001 for |ψ(+)〉 respectively. This GVM-PPKTP-Sagnac scheme is directly applicable to quantum communication experiments at telecom wavelength, especially in free space.

Few studies have investigated the free radical intermediates involved in the formation of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) from chlorophenol. This study clarified the reaction pathways during thermochemical formation of PCDDs from 2,3,6-trichlorophenol (TCP) over a Cu(II)O/silica matrix, which was used to simulate fly ash, at 298-523 K. The reaction was studied using electron paramagnetic resonance (EPR) spectroscopy and theoretical calculations. In situ EPR indicated the TCP radical (TCPR) formed by hydrogen abstraction of TCP. Five elementary processes including dimerization of TCPR, ortho-chloride abstraction, Smiles rearrangement, ring closure, and intra-annular elimination of Cl were proposed to occur during formation of PCDDs. The proposed mechanism was further confirmed by the detection of PCDD products from thermochemical experiments in a tube furnace. Several dominant congeners, including 1,2,6,9-tetrachlorodibenzo-p-dioxin (TeCDD), 1,2,6,7-TeCDD, 1,2,8,9-TeCDD, and 1,4,6,9-TeCDD were detected by gas chromatography/quadrupole time-of-flight mass spectrometry, and further confirmed by gas chromatography/high resolution mass spectrometry. The detected PCDD products agree with the proposed PCDD formation mechanism. Relatively high temperatures were found to lead to dechlorination of TCPR to form phenoxy radicals in addition to PCDD/Fs. These radicals will be attached to particles, which will increase their lifetimes. These reactions were further verified by molecular orbital theory calculations. The discovery of persistent phenoxy radicals is of environmental significance because of their potential toxicity. The details of this mechanism could be used for controlling PCDD/F formation during industrial thermal processes.