Probing an Excited-State Atomic Transition Using Hyperfine Quantum Beat Spectroscopy

We describe a method to observe the dynamics of an excited-state transition in a room-temperature atomic vapor using hyperfine quantum beats. Our experiment using cesium atoms consists of a pulsed excitation of the D2 transition and continuous-wave driving of an excited-state transition from the 6P3/2 state to the 7S1/2 state. We observe quantum beats in the fluorescence from the 6P3/2 state which are modified by the driving of the excited-state transition. The Fourier spectrum of the beat signal yields evidence of Autler-Townes splitting of the 6P3/2, F=5 hyperfine level and Rabi oscillations on the excited-state transition. A detailed model provides qualitative agreement with the data, giving insight to the physical processes involved

Atomic Faraday filter with equivalent noise bandwidth less than 1 GHz

We demonstrate an atomic bandpass optical filter with an equivalent noise bandwidth less than 1 GHz using the D1 line in a cesium vapor. We use the ElecSus computer program to find optimal experimental parameters and find that, for important quantities, the cesium D1 line clearly outperforms other alkali metals on either D-lines. The filter simultaneously achieves a peak transmission of 77%, a passband of 310 MHz, and an equivalent noise bandwidth of 0.96 GHz, for a magnetic field of 45.3 G and a temperature of 68.0°C. Experimentally, the prediction from the model is verified. The experiment and theoretical predictions show excellent agreement

Single-photon interference due to motion in an atomic collective excitation

We experimentally demonstrate the generation of heralded bi-chromatic single photons from an atomic collective spin excitation (CSE). The photon arrival times display collective quantum beats, a novel interference effect resulting from the relative motion of atoms in the CSE. A combination of velocity-selective excitation with strong laser dressing and the addition of a magnetic field allows for exquisite control of this collective beat phenomenon. The present experiment uses a diamond scheme with near-IR photons that can be extended to include telecommunications-wavelengths or modified to allow storage and retrieval in an inverted-Y scheme

Source and quantity of carbon influence its sequestration in Rostherne Mere (UK) sediment: a novel application of stepped combustion radiocarbon analysis

We explored the roles of phytoplankton production, carbon source, and human activity on carbon accumulation in a eutrophic lake (Rostherne Mere, UK) to understand how changes in nutrient loading, algal community structure and catchment management can influence carbon sequestration in lake sediments. Water samples (dissolved inorganic, organic and particulate carbon) were analysed to investigate contemporary carbon sources. Multiple variables in a 55-cm sediment core, which represents the last ~ 90 years of accumulation, were studied to determine historical production rates of algal communities and carbon sources. Fluctuations in net primary production, inferred from sedimentary diatom abundance and high-performance liquid chromatography (HPLC) pigment methods, were linked to nutrient input from sewage treatment works (STW) in the catchment. Stepped combustion radiocarbon (SCR) measurements established that lake sediment contains between 11% (~ 1929 CE) and 69% (~ 1978 CE) recalcitrant carbon, with changes in carbon character coinciding with peaks in accumulation rate and linked to STW inputs. Catchment disturbance was identified by radiocarbon analysis, and included STW construction in the 1930s, determined using SCR analysis, and recent nearby highway construction, determined by measurements on dissolved organic carbon from the lake and outflow river. The quantity of autochthonous carbon buried was related to diatom biovolume accumulation rate (DBAR) and decreased when diatom accumulation rate and valve size declined, despite an overall increase in net carbon production. HPLC pigment analysis indicated that changes in total C deposition and diatom accumulation were related to proliferation of non-siliceous algae. HPLC results also indicated that dominance of recalcitrant carbon in sediment organic carbon was likely caused by increased deposition rather than preservation factors. The total algal accumulation rate controlled the sediment organic carbon accumulation rate, whereas DBAR was correlated to the proportion of each carbon source buried

Carbon supported hybrid catalysts for controlled product selectivity in the hydrosilylation of alkynes

A series of Rh- and Ir-hybrid catalysts with varying tether lengths has been prepared by immobilization of RhI, RhIIIand IrIIIcomplexes on carbon blackviaradical grafting. The performance of the different catalysts was assessed for the hydrosilylation of phenylacetylene with Et3SiH. The efficiency of the catalysts was dependent on the length of the tethers to the surface. The RhIII- and IrIIIhybrids afforded the β(Z)-vinylsilanes, as observed for the analogous homogeneous RhIIIcatalyst. No distinct product selectivity was observed when using the homogeneous RhIprecursors as catalysts. However, on using the RhIIIhybrid catalysts derived from the RhIprecursors to promote hydrosilylation, the major products were the α-vinylsilanes and the origin of the difference in reactivity was found to be a chemical modification of the catalysts during immobilization. Substrate scope is demonstrated for a number of alkynes, and feasible mechanisms supported by DFT calculations are proposed

Preliminary results from a survey of oyster production areas in Ireland for norovirus

A survey of 18 oyster production areas in Ireland for norovirus (NoV) contamination was initiated in August 2006. The findings presented are the preliminary results from the first seven months of the survey. Prior to the survey commencing, a simple desk bask sanitary survey of each area was undertaken. This provided an assessment enabling each site to be ranked into 3 categories (low, medium and high) on the basis of the risk of NoV contamination. Samples were collected on a monthly basis and tested for the presence of NoV using semi-quantitative real-time PCR allowing relative quantitation of NoV levels. A correlation was observed between occurrence and levels of NoV detected and the risk categories ascribed to each production area. To date NoV was detected in 60.7, 30.0 and 2.5 percent of samples from the high, medium and low risk categorised areas, respectively. A strong seasonal bias towards increased winter contamination was observed with NoV detected in 15.5 and 50 % of samples in August and February, respectively. The preliminary results from this survey indicate that it may be possible to predict the relative risk of NoV contamination in a shellfish harvesting area. This in conjunction with targeted NoV monitoring using real-time PCR could aid the further development of risk management procedures in shellfisheries

Quantitative optical spectroscopy of 87^{87}Rb vapour in the Voigt geometry in DC magnetic fields up to 0.4T

We present a detailed spectroscopic investigation of a thermal ⁸⁷Rb atomic vapour in magnetic fields up to 0.4T in the Voigt geometry. We fit experimental spectra with our theoretical model ElecSus and find excellent quantitative agreement, with RMS errors of backsim0.3%. We extract the magnetic field strength and the angle between the polarisation of the light and the magnetic field from the atomic signal and find excellent agreement to within backsim1% with a commercial Hall probe. Finally, we present an investigation of the relative sensitivity of this technique to variations in the field strength and angle with a view to enabling atom-based high-field vector magnetometry

Engineering regioselectivity in the hydrosilylation of alkynes using heterobimetallic dual-functional hybrid catalysts

The synthesis and characterization of carbon black supported rhodium and iridium heterobimetallic catalysts, termed hybrid catalysts, and their application in the hydrosilylation of alkynes is described. An aryl diazonium grafting procedure was applied to simultaneously immobilize Rh and Ir pyrazole–triazole complexes with tethers of varying lengths to carbon black, yielding the hybrid catalysts. The complexes differ in metal centre oxidation state and co-ligands, which are CO or Cp*Cl for the Rh complexes and Cp*Cl for the Ir complexes. The immobilization results in simultaneous surface binding and modification of the Rh complexes bearing CO-ligands. In this process, the CO ligands are removed and the overall structure of the catalytically active complex is altered. Analysis of the hybrid catalysts by XPS and SEM/EDX shows that the catalysts bear both surface bound Rh- and Ir-complexes. The Rh content is substantially higher than the Ir content. This is due to more efficient binding of the modified Rh complexes to the carbon black, as they feature two potential binding sites. Synchrotron based X-ray absorption spectroscopy (XAS) at the Rh K- and Ir L3 edges further confirms the presence of the surface bound metal complexes. There is no indication that the presence of a secondary metal affects the electronic structure of the adjacent metal in the systems under investigation, for either the long or short tether derivatives. The performance of the different catalysts was assessed for promoting the hydrosilylation of alkynes, an important industrially relevant reaction. All catalysts are highly efficient. The modified Rh sites are α-selective in the product formation on activation of terminal alkynes, while the RhCp*Cl and IrCp*Cl sites are β(Z)-selective. When operating at mild conditions with high metal loadings, the surface bound Rh catalyst is the active species, while the Ir sites are inactive. At a lower overall surface coverage or higher temperature, the Ir sites become active, which allows engineering of the regioselectivity by adjusting surface coverages and metal loadings