High-power, frequency-quadrupled UV laser source resonant with the 1S0-3P1 narrow intercombination transition of cadmium at 326.2 nm.

We present a novel high-power, frequency-stabilized UV laser source at 326.2 nm, resonant with the Cd 1S0-3P1 narrow intercombination transition. We achieve a maximum produced power of 1 W at 326.2 nm by two successive frequency doubling stages of a narrow-linewidth (<1 kHz) seed laser at 1304.8 nm. Approximately 3.4 W of optical power at 652.4 nm is produced by a visible Raman fiber amplifier (VRFA) that amplifies and generates the second harmonic of the infrared radiation. The visible light is subsequently frequency-doubled down to 326.2 nm in a nonlinear bow-tie cavity using a Brewster-cut beta-barium-borate (BBO) crystal, with a maximum conversion efficiency of approximately 40% for 2.5 W of coupled red power. Full characterization of the laser source, together with spectroscopy signals of all Cd isotopes, spanning more than 4 GHz in the UV, are shown.

Watt-level blue light for precision spectroscopy, laser cooling and trapping of strontium and cadmium atoms.

High-power and narrow-linewidth laser light is a vital tool for atomic physics, being used for example in laser cooling and trapping and precision spectroscopy. Here we produce Watt-level laser radiation at 457.75 nm and 460.86 nm of respective relevance for the cooling transitions of cadmium and strontium atoms. This is achieved via the frequency doubling of a kHz-linewidth vertical-external-cavity surface-emitting laser (VECSEL), which is based on a novel gain chip design enabling lasing at > 2 W in the 915-928 nm region. Following an additional doubling stage, spectroscopy of the 1S0 → 1P1 cadmium transition at 228.87 nm is performed on an atomic beam, with all the transitions from all eight natural isotopes observed in a single continuous sweep of more than 4 GHz in the deep ultraviolet. The absolute value of the transition frequency of 114Cd and the isotope shifts relative to this transition are determined, with values for some of these shifts provided for the first time.

One Dimensional ZnO Nanostructures: Growth and Chemical Sensing Performances.

Recently, one-dimensional (1D) nanostructures have attracted the scientific community attention as sensitive materials for conductometric chemical sensors. However, finding facile and low-cost techniques for their production, controlling the morphology and the aspect ratio of these nanostructures is still challenging. In this study, we report the vapor-liquid-solid (VLS) synthesis of one dimensional (1D) zinc oxide (ZnO) nanorods (NRs) and nanowires (NWs) by using different metal catalysts and their impact on the performances of conductometric chemical sensors. In VLS mechanism, catalysts are of great interest due to their role in the nucleation and the crystallization of 1D nanostructures. Here, Au, Pt, Ag and Cu nanoparticles (NPs) were used to grow 1D ZnO. Depending on catalyst nature, different morphology, geometry, size and nanowires/nanorods abundance were established. The mechanism leading to the VLS growth of 1D ZnO nanostructures and the transition from nanorods to nanowires have been interpreted. The formation of ZnO crystals exhibiting a hexagonal crystal structure was confirmed by X-ray diffraction (XRD) and ZnO composition was identified using transmission electron microscopy (TEM) mapping. The chemical sensing characteristics showed that 1D ZnO has good and fast response, good stability and selectivity. ZnO (Au) showed the best performances towards hydrogen (H2). At the optimal working temperature of 350 °C, the measured response towards 500 ppm of H2 was 300 for ZnO NWs and 50 for ZnO NRs. Moreover, a good selectivity to hydrogen was demonstrated over CO, acetone and ethanol.

Seed-Assisted Growth of TiO2 Nanowires by Thermal Oxidation for Chemical Gas Sensing.

Herein, we report the catalyst assisted growth of TiO2 one-dimensional (1D) nanowires (NWs) on alumina substrates by the thermal oxidation technique. RF magnetron sputtering was used to deposit a thin Ti metallic layer on the alumina substrate, followed by an Au catalytic layer on the Ti metallic one. Thermal oxidation was carried out in an oxygen deficient environment. The optimal thermal growth temperature was 700 °C, in a mixture environment composed by Ar and O2. As a comparison, Ti films were also oxidized without the presence of the Au catalyst. However, without the Au catalyst, no growth of nanowires was observed. Furthermore, the effect of the oxidation temperature and the film thickness were also investigated. SEM, TEM, and EDX studies demonstrated the presence of Au nanoparticles on top of the NWs, indicating that the Au catalyst drove the growth process. Raman spectroscopy revealed the Rutile crystalline phase of TiO2 NWs. Gas testing measurements were carried out in the presence of a relative humidity of 40%, showing a reversible response to ethanol and H2 at various concentrations. Thanks to the moderate temperature and the easiness of the process, the presented synthesis technique is suitable to grow TiO2 NWs for many different applications.

Integration of VLS-Grown WO3 Nanowires into Sensing Devices for the Detection of H2S and O3.

The inspiration behind this research is the development of tungsten oxide (WO3) nanowires based, highly sensitive and selective sensing devices directly on the active sensing platform. WO3 one-dimensional nanowires were synthesized via the vapour-phase growth technique. This approach allows the production of well-aligned and uniform nanowires on alumina substrates with their diameter and length in the nanometer range. The morphological and structural properties of nanowires have been investigated by means of the field effect electron microscopy, grazing incidence X-ray diffraction, Raman spectroscopy, and X-ray photoelectron spectroscopy. Finally, the fabricated WO3 nanowire sensing devices and their gas sensing performance were investigated in the presence of different oxidizing and reducing gases (especially environmental gases) at different temperatures. The WO3 sensors demonstrate high performance toward H2S and O3 at the optimal working temperatures of 400 and 200 °C, respectively, with the detection limit in the ppb level.

Imaging Optical Frequencies with 100 µHz Precision and 1.1 µm Resolution.

We implement imaging spectroscopy of the optical clock transition of lattice-trapped degenerate fermionic Sr in the Mott-insulating regime, combining micron spatial resolution with submillihertz spectral precision. We use these tools to demonstrate atomic coherence for up to 15 s on the clock transition and reach a record frequency precision of 2.5×10^{-19}. We perform the most rapid evaluation of trapping light shifts and record a 150 mHz linewidth, the narrowest Rabi line shape observed on a coherent optical transition. The important emerging capability of combining high-resolution imaging and spectroscopy will improve the clock precision, and provide a path towards measuring many-body interactions and testing fundamental physics.

Squeezing on Momentum States for Atom Interferometry.

We propose and analyze a method that allows for the production of squeezed states of the atomic center-of-mass motion that can be injected into an atom interferometer. Our scheme employs dispersive probing in a ring resonator on a narrow transition in order to provide a collective measurement of the relative population of two momentum states. We show that this method is applicable to a Bragg diffraction-based strontium atom interferometer with large diffraction orders. This technique can be extended also to small diffraction orders and large atom numbers N by inducing atomic transparency at the frequency of the probe field, reaching an interferometer phase resolution scaling Δϕ∼N^{-3/4}. We show that for realistic parameters it is possible to obtain a 20 dB gain in interferometer phase estimation compared to the standard quantum limit. Our method is applicable to other atomic species where a narrow transition is available or can be synthesized.

Metal oxide nanostructures: preparation, characterization and functional applications as chemical sensors.

Preparation and characterization of different metal oxide (NiO, WO3, ZnO, SnO2 and Nb2O5) nanostructures for chemical sensing are presented. p-Type (NiO) and n-type (WO3, SnO2, ZnO and Nb2O5) metal oxide nanostructures were grown on alumina substrates using evaporation-condensation, thermal oxidation and hydrothermal techniques. Surface morphologies and crystal structures were investigated through scanning electron microscopy and Raman spectroscopy. Furthermore, different batches of sensors have been prepared, and their sensing performances towards carbon monoxide and nitrogen dioxide have been explored. Moreover, metal oxide nanowires have been integrated into an electronic nose and successfully applied to discriminate between drinking and contaminated water.

Atom Interferometry with the Sr Optical Clock Transition.

We report on the realization of a matter-wave interferometer based on single-photon interaction on the ultranarrow optical clock transition of strontium atoms. We experimentally demonstrate its operation as a gravimeter and as a gravity gradiometer. No reduction of interferometric contrast was observed for a total interferometer time up to ∼10 ms, limited by geometric constraints of the apparatus. Single-photon interferometers represent a new class of high-precision sensors that could be used for the detection of gravitational waves in so far unexplored frequency ranges and to enlighten the boundary between quantum mechanics and general relativity.

A composite structure based on reduced graphene oxide and metal oxide nanomaterials for chemical sensors.

A hybrid nanostructure based on reduced graphene oxide and ZnO has been obtained for the detection of volatile organic compounds. The sensing properties of the hybrid structure have been studied for different concentrations of ethanol and acetone. The response of the hybrid material is significantly higher compared to pristine ZnO nanostructures. The obtained results have shown that the nanohybrid is a promising structure for the monitoring of environmental pollutants and for the application of breath tests in assessment of exposure to volatile organic compounds.