Boosting infrared energy transfer in 3D nanoporous gold antennas.

The applications of plasmonics to energy transfer from free-space radiation to molecules are currently limited to the visible region of the electromagnetic spectrum due to the intrinsic optical properties of bulk noble metals that support strong electromagnetic field confinement only close to their plasma frequency in the visible/ultraviolet range. In this work, we show that nanoporous gold can be exploited as a plasmonic material for the mid-infrared region to obtain strong electromagnetic field confinement, co-localized with target molecules into the nanopores and resonant with their vibrational frequency. The effective optical response of the nanoporous metal enables the penetration of optical fields deep into the nanopores, where molecules can be loaded thus achieving a more efficient light-matter coupling if compared to bulk gold. In order to realize plasmonic resonators made of nanoporous gold, we develop a nanofabrication method based on polymeric templates for metal deposition and we obtain antenna arrays resonating at mid-infrared wavelengths selected by design. We then coat the antennas with a thin (3 nm) silica layer acting as the target dielectric layer for optical energy transfer. We study the strength of the light-matter coupling at the vibrational absorption frequency of silica at 1240 cm-1 through the analysis of the experimental Fano lineshape that is benchmarked against identical structures made of bulk gold. The boost in the optical energy transfer from free-space mid-infrared radiation to molecular vibrations in nanoporous 3D nanoantenna arrays can open new application routes for plasmon-enhanced physical-chemical reactions.

Compact hematite buffer layer as a promoter of nanorod photoanode performances.

The effect of a thin α-Fe2O3 compact buffer layer (BL) on the photoelectrochemical performances of a bare α-Fe2O3 nanorods photoanode is investigated. The BL is prepared through a simple spray deposition onto a fluorine-doped tin oxide (FTO) conducting glass substrate before the growth of a α-Fe2O3 nanorods via a hydrothermal process. Insertion of the hematite BL between the FTO and the nanorods markedly enhances the generated photocurrent, by limiting undesired losses of photogenerated charges at the FTO||electrolyte interface. The proposed approach warrants a marked improvement of material performances, with no additional thermal treatment and no use/dispersion of rare or toxic species, in agreement with the principles of green chemistry.

Nanoporous gold plasmonic structures for sensing applications.

The fabrication, characterization and functionalization of periodically patterned nanoporous gold layers is presented. The material shows plasmonic properties in the near infrared range, with excitation and propagation of surface plasmon polaritons. Functionalization shows a marked enhancement in the optical response in comparison with evaporated gold gratings, due to a great increase of the active surface. Due to its superior response, nanoporous gold patterns appear promising for the realization of compact plasmonic platforms for sensing purposes.

Ternary CdSxSe 1-x deposited on Ag(111) by ECALE: synthesis and characterization.

Morphology and electronic properties of CdS, CdSe, and the ternary compounds of formula CdSxSe(1-x) deposited on Ag(111) by ECALE have been characterized as a function of the composition. The number of the attainable x values is limited by the necessity of using well-defined CdS/CdSe deposition sequences. However, the quantitative analysis carried out by XPS and electrochemical stripping experiments indicates that the ECALE method has a good control on composition. The AFM images together with the electrochemical characterization indicate both two-dimensional and three-dimensional growth contributions. The photospectra recorded at CdS film electrodes in liquid junction with an alkaline (poly)sulfide electrolyte show good efficiency of photoconversion and band gap typical of the single crystal. Lower photoconversion efficiency and the presence of subband gap response are observed for CdSe; a possible reason is some crystalline disorder due to lower control of the layer-by-layer deposition in the case of Se. The dependence of band gap on composition of ternary CdSxSe(1-x) ECALE films is monotonic and in agreement with literature data reported for bulk materials.

Determination of 99Tc in urine by liquid scintillation counting to evaluate internal contamination.

A practical method is described which allows the radiochemical determination of 99Tc in urine. The radionuclide is recovered as tetraphenylarsonium pertechnetate by coprecipitation with tetraphenylarsonium perchlorate and its activity is counted by the liquid scintillation technique. The lower limit of detection, assumed equal to three standard deviations of the blank activity, is about 2 pCi in 50 ml of urine and permits an evaluation of an internal contamination of one investigation level even four months after intake. The urinary excretion function of 99Tc is calculated from experimental data reported in the literature for 99mTc and is used to establish derived investigation levels on the basis of annual limits on intake recommended by the International Commission on Radiological Protection. The illustrated method is sensitive enough to perform accurate evaluations every three months, a frequency suitable for radiological protection of workers.