Spectral dependence of irreversible light-induced fluorescence quenching: Chlorophyll forms with maximal emission at 700-702 and 705-710nm as spectroscopic markers of conformational changes in the core complex.

The spectral dependence of the irreversible non-photochemical fluorescence quenching associated with photoinhibition in vitro has been comparatively investigated in thylakoid membranes, PSII enriched particles and PSII core complexes isolated from spinach. The analysis of the fluorescence emission spectra of dark-adapted and quenched samples as a function of the detection temperature in the 280-80K interval, indicates that Chlorophyll spectral forms having maximal emission in the 700-702nm and 705-710nm ranges gain relative intensity in concomitance with the establishment of irreversible light-induced quenching, acting thereby as spectroscopic markers. The relative enhancement of the 700-702nm and 705-710nm forms emission could be due either to an increase of their stoichiometric abundance or to their intrinsically low fluorescence quantum yields. These two factors, that can also coexist, need to be promoted by light-induced alterations in chromophore-protein as well as chromophore-chromophore interactions. The bands centred at about 701 and 706nm are also observed in the PSII core complex, suggesting their, at least partial, localisation in proximity to the reaction centre, and the occurrence of light-induced conformational changes in the core subunits.

Investigation of Reduced Graphene Oxide and a Nb-Doped TiO2 Nanotube Hybrid Structure To Improve the Gas-Sensing Response and Selectivity.

The precise detection of flammable and explosive gases and vapors remains an important issue because of the increasing demand for renewable energy sources and safety requirements in industrial processes. Metal oxides (TiO2, SnO2, ZnO, etc.) are very attractive materials for the manufacturing of chemical gas sensors. However, their gas selectivity issues and further improvement in the sensing response remain a significant challenge. The incorporation of metal oxides with two-dimensional (2D) graphene oxide (GO) is considered to be a promising approach to obtaining hybrid structures with improved gas-sensing performance. Herein, we report the development of GO and niobium-doped titanium dioxide nanotube (NT) hybrid structures with a tunable selectivity and sensing response against hydrogen gas, achieved by properly controlling the degree of reduction and concentration of GO. The effects of these parameters are systematically studied in terms of the response amplitude and selectivity. It was found that, compared to undoped titanium dioxide nanotubes, the hybrid material with an optimal concentration of reduced-GO and the introduction of niobium shows an increase in hydrogen response of about an order of magnitude and a simultaneous reduction of the response to possible interfering compounds such as carbon monoxide and acetone, thus providing enhanced selectivity. This research may provide an efficient way to enhance the chemical sensing performance of metal oxide nanomaterials.