Automatic outdoor monitoring system for photovoltaic panels.

Long-term acquisition of solar panel performance parameters, for panels operated at maximum power point in their real environment, is of critical importance in the photovoltaic research sector. However, few options exist for the characterization of non-standard panels such as concentrated photovoltaic systems, heavily soiled or shaded panels or those operating under non-standard spectral illumination; certainly, it is difficult to find such a measurement system that is flexible and affordable enough to be adopted by the smaller research institutes or universities. We present here an instrument aiming to fill this gap, autonomously tracking and maintaining any solar panel at maximum power point while continuously monitoring its operational parameters and dissipating the produced energy without connection to the power grid.

Solution-phase synthesis of heteroatom-substituted carbon scaffolds for hydrogen storage.

This paper reports a bottom-up solution-phase process for the preparation of pristine and heteroatom (boron, phosphorus, or nitrogen)-substituted carbon scaffolds that show good surface areas and enhanced hydrogen adsorption capacities and binding energies. The synthesis method involves heating chlorine-containing small organic molecules with metallic sodium at reflux in high-boiling solvents. For heteroatom incorporation, heteroatomic electrophiles are added to the reaction mixture.

Nanoengineered carbon scaffolds for hydrogen storage.

Single-walled carbon nanotube (SWCNT) fibers were engineered to become a scaffold for the storage of hydrogen. Carbon nanotube fibers were swollen in oleum (fuming sulfuric acid), and organic spacer groups were covalently linked between the nanotubes using diazonium functionalization chemistry to provide 3-dimensional (3-D) frameworks for the adsorption of hydrogen molecules. These 3-D nanoengineered fibers physisorb twice as much hydrogen per unit surface area as do typical macroporous carbon materials.

Structural and magnetic studies of two-dimensional solvent-free manganeseII complexes prepared via ligand exchange reaction under solvothermal conditions.

Systematic investigation of the ligand exchange reactions between manganese(II) acetate and benzoic acid under solvothermal conditions led to the isolation of crystalline complexes {Mn5(OC(O)CH3)6(OC(O)C6H5)4}(infinity) ( 1) and {Mn5(OC(O)CH3)4(OC(O)C6H5)6}}(infinity) ( 2) in high (i.e., >90%) yields.