Undoped, high-quality diamond is, under almost all circumstances, one of the best insulators known. However, diamond covered with chemically bound hydrogen shows a pronounced conductivity when exposed to air. This conductivity arises from positive-charge carriers (holes) and is confined to a narrow near-surface region. Although several explanations have been proposed, none has received wide acceptance, and the mechanism remains controversial. Here, we report the interactions of hydrogen-terminated, macroscopic diamonds and diamond powders with aqueous solutions of controlled pH and oxygen concentration. We show that electrons transfer between the diamond and an electrochemical reduction/oxidation couple involving oxygen. This charge transfer is responsible for the surface conductivity and also influences contact angles and zeta potentials. The effect is not confined to diamond and may play a previously unrecognized role in other disparate systems.

The presence of sulfide/polysulfide redox couple is crucial in achieving stability of metal chalcogenide (e.g., CdS and CdSe)-based quantum dot-sensitized solar cells (QDSC). However, the interfacial charge transfer processes play a pivotal role in dictating the net photoconversion efficiency. We present here kinetics of hole transfer, characterization of the intermediates involved in the hole oxidation of sulfide ion, and the back electron transfer between sulfide radical and electrons injected into TiO(2) nanoparticles. The kinetic rate constant (10(7)-10(9) s(-1)) for the hole transfer obtained from the emission lifetime measurements suggests slow hole scavenging from CdSe by S(2-) is one of the limiting factors in attaining high overall efficiency. The presence of the oxidized couple, by addition of S or Se to the electrolyte, increases the photocurrent, but it also enhances the rate of back electron transfer.

In this report, we show for the first time that SnO2 nanowire based dye sensitized solar cells exhibit an open circuit voltage of 560 mV, which is 200 mV higher than that using SnO2 nanoparticle based cells. This is attributed to the more negative flat band potential of nanowires compared to the nanoparticles as determined by open circuit photo voltage measurements made at high light intensities. The nanowires were employed in hybrid structures consisting of highly interconnected SnO2 nanowire matrix coated with TiO2 nanoparticles, which showed an open circuit voltage of 720 mV and an efficiency of 4.1% compared to 2.1% obtained with pure SnO2 nanowire matrix. The electron transport time constants for SnO2 nanowire matrix were an order of magnitude lower and the recombination time constants are about 100 times higher than that of TiO2 nanoparticles. The higher efficiency observed for DSSCs based on hybrid structure is attributed to the band edge positions of SnO2 relative to that of TiO2 and faster electron transport in SnO2 nanowires.

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Fabrication of nanofibrous biomaterials based on natural materials (collagen, gelatin, etc.) through various techniques is an important research topic. Electrospinning, a well-established technique for nanofiber production has also been extended for producing nanofibrous structures of natural materials. Collagen nanofiber production utilizes hexafluoro isopropanol (HFIP) as a solvent for electrospinning. Research efforts are now focused on replacing HFIP with an environmentally benign solvent. In this study, electrospinning of Type I collagen of bovine skin with polycaprolactone (PCL) as a blend and an environmentally benign solvent, acetic acid, was carried out. The samples produced were subjected to contact angle measurements, porosity estimation, SEM, FTIR, TGA, and DSC. Nanofibers in the range of 100-200 nm were produced with an optimum porosity of 60%. The instrumental analyses confirm the physical interaction between collagen and PCL. Electrospinning of collagen in an environmentally benign solvent has been carried out and its usage in tissue engineering is being investigated by our research group.Correspondence to: A. Gnanamani (gnanamani3@gmail. com) and V. R. Giridev (Giridev vrgiridev@yahoo.com).

Charge injection from excited CdSe quantum dots into nanostructured TiO(2) film can be modulated by varying solution pH. At increasing solution pH, the conduction band of TiO(2) shifts 59 mV/pH unit to a more negative potential, thereby decreasing the driving force and thus decreasing the rate of nonradiative electron transfer from excited CdSe. The emission yield and the average emission lifetime increase with increasing pH, thus providing a way to monitor the variation in medium pH.

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ARTICLEthat seen with the organic electrolyte), and low capacity fade observed here are promising for the future development of silicon/IL-based batteries.