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https://www.selleckchem.com/products/5-cholesten-3beta-ol-7-one.html Semiconductor-metal heterojunction nanostructures possess an ability to store electrons upon photoexcitation through Fermi level equilibration. The unique role of capping ligands in modulating the equilibration of Fermi level in CdSe-Au heteronanostructures is explored by taking alkyl thiols and alkyl amines as examples. Alkyl thiol having its highest occupied molecular orbital (HOMO) above the valence band of the heterojunction nanostructure inhibits the exciton recombination by scavenging the photogenerated hole. This leads to the elevation in the Fermi level of Au and equilibration with the conduction band of CdSe. The Fermi level equilibrated electrons are further transferred to an acceptor molecule such as methyl viologen, demonstrating the potential of heterojunction nanostructures capped with hole accepting ligands for charge transport application in photovoltaics. In contrast, alkyl amine being a non-hole acceptor ligand with its HOMO placed below its valence band promotes rapid Au mediated exciton recombination, limiting its usefulness in charge transport application. Thus, the energetics of ligands on heterojunction nanostructures plays a decisive role in Fermi level equilibration.In this work, the reaction properties of mixed silver-nickel oxide AgNiO2 were investigated in the reaction of CO oxidation ranging from room temperature up to 350 °C. X-ray photoelectron spectroscopy revealed the presence of a single oxidized silver state and the combination of Ni2+ and Ni3+ species on the surface of the as-prepared mixed oxide. It was established that AgNiO2 was able to interact with CO at room temperature. It was accompanied by the simultaneous titration of the lattice (O2--like) and weakly charged (O--like) oxygen species. The interaction with CO below 100 °C resulted in the accumulation of carbonate-like species on the AgNiO2 surface. Above 150 °C, the surface structure of mixed oxide was f

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