An unprecedented octahedral {Cd30} nanocage supported by twelve pendant-armed tetraacetate macrocyclic ligands.

An unprecedented octahedral {Cd(30)} nanocage supported by twelve pendant-armed tetraacetate macrocyclic ligands was synthesized through the reaction of macrocyclic tetraethyl ester and Cd(OAc)(2)·2H(2)O in a 1 : 2 stoichiometry, where the surface photovoltage and photoluminescent properties have been studied for the nanocage.

Synthesis and plasmon-induced charge-transfer properties of monodisperse gold-doped titania microspheres.

Monodisperse gold-doped titania microspheres have been synthesized under high concentration of a titanium precursor (9.34 mM) by introducing a trace amount of chloroauric acid (CA) into the reaction system; the size of the microspheres can be easily tuned (from approximately 587 to approximately 392 nm) by varying the amount of the CA added. The plausible formation mechanism has been discussed in detail. Chloroauric acid was found to act as the stabilizing agent to induce the formation of monodisperse colloidal spheres. Gold-doped anatase titania spheres with approximately 7 nm gold nanodots on the surface were synthesized by calcination. Interestingly, results from surface photocurrent, surface photovoltage, and transient photovoltage measurements indicate that the gold nanodots exhibit different electronic properties when the gold-doped anatase titania spheres were illuminated by different wavelengths of light: one is an electron acceptor in the UV region, while the other is an electron donor in the visible region. Furthermore, the decay time of the injected plasmon-induced electrons was found to be on the millisecond timescale and increased with increasing amounts of gold doped.