Iron oxide nanowhiskers with dimensions of approximately 2 × 20 nm were successfully synthesized by selectively heating an iron oleate complex. Such nanostructures resulted from the difference in the ligand coordination microenvironments of the Fe(III) oleate complex, according to our electronic structure calculations and thermogravimetric analysis. A ligand-directed growth mechanism was subsequently proposed to rationalize the growth process. The formation of the nanowhiskers provides a unique example of shape-controlled nanostructures, offering additional insights into nanoparticle synthesis.

Organothiol (OT) adsorption onto gold nanoparticles (AuNPs) and gold powder was studied in 50% aqueous ethanol and in water. The OT solution rapidly acidifies upon addition of AuNPs or Au powder, and the number of protons released into the solution is proportional to the amount of OT adsorbed onto the gold surface. Theoretical calculations and normal Raman and surface-enhanced Raman spectroscopic (SERS) measurements show that the pK a of the OTs adsorbed onto AuNP can be more than 10 pK a units smaller than the pK a of OT in solution. The pH measurements suggest that there is a substantial fraction (up to 45%) of the protons derived from the surface-adsorbed OTs retained close to the gold surface, presumably as the counterion to the negatively charged, thiolate-covered AuNPs. Charge transfer between the surface-adsorbed thiolate and the AuNPs is demonstrated by the quenching of the OT UV−vis absorption when the OTs are adsorbed onto the synthesized AuNPs or bovine serum albumin-stabilized AuNPs.

An effective approach to synthesizing crystalline iron oxide nanoplates (~3 nm thick) and nanoflowers composed of ~5 nm small grains was reported. The formation of different-shaped nanoparticles in a similar system was achieved by controlling the nucleus concentration and growth rate.

A general approach to the synthesis and detailed characterization of magnetic ferrite nanocubes were reported, where the nanocubes were synthesized by the thermal decomposition of metal-oleate complexes following a step-heating method. The doping ions were introduced during the precursor preparation by forming M(2+)/Fe(3+) oleate mixed complex (M(2+) = Fe(2+), Mn(2+), Zn(2+), Cu(2+), Ca(2+), and Mg(2+)). The mechanistic studies showed that the presence of sodium oleate in combination with step-heating was critical for the formation of the cubic shapes for the doped magnetic ferrites. The nanocubes were extensively characterized, including morphology and crytsal structure by advanced transmission electron microscopy, doping level and distribution by energy dispersive X-ray spectroscopy and X-ray photoelectron spectroscopy, cation distribution within the spinel structures by Fourier transform infrared and Raman spectroscopy, and magnetic properties by alternating gradient magnetometer at room temperature.

We develop a systematic theory of multiparticle excitations in strongly interacting Fermi systems. Our work is the generalization of the time-honored work by Jackson, Feenberg, and Campbell for bosons, that provides, in its most advanced implementation, quantitative predictions for the dynamic structure function in the whole experimentally accessible energy/momentum regime. Our view is that the same physical effects, namely, fluctuations of the wave function at an atomic length scale are responsible for the correct energetics of the excitations in both Bose and Fermi fluids. Besides a comprehensive derivation of the fermion version of the theory and discussion of the approximations made, we present results for homogeneous 3 He and electrons in three dimensions. We find indeed a significant lowering of the zero-sound mode in 3 He and a broadening of the collective mode due to the coupling to two-particle-two-hole excitations in good agreement with experiments. The most visible effect in electronic systems is the appearance of a "double-plasmon" excitation.