We present a generalized cation-anion codoping methodology for the synthesis of monodisperse, doped metal-oxide nanocrystals (NCs) that exhibit near-infrared localized surface plasmon resonance (LSPR) with the highest reported quality factors. We demonstrate that, in addition to the use of common cation dopants, the incorporation of fluorine into the lattice as an anion dopant can further increase the free-carrier concentration within individual NCs; this supports the cooperative effects of mixed cation-anion doping in shifting the LSPR to higher energies. As a result, this method allows the LSPR of doped metal-oxide NCs to become tunable across a significantly broader wavelength range (1.5-3.3 μm), circumventing the prior limitations on the highest possible LSPR energies associated with single-element doping for a given oxide host. The strategy of cation-anion codoping can offer new possibilities for the chemical design of doped semiconductor and metal-oxide NCs with tailored LSPR characteristics.

We have developed a generalized seeded-growth methodology for the synthesis of monodisperse metal-doped plasmonic oxide heterodimer nanocrystals (NCs) with a near-unity morphological yield. Using indium-doped cadmium oxide (ICO) as an example, we show that a wide variety of preformed metal NCs (Au, Pt, Pd, FePt, etc.) can serve as the seeds for the tailored synthesis of metal-ICO heterodimers with exquisite size, shape, and composition control, facilitated by the delayed nucleation mechanism of the CdO phase. The metal-ICO heterodimers exhibit broadly tunable near-infrared localized surface plasmon resonances, and dual plasmonic bands are observed for Au-ICO heterodimers. We further demonstrate that the oxide domain of the Au-ICO heterodimers can be selectively and controllably transformed into a series of partially and completely hollow cadmium chalcogenide nanoarchitectures with unprecedented structural complexity, leaving the metal domain intact. Our work not only represents an exciting addition to the rapidly expanding library of chemical reactions that produce colloidal hybrid NCs, but it also provides a general route for the bottom-up chemical design of multicomponent metal-oxide-semiconductor NCs in a rational and sequential manner.

The structure and size of ligands attached to the surfaces of gold nanorods, such as adsorbed surfactants or grafted polymers, are important considerations that facilitate the use of such nanoparticles in the human body, in advanced materials for energy harvesting, or in devices for single molecule detection. Here, we report small-angle neutron scattering (SANS) measurements from surfactant or poly(ethylene glycol) (PEG) coated gold nanorods in solution, which quantitatively determine the location, structure, and composition of these surface layers. In addition, by synthesizing gold nanorods using seed crystals which are coated with deuterated cetyltrimethylammonium bromide (dCTAB), we are able to exploit the isotopic sensitivity of SANS to study, for the first time, the retention of surfactant from the seed crystals to the final gold nanorod product, finding that very little exchange of the deuterated with hydrogenated surfactant occurs. Finally, we demonstrate that, when Au NRs are PEGylated using standard techniques, the surfactant bilayer remains intact, and while mass spectrometry detects the presence of both surfactant and PEG, the composition as measured from SANS is predominantly that of the surfactant. These measurements not only provide new insight into the synthesis and functionalization of gold nanorods but provide a quantitative picture of the structure of grafted polymer and surfactant layers on gold nanorod surfaces which has implications for the fabrication of plasmonic and biomedical materials.

Three-dimensional (3D) hollow-porous vanadium pentoxide (V2 O5 ) quasi-microspheres are synthesized by a facile solvothermal method followed by annealing at 450 °C in air. The interconnected hollow-porous networks facilitate the kinetics of lithium-ion diffusion and improve the performance of V2 O5 to achieve a high capacity and remarkable rate capability as a cathode material for lithium batteries.

Ultrathin V2O5 nanosheets were successfully prepared through supercritical solvothermal reaction followed by annealing treatment. The formation of ultrathin nanosheets is owing to Ostwald ripening and the effect of supercritical fluids. As cathode material for lithium batteries, the ultrathin V2O5 nanosheets exhibit a capacity of 108 mA h g(-1) at a high rate of up to 10 C at 2.4-4 V and excellent cyclability with little capacity loss after 200 cycles. The enhanced rate performance is attributed to the shortened diffusion distance and the increased electrode-electrolyte contact area of the ultrathin nanosheet structure. It is also demonstrated that the supercritical solvothermal method is effective and facile to scalably synthesize ultrathin nanomaterials for lithium batteries.