Yiding Liu

Thermoresponsive Assembly of Charged Gold Nanoparticles and Their Reversible Tuning of Plasmon Coupling

Charged colloidal gold nanoparticles (AuNPs) can be assembled and disassembled in an aqueous solution in response to temperature change and display reversible thermoresponsive tuning of plasmon coupling. The reversible tuning was made possible by manipulating the electrostatic interaction through the temperature-dependent zeta potential of the charged AuNPs (see the extinction spectra of a typical AuNP dispersion).

Colorimetric stress memory sensor based on disassembly of gold nanoparticle chains.

We report the development of a stress-responsive colorimetric film that can memorize the stress it has experienced. The system is designed by taking advantage of the plasmonic shift associated with the disassembly of one-dimensional gold nanoparticle chains driven by the plastic deformation of the surrounding polymer matrix. By modifying the plasticity of the polymer, we demonstrate that the plasmonic shift and colorimetric change respond to a large range of stresses. This novel pressure indicating film can be used to capture and record the pressure distribution and magnitude between two contacting or impacting surfaces by outputting color information.

One-step seeded growth of Au nanoparticles with widely tunable sizes

A one-step seeded growth process has been developed for the synthesis of Au nanoparticles with tunable diameters from ~10 nm to ~200 nm. The delicately designed growth system suppresses self-nucleation by stabilizing a concentrated growth solution with strong coordinating ligands, leading to precise size control and convenient, scalable fabrication of Au nanoparticles.

Seed-Mediated Growth of Anatase TiO2 Nanocrystals with Core–Antenna Structures for Enhanced Photocatalytic Activity

We demonstrate that anatase TiO2 nanocrystals composed of a nanocrystal core and nanorod antennas can be produced via a nonaqueous colloidal seed-mediated growth method. Anatase TiO2 nanocrystals with defined morphologies were first prepared as seeds, and then secondary anatase TiO2 nanorods were grown on the defined facets of the seeds under appropriate conditions. Systematic studies on the growth mechanism reveal that the formation of core-antenna nanocrystals involves an epitaxial growth process with specific orientational preference governed by both thermodynamic and kinetic factors. By manipulating the reaction conditions including the precursor amount and introduction rate, the epitaxial growth behavior can be well controlled. By further varying the morphology of seed nanocrystals, we have also been able to produce core-antenna anatase TiO2 nanocrystals with complex spatial configurations in a highly predictable manner. The high structural configurability and predictability offered by this seed-mediated growth method may provide great opportunities in enhancing the performance of TiO2-based nanostructures in many energy-related applications. As a demonstration, we show by simply manipulating the core-antenna structures that the photocatalytic activity of the anatase nanocrystals can be improved from the relatively less active seed nanocrystals or pure nanorods to the extent that exceeds the activity of the commercial P25 titania.

High-yield halide-free synthesis of biocompatible Au nanoplates

We communicate an unconventional synthesis of Au nanoplates with high yield and excellent reproducibility through polyvinylpyrrolidone (PVP)-assisted H2O2 reduction. Unlike the ones prepared using halide-based surfactants, the PVP-capped Au nanoplates are found to afford fairly easy bio-functionalization, suggesting a vastly expanded spectrum of applications in bio-related fields.

Migration of Iron Oxide Nanoparticle through a Silica Shell by the Redox-Buffering Effect

This study demonstrates that mineral redox buffer, an important concept in geology, can be used to manipulate the migration of nanoparticles and produce nanostructures of unexpected morphologies. Using a silica shell as a redox buffer, we show that iron oxide nanoparticles can be relocated from inside to the outer surface of the silica shell. The migration of iron oxide through silica was initiated by manipulation of the oxygen fugacity conditions at an elevated temperature. During the treatment, iron oxide was absorbed and then separated from the silica shell by the formation and then decomposition of iron silicate (Fe2SiO4). Tuning the relative dimensions of the iron oxide core and silica shell allows control of the shape of the iron oxide-silica composite structures. It is believed that the discovery of the nanoscale redox buffering effect can be extended to control the morphological configuration of other multivalent metal oxide nanocomposite structures by this particular type of template synthesis through manipulation of the chemical-transport properties of nanoscale templates.