임병권 교수

Controlling the morphology of Pt nanostructures can provide a great opportunity to improve their catalytic properties and increase their activity on a mass basis. We synthesized Pd-Pt bimetallic nanodendrites consisting of a dense array of Pt branches on a Pd core by reducing K2PtCl4 with L-ascorbic acid in the presence of uniform Pd nanocrystal seeds in an aqueous solution. The Pt branches supported on faceted Pd nanocrystals exhibited relatively large surface areas and particularly active face

Abstract This article provides an overview of recent developments regarding synthesis of Pd nanocrystals with well‐controlled shapes in aqueous solutions. In a solution‐phase synthesis, the final shape taken by a nanocrystal is determined by the twin structures of seeds and the growth rates of different crystallographic facets. Here, the maneuvering of these factors in an aqueous system to achieve shape control for Pd nanocrystals is discussed. L ‐ascorbic acid, citric acid, and poly(vinyl pyrro

Metal nanocrystals with highly branched morphologies are an exciting new class of nanomaterials owing to their unique structures, physicochemical properties, and great potential as catalysts, sensing materials, and building blocks for nanoscale devices. Various strategies have recently been developed for the solution-phase synthesis of metal nanocrystals with branched morphologies, such as multipods and nanodendrites. In this Minireview, the procedures and mechanisms underlying the formation of

This paper describes the synthesis of Pd-Au bimetallic nanocrystals with controlled morphologies via a one-step seeded-growth method. Two different reducing agents, namely, L-ascorbic acid and citric acid, were utilized for the reduction of HAuCl(4) in an aqueous solution to control the overgrowth of Au on cubic Pd seeds. When L-ascorbic acid was used as the reducing agent, conformal overgrowth of Au on the Pd nanocubes led to the formation of Pd-Au nanocrystals with a core-shell structure. On t

Highly faceted Pt nanocrystals with a large number of interconnected arms in a quasi-octahedral shape were synthesized simply by reducing H2PtCl6 precursor with poly(vinyl pyrrolidone) in aqueous solutions containing a trace amount of FeCl3. The iron species (Fe(3+) or Fe(2+)) play a key role in inducing the formation of the multioctahedral structure by decreasing the concentration of Pt atoms and keeping a low concentration for the Pt seeds during the reaction. This condition favors the overgro

Shapes from water: Pd nanocrystals with controllable shapes are synthesized by reducing a Pd salt with citric acid in aqueous solution. Citric acid favors the formation of octahedra, icosahedra, or decahedra (see picture) owing to its strong binding to the {111} facets of Pd. Shape control of these nanocrystals is readily accomplished by adjusting the amounts of Na2PdCl4 precursor and citric acid added to the reaction mixture.

Pd-Pt core-shell nanoplates with hexagonal and triangular shapes were synthesized through the heterogeneous, epitaxial growth of Pt on Pd nanoplates. The Pd nanoplates were synthesized by reducing Na2PdCl4 precursor with PVP as a reducing agent, which then served as seeds for the nucleation of Pt atoms formed by reducing H2PtCl6 with citric acid. Characterization of the as-prepared Pd-Pt nanoplates by scanning transmission electron microscopy and high-resolution transmission electron microscopy

The evolution of sheet morphology for single-crystal ceria nanosheets with a thickness of about 2.2 nm and lateral dimensions up to 4 μm (see picture), involves two-dimensional self-organization of the initially formed ceria nanocrystals, followed by recrystallization. Ceria nanosheets exhibit an unusually large optical band gap energy due to the quantum size effect associated with their extremely small thickness.

In a seed-mediated synthesis, nanocrystal growth is often described by assuming the absence of homogeneous nucleation in the solution. Here we provide new insights into the nucleation and growth mechanisms underlying the formation of bimetallic nanodendrites that are characterized by a dense array of Pt branches anchored to a Pd nanocrystal core. These nanostructures can be easily prepared by a one-step, seeded growth method that involves the reduction of K2PtCl4 by L-ascorbic acid in the presen

Multilayered Au nanosheets are suggested as a novel class of material for fabricating stretchable electrodes suitable for organic-based electronic devices. The electrodes show no difference in resistivity during repeated stretching cycles of up to ϵ = 40%.

Abstract Paper‐based electronics has attracted growing interest owing to many advantages of papers including low‐cost, abundance, flexibility, biocompatibility, and environmental friendliness. Despite recent progress in paper electronics, however, development of a high‐performance paper‐based triboelectric nanogenerator (TENG), which is a power‐generating device that converts mechanical energy into electric energy by coupling triboelectrification and electrostatic induction, remains a challenge

This article describes a simple approach to anisotropic Au nanostructures with various shapes by reducing HAuCl 4 with poly(vinyl pyrrolidone) (PVP) in aqueous solutions without the use of any additional capping agent or reductant. In this approach, the commercially available PVP servers as a mild reducing agent thanks to its hydroxyl (-OH) end groups, enabling kinetic control over both nucleation and growth. As the volume of HAuCl 4 solution added to the reaction was increased, the morphology o

Identical or fraternal? Palladium–platinum alloy nanocrystals with well-defined twinned structures (see picture) were synthesized by co-reducing Pd and Pt salts. The evolution of twinned morphologies involves coalescence between initially formed small particles under the slow reduction process. Manipulation of the reduction kinetics allows ready control over crystallinity, and thus shape, of the nanocrystals.