Kohei Kusada 교수

We report the first discovery of pure face-centered-cubic (fcc) Ru nanoparticles. Although the fcc structure does not exist in the bulk Ru phase diagram, fcc Ru was obtained at room temperature because of the nanosize effect. We succeeded in separately synthesizing uniformly sized nanoparticles of both fcc and hcp Ru having diameters of 2-5.5 nm by simple chemical reduction methods with different metal precursors. The prepared fcc and hcp nanoparticles were both supported on γ-Al2O3, and their c

Pd(x)Ru(1-x) solid solution alloy nanoparticles were successfully synthesized over the whole composition range through a chemical reduction method, although Ru and Pd are immiscible at the atomic level in the bulk state. From the XRD measurement, it was found that the dominant structure of Pd(x)Ru(1-x) changes from fcc to hcp with increasing Ru content. The structures of Pd(x)Ru(1-x) nanoparticles in the Pd composition range of 30-70% consisted of both solid solution fcc and hcp structures, and

High-entropy alloy nanoparticles (HEA NPs) emerged as catalysts with superior performances that are not shown in monometallic catalysts. Although many kinds of synthesis techniques of HEA NPs have been developed recently, synthesizing HEA NPs with ultrasmall particle size and narrow size distribution remains challenging because most of the reported synthesis methods require high temperatures that accelerate particle growth. This work provides a new methodology for the fabrication of ultrasmall a

Rh and Ag are the elements neighboring Pd, which is well known as a hydrogen-storage metal. Although Rh and Ag do not possess hydrogen-storage properties, can Ag-Rh alloys actually store hydrogen? Ag-Rh solid-solution alloys have not been explored in the past because they do not mix with each other at the atomic level, even in the liquid phase. We have used the chemical reduction method to obtain such Ag-Rh alloys, and XRD and STEM-EDX give clear evidence that the alloys mixed at the atomic leve

For the first time, we synthesize solid-solution alloy nanoparticles of Ir and Cu with a size of ca. 2 nm, despite Ir and Cu being immiscible in the bulk up to their melting over the whole composition range. We performed a systematic characterization on the nature of the Ir_x Cu_1-x solid-solution alloys using powder X-ray diffraction, scanning transmission electron microscopy coupled with energy-dispersive X-ray spectroscopy and X-ray photoelectron spectroscopy. The results

The crystal structure significantly affects the physical and chemical properties of solids. However, the crystal structure-dependent properties of alloys are rarely studied because controlling the crystal structure of an alloy at the same composition is extremely difficult. Here, for the first time, we successfully demonstrate the synthesis of binary Ru-Pt (Ru/Pt = 7:3) and Ru-Ir (Ru/Ir = 7:3) and ternary Ru-Ir-Pt (Ru/Ir/Pt = 7:1.5:1.5) solid-solution alloy nanoparticles (NPs) with well-controll

There is untapped potential for materials whose crystal structures are unobtainable in the bulk state. Several examples of such structures have been found in nanomaterials, and these materials exhibit unique properties that arise from their unique electronic states and surface structures. Here, recent developments in the syntheses of these nanomaterials and their unique properties, such as hydrogen-storage ability and catalytic activity, are summarized. Firstly, the syntheses and properties of n

Platinum group metal (PGM) nanoparticles (NPs) have been investigated in a variety of research fields such as catalysis and electronics. Alloying has been recognized as one of the most efficient ways of improving or creating properties in metals. Among the types of alloys, solid-solution alloy NPs have the advantage of being capable of continuously changing their properties by tuning their composition. However, synthesizing PGM solid-solution alloy NPs with any combination and composition is not

Au and Ru are elements that are immiscible in the bulk state and have the largest gap in reduction potential among noble metals. Here, for the first time, Au _<i>x</i> Ru_1-<i>x</i> solid-solution alloy nanoparticles (NPs) were successfully synthesized over the whole composition range through a chemical reduction method. Powder X-ray diffraction and scanning transmission electron microscopy coupled with energy-dispersive X-ray spectroscopy showed that Au and Ru atoms are homo

Multi-element nanoparticles (NPs) consisting of five or more elements have been increasingly studied in the past five years. Their emergence is taking materials science one step further because they exhibit superior properties to those of conventional NPs in a range of respects, including catalysis. This Review focuses on the recent progress in multi-element NPs regarding synthesis, especially with regard to chemical synthesis, characterization, and properties. We begin with a brief introduction

Multielement alloy nanoparticles have attracted much attention due to their attractive catalytic properties derived from the multiple interactions of adjacent multielement atoms. However, mixing multiple elements in ultrasmall nanoparticles from a wide range of elements on the periodic table is still challenging because the elements have different properties and miscibility. Herein, we developed a benchtop 4-way flow reactor for chemical synthesis of ultra-multielement alloy (UMEA) nanoparticles

High-entropy oxide nanoparticles (HEO NPs) have been intensively studied because of their attractive properties, such as high stability and enhanced catalytic activity. In this work, for the first time, denary HEO NPs were successfully synthesized using a continuous supercritical hydrothermal flow process without calcination. Interestingly, this process allows the formation of HEO NPs on the order of seconds at a relatively lower temperature. The synthesized HEO NPs contained 10 metal elements,

Solid-solution alloy nanoparticles (NPs), where the constituents mix at the atomic level, show a variety of attractive properties due to their tunable electronic structures. However, it is still difficult to stably synthesize them, particularly nonequilibrium alloys that consist of combinations immiscible in the bulk. Here, we first report the successful syntheses of solid-solution alloy NPs including PdRu and PdRuIr, which are immiscible in the bulk, and of IrPdPtRhRu high-entropy alloy NPs thr

We succeeded in controlling the crystal structure of osmium (Os) nanoparticles (NPs). Although Os adopts only a hexagonal close-packed (hcp) structure in the bulk state, a face-centred cubic (fcc) Os was synthesized by a chemical reduction method using an Os acetylacetonate complex as a precursor.

Alloy nanoparticles (NPs), including core-shell, segregated and solid-solution types, show a variety of attractive properties such as catalytic and optical properties and are used in a wide range of applications. Precise control and good reproducibility in the syntheses of alloy NPs are highly demanded because these properties are tunable by controlling alloy structures, compositions, particle sizes, and so on. To improve the efficiency and reproducibility of their syntheses, continuous-flow syn