Tatsuya Tsukuda 교수

Bare metal clusters with fewer than ∼100 atoms exhibit intrinsically unique and size-specific properties, making them promising functional units or building blocks for novel materials. To utilize such clusters in functional materials, they need to be stabilized against coalescence by employing organic ligands, polymers, and solid materials. To realize rational development of cluster-based materials, it is essential to clarify how the stability and nature of clusters are modified by interactions

Au(25) clusters supported on hydroxyapatite oxidized styrene in toluene with 100% conversion and 92% selectivity to the epoxide, under optimum conditions and using anhydrous tert-butyl hydroperoxide (TBHP) as an oxidant.

Abstract Metal clusters consisting of fewer than 100 atoms (diameter <2 nm) are highly promising as a new class of building units for functional materials because of their novel and size-dependent properties. Nevertheless, basic and applied studies of metals clusters have been hampered by the lack of specific guidelines for design and precise synthetic methods. This account surveys recent investigations of gold clusters focusing on our effort toward an atomic-level understanding and contr

We synthesized a series of MAu₁₂ (dppe)₅ Cl₂ (MAu₁₂ ; M=Au, Pd, Pt, Rh, or Ir; dppe=1,2-bis(diphenylphosphino)ethane), which have icosahedral M@Au₁₂ superatomic cores, and systematically investigated their electronic structures, photoluminescence (PL) and photocatalytic properties. The energy gap between the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO) was expanded when doping an M element posi