早稲田大学 · Materials Science
Toru Asahi 교수의 연구실은 비백금 계 금속 기반 나노소재를 중심으로, 다공성 구조를 가진 비희토류 전이금속 화합물, 특히 복합질소 도핑 및 비정질 합금 나노소재의 설계 및 합성을 목표로 합니다. 주로 전기화학적 수소 생산을 위한 산소 발생 반응(OER) 촉매로 활용 가능한 메조다공성 나노구조를 제어적으로 합성하며, 전자적 특성과 표면 구조를 정밀하게 조절한 고성능 촉매를 개발하고 있습니다. 또한, 자기적 특성과 다공성 구조를 동시에 확보한 CoFe 기반 나노소재를 활용한 분리·정제 및 생물의학적 응용 기술도 함께 연구하고 있습니다.
표시된 성과는 수집된 데이터 기준으로 산출되며, 일부 차이가 있을 수 있습니다.
Porous nonprecious metal-based nanomaterials have gained considerable attention in heterogeneous catalysis owing to their low price, high specific surface area, efficient mass/electron transfer, tunable pore structure, and unique physicochemical properties. Controlling the phase and compositions of these porous nonprecious metal-based materials is critical to their applications. Porous nonprecious transition-metal borides (TMBs), typical metal–metalloid alloys, have recently received much intere
Controlling the morphology, composition, and crystalline phase of mesoporous nonnoble metal catalysts is essential for improving their performance. Herein, well-defined P- and B-codoped NiFe alloy mesoporous nanospheres (NiFeB-P MNs) with an adjustable Ni/Fe ratio and large mesopores (11 nm) are synthesized via soft-template-based chemical reduction and a subsequent phosphine-vapor-based phosphidation process. Earth-abundant NiFe-based materials are considered promising electrocatalysts for the
Amorphous bimetallic borides are an emerging class of catalytic nanomaterial that has demonstrated excellent catalytic performance due to its glass-like structure, abundant unsaturated active sites, and synergistic electronic effects. However, the creation of mesoporous Earth-abundant bimetallic metal borides with tunable metal proportion remains a challenge. Herein, we develop a sophisticated and controllable dual-reducing agent strategy to synthesize the mesoporous nickel-cobalt boron (NiCoB)
Mesoporous PtPdAu alloy films with the highest electrocatalytic activity are discovered by the active learning approach using Bayesian optimization.
2D heterostructures exhibit a considerable potential in electrolytic water splitting due to their high specific surface areas, tunable electronic properties, and diverse hybrid compositions. However, the fabrication of well-defined 2D mesoporous amorphous-crystalline heterostructures with highly active heterointerfaces remains challenging. Herein, an efficient 2D heterostructure consisting of amorphous nickel boron oxide (Ni-B<sub>i</sub> ) and crystalline mesoporous iridium (meso-Ir) is designe
Construction of a well-defined mesoporous nanostructure is crucial for applying nonnoble metals in catalysis and biomedicine owing to their highly exposed active sites and accessible surfaces. However, it remains a great challenge to controllably synthesize superparamagnetic CoFe-based mesoporous nanospheres with tunable compositions and exposed large pores, which are sought for immobilization or adsorption of guest molecules for magnetic capture, isolation, preconcentration, and purification. H
We report on the self-disproportionation of enantiomers (SDE) of non-racemic thalidomide (<b>1</b>) and 3'-fluorothalidomide (<b>2</b>) under the conditions of gravity-driven achiral silica-gel chromatography. The presence of a fluorine atom on the chiral center dramatically alters the structure and polarity of <b>1</b> and <b>2</b>, resulting in the opposite SDE profile on silica-gel.