The University of Tokyo · 재료과학
Yasushi Hirose 교수의 연구실은 초고속 분광학을 기반으로 한 분자 동역학 및 전자 구조 분석을 통해 광학적·전기적 성질을 가진 신소재의 기초 메커니즘을 규명하고 있습니다. 특히 광자기 이성질화 반응, 전도성 산화물의 전자 질량 이방성, 수용체 환경에서의 분자 리허설 동역학, 그리고 극자외선 영역에서의 투명 전도 산화물 등 고성능 온디바이스 응용을 위한 신소재 설계에 초점을 맞추고 있습니다. 다양한 스펙트로스코피 기법과 이종 결정막 합성 기술을 융합하여 물질의 나노스케일 거동을 정량적으로 분석합니다.
표시된 성과는 수집된 데이터 기준으로 산출되며, 일부 차이가 있을 수 있습니다.
We considered the trans → cis photoisomerization dynamics of the S2-excited azobenzene derivatives in terms of the potential energy gap between the n-π* (S1) and the π-π* (S2) state. The photoisomerization dynamics of trans-4-aminoazobenzene (trans-4-AAB) which has an energy gap (3000−4000 cm-1) rather smaller than that of trans-azobenzene (∼10000 cm-1) due to an amino-substitution was investigated using UV−vis transient absorption spectroscopy. The recorded transient absorption spectra of the π
Electron mass anisotropy in the Nb-doped anatase ${\text{TiO}}_{2}$ (TNO) was determined by polarized infrared spectroscopy measurements for (012)-oriented TNO epitaxial films. The electron mass along the $c$ axis, ${m}_{⟨001⟩}^{\ensuremath{\ast}}$, derived by Drude analyses, was found to be $0.5--3.3\text{ }{m}_{0}$, which was 3--6 times larger than that along the $a$ axis, ${m}_{⟨100⟩}^{\ensuremath{\ast}}$, $0.2--0.6\text{ }{m}_{0}$. This large anisotropy was attributed to not only the anisotr
The ultrafast relaxation dynamics of a widely used viscosity probe molecule, auramine O (AuO), was investigated in water and a water/aerosol−OT (AOT)/n−heptane reversed micelle. We discussed the contribution of specific interactions between AuO and the local environment to the relaxation dynamics. The transient absorption spectra of AuO showed that the nonradiative relaxation process of the photoexcited AuO in the AOT-reversed micelle was approximately 1 order slower than that in bulk water and
Transparent conductive oxides (TCOs) are key materials for highly efficient optoelectronic devices such as light-emitting diodes (LEDs) and photovoltaic cells. While high-performance TCOs have been developed for use in the visible light spectrum, few materials are identified as TCOs feasible for deep ultraviolet (DUV) devices, especially at wavelengths shorter than 280 nm (UV-C region). Herein, we demonstrate that an alloy of rutile SnO2 and isostructural GeO2, rutile Sn1–xGexO2 (SGO), is a prom