Hokkaido University · 화학
마수치 교수의 연구실은 산화질화물 퍼보스카이트 소재를 중심으로, 고도로 안정된 비금속성 편광 물질의 합성 및 응용을 연구하고 있습니다. 특히, 낮은 온도에서의 질소 도핑 반응 메커니즘과 고압 환경에서의 광학적 압력 센서로 활용 가능한 발광 물질 개발에 초점을 맞추고 있으며, 고성능 유기-무기 복합 소재의 설계 및 물성 제어를 위한 신소재 합성 기법을 개발하고 있습니다.
표시된 성과는 수집된 데이터 기준으로 산출되며, 일부 차이가 있을 수 있습니다.
Oxynitride perovskites, having oxide and nitride anions together in a compound, are a new class of dielectric material. The shaping process in either bulk ceramics or thin films is an essential factor for investigating and utilizing the dielectric properties of these materials. In this perspective, recent studies on the shaping of dielectric oxynitride perovskites are reviewed with a consideration of the powder preparation and thermal stability for sintering, several sintering methods, ultra-hig
Perovskite-type oxynitride BaTaO<sub>2</sub>N has been attracting attention for its large dielectric constant, which is almost independent of the temperature by measurements on its ceramics. Its dielectric characteristics are attributed to polar nanoregions (PNRs) in the average cubic crystal structure. Polarization saturation to produce a butterfly-like piezoresponse force microscopy (PFM) signal was observed on BaTaO<sub>2</sub>N crystals in the present study. Reddish crystallites of BaTaO<sub
A new tetragonal BaCN<sub>2</sub> polymorph was obtained <italic>via</italic> a simple nitridation reaction of BaCO<sub>2</sub>, and the Eu doped product showed a red emission with an extremely wide range of red-shift of the emission wavelength with decreasing temperature.
We report a new material, BaCN2:Eu 2+ for a very sensitive optical pressure sensor, 50 times more sensitive than ruby. Photoluminescence spectra of the BaCN2:Eu 2+ phosphor was measured under hydrostatic pressures from ambient pressure to 5.34 GPa at room temperature. The peak wavelength of the luminescence was drastically red-shifted at a rate of 19 nm/GPa, which is approximately 50 times larger than that of the ruby, most commonly used as a pressure sensor in the high-pressure experiments. Thi
The perovskite-type oxynitride SrTaO2N was synthesized from Sr2Ta2O7 and carbon nitride (C3N4) and the formation mechanism was investigated using X-ray diffraction and thermogravimetry combined with mass spectrometry. In this process, ammonia is not required for the nitridation of the oxide. The C3N4 thermally decomposes to gaseous C2N2, which forms SrCN2 and Ta3N5 intermediates on the Sr2Ta2O7. These intermediates then react with the oxide to form SrTaO2N at 800 °C, which is 200 °C lower than t
Solid phase sintering of dielectric oxynitride perovskites above 1000 °C is accompanied by their decomposition. Post-ammonolysis is required to recover their stoichiometric nitrogen content and dielectric properties. In the present work, the oxynitride perovskite SrTaO<sub>2</sub>N was sintered with a BaCN<sub>2</sub> flux at approximately 900 °C avoiding its thermal decomposition. The resulting solid product with a relative density of 68.9% showed relative dielectric constants in the range from