Project/Area Number |
14205122
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Research Category |
Grant-in-Aid for Scientific Research (A)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
工業物理化学
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Research Institution | Kyushu University (2003-2005) Shizuoka University (2002) |
Principal Investigator |
NAGAMURA Toshihiko Kyushu University, Department of Applied Chemistry, Faculty of Engineering, Professor, 大学院・工学研究院, 教授 (90117200)
|
Co-Investigator(Kenkyū-buntansha) |
TANAKA Keiji Kyushu University, Department of Applied Chemistry, Faculty of Engineering, Associate Professor, 大学院・工学研究院, 助教授 (20325509)
ITO Fuyuki Kyushu University, Department of Applied Chemistry, Faculty of Engineering, Research Associate, 大学院・工学研究院, 助手 (80403921)
川井 秀記 静岡大学, 電子工学研究所, 助手 (80324341)
稲垣 由夫 富士写真フィルム(株), 足柄研究所, 主任研究員
|
Project Period (FY) |
2002 – 2005
|
Project Status |
Completed (Fiscal Year 2005)
|
Budget Amount *help |
¥54,730,000 (Direct Cost: ¥42,100,000、Indirect Cost: ¥12,630,000)
Fiscal Year 2005: ¥5,460,000 (Direct Cost: ¥4,200,000、Indirect Cost: ¥1,260,000)
Fiscal Year 2004: ¥9,100,000 (Direct Cost: ¥7,000,000、Indirect Cost: ¥2,100,000)
Fiscal Year 2003: ¥16,900,000 (Direct Cost: ¥13,000,000、Indirect Cost: ¥3,900,000)
Fiscal Year 2002: ¥23,270,000 (Direct Cost: ¥17,900,000、Indirect Cost: ¥5,370,000)
|
Keywords | Nano materials / Fluorescence lifetime / Surface plasmon resonance / Polymer properties / Guided wave mode / 酸化還元クロモフォア / 高分子化合物 / ESRスペクトル / 光通信波長域での吸収制御 / イオン対間光誘起電子移動 / フェムト秒パルス / 導波モード薄膜 / 電場増強エバネッセント光 / DNA誘導体超薄膜 / 蛍光の超高感度計測 / 高性能ガスセンシング / 電子移動消光 / 有機超薄膜 / 時間分割蛍光測定 / ピコ秒レーザー / 電場増強 |
Research Abstract |
We have achieved highly sensitive time-resolved fluorescence measurements of ultra-thin films upon guided wave mode or surface plasmon resonance excitation and their applications to chemical sensing, molecular photonics and non-contact evaluation of molecular motion in very thin polymer films. Major achievements are as follows : 1.A novel time-resolved fluorescence measurement system was developed by using enhanced evanescent light at surface plasmon resonance (SPR) or guided wave mode (GWM) as an excitation light source. 2.We demonstrated that highly sensitive, fast responsive and highly reversible sensing of nitrogen dioxide, nitric oxide, and nitrous oxide at a ppm-to-sub-ppm level has been achieved by fluorescence measurements upon excitation of various dye-doped deoxyribonucleic acid (DNA) and hydrophobic DNA thin films spin-coated on a thin silver film by electric field enhanced evanescent light at SPR. 3.Ultrafast and large absorption change in the optical telecommunication wavelen
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gth region was achieved in solid films by making transitory expansion of a π-electronic system with photoinduced electron transfer and reverse reactions between redox-active ion pairs. This polymer film may be applied to terahertz all optical information processing in the telecommunication system. 4.Fluorescence lifetimes of dyes dispersed in ultrathin films of poly(vinyl alcohol) or polytricyclodecane were examined by GWM or SPR excitation. The fluorescent behavior of the dyes at interface or surface of ultrathin films was strongly suggested to be different from that in the bulk state. 5.Highly sensitive ultrafast all-optical light modulation was proposed on the basis of photoinduced complex refractive-index changes in composite GWM geometry composed of a low-refractive-index polymer and a photoresponsive polymer. The present device can give highly enhanced changes of probe light as compared with simple transmission-type devices or the GWM geometry in a metal thin film. A photoelectrochromic polymer (shown above 3) was employed in this geometry to demonstrate ultrafast reflectance control upon femtosecond laser excitation. Less
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