| Project/Area Number |
16310098
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| Research Category |
Grant-in-Aid for Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Microdevices/Nanodevices
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| Research Institution | Japan Advanced Institute of Science and Technology |
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Principal Investigator |
MURATA Hideyuki Japan Advanced Institute of Science and Technology, School of Materials Science, Associate Professor (10345663)
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| Co-Investigator(Kenkyū-buntansha) |
土本 晃久 北陸先端科学技術大学院大学, 材料科学研究科, 助手 (80313716)
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| Project Period (FY) |
2004 – 2007
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| Project Status |
Completed (Fiscal Year 2007)
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| Budget Amount *help |
¥16,180,000 (Direct Cost: ¥16,000,000、Indirect Cost: ¥180,000)
Fiscal Year 2007: ¥780,000 (Direct Cost: ¥600,000、Indirect Cost: ¥180,000)
Fiscal Year 2006: ¥1,000,000 (Direct Cost: ¥1,000,000)
Fiscal Year 2005: ¥1,800,000 (Direct Cost: ¥1,800,000)
Fiscal Year 2004: ¥12,600,000 (Direct Cost: ¥12,600,000)
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| Keywords | Conjugated Polymer / Vapor Deposition Polymerization / Organic Device / Chemical modification of silicon / ポリアゾメチン / 高分子EL素子 / 水素終端シリコン基板 / アミノ基終端シリコン基板 / 垂直配向単分子膜 |
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| Research Abstract |
Attaching functional organic layers to semiconductor surfaces may have applications in a number of areas, including molecular and biomolecular electronics, sensors and lithography. In this study, we have developed a novel, two-step strategy for the covalent bond formation between aromatic molecules and silicon surfaces. In the first step, a H-terminated Si (III)surface reacts with amino radicals to give a NH_2-terminated Si (III) surface at room temperature. The amino radicals were generated by the thermal decomposition of ammonia gas with Tungsten filament heated at 1000-1200℃. The formation of NH_2-terminated surface and the monolayer was confirmed by X-ray photoelectron spectroscopy (XPS) and Multi Internal Reflection Fourier Transfer Infrared Spectroscopy (MIR FT-IR). In the second step, the reaction of amino-terminated Si surface with an aromatic dialdehydes (1,4-bis (4-formylstyryl)benzene) (BFSB) was carried out by vacuum deposition of BFSB on the substrate heated at 130℃ under high vacuum. The reaction of amino-terminated surface between BFSB and the monolayer formation was confirmed by XPS and MIR FT-IR. Distinct images such as an island structure with the diameter of around 5 nm can be seen in non-contact atomic force microscopy (nc-AFM) images. The islands consist of several dots with the height of each dot was about 2.3 nm. According to the molecular orbital calculation (MOPAC), the length of BFSB molecule is about 2.2 nm. These results suggest that the each dot corresponds to the vertically aligned BFSB molecules. On the other hand, no photoluminescence from BFSB was observed on silicon surface, due to an energy transfer. Next, we have investigated the formation of organic monolayer on indium-tin-oxide (ITO) electrode and the effect to device performance of OLEDs. We have found that the carrier injection efficiency was enhanced by modification of ITO by organic monolayers depending on their chemical structure.
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