Radical/Ion-Containing Block Copolymers: Self-Assembly and Application toward Organic Devices
Project/Area Number |
23550139
|
Research Category |
Grant-in-Aid for Scientific Research (C)
|
Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Polymer chemistry
|
Research Institution | Waseda University |
Principal Investigator |
SUGA Takeo 早稲田大学, 高等研究所, 助教 (10409659)
|
Project Period (FY) |
2011 – 2013
|
Project Status |
Completed (Fiscal Year 2013)
|
Budget Amount *help |
¥5,330,000 (Direct Cost: ¥4,100,000、Indirect Cost: ¥1,230,000)
Fiscal Year 2013: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2012: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2011: ¥2,730,000 (Direct Cost: ¥2,100,000、Indirect Cost: ¥630,000)
|
Keywords | ミクロ相分離 / ブロック共重合体 / ラジカル / イオン液体 / 精密重合 / 有機メモリ / 走査プローブ顕微鏡 / クリック反応 / 国際研究者交流 ドイツ / 自己組織化 / 国際研究者交流 アメリカ |
Research Abstract |
A well-defined mesostructure of block copolymer templates was successfully functionalized with redox-active radicals and charge-compensating ionic groups via ionic liquid-assisted self-assembly. The obtained PS-b-PEO layer containing TEMPO-IL 1 exhibited morphology-driven modulation of charge-transport (on/off switching) in an organic thin film device. Location of radical and ionic molecules was correlated with resistive memory characteristics (rewritable/WORM, etc). We applied Kelvin Probe Force Microscopy (KPFM) technique and conductive AFM to visualize local surface potential and local conductivity change of microdomains under the programmed bias. Radical- and ion-functionalized block copolymers were also synthesized via controlled radical polymerization and ring-opening metathesis polymerization, and utilized as the active layer for organic memory.
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Report
(4 results)
Research Products
(60 results)