Potential-driven reversible regulation of hierarchical dynamics of nano-entities and functionalization of electrified interfaces
Project/Area Number |
16350077
|
Research Category |
Grant-in-Aid for Scientific Research (B)
|
Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Functional materials chemistry
|
Research Institution | Nagasaki University |
Principal Investigator |
SAGARA Takamasa Nagasaki University, Faculty of Engineering, Department of Applied Chemistry, Professor, 工学部, 教授 (20192594)
|
Project Period (FY) |
2004 – 2006
|
Project Status |
Completed (Fiscal Year 2006)
|
Budget Amount *help |
¥15,100,000 (Direct Cost: ¥15,100,000)
Fiscal Year 2006: ¥2,100,000 (Direct Cost: ¥2,100,000)
Fiscal Year 2005: ¥2,700,000 (Direct Cost: ¥2,700,000)
Fiscal Year 2004: ¥10,300,000 (Direct Cost: ¥10,300,000)
|
Keywords | Electrode surface / Ultra-thin films / Surface and Interfacial Properties / Metal nanoparticle / Dendrimer / Viologen / Dynamics / Phase transition / ナノ材料 / 吸脱着 / 赤外反射分光法 / 蛍光性デンドリマー / 両親媒性長鎖分子 / 長鎖分子集合組織 |
Research Abstract |
1. In situ characterization methods being indispensable as basic techniques in this research were developed for the measurements of adsorption state, molecular orientation, micro-environment and molecular assembling structure as well as their potential dependent dynamics on electrode surfaces: (1) Electroreflectance methods were sophisticated, for example, to elucidate the adsorption orientation of macromolecules and to track the potential step transients of the surface processes, (2) An 1R reflection instrument was constructed, and (3) The fluorescence spectral analysis and moving imaging microscopic observation were developed. 2. The title research targets at electrified interfaces included liquid alkane thin films, surface assemblies of amphiphiles, viologen adsorption layers, a fluorescent dendrimer, and surface-modified Au nanoparticles. Representative achievements are listed below. (1) Alkane molecules were found to be potential-responsible on a Au(III) electrode. The dynamics extended to far distances from the electrode surface to the bulk of the aqueous solution. (2) Systematic understandings of potential-driven assembling structural changes of pyridyl and imidazolyl terminated amphiphiles on a Au(III) electrode surface were established. (3) Two-dimensional faradaic phase transition behavior of various viologen molecules on a HOPG electrode was described in terms of interplay of multiple modes of intermolecular interactions. (4) An anomalous effect of dendrimer adsorption upon redox reaction was found. Potential dependent reshape of dendrimer also was analyzed. (5) Potential-driven dynamics of Au nanoparticles were elucidated, together with adsorption-desorption and charging-discharging processes as well as anion effects. 3. These results would be quite useful for design of dynamics and interfacial functionalization in the near future.
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Report
(4 results)
Research Products
(31 results)