| Dynamics of Block Copolymer Nanocomposites | |
| Mochrie, Simon G. J. | |
| 关键词: x-ray photon correlation spectroscopy; nanoparticles; nanocomposites; block copolymers; | |
| DOI : 10.2172/1154906 RP-ID : DOE-YALE-SC0004162 PID : OSTI ID: 1154906 |
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| 美国|英语 | |
| 来源: SciTech Connect | |
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【 摘 要 】
A detailed study of the dynamics of cadmium sulfide nanoparticles suspended in polystyrene homopolymer matrices was carried out using X-ray photon correlation spectroscopy for temperatures between 120 and 180 ?��C. For low molecular weight polystyrene homopolymers, the observed dynamics show a crossover from diffusive to hyper-diffusive behavior with decreasing temperatures. For higher molecular weight polystyrene, the nanoparticle dynamics appear hyper-diffusive at all temperatures studied. The relaxation time and characteristic velocity determined from the measured hyper-diffusive dynamics reveal that the activation energy and underlying forces determined are on the order of 2.14 ?? 10-19 J and 87 pN, respectively. We also carried out a detailed X-ray scattering study of the static and dynamic behavior of a styrene??? isoprene diblock copolymer melt with a styrene volume fraction of 0.3468. At 115 and 120 ?��C, we observe splitting of the principal Bragg peak, which we attribute to phase coexistence of hexagonal cylindrical and cubic double- gyroid structure. In the disordered phase, above 130 ?��C, we have characterized the dynamics of composition fluctuations via X-ray photon correlation spectroscopy. Near the peak of the static structure factor, these fluctuations show stretched-exponential relaxations, characterized by a stretching exponent of about 0.36 for a range of temperatures immediately above the MST. The corresponding characteristic relaxation times vary exponentially with temperature, changing by a factor of 2 for each 2 ?��C change in temperature. At low wavevectors, the measured relaxations are diffusive with relaxation times that change by a factor of 2 for each 8 ?��C change in temperature.
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