The morphology and the microscopic internal dynamics of a bidimensional gel formed by spontaneous aggregation of gold nanoparticles confined at the water surface are investigated by a suite of techniques, including grazing-incidence x-ray photon correlation spectroscopy (GI-XPCS). The range of concentrations studied spans across the percolation transition for the formation of the gel. The dynamical features observed by GI-XPCS are interpreted in view of the results of microscopic imaging; an intrinsic link between the mechanical modulus and internal dynamics is demonstrated for all the concentrations. Our work presents an example of a transition from a stretched to a compressed correlation function actively controlled by quasistatically varying the relevant thermodynamic variable. Moreover, by applying a model proposed some time ago by Duri and Cipelletti [Europhys. Lett. 76, 972 (2006)]we are able to build a master curve for the shape parameter, whose scaling factor allows us to quantify a “long-time displacement length.” This characteristic length is shown to converge, as the concentration is increased, to the “short-time localization length” determined by pseudo-Debye-Waller analysis of the initial contrast. Finally, the intrinsic dynamics of the system is then compared with that induced by means of a delicate mechanical perturbation applied to the interface.
Controlling the dynamics of a bidimensional gel above and below its percolation transition / Orsi, Davide; B., Ruta; Y., Chushkin; A., Pucci; G., Ruggeri; Baldi, Giacomo; Rimoldi, Tiziano; Cristofolini, Luigi. - In: PHYSICAL REVIEW E, STATISTICAL, NONLINEAR, AND SOFT MATTER PHYSICS. - ISSN 1539-3755. - 89:4(2014), pp. 042308-1-042308-11. [10.1103/PhysRevE.89.042308]
Controlling the dynamics of a bidimensional gel above and below its percolation transition
ORSI, Davide;BALDI, GIACOMO;RIMOLDI, Tiziano;CRISTOFOLINI, Luigi
2014-01-01
Abstract
The morphology and the microscopic internal dynamics of a bidimensional gel formed by spontaneous aggregation of gold nanoparticles confined at the water surface are investigated by a suite of techniques, including grazing-incidence x-ray photon correlation spectroscopy (GI-XPCS). The range of concentrations studied spans across the percolation transition for the formation of the gel. The dynamical features observed by GI-XPCS are interpreted in view of the results of microscopic imaging; an intrinsic link between the mechanical modulus and internal dynamics is demonstrated for all the concentrations. Our work presents an example of a transition from a stretched to a compressed correlation function actively controlled by quasistatically varying the relevant thermodynamic variable. Moreover, by applying a model proposed some time ago by Duri and Cipelletti [Europhys. Lett. 76, 972 (2006)]we are able to build a master curve for the shape parameter, whose scaling factor allows us to quantify a “long-time displacement length.” This characteristic length is shown to converge, as the concentration is increased, to the “short-time localization length” determined by pseudo-Debye-Waller analysis of the initial contrast. Finally, the intrinsic dynamics of the system is then compared with that induced by means of a delicate mechanical perturbation applied to the interface.File | Dimensione | Formato | |
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