Hornfeck Wolfgang, Menke Dirk, Forthaus Martin, Subatzus Sebastian, Franke Markus, Schöpe Hans-Joachim, Palberg Thomas, Perlich Jan, Herlach Dieter
Institut für Materialphysik im Weltraum, Deutsches Zentrum für Luft- und Raumfahrt (DLR), 51170 Köln, Germany.
Institut für Physik, Johannes-Gutenberg-Universität, Staudingerweg 7, 55128 Mainz, Germany.
J Chem Phys. 2014 Dec 7;141(21):214906. doi: 10.1063/1.4902904.
A suspension of charged colloidal silica spheres exhibiting a bi-modal size distribution of particles, thereby mimicking a binary mixture, was studied using time-resolved ultra-small-angle synchrotron X-ray scattering (USAXS). The sample, consisting of particles of diameters d(A) = (104.7 ± 9.0) nm and d(B) = (88.1 ± 7.8) nm (d(A)/d(B) ≈ 1.2), and with an estimated composition A(0.6(1))B(0.4(1)), was studied with respect to its phase behaviour in dependance of particle number density and interaction, of which the latter was modulated by varying amounts of added base (NaOH). Moreover, its short-range order in the fluid state and its eventual solidification into a long-range ordered colloidal crystal were observed in situ, allowing the measurement of the associated kinetics of nucleation and crystal growth. Key parameters of the nucleation kinetics such as crystallinity, crystallite number density, and nucleation rate density were extracted from the time-resolved scattering curves. By this means an estimate on the interfacial energy for the interface between the icosahedral short-range ordered fluid and a body-centered cubic colloidal crystal was obtained, comparable to previously determined values for single-component colloidal systems.
使用时间分辨超小角同步加速器X射线散射(USAXS)研究了一种带电胶体二氧化硅球体的悬浮液,该悬浮液呈现出双峰尺寸分布的颗粒,从而模拟二元混合物。该样品由直径为d(A) = (104.7 ± 9.0) nm和d(B) = (88.1 ± 7.8) nm(d(A)/d(B) ≈ 1.2)的颗粒组成,估计组成为A(0.6(1))B(0.4(1)),研究了其在颗粒数密度和相互作用依赖下的相行为,其中后者通过改变添加碱(NaOH)的量来调节。此外,原位观察了其在流体状态下的短程有序以及最终固化成长程有序胶体晶体的过程,从而能够测量相关的成核和晶体生长动力学。从时间分辨散射曲线中提取了成核动力学的关键参数,如结晶度、微晶数密度和成核速率密度。通过这种方法,获得了二十面体短程有序流体与体心立方胶体晶体之间界面的界面能估计值,与先前确定的单组分胶体系统的值相当。