Soft colloids make strong glasses Export

@article{citeulike:6071890, abstract = {Glass formation in colloidal suspensions has many of the hallmarks of glass formation in molecular materials1, 2, 3, 4, 5. For hard-sphere colloids, which interact only as a result of excluded volume, phase behaviour is controlled by volume fraction, ; an increase in drives the system towards its glassy state, analogously to a decrease in temperature, T, in molecular systems. When increases above *  0.53, the viscosity starts to increase significantly, and the system eventually moves out of equilibrium at the glass transition, g  0.58, where particle crowding greatly restricts structural relaxation1, 2, 3, 4. The large particle size makes it possible to study both structure and dynamics with light scattering1 and imaging3, 4; colloidal suspensions have therefore provided considerable insight into the glass transition. However, hard-sphere colloidal suspensions do not exhibit the same diversity of behaviour as molecular glasses. This is highlighted by the wide variation in behaviour observed for the viscosity or structural relaxation time, , when the glassy state is approached in supercooled molecular liquids5. This variation is characterized by the unifying concept of fragility5, which has spurred the search for a 'universal' description of dynamic arrest in glass-forming liquids. For 'fragile' liquids, is highly sensitive to changes in T, whereas non-fragile, or 'strong', liquids show a much lower T sensitivity. In contrast, hard-sphere colloidal suspensions are restricted to fragile behaviour, as determined by their  dependence1, 6, ultimately limiting their utility in the study of the glass transition. Here we show that deformable colloidal particles, when studied through their concentration dependence at fixed temperature, do exhibit the same variation in fragility as that observed in the T dependence of molecular liquids at fixed volume. Their fragility is dictated by elastic properties on the scale of individual colloidal particles. Furthermore, we find an equivalent effect in molecular systems, where elasticity directly reflects fragility. Colloidal suspensions may thus provide new insight into glass formation in molecular systems.}, author = {Mattsson, Johan and Wyss, Hans M. and Fernandez-Nieves, Alberto and Miyazaki, Kunimasa and Hu, Zhibing and Reichman, David R. and Weitz, David A.}, booktitle = {Nature}, citeulike-article-id = {6071890}, citeulike-linkout-0 = {http://dx.doi.org/10.1038/nature08457}, citeulike-linkout-1 = {http://dx.doi.org/10.1038/nature08457}, day = {05}, doi = {10.1038/nature08457}, issn = {0028-0836}, journal = {Nature}, keywords = {colloids, glass, soft-sphere, supercooled}, month = {November}, number = {7269}, pages = {83--86}, posted-at = {2009-11-13 15:47:57}, priority = {2}, publisher = {Nature Publishing Group}, title = {Soft colloids make strong glasses}, url = {http://dx.doi.org/10.1038/nature08457}, volume = {462}, year = {2009} }

TY - JOUR ID - citeulike:6071890 L3 - citeulike-article-id:6071890 N2 - Glass formation in colloidal suspensions has many of the hallmarks of glass formation in molecular materials1, 2, 3, 4, 5. For hard-sphere colloids, which interact only as a result of excluded volume, phase behaviour is controlled by volume fraction, ; an increase in drives the system towards its glassy state, analogously to a decrease in temperature, T, in molecular systems. When increases above *  0.53, the viscosity starts to increase significantly, and the system eventually moves out of equilibrium at the glass transition, g  0.58, where particle crowding greatly restricts structural relaxation1, 2, 3, 4. The large particle size makes it possible to study both structure and dynamics with light scattering1 and imaging3, 4; colloidal suspensions have therefore provided considerable insight into the glass transition. However, hard-sphere colloidal suspensions do not exhibit the same diversity of behaviour as molecular glasses. This is highlighted by the wide variation in behaviour observed for the viscosity or structural relaxation time, , when the glassy state is approached in supercooled molecular liquids5. This variation is characterized by the unifying concept of fragility5, which has spurred the search for a 'universal' description of dynamic arrest in glass-forming liquids. For 'fragile' liquids, is highly sensitive to changes in T, whereas non-fragile, or 'strong', liquids show a much lower T sensitivity. In contrast, hard-sphere colloidal suspensions are restricted to fragile behaviour, as determined by their  dependence1, 6, ultimately limiting their utility in the study of the glass transition. Here we show that deformable colloidal particles, when studied through their concentration dependence at fixed temperature, do exhibit the same variation in fragility as that observed in the T dependence of molecular liquids at fixed volume. Their fragility is dictated by elastic properties on the scale of individual colloidal particles. Furthermore, we find an equivalent effect in molecular systems, where elasticity directly reflects fragility. Colloidal suspensions may thus provide new insight into glass formation in molecular systems. IS - 7269 JF - Nature SN - 0028-0836 EP - 86 TI - Soft colloids make strong glasses PB - Nature Publishing Group VL - 462 T2 - Nature SP - 83 KW - colloids KW - glass KW - soft-sphere KW - supercooled AU - Mattsson, Johan AU - Wyss, Hans AU - Fernandez-Nieves, Alberto AU - Miyazaki, Kunimasa AU - Hu, Zhibing AU - Reichman, David AU - Weitz, David PY - 2009/11/05/ UR - http://dx.doi.org/10.1038/nature08457 ER -