Formation of Laves phases in buoyancy matched hard sphere suspensions

被引:12
作者
Schaertl, N. [1 ,2 ]
Botin, D. [3 ]
Palberg, T. [3 ]
Bartsch, E. [1 ,2 ]
机构
[1] Albert Ludwigs Univ Freiburg, Inst Makromol Chem, D-79104 Freiburg, Germany
[2] Albert Ludwigs Univ Freiburg, Inst Phys Chem, D-79104 Freiburg, Germany
[3] Johannes Gutenberg Univ Mainz, Inst Phys, D-55128 Mainz, Germany
关键词
ENTROPY-DRIVEN FORMATION; BINARY-MIXTURES; SUPERLATTICE FORMATION; DENSITY-FLUCTUATIONS; CRYSTALLIZATION; STABILITY; CRYSTALS; BEHAVIOR; TRANSITION; RHEOLOGY;
D O I
10.1039/c7sm02348k
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Colloidal Laves phases (LPs) are promising precursors for photonic materials. Laves phases have not yet been observed to form in experiments on colloidal suspensions of hard spheres (HS), even though they have been reported in computer simulations. LP formation so far has been achieved only for binary mixtures of colloidal charged spheres or ligand-stabilized nano-particles after drying. Using static light scattering, we monitored LP formation and annealing in a binary mixture of buoyant hard sphere approximants (size ratio Gamma = 0.77, number or molar fraction of small spheres x(S) = 0.76) for volume fractions in the fluid-crystal coexistence regions. All samples spontaneously formed MgZn2 type LPs on the time scale of weeks to months via bulk nucleation and growth. Irrespective of the initial suspension volume fractions, the LP volume fraction at coexistence is Phi(COEX) = 0.59 which is significantly below the close packing limit Phi(MAX) = 0.615 and remarkably close to the expectation from simulation. At low volume fractions, crystals anneal to high quality during coarsening which is in line with recent theoretical expectations for the thermodynamic stability of different LP types. At large volume fractions, however, the diffractograms evolve towards a more MgCu2-like appearance which we attribute to the formation of randomly stacked LPs. Such structures are not known from atomic systems.
引用
收藏
页码:5130 / 5139
页数:10
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