Evaporative self-assembly of the binary mixture of soft colloids†

被引:10
|
作者
Jose, Merin [1 ]
Mayarani, Muraleedharapai [1 ]
Basavaraj, Madivala G. [2 ]
Satapathy, Dillip K. [1 ]
机构
[1] IIT Madras, Dept Phys, Soft Mat Lab, Chennai, Tamil Nadu, India
[2] IIT Madras, Dept Chem Engn, PECS Lab, Chennai, Tamil Nadu, India
关键词
AIR-WATER-INTERFACE; PARTICLES; MICROGELS; CRYSTALS;
D O I
10.1039/d1cp00440a
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
We have reported experimental studies on the self-assembly and degree of ordering of a binary mixture of soft colloids in monolayer deposits obtained by controlled evaporation. A sessile drop containing soft colloids is evaporated on a solid surface to achieve a loosely-packed two-dimensional deposit with a hexagonal arrangement. The soft microgel particles possess a hard core with a compliant corona, which plays a crucial role in retaining the crystallinity of the binary particle monolayer. The ordered arrangement of the binary mixture is observed even when the bulk diameter of one type of particle is 25% higher than the other, irrespective of their mixing ratio (1 : 3, 1 : 1, and 3 : 1). The microgel particles of both sizes are found to be homogeneously distributed throughout the deposit, completely suppressing the size-dependent particle segregation. Furthermore, in contrast to the self-assembly of bidisperse hard colloids, wherein the lattice distorts to accommodate particles of disparate sizes, in soft colloids, the particles deform at the interface to preserve the crystalline lattice. Moreover, unlike the gradual order-to-disorder transition observed in the deposits consisting of monodisperse microgel particles, the deposits of a binary mixture of microgels exhibit no noticeable trend. The areal disorder parameter, pair correlation function and the shape factor which quantifies the local ordering of particles in the deposit indicate the absence of a distinct order-to-disorder transition for the binary mixtures.
引用
收藏
页码:7115 / 7124
页数:10
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