School of Polymer Science and Polymer Engineering, The University of Akron, Akron, Ohio 44325, United States.
Department of Civil Engineering and Geological Sciences, University of Notre Dame, Notre Dame, Indiana 46556, United States.
J Phys Chem B. 2021 Nov 11;125(44):12392-12397. doi: 10.1021/acs.jpcb.1c08019. Epub 2021 Oct 27.
Unexpected hydrogel and coacervate are observed for dilute (1 mM) uranyl peroxide molecular cluster (LiK(OH)[UO(O)(OH)], U) solution in the presence of di- or trivalent salts. We report the mechanism as the formation of anisotropic two-dimensional (2-D) single-layer nanosheets, driven by counterion-mediated attraction due to the size disparity between U and small counterions. With weak monovalent cations, the nanosheets are bendable, resulting in hollow, spherical blackberry-type supramolecular assemblies in a homogeneous solution. With extra strong divalent or trivalent cations, the tough, free-standing sheets lead to gelation at ∼1 mM U. These stiff nanosheets are difficult to bend into spherical blackberry-type structures; instead, they stay in solution and form hydrogel based on their significant excluded volumes. At higher ionic strength, the large, thin filmlike nanosheet structures stack together more compactly and consequently lead to the transition from gel phase to a coacervate phase, another surprise since it was formed without the presence of bulky polycations.
在二价或三价盐存在的情况下,我们观察到稀(1mM)过氧铀酰分子簇(LiK(OH)[UO(O)(OH)],U)溶液中出现了意想不到的水凝胶和凝聚物。我们报告的机制是由于 U 和小抗衡离子之间的尺寸差异,由抗衡离子介导的吸引力驱动形成各向异性的二维(2-D)单层纳米片。对于弱单价阳离子,纳米片具有可弯曲性,导致在均相溶液中形成中空、球形黑莓型超分子组装体。对于额外的强二价或三价阳离子,坚韧的、独立的薄片在约 1mM U 时导致凝胶化。这些刚性纳米片很难弯曲成球形黑莓型结构;相反,它们留在溶液中,并基于其显著的排斥体积形成水凝胶。在较高的离子强度下,大而薄的薄膜状纳米片结构更紧密地堆积在一起,从而导致从凝胶相到凝聚相的转变,这是另一个惊喜,因为它是在没有大的聚阳离子存在的情况下形成的。