McKetta Department of Chemical Engineering, University of Texas at Austin, Austin, Texas 78712-1589, United States.
Department of Chemistry, University of Texas at Austin, Austin, Texas 78712-1589, United States.
Nano Lett. 2020 May 13;20(5):4007-4013. doi: 10.1021/acs.nanolett.0c01311. Epub 2020 May 1.
Nanocrystal gelation provides a powerful framework to translate nanoscale properties into bulk materials and to engineer emergent properties through the assembled microstructure. However, many established gelation strategies rely on chemical reactions and specific interactions, e.g., stabilizing ligands or ions on the nanocrystals' surfaces, and are therefore not easily transferable. Here, we report a general gelation strategy via nonspecific and purely entropic depletion attractions applied to three types of metal oxide nanocrystals. The gelation thresholds of two compositionally distinct spherical nanocrystals agree quantitatively, demonstrating the adaptability of the approach for different chemistries. Consistent with theoretical phase behavior predictions, nanocrystal cubes form gels at a lower polymer concentration than nanocrystal spheres, allowing shape to serve as a handle to control gelation. These results suggest that the fundamental underpinnings of depletion-driven assembly, traditionally associated with larger colloidal particles, are also applicable at the nanoscale.
纳米晶凝胶化提供了一个强大的框架,可以将纳米级性质转化为体材料,并通过组装的微结构来设计涌现性质。然而,许多已建立的凝胶化策略依赖于化学反应和特定相互作用,例如,在纳米晶体表面上的稳定配体或离子,因此不容易转移。在这里,我们报道了一种通过非特异性和纯粹的熵耗散吸引力的通用凝胶化策略,该策略适用于三种类型的金属氧化物纳米晶体。两种组成不同的球形纳米晶体的凝胶化阈值在数量上是一致的,这证明了该方法对于不同化学物质的适应性。与理论相行为预测一致,纳米晶立方体形成为凝胶的聚合物浓度低于纳米晶球形,这使得形状可以作为控制凝胶化的手段。这些结果表明,传统上与较大胶体颗粒相关的耗散驱动组装的基本原理也适用于纳米尺度。