State Key Laboratory of Chemical Resource Engineering & State Key Laboratory of Organic-Inorganic Composites, Beijing University of Chemical Technology , Beijing, China.
ACS Appl Mater Interfaces. 2015 Aug 26;7(33):18824-31. doi: 10.1021/acsami.5b05555. Epub 2015 Aug 14.
The zigzag film growth behavior in the layer-by-layer (LbL) assembly method is a ubiquitous phenomenon for which the growth mechanism was rarely investigated, especially for small molecules. To interpret the zigzag increasing manner, we hypothesized that the desorption kinetics of small molecules was dominant for the film growth behavior and demonstrated this hypotheis by introducing the high-gravity technique into the LbL assembly of a typical polyelectrolyte/small molecule system of polyethylenimine (PEI) and meso-tetra(4-carboxyphenyl)porphine (Por). The results showed that the high-gravity technique remarkably accelerated the desorption process of Por; the high-gravity LbL assembly provides a good platform to reveal the desorption kinetics of Por, which is tedious to study in conventional situation. We found that as much as 50 min is required for Por molecules to reach desorption equilibrium from the substrate to the bulk PEI solution for the conventional dipping method; however, the process could be accelerated and require only 100 s if a high-gravity field is used. Nonequilibrated desorption at 10 min for normal dipping and at 30 s for high-gravity-field-assisted assembly both exhibited a zigzag film growth, but after reaching desorption equilibrium at 100 s under a high-gravity field, film growth began to cycle between assembly and complete disassembly instead of LbL assembly. For the first time we have proven that the high-gravity technique can also accelerate the desorption process and demonstrated the desorption-dependent mechanism of small molecules for zigzag film growth behaviors.
层层自组装过程中的锯齿形膜生长行为是一种普遍现象,但对于小分子,其生长机制很少被研究。为了解释锯齿形增长方式,我们假设小分子的解吸动力学对于膜生长行为起主导作用,并通过将高重力技术引入典型聚电解质/小分子体系聚乙烯亚胺(PEI)和间四(4-羧基苯基)卟啉(Por)的层层自组装中验证了这一假设。结果表明,高重力技术显著加速了 Por 的解吸过程;高重力层层自组装为揭示 Por 的解吸动力学提供了一个良好的平台,而在常规情况下研究这一动力学非常繁琐。我们发现,对于常规浸渍法,Por 分子从基底到达大块 PEI 溶液达到解吸平衡需要长达 50 分钟的时间;然而,如果使用高重力场,这个过程可以加速,只需要 100 秒。对于常规浸渍法的 10 分钟非平衡解吸和高重力场辅助组装的 30 秒非平衡解吸都表现出锯齿形膜生长,但在高重力场下达到 100 秒的解吸平衡后,膜生长开始在组装和完全解组装之间循环,而不是进行层层自组装。我们首次证明高重力技术也可以加速解吸过程,并证明了小分子锯齿形膜生长行为的解吸依赖性机制。