Two Nanoparticle Populations Simultaneously Directed Using Triptych Triblock Terpolymers

IF 4.4 2区 化学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY ACS Applied Polymer Materials Pub Date : 2024-09-05 DOI:10.1021/acs.chemmater.4c0152410.1021/acs.chemmater.4c01524
Mengxue Zhang, Xiaomeng Li, Chuanbing Tang and Morgan Stefik*, 
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Abstract

Multicomponent nanocomposites are important for diverse fields spanning energy conversion to optoelectronics and catalysis. Polymer structure-directing agents typically direct the placement of hydrophilic nanoparticles (HNPs) using hydrophilic interactions; however, this approach is generally limited to random mixtures when combining two types of HNPs. A new approach is shown where two distinct intermolecular interaction modalities enable independent control of two, respectively, functionalized nanoparticle populations. Specifically, the orthogonal interactions of the hydrophilic-fluorophobic structure-directing agents enabled independent control of the placement of both HNPs and fluorophobic nanoparticles (FNPs). This dual-nanoparticle assembly was first examined using a diblock poly(hydrophilic-b-fluorophobic) structure-directing agents where achieving well-defined assemblies required >32 wt % HNPs to preserve micelle templates. The addition of a glassy lipophilic block led to a triptych triblock poly(hydrophilic-b-lipophilic-b-fluorophobic) design that enabled vitrification of FNP-loaded micelles for robust dual-nanoparticle control with well-defined assemblies regardless of the FNP/HNP fractions. A novel micelle-chain morphology occurred with ≥ 89 wt % FNPs which may support unique transport applications. This micelle-chain morphology was associated with the depletion of chains at the core–corona interface, promoting micelle aggregation. Equilibration experiments were used to probe for dynamic exchange processes during various stages of processing from sequential solvent conditions. These mixing experiments identified that polymer chains and FNPs underwent dynamic exchange in acetone (plasticizer) but did not after transferring to water (nonplasticizer), thus confirming glassy kinetic entrapment at the final stage of processing. This collection of experiments highlights how triptych block polymers offer a new approach toward independent control over two types of nanoparticles.

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使用三嵌段三元共聚物同时引导两个纳米粒子群
多组分纳米复合材料在能源转换、光电子学和催化等多个领域都非常重要。聚合物结构引导剂通常利用亲水性相互作用来引导亲水性纳米粒子(HNPs)的放置;然而,当结合两种类型的 HNPs 时,这种方法通常仅限于随机混合物。本文展示了一种新方法,通过两种不同的分子间相互作用方式,可以分别独立地控制两种功能化纳米粒子群。具体来说,亲水-疏氟结构导向剂的正交相互作用能够独立控制 HNPs 和疏氟纳米粒子(FNPs)的位置。首先使用二嵌段聚(亲水-疏水-疏氟)结构引导剂对这种双纳米粒子组装进行了研究,要实现定义明确的组装,需要 32 wt % 的 HNPs 来保留胶束模板。加入玻璃状亲脂嵌段后,就产生了三元三嵌段聚(亲水-亲脂-疏水-疏氟)设计,从而实现了 FNP 负载胶束的玻璃化,无论 FNP/HNP 分量如何,都能以定义明确的组装实现稳健的双纳米粒子控制。FNP 含量≥ 89 wt % 时,会出现一种新颖的胶束链形态,可支持独特的运输应用。这种胶束链形态与核心-电晕界面上的链耗尽有关,从而促进了胶束的聚集。平衡实验用于探测连续溶剂条件下不同加工阶段的动态交换过程。这些混合实验发现,聚合物链和 FNPs 在丙酮(增塑剂)中发生了动态交换,但转移到水(非增塑剂)中后却没有发生,从而证实了在加工的最后阶段存在玻璃态动力学夹持。这组实验强调了三元嵌段聚合物是如何为独立控制两种类型的纳米粒子提供新方法的。
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来源期刊
CiteScore
7.20
自引率
6.00%
发文量
810
期刊介绍: ACS Applied Polymer Materials is an interdisciplinary journal publishing original research covering all aspects of engineering, chemistry, physics, and biology relevant to applications of polymers. The journal is devoted to reports of new and original experimental and theoretical research of an applied nature that integrates fundamental knowledge in the areas of materials, engineering, physics, bioscience, polymer science and chemistry into important polymer applications. The journal is specifically interested in work that addresses relationships among structure, processing, morphology, chemistry, properties, and function as well as work that provide insights into mechanisms critical to the performance of the polymer for applications.
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