Two Nanoparticle Populations Simultaneously Directed Using Triptych Triblock Terpolymers

IF 7.2 2区 材料科学 Q2 CHEMISTRY, PHYSICAL
Mengxue Zhang, Xiaomeng Li, Chuanbing Tang and Morgan Stefik*, 
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引用次数: 0

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.

Abstract Image

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
Chemistry of Materials
Chemistry of Materials 工程技术-材料科学:综合
CiteScore
14.10
自引率
5.80%
发文量
929
审稿时长
1.5 months
期刊介绍: The journal Chemistry of Materials focuses on publishing original research at the intersection of materials science and chemistry. The studies published in the journal involve chemistry as a prominent component and explore topics such as the design, synthesis, characterization, processing, understanding, and application of functional or potentially functional materials. The journal covers various areas of interest, including inorganic and organic solid-state chemistry, nanomaterials, biomaterials, thin films and polymers, and composite/hybrid materials. The journal particularly seeks papers that highlight the creation or development of innovative materials with novel optical, electrical, magnetic, catalytic, or mechanical properties. It is essential that manuscripts on these topics have a primary focus on the chemistry of materials and represent a significant advancement compared to prior research. Before external reviews are sought, submitted manuscripts undergo a review process by a minimum of two editors to ensure their appropriateness for the journal and the presence of sufficient evidence of a significant advance that will be of broad interest to the materials chemistry community.
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