Tuning Enantioselective Recognition and Synergistic Catalytic Activity by the Heterojunction of a Chiral Polysaccharide Hydrogel Interface Electric Field.

IF 15.8 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
ACS Nano Pub Date : 2025-07-08 DOI:10.1021/acsnano.5c06687
Xiaohui Niu,Yuewei Wang,Jianying Zhang,Xing Yang,Hongxia Li,Kunjie Wang
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引用次数: 0

Abstract

The demand for high conductivity often forces hydrogels to sacrifice their chiral ordered structure, and the addition of conductive materials may destroy the spatial arrangement of chiral components and reduce the stereoselectivity. To solve this problem, we introduced the heterojunction structure with good electron transport characteristics into the chiral hydrogel to obtain CoFe Prussian blue analogue/MoS2@Chitosan hydrogel (PBA/MoS2@CSH), and it exhibits interface catalytic activity and enantioselective recognition performance. The experimental and theoretical calculation results show that chitosan and its cross-linked PBA/MoS2 compounds complement each other. The chiral microenvironment of the former has different effects on tryptophan enantiomers. The heterojunction between the latter can accelerate the electron transfer during the catalytic oxidation process of tryptophan adsorbed by chitosan by forming a directional interface electric field, thus amplifying the electrochemical signal and increasing the enantioselectivity effect. The collaborative design of chiral hydrogels and heterojunctions is expected to break through the functional boundaries of traditional materials, and endow the materials with multiple functions through the complementarity of the dynamic responsiveness of the chiral structure and the interfacial effects of the heterojunction.
手性多糖水凝胶界面电场异质结调节对映选择性识别和协同催化活性。
对高导电性的要求往往迫使水凝胶牺牲其手性有序结构,而导电材料的加入可能会破坏手性组分的空间排列,降低其立体选择性。为了解决这一问题,我们将具有良好电子传递特性的异质结结构引入手性水凝胶中,得到了CoFe普鲁士蓝类似物/MoS2@Chitosan水凝胶(PBA/MoS2@CSH),该水凝胶具有界面催化活性和对端选择性识别性能。实验和理论计算结果表明,壳聚糖及其交联的PBA/MoS2化合物具有互补性。前者的手性微环境对色氨酸对映体有不同的影响。后者之间的异质结可以通过形成定向界面电场,加速壳聚糖吸附色氨酸催化氧化过程中的电子转移,从而放大电化学信号,增强对映选择性效应。手性水凝胶与异质结的协同设计有望突破传统材料的功能界限,通过手性结构的动态响应性与异质结的界面效应的互补,赋予材料多种功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Nano
ACS Nano 工程技术-材料科学:综合
CiteScore
26.00
自引率
4.10%
发文量
1627
审稿时长
1.7 months
期刊介绍: ACS Nano, published monthly, serves as an international forum for comprehensive articles on nanoscience and nanotechnology research at the intersections of chemistry, biology, materials science, physics, and engineering. The journal fosters communication among scientists in these communities, facilitating collaboration, new research opportunities, and advancements through discoveries. ACS Nano covers synthesis, assembly, characterization, theory, and simulation of nanostructures, nanobiotechnology, nanofabrication, methods and tools for nanoscience and nanotechnology, and self- and directed-assembly. Alongside original research articles, it offers thorough reviews, perspectives on cutting-edge research, and discussions envisioning the future of nanoscience and nanotechnology.
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