对映选择合成
多糖
电场
异质结
催化作用
接口(物质)
材料科学
分子识别
纳米技术
组合化学
化学
光电子学
分子
有机化学
物理
量子力学
吉布斯等温线
作者
Xiaohui Niu,Yuewei Wang,Jianying Zhang,Xing Yang,Hongxia Li,Kunjie Wang
出处
期刊:ACS Nano
[American Chemical Society]
日期:2025-07-08
卷期号:19 (28): 26019-26030
被引量:5
标识
DOI:10.1021/acsnano.5c06687
摘要
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.
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