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用于先进传感应用的羟基化共价有机框架纳米纤维的结构诱导选择性:一项实验与密度泛函理论研究

Structure-Induced Selectivity of Hydroxylated Covalent Organic Framework Nanofibers for Advanced Sensing Applications: An Experimental and Density Functional Theory Study.

作者信息

Torad Nagy L, Yang Tzu-Ling, A Darwish Moustafa, Raghunath Putikam, Qurashi Ahsanulhaq, Ahmed Lamiaa Reda, Lin Ming-Chang, Yamauchi Yusuke, Yuliarto Brian, Kaveevivitchai Watchareeya, Abu Haija Mohammad, El-Mahdy Ahmed F M

机构信息

Department of Chemistry, Khalifa University of Science and Technology, P.O. Box 127788, Abu Dhabi, United Arab Emirates.

Center for Catalysis and Separation (CeCaS), Khalifa University of Science and Technology, P.O. Box 127788, Abu Dhabi, United Arab Emirates.

出版信息

ACS Appl Mater Interfaces. 2025 May 7;17(18):27188-27203. doi: 10.1021/acsami.5c03407. Epub 2025 Apr 26.

Abstract

This study reports on the rational design of hydroxyl-functionalized covalent organic framework nanofibers (HO-COFs: PyTA-2,3-NA(OH) and PyTA-2,6-NA(OH)) by a scalable solvothermal method. The resulting PyTA-2,3-NA(OH) HO-COF is more hydrophilic than the PyTA-2,6-NA(OH) HO-COF, which can effectively enhance the sensitivity of the sensor toward basic ethylenediamine (EDA). The fabricated HO-COF nanofiber-based quartz crystal microbalance sensor exhibits a rapid sensing response and a distinguished selectivity toward EDA vapor, arising from the strong hydrogen bonding interactions with the NH groups of EDA, as investigated by a wide variety of chemical analysis techniques and density functional theory calculations. The presence of exposed neighboring hydroxyl groups that face the same direction in the PyTA-2,3-NA(OH) HO-COF and the NH groups present in EDA exhibited efficient interactions. The PyTA-2,3-NA(OH) nanofiber with neighboring hydroxyl groups exhibits 1.6 times higher sensitivity to 100 ppm (ppm) EDA than PyTA-2,6-NA(OH) with hydroxyl groups in opposite directions, with a low limit of detection of 2.9 ppm. The PyTA-2,3-NA(OH) nanofiber structure has abundant active neighboring hydroxyl groups facing the same direction, making them favorable active sites for binding EDA molecules through strong hydrogen bond interactions. The color of the HO-COF changed after exposure to EDA vapor, as investigated by colorimetric assessment and naked-eye detection. These HO-COF nanofibers exhibit remarkable selectivity for EDA in the presence of other interfering chemical vapors and show high stability with only a 6.4% drop in sensitivity after 6 months. The adsorption of EDA on PyTA-2,3-NA(OH) nanofibers follows a pseudo-first-order kinetic model, with an adsorption rate about 8.0 times faster than PyTA-2,6-NA(OH) nanofibers. The findings of this study highlight the potential use of COFs, particularly those nanofibers with close neighboring hydroxyl groups, as effective sensing materials for the selective detection of harmful EDA.

摘要

本研究报告了通过可扩展的溶剂热法对羟基官能化共价有机框架纳米纤维(HO-COFs:PyTA-2,3-NA(OH)和PyTA-2,6-NA(OH))进行的合理设计。所得的PyTA-2,3-NA(OH) HO-COF比PyTA-2,6-NA(OH) HO-COF更具亲水性,这可以有效提高传感器对碱性乙二胺(EDA)的灵敏度。所制备的基于HO-COF纳米纤维的石英晶体微天平传感器对EDA蒸汽表现出快速的传感响应和出色的选择性,这源于与EDA的NH基团的强氢键相互作用,通过多种化学分析技术和密度泛函理论计算进行了研究。在PyTA-2,3-NA(OH) HO-COF中存在面向同一方向的相邻暴露羟基,与EDA中存在的NH基团表现出有效的相互作用。具有相邻羟基的PyTA-2,3-NA(OH)纳米纤维对100 ppm EDA的灵敏度比具有相反方向羟基的PyTA-2,6-NA(OH)高1.6倍,检测下限低至2.9 ppm。PyTA-2,3-NA(OH)纳米纤维结构具有大量面向同一方向的相邻活性羟基,使其成为通过强氢键相互作用结合EDA分子的有利活性位点。通过比色评估和肉眼检测发现,暴露于EDA蒸汽后HO-COF的颜色发生了变化。这些HO-COF纳米纤维在存在其他干扰化学蒸汽的情况下对EDA表现出显著的选择性,并且显示出高稳定性,6个月后灵敏度仅下降6.4%。EDA在PyTA-2,3-NA(OH)纳米纤维上的吸附遵循准一级动力学模型,吸附速率比PyTA-2,6-NA(OH)纳米纤维快约8.0倍。本研究结果突出了COFs,特别是那些具有紧密相邻羟基的纳米纤维,作为选择性检测有害EDA的有效传感材料的潜在用途。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b5/12067381/e8e04d6ad2e4/am5c03407_0010.jpg

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