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用于过氧化氢电化学传感的双金属纳米结构在钴基金属有机框架上的直接电沉积

Direct Electrodeposition of Bimetallic Nanostructures on Co-Based MOFs for Electrochemical Sensing of Hydrogen Peroxide.

作者信息

Xie Yixuan, Shi Xianhua, Chen Linxi, Lu Jing, Lu Xiange, Sun Duanping, Zhang Luyong

机构信息

Center for Drug Research and Development, Guangdong Provincial Key Laboratory of Pharmaceutical Bioactive Substances, Guangdong Pharmaceutical University, Guangzhou, China.

National and Local United Engineering Lab of Druggability and New Drugs Evaluation, School of Pharmaceutical Sciences, Sun Yat-Sen University, Guangzhou, China.

出版信息

Front Chem. 2022 Mar 11;10:856003. doi: 10.3389/fchem.2022.856003. eCollection 2022.

DOI:10.3389/fchem.2022.856003
PMID:35360537
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8961982/
Abstract

Hydrogen peroxide (HO) is the most significant reactive oxygen species in biological systems. Here, we reported an electrochemical sensor for the detection of HO on the basis of bimetallic gold-platinum nanoparticles (AuPt NPs) supported by Co-based metal organic frameworks (Co-MOFs). First, AuPt NPs, with optimal electrocatalytic activity and accessible active surface, can be deposited on the surface of the Co-MOF-modified glassy carbon electrodes (AuPt/Co-MOFs/GCE) by one-step electrodeposition method. Then, the electrochemical results demonstrated that the two-dimensional (2D) Co-MOF nanosheets as the supporting material displayed better electrocatalytic properties than the 3D Co-MOF crystals for reduction of HO. The fabricated AuPt/2D Co-MOF exhibited high electrocatalytic activity, and the catalytic current was linear with HO concentration from 0.1 μM to 5 mM, and 5-60 mM with a low detection limit of 0.02 μM (S/N = 3). The remarkable electroanalytical performance of AuPt/2D Co-MOF can be attributed to the synergistic effect of the high dispersion of the AuPt NPs with the marvelous electrochemical properties and the 2D Co-MOF with high-specific surface areas. Furthermore, this sensor has been utilized to detect HO concentrations released from the human Hela cells. This work provides a new method for improving the performance of electrochemical sensors by choosing the proper support materials from diverse crystal morphology materials.

摘要

过氧化氢(HO)是生物系统中最重要的活性氧物种。在此,我们报道了一种基于钴基金属有机框架(Co-MOFs)负载的双金属金铂纳米颗粒(AuPt NPs)检测HO的电化学传感器。首先,具有最佳电催化活性和可及活性表面的AuPt NPs可通过一步电沉积法沉积在Co-MOF修饰的玻碳电极(AuPt/Co-MOFs/GCE)表面。然后,电化学结果表明,作为支撑材料的二维(2D)Co-MOF纳米片在还原HO方面比三维Co-MOF晶体表现出更好的电催化性能。制备的AuPt/2D Co-MOF表现出高电催化活性,催化电流与HO浓度在0.1 μM至5 mM范围内呈线性关系,在5 - 60 mM范围内也呈线性关系,检测限低至0.02 μM(S/N = 3)。AuPt/2D Co-MOF卓越的电分析性能可归因于具有出色电化学性质的AuPt NPs的高分散性与具有高比表面积的2D Co-MOF的协同效应。此外,该传感器已用于检测人Hela细胞释放的HO浓度。这项工作通过从不同晶体形态材料中选择合适的支撑材料,为提高电化学传感器的性能提供了一种新方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7125/8961982/d78542761c0c/fchem-10-856003-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7125/8961982/9f62bdb156a1/FCHEM_fchem-2022-856003_wc_sch1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7125/8961982/bb1ed8165d48/fchem-10-856003-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7125/8961982/5e4109cdfd44/fchem-10-856003-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7125/8961982/aa76c466ed40/fchem-10-856003-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7125/8961982/4d4527f4fc6c/fchem-10-856003-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7125/8961982/d78542761c0c/fchem-10-856003-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7125/8961982/9f62bdb156a1/FCHEM_fchem-2022-856003_wc_sch1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7125/8961982/bb1ed8165d48/fchem-10-856003-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7125/8961982/5e4109cdfd44/fchem-10-856003-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7125/8961982/aa76c466ed40/fchem-10-856003-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7125/8961982/4d4527f4fc6c/fchem-10-856003-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7125/8961982/d78542761c0c/fchem-10-856003-g005.jpg

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