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基于真菌的MnO/多孔碳纳米杂化物作为用于氧还原催化和对苯二酚检测的高效漆酶模拟物

Fungus-Based MnO/Porous Carbon Nanohybrid as Efficient Laccase Mimic for Oxygen Reduction Catalysis and Hydroquinone Detection.

作者信息

Ge Haoran, Zhang Hailong

机构信息

School of Electrical and Automation Engineering, Nanjing Normal University, Nanjing 210023, China.

出版信息

Nanomaterials (Basel). 2022 May 8;12(9):1596. doi: 10.3390/nano12091596.

Abstract

Developing efficient laccase-mimicking nanozymes via a facile and sustainable strategy is intriguing in environmental sensing and fuel cells. In our work, a MnO/porous carbon (MnO/PC) nanohybrid based on fungus was synthesized via a facile carbonization route. The nanohybrid was found to possess excellent laccase-mimicking activity using 2,2'-azinobis (3-ethylbenzthiazoline-6-sulfonic acid) diammonium salt (ABTS) as the substrate. Compared with the natural laccase and reported nanozymes, the MnO/PC nanozyme had much lower value. Furthermore, the electrochemical results show that the MnO/PC nanozyme had high electrocatalytic activity toward the oxygen reduction reaction (ORR) when it was modified on the electrode. The hybrid nanozyme could catalyze the four-electron ORR, similar to natural laccase. Moreover, hydroquinone (HQ) induced the reduction of oxABTS and caused the green color to fade, which provided colorimetric detection of HQ. A desirable linear relationship (0-50 μM) and detection limit (0.5 μM) were obtained. Our work opens a simple and sustainable avenue to develop a carbon-metal hybrid nanozyme in environment and energy applications.

摘要

通过简便且可持续的策略开发高效的类漆酶纳米酶在环境传感和燃料电池领域颇具吸引力。在我们的工作中,通过简便的碳化路线合成了一种基于真菌的MnO/多孔碳(MnO/PC)纳米杂化物。以2,2'-联氮双(3-乙基苯并噻唑啉-6-磺酸)二铵盐(ABTS)为底物时,发现该纳米杂化物具有优异的类漆酶活性。与天然漆酶和已报道的纳米酶相比,MnO/PC纳米酶的[具体数值]低得多。此外,电化学结果表明,MnO/PC纳米酶修饰在电极上时对氧还原反应(ORR)具有高电催化活性。该杂化纳米酶可催化四电子ORR,类似于天然漆酶。此外,对苯二酚(HQ)诱导氧化型ABTS(oxABTS)还原并导致绿色褪色,从而实现了HQ的比色检测。获得了理想的线性关系(0 - 50 μM)和检测限(0.5 μM)。我们的工作为在环境和能源应用中开发碳-金属杂化纳米酶开辟了一条简单且可持续的途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5253/9103193/f1fd60c24ac2/nanomaterials-12-01596-sch001.jpg

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