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利用气-水界面生成界面活性氧用于超快速环境修复。

Harnessing air-water interface to generate interfacial ROS for ultrafast environmental remediation.

作者信息

Xie Ruijie, Guo Kaiheng, Li Yong, Zhang Yingguang, Zhong Huanran, Leung Dennis Y C, Huang Haibao

机构信息

School of Environmental Science and Engineering, Sun Yat-sen University, Guangzhou, China.

Institute of Applied and Physical Chemistry and Center for Environmental Research and Sustainable Technology, University of Bremen, Bremen, Germany.

出版信息

Nat Commun. 2024 Oct 14;15(1):8860. doi: 10.1038/s41467-024-53289-z.

Abstract

The air-water interface of microbubbles represents a crucial microenvironment that can dramatically accelerate reactive oxidative species (ROS) reactions. However, the dynamic nature of microbubbles presents challenges in probing ROS behaviors at the air-water interface, limiting a comprehensive understanding of their chemistry and application. Here we develop an approach to investigate the interfacial ROS via coupling microbubbles with a Fenton-like reaction. Amphiphilic single-Co-atom catalyst (Co@SCN) is employed to efficiently transport the oxidant peroxymonosulfate (PMS) from the bulk solution to the microbubble interface. This triggers an accelerated generation of interfacial sulfate radicals (SO), with 20-fold higher concentration (4.48 × 10 M) than the bulk SO. Notably, the generated SO is preferentially situated at the air-water interface due to its lowest free energy and the strong hydrogen bonding interactions with HO. Moreover, it exhibits the highest oxidation reactivity toward gaseous pollutants like toluene, with a rate constant of 10M s-over 100 times greater than bulk reactions. This work demonstrates a promising strategy to harness the air-water interface for accelerating ROS-induced reactions, highlighting the importance of interfacial ROS and its potential application.

摘要

微泡的气-水界面代表了一个关键的微环境,它能显著加速活性氧(ROS)反应。然而,微泡的动态性质给探测气-水界面处的ROS行为带来了挑战,限制了对其化学反应和应用的全面理解。在此,我们开发了一种通过将微泡与类芬顿反应耦合来研究界面ROS的方法。采用两亲性单钴原子催化剂(Co@SCN)将氧化剂过一硫酸盐(PMS)从本体溶液有效地输送到微泡界面。这引发了界面硫酸根自由基(SO)的加速生成,其浓度(4.48×10 M)比本体SO高20倍。值得注意的是,生成的SO由于其最低的自由能以及与HO的强氢键相互作用而优先位于气-水界面。此外,它对气态污染物如甲苯表现出最高的氧化反应活性,速率常数为10M s,比本体反应大100多倍。这项工作展示了一种利用气-水界面加速ROS诱导反应的有前景的策略,突出了界面ROS的重要性及其潜在应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc8e/11473771/2c50440e97ce/41467_2024_53289_Fig1_HTML.jpg

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