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通过碳包覆二氧化钛上的界面氧空位实现自驱动活性氧生成及其广泛应用

Self-Driven Reactive Oxygen Species Generation via Interfacial Oxygen Vacancies on Carbon-Coated TiO with Versatile Applications.

作者信息

Lyu Pin, Zhu Jian, Han Chongchong, Qiang Lei, Zhang Linlin, Mei Bingbao, He Jiehong, Liu Xiaoyan, Bian Zhenfeng, Li Hexing

机构信息

The Education Ministry Key Laboratory of Resource Chemistry, International Joint Laboratory of Resource Chemistry, College of Chemistry and Materials Science, Shanghai Normal University, Shanghai 200234, P.R. China.

Department of Nuclear Medicine, Xinhua Hospital Affiliated to Shanghai Jiao Tong University, Shanghai Jiao Tong University, Shanghai 200092, P.R. China.

出版信息

ACS Appl Mater Interfaces. 2021 Jan 13;13(1):2033-2043. doi: 10.1021/acsami.0c19414. Epub 2020 Dec 30.

Abstract

The effective activation and utilization of O have always been the focus of scientists because of its wide applications in catalysis, organic synthesis, life and medical science. Here, a novel method for activating O spontaneously via interfacial oxygen vacancies on carbon-coated TiO to generate reactive oxygen species (ROS) with versatile applications is reported. The interfacial oxygen vacancies can be stabilized by the carbon layer and hold its intrinsic properties for spontaneous oxygen activation without light irradiation, while common surface oxygen vacancies on TiO are always consumed by the capture of HO to form the surface hydroxyls. Thus, O absorbed at the interface of carbon and TiO can be directly activated into singlet oxygen (O) or superoxide radicals (·O), confirmed both experimentally and theoretically. These reactive oxygen species exhibit excellent performance in oxidation reactions and inhibition of MCF-7 cancer cells, providing new insight into the effective utilization of O via oxygen vacancies on metal oxides.

摘要

由于O在催化、有机合成、生命科学和医学等领域具有广泛应用,其有效活化和利用一直是科学家们关注的焦点。在此,报道了一种通过碳包覆TiO上的界面氧空位自发活化O以生成具有多种用途的活性氧物种(ROS)的新方法。界面氧空位可被碳层稳定,并在无光照的情况下保持其自发氧活化的固有特性,而TiO上常见的表面氧空位总是被HO捕获消耗以形成表面羟基。因此,在碳与TiO界面处吸附的O可直接被活化成单线态氧(O)或超氧自由基(·O),这在实验和理论上均得到证实。这些活性氧物种在氧化反应和抑制MCF-7癌细胞方面表现出优异性能,为通过金属氧化物上的氧空位有效利用O提供了新的见解。

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