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用于提高降解性能的富氧空位CuO/Cu(OH)NO异质结构纳米片的等离子体合成

Plasma synthesis of oxygen vacancy-rich CuO/Cu(OH)NO heterostructure nanosheets for boosting degradation performance.

作者信息

Yang Zikun, Peng Xiangfeng, Zheng Jingxuan, Wang Zhao

机构信息

National Engineering Research Center of Industry Crystallization Technology, School of Chemical Engineering and Technology, Tianjin University, China.

出版信息

Phys Chem Chem Phys. 2023 Nov 1;25(42):29108-29119. doi: 10.1039/d3cp03918h.

DOI:10.1039/d3cp03918h
PMID:37869910
Abstract

Defect regulation and the construction of a heterojunction structure are effective strategies to improve the catalytic activity of catalysts. In this work, the rapid conversion of CuO to Cu(OH)NO was achieved by fixing nitrogen in air as NO using dielectric barrier discharge (DBD) plasma. This innovative approach resulted in the successful synthesis of a CuO/Cu(OH)NO nanosheet heterostructure. Notably, the samples prepared using plasma exhibit thinner thickness and larger specific surface area. Importantly, oxygen vacancies are introduced, simultaneously forming heterojunction interfaces within the CuO/Cu(OH)NO structure. CuO/Cu(OH)NO using plasma effectively degraded 96% of methyl orange within 8 min in the dark. The degradation rate is 81 and 23 times that of CuO and Cu(OH)NO using hydrothermal methods, respectively. The high catalytic activity is attributed to the large specific surface area, the abundance of active sites, and the synergy between oxygen vacancies and the strong heterojunction interfacial interactions, which accelerate the transfer of electrons and the production of reactive oxygen species (˙O and ˙OH). The mechanism of plasma preparation was proposed on account of microstructure characterization and online mass spectroscopy, which indicated that gas etching, gas expansion, and the repulsive force of electrons play key roles in plasma exfoliation.

摘要

缺陷调控和异质结结构的构建是提高催化剂催化活性的有效策略。在本工作中,通过在空气中利用介质阻挡放电(DBD)等离子体将氮固定为NO,实现了CuO快速转化为Cu(OH)NO。这种创新方法成功合成了CuO/Cu(OH)NO纳米片异质结构。值得注意的是,使用等离子体制备的样品厚度更薄且比表面积更大。重要的是,引入了氧空位,同时在CuO/Cu(OH)NO结构内形成了异质结界面。使用等离子体的CuO/Cu(OH)NO在黑暗中8分钟内有效降解了96%的甲基橙。降解速率分别是使用水热法制备的CuO和Cu(OH)NO的81倍和23倍。高催化活性归因于大比表面积、丰富的活性位点以及氧空位与强异质结界面相互作用之间的协同作用,这加速了电子转移和活性氧物种(˙O和˙OH)的产生。基于微观结构表征和在线质谱提出了等离子体制备的机制,表明气体蚀刻、气体膨胀和电子的排斥力在等离子体剥离中起关键作用。

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