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空位诱导的 MoS2 纳米片铁磁性

Vacancy-induced ferromagnetism of MoS2 nanosheets.

机构信息

National Synchrotron Radiation Laboratory, University of Science and Technology of China , Hefei 230029, P. R. China.

出版信息

J Am Chem Soc. 2015 Feb 25;137(7):2622-7. doi: 10.1021/ja5120908. Epub 2015 Feb 10.

Abstract

Outstanding magnetic properties are highly desired for two-dimensional ultrathin semiconductor nanosheets. Here, we propose a phase incorporation strategy to induce robust room-temperature ferromagnetism in a nonmagnetic MoS2 semiconductor. A two-step hydrothermal method was used to intentionally introduce sulfur vacancies in a 2H-MoS2 ultrathin nanosheet host, which prompts the transformation of the surrounding 2H-MoS2 local lattice into a trigonal (1T-MoS2) phase. 25% 1T-MoS2 phase incorporation in 2H-MoS2 nanosheets can enhance the electron carrier concentration by an order, introduce a Mo(4+) 4d energy state within the bandgap, and create a robust intrinsic ferromagnetic response of 0.25 μB/Mo by the exchange interactions between sulfur vacancy and the Mo(4+) 4d bandgap state at room temperature. This design opens up new possibility for effective manipulation of exchange interactions in two-dimensional nanostructures.

摘要

具有优异磁性的二维超薄半导体纳米片是人们非常期望的。在这里,我们提出了一种相整合策略,以在非磁性 MoS2 半导体中诱导出稳定的室温铁磁性。采用两步水热法在 2H-MoS2 超薄纳米片主体中有意引入硫空位,促使周围的 2H-MoS2 局域晶格转变为三角(1T-MoS2)相。在 2H-MoS2 纳米片中掺入 25%的 1T-MoS2 相,可以将电子载流子浓度提高一个数量级,在能带内引入 Mo(4+) 4d 态,并通过室温下硫空位和 Mo(4+) 4d 带隙态之间的交换相互作用产生 0.25 μB/Mo 的强本征铁磁响应。该设计为有效控制二维纳米结构中的交换相互作用开辟了新的可能性。

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