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Mesoporous oxide-diluted magnetic semiconductors prepared by co implantation in nanocast 3D-ordered In2O3-y materials

机译:纳米浇铸3D顺序In2O3-y材料中共注入制备的介孔氧化物稀释的磁性半导体

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Mesoporous In2O3-y materials have been implanted using Co ions to induce a moderate ferromagnetic response at room temperature, forming a >mesoporous oxide-diluted magnetic semiconductor> (MODMS). X-ray photoemission spectroscopy (XPS) reveals that implantation results in up to 1 at. % Co (for 6 × 1015 ions/cm2 at 40 keV) and 15 at. % Co (for 1 × 1017 ions/cm2 at 60 keV). This is in both cases accompanied by a pronounced increase in the amount of oxygen vacancies with respect to the pristine, nonimplanted, In2O 3-y. Further increase in the ion fluence (up to 2 × 10 17 ions/cm2 at 60 keV) results in the collapse of the mesoporous structure, i.e., loss of the 3D-ordered porous configuration. XPS also reveals that virtually no metallic Co is formed at 40 keV, while a mixture of Co2+ and Co0 states is detected after implantation at 60 keV. Most of the Co2+ is incorporated in the bixbyite structure of the In2O3-y matrix. These results are consistent with previous models suggesting that the origin of the obtained ferromagnetic response in oxide-diluted magnetic semiconductors can be ascribed to ferromagnetic exchange interactions mediated by oxygen vacancies. This work constitutes the first report on MODMS prepared by nanocasting followed by implantation of transition metal ions. © 2013 American Chemical Society.
机译:已经使用Co离子注入了介孔In2O3-y材料,以在室温下感应出适度的铁磁响应,从而形成了>介孔氧化物稀释的磁性半导体>(MODMS)。 X射线光电子能谱(XPS)揭示,植入最多可导致1 at。 %Co(40 keV时为6×1015离子/ cm2)和15 at。 %Co(60 keV时1×1017离子/ cm2)。在这两种情况下,相对于未植入的原始In2O 3-y,原始的氧空位数量均明显增加。离子通量的进一步增加(在60 keV时高达2×10 17离子/ cm2)导致中孔结构的崩溃,即3D有序多孔结构的丧失。 XPS还揭示出,在40 keV注入时几乎没有形成金属Co,而在60 keV注入后检测到了Co2 +和Co0的混合态。大多数的Co2 +被掺入In2O3-y基体的方铁矿结构中。这些结果与先前的模型一致,表明先前的模型表明在氧化物稀释的磁性半导体中获得的铁磁响应的起源可以归因于由氧空位介导的铁磁交换相互作用。这项工作是有关MODMS的第一份报告,该报告是通过纳米浇铸,然后注入过渡金属离子制备的。 ©2013美国化学学会。

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