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Doping with Graphitic Nitrogen Triggers Ferromagnetism in Graphene

机译:掺杂氮元素会触发石墨烯中的铁磁性

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摘要

Nitrogen doping opens possibilities for tailoring the electronic properties and band gap of graphene toward its applications, e.g., in spintronics and optoelectronics. One major obstacle is development of magnetically active N-doped graphene with spin-polarized conductive behavior. However, the effect of nitrogen on the magnetic properties of graphene has so far only been addressed theoretically, and triggering of magnetism through N-doping has not yet been proved experimentally, except for systems containing a high amount of oxygen and thus decreased conductivity. Here, we report the first example of ferromagnetic graphene achieved by controlled doping with graphitic, pyridinic, and chemisorbed nitrogen. The magnetic properties were found to depend strongly on both the nitrogen concentration and type of structural N-motifs generated in the host lattice. Graphenes doped below 5 at. % of nitrogen were nonmagnetic; however, once doped at 5.1 at. % of nitrogen, N-doped graphene exhibited transition to a ferromagnetic state at ~69 K and displayed a saturation magnetization reaching 1.09 emu/g. Theoretical calculations were used to elucidate the effects of individual chemical forms of nitrogen on magnetic properties. Results showed that magnetic effects were triggered by graphitic nitrogen, whereas pyridinic and chemisorbed nitrogen contributed much less to the overall ferromagnetic ground state. Calculations further proved the existence of exchange coupling among the paramagnetic centers mediated by the conduction electrons.
机译:氮掺杂为定制石墨烯的电子性能和带隙提供了可能性,以适应石墨烯在自旋电子学和光电子学中的应用。一个主要障碍是开发具有自旋极化导电行为的磁活性N掺杂石墨烯。然而,迄今为止,氮对石墨烯的磁性的影响仅在理论上得到了解决,并且除含有大量氧气从而降低电导率的系统外,尚未通过实验证明通过N掺杂触发磁性。在这里,我们报告了通过石墨,吡啶和化学吸附氮的受控掺杂获得的铁磁石墨烯的第一个示例。发现磁性能强烈依赖于氮浓度和在主晶格中产生的结构性N-基序的类型。石墨烯的掺杂浓度低于5 at。氮的百分比是非磁性的;但是,曾经在5.1 at处掺杂。在约69K的氮中,N掺杂的石墨烯的百分比显示出转变为铁磁态,并且饱和磁化强度达到1.09emu / g。理论计算用于阐明氮的各种化学形式对磁性能的影响。结果表明,磁性效应是由石墨氮触发的,而吡啶氮和化学吸附氮对整体铁磁基态的影响则要小得多。计算进一步证明了由传导电子介导的顺磁中心之间存在交换耦合。

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  • 来源
    《Journal of the American Chemical Society》 |2017年第8期|3171-3180|共10页
  • 作者单位

    Regional Centre of Advanced Technologies and Materials, Department of Physical Chemistry, Faculty of Science, Palacký University in Olomouc, 17. listopadu 1192/12, 771 46 Olomouc, Czech Republic;

    Regional Centre of Advanced Technologies and Materials, Department of Physical Chemistry, Faculty of Science, Palacký University in Olomouc, 17. listopadu 1192/12, 771 46 Olomouc, Czech Republic;

    Department of Inorganic Chemistry, University of Chemistry and Technology Prague, Technická 5, 166 28 Prague 6, Czech Republic;

    Department of Inorganic Chemistry, University of Chemistry and Technology Prague, Technická 5, 166 28 Prague 6, Czech Republic;

    Regional Centre of Advanced Technologies and Materials, Department of Physical Chemistry, Faculty of Science, Palacký University in Olomouc, 17. listopadu 1192/12, 771 46 Olomouc, Czech Republic;

    Division of Chemistry & Biological Chemistry, School of Physical and Mathematical Sciences, Nanyang Technological University, 637371 Singapore;

    Regional Centre of Advanced Technologies and Materials, Department of Physical Chemistry, Faculty of Science, Palacký University in Olomouc, 17. listopadu 1192/12, 771 46 Olomouc, Czech Republic;

    Regional Centre of Advanced Technologies and Materials, Department of Physical Chemistry, Faculty of Science, Palacký University in Olomouc, 17. listopadu 1192/12, 771 46 Olomouc, Czech Republic;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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  • 入库时间 2022-08-18 03:07:55

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