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Magneto-Ionics in Single-Layer Transition Metal Nitrides

机译:单层过渡金属氮化物中的磁离子

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Magneto-ionics allows for tunable control of magnetism by voltage-driven transport of ions, traditionally oxygen or lithium and, more recently, hydrogen, fluorine, or nitrogen. Here, magneto-ionic effects in single-layer iron nitride films are demonstrated, and their performance is evaluated at room temperature and compared with previously studied cobalt nitrides. Iron nitrides require increased activation energy and, under high bias, exhibit more modest rates of magneto-ionic motion than cobalt nitrides. Ab initio calculations reveal that, based on the atomic bonding strength, the critical field required to induce nitrogen-ion motion is higher in iron nitrides (≈6.6 V nm~(–1)) than in cobalt nitrides (≈5.3 V nm~(–1)). Nonetheless, under large bias (i.e., well above the magneto-ionic onset and, thus, when magneto-ionics is fully activated), iron nitride films exhibit enhanced coercivity and larger generated saturation magnetization, surpassing many of the features of cobalt nitrides. The microstructural effects responsible for these enhanced magneto-ionic effects are discussed. These results open up the potential integration of magneto-ionics in existing nitride semiconductor materials in view of advanced memory system architectures.
机译:磁离子技术允许通过电压驱动的离子传输来调节磁性,传统上是氧或锂,最近是氢、氟或氮。本文展示了单层氮化铁薄膜中的磁离子效应,并在室温下对其性能进行了评估,并与之前研究的氮化钴薄膜进行了比较。氮化铁需要增加活化能,并且在高偏压下,比氮化钴表现出更温和的磁离子运动速率。从头算计算表明,基于原子键强度,在氮化铁中诱导氮离子运动所需的临界场较高(≈比氮化钴高6.6V nm~(-1))(≈5.3 V nm~(-1))。尽管如此,在大偏压下(即远高于磁离子起始点,因此,当磁离子完全激活时),氮化铁薄膜表现出增强的矫顽力和更大的饱和磁化强度,超过了氮化钴的许多特征。讨论了这些增强磁离子效应的微观结构效应。从先进的存储系统结构来看,这些结果开启了磁离子在现有氮化物半导体材料中的潜在集成。

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