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首页> 外文期刊>Angewandte Chemie >Hydrogen Treatment for Superparamagnetic VO2 Nanowires with Large Room-Temperature Magnetoresistance
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Hydrogen Treatment for Superparamagnetic VO2 Nanowires with Large Room-Temperature Magnetoresistance

机译:具有大室温磁阻的超顺磁性VO2纳米线的氢处理

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摘要

One-dimensional (1D) transition metal oxide (TMO) nanostructures are actively pursued in spintronic devices owing to their nontrivial d electron magnetism and confined electron transport pathways. However, for TMOs, the realization of 1D structures with long-range magnetic order to achieve a sensitive magnetoelectric response near room temperature has been a longstanding challenge. Herein, we exploit a chemical hydric effect to regulate the spin structure of 1D V-V atomic chains in monoclinic VO2 nanowires. Hydrogen treatment introduced V3+ (3d(2)) ions into the 1D zigzag V-V chains, triggering the formation of ferromagnetically coupled V3+-V4+ dimers to produce 1D superparamagnetic chains and achieve large room-temperature negative magnetoresistance (-23.9%, 300 K, 0.5 T). This approach offers new opportunities to regulate the spin structure of 1D nanostructures to control the intrinsic magnetoelectric properties of spintronic materials.
机译:一维(1D)过渡金属氧化物(TMO)纳米结构由于其非平凡的d电子磁性和受限的电子传输路径而在自旋电子器件中得到了积极的追求。然而,对于TMO,实现具有长距离磁阶的一维结构以在室温附近实现敏感的磁电响应一直是一项长期的挑战。在本文中,我们利用化学水合效应来调节单斜VO2纳米线中1D V-V原子链的自旋结构。氢处理将V3 +(3d(2))离子引入一维之字形VV链中,触发铁磁耦合的V3 + -V4 +二聚体的形成,从而产生一维超顺磁链并实现大的室温负磁致电阻(-23.9%,300 K,0.5 T)。这种方法为调节一维纳米结构的自旋结构以控制自旋电子材料的固有磁电性质提供了新的机会。

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