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通过可逆电压驱动的元素选择性氧化还原过程实现纳米多孔铜镍合金中的可调磁性

Tunable Magnetism in Nanoporous CuNi Alloys by Reversible Voltage-Driven Element-Selective Redox Processes.

作者信息

Quintana Alberto, Menéndez Enric, Isarain-Chávez Eloy, Fornell Jordina, Solsona Pau, Fauth François, Baró Maria Dolors, Nogués Josep, Pellicer Eva, Sort Jordi

机构信息

Departament de Física, Universitat Autònoma de Barcelona, Cerdanyola del Vallès, E-08193, Barcelona, Spain.

CELLS-ALBA, BP1413, Cerdanyola del Vallès, 08290, Barcelona, Spain.

出版信息

Small. 2018 May;14(21):e1704396. doi: 10.1002/smll.201704396. Epub 2018 Apr 18.

DOI:10.1002/smll.201704396
PMID:29667302
Abstract

Voltage-driven manipulation of magnetism in electrodeposited 200 nm thick nanoporous single-phase solid solution Cu Ni (at%) alloy films (with sub 10 nm pore size) is accomplished by controlled reduction-oxidation (i.e., redox) processes in a protic solvent, namely 1 m NaOH aqueous solution. Owing to the selectivity of the electrochemical processes, the oxidation of the CuNi film mainly occurs on the Cu counterpart of the solid solution, resulting in a Ni-enriched alloy. As a consequence, the magnetic moment at saturation significantly increases (up to 33% enhancement with respect to the as-prepared sample), while only slight changes in coercivity are observed. Conversely, the reduction process brings Cu back to its metallic state and, remarkably, it becomes alloyed to Ni again. The reported phenomenon is fully reversible, thus allowing for the precise adjustment of the magnetic properties of this system through the sign and amplitude of the applied voltage.

摘要

通过在质子溶剂(即1 m NaOH水溶液)中进行可控的还原-氧化(即氧化还原)过程,实现了对电沉积的200 nm厚纳米多孔单相固溶体CuNi(原子百分比)合金薄膜(孔径小于10 nm)中磁性的电压驱动操纵。由于电化学过程的选择性,CuNi薄膜的氧化主要发生在固溶体的Cu组分上,从而形成富Ni合金。结果,饱和磁矩显著增加(相对于制备态样品增强高达33%),而矫顽力仅观察到轻微变化。相反,还原过程使Cu回到其金属态,并且值得注意的是,它再次与Ni合金化。所报道的现象是完全可逆的,因此可以通过施加电压的符号和幅度精确调节该系统的磁性。

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