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调控纳米尺度下氧离子输运以实现对磁性的高循环磁离子控制。

Regulating Oxygen Ion Transport at the Nanoscale to Enable Highly Cyclable Magneto-Ionic Control of Magnetism.

机构信息

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

Institut de Ciència de Materials de Barcelona, CSIC, Campus UAB, 08193 Bellaterra, Barcelona, Spain.

出版信息

ACS Nano. 2023 Apr 11;17(7):6973-6984. doi: 10.1021/acsnano.3c01105. Epub 2023 Mar 27.

DOI:10.1021/acsnano.3c01105
PMID:36972329
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10100572/
Abstract

Magneto-ionics refers to the control of magnetic properties of materials through voltage-driven ion motion. To generate effective electric fields, either solid or liquid electrolytes are utilized, which also serve as ion reservoirs. Thin solid electrolytes have difficulties in (i) withstanding high electric fields without electric pinholes and (ii) maintaining stable ion transport during long-term actuation. In turn, the use of liquid electrolytes can result in poor cyclability, thus limiting their applicability. Here we propose a nanoscale-engineered magneto-ionic architecture (comprising a thin solid electrolyte in contact with a liquid electrolyte) that drastically enhances cyclability while preserving sufficiently high electric fields to trigger ion motion. Specifically, we show that the insertion of a highly nanostructured (amorphous-like) Ta layer (with suitable thickness and electric resistivity) between a magneto-ionic target material (.., CoO) and the liquid electrolyte increases magneto-ionic cyclability from <30 cycles (when no Ta is inserted) to more than 800 cycles. Transmission electron microscopy together with variable energy positron annihilation spectroscopy reveals the crucial role of the generated TaO interlayer as a solid electrolyte (., ionic conductor) that improves magneto-ionic endurance by proper tuning of the types of voltage-driven structural defects. The Ta layer is very effective in trapping oxygen and hindering O ions from moving into the liquid electrolyte, thus keeping O motion mainly restricted between CoO and Ta when voltage of alternating polarity is applied. We demonstrate that this approach provides a suitable strategy to boost magneto-ionics by combining the benefits of solid and liquid electrolytes in a synergetic manner.

摘要

磁离子学是指通过电压驱动离子运动来控制材料的磁性。为了产生有效的电场,需要使用固体或液体电解质作为离子源。然而,固体电解质存在两个问题:(i)难以承受高电场而不产生电穿孔;(ii)在长期驱动过程中难以保持稳定的离子传输。相比之下,液体电解质的循环性能较差,因此限制了其应用。在这里,我们提出了一种纳米工程化的磁离子架构(由与液体电解质接触的薄固体电解质组成),该架构极大地提高了循环性能,同时保持了足够高的电场以触发离子运动。具体来说,我们发现,在磁离子靶材料(例如 CoO)和液体电解质之间插入一层具有合适厚度和电阻率的高度纳米结构化(非晶态类似)Ta 层,可以将磁离子的循环性能从<30 次(未插入 Ta 时)提高到 800 次以上。透射电子显微镜和变能正电子湮没谱表明,生成的 TaO 中间层作为固体电解质(离子导体)的关键作用,通过适当调整电压驱动结构缺陷的类型,提高了磁离子的耐久性。Ta 层非常有效地捕获氧,并阻止 O 离子进入液体电解质,因此当施加交替极性电压时,O 离子的运动主要限制在 CoO 和 Ta 之间。我们证明,这种方法通过协同结合固体和液体电解质的优点,为提高磁离子学提供了一种合适的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3eff/10100572/ba05ea85def7/nn3c01105_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3eff/10100572/d75f8a04d780/nn3c01105_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3eff/10100572/da7bc88758d8/nn3c01105_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3eff/10100572/7653c3500c9b/nn3c01105_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3eff/10100572/48cc7a9cbaf8/nn3c01105_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3eff/10100572/6cd07db81c9d/nn3c01105_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3eff/10100572/9634b123cb82/nn3c01105_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3eff/10100572/ba05ea85def7/nn3c01105_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3eff/10100572/d75f8a04d780/nn3c01105_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3eff/10100572/da7bc88758d8/nn3c01105_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3eff/10100572/7653c3500c9b/nn3c01105_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3eff/10100572/48cc7a9cbaf8/nn3c01105_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3eff/10100572/6cd07db81c9d/nn3c01105_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3eff/10100572/9634b123cb82/nn3c01105_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3eff/10100572/ba05ea85def7/nn3c01105_0007.jpg

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