Mehran Sedrpooshan, P. Ternero, C. Bulbucan, Adam Burke, M. Messing, R. Westerström
{"title":"Single-Step Generation of 1D FeCo Nanostructures","authors":"Mehran Sedrpooshan, P. Ternero, C. Bulbucan, Adam Burke, M. Messing, R. Westerström","doi":"10.1088/2632-959x/ad3e1c","DOIUrl":null,"url":null,"abstract":"\n Magnetic one-dimensional structures are attractive nanomaterials due to the variety of potential applications they can provide. The fabrication of bimetallic 1D structures further expands the capabilities of such structures by tailoring the magnetic properties. Here, a single-step template-free method is presented for the fabrication of 1D FeCo alloy nanochains. In this approach, charged single-crystalline FeCo nanoparticles are first generated by the co-ablation of pure Fe and Co electrodes under a carrier gas at ambient pressures and attracted to a substrate using an electric field. When reaching the surface, the particles are self-assembled into parallel nanochains along the direction of an applied magnetic field. The approach allows for monitoring the self-assembly particle by particle as they are arranged into linear 1D chains with an average length controlled by the deposited particle concentration. Facilitated by the self-assembly, the magnetic properties of the structures can be studied in detail. Magnetometry measurements revealed that arranging nanoparticles into nanochains results in a 100% increase in the remanent magnetization, indicating significant shape anisotropy. Furthermore, by combining X-ray microscopy and micromagnetic simulations, we have studied the local magnetization configuration along the nanochains. Our findings show that variations in magnetocrystalline anisotropy along the structure play a crucial role in the formation of magnetic domains.","PeriodicalId":484840,"journal":{"name":"Nano express","volume":"14 3","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-04-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nano express","FirstCategoryId":"0","ListUrlMain":"https://doi.org/10.1088/2632-959x/ad3e1c","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Magnetic one-dimensional structures are attractive nanomaterials due to the variety of potential applications they can provide. The fabrication of bimetallic 1D structures further expands the capabilities of such structures by tailoring the magnetic properties. Here, a single-step template-free method is presented for the fabrication of 1D FeCo alloy nanochains. In this approach, charged single-crystalline FeCo nanoparticles are first generated by the co-ablation of pure Fe and Co electrodes under a carrier gas at ambient pressures and attracted to a substrate using an electric field. When reaching the surface, the particles are self-assembled into parallel nanochains along the direction of an applied magnetic field. The approach allows for monitoring the self-assembly particle by particle as they are arranged into linear 1D chains with an average length controlled by the deposited particle concentration. Facilitated by the self-assembly, the magnetic properties of the structures can be studied in detail. Magnetometry measurements revealed that arranging nanoparticles into nanochains results in a 100% increase in the remanent magnetization, indicating significant shape anisotropy. Furthermore, by combining X-ray microscopy and micromagnetic simulations, we have studied the local magnetization configuration along the nanochains. Our findings show that variations in magnetocrystalline anisotropy along the structure play a crucial role in the formation of magnetic domains.
磁性一维结构是一种极具吸引力的纳米材料,因为它们可以提供多种潜在应用。通过定制磁性能,双金属一维结构的制造进一步扩展了此类结构的功能。本文介绍了一种单步无模板法制备一维铁钴合金纳米链。在这种方法中,带电的单晶铁钴纳米颗粒首先是在环境压力下通过纯铁和钴电极在载气中的共熔产生的,然后利用电场吸引到基底上。当颗粒到达表面时,会沿着外加磁场的方向自组装成平行的纳米链。这种方法可以逐个监测颗粒的自组装情况,因为颗粒被排列成线性一维链,其平均长度受沉积颗粒浓度的控制。通过自组装,可以对结构的磁特性进行详细研究。磁力测量显示,将纳米粒子排列成纳米链会导致剩磁增加 100%,这表明形状各向异性非常明显。此外,我们还结合 X 射线显微镜和微磁模拟,研究了纳米链的局部磁化配置。我们的研究结果表明,磁晶各向异性沿结构的变化在磁畴的形成中起着至关重要的作用。