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自组装的 Pt 薄膜顶部的 Co 纳米颗粒形成纳米尺度的合金。

Nanoscaled alloy formation from self-assembled elemental Co nanoparticles on top of Pt films.

机构信息

Institut für Festkörperphysik, Universität Ulm, Albert-Einstein-Allee 11, 89069 Ulm, Germany.

出版信息

Beilstein J Nanotechnol. 2011;2:473-85. doi: 10.3762/bjnano.2.51. Epub 2011 Aug 23.

DOI:10.3762/bjnano.2.51
PMID:22003453
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3190617/
Abstract

The thermally activated formation of nanoscale CoPt alloys was investigated, after deposition of self-assembled Co nanoparticles on textured Pt(111) and epitaxial Pt(100) films on MgO(100) and SrTiO(3)(100) substrates, respectively. For this purpose, metallic Co nanoparticles (diameter 7 nm) were prepared with a spacing of 100 nm by deposition of precursor-loaded reverse micelles, subsequent plasma etching and reduction on flat Pt surfaces. The samples were then annealed at successively higher temperatures under a H(2) atmosphere, and the resulting variations of their structure, morphology and magnetic properties were characterized. We observed pronounced differences in the diffusion and alloying of Co nanoparticles on Pt films with different orientations and microstructures. On textured Pt(111) films exhibiting grain sizes (20-30 nm) smaller than the particle spacing (100 nm), the formation of local nanoalloys at the surface is strongly suppressed and Co incorporation into the film via grain boundaries is favoured. In contrast, due to the absence of grain boundaries on high quality epitaxial Pt(100) films with micron-sized grains, local alloying at the film surface was established. Signatures of alloy formation were evident from magnetic investigations. Upon annealing to temperatures up to 380 °C, we found an increase both of the coercive field and of the Co orbital magnetic moment, indicating the formation of a CoPt phase with strongly increased magnetic anisotropy compared to pure Co. At higher temperatures, however, the Co atoms diffuse into a nearby surface region where Pt-rich compounds are formed, as shown by element-specific microscopy.

摘要

我们研究了在自组装 Co 纳米粒子沉积在分别具有织构化 Pt(111)和外延 Pt(100)膜的 MgO(100)和 SrTiO(3)(100)衬底上之后,纳米级 CoPt 合金的热激活形成。为此,通过沉积载有前体的反胶束、随后在平坦的 Pt 表面进行等离子体刻蚀和还原,制备了直径为 7nm、间距为 100nm 的金属 Co 纳米粒子。然后,将样品在 H(2)气氛下依次在更高的温度下退火,并对其结构、形貌和磁性能的变化进行了表征。我们观察到 Co 纳米粒子在具有不同取向和微观结构的 Pt 薄膜上的扩散和合金化存在明显差异。在具有小于粒子间距(100nm)的晶粒尺寸(20-30nm)的织构化 Pt(111)薄膜上,表面局部纳米合金的形成受到强烈抑制,而 Co 通过晶界掺入薄膜中则更为有利。相比之下,由于高质量外延 Pt(100)薄膜上不存在晶界,且晶粒尺寸达到微米级,因此在薄膜表面上形成了局部合金化。合金形成的特征从磁性研究中显而易见。在退火至 380°C 以下的温度时,我们发现矫顽力和 Co 轨道磁矩都有所增加,这表明形成了具有与纯 Co 相比显著增加的磁各向异性的 CoPt 相。然而,在更高的温度下,Co 原子扩散到附近的表面区域,在那里形成富 Pt 的化合物,这一点通过元素特异性显微镜得到了证实。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/030c/3190617/2049d7d1fe03/Beilstein_J_Nanotechnol-02-473-g011.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/030c/3190617/61d94e9f4fe5/Beilstein_J_Nanotechnol-02-473-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/030c/3190617/aa17b27f0e9b/Beilstein_J_Nanotechnol-02-473-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/030c/3190617/2f683462c2f4/Beilstein_J_Nanotechnol-02-473-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/030c/3190617/431330ddb5d2/Beilstein_J_Nanotechnol-02-473-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/030c/3190617/10c60fd71e9e/Beilstein_J_Nanotechnol-02-473-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/030c/3190617/371ba23a5204/Beilstein_J_Nanotechnol-02-473-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/030c/3190617/08be994a627a/Beilstein_J_Nanotechnol-02-473-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/030c/3190617/2049d7d1fe03/Beilstein_J_Nanotechnol-02-473-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/030c/3190617/7aa579aff50a/Beilstein_J_Nanotechnol-02-473-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/030c/3190617/6cf9ef5f8bda/Beilstein_J_Nanotechnol-02-473-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/030c/3190617/61d94e9f4fe5/Beilstein_J_Nanotechnol-02-473-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/030c/3190617/aa17b27f0e9b/Beilstein_J_Nanotechnol-02-473-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/030c/3190617/2f683462c2f4/Beilstein_J_Nanotechnol-02-473-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/030c/3190617/431330ddb5d2/Beilstein_J_Nanotechnol-02-473-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/030c/3190617/10c60fd71e9e/Beilstein_J_Nanotechnol-02-473-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/030c/3190617/371ba23a5204/Beilstein_J_Nanotechnol-02-473-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/030c/3190617/08be994a627a/Beilstein_J_Nanotechnol-02-473-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/030c/3190617/2049d7d1fe03/Beilstein_J_Nanotechnol-02-473-g011.jpg

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