Crystallization dynamics of amorphous yttrium iron garnet thin films

被引:0
|
作者
Sailler, Sebastian [1 ]
Skobjin, Gregor [1 ]
Schlorb, Heike [2 ]
Boehm, Benny [3 ]
Hellwig, Olav [3 ,4 ]
Thomas, Andy [2 ,5 ]
Goennenwein, Sebastian T. B. [1 ]
Lammel, Michaela [1 ]
机构
[1] Univ Konstanz, Dept Phys, D-78457 Constance, Germany
[2] Leibniz Inst Solid State & Mat Sci, D-01069 Dresden, Germany
[3] Tech Univ Chemnitz, Inst Phys, D-09126 Chemnitz, Germany
[4] Tech Univ Chemnitz, Ctr Mat Architectures & Integrat Nanomembranes MAI, D-09107 Chemnitz, Germany
[5] TUD Dresden Univ Technol, Inst Festkorper und Materialphys IFMP, D-01069 Dresden, Germany
来源
PHYSICAL REVIEW MATERIALS | 2024年 / 8卷 / 04期
关键词
SOLID-PHASE EPITAXY; GROWTH-KINETICS; YIG-FILMS; CRYSTAL; LAYERS; RECRYSTALLIZATION; MICROSTRUCTURE; DIFFRACTION;
D O I
10.1103/PhysRevMaterials.8.043402
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Yttrium iron garnet (YIG) is a prototypical material in spintronics due to its exceptional magnetic properties. To exploit these properties, high quality thin films need to be manufactured. Deposition techniques like sputter deposition or pulsed laser deposition at ambient temperature produce amorphous films, which need a postannealing step to induce crystallization. However, not much is known about the exact dynamics of the formation of crystalline YIG out of the amorphous phase. Here, we conduct extensive time and temperature series to study the crystallization behavior of YIG on various substrates and extract the crystallization velocities as well as the activation energies needed to promote crystallization. We find that the type of crystallization as well as the crystallization velocity depend on the lattice mismatch to the substrate. We compare the crystallization parameters found in literature with our results and find excellent agreement with our model. Our results allow us to determine the time needed for the formation of a fully crystalline film of arbitrary thickness for any temperature.
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页数:9
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