Title of article :
Enhancing magnetocrystalline anisotropy of the Fe70Pd30 magnetic shape memory alloy by adding Cu Original Research Article
Author/Authors :
S. Kauffmann-Weiss، نويسنده , , Christian S. Hamann، نويسنده , , M.E. Gruner، نويسنده , , L. Schultz، نويسنده , , A. Ludwig، نويسنده , , S. F?hler، نويسنده ,
Issue Information :
دوهفته نامه با شماره پیاپی سال 2012
Pages :
11
From page :
6920
To page :
6930
Abstract :
Fe–Pd–Cu thin films are of great interest for applications in magnetic shape memory microsystems due to their increased martensitic transformation temperature. Here we analyse the consequences of Cu addition to Fe–Pd on the binding energy and magnetic properties by a combination of thin film experiments and first-principles calculations. Strained epitaxial growth of Fe70Pd30-xCux with x = 0, 3, 7 is used to freeze intermediate stages during the martensitic transformation. This makes a large range of tetragonal distortion susceptible for analysis, ranging from body-centred cubic to beyond face-centred cubic (1.07 < c/abct < 1.57). We find that Cu enhances the quality of epitaxial growth, while spontaneous polarization and Curie temperature are reduced only moderately, in agreement with our calculations. Beyond c/abct > 1.41 the samples undergo structural relaxations through adaptive nanotwinning. Cu enhances the magnetocrystalline anisotropy constant K1 at room temperature, which reaches a maximum of −2.4 × 105 J m−3 around c/abct = 1.33. This value exceeds those of binary Fe70Pd30 and the prototype Ni–Mn–Ga magnetic shape memory system. Since K1 represents the maximum driving energy for variant reorientation in magnetic shape memory systems, we conclude that Fe–Pd–Cu alloys offer a promising route towards microactuator applications with significantly improved work output.
Keywords :
Adaptive nanotwins , Epitaxial films , Bain path , First-principles calculations , Magnetic properties
Journal title :
ACTA Materialia
Serial Year :
2012
Journal title :
ACTA Materialia
Record number :
1146653
Link To Document :
بازگشت