4.8 Article

Self-Arranged Misfit Dislocation Network Formation upon Strain Release in La0.7Sr0.3MnO3/LaAlO3(100) Epitaxial Films under Compressive Strain

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 8, 期 26, 页码 16823-16832

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.6b02896

关键词

strain relaxation; misfit dislocation arrangement; nanophase modulation; nanotemplate

资金

  1. Spanish MINECO [MAT2011-29081-C02, MAT2012-33207, MAT2013-47869-C4-1-P, CSD2008-00023]
  2. European Union Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie [645658]
  3. Generalitat de Catalunya [2014 SGR 501, 2014 SGR 1216]
  4. Ministry of Education and Science through program Salvador de Madariaga [PRX14/00297]
  5. Ministry of Education, Science, and Technological Development of the Republic of Serbia [III45018]
  6. National Science Foundation through the MIT Center of Materials Science and Engineering MRSEC [DMR-1419807]
  7. MRSEC Program of the National Science Foundation [DMR-1419807]

向作者/读者索取更多资源

Lattice-mismatched epitaxial films of La0.7Sr0.3MnO3 (LSMO) on LaAlO3 (001) substrates develop a crossed pattern of misfit dislocations above a critical thickness of 2.5 nm. Upon film thickness increases, the dislocation density progressively increases, and the dislocation spacing distribution becomes narrower. At a film thickness of 7.0 nm, the misfit dislocation density is close to the saturation for full relaxation. The misfit dislocation arrangement produces a 2D lateral periodic structure modulation (A 16 nm) alternating two differentiated phases: one phase fully coherent with the substrate and a fully relaxed phase. This modulation is confined to the interface region between film and substrate. This phase separation is clearly identified by X-ray diffraction and further proven in the macroscopic resistivity measurements as a combination of two transition temperatures (with low and high Tc). Films thicker than 7.0 nm show progressive relaxation, and their macroscopic resistivity becomes similar than that of the bulk material. Therefore, this study identifies the growth conditions and thickness ranges that facilitate the formation of laterally modulated nanocomposites with functional properties notably different from those of fully coherent or fully relaxed material.

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