4.8 Article

Competition between Covalent Bonding and Charge Transfer at Complex-Oxide Interfaces

期刊

PHYSICAL REVIEW LETTERS
卷 112, 期 19, 页码 -

出版社

AMER PHYSICAL SOC
DOI: 10.1103/PhysRevLett.112.196802

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资金

  1. U.S. Department of Energy (DOE)
  2. Basic Energy Sciences (BES)
  3. Materials Sciences and Engineering Division
  4. Materials Sciences and Engineering Division through the Center for Nanophase Materials Sciences (CNMS)
  5. Scientific User Facilities Division
  6. DOE-BES
  7. ERC starting Investigator Award [239739 STEMOX]
  8. Juan de la Cierva program (MICINN-Spain) [JCI-2011-09428]
  9. Spanish MICINN/MINECO [MAT2011-27470-C02]
  10. Consolider Ingenio (Imagine) [CSD2009-00013]
  11. CAM (PHAMA) [S2009/MAT-1756]
  12. National Center for Supercomputing Applications (U. S. Department of Energy) [DEAC02-05CH11231]

向作者/读者索取更多资源

Here we study the electronic properties of cuprate-manganite interfaces. By means of atomic resolution electron microscopy and spectroscopy, we produce a subnanometer scale map of the transition metal oxidation state profile across the interface between the high Tc superconductor YBa2Cu3O7-delta and the colossal magnetoresistance compound (La,Ca)MnO3. A net transfer of electrons from manganite to cuprate with a peculiar nonmonotonic charge profile is observed. Model calculations rationalize the profile in terms of the competition between standard charge transfer tendencies (due to band mismatch), strong chemical bonding effects across the interface, and Cu substitution into the Mn lattice, with different characteristic length scales.

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