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Engineering Carrier Effective Masses in Ultrathin Quantum Wells of IrO_{2}.
Kawasaki, Jason K; Kim, Choong H; Nelson, Jocienne N; Crisp, Sophie; Zollner, Christian J; Biegenwald, Eric; Heron, John T; Fennie, Craig J; Schlom, Darrell G; Shen, Kyle M.
Afiliação
  • Kawasaki JK; Kavli Institute at Cornell for Nanoscale Science, Cornell University, Ithaca, New York 14853, USA.
  • Kim CH; Laboratory for Atomic and Solid State Physics, Cornell University, Ithaca, New York 14853, USA.
  • Nelson JN; Department of Materials Science and Engineering, Cornell University, Ithaca, New York 14853, USA.
  • Crisp S; Department of Materials Science and Engineering, University of Wisconsin, Madison, Wisconsin 53706, USA.
  • Zollner CJ; Center for Correlated Electron Systems, Institute for Basic Science, Seoul, Korea.
  • Biegenwald E; Department of Physics and Astronomy, Seoul National University, Seoul, Korea.
  • Heron JT; Laboratory for Atomic and Solid State Physics, Cornell University, Ithaca, New York 14853, USA.
  • Fennie CJ; Laboratory for Atomic and Solid State Physics, Cornell University, Ithaca, New York 14853, USA.
  • Schlom DG; Department of Applied and Engineering Physics, Cornell University, Ithaca, New York 14853, USA.
  • Shen KM; Department of Materials Science and Engineering, Cornell University, Ithaca, New York 14853, USA.
Phys Rev Lett ; 121(17): 176802, 2018 Oct 26.
Article em En | MEDLINE | ID: mdl-30411938
ABSTRACT
The carrier effective mass plays a crucial role in modern electronic, optical, and catalytic devices and is fundamentally related to key properties of solids such as the mobility and density of states. Here we demonstrate a method to deterministically engineer the effective mass using spatial confinement in metallic quantum wells of the transition metal oxide IrO_{2}. Using a combination of in situ angle-resolved photoemission spectroscopy measurements in conjunction with precise synthesis by oxide molecular-beam epitaxy, we show that the low-energy electronic subbands in ultrathin films of rutile IrO_{2} have their effective masses enhanced by up to a factor of 6 with respect to the bulk. The origin of this strikingly large mass enhancement is the confinement-induced quantization of the highly nonparabolic, three-dimensional electronic structure of IrO_{2} in the ultrathin limit. This mechanism lies in contrast to that observed in other transition metal oxides, in which mass enhancement tends to result from complex electron-electron interactions and is difficult to control. Our results demonstrate a general route towards the deterministic enhancement and engineering of carrier effective masses in spatially confined systems, based on an understanding of the three-dimensional bulk electronic structure.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article