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Modified Oxygen Defect Chemistry at Transition Metal Oxide Heterostructures Probed by Hard X-ray Photoelectron Spectroscopy and X-ray Diffraction

Journal Article · · Chemistry of Materials
 [1];  [2];  [1];  [3];  [4];  [1];  [1]
  1. Massachusetts Inst. of Technology (MIT), Cambridge, MA (United States)
  2. Argonne National Lab. (ANL), Argonne, IL (United States)
  3. Synchrotron SOLEIL, Saint-Aubin (France)
  4. Synchrotron SOLEIL, Saint-Aubin (France); Sorbonne Univ., Paris (France)
Transition metal oxide hetero-structures are interesting due to the distinctly different properties that can arise from their interfaces, such as superconductivity, high catalytic activity and magnetism. Oxygen point defects can play an important role at these interfaces in inducing potentially novel properties. The design of oxide hetero-structures in which the oxygen defects are manipulated to attain specific functionalities requires the ability to resolve the state and concentration of local oxygen defects across buried interfaces. In this work, we utilized a novel combination of hard x-ray photoelectron spectroscopy (HAXPES) and high resolution xray diffraction (HRXRD) to probe the local oxygen defect distribution across the buried interfaces of oxide heterolayers. This approach provides a non-destructive way to qualitatively probe locally the oxygen defects in transition metal oxide hetero-structures. We studied two trilayer structures as model systems - the La0.8Sr0.2CoO3-δ/(La0.5Sr0.5)2CoO4/La0.8Sr0.2CoO3-δ (LSC113/LSC214) and the La0.8Sr0.2CoO3-δ/La2NiO4+δ/La0.8Sr0.2CoO3-δ (LSC113/LNO214) on SrTiO3(001) single crystal substrates. We found that the oxygen defect chemistry of these transition metal oxides was strongly impacted by the presence of interfaces and the properties of the adjacent phases. Under reducing conditions, the LSC113 in the LSC113/LNO214 tri-layer had less oxygen vacancies than the LSC113 in the LSC113/LSC214 tri-layer and the LSC113 single phase film. On the other hand, LSC214 and LNO214 were more reduced in the two tri-layer structures when in contact with the LSC113 layer compared to their single phase counterparts. Furthermore, the results point out a potential way to modify the local oxygen defect states at oxide hetero-interfaces.
Research Organization:
Argonne National Lab. (ANL), Argonne, IL (United States)
Sponsoring Organization:
USDOE Office of Science (SC), Basic Energy Sciences (BES) (SC-22)
Grant/Contract Number:
AC02-06CH11357
OSTI ID:
1455048
Journal Information:
Chemistry of Materials, Journal Name: Chemistry of Materials Journal Issue: 10 Vol. 30; ISSN 0897-4756
Publisher:
American Chemical Society (ACS)Copyright Statement
Country of Publication:
United States
Language:
English

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Cited By (6)

Improving the Activity for Oxygen Evolution Reaction by Tailoring Oxygen Defects in Double Perovskite Oxides journal June 2019
Nanostructured Materials and Interfaces for Advanced Ionic Electronic Conducting Oxides journal May 2019
Uncovering the Effect of Lattice Strain and Oxygen Deficiency on Electrocatalytic Activity of Perovskite Cobaltite Thin Films journal January 2019
Anionic defect engineering of transition metal oxides for oxygen reduction and evolution reactions journal January 2019
Heterointerface engineering for enhancing the electrochemical performance of solid oxide cells journal January 2020
Nanostructured Materials and Interfaces for Advanced Ionic Electronic Conducting Oxides text January 2019

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