Published July 2019 | Version v1
Journal article

Spin states investigation of delafossite oxides by means of X-ray absorption and photoemission spectroscopy

  • 1. Technology Innovation Division, Panasonic Corporation, 3-1-1 Yagumo-nakamachi, Moriguchi 570-8501 (Japan)
  • 2. Department of Applied Chemistry, College of Life Sciences, Ritsumeikan University, 1-1-1 Noji-Higashi, Kusatsu 525-8577 (Japan)
  • 3. Research Organization of Science and Technology, Ritsumeikan University, 1-1-1 Noji-Higashi, Kusatsu 525-8577 (Japan)

Description

Highlights: • We investigated the local atomic structure of delafossite oxides including AgCoO2 and CuCoO2. • Shortening of Co-O bond length indicated that Co 3d orbitals were in low spin states. • Non-splitting of Co 3s core level spectra also agreed with the low spin states. • Fully-filled t2g orbital and its metallic surface states is likely associated with high catalytic activity. -- Abstract: The d-electron occupancy of transition metal (TM) oxides is one of the most dominant factors in the catalytic activity in the oxygen evolution reaction (OER). To investigate the spin states and the local atomic structure around the TM atoms in delafossite oxides, CuCrO2, CuMnO2, AgFeO2, CuFeO2, AgCoO2, and CuCoO2, were investigated using X-ray absorption spectroscopy. Based on Shannon radii, the extracted TM-O bond lengths showed that TM = Co delafossite oxides are in the low spin (LS) state, while the other delafossite oxides are in the high spin state. Furthermore, non-splitting of Co 3s core level spectra were observed in photoemission spectroscopy, also indicating LS states. In the LS states, Fully-filled t2g orbital and its metallic surface states distributing normal to (001) surface is likely associated with high OER activity in TM = O delafossite oxides.

Additional details

Identifiers

DOI
10.1016/j.jssc.2019.03.023;
PII
S0022459619301331;

Publishing Information

Journal Title
Journal of Solid State Chemistry (Print)
Journal Volume
275
Journal Page Range
p. 83-87
ISSN
0022-4596
CODEN
JSSCBI

Optional Information

Copyright
Copyright (c) 2019 Published by Elsevier Inc.