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X-ray photoelectron (XPS) and Diffuse Reflectance Infra Fourier Transformation (DRIFT) study of Ba{sub 0.5}Sr{sub 0.5}Co{sub x}Fe{sub 1-x}O{sub 3-{delta}} (BSCF: x=0-0.8) ceramics

Journal Article · · Journal of Solid State Chemistry
 [1];  [1]
  1. Kazuo Inamori School of Engineering, Alfred University, Alfred, NY 14802 (United States)
The X-ray photoelectron spectra (XPS) of sintered BSCF ceramics (Ba{sub 0.5}Sr{sub 0.5}Co{sub x}Fe{sub 1-x}O{sub 3-{delta}},0{<=}x{<=}0.8) were measured at room temperature (RT). Peak areas of Fe{sub 2p1}, Fe{sub 2p3}, Fe{sub 3p} and Co{sub 3p} increased systematically with increasing cobalt concentration, while their binding energies (BEs) remained the same (723.3, 710.0, 55.0 and 60.9 eV, respectively). However, the BEs of lattice oxygen in O{sub 1s} (528.1 eV) and Ba{sub 4d} for the BaO bond (87.9V and 90.2 eV) increased with increasing cobalt concentration. The shoulder peak of Ba{sub 3d}/Co{sub 2p} increased from 778.0 to 778.7 eV, which implies that this peak can be attributed to another Ba XPS peak (described as Ba{sub 2nd} in this study) due to the overlapping area between barium cations and oxygen anions. The overall peak areas of Ba{sub 4d} increased up to x=0.4, and then decreased, which coincides with the behavior of the Diffuse Reflectance Infrared Fourier Transform (DRIFT) bands representing adsorbed CO{sub 3}{sup 2-} ({nu}CO{sub 3}{sup 2-}) and structurally bonded CO{sub 3}{sup 2-} ({nu}{sub 2}, {nu}{sub 3}) (800-1200 and 862/1433 cm{sup -1}, respectively). - Graphical abstract: The bonding of CO{sub 3}{sup 2-} to the surface of BSCF perovskite and the bonding state between cations vs. oxygen have been suggested. Highlights: > XPS and DRIFT were measured on BSCF (BSCF: x=0-0.8) samples. > The identity of Ba{sub 3d}/Co{sub 2p} XPS shoulder peak at {approx}778.0 was suggested. > The bonding behavior of CO{sub 3}{sup 2-} to the BSCF prevoskite structure was studied substantially.
OSTI ID:
21580214
Journal Information:
Journal of Solid State Chemistry, Journal Name: Journal of Solid State Chemistry Journal Issue: 8 Vol. 184; ISSN 0022-4596; ISSN JSSCBI
Country of Publication:
United States
Language:
English