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Title: Preparation and neutron diffraction study of Dion-Jacobson type oxynitrides LiLaTa{sub 2}O{sub 7−3x}N{sub 2x} (x = 0.09, 0.29)

Journal Article · · Materials Research Bulletin
 [1];  [2];  [3];  [1]
  1. Department of Chemistry, Yeungnam University, Gyeongsan 712-749 (Korea, Republic of)
  2. Department of Chemistry, Division of Energy Systems Research, Ajou University, Suwon 443-749 (Korea, Republic of)
  3. Korea Basic Science Institute, Daegu 701-702 (Korea, Republic of)

Highlights: ► Dion-Jacobson oxynitrides LiLaTa{sub 2}O{sub 7−3x}N{sub 2x}□{sub x} (x < 0.3) by ammonolysis of LiLaTa{sub 2}O{sub 7}. ► Enhanced thermal stability and band gap narrowing by the oxynitride modification. ► Locations of N and □ within LiLaTa{sub 2}O{sub 7−3x}N{sub 2x} by neutron diffraction and {sup 7}Li MAS NMR. -- Abstract: Ammonolytic heating of Dion-Jacobson type layered perovskite LiLaTa{sub 2}O{sub 7} produced oxynitride derivatives LiLaTa{sub 2}O{sub 7−3x}N{sub 2x}□{sub x}via the substitution, 3O{sup 2−} → 2N{sup 3−} + □. The nitridation level increased with raising the temperature and/or increasing the time of reaction, reaching the limit at x ≈ 0.3 by the ammonolysis at 650 °C for 48 h. Upon the nitridation, tetragonal pristine lattice underwent a axis expansion together with c axis contraction. Neutron Rietveld refinement of LiLaTa{sub 2}O{sub 7} and LiLaTa{sub 2}O{sub 7−3x}N{sub 2x} (x = 0.09, 0.29) revealed that the Li-centered tetrahedra are gradually compressed along the 2-fold rotation axis, with the increase of x. Solid state {sup 7}Li nuclear magnetic resonance spectroscopy suggested that the anion vacancy resides mostly on the interlayer surface of perovskite block. As measured from the diffuse-reflectance spectroscopy, the nitridation induced marked reduction in the band gap magnitude, from 4.11 eV (x = 0) to 3.35 eV (x = 0.09) to 2.76 eV (x = 0.29).

OSTI ID:
22217694
Journal Information:
Materials Research Bulletin, Vol. 48, Issue 2; Other Information: Copyright (c) 2012 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.; Country of input: International Atomic Energy Agency (IAEA); ISSN 0025-5408
Country of Publication:
United States
Language:
English