Published February 2013 | Version v1
Journal article

Preparation and neutron diffraction study of Dion-Jacobson type oxynitrides LiLaTa2O7−3xN2x (x = 0.09, 0.29)

  • 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)

Description

Highlights: ► Dion-Jacobson oxynitrides LiLaTa2O7−3xN2x□x (x < 0.3) by ammonolysis of LiLaTa2O7. ► Enhanced thermal stability and band gap narrowing by the oxynitride modification. ► Locations of N and □ within LiLaTa2O7−3xN2x by neutron diffraction and 7Li MAS NMR. -- Abstract: Ammonolytic heating of Dion-Jacobson type layered perovskite LiLaTa2O7 produced oxynitride derivatives LiLaTa2O7−3xN2x□xvia the substitution, 3O2− → 2N3− + □. 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 LiLaTa2O7 and LiLaTa2O7−3xN2x (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 7Li 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).

Availability note (English)

Available from http://dx.doi.org/10.1016/j.materresbull.2012.11.069

Additional details

Identifiers

DOI
10.1016/j.materresbull.2012.11.069;
PII
S0025-5408(12)00911-7;

Publishing Information

Journal Title
Materials Research Bulletin
Journal Volume
48
Journal Issue
2
Journal Page Range
p. 813-818
ISSN
0025-5408
CODEN
MRBUAC

Optional Information

Copyright
Copyright (c) 2012 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.