Antiphase inversion domains in lithium cobaltite thin films deposited on single-crystal sapphire substrates
Creators
- 1. Nanostructures Research Laboratory, Japan Fine Ceramics Center, Nagoya 456-8587 (Japan)
- 2. WPI Advanced Institute for Materials Research, Tohoku University, Sendai 980-8577 (Japan)
- 3. Institute of Engineering Innovation, The University of Tokyo, Tokyo 113-8656 (Japan)
- 4. Toyota Motor Corporation, Susono, Shizuoka 410-1193 (Japan)
Description
Antiphase inversion domains in LiCoO2 thin films prepared by pulsed laser deposition on sapphire single-crystal substrates are analyzed using a combination of (scanning) transmission electron microscopy and first-principles calculations. Domains form epitaxially on the substrates with orientation relationships of [112¯0]LiCoO2(0001)LiCoO2//[11¯00]α-Al2O3(0001)α-Al2O3 and [1¯1¯20]LiCoO2(0001)LiCoO2//[11¯00]α-Al2O3(0001)α-Al2O3. In addition, substrate/film interfaces with the above orientation relationships always have the same stacking sequence of Al–O–Co–O–Li–O. This is confirmed to be the most energetically stable stacking arrangement according to first-principles calculations. Individual domains form as a result of steps one (0 0 0 1) O–Al–O spacing in height on the otherwise flat substrate surface. Because the orientation of adjacent (0 0 0 1) AlO6 octahedra in Al2O3 are rotated by 180°, while LiO6 and CoO6 octahedra in LiCoO2 are all aligned in the same direction, substrate steps produce LiCoO2 domains rotated 180° relative to their neighbors. The similar size of oxygen octahedra in the two materials also means that the step height is close to the layer spacing in LiCoO2, so that (0 0 0 1) Li and Co layers of adjacent domains are shifted by one layer relative to each other at each domain boundary, aligning Li layers with Co layers across the boundary. The combination of these two effects generates antiphase inversion domains. The domain boundaries effectively sever Li-ion diffusion pathways in the (0 0 0 1) planes between domains and thus are expected to have a detrimental effect on Li-ion conductivity
Availability note (English)
Available from http://dx.doi.org/10.1016/j.actamat.2013.09.004Additional details
Identifiers
- DOI
- 10.1016/j.actamat.2013.09.004;
- PII
- S1359-6454(13)00677-0;
Publishing Information
- Journal Title
- Acta Materialia
- Journal Volume
- 61
- Journal Issue
- 20
- Journal Page Range
- p. 7671-7678
- ISSN
- 1359-6454
- CODEN
- ACMAFD
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 45038123
- Subject category
- S36: MATERIALS SCIENCE;
- Descriptors DEI
- ALUMINIUM OXIDES; COBALT OXIDES; DEPOSITS; ENERGY BEAM DEPOSITION; INTERFACES; LASER RADIATION; LAYERS; LITHIUM; LITHIUM IONS; LITHIUM OXIDES; MONOCRYSTALS; PULSED IRRADIATION; SAPPHIRE; SUBSTRATES; SURFACES; THIN FILMS; TRANSMISSION ELECTRON MICROSCOPY
- Descriptors DEC
- ALKALI METAL COMPOUNDS; ALKALI METALS; ALUMINIUM COMPOUNDS; CHALCOGENIDES; CHARGED PARTICLES; COBALT COMPOUNDS; CORUNDUM; CRYSTALS; DEPOSITION; ELECTROMAGNETIC RADIATION; ELECTRON MICROSCOPY; ELEMENTS; FILMS; IONS; IRRADIATION; LITHIUM COMPOUNDS; METALS; MICROSCOPY; MINERALS; OXIDE MINERALS; OXIDES; OXYGEN COMPOUNDS; RADIATIONS; SURFACE COATING; TRANSITION ELEMENT COMPOUNDS
Optional Information
- Copyright
- Copyright (c) 2013 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.