Electrochemical oxygen intercalation into Sr2IrO4. (January 2018)

• Record Type: Journal Article
• Authors: Fruchter, L.; Brouet, V.; Colson, D.; Moussy, J.-B.; Forget, A.; Li, Z.Z.
• Is Part Of: Journal of physics and chemistry of solids. Volume 112(2018)
• Page Start: 1
• Page End: 7
• Publication Date: 2018-01
• Subjects: Solids -- Periodicals; Solides -- Périodiques; Solids; Periodicals; 530.41
• DOI: 10.1016/j.jpcs.2017.08.032
• Languages: English
• ISSNs: 0022-3697

Abstract

Abstract: Oxygen was electrochemically intercalated into Sr2 IrO4 sintered samples, single crystals and a thin film. We estimate the diffusion length to a few μ m and the concentration of the intercalated oxygen to δ ≃ 0.01. The latter is thus much smaller than for the cuprate and nickelate parent compounds, for which δ > 0.1 is obtained, which could be a consequence of larger steric effects. The influence of the oxygen doping state on resistivity is small, indicating also a poor charge transfer to the conduction band. It is shown that electrochemical intercalation of oxygen may also contribute to doping, when gating thin films with ionic liquid in the presence of water. Highlights: Bulk intercalation of oxygen is observed from single crystal (001) surface. Diffusion length is evaluated a few microns; oxygen excess less than 1% per Ir. A non-linear diffusion mechanism is proposed. The charge transfer from the intercalated oxygen to the conduction band is weak. Thin films gating with water-contaminated ionic liquid involves oxygen electrochemical doping.