AI Article Synopsis

  • Oxygen vacancies in complex oxides like LaSrCuO (LSCO) can be manipulated to enhance properties like superconductivity and oxygen diffusivity.
  • Researchers utilized first-principles calculations to investigate how Sr doping and external strain affect oxygen vacancy movement on an atomic level.
  • In doped scenarios, small strains or attractions can significantly lower energy barriers for oxygen mobility, while in fully compensated cases, most vacancies become trapped and unable to move due to high formation energy.

Article Abstract

In many complex oxides, the oxygen vacancy formation is a promising route to modify the material properties such as a superconductivity and an oxygen diffusivity. Cation substitutions and external strain have been utilized to control the concentration and diffusion of oxygen vacancies, but the mechanisms behind the controls are not fully understood. Using first-principles calculations, we find how Sr doping and external strain greatly enhances the diffusivity of oxygen vacancies in LaSrCuO (LSCO) in the atomic level. In hole-doped case (2x > δ), the formation energy of an apical vacancy in the LaO layer is larger than its equatorial counterpart by 0.2 eV that the bottleneck of diffusion process is for oxygen vacancies to escape equatorial sites. Such an energy difference can be reduced and even reversed by either small strain (< 1.5%) or short-range attraction between Sr and oxygen vacancy, and in turn, the oxygen diffusivity is greatly enhanced. For fully compensated hole case (2x ≦ δ), the formation energy of an apical vacancy becomes too high that most oxygen vacancies cannot move but would be trapped at equatorial sites. From our electronic structure analysis, we found that the contrasting change in the formation energy by Sr doping and external strain is originated from the different localization natures of electron carrier from both types of oxygen vacancies.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9352678PMC
http://dx.doi.org/10.1038/s41598-022-17376-9DOI Listing

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