1. Robust electronic phase transition against cation disorder in high-entropy pyrochlore iridates.
- Author
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Contant, D., McNally, G. M., Krajewska, A., Takagi, H., and Takayama, T.
- Subjects
PHASE transitions ,MAGNETIC insulators ,TRANSITION temperature ,MAGNETIC transitions ,INFORMATION display systems ,TRANSITION metals - Abstract
High-entropy pyrochlore iridates A
2 Ir2 O7 with multiple trivalent A cations were synthesized. The parent ternary A2 Ir2 O7 displays a variety of electronic phases depending on the size of A cations; Pr2 Ir2 O7 with a large A cation shows semimetallic behavior down to low temperatures, whereas A2 Ir2 O7 with smaller A cations, such as Nd2 Ir2 O7 and Eu2 Ir2 O7 , displays a (semi)metal to magnetic insulator transition as a function of temperature. By further reducing the A cation size, smaller than Y3+ , A2 Ir2 O7 becomes a Mott insulator, and long-range magnetic order takes place below room temperature. The metal–insulator transition and magnetic ordering turned out to be robust against strong disorder induced by the mixing of more than five A-cations in the high-entropy A2 Ir2 O7 . The transition temperatures were found to scale with the average ionic radius of multiple A-cations. In contrast, high-entropy A2 Ir2 O7 including Bi3+ exhibits metallic behavior down to 2 K, which is likely associated with the presence of oxygen vacancies as in the parent Bi2 Ir2 O7 . Although these indicate that the overall electronic structure of A2 Ir2 O7 remains intact in the presence of high-entropy configuration at the A-site, the transport properties suggest that fine details of the band structure may be modulated by local distortion. Strong disorder at the A-site of complex oxides may be exploited as a tool to control electronic properties. [ABSTRACT FROM AUTHOR]- Published
- 2024
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