Abstract

We demonstrate how chemical pressure affects the structural and electronic phase transitions of the quadruple perovskite CaMn7O12 by Sr doping, a compound that exhibits a charge-ordering transition above room temperature making it a candidate for oxide electronics. We have synthesized Ca1−xSrxMn7O12 (0 ≤ x ≤ 0.6) thin films by oxide molecular beam epitaxy on (LaAlO3)0.3(SrAl0.5Ta0.5O3)0.7 (LSAT) substrates. The substitution of Sr for Ca results in a linear expansion of the lattice, as revealed by X-ray diffraction. Temperature-dependent resistivity and X-ray diffraction measurements are used to demonstrate that the coupled charge-ordering and structural phase transitions can be tuned with Sr doping. An increase in Sr concentration acts to decrease the phase transition temperature (T*) from 426 K at x = 0 to 385 K at x = 0.6. The presence of a tunable electronic phase transition, above room temperature, points to the potential applicability of Ca1−xSrxMn7O12 in sensors or oxide electronics, for example, via charge doping.

Highlights

  • There is growing interest in quadruple perovskites, (AA 3)B4O12,1–3 due to the wide range of physical properties found in this material class

  • An orbital-ordering transition is observed at ∼250 K (T OO) through scattering and Raman spectroscopy measurements.[17,18]

  • Similar transitions are observed in bulk SrMn7O12, with little change in the magnetic transition temperatures but a decrease of ∼60 K reported in T *

Read more

Summary

Introduction

There is growing interest in quadruple perovskites, (AA 3)B4O12,1–3 due to the wide range of physical properties found in this material class. (Received 3 July 2017; accepted 23 August 2017; published online 18 September 2017)

Results
Conclusion

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.