Tolerance Factor Control of Uniaxial Negative Thermal Expansion in a Layered Perovskite

Chris Ablitt(Thomas Young Centre), Harriet McCay(University of Oxford), Sarah Craddock(University of Oxford), Lauren Cooper(University of Warwick), Emily Reynolds(University of Oxford), Arash A. Mostofi(Thomas Young Centre), Nicholas C. Bristowe(University of Kent), Claire A. Murray(Diamond Light Source), Mark S. Senn(University of Warwick)
Chemistry of Materials
December 16, 2019
Cited by 26Open Access
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Abstract

By tuning the tolerance factor, t, of the Ruddlesden–Popper oxide Ca2MnO4 through isovalent substitutions, we show that the uniaxial coefficient of linear thermal expansion (CLTE) of these systems can be systematically changed through large negative to positive values. High-resolution X-ray diffraction measurements show that the magnitude of uniaxial negative thermal expansion (NTE) increases as t decreases across the stability window of the NTE phase. Transitions to phases with positive thermal expansion (PTE) are found to occur at both the high-t and low-t limits of stability. First-principles calculations demonstrate that reducing t enhances the contribution to thermal expansion from the lowest frequency phonons, which have the characteristics of octahedral tilts and have negative mode Grüneisen parameter components along the NTE axis. By tuning t to the lower edge of the NTE phase stability window, we are hence able to maximize the amplitudes of these vibrations and thereby maximize NTE with a CLTE of −8.1 ppm/K at 125 K. We also illustrate, at the other end of the phase diagram, that an enhancement in compliance of these materials associated with the rotational instability provides another mechanism by which NTE could be yet further enhanced in this and related systems.


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