Imperial College London

ProfessorArashMostofi

Faculty of EngineeringDepartment of Materials

Professor of Theory and Simulation of Materials
 
 
 
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Contact

 

+44 (0)20 7594 8154a.mostofi Website

 
 
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Location

 

Bessemer B332Royal School of MinesSouth Kensington Campus

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Summary

 

Publications

Citation

BibTex format

@article{Mostofi:2018:10.3389/fchem.2018.00455,
author = {Mostofi, AA and Ablitt, C and Senn, M and Bristowe, N},
doi = {10.3389/fchem.2018.00455},
journal = {Frontiers in Chemistry},
title = {Control of uniaxial negative thermal expansion in layered Perovskites by tuning layer thickness},
url = {http://dx.doi.org/10.3389/fchem.2018.00455},
volume = {6},
year = {2018}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - Uniaxial negative thermal expansion (NTE) is known to occur in low n members of the An+1BnO3n+1 Ruddlesden–Popper (RP) layered perovskite series with a frozen rotation of BO6 octahedra about the layering axis. Previous work has shown that this NTE arises due to the combined effects of a close proximity to a transition to a competing phase, so called “symmetry trapping”, and highly anisotropic elastic compliance specific to the symmetry of the NTE phase. We extend this analysis to the broader RP family (n = 1, 2, 3, 4, …, ∞), demonstrating that by changing the fraction of layer interface in the structure (i.e., the value of 1/n) one may control the anisotropic compliance that is necessary for the pronounced uniaxial NTE observed in these systems. More detailed analysis of how the components of the compliance matrix develop with 1/n allows us to identify different regimes, linking enhancements in compliance between these regimes to the crystallographic degrees of freedom in the structure. We further discuss how the perovskite layer thickness affects the frequencies of soft zone boundary modes with large negative Grüneisen parameters, associated with the aforementioned phase transition, that constitute the thermodynamic driving force for NTE. This new insight complements our previous work—showing that chemical control may be used to switch from positive to negative thermal expansion in these systems—since it makes the layer thickness, n, an additional design parameter that may be used to engineer layered perovskites with tuneable thermal expansion. In these respects, we predict that, with appropriate chemical substitution, the n = 1 phase will be the system in which the most pronounced NTE could be achieved.
AU - Mostofi,AA
AU - Ablitt,C
AU - Senn,M
AU - Bristowe,N
DO - 10.3389/fchem.2018.00455
PY - 2018///
SN - 2296-2646
TI - Control of uniaxial negative thermal expansion in layered Perovskites by tuning layer thickness
T2 - Frontiers in Chemistry
UR - http://dx.doi.org/10.3389/fchem.2018.00455
UR - http://hdl.handle.net/10044/1/64756
VL - 6
ER -