A spatially resolved optical method to measure thermal diffusivity.


Journal

The Review of scientific instruments
ISSN: 1089-7623
Titre abrégé: Rev Sci Instrum
Pays: United States
ID NLM: 0405571

Informations de publication

Date de publication:
01 Apr 2023
Historique:
received: 12 05 2022
accepted: 21 03 2023
medline: 12 12 2023
pubmed: 12 12 2023
entrez: 11 12 2023
Statut: ppublish

Résumé

We describe an optical method to directly measure the position-dependent thermal diffusivity of reflective single crystal samples across a broad range of temperatures for condensed matter physics research. Two laser beams are used, one as a source to locally modulate the sample temperature, and the other as a probe of sample reflectivity, which is a function of the modulated temperature. Thermal diffusivity is obtained from the phase delay between source and probe signals. We combine this technique with a microscope setup in an optical cryostat, in which the sample is placed on a three-axis piezo-stage, allowing for spatially resolved measurements. Furthermore, we demonstrate experimentally and mathematically that isotropic in-plane diffusivity can be obtained when overlapping the two laser beams instead of separating them in the traditional way, which further enhances the spatial resolution to a micron scale, especially valuable when studying inhomogeneous or multidomain samples. We discuss in detail the experimental conditions under which this technique is valuable and demonstrate its performance on two stoichiometric bilayer ruthenates: Sr3Ru2O7 and Ca3Ru2O7. The spatial resolution allowed us to study the diffusivity in single domains of the latter, and we uncovered a temperature-dependent in-plane diffusivity anisotropy. Finally, we used the enhanced spatial resolution enabled by overlapping the two beams to measure the temperature-dependent diffusivity of Ti-doped Ca3Ru2O7, which exhibits a metal-insulator transition. We observed large variations of transition temperature over the same sample, originating from doping inhomogeneity and pointing to the power of spatially resolved techniques in accessing inherent properties.

Identifiants

pubmed: 38081228
pii: 2877865
doi: 10.1063/5.0098800
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2023 Author(s). All article content, except where otherwise noted, is licensed under a Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).

Auteurs

F Sun (F)

Max Planck Institute for Chemical Physics of Solids, 01187 Dresden, Germany.

S Mishra (S)

Max Planck Institute for Chemical Physics of Solids, 01187 Dresden, Germany.

P H McGuinness (PH)

Max Planck Institute for Chemical Physics of Solids, 01187 Dresden, Germany.

Z H Filipiak (ZH)

Max Planck Institute for Chemical Physics of Solids, 01187 Dresden, Germany.

I Marković (I)

Max Planck Institute for Chemical Physics of Solids, 01187 Dresden, Germany.

D A Sokolov (DA)

Max Planck Institute for Chemical Physics of Solids, 01187 Dresden, Germany.

N Kikugawa (N)

National Institute for Materials Science, Ibaraki 305-0003, Japan.

J W Orenstein (JW)

Department of Physics, University of California, Berkeley, California 94720, USA.
Materials Science Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720, USA.

S A Hartnoll (SA)

Department of Applied Mathematics and Theoretical Physics, University of Cambridge, Cambridge CB3 0WA, United Kingdom.

A P Mackenzie (AP)

Max Planck Institute for Chemical Physics of Solids, 01187 Dresden, Germany.
School of Physics and Astronomy, University of St Andrews, St Andrews KY16 9SS, United Kingdom.

V Sunko (V)

Max Planck Institute for Chemical Physics of Solids, 01187 Dresden, Germany.
Department of Physics, University of California, Berkeley, California 94720, USA.

Classifications MeSH