Bi-directional tuning of thermal transport in SrCoOx with electrochemically induced phase transitions
Abstract
Unlike the wide-ranging dynamic control of electrical conductivity, there does not exist an analogous ability to tune thermal conductivity by means of electric potential. The traditional picture assumes that atoms inserted into a material’s lattice act purely as a source of scattering for thermal carriers, which can only reduce thermal conductivity. In contrast, here we show that the electrochemical control of oxygen and proton concentration in an oxide provides a new ability to bi-directionally control thermal conductivity. On electrochemically oxygenating the brownmillerite SrCoO2.5 to the perovskite SrCoO3–δ, the thermal conductivity increases by a factor of 2.5, whereas protonating it to form hydrogenated SrCoO2.5 effectively reduces the thermal conductivity by a factor of four. This bi-directional tuning of thermal conductivity across a nearly 10 ± 4-fold range at room temperature is achieved by using ionic liquid gating to trigger the ‘tri-state’ phase transitions in a single device. We elucidated the effects of these anionic and cationic species, and the resultant changes in lattice constants and lattice symmetry on thermal conductivity by combining chemical and structural information from X-ray absorption spectroscopy with thermoreflectance thermal conductivity measurements and ab initio calculations. This ability to control multiple ion types, multiple phase transitions and electronicmore »
- Authors:
-
- Massachusetts Inst. of Technology (MIT), Cambridge, MA (United States). Dept. of Materials Science and Engineering, and Lab. for Electrochemical Interfaces
- Massachusetts Inst. of Technology (MIT), Cambridge, MA (United States). Dept. of Materials Science and Engineering
- Massachusetts Inst. of Technology (MIT), Cambridge, MA (United States). Dept. of Nuclear Science and Engineering, and Lab. for Electrochemical Interfaces
- Massachusetts Inst. of Technology (MIT), Cambridge, MA (United States). Dept. of Nuclear Science and Engineering
- Brookhaven National Lab. (BNL), Upton, NY (United States). National Synchrotron Light Source II (NSLS-II)
- Massachusetts Inst. of Technology (MIT), Cambridge, MA (United States). Dept. of Materials Science and Engineering, Dept. of Nuclear Science and Engineering, and Lab. for Electrochemical Interfaces
- Publication Date:
- Research Org.:
- Brookhaven National Lab. (BNL), Upton, NY (United States)
- Sponsoring Org.:
- USDOE Office of Science (SC), Basic Energy Sciences (BES)
- OSTI Identifier:
- 1615584
- Report Number(s):
- BNL-213857-2020-JAAM
Journal ID: ISSN 1476-1122
- Grant/Contract Number:
- SC0012704
- Resource Type:
- Accepted Manuscript
- Journal Name:
- Nature Materials
- Additional Journal Information:
- Journal Volume: 19; Journal Issue: 6; Journal ID: ISSN 1476-1122
- Publisher:
- Springer Nature - Nature Publishing Group
- Country of Publication:
- United States
- Language:
- English
- Subject:
- 36 MATERIALS SCIENCE
Citation Formats
Lu, Qiyang, Huberman, Samuel, Zhang, Hantao, Song, Qichen, Wang, Jiayue, Vardar, Gulin, Hunt, Adrian, Waluyo, Iradwikanari, Chen, Gang, and Yildiz, Bilge. Bi-directional tuning of thermal transport in SrCoOx with electrochemically induced phase transitions. United States: N. p., 2020.
Web. doi:10.1038/s41563-020-0612-0.
Lu, Qiyang, Huberman, Samuel, Zhang, Hantao, Song, Qichen, Wang, Jiayue, Vardar, Gulin, Hunt, Adrian, Waluyo, Iradwikanari, Chen, Gang, & Yildiz, Bilge. Bi-directional tuning of thermal transport in SrCoOx with electrochemically induced phase transitions. United States. https://doi.org/10.1038/s41563-020-0612-0
Lu, Qiyang, Huberman, Samuel, Zhang, Hantao, Song, Qichen, Wang, Jiayue, Vardar, Gulin, Hunt, Adrian, Waluyo, Iradwikanari, Chen, Gang, and Yildiz, Bilge. Mon .
"Bi-directional tuning of thermal transport in SrCoOx with electrochemically induced phase transitions". United States. https://doi.org/10.1038/s41563-020-0612-0. https://www.osti.gov/servlets/purl/1615584.
@article{osti_1615584,
title = {Bi-directional tuning of thermal transport in SrCoOx with electrochemically induced phase transitions},
author = {Lu, Qiyang and Huberman, Samuel and Zhang, Hantao and Song, Qichen and Wang, Jiayue and Vardar, Gulin and Hunt, Adrian and Waluyo, Iradwikanari and Chen, Gang and Yildiz, Bilge},
abstractNote = {Unlike the wide-ranging dynamic control of electrical conductivity, there does not exist an analogous ability to tune thermal conductivity by means of electric potential. The traditional picture assumes that atoms inserted into a material’s lattice act purely as a source of scattering for thermal carriers, which can only reduce thermal conductivity. In contrast, here we show that the electrochemical control of oxygen and proton concentration in an oxide provides a new ability to bi-directionally control thermal conductivity. On electrochemically oxygenating the brownmillerite SrCoO2.5 to the perovskite SrCoO3–δ, the thermal conductivity increases by a factor of 2.5, whereas protonating it to form hydrogenated SrCoO2.5 effectively reduces the thermal conductivity by a factor of four. This bi-directional tuning of thermal conductivity across a nearly 10 ± 4-fold range at room temperature is achieved by using ionic liquid gating to trigger the ‘tri-state’ phase transitions in a single device. We elucidated the effects of these anionic and cationic species, and the resultant changes in lattice constants and lattice symmetry on thermal conductivity by combining chemical and structural information from X-ray absorption spectroscopy with thermoreflectance thermal conductivity measurements and ab initio calculations. This ability to control multiple ion types, multiple phase transitions and electronic conductivity that spans metallic through to insulating behaviour in oxides by electrical means provides a new framework for tuning thermal transport over a wide range.},
doi = {10.1038/s41563-020-0612-0},
journal = {Nature Materials},
number = 6,
volume = 19,
place = {United States},
year = {Mon Feb 24 00:00:00 EST 2020},
month = {Mon Feb 24 00:00:00 EST 2020}
}
Web of Science
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