Destabilized Calcium Hydride as a Promising High-Temperature Thermal Battery

Calcium hydride (CaH2) is considered an ideal candidate for thermochemical energy storage (thermal battery) due to its high energy density and low cost. Its very high operating temperature and poor cycling stability are the main factors that hinder its development and implementation as a thermal bat...

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Main Authors: Balakrishnan, Sruthy, Sofianos, M. Veronica, Paskevicius, Mark, Rowles, Matthew, Buckley, Craig
Format: Journal Article
Language:English
Published: AMER CHEMICAL SOC 2020
Subjects:
Online Access:http://purl.org/au-research/grants/arc/FT160100303
http://hdl.handle.net/20.500.11937/90586
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author Balakrishnan, Sruthy
Sofianos, M. Veronica
Paskevicius, Mark
Rowles, Matthew
Buckley, Craig
author_facet Balakrishnan, Sruthy
Sofianos, M. Veronica
Paskevicius, Mark
Rowles, Matthew
Buckley, Craig
author_sort Balakrishnan, Sruthy
building Curtin Institutional Repository
collection Online Access
description Calcium hydride (CaH2) is considered an ideal candidate for thermochemical energy storage (thermal battery) due to its high energy density and low cost. Its very high operating temperature and poor cycling stability are the main factors that hinder its development and implementation as a thermal battery for concentrated solar power (CSP) plants. In this work, CaH2 was thermodynamically destabilized with aluminum oxide (Al2O3) at a 1:1 molar ratio to release hydrogen at a lower temperature than the hydride alone. Temperature-programmed desorption measurements showed that the addition of Al2O3 destabilized the reaction thermodynamics of hydrogen release from CaH2 by reducing the decomposition temperature to ∼600 °C in comparison to ∼1000 °C for pure CaH2 at 1 bar of H2 pressure. The experimental enthalpy and entropy of this system were determined by pressure composition isotherm measurements between 612 and 636 °C. The enthalpy was measured to be ΔHdes = 100 ± 2 kJ mol-1 of H2, and the entropy was measured to be ΔSdes = 110 ± 2 J·K-1 mol-1 of H2. The XRD after TPD and in situ XRD data confirmed the main product as Ca12Al14O33. The system exhibited a loss of capacity during hydrogen cycling at 636 °C, which was found to be due to sintering of excess Al2O3, as confirmed by X-ray diffraction and scanning electron microscopy. The hydrogen cycling capacity was significantly improved by reducing the initial amount of Al2O3 to a 2:1 molar ratio of CaH2 to Al2O3, deeming it as a highly promising high-temperature thermal battery for the next generation of CSP plants.
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spelling curtin-20.500.11937-905862023-03-23T05:20:20Z Destabilized Calcium Hydride as a Promising High-Temperature Thermal Battery Balakrishnan, Sruthy Sofianos, M. Veronica Paskevicius, Mark Rowles, Matthew Buckley, Craig Science & Technology Physical Sciences Technology Chemistry, Physical Nanoscience & Nanotechnology Materials Science, Multidisciplinary Chemistry Science & Technology - Other Topics Materials Science CONCENTRATING SOLAR POWER X-RAY-DIFFRACTION ENERGY-STORAGE TECHNOLOGIES Calcium hydride (CaH2) is considered an ideal candidate for thermochemical energy storage (thermal battery) due to its high energy density and low cost. Its very high operating temperature and poor cycling stability are the main factors that hinder its development and implementation as a thermal battery for concentrated solar power (CSP) plants. In this work, CaH2 was thermodynamically destabilized with aluminum oxide (Al2O3) at a 1:1 molar ratio to release hydrogen at a lower temperature than the hydride alone. Temperature-programmed desorption measurements showed that the addition of Al2O3 destabilized the reaction thermodynamics of hydrogen release from CaH2 by reducing the decomposition temperature to ∼600 °C in comparison to ∼1000 °C for pure CaH2 at 1 bar of H2 pressure. The experimental enthalpy and entropy of this system were determined by pressure composition isotherm measurements between 612 and 636 °C. The enthalpy was measured to be ΔHdes = 100 ± 2 kJ mol-1 of H2, and the entropy was measured to be ΔSdes = 110 ± 2 J·K-1 mol-1 of H2. The XRD after TPD and in situ XRD data confirmed the main product as Ca12Al14O33. The system exhibited a loss of capacity during hydrogen cycling at 636 °C, which was found to be due to sintering of excess Al2O3, as confirmed by X-ray diffraction and scanning electron microscopy. The hydrogen cycling capacity was significantly improved by reducing the initial amount of Al2O3 to a 2:1 molar ratio of CaH2 to Al2O3, deeming it as a highly promising high-temperature thermal battery for the next generation of CSP plants. 2020 Journal Article http://hdl.handle.net/20.500.11937/90586 10.1021/acs.jpcc.0c04754 English http://purl.org/au-research/grants/arc/FT160100303 http://purl.org/au-research/grants/arc/LP150100730 AMER CHEMICAL SOC fulltext
spellingShingle Science & Technology
Physical Sciences
Technology
Chemistry, Physical
Nanoscience & Nanotechnology
Materials Science, Multidisciplinary
Chemistry
Science & Technology - Other Topics
Materials Science
CONCENTRATING SOLAR POWER
X-RAY-DIFFRACTION
ENERGY-STORAGE
TECHNOLOGIES
Balakrishnan, Sruthy
Sofianos, M. Veronica
Paskevicius, Mark
Rowles, Matthew
Buckley, Craig
Destabilized Calcium Hydride as a Promising High-Temperature Thermal Battery
title Destabilized Calcium Hydride as a Promising High-Temperature Thermal Battery
title_full Destabilized Calcium Hydride as a Promising High-Temperature Thermal Battery
title_fullStr Destabilized Calcium Hydride as a Promising High-Temperature Thermal Battery
title_full_unstemmed Destabilized Calcium Hydride as a Promising High-Temperature Thermal Battery
title_short Destabilized Calcium Hydride as a Promising High-Temperature Thermal Battery
title_sort destabilized calcium hydride as a promising high-temperature thermal battery
topic Science & Technology
Physical Sciences
Technology
Chemistry, Physical
Nanoscience & Nanotechnology
Materials Science, Multidisciplinary
Chemistry
Science & Technology - Other Topics
Materials Science
CONCENTRATING SOLAR POWER
X-RAY-DIFFRACTION
ENERGY-STORAGE
TECHNOLOGIES
url http://purl.org/au-research/grants/arc/FT160100303
http://purl.org/au-research/grants/arc/FT160100303
http://hdl.handle.net/20.500.11937/90586