TY - JOUR
T1 - Compact Thermochemical Heat Storage Based on Hydrothermal Dehydration of Cobalt Hydroxide
AU - Dwivedi, A.
AU - Veerabagu, M.
AU - Rajagopalan, N.
AU - Sinha, S.
N1 - The authors acknowledge support from the Institute for Sustainability, Energy and Environment (iSEE) at the University of Illinois Urbana-Champaign for part of this work. TGA, DSA, XRD, XPS analyses and, TEM and SEM imaging were carried out in part in the Materials Research Laboratory Central Research Facilities, University of Illinois.
PY - 2025
Y1 - 2025
N2 - Heat storage for waste heat sources at 200–250 C, where most power is available, remains challenging due to the lack of suitable storage materials. Here, we explore thermochemical heat storage at these temperatures based on cobalt oxide/hydroxide chemistry under hydrothermal conditions that is uniquely closed to mass flows. The closed system removes the need to separate and store individual products and is therefore, expected to be simpler and more compact than existing chemistries that require separation and storage of the product gas. The hydrothermal dehydration of cobalt hydroxide is attractive among other metal hydroxides due to its relatively modest pressure requirement and a temperature that is well-matched to low-temperature waste heat recovery. We find the theoretical round-trip energetic and exergetic efficiencies to be ~60% and ~50% respectively. In cycling experiments of hydrothermal dehydration and hydration, characterized using TGA, XRD, and XPS, we find the dehydration kinetics to be reasonably fast but the hydration to be limited to 40% on repeated conversion. TGA and TEM analysis of the product further suggest that this limit arises from the diffusion resistance of water through the cobalt hydroxide layer on the surface of the reacting oxide. Doping with Mg can yield a higher conversion limit. This work yields fundamental insights into a chemistry for novel thermochemical heat storage useful for low-to-mid temperature waste heat recovery.
AB - Heat storage for waste heat sources at 200–250 C, where most power is available, remains challenging due to the lack of suitable storage materials. Here, we explore thermochemical heat storage at these temperatures based on cobalt oxide/hydroxide chemistry under hydrothermal conditions that is uniquely closed to mass flows. The closed system removes the need to separate and store individual products and is therefore, expected to be simpler and more compact than existing chemistries that require separation and storage of the product gas. The hydrothermal dehydration of cobalt hydroxide is attractive among other metal hydroxides due to its relatively modest pressure requirement and a temperature that is well-matched to low-temperature waste heat recovery. We find the theoretical round-trip energetic and exergetic efficiencies to be ~60% and ~50% respectively. In cycling experiments of hydrothermal dehydration and hydration, characterized using TGA, XRD, and XPS, we find the dehydration kinetics to be reasonably fast but the hydration to be limited to 40% on repeated conversion. TGA and TEM analysis of the product further suggest that this limit arises from the diffusion resistance of water through the cobalt hydroxide layer on the surface of the reacting oxide. Doping with Mg can yield a higher conversion limit. This work yields fundamental insights into a chemistry for novel thermochemical heat storage useful for low-to-mid temperature waste heat recovery.
KW - hydrothermal dehydration
KW - low temperature heat storage
KW - oxide hydration
KW - Thermochemical
KW - waste heat
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U2 - 10.1080/15567265.2025.2458857
DO - 10.1080/15567265.2025.2458857
M3 - Article
AN - SCOPUS:105001477140
SN - 1556-7265
VL - 29
SP - 36
EP - 46
JO - Nanoscale and Microscale Thermophysical Engineering
JF - Nanoscale and Microscale Thermophysical Engineering
IS - 1
ER -