A thermochemical mechanism for thermal energy storage, in which heat is used to drive the endothermic chemical reaction (charging mode) and is released in the reverse reaction (discharging mode), is claimed to offer high energy densities [
15], especially if one of the products in the regeneration stage is in the vapour phase [
16]. Alternatively, heat can be stored in the form of sensible or latent heat via a change of the storage medium temperature or phase, respectively [
12,
15]. The former is the simplest and cheapest of all thermal energy storage mechanisms, yet the low thermal capacity of the available storage materials would require a large size of the storage equipment. The latter, on the other hand, offers higher storage density and isothermal nature of the storage process. The greatest challenges of phase change materials are degradation of their cycling performance and high cost [
12,
15]. As the thermochemical mechanism allows long-term energy storage, as long as the reactants are stored separately, and the stored energy is almost completely recovered, it is regarded as a viable and effective route for long-term thermal energy storage and transport [
15]. A calcium looping (CaL) process, which involves either hydration or carbonation of CaO, was first proposed for energy storage in the mid-1970s [
16,
17] and has been considered among the best candidates for energy storage [
14,
15], especially when linked with concentrating solar power plants [
18]. The carbonation reaction offers nearly 50% higher theoretical thermal energy density (1222 kWh·m
–3) compared to the hydration reaction (833 kWh·m
–3). However, some technical challenges need to be resolved prior to the large-scale deployment of CaL for energy storage, including the lack of electricity storage capability [
19], loss of sorbent performance over time in continuous operation [
16], and the requirement for temporary CO
2 storage [
15].