Thermochemical energy storage performance of zinc destabilized calcium hydride at high-temperatures

Abstract

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CaH2 has 20 times the energy density of molten salts and was patented in 2010 as a potential solar thermal energy storage material. Unfortunately, its high operating temperature (>1000 °C) and corrosivity at that temperature make it challenging to use as a thermal energy storage (TES) material in concentrating solar power (CSP) plants. To overcome these practical limitations, here we propose the thermodynamic destabilization of CaH2 with Zn metal. It is a unique approach that reduces the decomposition temperature of pure CaH2 (1100 °C at 1 bar of H2 pressure) to 597 °C at 1 bar of H2 pressure. Its new decomposition temperature is closer to the required target temperature range for TES materials used in proposed third-generation high-temperature CSP plants. A three-step dehydrogenation reaction between CaH2 and Zn (1 : 3 molar ratio) was identified from mass spectrometry, temperature-programmed desorption and in situ X-ray diffraction studies. Three reaction products, CaZn13, CaZn11 and CaZn5, were confirmed from in situ X-ray diffraction studies at 190 °C, 390 °C and 590 °C, respectively. The experimental enthalpy and entropy of the second hydrogen release reaction were determined by pressure composition isotherm measurements, conducted between 565 and 614 °C, as ΔHdes = 131 ± 4 kJ mol-1 H2 and ΔSdes = 151 ± 4 J K-1 mol-1 H2. Hydrogen cycling studies of CaZn11 at 580 °C showed sufficient cycling capacity with no significant sintering occurring during heating, as confirmed by scanning electron microscopy, demonstrating its great potential as a TES material for CSP applications. Finally, a cost comparison study of known destabilized CaH2 systems was carried out to assess the commercial potential.