This content will become publicly available on September 19, 2026
                            
                            Redox‐Active Oxide/molten Salt Composites for Hybrid Thermal‐Chemical Energy Storage
                        
                    
    
            Structurally stabilized composites are promising for using phase change materials in high‐temperature thermal energy storage (TES). However, conventional skeleton materials, which typically comprise 30–50 wt% of the composite, mainly provide sensible heat storage and contribute minimally to overall energy density. This study introduces a new class of redox‐active oxide‐molten salt (ROMS) composites that overcome this limitation by combining sensible, latent, and thermochemical heat storage in a single particle. Specifically, porous, redox‐active Ca2AlMnO5+δ(CAM) complex oxide particles were demonstrated as a suitable support matrix, with the pores filled by eutectic NaCl/CaCl2salt. X‐ray diffraction confirms excellent phase compatibility between CAM and the salt. Scanning electron microscopy/energy dispersive X‐ray spectroscopy and nano X‐ray tomography show good salt infiltration and wettability within the CAM pores. Thermogravimetric analysis reveals that a 60 wt% CAM/40 wt% salt composite achieves an energy density of 267 kJ kg−1over a narrow 150 °C window, with ≈50 kJ kg−1from thermochemical storage. Additionally, the composite shows higher thermal conductivity than salt alone, enabling faster energy storage and release. ROMS composites thus represent a novel and efficient solution for high‐performance TES. 
        more » 
        « less   
        
    
                            - Award ID(s):
- 1943813
- PAR ID:
- 10637665
- Publisher / Repository:
- Wiley
- Date Published:
- Journal Name:
- Advanced Energy and Sustainability Research
- ISSN:
- 2699-9412
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
- 
            Abstract The structural and compositional flexibility of perovskite oxides and their complex yet tunable redox properties offer unique optimization opportunities for thermochemical energy storage (TCES). To improve the relatively inefficient and empirical‐based approaches, a high‐throughput combinatorial approach for accelerated development and optimization of perovskite oxides for TCES is reported here. Specifically, thermodynamic‐based screening criteria are applied to the high‐throughput density functional theory (DFT) simulation results of over 2000 A/B‐site doped SrFeO3−δ. 61 promising TCES candidates are selected based on the DFT prediction. Of these, 45 materials with pure perovskite phases are thoroughly evaluated. The experimental results support the effectiveness of the high‐throughput approach in determining both the oxygen capacity and the oxidation enthalpy of the perovskite oxides. Many of the screened materials exhibit promising performance under practical operating conditions: Sr0.875Ba0.125FeO3−δexhibits a chemical energy storage density of 85 kJ kgABO3−1under an isobaric condition (with air) between 400 and 800 °C whereas Sr0.125Ca0.875Fe0.25Mn0.75O3−δdemonstrates an energy density of 157 kJ kgABO3−1between 400 °C/0.2 atm O2and 1100 °C/0.01 atm O2. An improved set of optimization criteria is also developed, based on a combination of DFT and experimental results, to improve the effectiveness for accelerated development of redox‐active perovskite oxides.more » « less
- 
            Abstract Long duration energy storage (LDES) is an economically attractive approach to accelerating clean renewable energy deployment. The newly emerged solid oxide iron–air battery (SOIAB) is intrinsically suited for LDES applications due to its excellent low‐rate performance (high‐capacity with high efficiency) and use of low‐cost and sustainable materials. However, rechargeability and durability of SOIAB are critically limited by the slow kinetics in iron/iron‐oxide redox couples. Here the use of combined proton‐conducting BaZr0.4Ce0.4Y0.1Yb0.1O3(BZC4YYb) and reduction‐promoting catalyst Ir to address the kinetic issues, is reported. It is shown that, benefiting from the facilitated H+diffusion and boosted FeOx‐reduction kinetics, the battery operated under 550 °C, 50% Fe‐utilization and 0.2 C, exhibits a discharge specific energy density of 601.9 Wh kg–1‐Fe with a round‐trip efficiency (RTE) of 82.9% for 250 h of a cycle duration of 2.5 h. Under 500 °C, 50% Fe‐utilization and 0.2 C, the same battery exhibits 520 Wh kg–1‐Fe discharge energy density with an RTE of 61.8% for 500 h. This level of energy storage performance promises that SOIAB is a strong candidate for LDES applications.more » « less
- 
            Abstract All‐solid‐state flexible asymmetric supercapacitors (ASCs) are developed by utilization of graphene nanoribbon (GNR)/Co0.85Se composites as the positive electrode, GNR/Bi2Se3composites as the negative electrode, and polymer‐grafted‐graphene oxide membranes as solid‐state electrolytes. Both GNR/Co0.85Se and GNR/Bi2Se3composite electrodes are developed by a facile one‐step hydrothermal growth method from graphene oxide nanoribbons as the nucleation framework. The GNR/Co0.85Se composite electrode exhibits a specific capacity of 76.4 mAh g−1at a current density of 1 A g−1and the GNR/Bi2Se3composite electrode exhibits a specific capacity of 100.2 mAh g−1at a current density of 0.5 A g−1. Moreover, the stretchable membrane solid‐state electrolytes exhibit superior ionic conductivity of 108.7 mS cm−1. As a result, the flexible ASCs demonstrate an operating voltage of 1.6 V, an energy density of 30.9 Wh kg−1at the power density of 559 W kg−1, and excellent cycling stability with 89% capacitance retention after 5000 cycles. All these results demonstrate that this study provides a simple, scalable, and efficient approach to fabricate high performance flexible all‐solid‐state ASCs for energy storage.more » « less
- 
            Thermochemical energy storage is promising for building applications as it offers high energy density and near-lossless storage. For example, inorganic salt hydrates that undergo reversible solid-gas thermochemical reactions can be used for thermal load shifting and/or shedding in buildings. However, this technology is still in early stages of development and drawbacks need to be addressed to make such a thermal battery viable. As salt hydrates differ in their morphology, crystal and/or particle size, and hygrothermal stability, it is critical to characterize thermochemical reactions accurately under specific operating conditions. Not only is the amount of heat delivered important, but so is the rate at which this heat is extracted for thermal end-use in buildings. However, the latter is not well reported in the literature, which is largely focused on energy storage rather than power density during the hydration reaction (battery discharge). To address this gap and the lack of standardized measurement methods, this work lays out a systematic simultaneous thermal analysis (STA) method for characterizing five different salt hydrate thermochemical materials (TCM). The effects of particle size, temperature and vapor pressure are analyzed to obtain the energy storage density and thermal power density across a full hydration-dehydration cycle under controlled conditions.more » « less
 An official website of the United States government
An official website of the United States government 
				
			 
					 
					
