Efficient Energy Storage Research Articles

Solid Foam Insertion to Increase PCM-Based Thermal Energy Storage System Efficiency: Experimental Test and Numerical Simulation of Spherical Macrocapsules

Phase change materials (PCMs) are an interesting solution to increase the efficiency of thermal energy storage (TES) systems. The present work explores, with an experimental and computational study, the behavior of a paraffin wax encapsulated in a spherical containment system during the melting and solidification phases. The experimental tests were conducted by immersing the spherical capsule in a thermostatic water bath at different temperatures and measuring the temperatures at four different points inside the capsule. A two-dimensional CFD model of the sphere was then applied to investigate the effect of the insertion of a solid foam into the sphere to increase the system’s responsiveness under demanding conditions. In addition, an analysis of the solidification process considering two different wall materials (HDPE and aluminum) with different thermal conductivity was performed. The results suggest that embedded foams can represent a useful tool to increase the efficiency of a PCM-based TES, but, at the same time, they also highlight that a considerable increase in thermal conductivity is required to achieve significant advantages with respect to pure PCM systems.

The Role of Photo in Oxygen Evolution Reaction: A Review.

Photo enhanced oxygen evolution reaction has recently emerged as an advanced strategy with great application prospects for highly efficient energy conversion and storage. In the course of photo enhanced oxygen evolution reactions, the other works focus has predominantly centered on catalysts while inadvertently overlooking the pivotal role of photo. Consequently, this manuscript embarks upon a comprehensive review of recent advancements in photo-driven, aiming to illuminate this critical dimension. A detailed introduction to the photothermal effect, photoelectronic effect, photon-induced surface plasmon resonance, photo and heterojunction, photo-induced reversible geometric conversion, photo-induced energy barrier reduction, photo-induced chemical effect, photo-charging, and the synthesis of laser/photo-assisted catalysts, offering prospects for the development of each case is provided. A detailed introduction to the photothermal effect, photoelectronic effect, photon-induced surface plasmon resonance, photo and heterojunction, photo-induced reversible geometric conversion, photo-induced energy barrier reduction, photo-induced chemical effect, photo-charging, and the synthesis of laser/photo-assisted catalysts is provided. At the same time, the overpotential and Tafel slope of some catalysts mentioned above at 10mAcm-2 is collected, and calculated the lifting efficiency of light on them, offering prospects for the development of each case.

Energy storage properties influenced by relaxor ferroelectric properties dependent on the growth direction of epitaxial Bi2SiO5 thin films

Ferroelectric Bi2SiO5 (BSO) thin films were deposited by pulsed laser deposition on Nb-doped (100), (110) and (111) SrTiO3 (Nb:STO) substrates, resulting in (001)-, (113)- and (204)-oriented epitaxial films. Due to the crystallinity of BSO, in which the Bi2O2 layers are formed perpendicular to the c-axis direction, the (001)-oriented epitaxial BSO thin film showed the lowest remanent polarization and the best leakage current characteristics. On the other hand, the (113)- and (204)-oriented films showed an increase in remanent polarization due to the improvement of a-oriented crystallinity. Through experiments using vertical and lateral piezoresponse force microscopy, it has been confirmed that the distribution of in-plane-oriented domains reducing remanent polarization decreases in the order of (001)-, (113)- and (204)-oriented epitaxial BSO thin films. The epitaxial BSO thin films that exhibit ferroelectric hysteresis loops similar to the relaxor ferroelectric thin films tended to have improved energy storage characteristics as a result of improved remanent polarization and saturation polarization. In particular, the (113)-oriented epitaxial BSO thin film showed a high recoverable energy density of about 41.6 J cm−3 and an energy storage efficiency of about 85.6%.

Evolving Thermal Energy Storage Using Hybrid Nanoparticle: An Experimental Investigation on Salt Hydrate Phase Change Materials for Greener Future

Thermal energy storage (TES) assisted with phase change materials (PCM)s seeks greater attention to bridge the gap between energy demand and supply. PCM has its footprint toward efficient storage of solar energy. Inorganic salt hydrate PCMs are propitious over organic PCMs in terms of energy storage ability, thermal conductivity, and fireproof, however the major issue of supercooling and poor optical absorbance remains. This research investigates commercialized inorganic salt hydrate PCM with phase transition temperature of 50 °C, thermal conductivity of 0.593 W m−1 K which is favoured with melting enthalpy of 190 J g−1, and 2–3 °C of supercooling. Mixture of graphene: silver at a proportion of (1:1) is used as the hybrid nanomaterial to further enhance the thermal conductivity, optical absorbance, and thermal stability. Hybrid nanocomposites are developed via two‐step process involving direct mixing and ultrasonication. Morphological behaviour, chemical stability, optical property, thermal property, thermal reliability, and stability of the developed nanocomposite samples are experimentally analysed. As a result, sustainable TES materials with thermal conductivity of 0.937 W m−1 K, optical absorbance of 0.8, increased energy storage potential is formulated. Subsequently a numerical simulation is conducted to illustrate the potential of the developed nanocomposite in transfer of heat energy.

Effect of Aggregation Structure on Capacitive Energy Storage in Conducting Polymer Films.

Conducting polymers (CPs), a significant class of electrochemical capacitor electrode materials, exhibit exceptional capacitive energy storage performance in aqueous electrolytes. Current research primarily concentrates on enhancing the electrical conductivity and capacitive performance of CPs via molecular design and structural control. However, the absence of a comprehensive understanding of the impact of molecular chain spatial order on ion/electron transport and capacitive performance impedes the development and optimization of advanced electrode materials. Here, a solvent treatment strategy is employed to modulate the molecular chain spatial order of PEDOT:PSS films. The results of electrochemical performance tests and Grazing Incidence Wide Angle X-ray Scattering (GIWAXS) show that PEDOT:PSS films with both face-on and edge-on orientations exhibit exceptional electronic conductivity and ion diffusion efficiency, with capacitive performance 1.33 times higher than that of PEDOT:PSS films with only edge-on orientation. Consequently, molecular chain orientations conducive to charge transport not only enhance inter-chain coupling, but also effectively reduce ion transport resistance, enabling efficient capacitive energy storage. This research provides novel insights for the design and development of higher performance CPs-based electrode materials.

Simultaneously enhanced of energy storage and energy harvesting performances of [(Bi0.5Na0.5)TiO3–BaTiO3] ceramics by addition of SrTiO3

As is well known, relaxor dielectrics are characterized by high energy storage efficiency (η), while high recoverable energy storage density (Wrec) can be achieved by anti-ferroelectric ceramics. Herein, our approach is to find relaxor- anti-ferroelectric coexistence phases of (Bi0.5Na0.5)TiO3- BaTiO3 ceramics for achieving high performance in energy storage and energy harvesting as well. Therefore, [(0.9-x) ( Bi0.5Na0.5)TiO3-xSrTiO3-0.1BaTiO3] (abbreviation (0.9-x) NBT-0.1BT-xST) (0.0 ≤ x ≤ 0.4) were synthesized via the solid-state reaction route in air. The tolerance factor (τ) increased from 0.9901 to 0.9998 when ST-content increased from 0.0 to 0.4, indicating an increase in crystal lattice symmetry. The FT-IR de-convolution vibration modes shown in the TiO6 octahedra exhibit two peaks at ∼550 and 650 cm−1, which indicate present coexistence phases of the crystal structure. Ferroelectric to relaxor phase crossover has been detected by the addition of ST with the present anti-ferroelectric phase in particular dopant ST = 0.2. The increasing into the diffused phase transition (γ) is signified by enhancement of the relaxor degree of NBT-BT at high content of ST. The rapidly suppressed remnant polarization (Pr) at high content of ST is due to substitute iso-valence (Sr2+) by tri-valence (Bi3+) and mono-valence (Na1+). Ultrahigh Wrec = 1.13 J/ cm3 with excellent η = 92.62% were obtained at ST = 0.3 at low electric field (E = 110 kV cm−1). A remarkable response of the strain with a high converse piezoelectric coefficient ( d33* = 390.47 pm V−1) at ST = 0.2 was obtained due to decreasing the non-revisable 180° domain switching. Based on the obtained results, the addition of ST to NBT-BT ceramics can provide a head start in the implementation of ceramic capacitors for potential effective into energy harvesting and energy storage applications.

Improved Energy Storage Performance of Composite Films Based on Linear/Ferroelectric Polarization Characteristics

The development and integration of high-performance electronic devices are critical in advancing energy storage with dielectric capacitors. Poly(vinylidene fluoride-trifluoroethylene-chlorofluoroethylene) (PVTC), as an energy storage polymer, exhibits high-intensity polarization in low electric strength fields. However, a hysteresis effect can result in significant residual polarization, leading to a severe energy loss, which impacts the resultant energy storage density and charge/discharge efficiency. In order to modify the polarization properties of the polymer, a biaxially oriented polypropylene (BOPP) film with linear characteristics has been selected as an insulating layer and combined with the PVTC ferroelectric polarization layer to construct PVTC/BOPP bilayer films. The hetero-structure and polarization characteristics of the bilayer film have been systematically studied. Adjusting the BOPP volume content to 67% resulted in a discharge energy density of 10.1 J/cm3 and an energy storage efficiency of 80.9%. The results of this study have established the mechanism for a composite structure regulation of macroscopic energy storage performance. These findings can provide a basis for the effective application of ferroelectric polymer-based composites in dielectric energy storage.

Emerging Two–Dimensional Intercalation Pseudocapacitive Electrodes for Supercapacitors

AbstractThe growing need for efficient energy storage has spurred advancements in supercapacitors (SCs), aiming to offer high power and energy density simultaneously. While SCs offer longer cycles and higher power density values, their low energy densities limit practical applications. In response, pseudocapacitive materials have emerged, leveraging reversible Faradaic reactions at or near the surface for enhanced energy storage. This approach surpasses the constraints of the electrical double layer in SCs and the mass transfer constraints of batteries. Progress in asymmetric supercapacitors and high mass loading has improved energy density values, yet maintaining high mass loading without compromising power density remains a hurdle. Advancements in pseudocapacitance through intercalation during charging/discharging processes, especially in layered structures like graphite, graphene, transition metal oxides (TMOs) transition metal dichalcogenides (TMDCs), MXenes, and metal–organic frameworks (MOFs) have proven significant. The intercalated species induce reversible or irreversible structural changes, contributing to the physicochemical characteristics of the electrode materials. Exploring the intercalation mechanism in bulk two‐dimensional (2D) materials reveals distinct differences that enhance our understanding and improve electrochemical properties for superior energy storage. Finally, an in‐depth exploration of the intercalation pseudocapacitance in 2D materials such as TMDCs and MXenes underscores their significance, setting a benchmark for future electrochemical studies in the subsequent advancement of SCs research.

Synthesis and characterization of magnesium ferrite-activated carbon composites derived from orange peels for enhanced supercapacitor performance

Supercapacitors have emerged as highly efficient energy storage devices, relying on electrochemical processes. The performance of these devices can be influenced by several factors, with key considerations including the selection of electrode materials and the type of electrolyte utilized. Transition metal oxide electrodes are commonly used in supercapacitors, as they greatly influence the electrochemical performance of these devices. Nonetheless, ferrites' low energy density poses a limitation. Hence, it is crucial to create electrode materials featuring unique and distinct structures, while also exploring the ideal electrolyte types, to enhance the electrochemical performance of supercapacitors incorporating magnesium ferrites (MF). In this study, we effectively prepared magnesium ferrites (MgFe2O4) supported on activated carbon (AC) derived from orange peels (OP) using a simple hydrothermal method. The resulting blends underwent comprehensive characterization employing various methods, including FTIR, XRD, TEM, SEM, EDX, and mapping analysis. Moreover, the electrochemical performance of MgFe2O4@AC composites was evaluated using GCD and CV techniques. Remarkably, the MF45-AC electrode material showed exceptional electrochemical behavior, demonstrating a specific capacitance of 870 F·g−1 within current density of 1.0 A g−1 and potential windows spanning from 0 to 0.5 V. Additionally, the prepared electrodes displayed exceptional cycling stability, with AC, MF, and MF45-AC retaining 89.6%, 94.2%, and 95.1% of their initial specific capacitance, respectively, even after 5000 cycles. These findings underscore the potential of MF-AC composites as superior electrode materials for supercapacitors. The development of such composites, combined with tailored electrolyte concentrations, holds significant promise for advancing the electrochemical performance and energy density of supercapacitor devices.

Efficient and flexible thermal-integrated pumped thermal energy storage through composition adjustment

Thermal-integrated pumped thermal electricity storage (TI-PTES) could realize efficient energy storage for fluctuating and intermittent renewable energy. However, the boundary conditions of TI-PTES may frequently change with the variation of times and seasons, which causes a tremendous deterioration to the operating performance. To realize efficient and flexible energy storage in operating conditions, a novel composition-adjustable TI-PTES is proposed, and the operating performance is investigated and compared with composition-fixed TI-PTES. Simulation results show that, compared to composition-fixed TI-PTES, the energy storage efficiency of TI-PTES could be enhanced by the absolute value of 4.4–18.3% by introducing composition adjustment method under various boundary conditions. Besides, tuning sub-system composition could simultaneously adjust the capacities of power input, heat storage and power output, realizing a more flexible operating range for TI-PTES. A case study for an isolated energy community shows that composition-adjustable TI-PTES could realize 100% conversion of off-peak electric energy and reduce daily investment by 35.6% compared with composition-fixed TI-PTES.

A Highly Robust and Conducting Ultramicroporous 3D Fe(II)-Based Metal-Organic Framework for Efficient Energy Storage.

Exploitation of metal-organic framework (MOF) materials as active electrodes for energy storage or conversion is reasonably challenging owing to their poor robustness against various acidic/basic conditions and conventionally low electric conductivity. Keeping this in perspective, herein, a 3D ultramicroporous triazolate Fe-MOF (abbreviated as Fe-MET) is judiciously employed using cheap and commercially available starting materials. Fe-MET possesses ultra-stability against various chemical environments (pH-1 to pH-14 with varied organic solvents) and is highly electrically conductive (σ=0.19Sm-1) in one fell swoop. By taking advantage of the properties mentioned above, Fe-MET electrodes give prominence to electrochemical capacitor (EC) performance by delivering an astounding gravimetric (304Fg-1) and areal (181mFcm-2) capacitance at 0.5Ag-1 current density with exceptionally high cycling stability. Implementation of Fe-MET as an exclusive (by not using any conductive additives) EC electrode in solid-state energy storage devices outperforms most of the reported MOF-based EC materials and even surpasses certain porous carbon and graphene materials, showcasing superior capabilities and great promise compared to various other alternatives as energy storage materials.

Properties of Carbon Fibers as Supercapacitor Electrodes via Electrospinning Using a Blending Solution of Polyacrylonitrile and Bisphenol A

Supercapacitors have attracted attention as efficient energy storage systems owing to their high power density and cycling stability. The use of appropriate electrode materials is important for high-performance supercapacitors, and various carbon materials have been studied as supercapacitor electrodes. In this study, carbon nanofibers with high specific surface areas were fabricated via a simple electrospinning process. Carbon nanofibers were fabricated by adjusting the ratio of polyacrylonitrile (PAN) to bisphenol A (BPA) and evaluated as electrode materials for supercapacitors. With the addition of BPA, improved specific surface area and oxygen functional groups were observed compared with nanofibers using only PAN. Therefore, BPA3, which had the highest specific surface area, exhibited a 28% improvement in capacitance (162 F/g) compared with BPA0 fabricated using only PAN. Carbon nanofibers fabricated by adjusting the ratio of BPA to PAN are promising electrodes for supercapacitors owing to their high capacitance and stability.

Moderation of [Bi3+/Na1+] molar ratio for enhancement of dielectric and energy storage properties of NaNbO3 ceramics

Lead-free (Na1−3xBix)(Nb0.75Ti0.25)O3 (x = 0.0, 0.05, 0.1, 0.125 and 0.15) (NN-BT) ceramics were synthesized using solid-state reaction technique. The effect of Bi3+ into the crystal structure, dielectric, ferroelectric and energy storage properties of NNT ceramics were investigated. Pure NNT shows present perovskite structure with orthorhombic crystal structure at x ≤ 0.125, while Na3NbO8-NaNbO3 composite phase has been detected at x = 0.15. The tolerance factor (τ) decreased from 0.97 (x = 0.0) to 0.82 (0.15) which signified the composition deviated from perovskite structure at 0.15. Significant enhancement of dielectric constant at room temperature has been achieved by increasing Bi-content and the maximum value (∼1500) obtained at 0.1. The largest value of maximum polarization (Pmax) and smallest value of remnant polarization (Pr) were achieved at x = 0.1 due to orthorhombic NaNbO3 and rhombohedral (Na0.5Bi0.5)TiO3 coexistence phases. The substitution of monovalent (Na1+) by trivalent (Bi3+) lead to create sodium vacancies into the A-sites of NNT lattice subsequently increased the cations disorder and charge misfit. The maximum recoverable energy storage density (Wrec = 17.5 J cm−3) and energy storage efficiency (η = 80%) were achieved at x = 0.1, E ∼ 700 kV cm−1. Partially, (NNTB0.1) exhibit an outstanding stability of energy storage properties in terms of temperature range (25 to 150 °C) and frequency stability (2–20Hz). The present results imply the moderation ratio of Bi/Na plays an important role for enhancement of energy storage properties of NaNbO3 anti-ferroelectric ceramics.

High-performance Ti-doped strontium cobaltite perovskites as oxygen electrodes in solid oxide cells

Oxygen electrodes play a vital role in realizing high-performance solid oxide cells (SOCs) with high roundtrip efficiency, large-scale capacity, and long-term stability energy storage. This paper constructs Ti-doped strontium cobaltite perovskites (SrCo1-xTixO3-δ, SCTx, x = 0.2, 0.3, 0.4, 0.5) as newly stable oxygen electrodes for SOCs. The changes of oxygen vacancy in SCTx with Ti-doped concentration are investigated by X-ray photoelectron spectroscopy (XPS). The results show that the content of oxygen vacancy decreases with the enrichment of Ti doping. The area-specific resistance (ASR) of the symmetrical cell with SrCo0.8Ti0.2O3-δ (SCT2) electrode is only 0.013 Ω cm2 at 850 °C in air. The single cell with SCT2 oxygen electrode achieves the peak power density of 1.313 W cm−2 at 850 °C under humidified H2 conditions in fuel cells mode, and the current density reaches 2.95 A cm−2 under an electrolytic voltage of 1.9 V at 850 °C for CO2 electrolysis. The Density functional theory (DFT) calculations confirm that the oxygen vacancy formation energy is the lowest when the ratio of Ti to Co is 2:8, verifying the superior property of SCT2. This study comes up with a creation for developing high-stability and high-activity oxygen electrode materials that can be used for energy storage systems.

Investigating the energy storage mechanism of modified PEDOT:PSS for enhanced electrochemical performance

In this study, first principles calculations are performed to investigate the relevant energy storage mechanisms of PEDOT:PSS membranes and WO3/MnO2. The calculation results indicate that the modified PEDOT:PSS reduces the interaction force between cation and inorganic material lattice, weakens the adsorption energy, and accelerates the electrochemical reaction kinetics. Simultaneously, the prepared composite material exhibits a higher state density and more energy orbitals. The cations of the electrolyte can be stored in the s and p orbitals of the material, leading to significant hybridization of electron clouds in these orbitals and improving the conductivity of the material. Based on the above calculation results, a WO3/MnO2 self-healing electrochromic energy storage device is prepared. The device has a high specific capacitance (10.81 mF cm−2) and excellent cycle retention performance (97% retention rate after 1000 cycles), which ensures its efficient energy storage and reliable durability. Furthermore, the device has the self-healing capability to restore most of its functions even in the event of damage, ensuring its long-term utilization.

Cobalt Ion-Stabilized VO2 for Aqueous Ammonium Ion Hybrid Supercapacitors.

Aqueous ammonium ion hybrid supercapacitor (A-HSC) is an efficient energy storage device based on nonmetallic ion carriers (NH4+), which combines advantages such as low cost, safety, and sustainability. However, unstable electrode structures are prone to structural collapse in aqueous electrolytes, leading to fast capacitance decay, especially in host materials represented by vanadium-based oxidation. Here, the Co2+ preintercalation strategy is used to stabilize the VO2 tunnel structure and improve the electrochemical stability of the fast NH4+ storage process. In addition, the understanding of the NH4+ storage mechanism has been deepened through ex situ structural characterization and electrochemical analysis. The results indicate that Co2+ preintercalation effectively enhances the conductivity and structural stability of VO2, and inhibits the dissolution of V in aqueous electrolytes. In addition, the charge storage mechanisms of NH4+ intercalation/deintercalation and the reversible formation/fracture of hydrogen bonds were revealed.

Superior energy-storage density and ultrahigh efficiency in KNN-based ferroelectric ceramics via high-entropy design

The rapidly advancing energy storage performance of dielectric ceramics capacitors have garnered significant interest for applications in fast charge/discharge and high-power electronic techniques. Simultaneously improving the recoverable energy storage density Wrec and efficiency η becomes more prominent at the present time for their practical applications. Herein, a high-entropy concept is implemented on the (K0.5Na0.5)NbO3 (KNN)-based ferroelectric ceramics to design the high-performance dielectric capacitors. First, the strong lattice distortion can absorb some electric energy during the electrical loading process and result in the delayed polarization saturation. Additionally, the large composition fluctuations induce the weak correlation between polar nanoregions and enhance the η. Finally, the high-entropy design and viscous polymer processing method reduce the grain size and improve the Eb. In consequence, excellent Wrec of 11.14 J/cm3 with high η of 87.1% are achieved under an electric field of 750 kV/cm in the high-entropy component. These results demonstrate that the high-entropy concept is a potential avenue to design the KNN-based high-performance dielectric energy storage capacitors.

Study on the photothermal conversion enhancement performance and application of the metal-polyphenol phase-change microcapsules modified by molybdenum disulfide

Aiming to improving photothermal conversion and heat storage efficiency, layered molybdenum disulfide (MoS2) was prepared with hydrothermal method, which was used as the thermally conductive and photothermal conversion material to modify metal-polyphenol (MPN) /paraffin (PA) microcapsules. The fabricated phase-change microcapsules (MoS2/MPN@PA-MEPCM) exhibits excellent thermal conductivity, photothermal conversion and heat storage performance. The effect of the additive amount of MoS2 on the leakage performance, microstructure, thermal conductivity, heat storage capacity, thermal stability and photothermal conversion performance of MoS2/MPN@PA-MEPCM was investigated. Furthermore, the enhancement mechanisms of the thermal conductivity and photothermal conversion were analyzed. The results show that when the additive amount of MoS2 is 10 wt%, the phase-change enthalpy of MoS2/MPN@PA-MEPCM reaches 127.1 J/g with an encapsulation ratio of 53.74 %. Compared to MPN@PA-MEPCM, the thermal conductivity of MoS2/MPN@PA-MEPCM increases by 88.45 % and the photothermal conversion and heat storage efficiency reaches 90.78 %. When the solar radiation intensity is 800 W/m2 and 1000 W/m2, the thermal efficiency of PFPSC is 57.17 % and 59.45 % respectively, which is higher than that of FPSC. The operation time of PFPSC is extended by 2435 s and 2750 s, respectively, improving the operational stability of flat plate solar water heaters. The developed microcapsules in this study demonstrate significant potential for highly efficient solar energy utilization and thermal energy storage in the fields of seawater desalination, solar water heating system and building heating.

Performance of a rotating latent heat thermal energy storage unit with heat transfer from different surfaces

Due to the rapid growth in the demand for fast and efficient latent heat thermal energy storage system, multiple heat transfer enhancement techniques have been proposed and widely investigated. Actively or passively, rotation of the energy storage unit affects the internal natural convection and the heat transfer performance. Hence, this study is conducted to evaluate the potential of the heat transfer enhancement by rotation. A two-dimensional model with the phase change material filled in the annular space of a double tube energy storage unit is developed. The numerical simulations for the heat transfer through the internal or external surfaces of the annular space are respectively conducted. Both solidification and melting of the phase change material are taken into account by the enthalpy-porosity method. According to different heat transfer surfaces and the occurrence of solidification or melting, four arrangements are formed. It is found that the rotation of the thermal energy storage unit can reduce the solidification time as high as 46 % compared to its still counterpart, but variation of the rotation speed only produces a minor influence. The effect of rotation on the melting depends on the heat transfer direction (or surface). When the heat is transferred into the solid phase change material through the internal wall, the melting time can be gradually reduced as the rotation speed increases with a maximum of 69 %. However, when the heat is transferred through the external wall, influence of the rotation results in adverse effect. This study can guide the design of innovative high performance latent heat thermal energy storage system containing rotation unit.

Design of reactive particle fluidized bed heat exchangers for gas–solid thermochemical energy storage

Concentrated solar power (CSP) systems integrated with a supercritical carbon dioxide (sCO2) Brayton power cycle are regarded as the primary future direction for CSP technologies. Calcium-based particles can be a suitable storage medium to achieve high temperatures exceeding 750 ℃. However, there have been few studies on reactive particle/sCO2 heat exchangers (HXs) to drive high-performance power cycles with high energy storage efficiencies. In this paper, the mechanisms by which chemically reactive particles release energy in a fluidized bed (FB) heat exchanger has been investigated to evaluate the performance of thermochemical storage systems. A 1-MWt thermal duty fluidized bed heat exchanger with sCO2 as the working fluid operating at 988 K was designed in different configurations, featuring single stage and multistage counter-flow HXs. A detailed shell and tube model combining the chemical reaction kinetics and the heat transfer between the fluidized particle and sCO2 FB HX design was developed. A comparison of sensible and chemical heat materials shows that thermochemical energy storage is advantageous due to the relatively short tube length and slow particle mass flow rate. The tube length and particle mass flow rate are reduced by 3.5 and 11.5 times, respectively. The average chemical conversion is 97.30 % for a one-stage heat exchanger, which is lower than the 99.95 % conversion achieved by the two-stage heat exchanger. Additionally, a sensitivity analysis was carried out to understand the impacts of key operating parameters on the process performance. These findings provide insights into the operational stability and efficiency of the system, contributing to the development of advanced heat exchangers for thermochemical energy storage applications.