Energy Storage Performance Research Articles

Titanium dioxide/graphene oxide synergetic reinforced composite phase change materials with excellent thermal energy storage and photo-thermal performances

The development of advanced composite solid-solid phase change materials (SSPCMs) is urgent to explore for improving solar energy harvesting and storage. Herein, novel composite SSPCMs with synergetic cross-linking structure were fabricated through polymerization using GO and TiO2 constructed on the polyurethane framework skeleton. GO and TiO2 synergetic enhanced polymer framework played a role as skeletal structure to encapsulate PEG in the molecular chains, and provided as highly thermal conductive pathways for the composite SSPCMs. TiO2 nanoparticles performed as extended surface on the skeletal structure for further improvement in thermal conductivity. The composite SSPCMs exhibited a remarkably improved thermal conductivity as high as 0.7 W/(m‧K) and fast thermal response rate. The good light adsorption property of TiO2 enhanced the light absorbance efficiency of the composite SSPCMs by 94.4%. And the photo-thermal conversion efficiency of the composite SSPCMs highly reached 93.5%. Meanwhile, the composite SSPCMs exhibited excellent anti-leakage performance and shape stability under high temperature. Consequently, the as-prepared composite SSPCMs possessed a potential for applications in thermal energy storage and solar energy utilization systems.

The phase composition, dielectric, and energy storage performance of A-site vacancy modulated BaTiO3 ceramics with Bi(In1/2(Li0.5Ta0.5)1/2)O3 modification

The (1-x)Ba0.94Ce0.04TiO3-xBi(In1/2(Li0.5Ta0.5)1/2)O3 (BCT-BILT) relaxor ferroelectric ceramic system was explored based on the A-site vacancy design and defect dipole engineering. The impacts of different doping concentrations on the phase composition, dielectric and energy storage performance of the BCT-BILT ceramics were studied and discussed in detail. The pure BCT and 0.95BCT-0.05BILT samples exhibited a mixed crystal structure of tetragonal (T) and pseudo-cubic (PC) phase, while the BCT-BILT samples with x > 0.05 possessed a cubic (C) phase, accompanied by the secondary phases of BaBi2Ta2O9 and BaTa2O6. With an increase in the BILT doping concentration, the surface morphologies of the ceramics were continuously modulated, and the dielectric loss had been reduced to 0.001 at 1 kHz, which was beneficial to improve the energy storage properties. Compared to the pure BCT, the breakdown field strength was significantly enhanced owing to the formation of Aurivillius phase BaBi2Ta2O9 and the increased dielectric relaxation. Ultimately, the highest energy storage density of Wrec = 0.7 J/cm3 and high energy conversion efficiency of η = 95 % was realized at the composition of x = 0.05 under a small electric field of 130 kV/cm. Furthermore, the good temperature stability with the ΔWrec/Wrec30°C < 9 % and Δη/η30°C < 6.5 % was acquired for the samples with x = 0.20–0.30 in the temperature range of 30–120 °C, owing to the synergistic roles of the defect dipoles, impurities BaBi2Ta2O9, and polar nanoregions (PNRs). The 0.95BCT-0.05BILT ceramic obtains discharge energy density Wdis of 0.35 J/cm3 and fast discharge speed t0.9 of 312 ns at 60 kV/cm, current density CD of 255.4 A/cm2 and power density PD of 10.2 MW/cm3 at 80 kV/cm. This work is of guiding significance for designing and optimizing energy storage performance of lead-free relaxors from the perspective of defect building and engineering.

B-site engineering in rare earth ferrites: Composition and polymorphic control of electrical and photocatalytic functionalities

Rare-earth perovskites possess structural features conducive to co-existence of interesting functionalities. This study establishes structural tunability of B-site tailored GdFeO3 and its implications. Isovalent introduction of In3+ at B-site by hybrid synthesis approach yielded GdInxFe1-xO3 (0.0 ≤ x ≤ 1.0) system. The synthesis-route adopted could enable stabilization of metastable C-type and hexagonal (H) polymorphs that eventually led to thermodynamically stable phases in H (hexagonal), O (orthorhombic) and biphasic (H + O) phases. Gradual evolution of phases with respect to temperature as well as composition were studied with XRD, HT-XRD and Raman spectroscopy. Density functional theory was employed to explain prevalence of wide biphasic-field and it was attributed to non-favourable energetics of Fe3+ at trigonal-bipyramidal site in H-polymorph. The system exhibits structure and composition-dependent electrical behaviour and tunable band gap. Detailed study highlighted a very low leakage current(I) and low dielectric loss in In3+-rich polymorphs(H). Typically, GdInO3 shows I of 4 × 10−9A/cm2, high dielectric constant (ε) of 106 with a stable loss of 0.009. The energy storage performance showed decrease in recoverable E-density (Wrec) and increase in energy storage efficiency with In3+-content. Optimum properties were observed for equimolar composition, GdIn0.5Fe0.5O3 (Wrec= 560 mJ/cm3; ɳ= 82 %). An intriguing observation is effect of structure on visible light-catalysed degradation of methylene blue with O-polymorphs showing excellent photodegradation (̴ 99 % dye/180 min) while H-polymorphs performing abysmally. This is explained based on band gaps, surface charges and plausible difference in generation of photo-induced charge carriers.

Component design for stabilizing P phase in NaNbO3-based ceramics and the energy storage performance

Antiferroelectric (AFE) ceramic dielectrics are widely recognized for their high potential in high-power pulse equipment applications. Lead-free NaNbO3 (NN) antiferroelectric ceramics have emerged as a prominent research topic in the field of energy storage due to their abundant phase structure, affordability, and moderate bandgap. The metastable ferroelectric Q phase results in a square hysteresis loop for NN at room temperature. However, 0.96NaNbO3-0.04 CaZrO3 (NNCZ) exhibits a typical double hysteresis loop at room temperature with the main crystalline phase being the antiferroelectric P phase, which has poor energy storage performance. In this study, Bi0.5Na0.5TiO3 (BNT) is used to optimize the energy storage performance and stabilize the P phase in NNCZ simultaneously. The dielectric constant and temperature-dependence XRD results that from −100 °C to 350 °C, x = 0.05 undergoes a phase transition from AFE P to AFE R and then to PE S. The solid solution of BNT decreased the sintering temperature of NN-based ceramics and decreased average grain size, thereby facilitating domain size reduction and improving the sample's energy storage efficiency from ∼30 % to ∼60 %, with an effective energy storage density reaching 1.51 J/cm3. The above results demonstrate that enhancing energy storage efficiency can be achieved through component design by reducing average grain size.

Excellent energy-storage performance in BNT-BT lead-free ceramics through optimized electromechanical breakdown

Dielectric capacitors with high recoverable energy storage density (Wrec) are in urgent demand for clean energy technologies. However, their lower breakdown strength (Eb) strongly limits their energy storage performance. We, herein, propose a facile method to enhance Eb by enhancing mechanical strength via second phase modulation. The efficiency of this method is validated in the (1-x)(0.94Na0.5Bi0.5TiO3-0.06BaTiO3)-xSr(Ta0.5Sb0.5)O3 ((BNT-BT)-xSTS, x = 0.1, 0.15, 0.2, 0.25, and 0.3) ceramics. The introduction of Sr(Ta0.5Sb0.5)O3 (STS) increases the relaxor degree, refines grain size, and most importantly, creates a second phase of BiSb2O7, which hinders dislocation movement and improves mechanical strength. Our results show that the breakdown strength strongly depends on the mechanical strength. The highest hardness of 7.42 GPa accompanied by the largest Eb of 620 kV/cm was obtained in (BNT-BT)-0.25STS sample. The sample exhibits the best energy storage properties of a large Wrec = 8.3 J/cm3, a high efficiency of 82.3 %, and excellent temperature/frequency stability. Furthermore, the sample also exhibits good charge/discharge stability and ultra-fast transient discharge time (62.26 ns). This work provides a theoretical guidance for developing lead-free dielectrics with superior energy-storage performance.

Thermodynamic performance of air-cooled seasonal cold energy storage for space cooling: A case study

With the improvement in people's living standards, there is a growing demand for cooling, making it urgent to develop a low-carbon and energy-efficient refrigeration system. Therefore, this paper proposes an air-cooled seasonal energy storage (ACSES) system. The heat transfer model of the system is constructed. The impact of relevant parameters on the system's cold storage performance was analyzed. The results show that larger glycol flow rates, windward velocity, number of tube passes and tube rows, and the volume ratio of ethylene glycol to water (VR) are beneficial for improving cold storage performance. However, excessively large parameters do not significantly enhance cold storage performance. The influence of ambient temperature on cold storage performance is greater than that of ice thickness. When VR is 0.02, the cold storage performance is relatively superior. To demonstrate the energy-saving performance of the system, the energy consumption saving rate (ECSR) indicator was proposed. The ECSR of the ACSES system is 72.75 %. The system can significantly conserve resources and reduce energy consumption.

Growth of Ni-Ga oxalate nanoparticles on 3D current collector as a supercapacitive electrode

Metal oxalate materials have been explored for electrochemical energy storage (EES) applications. Herein, Ni-incorporated gallium oxalate (Ni-Ga-C2O4) based binder-free electrode was fabricated through a facile process. The electrode gathers the benefit of Ni foam contributed as a conductive substrate and also acting as a Ni source with binder-free approach. The Ni-Ga-C2O4 crystalline phase formation was confirmed through X-ray diffraction spectroscopy (XRD). The morphological properties and elemnetal quantification were studied via scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), and transmission electron spectroscopy (TEM). Importantly, electrochemical energy storage investigation revealed the Ni-Ga-C2O4 electrode exhibits battery behavior with capacity retention of 85.5 % and possessed the highest specific capacity of 319 C g−1 at 1 A g−1. Overall, the additional contribution of Ni during the synthesis has boosted the physicochemical properties and electrochemical energy storage performance of the Ni-Ga-C2O4 electrode.

Constructing superparaelectric state for NaNbO3-based ceramics electrostatic supercapacitors

A crucial prerequisite for developing high-performance energy storage devices for high pulsed power systems is the urgent necessity to acquire dielectric ceramics with high recoverable energy density (Wrec) and ultrahigh energy efficiency (η), particularly through an environmentally friendly lead-free approach. Here, superparaelectric state with ultra-small nanodomains in NaNbO3-based ceramics is successfully induced by implementing a superparaelectric modulation strategy. This innovation not only reduces the curvature value of the polarization–electric field (P-E) curve, but also produces negligible remanent polarization (Pr) and a linear-like P-E curve, obtaining outstanding efficiency (η) of 92.2 % and high energy storage density (Wrec) of 7.05 J/cm3. This achievement not only opens new avenues for enhancing the energy storage performance of dielectric ceramics but also heralds extensive applications of this material in high-pulse power electronic devices.

Preparation of MoS2 nanosheets/nitrogen-doped carbon nanotubes/MoS2 nanoparticles and their electrochemical energy storage properties

Inferior electrical conductivity, huge volume swell, shuttle effect and slow redox reactions in Li-S batteries restrict their practical applications. In this study, molybdenum disulfide nanosheets anchored on nitrogen-doped carbon nanotubes encapsulating molybdenum disulfide nanoparticles (MoS2/NC/MoS2 NTs) were prepared by heat treatment, ammonia etching, high-temperature sulfurization, and solvent-thermal in-situ growth using polypyrrole-coated molybdenum trioxide nanorods (MoO3 NRs) as templates. The hollow structure of nitrogen-doped carbon nanotubes and the high specific surface area are conducive to increasing sulfur loading, increasing the contact area of electrolyte, accelerating the electron transport, and shortening the lithium ion transport route. The MoS2 nanosheets on the outer layer of the nitrogen-doped carbon tubes and the MoS2 particles wrapped inside can anchor polysulfides by chemisorption, slowing down the shuttle effect and enhancing the energy storage performance of lithium-sulfur batteries. The MoS2/NC/MoS2/S nanotubes (MoS2/NC/MoS2/S NTs) maintain a capacity of 498.9 mAh g−1 over 500 cycles at 1.0 A g−1, with an average single-cycle capacity decay rate of 0.061 %. The density functional theory calculations, the adsorption experiments, and the X-ray photoelectron spectroscopy results all confirm that the MoS2/NC/MoS2 NTs are able to anchor lithium polysulfides through strong adsorption, thus effectively mitigating the shuttle effect of polysulfides. The synthesis of MoS2/NC/MoS2/S NTs in this study is of important significance for the development of advanced lithium-sulfur batteries.

Engineering Mn Vacancies to Enhance Ion Kinetics in Layered Manganese Silicate for High-Energy and Durable Intercalation Pseudocapacitance.

Transition metal silicates (TMSs) are potential electrodes for aqueous metal-ion intercalation pseudocapacitors owing to their superior theoretical capacity and high structural stability. However, the narrow interlayer spacing and intrinsic inert basal plane of TMSs lead to sluggish ions and charge transfer, causing an undesirable energy storage performance. Herein, rich Mn vacancies are introduced in layered manganous silicates (M2-xS@FA) to expedite K+ diffusion, while enhancing charge storage capacity and prolonging lifespan. In situ characterizations validate the K+ intercalation pseudocapacitance mechanism with evident crystal structure and valence state variations in M2-xS@FA. Both theoretical calculations and electrochemical experimental evaluations elucidate the imperative role of Mn vacancies in enhancing K+ diffusion kinetics and electron transfer through increased interlayer spacing and activated basal plane. Mn vacancies further boost the charge storage capacity by providing additional K+ storage sites, while simultaneously reinforcing local atomic bonding within M2-xS@FA, thereby augmenting structural stability. The assembled aqueous asymmetric solid-state cell, featuring a M2-xS@FA cathode, demonstrates exceptional power and energy densities (144.08 W h kg-1 at 375.80 W kg-1) and ultralong lifespan (100% capacity retention after 10,000 cycles). This work heralds a paradigm whereby modulating cation vacancies in layered TMSs significantly enhances K+ storage and stability for high-energy intercalation pseudocapacitance.

Crystalline/Amorphous Co2P2O7 cathode with outstanding areal capacity for High-Performance Zinc-Cobalt battery

It is still a challenge to develop aqueous rechargeable Zn-based alkaline batteries with high energy density, power density and excellent stability. Herein, a crystalline/amorphous Co2P2O7 self-supporting on the Ni foam is fabricated as a cathode material of aqueous Zn-based alkaline batteries. The unique crystalline/amorphous structure endows the electrode material with more exposed active sites, higher redox species coverage, larger electrochemical surface area (ECSA), smaller charge-transfer resistance, lower reaction energy barriers and faster electrochemical reaction kinetics process, which clarifies an explicit structure–property relationship simultaneously. As a result, the crystalline/amorphous Co2P2O7 (CP-P-450) electrode assembled as CP-P-450//Zn battery achieves an extraordinary areal capacity of 2.49 mAh cm−2 at 5 mA cm−2, satisfactory rate performance, excellent cyclic durability (96.6 % retention after 4000 cycles) and impressive energy density (4.16 mAh cm−2) and peak power density (115.94 mW cm−2). The quasi-solid CP-P-450//Zn battery can drive a variety of electrical appliances working well even under abuse tests, demonstrating excellent safety and application potential. This study provides an effective strategy towards excellent comprehensive energy storage performance of aqueous Zn-based alkaline batteries through structuring the crystalline/amorphous phase in cathodes.

Synergistic effect of Sn doped manganese oxide and conductive reduced graphene oxide for zinc ion battery

Manganese based oxide is a kind of promising water zinc ion batteries (ZIBs) cathode electrode material. It has the advantages of lower cost and higher operating voltage range, but this kind of material has poor conductivity, easy collapse of structure during the reaction process, and the material dissolves, etc., which is widely concerned and studied by researchers. In this paper, Sn-doped manganese oxides coated with reduced graphene oxide (rGO) nanorod-like materials (2%Sn-MnOx/rGO) were prepared by in situ solvothermal autogenous growth method. The abundant Sn active sites are highly dispersed, and the introduction of graphene increased the conductivity of 2%Sn-MnOx, reduced the dissolution of Mn2+. The ZIBs assembled with 2%Sn-MnOx/rGO cathode material has a maximum specific capacity of 352.3 mAh g−1 at 0.1 A g−1, and the rate performance is 211.3 mAh g−1 at 1.0 A g−1. Moreover, at 1.0 A g−1, the capacity is still 108.5 mAh g−1 after 1000 cycles. In addition, 2%Sn-MnOx/rGO successfully assembled a flexible quasi-solid ZIB. The synergistic effect introduced by metal Sn doping and graphene can provide a good improvement effect for the energy storage performance and application of manganese-based oxides in water zinc electricity, which is a feasible optimization strategy.

A comprehensive performance comparison between compressed air energy storage and compressed carbon dioxide energy storage

Currently, working fluids for adiabatic compressed energy storage primarily rely on carbon dioxide and air. However, it remains an unresolved issue to which of these two systems performs better. Therefore, this paper compares the advantages and disadvantages of both systems in terms of thermodynamic and economic performances under the given boundary conditions. To accurately obtain the performance of energy storage systems, quasi-dynamic models are established for key components. On this foundation, corresponding thermodynamic-economic models are developed. The results indicate that at thermal storage temperatures of 120 ℃, 140 ℃, and 160 ℃, 100 MW×5h compressed carbon dioxide energy storage systems have higher round-trip efficiencies than compressed air energy storage systems. However, the compressed carbon dioxide energy storage also faces the difficulties of higher cost and longer payback period. Specifically, at the thermal storage temperature of 140 ℃, round-trip efficiencies of compressed air energy storage and compressed carbon dioxide energy storage are 59.48 % and 65.16 % respectively, with costs of $11.54 × 107 and $13.45 × 107, and payback periods of 11.86 years and 12.57 years respectively. Compared to compressed air energy storage system, compressed carbon dioxide energy storage system has 9.55 % higher round-trip efficiency, 16.55 % higher cost, and 6 % longer payback period. At other thermal storage temperatures, similar phenomenons can be observed for these two systems. After comprehensively considering the obtained thermodynamic and economic performances, the overall performance of compressed air energy storage is superior to that of compressed carbon dioxide energy storage. In addition, in practical engineering, key components of compressed air energy storage are more mature than those of compressed carbon dioxide energy storage, and air has higher safety than carbon dioxide. In the future work, the comparison for performances between different types of compressed carbon dioxide energy storage and compressed air energy storage should be taken into account, and dynamic models of the systems should be developed. Additionally, the industry chain of compressed carbon dioxide energy storage should be accelerated to reduce equipment costs, enabling it to compete with compressed air energy storage.

Design and fabrication of nitrogen-doped graphene-promoted Na3MnTi(PO4)3@C cathode with three-electron reactions for sodium-ion storage

As a novel cathode material for sodium-ion batteries, Na3MnTi(PO4)3 (denoted as NMTP) has received great attention because of its abundant natural resources, excellent safety, low toxicity as well as three-electron reactions. Unfortunately, the pure NMTP cathode displays a bad conductivity, resulting in an inferior electrochemical performance for sodium energy storage. Herein, we introduce a good route to fabricate the nitrogen-doped graphene-decorated NMTP@C (denoted as NG-NMTP@C) composite with superior rate property and superior cycle stability for the first time. In this fabricated material, the nitrogen-doped graphene nanosheets are dispersed into the NMTP@C particles. Compared to NMTP@C, the prepared NG-NMTP@C cathode possesses better cycle stability and higher capacity. It shows the capacity of 173.1 mAh g−1 at 0.1 C and presents the high capacity retention of around 97.1 % at 10.0 C over 400 cycles. Therefore, this fabricated NG-NMTP@C nanocomposite can be employed as the novel positive electrode in sodium-ion storage.

Thermal energy storage, heat transfer, and thermodynamic behaviors of nano phase change material in a concentric double tube unit with triple tree fins

The contribution of this study is the proposal of a synergistic composite enhancement strategy involving tree fins and nanomaterials to improve the low thermal performance of phase change material (lauric acid) in a typical double tube latent heat thermal energy storage unit. The effects of nanoparticle concentrations and tree fin branching angles on the fluid dynamics, melting time, heat transfer, energy storage, and entropy generation characteristics were investigated. By employing tree fins, the melting time was respectively reduced by up to 60.20% and 36.05% compared to the finless case and the rectangular fins, while the energy storage power was respectively boosted by up to 143.36% and 37.45%. The increase of nanoparticle concentration was beneficial for melting heat transfer, and the dendritic fins with a bottom angle of 90° and a top angle of 30° yielded the highest energy storage performance. The total entropy generation of the melting process was mainly governed by the thermal entropy generation, and it showed a decreasing trend with the increase of time. In contrast to the finless configuration, the incorporation of fins diminished the integrated entropy generation value. Similarly, an elevation in nanoparticle concentration also led to a reduction of the integrated entropy generation value.

Enhanced Energy Storage Properties of Highly Polarized BMT-Based Thin Films through the Multiscale Structure Synergistic Regulation Strategy.

For solving the trade-off relationship of the polarization and breakdown electric field, ferroelectric films with high polarization are playing a critical role in energy storage capacitor applications, especially at moderate/low electric fields. In this work, we propose a multiscale structure (including defect, domain, and grain structures) synergetic optimization strategy to optimize the polarization behavior and energy storage performances of BiMg0.5Ti0.5O3 (BMT) ferroelectric films by introducing Sr0.7La0.2TiO3 (SLT) without compromising the breakdown strength. At a moderate electric field of 2917 kV/cm, a high discharge density of 72.2 J/cm3 has been achieved in 0.9BMT-0.1SLT films, together with good frequency, thermal, and cycle stabilities for energy storage. Importantly, the phase difference Δφ is utilized to quantitatively evaluate the polarization switching mobility of the ferroelectric domain/PNRs at an external electric field stimulation. This research demonstrates that a multiscale structure optimization strategy could effectively regulate the energy storage performance, and ecofriendly BMT-based materials are promising candidates for next-generation energy storage capacitors, especially at moderate/low electric fields.

Superior energy storage performance of Sr0.7Bi0.2TiO3-modified Na0.5Bi0.5TiO3-K0.7La0.1NbO3 lead-free ferroelectric ceramics

Na0.5Bi0.5TiO3 (NBT)-based ceramics exhibit significant potential as energy storage dielectric materials due to their high maximum polarization (Pmax). However, their limited energy storage density significantly restricts their practical applications. To address this, this study optimizes the dielectric energy storage characteristics of lead-free relaxor ferroelectric ceramics based on 0.91Na0.5Bi0.5TiO3-0.09 K0.7La0.1NbO3 (NBT-KLN) by incorporating Sr0.7Bi0.2TiO3 (SBT) relaxor additives. The introduction of SBT helps maintain large polarization and induces local disorderly fields, promoting the formation of polar nanoregions. Subsequently, a viscous polymer processing (VPP) technique was employed to reduce defects and enhance density, markedly improving the breakdown strength (BDS). The findings indicate that the BDS of the optimized 0.30SBT (VPP) ceramics increased to 440 kV/cm, while achieving a high energy storage efficiency (η) of 78 % and an elevated energy storage density (Wrec) of 6.29 J/cm3. Additionally, the 0.30SBT (VPP) ceramics demonstrate excellent temperature stability across a broad temperature range from 30 to 120 °C, making them ideal for long-term operation in variable environments. This study demonstrates superior results compared to previous research, thereby opening up new avenues for developing novel lead-free relaxor ferroelectric ceramics with superior energy storage characteristics.

Nickel-Copper Bimetallic Oxide Nanoparticles Prepared by Simple Coprecipitation Method as High Performance Electrode Materials for Asymmetric Supercapacitors.

Supercapacitors with transition bimetallic oxides as pseudocapacitive materials have been of wide concern for their excellent energy storage performance. In this work, a simple coprecipitation method was used to synthesize the precursor, followed by calcination to prepare Ni-Cu bimetallic oxide materials. The structure, morphology and properties of the materials prepared by different precipitating agents and different calcination temperatures of NCO-H2C2O4 precursor were investigated. The optimum precipitant was determined to be H2C2O4, and Ni-Cu nanoparticles with regular lamellar microstructure were obtained at the calcination temperature of 400 °C. The nanostructure and morphology provide a large active channel for the rapid diffusion of electrolyte ions, and the specific capacitance of NCO-H2C2O4-400 electrode material can reach 740.31 F/g Cs at 1 A/g. The investigation of charge storage mechanism shows that the contribution rate of capacitance and diffusion control is about 37.9% and 67.2%, respectively. The electrochemical test results of the asymmetric supercapacitors (ASC) constructed with NCO-H2C2O4-400 and activated carbon show that the specific capacitance, energy density, and power density of the capacitor are 52.66 F/g, 16.45 Wh/kg, and 759.51 W/kg, respectively. Even after 5000 charge/discharge cycles at 5 A/g, it can still keep 90.57% of its initial capacity. This work not only provides competitive electrode materials for energy storage devices but also provides a feasible strategy for producing complex transition metal oxide materials with high capacitance performance.

Optimizing Energy Storage and Hybrid Inverter Performance in Smart Grids Through Machine Learning

Optimizing Energy Storage and Hybrid Inverter Performance in Smart Grids Through Machine Learning

Facile and scalable fabrication of flexible microsupercapacitor based on boron modified 2D/2D 1 T MoS2/MXene hybrids

Micro-supercapacitors (MSCs) with outstanding flexibility and electrochemical performance are critical for portable and miniaturized electronics. This study utilizes the potential utilization of Boron-modified MoS2/MXene heterostructure for fabricating highly efficient and durable microsupercapacitors. The Boron incorporation and hybrid formation significantly enhance the electrochemical performance of 1 T MoS2 and MXene (Ti3C2Tx) by activating their basal plane. The boron modified MoS2/Ti3C2Tx(B-1 T MoS2/Ti3C2Tx_) demonstrates excellent energy storage performance with a capacitance of around 420 Fg−1 in two-electrode system. Laser scribed graphene (LSG), chosen for its superior wettability, serves as the current collector facilitating the development of these MSC based on B-1 T MoS2/Ti3C2Tx. The resulting MSC demonstrates a high areal capacitance of nearly 72.31 mF/cm2 and excellent stability over 10,000 cycles. Density functional theory (DFT) simulations support these findings, indicating that hybridization with Ti3C2Tx and B substitution enhances the conductivity of the 1 T-MoS2 system. The quantum capacitance of B-substituted hybrid system surpasses that of the pristine material, validating the experimental observations of enhanced charge storage performance.