Large-scale Energy Storage Systems Research Articles

CVD Grown CNTs-Modified Electrodes for Vanadium Redox Flow Batteries.

Vanadium redox flow batteries (VRFBs) are of considerable importance in large-scale energy storage systems due to their high efficiency, long cycle life and easy scalability. In this work, chemical vapor deposition (CVD) grown carbon nanotubes (CNTs)-modified electrodes and Nafion 117 membrane are utilised for formulating a vanadium redox flow battery (VRFB). In a CVD chamber, the growth of CNTs is carried out on an acid-treated graphite felt surface. Cyclic voltammetry of CNT-modified electrode and acid-treated electrode revealed that CNTs presence improve the reaction kinetics of V3+/V2+ and VO2+/VO2+ redox pairs. Battery performance is recorded for analysing, the effect of modified electrodes, varying electrolyte flow rates, varying current densities and effect of removing the current collector plates. CNTs presence enhance the battery performance and offered 96.30% of Coulombic efficiency, 79.33% of voltage efficiency and 76.39% of energy efficiency. In comparison with pristine electrodes, a battery consisting CNTs grown electrodes shows a 14% and 15% increase in voltage efficiency and energy efficiency, respectively. Battery configured without current collector plates performs better as compared to with current collector plates which is possibly due to decrease in battery resistance.

Dendrite suppression enabled longevous sodium metal batteries by sodiophilic Zein/MXene nanofiber modulated polypropylene separator

Sodium metal batteries with low-cost and high-energy density are considered as the most promising candidate for large-scale energy storage systems. However, dendritic growth of sodium metal anode (SMA) severely hampered their viability. Here, we propose the use of polypropylene separators coated by electrospinning nanofibers containing corn protein (Zein) molecules and MXene (V2CTx) sheets on polyacrylonitrile (PAN) skeletons (denoted as PZM) to tackle these issues. The abundant sodiophilic functional groups on Zein and V2CTx as well as the porous network of electrospinning nanofibers can facilitate homogeneous Na metal deposition and achieve dendrite-free SMA. Additionally, the oxygen- and nitrogen-containing functional moieties on the nanofibers benefit the electrolyte up take (395 %), ion-conductivity (1.43 mS cm−1), Na+transference number (0.77) and inorganic-rich SEI. The PZM separator enables Na metal electrodes in symmetric cells to cycle over 3500 h with a stable overpotential of 10 mV at 1 mA cm−2/1 mAh cm−2 and over 1200 h at 5 mA cm−2/10 mAh cm−2. When tested in Na3V2(PO4)3@C||Na full cells, the PZM separator enables a high capacity of 86.2 mAh g−1 over 1000 cycles with an excellent capacity retention of 87.8 %. The proposed biomaterial-based separator modification strategy can spur the development of feasible sodium metal batteries.

Ultralong Cycling and Interfacial Regulation of Bilayer Heterogeneous Composite Solid-State Electrolytes in Lithium Metal Batteries.

Under the background of "carbon neutral", lithium-ion batteries (LIB) have been widely used in portable electronic devices and large-scale energy storage systems, but the current commercial electrolyte is mainly liquid organic compounds, which have serious safety risks. In this paper, a bilayer heterogeneous composite solid-state electrolyte (PLPE) was constructed with the 3D LiX zeolite nanofiber (LiX-NF) layer and in-situ interfacial layer, which greatly extends the life span of lithium metal batteries (LMB). LiX-NF not only offers a continuous fast path for Li+, but also zeolite's Lewis acid-base interaction can immobilize large anions, which significantly improves the electrochemical performance of the electrolyte. In addition, the in-situ interfacial layer at the electrode-electrolyte interface can effectively facilitate the uniform deposition of Li+ and inhibit the growth of lithium dendrites. As a result, the Li/Li battery assembled with PLPE can be stably cycled for more than 2500 h at 0.1 mA cm-2. Meanwhile, the initial discharge capacity of the LiFePO4/PLPE/Li battery can be 162.43 mAh g-1 at 0.5 C, and the capacity retention rate is 82.74% after 500 cycles. These results emphasize that this bilayer heterogeneous composite solid-state electrolyte has distinct properties and shows excellent potential for application in LMB.

Unlocking zinc storage in silver vanadate structures for high-performance aqueous zinc batteries

Zinc-ion batteries (ZIBs) are being increasingly recognized as promising candidates for large-scale energy-storage systems owing to their stability in air, abundance of elemental zinc, low cost, and ease of handling. Although various cathode materials have been explored for ZIBs, silver vanadate stands out for its highly stable structure. However, the presence of silver in silver vanadate may hinder its electrochemical performance, necessitating activation over several cycles. In this study, we introduce an ion-exchange reaction to directly activate silver vanadate. The resulting ion-exchanged zinc vanadate demonstrates superior performance compared with silver vanadate, showcasing stable cycling behavior and high-rate capability. Remarkably, it maintains a capacity retention of 71 % even after 400 cycles. Analysis of the zinc intercalation mechanism reveals a combination of capacitive and diffusion-based processes contributing to energy storage in ZIBs. Post-cycling examinations reveal the presence of dendritic zinc anodes and confirm the stability and safety of the framework, with no silver migration to the anode side. These findings highlight the potential of ZIBs as next-generation energy-storage solutions and underscore the need for continued research in optimizing electrode materials and electrolytes for practical applications.

Biomass derived hard carbon materials for sodium ion battery anodes: Exploring the influence of carbon source on structure and sodium storage performance

Compared to the scarce resources of lithium-ion batteries, sodium ion batteries have gradually become an ideal carrier for large-scale energy storage systems due to their abundant raw material resources. In recent years, hard carbon as an anode material for sodium ion batteries has attracted much attention. Biomass materials have become an ideal hard carbon precursor due to their natural and renewable advantages. This article evaluates the effect of hard carbon derived from three types of biomass waste (peanut shell, coffee grounds, and sugarcane bagasse) on the electrochemical performance of sodium ion batteries through pre carbonization pyrolysis method. The three materials exhibit different structures and surface functional group contents. Compared with coffee grounds and sugarcane bagasse, peanut shell-derived hard carbon has lower structural ordering and smaller specific surface area, and exhibits a higher initial Coulombic efficiency of 53.84 %. The initial reversible capacity of the HC-P electrode is 203.6 mAh/g, and the Coulombic efficiency of the electrode is close to 100 % with a reversible capacity of 127.1 mAh/g and a capacity retention of 81.4 % after cycling 100 at 1C current. The excellent electrochemical properties of HC-P can be attributed to its higher C=O bond content, larger layer spacing and lamellar structure.

In situ constructing a porous organic component-zincophilic Cu clusters layer on zinc anode for high performance aqueous zinc ion batteries

Aqueous zinc ion batteries (AZIBs) with Zn metal anodes stand out as a promising candidate for large-scale energy storage systems, owing to their high safety, low cost, and environmental friendliness. However, the commercialization of AZIBs is plagued by issues such as Zn dendrite growth and side reactions. Herein, an organic component-Cu metal composite layer is constructed on Zn anode (Org-Cu@Zn) by a novel, one-step and in situ spontaneous displacement reaction. The outer porous organic layer with functional groups may serve as migration sites and transport channels for Zn2+ ions, promoting transfer kinetics. The inner zincophilic Cu clusters layer diminishes the interfacial resistance, facilitating Zn2+ ions diffusion and even Zn deposition. Compared to the bare Zn, the unique dual-layer structure exhibits stronger zincophilicity, smaller interface resistance, lower nucleation energy barrier, and stronger anti-corrosion capability, thus effectively suppressing the Zn dendrite growth and side reactions. Remarkably, the Org-Cu@Zn electrode shows an ultra-long lifespan of 3600 h (1800 cycles) with an average Coulombic efficiency of 99.7 %, realizes long cycling stability over 4300 h (1 mA cm−2) and 1350 h (5 mA cm−2), and assures the stable operation of Org-Cu@Zn||ZVO full cells with coin-type configurations.

GRAVITY ENERGY STORAGE TECHNOLOGIES: A Review of the Solid Gravity Energy Storage Applications

The use of renewable energy sources is increasing to reduce the carbon footprint. Renewable energy sources provide limited electricity generation and cannot meet the variable energy demand. Large-scale energy storage systems are needed for sustainability. The applicability of energy storage technology depends on many factors such as energy source, site availability, energy density, storage time, storage capacity, system cost, environmental impact, reliability, durability, and system integration capacity. Solid gravity storage technology is seen as a promising new alternative for large-scale energy storage. There are various types of SGES systems classified according to the application method. In this paper, studies on various SGES methods are reviewed. Studies on the applicability factors of SGES systems and their integration into the electricity grid are evaluated. SGES technology has advantages in terms of geographical compatibility, storage volume, security, and energy conversion efficiency. It has been observed that successful results have been obtained in the theoretical studies. However, there is a need for the development of physical simulations and more comprehensive techno-economic analyses.

Suppressing the Jahn–Teller effect in Mn-based Prussian blue analogues by linear (N[dbnd]O) anions

Manganese-based Prussian blue analogues (PBAs) have been touted as a promising cathode material for sodium-ion batteries (SIBs) due to their low cost, long cycle life and high energy density. However, manganese-based PBAs perform poorly during cycling due to the Jahn-Teller effect. In this study, highly stable manganese nitrosylpentacyanoferrate (Mn[Fe(CN)5NO]) particles were synthesized using a simple hydrothermal method. The presence of nitroso group breaks the symmetry of the crystals to some extent, which is favorable to reduce the Jahn-Teller effect. Through experiments and DFT calculations, we confirm that the presence of linear (NO) anions reduces the lattice volume fluctuations of the samples during charging and discharging, thus contributing to the mitigation of the Jahn-Teller effect. The electrochemical properties of Mn[Fe(CN)5NO] were significantly improved compared to manganese hexacyanoferrate (MnFe[CN]6). Mn[Fe(CN)5NO] exhibited excellent sodium storage performance with an initial discharge capacity as high as 144.5 mAh/g at 20 mA g-1and capacity retention as high as 82.1 % after 400 cycles at 100 mA g−1. This Mn[Fe(CN)5NO] sample provides a promising cathode for sodium-ion batteries in large-scale energy storage systems.

Hydrophobic and zincophilic organic hierarchical nano-membranes with ordered molecular packing for stable zinc metal anodes

Rechargeable aqueous Zn metal batteries hold significant potentials as one of the next-generation energy-storage devices due to their low cost and high safety. However, the uncontrollable dendrite growth and low efficiency in plating/stripping of Zn anodes hinder the commercial application of aqueous Zn-ion batteries (AZIBs). Herein, inspired by hydrophobic lotus, a multifunctional organic hierarchical nano-membrane serving as an artificial protective layer is constructed through the gas-liquid interface method, using self-assembled organic nanosheets (NOS). The organic nano-membrane exhibits ordered molecular packing, accompanied by uniform distribution of zincophilic carbonyl (CO) groups on the Zn metal surface. These groups function as active sites, homogenizing Zn2+ flux and accelerating Zn2+ deposition. Simultaneously, the hydrophobic membrane isolates active water, thereby restraining side reactions, effectively suppressing corrosion and extremely inhibiting dendrite growth. Consequently, NOS@Zn anode exhibits stable cycling over 2400 h and an average coulombic efficiency (CE) of 99.69 % (600 cycles) at 1 mA cm−2. Furthermore, NOS@Zn||CNT-MnO2 full cell presents remarkable capacity retention, approximately 5 times higher than that of Zn||CNT-MnO2 after 3000 cycles at 2 A g−1. This work develops an innovative organic interface modification material paving the way for dendrite-free Zn metal anodes and advancing the practical application of large-scale Zn-based energy storage systems.

Borate modified Co-free LiNi0.5Mn1.5O4 cathode material: A pathway to superior interface and cycling stability in LNMO/graphite full-cells

Cobalt-free LiNi0.5Mn1.5O4 (LNMO) holds great promise as a next-generation cathode material for high-energy and high-power density lithium-ion batteries (LIBs), making it a key contender for large-scale energy storage systems (ESS) and transportation applications. Despite its potential, the commercial utilization of LNMO has been impeded by its rapid capacity deterioration attributed to an unstable LNMO/electrolyte interface caused by the intrinsically high operating voltage of LNMO. Here, we present a pragmatic and scalable strategy to improve the LNMO/electrolyte interface through borate-based surface coating of the LNMO. Optimizing the coating process yielded high-rate capability and stable LNMO/electrolyte interface analyzed by extended float tests. Borate-LNMO materials show superior cycling stability at 25 °C and 45 °C, attributed to a robust cathode electrolyte interphase (CEI) formation. The bare LNMO and 0.25-B2O3-LNMO demostrated a cycling stability of around 41.20 % and 62.50 % respectively after 1000 cycles in LNMO/graphite full-cells. Post-mortem X-ray photoelectron spectroscopy (XPS) analysis revealed fewer side reaction products on borate-LNMO cathodes compared to bare LNMO. Additionally, scanning electron microscopy (SEM) revealed a thicker and denser solid-electrolyte interphase (SEI) on cycled graphite anodes from bare LNMO cells, while a thin and robust SEI was observed on graphite from borate-LNMO cells. Finally, we have conclusively demonstrated that the primary aging mechanism in LNMO/graphite full cells stems from the instability at the LNMO/electrolyte or/and graphite/electrolyte interface, rather than material-related degradation phenomenon. These compelling outcomes underscore the potential of cathode material surface coating in general and especially of borate coating on LNMO as a promising and cost-effective enabler for the use of LNMO in next-generation LIBs.

Effect of geothermal heat transfer on performance of the adiabatic compressed air energy storage systems with the salt cavern gas storage

The temperature and pressure of compressed air influence the output performance of the adiabatic compressed air energy storage system with salt cavern gas storage. However, current studies often overlook the impact of geothermal heat transfer on system performance. In this paper, a mathematical model of the energy storage system with salt cavern gas storage is developed, considering the geothermal heat transfer in wellbore and salt carven. The model is used to illustrate the effects of geothermal heat transfer on the system performance through a sensitivity analysis of some key parameters. The results show that geothermal heat transfer will significantly reduce the gas and energy storage capacity, with a maximum reduction of 15.3 % and 11.1 % at a depth of 2000 m, respectively. Furthermore, this reduction would increase with the depth of the salt cavern. The geothermal energy reduces the round-trip efficiency from 68.7 % to 66.26 % and the energy storage density from 5.18 kWh·m−3 to 4.32 kWh·m−3. For common salt cavern gas storage at a depth of about 600 m ∼ 1200 m, the negative impacts of geothermal heat transfer on round-trip efficiency and energy storage density are less than 2.2 % and 0.5 kWh·m−3, respectively. Sensitivity analysis also demonstrates that the primary factors influencing the system’s performance are the thermal conductivity of the surrounding rock, the volume of the salt cavern, and the length of the wellbores. The secondary factors include the heat transfer coefficient on the inner wall of the salt cavern, the inner pipe radius, and the roughness of the inner pipe. Irrelevant factors include the thermal conductivity of the protective fluid and the thermal conductivity of the cement layer. The proposed comprehensive mathematical model of the system and simulation findings aid in forecasting the performance of storage systems and offer theoretical guidance for the design of large-scale compressed air energy storage systems.

Layer‑by‑layer assembled binder-free hydrated vanadium oxide-acetylene black electrode for flexible aqueous zinc ion battery

Vanadium oxides are potential positive electrode materials for aqueous zinc ion batteries (ZIBs) owing to their advantages of high theoretical capacity, low cost, and so on. Developments of methods for preparing binder-free vanadium oxide electrodes on a large scale and further investigation of their Zn2+ storage mechanisms are essential for expanding their uses in large-scale energy storage systems and wearable electronics. In this work, binder-free electrodes with hydrated vanadium oxide (V2O5·nH2O, denoted as VOH)-acetylene black (AB) on carbon cloth (VOH-AB/CC) are fabricated by a simple and scalable method which combined low-temperature hydrothermal treatment with layer-by-layer drop/spray-coating process. The AB can greatly improve the electrical conductivity of VOH, thereby enhancing the electrochemical performance. The as-prepared electrode with 20 wt% of AB (VOH-AB2/CC) delivers a high capacity of 280 mA h g−1 at 1 A/g and a good rate capability of 205 mA h g−1 at 4 A/g, which is better than many of the reported binder-free vanadium base electrodes. Besides, excellent cycling performance with 89 % retention rate after 3000 cycles at 4 A/g is achieved on the VOH-AB2/CC electrode. Furthermore, a storage mechanism of Zn2+/H+/H2O insertion accompanied by the formation of basic zinc salt precipitate during the discharging process is proposed by the aid of ex-situ XRD and XPS techniques. Additionally, the flexible Quasi-Solid-State ZIB constructed using VOH-AB/CC as positive electrode can work well at different bending states and two ZIBs connected in series can lighten a light-emitting diode even under bending state. This work provides a low-cost, time-saving, environmental-friendly and scalable method to fabricate binder-free hydrated vanadium oxide electrodes for flexible aqueous ZIBs.

Electropolymerization of a Carbonyl-Modified Dihydropyrazine Derivative for Aqueous Zinc Batteries with Ultrahigh Cycling Stability.

The design of aqueous zinc-ion batteries (ZIBs) that have high specific capacity and long-term stability is essential for future large-scale energy storage systems. Cathode materials with extended π-conjugation and abundant active sites are desirable to enhance the charge storage performance and the cycling stability of the aqueous ZIB. Based on this concept, 6,9-dihydropyrazino[2,3-g]quinoxaline-2,3,7,8(1H,4H)-tetrone was chosen as the monomer to be electropolymerized onto carbon cloth (PDHPQ-Tetrone/CC). When used as the cathode material for aqueous ZIBs, an exceptional cycling life (>20,000 cycles) at a current density of 10 A g-1 was achieved, with the specific capacity maintained at 82.8% and with the Coulombic efficiency at around 100% throughout cycling. At the charge-discharge current density of 0.1 A g-1, the ZIB with PDHPQ-Tetrone/CC achieved a high specific capacity of 248 mAh g-1. Kinetic analyses showed that both surface-capacitive-controlled processes and semi-infinite diffusion-controlled processes contribute to the stored charge. The charge storage mechanism was investigated with ex situ characterizations and involves the redox processes of carbonyl/hydroxyl and amino/imino groups coupled with insertion and extraction of both Zn2+ and H+.

1T/2H Mixed-phase MoS2 with enlarged interlayer spacing induced via bacteria-derived carbon for long-lifespan pseudocapacitors

Pseudocapacitors (PCs) are considered prospective candidates for large-scale aqueous energy storage systems due to their high power density. However, the poor cycling stability resulting from sluggish metal ion transport kinetics and the instability of the electrode structure hinders their further applications. To address this issue, an effective strategy of 1T/2H mixed-phase MoS2 directly grown on the electrochemically activated carbon (EC) induced via bacteria-derived carbon (BC) from bacillus subtilis is proposed to achieve efficient anodes for potassium ion capacitors. The inherent nitrogen elements found in the bacteria-derived carbon, along with a trace amount of amines and their derivatives generated from amino acid decarboxylation, act as support by inserting into the MoS2 interlayer. Amines and their derivatives as intercalators could suppress the MoS2 layer stacking and mitigate structure damage, which is responsible for preventing rapid capacity fading. Thus, the mixed-phase MoS2 with an expanded interlayer spacing of 0.94 nm achieves a remarkable durability with a capacitance retention of 110.2 % after 40,000 cycles at 10 A g−1. Density Functional Theory (DFT) reveals that the mixed-phase MoS2 could improve electron transfer ability and cyclic stability, in which the rich vacancies introduced by bacteria-derived carbon could enhance the K+ adsorption. To highlight, the asymmetric capacitor device (ASC) adopting mixed-phase MoS2 anode shows a long lifespan (88 % capacitance retention over 10,000 cycles). This work will provide a green approach to boost cycling performance of MoS2 anodes and shed light on developing high-performance MoS2-based materials for electrochemical energy storage.

Stable Zinc Electrode Reaction Enabled by Combined Cationic and Anionic Electrolyte Additives for Non-Flow Aqueous Zn─Br2 Batteries.

Aqueous zinc-bromine batteries hold immense promise for large-scale energy storage systems due to their inherent safety and high energy density. However, achieving a reliable zinc metal electrode reaction is challenging because zinc metal in the aqueous electrolyte inevitably leads to dendrite growth and related side reactions, resulting in rapid capacity fading. Here, it is reported that combined cationic and anionic additives in the electrolytes using CeCl3 can simultaneously address the multiple chronic issues of the zinc metal electrode. Trivalent Ce3+ forms an electrostatic shielding layer to prevent Zn2+ from concentrating at zinc metal protrusions, while the high electron-donating nature of Cl- mitigates H2O decomposition on the zinc metal surface by reducing the interaction between Zn2+ and H2O. These combined cationic and anionic effects significantly enhance the reversibility of the zinc metal reaction, allowing the non-flow aqueous Zn─Br2 full-cell to reliably cycle with exceptionally high capacity (>400mAh after 5000 cycles) even in a large-scale battery configuration of 15×15cm2.

Nonflammable Succinonitrile-Based Deep Eutectic Electrolyte for Intrinsically Safe High-Voltage Sodium-Ion Batteries.

Intrinsically safe sodium-ion batteries are considered as a promising candidate for large-scale energy storage systems. However, the high flammability of conventional electrolytes may pose serious safety threats and even explosions. Herein, a strategy of constructing a deep eutectic electrolyte is proposed to boost the safety and electrochemical performance of succinonitrile (SN)-based electrolyte. The strong hydrogen bond between S═O of 1,3,2-dioxathiolane-2,2-dioxide (DTD) and the α-H of SN endows the enhanced safety and compatibility of SN with Lewis bases. Meanwhile, the DTD participates in the inner Na+ sheath and weakens the coordination number of SN. The unique solvation configuration promotes the formation of robust gradient inorganic-rich electrode-electrolyte interphase, and merits stable cycling of half-cells in a wide temperature range, with a capacity retention of 82.8% after 800 cycles (25°C) and 86.3% after 100 cycles (60°C). Correspondingly, the full cells deliver tremendous improvement in cycling stability and rate performance.

High-energy and durable aqueous Zn batteries enabled by multi-electron transfer reactions

Aqueous Zn batteries (AZBs) have emerged as a highly promising technology for large-scale energy storage systems due to their eco-friendly, safe, and cost-effective characteristics. The current requirements for high-energy AZBs attract extensive attention to reasonably designed cathode materials with multi-electron transfer mechanisms. This review systematically overviews the development and challenges of typical cathode hosts capable of multiple electron transfer reactions for high-performance Zn batteries. Moreover, we also summarize how to trigger the multi-electron transfer chemistry of cathodes, including transition metal oxides, halogens, and organics, to further boost the energy storage capability of AZBs. Finally, perspectives on critical issues and future directions of the multi-electron transfer battery systems offer novel insights for advanced Zn batteries.

Constructing hierarchical MoS2/WS2 heterostructures in dual carbon layer for enhanced sodium ions batteries performance

The escalating global demand for clean energy has spurred substantial interest in sodium-ion batteries (SIBs) as a promising solution for large-scale energy storage systems. However, the insufficient reaction kinetics and considerable volume changes inherent to anode materials present significant hurdles to enhancing the electrochemical performance of SIBs. In this study, hierarchical MoS2/WS2 heterostructures were constructed into dual carbon layers (HC@MoS2/WS2@NC) and assessed their suitability as anodes for SIBs. The internal hard carbon core (HC) and outer nitrogen-doped carbon shell (NC) effectively anchor MoS2/WS2, thereby significantly improving its structural stability. Moreover, the conductive carbon components expedite electron transport during charge–discharge processes. Critically, the intelligently engineered interface between MoS2 and WS2 modulates the interfacial energy barrier and electric field distribution, promoting faster ion transport rates. Capitalizing on these advantageous features, the HC@MoS2/WS2@NC nanocomposite exhibits outstanding electrochemical performance when utilized as an anode in SIBs. Specifically, it delivers a high capacity of 415 mAh/g at a current density of 0.2 A/g after 100 cycles. At a larger current density of 2 A/g, it maintains a commendable capacity of 333 mAh/g even after 1000 cycles. Additionally, when integrated into a full battery configuration with a Na3V2(PO4)3 cathode, the Na3V2(PO4)3//HC@MoS2/WS2@NC full cell delivers a high capacity of 120 mAh/g after 300 cycles at 1 A/g. This work emphasizes the substantial improvement in battery performance that can be attained through the implementation of dual carbon confinement, offering a constructive approach to guide the design and development of next-generation anode materials for SIBs.

Controlling intermolecular interaction and interphase chemistry enabled highly stable aqueous ammonium-ion batteries

Aqueous ammonium-ion batteries (AIBs) show great potential in the large scale energy storage systems due to the advantages of low cost, high safety and environmental friendliness. However, they face the challenges of low output voltage and unsatisfactory electrochemical performance because of the narrow voltage window and unstable interfacial structure in conventional aqueous electrolytes. Herein, we design an aqueous AIB based on hydrogen-bond anchored electrolyte, Mn-based Prussian blue analogues (MnHCF) cathode and NaTi2(PO4)3@carbon (NTP@C) anode. In this electrolyte, the intermolecular hydrogen-bond interaction is constructed between water and sulfolane molecules, leading to the decreased water activity and wide voltage window. Furthermore, the coordination environment of NH4+ ions between sulfolane and CF3SO3- anions produces a unique solvation structure with low hydrated degree, which favors the formation of protective interfacial layer between electrode and electrolyte. Accordingly, the dissolution of MnHCF is largely inhibited and the side reactions between electrode and electrolyte are suppressed. As a result, the MnHCF electrode displays stable cycling performance and high Coulombic efficiency compared with the cases in conventional aqueous electrolytes. Moreover, the constructed full cells demonstrate high output voltage and superior stability. This work provides a synergistic route to design high-performance aqueous AIBs.

Numerical thermal control design for applicability to a large-scale high-capacity lithium-ion energy storage system subjected to forced cooling

Overheating and non-uniform temperature distributions within the energy storage system (ESS) often reduce the electric capacity and cycle lifespan of lithium-ion batteries. In this numerical work, the thermal design inside the battery cabinet is explored. The battery cabinet has seven-level configurations with the suction fans located on the top of the ESS to efficiently realize heat dissipation. First, the numerical modeling is validated by the available experimental data, and the discrepancy in the maximum temperature increase between the experimental and computational results is found to be 3.2% or 0.64 K. Then, the optimum airflow rates of the fans are determined, where the single-cell model is also compared with the model of seven-level modules (i.e., 1/3ESS cabinet). Finally, the airflow channel widths, air gaps between the battery modules, as well as the air gaps between the 7th level module and the fans are examined. It is indicated for the precise model of 1/3ESS cabinet that: i) The maximum temperature rise of 4.63 K, and the maximum temperature variation of 2.14 K from cell to cell & the temperature uniformity of 2.82 K from module to module are all controlled with the requirements of operating temperature < 313.15 K, and temperature differences < 5.0 K, respectively; ii) The airflow channel width of 3.0 mm and the air gap of 10 mm between two adjacent modules & air gap of 20 mm between 7th level module and six parallel-fans are designed, and the ESS cabinet can increase the batteries of one level caused by the saved inside space.