Large-scale Energy Storage Systems Research Articles

Progress on Copper-Based AnodeMaterials for Sodium-Ion Batteries.

Fossil fuels have clearly failed to meet people's growingenergy needs due to their limited reserves, potential pollution of the environment, and high costs.The development of cleaner, renewable energy sources as well as secondary batteries for energy storage is imminent, in a modern society where energy demand is soaring. Sodium-ion batteries (SIBs) have become the focus of large-scale energy storage systems as a promising alternative to lithium-ion batteries. The development of SIBs relies on the construction of high performance electrode materials. The design of low cost and high performance anode materials is a key link in this regard. Copper-based anodes are characterised by high theoretical capacity, abundant reserves, low cost and environmental friendliness. A variety of copper-based anode materials, which include cobalt oxides, sulfides, selenides and phosphides, have been synthesised and evaluated in the scientific literature for sodium storage. In detail, the preparation methods, response mechanisms, strengths and weaknesses, the relationship between morphology structure and electrochemical performance are discussed, as well as highlighting strategies to improve the electrochemical performance of copper-based anode materials. Finally, we offer our perspective on the challenges and potential for the development of copper-based anodes as a means of developing practical and high performing SIBs.

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+.

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.

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.

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 structures 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 was 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.

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.

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) layer 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.

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.

Two-dimensional/three-dimensional hierarchical self-supporting potassium ammonium vanadate@MXene hybrid film for superior performance aqueous zinc ion batteries

Currently, aqueous zinc ion batteries (AZIBs) have grown to be a good choice for large-scale energy storage systems due to their high theoretical specific capacity, low redox potential, low cost, and non-toxicity of the aqueous electrolyte. However, it is still challenging to obtain high specific capacity and stability suitable cathodes. Herein, hierarchical self-supporting potassium ammonium vanadate@MXene (KNVO@MXene) hybrid films were prepared by vacuum filtration method. Due to the three-dimensional nanoflower structure of KNVO with dual ions intercalation, high conductivity of two-dimensional Ti3C2Tx MXene, and the hierarchical self-supporting structure, the AZIB based on the KNVO@MXene hybrid film cathode possessed superior specific capacity (481 mAh/g at 0.3 A/g) and cycling stability (retaining 125 mAh/g after 1000 cycles at a high current density of 10 A/g). In addition, the storage mechanism was revealed by various ex-situ characterizations. Hence, a new viewpoint for the preparation of AZIB self-supporting cathode materials is presented.

Improved rule-based power distribution algorithm for hybrid battery storage systems and real-world validation

Large-scale battery energy storage systems (BESS) can serve many applications and are already widely used for grid services. The rapidly growing BESS market and the recent interest in their deployment accentuate the need for safe, reliable, and highly available energy management systems (EMS) for automated control. However, the EMS and their integrated power distribution algorithms (PDA) can still be optimized to adapt various characteristics of the BESS. This study investigates a new version of a PDA with a particular focus on battery aging and system efficiency. The rule-based PDA has been validated on a 6 MW/7.5 MWh BESS system with five battery technologies providing frequency containment reserve to the German power grid. The results underline the PDA's capability to exploit the individual strengths of each battery technology. The PDA sets objectives for the state of charge, energy throughput, and power of the batteries to extend battery life. The distribution of energy throughputs among batteries can be selected in advance through the new implementation of the PDA. At the same time, the inverters are significantly less often activated and used in the optimal efficiency range, increasing the overall system efficiency to approximately 82 %. The optimized switching behavior leads to less frequent power switching between individual battery units and longer phases with more constant power. In addition, the operational efficiency of BESS can be improved by the choice of battery technology and the overall system layout on the hardware side. The improvements on the software side are only possible by increasing the overall power requests through multi-use operation by about 6 % compared to our benchmark test. The results can be used by BESS operators to increase operational profits due to longer battery life and fewer efficiency losses.

Two-in-one strategy for optimizing chemical and structural properties of carbon felt electrodes for vanadium redox flow batteries

ABSTRACT Vanadium redox flow batteries (VRFBs) have received significant attention for use in large-scale energy storage systems (ESSs) because of their long cycle life, flexible capacity, power design, and safety. However, the poor electrochemical activity of the conventionally used carbon felt electrode results in low energy efficiency of the VRFBs and consequently impedes their commercialization. In this study, a carbon felt (CF) electrode with numerous nanopores and robust oxygen-containing functional groups at its edge sites is designed to improve the electrochemical activity of a carbon felt electrode. To achieve this, Ni metal nanoparticles were initially precipitated on the surface of the CF electrode, followed by etching of the precipitated Ni nanoparticles on the CF electrode using sulfuric acid. The resulting CF electrode had a specific surface area eight times larger than that of the pristine CF electrode. In addition, the oxygen-containing functional groups anchored at the graphite edge sites of the nanopores can act as robust electrocatalysts for VO2+/VO2 + and V2+/V3+ redox reactions. Consequently, the VRFB cell with the resulting carbon felt electrode can deliver a high energy efficiency of 86.2% at the current density of 60 mA cm−2, which is 20% higher than that of the VRFB cell with the conventionally heat-treated CF electrode. Furthermore, the VRFB cell with the resultant carbon felt electrodes showed stable cycling performance with no considerable energy efficiency loss over 200 charge-discharge cycles. In addition, even at a high current density of 160 mA cm−2 , the developed carbon felt electrode can achieve an energy efficiency of 70.1%.

A self-regulated interface enabled by trivalent gadolinium ions toward highly reversible zinc metal anodes

Aqueous zinc-ion batteries (AZIBs) have become an ideal candidate for large-scale energy storage systems owing to their inherent safety and highly competitive capacity. However, severe dendrite growth and side reactions on the surface of zinc metal anodes lead to quick performance deterioration, seriously impeding the commercialization of AZIBs. In this work, a self-regulated zinc metal/electrolyte interface is constructed to solve these problems by incorporating the trivalent Gd3+ additive with a lower effective reduction potential into the aqueous ZnSO4 electrolyte. It is revealed that the inert Gd3+ ions preferentially adsorb on the active sites of the zinc anode, and the induced electrostatic shielding layer is beneficial to uniform Zn deposition. Meanwhile, the adsorbed Gd3+ ions act as a buffer interface to lower the direct contact of the zinc anode with water molecules, thereby suppressing the interfacial parasitic reaction. These features endow the Zn//Zn battery using 0.2 M Gd3+ ions with 2940 h of cycling life at 5 mA cm−2 and a cumulative plating capacity (CPC) of 6.2 Ah cm−2 at 40 mA cm−2. When assembling with a MnO2 cathode, the full cell using the modified electrolyte exhibits a high capacity of 268.9 mAh/g at 0.2 A/g, as well as improved rate capability and cycle stability. The results suggest the great potential of a rare earth ion additive in reinforcing Zn metal anodes for developing practical AZIBs.

Enhanced Aluminum-Ion Storage Properties of N-Doped Titanium Dioxide Electrode in Aqueous Aluminum-Ion Batteries.

Aqueous aluminum-ion batteries (AIBs) have great potential as devices for future large-scale energy storage systems due to the cost efficiency, environmentally friendly nature, and impressive theoretical energy density of Al. However, currently, available materials used as anodes for aqueous AIBs are scarce. In this study, a novel sol-gel method was used to synthesize nitrogen-doped titanium dioxide (N-TiO2) as a potential anode material for AIBs in water. The annealed N-TiO2 showed a high discharge capacity of 43.2 mAh g-1 at a current density of 3 A g-1. Analysis of the electrode kinetics revealed that the N-TiO2 anodes exhibited rapid diffusion of aluminum ions, low resistance to charge transfer, and high electronic conductivity, enabling good rate performance. The successful implementation of a nitrogen-doping strategy provides a promising approach to enhance the electrochemical characteristics of electrode materials for aqueous AIBs.

An Efficient and Compact Equalizer Based on Forward-Flyback Conversion for Large-Scale Energy Storage Systems

An effective battery equalizer is of great significance to eliminate inconsistencies and improve the performance of large-scale battery packs. Nevertheless, the existing balancing circuits have various problems such as slow balancing speed, high cost, bulky size, complex control, etc. Therefore, this paper designs an efficient and compact transformer-based equalizer, which works at forward-flyback conversion. Distinguished from the conventional transformer-based equalizers, the proposed equalizer requires only one MOSFET and one transformer winding equipped with each cell. Two complementary PWM signals can control all MOSFETs used in the proposed equalizer. The equalizer can automatically equalize all cells without the need for additional voltage sensing and demagnetization circuits, reducing the cost and volume. It can directly transfer energy between any two adjacent modules, improving the equalization efficiency and speed. An experimental prototype of eight series-connected cells was set up. The experimental results and systematic comparison with the existing balancing topologies show that the proposed equalizer is appropriate for balancing large-scale energy storage systems. The energy delivery efficiency among cells can be as high as 93.15% over various loading conditions.

Facile Electrolytic (111)‐Textured Copper Foil for Dendrite‐Free Zinc Metal Batteries

AbstractAqueous Zn metal batteries are emerging as a promising candidate for the next‐generation largescale energy storage system due to their high safety, low lost, and eco‐friendliness. Nevertheless, their practical application is restricted by the uncontrollable Zn dendrite growth and the limited utilization of the Zn metal anode. Herein, a room temperature electrodeposition strategy based on an optimized rate relationship between the diffusion and consumption of Cu2+ to prepare a (111)‐textured Cu current collector for the construction of the dendrite‐free Zn metal anode with high reversibility is developed. Attributed to the high lattice match between the (002) facet of Zn with the (111) facet of Cu, the deposition of Zn along its [001] orientation is achieved on the (111)‐textured Cu. The (002) facets horizontally aligned with the current collector endow Zn with the dendrite‐free planar construction and superior corrosion resistance, resulting in a high reversibility with a long life‐span over 2186 cycles. Impressively, the resultant Zn anodes can stabilize the operation of pouch cells with an extremely demanding negative‐to‐positive capacity ratio of 2. This work provides a new avenue for the development of the current collectors for the low‐cost sustainable energy storage.