Rechargeable Research Articles

Fully sp2 Carbon-conjugated Covalent Organic Frameworks with Multiple Active Sites for Advanced Lithium-ion Battery Cathodes.

Covalent organic frameworks (COFs) hold great promise for rechargeable batteries. However, the synthesis of COFs with abundant active sites, excellent stability, and increased conductivity remains a challenge. Here, chemically stable fully sp2 carbon-conjugated COFs (sp2c-COFs) with multiple active sites are designed by the polymerization of benzo[1,2-b:3,4-b':5,6-b'']trithiophene-2,5,8-tricarbaldehyde) (BTT) and s-indacene-1,3,5,7(2H,6H)-tetrone (ICTO) (denoted as BTT-ICTO). The morphology and structure of the COF are precisely regulated from "butterfly-shaped" to "cable-like" through an in-situ controllable growth strategy, significantly promoting the exposure and utilization of active sites. When the unique "cable-like" BTT-ICTO@CNT is employed as lithium-ion batteries (LIBs) cathode, it exhibits exceptional capacity (396 mAh g-1 at 0.1 A g-1 with 97.9% active sites utilization rate), superb rate capacity (227 mAh g-1 at 5.0 A g-1), and excellent cycling performance (184 mAh g-1 over 8000 cycles at 2.0 A g-1 with 0.00365% decay rate per cycle). The lithium storage mechanism of BTT-ICTO is exhaustively revealed by in-situ Fourier transform infrared, in-situ Raman, and density functional theory calculations. This work provides in-depth insights into fully sp2c-COFs with multiple active sites for high-performance LIBs.

Sustainability assessment of rooftop solar photovoltaic systems: A case study

The study combined conventional life cycle assessment (LCA) with energy benefit and economic feasibility analysis for a 1 MW rooftop solar photovoltaic (PV) system. The study analyzed two solar PV system scenarios: in Case 1, the solar PV system was connected directly to the college's internal grid, while in Case 2, it was integrated with a battery storage system. The environmental impact was assessed in terms of global warming (GWp) and other impact indicators using the ReCiPe (H) midpoint and endpoint methodology. The study found a 73% increase in GWp, a 739% increase in mineral resource scarcity, and an increase in all toxicity indicators observed in Case 2, primarily due to battery utilization. Endpoint impact indicators also increased, affecting human health, ecosystems, and resources. The study also evaluated the energy benefits using energy payback time (EPBT) and energy return on investment (EROI), as well as the economic feasibility using the levelized cost of electricity (LCOE). The EPBT increased from 3.71 years in Case 1 to 6.74 years in Case 2, while the EROI decreased from 5.38 in Case 1 to 2.96 in Case 2, indicating a reduced energy feasibility with the battery storage system. Additionally, the LCOE increased from 3.17 Rs/kWh to 16.96 Rs/kWh in Case 2, primarily due to the high cost of the battery and its replacement. This study shows that converting solar power to firm power in the current scenario has a higher environmental, energy, and economic impact.

Multi-layered carbon accommodation of MnO2 enabling fast kinetics for highly stable zinc ion batteries

Large-scale durable aqueous zinc ion batteries for stationary storage are realized by spray-coating conductive PEDOT(Poly(3,4-ethylenedioxythiophene)) wrapping MnO2/carbon microspheres hybrid cathode in this work. The porous carbon microspheres with multiple layers deriving from sucrose provide suitable accommodation for MnO2 active materials, exposing more redox active sites and enhancing the contact surface between electrolyte and active materials. As a result, MnO2/microspheres are adhered to the current collector by a conductive PEDOT coating without any binder. The ternary design retards the structural degradation during cycling and shortens the electron and ion transport path, rendering the full batteries high capacity and long cycle stability. The resulting batteries perform the capacity of 277, 227, 110, 85 and 50 mAh/g at 0.2, 0.5, 1, 2 and 5 A/g, respectively. After 3000 cycles the initial capacity retains 86%, and 80% after 5000 cycles. GITT indicates PEDOT wrapping MnO2/microspheres cathode enables better ion intercalating kinetics than conventional MnO2. The work could represent a novel and significant step forward in the studies on the large-scale application of zinc ion batteries.

Construction of an n-Type Fluorinated ZnO Interfacial Phase for a Stable Anode of Aqueous Zinc-Ion Batteries.

Aqueous rechargeable zinc-ion batteries have become an ideal solution for the next generation of energy storage systems due to their low cost and high safety. However, the uncontrollable zinc dendrites and harmful side reactions of metal zinc anodes hinder the further development of aqueous zinc-ion batteries. In this work, the artificial fluoride zinc oxide (F-ZnO) interface phase is integrated in situ on the surface of zinc foil. The F-ZnO interface phase significantly inhibits the side reactions on the surface of the zinc electrode by reducing the direct contact between the electrolyte and the surface of the zinc foil. In addition, F-ZnO modified by a small amount of F doping shows enhanced conductivity and electron transport capacity, avoiding the accumulation of high concentration Zn2+ on the anode surface, and ultimately promoting the efficient nucleation and orderly deposition of a zinc anode. The cycle life of the symmetrical cell based on F-ZnO is as high as 2600 cycles at an area current density of 4 mA cm-2, which is much better than that of a commercial pure Zn electrode. The modified F-ZnO@Zn anode truly achieves the purpose of prolonging the anode's life.

Optimizing quasi-dynamic wireless charging for urban electric buses: A two-scenario mathematical framework with grid and PV-battery systems

This paper presents a mathematical optimization framework for the strategic placement of quasi-dynamic wireless charging (QWC) stations within road networks to address the charging needs of battery electric buses (BEBs). This study evaluates two scenarios for powering the buses. In the first scenario, a grid-connected system is considered. The optimization aims to minimize annual costs related to capital, operation, and energy losses of the electric bus fleet. This involves determining the optimal locations for QWC stations, the length of power transmitters, and the corresponding battery capacities for the BEBs. Using MATLAB-based optimization tools Casadi and Yalmip, with solvers Bonmin and Fmincon, the optimal configuration includes a 13 kWh battery capacity and a 300 m power transmitter distributed across five bus stop areas. The second scenario employs a chance-constrained optimization approach for an isolated solar photovoltaic (PV) and battery energy storage system (BESS). This system is designed to reliably meet the BEBs' energy requirements throughout the day, considering different seasonal data (winter, summer, all seasons/year-round). The optimization results for the PV and BESS capacities vary with the seasons: 394.247 kW and 2012.6 kWh using summer data, 1762.1 kW and 2738.2 kWh using winter data, and 1610.8 kW and 2741.9 kWh using year-round data. Additionally, the paper examines the impact of varying bus fleet sizes on the optimal battery size and power transmitter combination using a real-world example of the bus route between Khalifa City and Abu Dhabi Downtown in the UAE. The findings suggest that larger batteries with fewer or no charging stations are more economical for smaller fleets. Conversely, as the fleet size increases, a combination of smaller battery sizes and a greater number (and length) of QWC (power transmitters) becomes more cost-effective. This research offers significant insights into the efficient deployment of QWC stations and the integration of renewable energy and energy storage for sustainable urban electric bus networks. The proposed optimization models provide a systematic approach to designing and operating charging infrastructure, contributing to sustainable urban transportation systems. Moreover, the study highlights the influence of seasonal data on PV system sizing and costs.

Approaching Theoretical Capacity: 0D/2D Amorphous/Crystalline Bi‐Based Heterostructures Anode for Aqueous Alkaline Rechargeable Batteries

Approaching Theoretical Capacity: 0D/2D Amorphous/Crystalline Bi‐Based Heterostructures Anode for Aqueous Alkaline Rechargeable Batteries

Highly Performing Sodium Metal Batteries Reinforced by a Self-Regulated Dual-Layered Solid Electrolyte Interphase via a Metal-Organic Framework.

Sodium-metal batteries, heralded for high energy density and cost-effectiveness, are compromised by an unstable solid electrolyte interphase (SEI) and dendrite formation, which hinder practical applications. Herein, a zirconium-based metal-organic framework nanostructure coating (ZMOF-NSC) was constructed in a low-loss, flexible manner. Comprehensive studies show that ZMOF-NSC, with its periodically ordered nanochannels and organized pore structures, enhances ion transport and decreases the Na+ migration energy barrier, thus ensuring uniform ion flux and achieving uniform spherical deposition. Additionally, ZMOF-NSC facilitates partial desolvation, catalyzing the formation of an inorganic-rich, dual-layered SEI that effectively protects the anode and suppresses dendrite formation. Consequently, the ZMOF-NSC@Na symmetric battery exhibits an impressive lifespan of over 2500 h, demonstrating extended operational longevity. The Na3V2(PO4)3∥ZMOF-NSC@Na batteries demonstrate exceptional cycling stability with 81% capacity retention after 2000 cycles at 10 C, maintaining stability over 3000 cycles at 20 C. Moreover, the NVP∥ZMOF-NSC@Na battery achieves an energy density of 370 Wh kg-1 and a power density of 10,484 W kg-1, indicating superior durability and performance. This significant finding highlights the significant potential of structured MOFs to induce a dual-layered SEI, advancing the commercialization of durable, dendrite-free sodium metal batteries. The precise design of self-assembled pore structures and surface active sites in MOFs demonstrates significant potential in advancing the commercialization of durable, dendrite-free electrodes of metal-based rechargeable batteries.

A modified Runge–Kutta optimization for optimal photovoltaic and battery storage allocation under uncertainty and load variation

A modified Runge–Kutta optimization for optimal photovoltaic and battery storage allocation under uncertainty and load variation

One-step fabrication of Polyvinylidene fluoride membranes enriched with electroactive β-Phase for secondary battery separators via simultaneous near infrared radiation and electrospinning

This study reports a one-step fabrication method to prepare polyvinylidene fluoride (PVDF) membranes enriched with electroactive β-Phase in application for secondary battery separator using near infrared radiation (NIR) heated electrospinning techniques. The electrospun PVDF fibrous membranes with NIR heating applied were investigated by various characterizations and measurements. The results present that NIR heating during electrospinning not only increased the β phase content and mechanical strength of the PVDF membranes but also improved the electrochemical performances, suggesting its potential suitability in the battery separator applications.

Progress and Prospect of Sn‐based Metal‐organic Framework Derived Anode Materials for Metal‐ion Batteries

AbstractIn order to realize the growing demand for superior energy storage devices and electric vehicles, commercial anode candidates for next‐generation rechargeable batteries need to meet the characteristics of low cost, high energy density, high capacity, and stable performance. The emerging tin‐based anodes show great potential for high performance metal‐ion battery anodes due to their high theoretical capacity, low cost, green harmless and high safety. Tin based anode materials include tin gold based materials, tin alloy materials, tin based oxides, tin based phosphide, tin based sulfides, multi‐component composite materials, etc. However, the change in volume and structure of tin‐based anode materials during the cycle has become the biggest obstacle to its development. Metal‐organic frameworks (MOFs) provide a wide range of possibilities for achieving high rate capacity and excellent cycle stability by finely regulating the structure and composition of tin‐based materials at the molecular level. The latest progress of tin‐based materials derived from MOFs as anode materials for metal‐ion batteries (including lithium ion batteries, sodium ion batteries, potassium ion batteries, magnesium ion batteries) was reviewed in this paper. Firstly, the preparation method and morphology control of tin‐based MOF are briefly introduced, and the structural characteristics, storage mechanism and modification of tin‐based MOF derived materials are emphatically discussed. Finally, we summarized the existing modification measures and challenges of these anode materials, and put forward the prospect of the future.

Recent progress of Prussian blue analogues as cathode materials for metal ion secondary batteries

Recent progress of Prussian blue analogues as cathode materials for metal ion secondary batteries

Fault Characterization for AC/DC Distribution Networks Considering the Control Strategy of Photovoltaic and Energy Storage Battery

In order to cope with the failure of existing fault analysis schemes for AC/DC distribution networks with a high proportion of distributed generations, this paper proposes a fault characteristic analysis method for AC/DC distribution networks that considers the influence of distributed generation control strategies. Firstly, a transient model for the AC/DC distribution network connected to distributed generations is built. Then, the fault characteristics of the AC/DC distribution network in different stages, such as the capacitor discharge stage, inductive renewal stage, and steady state stage, is analyzed. Finally, detailed simulation analysis is conducted using PSCAD/EMTDC to validate the effectiveness of the developed scheme by the superior approximation performance between simulated curves and calculated curves.

Co-Regulating Solvation Structure and Hydrogen Bond Network via Bio-Inspired Additive for Highly Reversible ZincAnode.

The feasibility of aqueous zinc-ion batteries for large-scale energy storage is hindered by the inherent challenges of Zn anode. Drawing inspiration from cellular mechanisms governing metal ion and nutrient transport, erythritol is introduced, a zincophilic additive, into the ZnSO4 electrolyte. This innovation stabilizes the Zn anode via chelation interactions between polysaccharides and Zn2+. Experimental tests in conjunction with theoretical calculation results verified that the erythritol additive can simultaneously regulate the solvation structure of hydrated Zn2+ and reconstruct the hydrogen bond network within the solution environment. Additionally, erythritol molecules preferentially adsorb onto the Zn anode, forming a dynamic protective layer. These modifications significantly mitigate undesirable side reactions, thus enhancing the Zn2+ transport and deposition behavior. Consequently, there is a notable increase in cumulative capacity, reaching 6000mA h cm⁻2 at a current density of 5mA cm-2. Specifically, a high average coulombic efficiency of 99.72% and long cycling stability of >500 cycles are obtained at 2mA cm-2 and 1mA h cm-2. Furthermore, full batteries comprised of MnO2 cathode and Zn anode in an erythritol-containing electrolyte deliver superior capacity retention. This work provides a strategy to promote the performance of Zn anodes toward practical applications.

MXene Supported Electrodeposition Engineering of Layer Double Hydroxide for Alkaline Zinc Batteries.

The main challenges faced by aqueous rechargeable nickel-zinc batteries are their comparatively low energy density and poor cycling stability. Moreover, the preparation procedures of these cathodes are complex and not easily scalable. Herein, we utilized MXenetoimprove the electrodeposition preparation of NiCo layered double hydroxides (LDH). Benefiting from the improved interfacial contact between nickel foam (NF) and platting solution and the enhanced ionic conductivity of platting product based on MXene additives, the resulting binder-free NiCo LDH electrode can achieve ultrahigh areal loading (~65 mg cm-2) with abundant active surface for redox reactions and maintained short transport pathway for ion diffusion and charge transfer. Furthermore, the as-fabricated alkaline NiCo LDH-based battery delivers high discharge capacity, up to 20.2 mAh cm-2 (311 mAh g-1), accompanied by remarkable rate performance (9.6 mAh cm-2 or 148 mAh g-1 at 120 mA cm-2). Due to the high structural and chemical stability of MXenes/LDH-based electrode, excellent cycling life can also be achieved with 88.6% capacity retention after 10000 cycles. In addition, ultrahigh areal energy density (31.2 mWh cm-2) and gravimetric energy density (465 Wh kg-1) can be simultaneously achieved. This work has inspired the design of advanced cathode materials to develop high-performance aqueous zinc batteries.

A Microscopically Heterogeneous Colloid Electrolyte for Extremely Fast-Charging and Long-Calendar-Life Silicon-Based Lithium-Ion Batteries.

Fast-charging capability and calendar life are critical metrics in rechargeable batteries, especially in silicon-based batteries that are susceptible to sluggish Li+desolvation kinetics and HF-induced corrosion. No existing electrolyte simultaneously tackles both these pivotal challenges. Here we report a microscopically heterogeneous covalent organic nanosheet (CON) colloid electrolyte for extremely fast-charging and long-calendar-life Si-based lithium-ion batteries. Theoretical calculations and operando Raman spectroscopy reveal the fundamental mechanism of the multiscale noncovalent interaction, which involves the mesoscopic CON attenuating the microscopic Li+-solvent coordination, thereby expediting the Li+desolvation kinetics. This electrolyte design enables extremely fast-charging capabilities of the full cell, both at 8C (83.1% state of charge) and 10C (81.3% state of charge). Remarkably, the colloid electrolyte demonstrates record-breaking cycling performance at 10C (capacity retention of 92.39% after 400 cycles). Moreover, benefiting from the robust adsorption capability of mesoporous CON towards HF and water, a notable improvement is observed in the calendar life of the full cell. This study highlights the role of microscopically heterogeneous colloid electrolytes in enhancing the fast-charging capability and calendar life of Si-based Li-ion batteries. Our work offers fresh perspectives on electrolyte design with multiscale interactions, providing insightful guidance for the development of alkali-ion/metal batteries operating under harsh environments.

Ab Initio Prediction of Two-Dimensional GeSiBi2 Monolayer as Potential Anode Materials for Sodium-Ion Batteries.

The conceptualization and deployment of electrode materials for rechargeable sodium-ion batteries are key concerns for next-generation energy storage systems. In this contribution, the configuration stability of single-layer GeSiBi2 is systematically discussed based on first-principles calculations, and its potential as an anode material is further investigated. It is demonstrated that the phonon spectrum confirms the dynamic stability and the adsorption energy identifies a strong interaction between Na atoms and the substrate material. The electronic bands indicative of inherent metallicity contribute to the enhancement of electronic conductivity after Na adsorption. The multilayer adsorption of Na provides a theoretical capacity of 361.7 mAh/g, which is comparable to that of other representative two-dimensional anode materials. Moreover, the low diffusion barriers of 0.19 and 0.15 eV further guarantee the fast diffusion kinetics. These contributions signal that GeSiBi2 can be a compatible candidate for sodium-ion batteries anodes.

Developing a Multifunctional Cathode for Photoassisted Lithium-Sulfur Battery.

Integration of solar cell and secondary battery cannot only promote solar energy application but also improve the electrochemical performance of battery. Lithium-sulfur battery (LSB) is an ideal candidate for photoassisted batteries owing to its high theoretical capacity. Unfortunately, the researches related the combination of solar energy and LSB are relatively lacking. Herein, a freestanding photoelectrode is developed for photoassisted lithium-sulfur battery (PALSB) by constructing a heterogeneous structured Au@N-TiO2 on carbon cloths (Au@N-TiO2/CC), which combines multiple advantages. The Au@N-TiO2/CC photoelectrode can produce the photoelectrons to facilitate sulfur reduction during discharge process, while generating holes to accelerate sulfur evolution during charge process, improving the kinetics of electrochemical reactions. Meanwhile, Au@N-TiO2/CC can work as an electrocatalyst to promote the conversion of intermediate polysulfides during charge/discharge process, mitigating induced side reactions. Benefiting from the synergistic effect of electrocatalysis and photocatalysis, PALSB assembled with an Au@N-TiO2/CC photoelectrode obtains ultrahigh specific capacity, excellent rate performance, and outstanding cycling performance. What is more, the Au@N-TiO2/CC assembled PALSB can be directly charged under light illumination. This work not only expands the application of solar energy but also provides a new insight to develop advanced LSBs.

Al–Ta dual-substituted Li7La3Zr2O12 ceramic electrolytes with two-step sintering for Stable All-solid-state Lithium Batteries

Cubic phase Li7La3Zr2O12 (LLZO) is a promising electrolyte material for all-solid-state rechargeable lithium-ion batteries. The homogeneous densification of the garnet solid electrolyte ceramic material is crucial for enhancing its ionic conductivity performance. Herein, an Al/Ta co-doped strategy is employed to stabilize the cubic phase structure of LLZO and is combined with a two-step sintering method to enhance densification, in order to investigate its effect on microstructure, ionic conductivity, and electrochemical properties. During the formation process, amorphous Li2O reacts with doped Al2O3 to create a Li–Al–O liquid phase at the grain boundaries. Combined with two-step sintering to ensure that the desired material transformation is achieved, resulting in a dense microstructure and better mechanical properties. The solid electrolyte Li6.4Al0.1La3Zr1.7Ta0.3O12 under two-step sintering (LLZATO-2) is successfully synthesized, delivering an ionic conductivity up to 7.33 × 10−4 S cm−1 at room temperature and an activation energy of 0.22 eV. This work also highlights the critical role of co-doping combined with two-step sintering in preparing well-performing solid-state electrolytes and all-solid-state lithium-ion batteries.

A Coplanar Edible Rechargeable Battery with Enhanced Capacity

A Coplanar Edible Rechargeable Battery with Enhanced Capacity

Oxygen-bridging Fe, Co dual-metal dimers boost reversible oxygen electrocatalysis for rechargeable Zn–air batteries

Rechargeable zinc-air batteries (ZABs) are regarded as a remarkably promising alternative to current lithium-ion batteries, addressing the requirements for large-scale high-energy storage. Nevertheless, the sluggish kinetics involving oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) hamper the widespread application of ZABs, necessitating the development of high-efficiency and durable bifunctional electrocatalysts. Here, we report oxygen atom-bridged Fe, Co dual-metal dimers (FeOCo-SAD), in which the active site Fe-O-Co-N6 moiety boosts exceptional reversible activity toward ORR and OER in alkaline electrolytes. Specifically, FeOCo-SAD achieves a half-wave potential (E1/2) of 0.87 V for ORR and an overpotential of 310 mV at a current density of 10 mA cm-2 for OER, with a potential gap (ΔE) of only 0.67 V. Meanwhile, FeOCo-SAD manifests high performance with a peak power density of 241.24 mW cm-2 in realistic rechargeable ZABs. Theoretical calculations demonstrate that the introduction of an oxygen bridge in the Fe, Co dimer induced charge spatial redistribution around Fe and Co atoms. This enhances the activation of oxygen and optimizes the adsorption/desorption dynamics of reaction intermediates. Consequently, energy barriers are effectively reduced, leading to a strong promotion of intrinsic activity toward ORR and OER. This work suggests that oxygen-bridging dual-metal dimers offer promising prospects for significantly enhancing the performance of reversible oxygen electrocatalysis and for creating innovative catalysts that exhibit synergistic effects and electronic states.