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Tiny NiSnO3 nanoparticles with the assistance of polyvinylpyrrolidone (PVP) are prepared to uniformly and stably "bond" on the surface of graphene to form a stable NiSnO3/RGO-PVP structure. At the same time, the excellent performance of lithium-ion batteries (LIBs) with the use of NiSnO3/RGO-PVP structure is verified through a dual combination of experiment and theory. The resulting NiSnO3/RGO-PVP structure enhanced the performance of LIBs with high cycling stability and better rate capability; even after undergoing rate performance tests at different high current densities, the NiSnO3/RGO-PVP electrode can still reach a capacity of 624 mA h g−1 at 200 mA g−1 after 400 cycles. The superior electrochemical performance of NiSnO3/RGO-PVP nanocomposites can be attributed to the synergistic effects between tiny NiSnO3 nanoparticles synthesized with the assistance of PVP and RGO, which can be verified through first-principles calculations based on DFT. The charge transfer between NiSnO3 and RGO through an electron density difference indicates a strong interaction between the two. Meanwhile, the low adsorption energies (−3.914, −0.77, and −0.65 eV), low diffusion barriers (0.025, 0.49, and 0.141 eV), and high diffusion coefficients (1.79 × 10−3, 5.38 × 10−11, and 2.97 × 10−5 cm2 s−1) of lithium ions at three different positions indicate the excellent rate performance of the NiSnO3/RGO-PVP heterostructure, which is consistent with experimental results. This work analyzes the excellent electrochemical performance of NiSnO3/RGO-PVP from the experimental results and supports the reliability of the experimental results through theoretical calculations. [ABSTRACT FROM AUTHOR]

Metal–Organic Polymers (MOPs) have attracted growing attention for lithium-ion battery (LIB) applications due to their merits in orderly ionic transportation and robust structure stability in electrochemical reactions. However, they suffer from poor electronic conductivity. In this work, we apply first-principles density functional theory to explore the potential of three one-dimensional (1D) electrically conductive C6H2S4TM (TM = Fe, Co, and Ni) MOPs with the π–d conjugated coordination as anode materials for Li+ ions storage. Our theoretical results reveal that these 1D MOPs possess a superior theoretical capacity of over 748 mA h g−1. In particular, the 1D C6H2S4Ni MOP shows an exceptional theoretical specific capacity of 1110 mA h g−1 based on the three-electron transferring reaction, which significantly outperforms the traditional graphite-based anode material in LIBs. Moreover, the resonant charge transfer between Ni metal and ligand within the 1D C6H2S4Ni MOP reduces the diffusion energy barrier of the Li atoms when they migrate on the surface of the MOP. The ultrahigh theoretical specific capacity of the C6H2S4Ni MOP predicts that it can be a promising anode material for LIBs. [ABSTRACT FROM AUTHOR]

This study presents a novel approach to developing high-performance lithium-ion battery electrodes by loading titania-carbon hybrid spherogels with sulfur. The resulting hybrid materials combine high charge storage capacity, electrical conductivity, and core-shell morphology, enabling the development of next-generation battery electrodes. We obtained homogeneous carbon spheres caging crystalline titania particles and sulfur using a template-assisted sol-gel route and carefully treated the titania-loaded carbon spherogels with hydrogen sulfide. The carbon shells maintain their microporous hollow sphere morphology, allowing for efficient sulfur deposition while protecting the titania crystals. By adjusting the sulfur impregnation of the carbon sphere and varying the titania loading, we achieved excellent lithium storage properties by successfully cycling encapsulated sulfur in the sphere while benefiting from the lithiation of titania particles. Without adding a conductive component, the optimized material provided after 150 cycles at a specific current of 250 mA g-1 a specific capacity of 825 mAh g-1 with a Coulombic efficiency of 98%.

Transport properties are essential for the understanding and modeling of electrochemical cells, in particular complex systems like lithium-ion batteries. In this study, we demonstrate how a certain degree of freedom in the choice of variables allows us to efficiently determine a complete set of transport properties. We apply the entropy production invariance condition to different sets of electrolyte variables and obtain a general set of formulas. We demonstrate the application of these formulas to an electrolyte typical for lithium-ion batteries, 1M lithium hexafluoro-phosphate in a 1:1 wt. % mixture of ethylene and diethyl carbonates. While simplifications can be introduced, they provide inadequate predictions of conductivity and transport numbers, and we argue that a full matrix of Onsager coefficients is needed for adequate property predictions. Our findings highlight the importance of a complete set of transport coefficients for accurate modeling of complex electrochemical systems and the need for careful consideration of the choice of variables used to determine these properties. [ABSTRACT FROM AUTHOR]

With the growing prevalence of neuromorphic computing algorithms, there is a growing need for electronic synaptic devices. In this study, using Li4+ x Ti5O12 (LTO) as the resistive switching layer, C as the lithium ions storage layer, and Li1+ x Al x Ti2− x (PO4)3 (LATP) as ions transmission layer, a synaptic device is designed with the structure of Pt/C/LATP/LTO/PtSi to imitate the lithium-ion battery. Variation of the thickness of the LATP layer in the LTO device is explored to show the impact on the device's synaptic performance. With a LATP thickness of 100 nm, the LTO synaptic device exhibits a high potentiation/depression cyclic stability of over 50 cycles, improved potentiation/depression linearity and smoothness. The synaptic potentiation/depression is ascribed to migration of lithium ions from the LTO layer. A conductance relaxation characteristic of the device is explained by battery self-discharge phenomenon. The battery effect in the LTO device also led to generation of electromotive force. The study of battery-imitating LTO synaptic device offers new perspectives on the connection between battery and analog synaptic device. [ABSTRACT FROM AUTHOR]

Herein, initially, we present a general overview of the global financial support for chemistry devoted to materials science, specifically intercalation layered compounds (ILCs). Subsequently, the strategies to synthesise these host structures and the corresponding guest-host hybrid assemblies are exemplified on the basis of some families of materials, including pillared clays (PILCs), porous clay heterostructures (PCHs), zirconium phosphate (ZrP), layered double hydroxides (LDHs), graphite intercalation compounds (GICs), graphene-based materials, and MXenes. Additionally, a non-exhaustive survey on their possible application in the field of energy through electrochemical storage, mostly as electrode materials but also as electrolyte additives, is presented, including lithium technologies based on lithium ion batteries (LIBs), and beyond LiBs with a focus on possible alternatives such XIBs (X = Na (NIB), K (KIB), Al (AIB), Zn (ZIB), and Cl (CIB)), reversible Mg batteries (RMBs), dual-ion batteries (DIBs), Zn-air and Zn-sulphur batteries and supercapacitors as well as their relevance in other fields related to (opto)electronics. This selective panorama should help readers better understand the reason why ILCs are expected to meet the challenge of tomorrow as electrode materials. [ABSTRACT FROM AUTHOR]

Fe2NiSe4@holey-graphene (FNS@HG) has been prepared by in situ growth and simultaneous perforation via a carbothermal reaction. The generation of nanoholes on the graphene sheets significantly reduced the diffusion distance of electrolyte ions, enhancing the rate capability of FNS@HG as an anode material for sodium-ion batteries. [ABSTRACT FROM AUTHOR]

Na 2 Ti 4 O 9 (NTO), an important chemical material, is used in chemical pigments, lithium ion batteries, catalyst carriers, and other fields. Nanoscale NTO crystal was firstly obtained by solvothermal process in this study, and the reactant conditions (time, temperature, solvent, and concentration of NaOH solution) for preparing NTO crystal were investigated. The result reveals that the as-prepared NTO crystal with one-dimensional (1D) rod-like morphology can be obtained in a solvent environment with H 2 O to C 2 H 5 OH via solvothermal process. And then investigating the formation mechanism of 1D NTO crystal based on the solvothermal soft chemical method. In addition, NTO crystal was utilized as the precursor for BaTiO 3 (BT) crystal at desired condition. The [010]-oriented BT polycrystals were directly obtained with NTO precursor via hydrothermal process in low concentration of Ba(OH) 2 solution. The transformation mechanism between BT polycrystals and NTO precursor was revealed, and the process of obtaining functional materials directly from NTO precursor was discussed. The study provides a novel way for the development of small-size barium titanate based functional materials. [ABSTRACT FROM AUTHOR]

Addressing the need for multiple health indicators is critical to improving prediction accuracy and reducing the limitation of reliance on a single health indicator. This paper presents an AutoML model for accurately forecasting the life span of lithium-ion batteries (LIBs) in electric vehicles. Unlike previous studies focusing solely on constant current (CC) and constant voltage (CV) charging, our AutoML approach includes ICA and direct analysis to generate eight novel multi-dimensional health indicators. These novel comprehensive indicators characterizing battery aging, including the position values of CC charging (IC_CC_P), the peak of CV charging (IC_CV_ H), and the peak/position of CC discharging (IC_D_H, IC_D_ P), are chosen based on correlation analysis and combined with four health indicators from direct analysis, i.e., capacity, cycle, cluster, and checkpoint, to improve prediction accuracy. K-means clustering is employed to group similar data points. At the same time, the ruptures library facilitates the implementation of a novel algorithm for change point detection, allowing for the identification of checkpoints within each battery dataset. Experimental validation using NASA's AMES LIB cycle life datasets demonstrates a significant performance improvement from existing recent methods, with 58.93 % lower mean absolute error (MAE) and 52.66 % lower root-mean-square error (RMSE) compared to recent AutoML-based methods. This shows a significant improvement in forecasting the RUL of electric vehicle LIBs using the proposed AutoML-based approach with novel multi-dimensional health indicators. [ABSTRACT FROM AUTHOR]

• CaCl 2 is an additive suitable for pyrometallurgical recovery of spent LIBs. • CaCl 2 has good chlorination ability and slag optimization ability. • SiO 2 and CO 2 in the system contribute to the increase in HCl yield. The difficulty of separating Li during pyrometallurgical smelting of spent lithium-ion batteries (LIBs) has limited the development of pyrometallurgical processes. Chlorination enables the conversion of Li from spent LIBs to the gas phase during the smelting process. In this paper, the effects of four solid chlorinating agents (KCl, NaCl, CaCl 2 and MgCl 2) on Li volatilization and metal (Co, Cu, Ni and Fe) recovery were investigated. The four solid chlorinating agents were systematically compared in terms of the direct chlorination capacities, indirect chlorination capacities, alloy physical losses and chemical losses in the slag. CaCl 2 was better suited for use as a solid chlorinating agent to promote Li volatilization due to its excellent results in these indexes. The temperature required for the release of HCl from MgCl 2 , facilitated by CO 2 and SiO 2 , was lower than 500 °C. The prematurely released HCl failed to participate in the chlorination reaction. This resulted in approximately 12 % less Li volatilization when MgCl 2 was used as a chlorinating agent compared to when CaCl 2 was used. In addition, the use of KCl as a chlorinating agent decreased the chemical dissolution loss of alloys in the slag. The performance of NaCl was mediocre. Finally, based on evaluations of the four indexes, recommendations for the selection and optimization of solid chlorinating agents were provided. [ABSTRACT FROM AUTHOR]

The accurate health status evaluation of lithium-ion batteries is crucial for preemptive identification of potential battery failures and averting hazardous incidents, given its essential role in indicating the extent of battery degradation. The challenge in determining the State of Health (SOH) arises from the absence of a precise and standardized definition, as well as the difficulty in measuring essential input variables. Therefore, this paper utilizes current and voltage data during the charge and discharge process as direct inputs for SOH estimation and proposes a deep learning-based lithium-ion battery SOH estimation approach. Specifically, it leverages Bayesian optimized Convolutional Neural Network (CNN) within a data-driven framework. Experimental results demonstrate that the proposed deep learning method achieves a Mean Absolute Error (MAE) of 1% and a Maximum Error (MAX) below 4% in estimation accuracy, highlighting its enhanced precision and robustness. [ABSTRACT FROM AUTHOR]

A variety of strategies have been developed to enhance the cycling stability of Si-based anodes in lithium-ion batteries. Although significant progress has been made in enhancing the cycling stability of Si-based anodes, the low initial Coulombic efficiency (ICE) remains a significant challenge to their commercial application. Herein, pitch-based carbon (C) coated Si nanoparticles (NPs) were wrapped by graphene (G) to obtain Si@C/G composite with a small specific surface area of 11.3 m2 g−1, resulting in a high ICE of 91.2% at 500 mA g−1. Moreover, the integrated utilization of graphene and soft carbon derived from the low-cost petroleum pitch strongly promotes the electrical conductivity, structure stability, and reaction kinetics of Si NPs. Consequently, the synthesized Si@C/G with a Si loading of 54.7% delivers large reversible capacity (1191 mAh g−1 at 500 mA g−1), long cycle life over 200 cycles (a capacity retention of 87.1%), and superior rate capability (952 mAh g−1 at 1500 mA g−1). When coupled with a homemade LiNi0.8Co0.1Mn0.1O2 (NCM811) cathode in a full cell, it exhibits a promising cycling stability for 200 cycles. This work presents an innovative approach for the manufacture of Si-based anode materials with commercial application. [ABSTRACT FROM AUTHOR]

[Display omitted] Owing to highly theoretical capacity of 3579 mAh/g for lithium-ion storage at ambient temperature, silicon (Si) becomes a promising anode material of high-performance lithium-ion batteries (LIBs). However, the large volume change (∼300 %) during lithiation/delithiation and low conductivity of Si are challenging the commercial developments of LIBs with Si anode. Herein, a sandwich structure anode that Si nanoparticles sandwiched between carbon nanotube (CNT) and silicon carbide (SiC) has been successfully constructed by acetylene chemical vapor deposition and magnesiothermic reduction reaction technology. The SiC acts as a stiff layer to inhibit the volumetric stress from Si and the inner graphited CNT plays as the matrix to cushion the volumetric stress and as the conductor to transfer electrons. Moreover, the combination of SiC and CNT can relax the surface stress of carbonaceous interface to synergistically prevent the integrated structure from the degradation to avoid the solid electrolyte interface (SEI) reorganization. In addition, the SiC (1 1 1) surface has a strong ability to adsorb fluoroethylene carbonate molecule to further stabilize the SEI. Consequently, the CNT/SiNPs/SiC anode can stably supply the capacity of 1127.2 mAh/g at 0.5 A/g with a 95.6 % capacity retention rate after 200 cycles and an excellent rate capability of 745.5 mAh/g at 4.0 A/g and 85.5 % capacity retention rate after 1000 cycles. The present study could give a guide to develop the functional Si anode through designing a multi-interface with heterostructures. [ABSTRACT FROM AUTHOR]

Lithium-ion batteries are widely used in portable electronic devices because of their high energy and power density. To enhance the energy density of these batteries, one strategy involves increasing the active material loading by increasing the thickness of the electrodes. In previous studies, we demonstrated that powder extrusion moulding (PEM) is a scalable and efficient method for producing additive-free LTO and LFP ceramic electrodes, which exhibit remarkable electrochemical performance with thicknesses up to 500 μm. This study focuses on the preparation and optimisation of the entire manufacturing process for thick ceramic electrodes of LiCoO 2 (LCO) with a high mass loading of 180 mg cm−2 using the PEM process. Different powder loadings of mixtures of LCO and a thermoplastic multi-component binder were explored to obtain a formulation suitable for rheology. The optimal formulation comprises 60 vol% of powder. After binder removal via a combination of solvent and thermal treatment, followed by air sintering, parts with varying porosities were obtained. Striking a balance between porosity and thermal degradation is crucial for achieving optimal electrochemical behaviour. Electrochemical evaluations of the electrodes sintered at 900 °C and 1000 °C revealed areal capacity values as high as 17 mAh cm−2 at C/25 and 7 mAh cm−2 at C/6.25, respectively. These values far exceed the 1−2 mAh cm−2 obtained from commercial LCO electrodes. These results indicate a strategy for the production of electrodes to fabricate lithium-ion batteries with a low ratio of inactive materials and, therefore, with higher energy densities. [ABSTRACT FROM AUTHOR]

Titanium niobium oxides (TNO) are chemically recovered from a mineral composed of cassiterite, columbotantalite, rutile and wollastonite. The process involves a series of steps, including pyrometallurgical processes, leaching, and liquid-liquid extraction. It takes advantage of the naturally occurring Ti in the extracted mineral, avoiding the separation of Ti and Nb to directly obtain the valuable Ti–Nb–O compounds. Two compositions can be obtained (Ti 2 Nb 10 O 29 or TiNb 2 O 7 , named TNO-cal and TNO-black, respectively) depending on the thermal treatment after the chemical separation from the original mineral. These compounds have been characterized to describe their composition, morphology and crystallographic properties. The recovered material, without any further purification or functionalization, has been studied as anodes in Lithium-ion batteries (LIBs). Different electrochemical behavior has been observed for voltage ranges of 1–3 V and 0.01–3 V, being the second range which gives best results. In the 1–3V range, TNO-black exhibits a reversible capacity of up to 101.4 mA h g−1 at 1C and maintains 97 % capacity retention after 200 cycles, this is mainly due to Li + insertion/de-insertion processes. Additionally, when expanding the voltage range down to 0.01V, TNO-black displays a specific capacity of approximately 139.1 mA h g−1 after 200 cycles at 1C, whereas TNO-cal reaches a specific capacity of 169 mA h g−1. Extended cycling experiments at a 1C rate for both electrodes reveal that after 200 cycles samples deliver efficiencies relative to the maximum discharge capacity values of 83.4 % (TNO-cal) and 64.4 % (TNO-black), with mean coulombic efficiencies of 97.5 %. These results demonstrate that the recovered materials can effectively function as anodes for LIBs, offering promising application potential, despite the presence of residual silica from the mining process. [ABSTRACT FROM AUTHOR]

As lithium-ion batteries are widely used in electric vehicles, safety accidents caused by battery failures emerge one after another. Nevertheless, failures caused by changes in the internal structure or characteristics of the battery, such as sudden and progressive failures, are still a serious problem for electric vehicles, challenging existing fault diagnosis methods. This paper first performs wavelet packet decomposition on the battery's raw voltage signal to obtain high-quality low-frequency and high-frequency characteristic signal components. Then performs singular value decomposition on the characteristic signal components to extract the corresponding singular value characteristic parameters, and introduces the Manhattan average distance algorithm to battery faults. Diagnosing and locating faulty battery units using the Laida criterion (3-σ criterion) outlier detection method. Finally, actual vehicle data were used to verify the reliability, stability, accuracy of the method, and compared with the traditional Manhattan distance, correlation coefficient, information entropy methods. The method in this paper has good fault detection effects on vehicles with sudden and progressive faults vehicles. [ABSTRACT FROM AUTHOR]

Wearable electronics are surging for various applications ranging from critical functions like personal health monitoring to communication and entertainment. To power these electronic devices, advanced high‐performing textile‐based batteries are reckoned. In this work, a 1D textile yarn battery is designed using silicon (Si) nanoparticles wrapped in molybdenum disulfide (MoS2) as an anode and layered Ni‐rich material Li[Ni0.8Co0.1Mn0.1]O2 (NCM) as a cathode. The anode materials design is selected to ensure the use of Si due to its high specific capacity but suppressing its known issue of volume expansion by layered MoS2 nanosheets and, at the same time, MoS2 providing channels for lithium‐ion (Li‐ion) transport during electrochemical cycles. The NCM cathode, on the other hand, is adopted as it has higher energy density and improved cycle life. The full yarn battery (FYB) delivered an excellent electrochemical performance (areal capacity of 3.13 mAh cm−2, power density of 421 mW cm−3, and energy density of 78.9 mWh cm−3) with a capacity retention of 86% at 0.1 C and coulombic efficiency of 91.3%. This work pointed out a new way to design and fabricate textile‐based batteries with high‐performance materials using simple, cost‐effective, and scalable approaches targeting to be used as energy sources for future wearable electronics. [ABSTRACT FROM AUTHOR]

Self-discharge and chemically induced mechanical effects degrade calendar and cycle life in intercalation-based electrochromic and electrochemical energy storage devices. In rechargeable lithium-ion batteries, self-discharge in cathodes causes voltage and capacity loss over time. The prevailing self-discharge model centers on the diffusion of lithium ions from the electrolyte into the cathode. We demonstrate an alternative pathway, where hydrogenation of layered transition metal oxide cathodes induces self-discharge through hydrogen transfer from carbonate solvents to delithiated oxides. In self-discharged cathodes, we further observe opposing proton and lithium ion concentration gradients, which contribute to chemical and structural heterogeneities within delithiated cathodes, accelerating degradation. Hydrogenation occurring in delithiated cathodes may affect the chemo-mechanical coupling of layered cathodes as well as the calendar life of lithium-ion batteries. [ABSTRACT FROM AUTHOR]

The application of micron silicon suboxide (μ-SiOx) as an anode material for commercial lithium-ion batteries (LIBs) is hindered by lower conductivity and significant volume expansion. To effectively address the inherent defects of μ-SiOx, in this study, we developed a strategy to confine μ-SiOx to N-doped-carbon networks modified by Sn nanoparticles to form a SiOx@NC/Sn composite, which utilizes tin salts for protein denaturation and NaCl as a pore-forming agent. The coexistence of Sn and N with carbon forms a conductive network, facilitating the migration of lithium ions and electrons and maintaining the structural stability of the SiOx@NC/Sn composite. SiOx@NC/Sn with a carbon content of 50.8% as the anode for LIBs exhibits long-term stability (801.1 mA h g−1 after 200 cycles at a current density of 0.2 A g−1) and rate capability (401.9 mA h g−1 at a current density of 5.0 A g−1). Moreover, the full cell demonstrates a capacity retention rate surpassing 75% after 100 cycles at 0.5C. This work provides a simple and low-cost strategy for preparing metal-modified and nitrogen doped-carbon materials for LIBs. [ABSTRACT FROM AUTHOR]

Lithium-ion batteries have the advantages of high energy density and high cycle times, and have been widely used in portable electronic devices, electric vehicles, and large-scale energy storage. However, lithium-ion batteries are prone to thermal runaway. Subsequently, electrolyte decomposition and combustion occur, leading to an increase in battery temperature and even causing fires or explosions. In order to explore the reaction mechanism of thermal runaway in lithium-ion battery electrolytes, the volatile and combustible organic solvents are selected as the research object. Three different organic solvents were established, namely pure ethylene carbonate (C 3 H 4 O 3) solvent and its mixture with dimethyl carbonate (C 3 H 6 O 3) and diethyl carbonate (C 5 H 10 O 3), respectively. The effect of heating on the thermal runaway of organic solvents was studied using reactive force field molecular dynamics (ReaxFF MD). All three organic solvents will produce a large amount of CH 2 free groups and flammable organic substances such as C 2 H 4 during pyrolysis, which is the main reason for thermal runaway of lithium-ion batteries. The research results may contribute to preventing and suppressing thermal runaway in lithium-ion batteries. [Display omitted] • EC pyrolysis yields significantly more CO 2 and H 2 O than DMC and DEC. • DMC hinders the decomposition of EC, while DEC promotes the pyrolysis of EC. • During pyrolysis, organic solvents yield abundant CH 2 radicals and flammable C 2 H 4. [ABSTRACT FROM AUTHOR]

Solid-state Li-ion batteries, based on Ni-rich oxide cathodes and Li-metal anodes, can theoretically reach a high specific energy of 393 Wh kg−1 and hold promise for electrochemical storage. However, Li intercalation-induced dimensional changes can lead to crystal defect formation in these cathodes, and contact mechanics problems between cathode and solid electrolyte. Understanding the interplay between cathode microstructure, operating conditions, micromechanics of battery materials, and capacity decay remains a challenge. Here, we present a microstructure-sensitive chemo-mechanical model to study the impact of grain-level chemo-mechanics on the degradation of composite cathodes. We reveal that crystalline anisotropy, state-of-charge-dependent Li diffusion rates, and lattice dimension changes drive dislocation formation in cathodes and contact loss at the cathode/electrolyte interface. These dislocations induce large lattice strain and trigger oxygen loss and structural degradation preferentially near the surface area of cathode particles. Moreover, contact loss is caused by the micromechanics resulting from the crystalline anisotropy of cathodes and the mechanical properties of solid electrolytes, not just operating conditions. These findings highlight the significance of grain-level cathode microstructures in causing cracking, formation of crystal defects, and chemo-mechanical degradation of solid-state batteries. The performance of solid-state batteries is affected by stress responses of their complex microstructure to volume changes from Li+ intercalation. Here, authors present a chemo-mechanical model to study the impact of grain-level chemo-mechanics on the degradation of composite positive electrodes. [ABSTRACT FROM AUTHOR]

Increasing the charging cut‐off voltage can significantly improve the capacity of LiCoO2 cathode. However, when the cut‐off voltage exceeds 4.5 V (vs Li/Li+), LiCoO2 undergoes irreversible phase transitions, leading to particle cracking and structural failure. Additionally, the decomposition of the electrolyte compromises the stability of the cathode/electrolyte interface, resulting in diminished battery capacity. Herein, the elements Al, Mg, and Zr are doped into single‐crystal LiCoO2 to enhance the structural stability of LiCoO2. Moreover, a 3 Å zeolite film is used to regulate the solvation structure to enhance the oxidation resistance of the electrolyte. This design enables a more stable cathode/electrolyte interface during high‐voltage cycling. At a cut‐off voltage of 4.8 V, the Li||LiCoO2 battery exhibits an initial discharge capacity of 236.2 mAh g−1 at 0.1 C and maintains 86.6% capacity retention after 100 cycles at 1 C. The pouch full cell, which utilizes a graphite anode and LiCoO2 cathode, operating within a charge–discharge range of 2.8–4.65 V, achieves a specific energy of 276 Wh kg−1 with 81% capacity retention after 200 cycles. This work introduces a desolvated electrolyte into the LiCoO2 battery system, providing a professional approach to addressing the challenges of high‐voltage LiCoO2. [ABSTRACT FROM AUTHOR]

Small molecule organic materials are widely used as anode materials for lithium‐ion batteries (LIBs) due to their high reversible capacity, designable structure, and environmental friendliness. However, they suffer from poor intrinsic electronic conductivity, severe dissolution, and low initial coulombic efficiency. Recently, metal–organic frameworks (MOFs) have demonstrated in metal‐ion batteries, outperforming some small molecule organic materials in terms of both cycling stability and rate capability. Herein, the first rational design and synthesis of a new cobalt‐based MOF (CoBPDCA), are reported employing cobalt(II) nitrate as the metal source and small organic molecules (2,2‐bipyridyl‐4,4‐dicarboxylic acid, BPDCA) as the ligands, which shows exceptional chemical stability and impressive electron conductivity. Most importantly, CoBPDCA electrodes deliver a high reversible capacity of 1112.9 mAh g−1 at 0.05 C (1 C = 1000 mA g−1) and outstanding high‐rate durability (166.3 mAh g−1 after 2500 cycles at 10 C). Employing a series of spectroscopic and morphological characterizations and density functional theory (DFT) calculations, it is revealed that these impressively electrochemical performances are contributed to the dual active redox centers of Co cations and BPDCA ligands (CN and CO groups), and the superb electron conductivity. This work might provide a new strategy and a deeper understanding of the other MOFs' development for LIBs. [ABSTRACT FROM AUTHOR]

Operating a lithium‐ion battery (LIB) in a wide temperature range is essential for ensuring a stable electricity supply amidst fluctuating temperatures caused by climate or terrain changes. Electrolyte plays a pivotal role in determining the temperature durability of batteries. However, specialized electrolytes designed for either low or high temperatures typically possess distinct features. Therefore, wide‐temperature electrolytes (WTEs) are necessary as they encompass a combination of diverse properties, which complicates the clear instruction of WTE design. Here we represent an artificial intelligence (Al)‐assisted workflow of WTE design through stepwise parameterizations and calculations. Linear mono‐nitriles are identified as ideal wide‐liquidus‐range solvents that can "softly" solvate lithium ions by weak interactions. In addition, the explainable modules revealed the halogenoid similarity of cyanide as fluorine on the electrolyte properties (e.g. boiling point and dielectric constant). With the further introduction of an ether bond, 3‐methoxypropionitrile (MPN) has been eventually determined as a main electrolyte solvent, enabling the battery operation from −60 to 120 °C. Particularly, a LiCoO2/Li cell using the proposed WTE can realize stable cycling with capacity retention reaching 72.3 % after 50 cycles under a high temperature of 100 °C. [ABSTRACT FROM AUTHOR]

Lithium-ion batteries (LIBs) have revolutionized portable electronics, yet their conventional graphite anodes face capacity limitations. Integrating graphene and 3D molybdenum disulfide (MoS2) offers a promising solution. Ensuring a uniform distribution of 3D MoS2 nanostructures within a graphene matrix is crucial for optimizing battery performance and preventing issues like agglomeration and capacity degradation. This study focuses on synthesizing a uniformly distributed paper wad structure by optimizing a composite of reduced graphene oxide RGO@MoS2 through structural and morphological analyses. Three composites with varying graphene content were synthesized, revealing that the optimized sample containing 30 mg RGO demonstrates beneficial synergy between MoS2 and RGO. The interconnected RGO network enhances reactivity and conductivity, addressing MoS2 aggregation. Experimental results exhibit an initially superior capacity of 911 mAh g−1, retained at 851 mAh g−1 even after 100 cycles at 0.1 A g−1 current density, showcasing improved rate efficiency and long-term stability. This research underscores the pivotal role of graphene content in customizing RGO@MoS2 composites for enhanced LIB performance. [ABSTRACT FROM AUTHOR]

In this study, CSs-g-C3N4 carbon and nitrogen composites based on glucose carbon spheres were successfully synthesized. A high-temperature and high-pressure hydrothermal reaction successfully induces the amidation of glucose with melamine, and led to the synthesis of CSs-g-C3N4 carbon and nitrogen composites. A series of characterization tests and electrochemical tests revealed the lithium storage mechanism of the CSs-g-C3N4 composites. The experimental results show that the CSs-g-C3N4 composites exhibit excellent cycling performance in lithium-ion battery anode applications. Specifically, after 300 cycles at a current density of 1 A g−1, the material still maintains a lithium storage capacity of 395.2 mA h g−1. This data fully demonstrates the superiority and stability of CSs-g-C3N4 composites as anode materials for lithium-ion batteries. In addition, the successful preparation of CSs-g-C3N4 composites not only demonstrates the technical feasibility of using g-C3N4 to prepare carbon and nitrogen composites, but also provides a new idea and direction for the research and development of anode materials for lithium-ion batteries. This achievement is expected to promote the wider application of g-C3N4 in the field of energy storage and further enhance the performance of lithium-ion batteries. [ABSTRACT FROM AUTHOR]

Li-rich Mn-based layered oxides provide a compelling amalgamation of high theoretical capacity and cost-effectiveness, positioning them as prime contenders for next-generation lithium-ion battery cathodes. However, their vulnerability to surface instability gives rise to a host of challenges, notably severe capacity and voltage fading. Consequently, the surface modification of Li-rich Mn-based layered oxides emerges as a viable solution to tackle this issue. Nevertheless, current methods exhibit various drawbacks, encompassing time-intensive procedures, environmental unfriendliness, and challenges in scalability. Hence, we present a technique employing ultrafast high-temperature heating technology to dynamically reshape the chemistry and structure of the surface of individual single-crystal Li1.2Mn0.54Ni0.13Co0.13O2 cathode particles (LMLO) within a rapid 8-second timeframe. Structural analysis reveals the seamless integration of the spinel structure onto the surface, intricately linked to the internal layered structure, accompanied by a notable abundance of oxygen vacancies. Leveraging the distinctive features of this modified structure, the material demonstrates enhanced discharge capacity, superior rate performance, and prolonged cycling stability compared to the unmodified counterpart. Significantly, in stark contrast to alternative preparation methods, this technique accomplishes the formation of the protective layer within a mere 8 seconds, showcasing unparalleled efficiency. Furthermore, it boasts safety and environmental friendliness, necessitates basic instrumentation, boasts ease of operation, and is well-suited for large-scale adoption. Consequently, this method is positioned to drive the commercialization of Li-rich Mn-based layered oxide cathode materials. [ABSTRACT FROM AUTHOR]

Electrodes are vital for lithium‐ion battery performance. The primary method for large‐scale electrode production involves wet slurry casting methods, which encounter challenges related to solvent usage, energy consumption, and mechanical stability. Dry processed (DP) electrodes are a promising alternative but struggle with rate capability and mechanical properties. Here, an approach of incorporating 1 wt.% flour into DP electrodes (DP–1%F) through a binder fibrillation strategy is introduced, which enhances the mechanical strength, rate performance, and cycling stability of the electrodes. The cross‐linking of protein and starch in flour, along with the fibrillation of Polytetrafluoroethylene (PTFE), enable the DP–1%F electrode to exhibit robust mechanical properties and high flexibility. Additionally, the incorporation of flour makes the DP electrode primarily create large pores, reducing electrode tortuosity, thereby endowing the DP–1%F electrode with improved kinetic behavior. The robust mechanical properties and improved kinetic behavior suppress the development of irreversible phase transitions and intragranular/intergranular cracks. These characteristics led to the superior cycling stability of the DP–1%F electrodes with a capacity retention of 80.3% after 260 cycles at 2C and 4.5 V (LiNi0.8Co0.1Mn0.1O2). The findings offer valuable insights for the development of high‐power, long‐life DP electrodes, addressing key challenges in lithium‐ion batteries. [ABSTRACT FROM AUTHOR]

Silicon (Si) is a promising anode material for high‐energy‐density lithium‐ion batteries. To achieve wide practical applications, it is highly desirable to build effective solidelectrolyte interphase (SEI) with high stability and high Li+ conductivity. Herein, a novel interface engineering strategy is demonstrated with the assistance of a surfactant and the self‐assembly of chitosan (CS) skin on Si surface. A high coating integrity of the Si particle is obtained compared to that without surfactants. Unlike traditional surface coatings, the positive charge of the applied CS layer enables it to selectively absorb PF6− anions in the electrolyte. The PF6− aggregates in Helmholtz layer lead to the formation of anion‐derived SEI enriched in LiF species. As the result, the prepared CS‐decorated Si anode exhibits a high initial coulombic efficiency of 92.2% and a high rate capability of 2200 mAh g−1 capacity at 10 C rate. After 500 charge–discharge cycles, it is still able to retain a reversible capacity 1621.3 mAh g−1. Furthermore, the excellent electrochemical property is demonstrated in full cells against NCM811 cathode. The novel interface engineering strategy provides a new SEI mechanism and demonstrates a feasible and effective way to develop high‐performance Si‐based lithium‐ion batteries. [ABSTRACT FROM AUTHOR]

In this work, a porous Co 3 O 4 anode material with capsule–shaped morphology is prepared by a simple solvothermal method and subsequent heat treatment process in air. The as–synthesized CoCO 3 precursor and Co 3 O 4 sample are systematically studied and analyzed by a series of testing technologies, such as XRD, FTIR, FESEM, (HR)TEM, TGA, XPS and N 2 adsorption/desorption measurement. As negative materials in Li–ion batteries, the Co 3 O 4 active material exhibits high charge/discharge specific capacity, good rate performance and satisfactory cycle stability. The excellent electrochemical properties are inevitably related to the structural characteristics of the electrode material itself, including regular morphology, rich pore structure, large specific surface area, high crystallinity, nanoscale particle size, etc. [ABSTRACT FROM AUTHOR]

A straightforward hydrothermal technique was employed to develop binder-free CaMoO 4 electrodes that can be utilized as electrodes in Li-ion batteries. Structural analysis was employed to validate the tetragonal scheelite structure and exceptional crystallinity of the electrodes. Examination with scanning electron microscopy revealed that the electrodes exhibited diverse morphologies, including nanorods, sheets, and flowers. The composition of CaMoO 4 was confirmed by analyzing the X-ray photoelectron spectroscopy data, which revealed distinct binding energy peaks corresponding to Ca, Mo, and O. The presence of these elements in the nanostructures was further confirmed by transmission electron microscopy and energy dispersive spectroscopy mapping. Electrochemical tests showed that CaMoO 4 (DIW@EG sample electrode) composite electrodes demonstrated an impressive primary discharge specific capacity of 2383 mAh g−1 and a high rate capacity of 1034 mAh g−1 at 0.5 A g−1 current density. Additionally, a full cell combining LCO with CaMoO 4 achieved a remarkable capacity of 321 mAh g−1 at a current density of 0.5 A g−1, presenting it as a viable substitute for the traditional LCO//graphite system. [ABSTRACT FROM AUTHOR]

Dual‐ion batteries (DIBs) represent a promising alternative for lithium ion batteries (LIBs) for various niche applications. DIBs with polymer‐based active materials, here poly(2,2,6,6‐tetramethylpiperidinyl‐N‐oxyl methacrylate) (PTMA), are of particular interest for high power applications, though they require appropriate electrolyte formulations. As the anion mobility plays a crucial role in transport kinetics, Li salts are varied using the well‐dissociating solvent γ‐butyrolactone (GBL). Lithium difluoro(oxalate)borate (LiDFOB) and lithium bis(oxalate)borate (LiBOB) improve cycle life in PTMA||Li metal cells compared to other Li salts and a LiPF6‐ and carbonate‐based reference electrolyte, even at specific currents of 1.0 A g−1 (≈10C), whereas LiDFOB reveals a superior rate performance, i. e. ≈90 % capacity even at 5.0 A g−1 (≈50C). This is attributed to faster charge‐transfer/mass transport, enhanced pseudo‐capacitive contributions during the de‐/insertion of the anions into the PTMA electrode and to lower overpotentials at the Li metal electrode. [ABSTRACT FROM AUTHOR]

Lithium‐ion batteries are commonly used for energy storage due to their long lifespan and high energy density, but the use of unsafe electrolytes poses significant health and safety concerns. An alternative source is necessary to maintain electrochemical efficacy. This research demonstrates new safe glyme‐based electrolytes for silica/carbon (SiOx/C) nanocomposite derived from Australian rice husk (RH). The quality of SiOx/C was preserved by using deep eutectic solvent‐based pre‐treatment and single‐step carbonization, which was confirmed through the X‐ray analysis of the crystalline phase of silica. The electrochemical assessment of SiOx/C anode using various glyme‐based electrolytes for LIBs was carried out. Among them, the resultant half cells based on diglyme electrolyte is superior to others with the first discharge capacity at 1274 mAh/g and a reversible discharge capacity of 759.7 mAh/g. Ex‐situ SEM and Time‐of‐Flight Secondary Ion Mass Spectrometry (ToF‐ SIMS) analysis of the electrode indicated that diglyme not only improves the capacity but also sustains the electrode architecture for longer cycle life with more LiF‐based components and also showed the absence of HF components. Importantly, the addition of fluoroethylene carbonate (FEC) additive enhanced the cycling stability. These results provide a new perspective on developing advanced SiOx/C anode using glyme electrolytes for Li‐ion batteries. [ABSTRACT FROM AUTHOR]

Electrolytes endowed with high oxidation/reduction interfacial stability, fast Li‐ion desolvation process and decent ionic conductivity over wide temperature region are known critical for low temperature and fast‐charging performance of energy‐dense batteries, yet these characteristics are rarely satisfied simultaneously. Here, we report anchored weakly‐solvated electrolytes (AWSEs), that are designed by extending the chain length of polyoxymethylene ether electrolyte solvent, can achieve the above merits at moderate salt concentrations. The −O−CH2−O− segment in solvent enables the weak four‐membered ring Li+ coordination structure and the increased number of segments can anchor the solvent by Li+ without largely sacrificing the ionic dissociation ability. Therefore, the single salt/single solvent AWSEs enable solvent co‐intercalation‐free behavior towards graphite (Gr) anode and high oxidation stability towards high‐nickel cathode (LiNi0.8Co0.1Mn0.1O2‐NCM811), as well as the formation of inorganic rich electrode/electrolyte interphase on both of them due to the anion‐rich solvation shells. The capacity retention of Gr||NCM811 Ah‐class pouch cell can reach 70.85 % for 1000 cycles at room‐temperature and 75.86 % for 400 cycles at −20 °C. This work points out a promising path toward the molecular design of electrolyte solvents for high‐energy/power battery systems that are adaptive for extreme conditions. [ABSTRACT FROM AUTHOR]

We introduce free-standing FeS2/carbon microlattice composites as electrodes for lithium-ion batteries through 3D printing. The computer-aided design allows for any shape. The microlattice features aligned microchannels, promoting ion transfer, while the carbon skeleton facilitates electron transfer. Overall, this study shows 3D printing is highly promising in advancing sustainable energy applications. [ABSTRACT FROM AUTHOR]

Tremendous efforts are made to enhance the energy density of lithium‐ion batteries, among which designing thick electrodes is a promising approach. Traditionally, kinetic effects are considered in constructing thick electrodes, such as decreasing the tortuosity to facilitate ion transport. This work innovatively investigates the coupling effect of kinetics and thermodynamics on electrode processes and conducts a competitive analysis between them by visualizing electrode processes. The results indicate that a sloping equilibrium potential curve facilitates the uniform utilization of electrodes, but severe kinetic constraints render the thermodynamic regulation ineffective. Thus, modifying the thermodynamic properties of the electrode to strengthen the regulatory effect is a promising approach. Kinetic constraints are the inherent factors limiting the capacity release of batteries. An in‐depth analysis reveals that ensuring the hybrid control of ions and electrons can significantly alleviate kinetic reaction heterogeneity. As a proof‐of‐concept, thick electrodes with vertical channels are constructed, enabling thermodynamics to regain dominance in the electrode process, ultimately achieving outstanding capacity retention of 63% at 4C. This work provides a more comprehensive perspective and represents a significant breakthrough in guiding electrode design to achieve a higher energy density. [ABSTRACT FROM AUTHOR]

The intrinsic low conductivity, low tap density, and huge volume expansion during lithium storage severely restrict the practicality of micron‐silicon suboxide (m‐SiOx). Here, a carbon and MXene dual confinement and dense structural engineering strategy is proposed to construct m‐SiOx composites (m‐SiOx@C/MXene) through in situ carbon coating and electrostatic self‐assembly process. This integrated structural achieves a conductivity of 157 S cm−1 for m‐SiOx@C/MXene, which is 7 and 2 orders of magnitude higher than m‐SiOx (5.3 × 10−5 S cm−1) and m‐SiOx@C (2.9 S cm−1), respectively. The tap density of m‐SiOx@C/MXene reaches 1.35 g cm−3, significantly greater than that of m‐SiOx (0.82 g cm−3) and m‐SiOx@C (0.75 g cm−3). The 29% volume expansion of m‐SiOx@C/MXene during lithium storage is much lower than the 228% and 162% of m‐SiOx and m‐SiOx@C. The synergistic effect of the above advantages enables m‐SiOx@C/MXene to exhibit excellent rate performance and cycle stability. When assembled into a full cell with the LiFePO4 (LFP) cathode, it features high capacity retention and energy density of 99.1% and 380 Wh kg−1 after 100 cycles at 0.2 C. This work provides new reference for the stable structural design of m‐SiOx or other materials with huge volume expansion during energy storage. [ABSTRACT FROM AUTHOR]

Silicon (Si)‐based anodes hold great potential for next‐generation lithium‐ion batteries (LIBs) due to their exceptional theoretical capacity. However, their practical application is hindered by the notably substantial volume expansion and unstable electrode/electrolyte interfaces during cycling, leading to rapid capacity degradation. To address these challenges, we have engineered a porous nitrogen/sulfur co‐doped carbon layer (CBPOD) to uniformly encapsulate Si, providing a multifunctional protective coating. This innovative design effectively passivates the electrode/electrolyte interface and mitigates the volumetric expansion of Si. The N/S co‐doping framework significantly enhances electronic and ionic conductivity. Furthermore, the carbonization process augments the elastic modulus of CBPOD and reconstructs the Si‐CBPOD interface, facilitating the formation of robust chemical bonds. These features collectively contribute to the high performance of the Si‐CBPOD anodes, which demonstrate a high reversible capacity of 1110.8 mAh g−1 after 1000 cycles at 4 A g−1 and an energy density of 574 Wh kg−1 with a capacity retention of over 75.6% after 300 cycles at 0.2 C. This study underscores the substantial potential of the CBPOD protective layer in enhancing the performance of Si anodes, providing a pathway for the development of composite materials with superior volumetric energy density and prolonged cyclic stability, thereby advancing high‐performance LIBs. [ABSTRACT FROM AUTHOR]

In scanning electrochemical microscopy (SECM), the addition of a redox active species plays an essential role. Those deliberately added mediators may alter results in SECM studies. In investigations of lithium‐ion battery (LIB) materials, especially of the positive electrode, the oxidation potentials of commonly used mediator substances such as ferrocene are located within the operation potential of the electrode. Thus, they possibly interfere with the regular charge/discharge processes. In situ studies are therefore in need of approaches reducing or eliminating the use of mediators. Within this publication, a novel mediator dosing (MD) concept is introduced. A capillary was closely positioned at the tip of the scanning probe. By gravity flow, stable flow rates of mediator solution of up to 32.4±0.6 μL h−1 were achieved. These low amounts were found to be sufficient to form a ferrocene zone at the probe tip enabling feedback mode SECM measurements with comparable quality to measurements directly in ferrocene solution. Proof of concept experiments were conducted by investigation of a thin‐film electrode with a micro‐structured surface. Furthermore, the MD concept was applied in imaging experiments of a commercially available LIB graphite electrode. [ABSTRACT FROM AUTHOR]

To address the urgent demand for sustainable battery manufacturing, this review contrasts traditional wet process with emerging dry electrode technologies. Dry process stands out because of its reduced energy and environmental footprint, offering considerable economic benefits and facilitating the production of high‐energy‐density electrodes. We spotlight technological innovations that exemplify the paradigm shift towards eco‐friendliness and cost‐efficiency. This review synthesizes the latest developments in dry electrode production, comparing the techniques with conventional methods, and outlines future research for further optimization toward a higher technology readiness level. We suggest that the evolution of battery manufacturing hinges on the synergy between process innovation and materials science, which is crucial for meeting the dual goals of environmental sustainability and economic practicality. [ABSTRACT FROM AUTHOR]

Advanced manufacturing research for sustainable battery life cycles is of utmost importance to reach net zero carbon emissions (European Commission, 2023a) as well as several of the United Nations Sustainable Development Goals (UNSDGs), for example: 30% reduction of CO2 emission, 10 million job opportunities and access to electricity for 600 million people (World Economic Forum, 2019). This editorial paper highlights international motivations for pursuing more sustainable manufacturing practices and discusses key research topics in battery manufacturing. Batteries will be central to our sustainable future as generation and storage become key components to on-demand energy supply. Four underlying themes are identified to address industrial needs in this field: 1. Digitalizing and automating production capabilities: data-driven solutions for production quality, smart maintenance, automation, and human factors, 2. Human-centric production: extended reality for operator support and skills development, 3. Circular battery life cycles: circular battery systems supported by service-based and other novel business models, 4. Future topics for battery value chains: increased industrial resilience and transparency with digital product passports, and next-generation battery chemistries. Challenges and opportunities along these themes are highlighted for transforming battery value chains through circularity and more sustainable production, with a particular emphasis on lithium-ion batteries (LIB). The paper concludes with directions for further research to advance a circular and sustainable battery value chain through utilizing the full potential of digitalization realising a cleaner, more energy-efficient society. [ABSTRACT FROM AUTHOR]

With the growing dependence on lithium-ion batteries, there is an urgent need to understand the potential developmental toxicity of LiPF6, a key component of these batteries. Although lithium's toxicity is well-established, the biological toxicity of LiPF6 has been minimally explored. This study leverages the zebrafish model to investigate the developmental impact of LiPF6 exposure. We observed morphological abnormalities, reduced spontaneous movement, and decreased hatching and swim bladder inflation rates in zebrafish embryos, effects that intensified with higher LiPF6 concentrations. Whole-mount in situ hybridization demonstrated that the specific expression of the swim bladder outer mesothelium marker anxa5b was suppressed in the swim bladder region under LiPF6 exposure. Transcriptomic analysis disclosed an upregulation of apoptosis-related gene sets. Acridine orange staining further supported significant induction of apoptosis. These findings underscore the environmental and health risks of LiPF6 exposure and highlight the necessity for improved waste management strategies for lithium-ion batteries. [ABSTRACT FROM AUTHOR]

Transition metal oxides are considered to be highly promising anode materials for high-energy lithium-ion batteries. While carbon matrices have demonstrated effectiveness in enhancing the electrical conductivity and accommodating the volume expansion of transition metal oxide-based anode materials in lithium-ion batteries (LIBs), achieving an optimized utilization ratio remains a challenging obstacle. In this investigation, we have devised a straightforward synthesis approach to fabricate CuO nano powder integrated with carbon matrix. We found that with the use of a sodium carboxymethyl cellulose (CMC) based binder and fluoroethylene carbonate additives, this anode exhibits enhanced performance compared to acrylonitrile multi-copolymer binder (LA133) based electrodes. CuO@CMC electrodes reveal a notable capacity ~1100 mA h g−1 at 100 mA g−1 following 170 cycles, and exhibit prolonged cycling stability, with a capacity of 450 mA h g−1 at current density 300 mA g−1 over 500 cycles. Furthermore, they demonstrated outstanding rate performance and reduced charge transfer resistance. This study offers a viable approach for fabricating electrode materials for next-generation, high energy storage devices. [ABSTRACT FROM AUTHOR]

Coal tar pitch (CTP) has become an ideal choice in the preparation of anode precursors for lithium-ion batteries (LIBs) and sodium-ion batteries (SIBs) because of its abundant carbon content, competitive pricing and adjustable structure properties. In this paper, sulfurized pitch-based carbon (SPC-800) was obtained by allowing CTP to react with sulfur at 350 °C and subsequently achieve carbonization at 800 °C. SPC-800 was more disordered and had a larger layer spacing than carbonized CTP (PC-800). Upon utilization as an anode for LIBs, SPC-800 possessed a higher reversible specific capacity (478.1 mAh g−1 at 0.1 A g−1), while utilization in SIBs displayed a capacity of 220.9 mAh g−1 at 20 mA g−1. This work is an important guide to the design of high-performance anodes suitable for use with both LIBs and SIBs. [ABSTRACT FROM AUTHOR]