Search Results (218)

The field of electrochemical devices, encompassing energy storage, fuel cells, electrolysis, and sensing, is fundamentally reliant on the electrode materials that govern their performance, efficiency, and sustainability. Traditional materials, while foundational, often face limitations such as restricted reaction kinetics, structural deterioration, and dependence on costly or scarce elements, driving the need for continuous innovation. Emerging electrode materials are designed to overcome these challenges by delivering enhanced reaction activity, superior mechanical robustness, accelerated ion diffusion kinetics, and improved economic feasibility. In energy storage, for example, the shift from conventional graphite in lithium-ion batteries has led to the exploration of silicon-based anodes, offering a theoretical capacity more than tenfold higher despite the challenge of massive volume expansion, which is being mitigated through nanostructuring and carbon composites. Simultaneously, the rise of sodium-ion batteries, appealing due to sodium’s abundance, necessitates materials like hard carbon for the anode, as sodium’s larger ionic radius prevents efficient intercalation into graphite. In electrocatalysis, the high cost of platinum in fuel cells is being addressed by developing Platinum-Group-Metal-free (PGM-free) catalysts like metal–nitrogen–carbon (M-N-C) materials for the oxygen reduction reaction (ORR). Similarly, for the oxygen evolution reaction (OER) in water electrolysis, cost-effective alternatives such as nickel–iron hydroxides are replacing iridium and ruthenium oxides in alkaline environments. Furthermore, advancements in materials architecture, such as MXenes—two-dimensional transition metal carbides with metallic conductivity and high volumetric capacitance—and Single-Atom Catalysts (SACs)—which maximize metal utilization—are paving the way for significantly improved supercapacitor and catalytic performance. While significant progress has been made, challenges related to fundamental understanding, long-term stability, and the scalability of lab-based synthesis methods remain paramount for widespread commercial deployment. The future trajectory involves rational design leveraging advanced characterization, computational modeling, and machine learning to achieve holistic, system-level optimization for sustainable, next-generation electrochemical devices. Full article

Sodium-ion batteries have emerged as a promising alternative to lithium-ion systems, due to the abundance and low cost of sodium resources. However, the demand for higher performance is always increasing, and developing new electrode materials and optimizing their behavior in full cells is necessary. Their electrochemical performance remains limited by challenges related to the anode materials. A fundamental understanding of electrode materials is essential to advance their practical application, for example, by designing strategies to minimize irreversible processes and enhance the reversible capacity. Thus, the properties of metals, including nanoparticles and clusters, are critical for various types of sodium batteries, such as sodium-ion microbatteries. Additionally, metallic nanoparticles exhibiting special properties are generated in situ at the negative electrode during the electrochemical cycling of certain batteries. This review focuses on their formation mechanisms, structural and electrochemical effects, and strategies to control their distribution and size. Particular attention is given to the interaction between metallic particles and carbon matrices, as well as their influence on capacity. Finally, current limitations and future perspectives for optimizing the properties of the metallic particles in advanced sodium battery anodes are highlighted. Full article

The depletion of global lithium reserves, coupled with the necessity for environmentally sustainable and economically accessible energy storage systems, has driven the development of sodium-ion batteries (SIBs) as a promising alternative to lithium-ion technologies. Among various anode materials for SIBs, hard carbon exhibits obvious advantages and significant commercial potential owing to its high energy density, low operating potential, and stable capacity retention during prolonged cycling. Biomass represents the most attractive source of non-graphitizable carbon from a practical standpoint, being readily available, renewable, and low-cost. However, the complex internal structure of biomass precursors creates significant challenges for precise control of microstructure and properties of the resulting hard carbon materials, requiring further research and optimization of synthesis methodologies. This work reports the synthesis of hard carbon from Sasa kurilensis via pyrolysis at 900 °C and investigates the effect of alkaline pretreatment on the structural and electrochemical characteristics of the anode material for SIBs. Sasa kurilensis is employed for the first time as a source for non-graphitizable carbon synthesis, whose unique natural vascular structure forms optimal hierarchical porosity for sodium-ion intercalation upon thermal treatment. The materials were characterized by X-ray diffraction, infrared and Raman spectroscopy, scanning electron microscopy, X-ray microtomography and low-temperature nitrogen adsorption–desorption. Electrochemical properties were evaluated by galvanostatic cycling in the potential range of 0.02–2 V at a current density of 25 mAhg⁻¹ in half-cells with sodium metal counter electrodes. The unmodified sample demonstrated a discharge capacity of 160 mAhg⁻¹ by the 6th cycle, with an initial capacity of 77 mAhg⁻¹. The alkaline-treated material exhibited lower discharge capacity (114 mAhg⁻¹) and initial Coulombic efficiency (40%) due to increased specific surface area, leading to excessive electrolyte decomposition. Full article

The demand for effective, economical, and sustainable anode materials for metal-ion batteries (MIBs) has increased significantly due to the rapid growth of energy storage technologies. Among various candidates, carbon-based materials have emerged as highly promising due to their abundance, structural versatility, and favorable electrochemical properties. This review highlights the current status and future directions of carbon-based anode materials in MIBs, with a particular focus on graphite, hard carbon, carbon nanotubes, heteroatom-doped carbons, carbon-based composites, and other related structures. Various synthesis strategies for these materials are presented, along with discussions on their physicochemical characteristics, including structural features that influence electrochemical performance. Furthermore, we provided an overview on the performance of newly developed carbon-based anode materials in lithium-, sodium-, potassium-, and other emerging metal-ion battery systems to assess the impact of different synthesis approaches. Special attention is given to surface engineering, heteroatom doping, and composite design that can address intrinsic challenges such as limited ion diffusion, low reversible capacity, and poor cycling stability in MIBs. This review does not cover any carbon materials which have been used as an additive. In addition, the review explores emerging opportunities enabled by advanced characterization techniques, computational modeling, and artificial intelligence for optimizing the design of next-generation carbon anode. Finally, this article provides future perspectives and insights into the design principles of novel carbon-based anode materials that can accelerate the development of high-performance, durable, and sustainable MIB technologies. Full article

Layered transition-metal oxides are among the most promising sodium-ion battery cathodes owing to their high specific capacities and structurally tunable frameworks. However, the prototypical P2-Na_0.67Ni_0.33Mn_0.67O₂ (NM) undergoes an irreversible P2 → O2 phase transition at high voltages, accompanied by severe lattice strain and capacity fade, which hinders practical deployment. Here, we propose a cooperative regulation strategy that couples Zn/Al co-doping with Na enrichment, and successfully synthesize P2-Na_0.80Ni_0.14Zn_0.14Mn_0.58Al_0.14O₂ (NMZA-N14). The optimized NMZA-N14 delivers an initial discharge capacity of 125 mAh g⁻¹ at 0.1C and demonstrates exceptional cycling and rate performance, retaining 98.6% of its capacity after 100 cycles at 0.2C and 93.6% after 200 cycles at 1C. Kinetic analyses indicate a higher Na⁺ diffusion coefficient and a lower charge-transfer resistance in NMZA-N14, evidencing substantially accelerated ion transport. In situ X-ray diffraction further reveals a reversible P2 → OP4 phase transition in the high-voltage regime with a unit-cell volume change of only ~2.27%, thereby avoiding the irreversible structural degradation observed in NM. This synergistic modulation markedly enhances structural stability and electrochemical kinetics, providing a viable pathway for the rational design of high-performance sodium-ion battery cathodes. Full article

Phase engineering has emerged as a powerful method for manipulating the structural and electrical characteristics of nanomaterials, resulting in significant enhancements in their electrochemical performance. This paper examines the correlation among morphology, crystal phase, and electrochemical performance of nanomaterials engineered for high-performance batteries and supercapacitors. The discourse starts with phase engineering methodologies in metal-based nanomaterials, including the direct synthesis of atypical phases and phase transformation mechanisms that provide metastable or mixed-phase structures. Special emphasis is placed on the impact of these synthetic processes on morphology and surface properties, which subsequently regulate charge transport and ion diffusion during electrochemical reactions. Additionally, the investigation of phase engineering in transition metal dichalcogenide (TMD) nanomaterials highlights how regulated phase transitions and heterophase structures improve active sites and conductivity. The optimized phase-engineered ZnCo₂O₄@Ti₃C₂ composite exhibited a high specific capacitance of 1013.5 F g⁻¹, a reversible capacity of 732.5 mAh g⁻¹, and excellent cycling stability, with over 85% retention after 10,000 cycles. These results confirm that phase and morphological control can substantially enhance charge transport and electrochemical durability, offering promising strategies for next-generation batteries and supercapacitors. The paper concludes by summarizing current advancements in phase-engineered nanomaterials for lithium-ion, sodium-ion, and lithium-sulfur batteries, along with supercapacitors, emphasizing the significant relationship between phase state, morphology, and energy storage efficacy. This study offers a comprehensive understanding of the optimal integration of phase and morphological control in designing enhanced electrode materials for next-generation electrochemical energy storage systems. Full article

Magnesium metal boasts a high theoretical volumetric specific capacity and abundant reserves. Magnesium batteries offer high safety and environmental friendliness. In recent years, magnesium-ion batteries (MIBs) with Mg or Mg alloys as anodes have garnered extensive interest and emerged as promising candidates for next-generation competitive energy storage technologies. However, MIBs are plagued by issues such as sluggish desolvation kinetics and slow migration kinetics, which lead to limitations including a limited electrochemical window and poor magnesium storage reversibility. Herein, the sodium vanadium phosphate @ carbon (Na₃V₂(PO₄)₃@C, hereafter abbreviated as NVP@C) cathode material was synthesized via a sol–gel method. The electrochemical performance and magnesium storage mechanism of NVP@C in a 0.5 M magnesium bis(trifluoromethanesulfonyl)imide/ethylene glycol dimethyl ether (Mg(TFSI)₂/DME) electrolyte were investigated. The as-prepared NVP@C features a pure-phase orthorhombic structure with a porous microspherical morphology. The discharge voltage of NVP@C is 0.75 V vs. activated carbon (AC), corresponding to 3.5 V vs. Mg/Mg²⁺. The magnesium storage process of NVP@C is tentatively proposed to follow a ‘sodium extraction → magnesium intercalation → magnesium deintercalation’ three-step intercalation–deintercalation mechanism, based on the characterization results of ICP-OES, ex situ XRD, and FTIR. No abnormal phases are generated throughout the process, and the lattice parameter variation is below 0.5%. Additionally, the vibration peaks of PO₄ tetrahedrons and VO₆ octahedrons shift reversibly, and the valence state transitions between V³⁺ and V⁴⁺/V⁵⁺ are reversible. These results confirm the excellent reversibility of the material’s structure and chemical environment. At a current density of 50 mA/g, NVP@C delivers a maximum discharge specific capacity of 62 mAh/g, with a capacity retention rate of 66% after 200 cycles. The observed performance degradation is attributed to the gradual densification of the CEI film during cycling, leading to increased Mg²⁺ diffusion resistance. This work offers valuable insights for the development of high-voltage MIB systems. Full article

In this research article, a silicon carbide (SiC) nanocluster has been designed and characterized as an anode electrode for lithium (Li), sodium (Na), potassium (K), beryllium (Be), magnesium (Mg), boron (B), aluminum (Al) and gallium (Ga)-ion batteries through the formation of SiLiC, SiNaC, SiKC, SiBeC, SiMgC, SiBC, SiAlC and SiGaC nanoclusters. A vast study on energy-saving by SiLiC, SiNaC, SiKC, SiBeC, SiMgC, SiBC, SiAlC and SiGaC complexes was probed using computational approaches accompanying density state analysis of charge density differences (CDDs), total density of states (TDOS) and molecular electrostatic potential (ESP) for hybrid clusters of SiLiC, SiNaC, SiKC, SiBeC, SiMgC, SiBC, SiAlC and SiGaC. The functionalization of Li, Na, K, Be, Mg, B, Al and Ga metal/metalloid elements can raise the negative charge distribution of carbon elements as electron acceptors in SiLiC, SiNaC, SiKC, SiBeC, SiMgC, SiBC, SiAlC and SiGaC nanoclusters. Higher Si/C content can increase battery capacity through SiLiC, SiNaC, SiKC, SiBeC, SiMgC, SiBC, SiAlC and SiGaC nanoclusters for energy storage processes and to improve the rate performance by enhancing electrical conductivity. Full article

Polyaniline (PANI), as a classical conducting polymer, has attracted significant attention in the field of energy storage due to its low cost, facile synthesis, environmental stability, and unique dual electronic/ionic conductivity. Particularly, one-dimensional (1D) nanostructures of PANI, such as nanowires and nanorods, exhibit superior electrochemical performance and cycling stability, attributed to their high surface area and efficient charge transport pathways. This review provides a comprehensive summary of recent advances in 1D PANI-based anode materials for lithium-ion, sodium-ion, and other types of rechargeable batteries. The specific capacity, rate performance, and long-term cycling behavior of these materials are discussed in detail. Moreover, strategies for performance enhancement through combination with carbon materials, metal oxides, and silicon, as well as chemical doping and structural modification, are systematically reviewed. Key challenges including electrochemical stability, structural durability, and large-scale fabrication are analyzed. Finally, the future directions in structural design, composite engineering, and commercialization of 1D PANI anode materials are outlined. This review aims to provide insight and guidance for the further development and practical application of PANI-based energy storage systems. Full article

Changing the topography of electrodes by ultrafast laser ablation has shown great potential in enhancing electrochemical performance in lithium-ion batteries. The generation of microstructured channels within the electrodes creates shorter pathways for lithium-ion diffusion and mitigates strain from volume expansion during electrochemical cycling. The topography modification enables faster charging, improved rate capability, and the potential to combine high-power and high-energy properties. In this study, we present a preliminary exploration of this approach for sodium-ion battery technology, focusing on the impact of laser-generated channels on hard carbon electrodes in sodium-metal half-cells. The performance was analyzed by employing different conditions, including different electrolytes, separators, and electrodes with varying compaction degrees. To identify key factors contributing to rate capability improvements, we conducted a comparative analysis of laser-structured and unstructured electrodes using methods including scanning electron microscopy, laser-induced breakdown spectroscopy, and electrochemical cycling. Despite being based on a limited sample size, the data reveal promising trends and serve as a basis for further optimization. Our findings suggest that laser structuring can enhance rate capability, particularly under conditions of limited electrolyte wetting or increased electrode density. This highlights the potential of laser structuring to optimize electrode design for next-generation sodium-ion batteries and other post-lithium technologies. Full article

In this study, we investigate the recovery of Li and Co from spent LiCoO₂ cathodes of spent lithium batteries using a combined approach of mechanochemical activation (MA) and ammoniacal leaching. High-energy ball milling disrupts the layered structure of LiCoO₂, introduces defects, and increases surface area, which strongly improves subsequent dissolution. Leaching experiments in an ammonia–ammonium sulphate–sulphite medium were optimized by varying the solid-to-liquid ratio, sodium sulfite concentration, and temperature. Under the best conditions (90 °C, 120 min, S/L = 10 g/L, 0.5 M Na₂SO₃), nearly complete recoveries were obtained: 99.5% Li and 96.5% Co. Kinetic modeling based on the shrinking-core model confirmed that dissolution of both metals is controlled by chemical reaction, with activation energies of 45.7 kJ·mol⁻¹ for Li and 60.7 kJ·mol⁻¹ for Co. Structural and morphological analyses (XRD, SEM) supported the enhanced reactivity of the activated material. The study demonstrates that MA coupled with optimized ammoniacal leaching provides an efficient process for LiCoO₂ recycling, without using aggressive mineral acids and long treatment times. Full article

O3-type NaNi_1/3Mn_1/3Fe_1/3O₂ (NFM) cathodes for sodium-ion batteries face critical challenges of sluggish Na⁺ diffusion and structural degradation during cycling. In this study, we implement an Sb³⁺ doping strategy that enhances structural stability and interfacial stability by modulating the NFM grain morphology to promote densification of primary particles and shorten Na⁺ migration paths. The optimized Sb-doped NFM1Sb (1%mol Sb) cathode exhibits excellent electrochemical performance, achieving 86.48% capacity retention after 200 cycles at 1 C and a high rate capability of 122.2 mAh g⁻¹ at 5 C. These improvements are attributed to the alleviation of stress concentration and suppression of microcrack formation during cycling. This work demonstrates the critical role of grain morphology regulation through heavy-metal doping in developing long-life and high-rate SIBs, providing a viable pathway toward next-generation energy storage systems. Full article

Searching anode materials is an important task for the development of sodium-ion batteries. In this regard, bronze-phase titanium dioxide, TiO₂(B), has been considered as one of the promising materials, owing to its crystal structure with open channels and voids facilitating Na⁺ diffusion and storage. However, the electrochemical de-/sodiation mechanism of TiO₂(B) has not been clearly comprehended, and further experiments are required. Herein, in situ and ex situ observations by a combination of X-ray photoelectron spectroscopy, X-ray diffraction, Raman spectroscopy, gas chromatography–mass spectrometry was used to provide additional insights into the electrochemical reaction scenario of bronze-phase TiO₂ in Na-ion batteries. The findings reveal that de-/sodiation of TiO₂(B) occurs through a reversible intercalation reaction and without the involvement of the conversion reaction (no metallic titanium is formed and no oxygen is released). At the same time, upon the first Na⁺ uptake process, crystalline TiO₂(B) becomes partially amorphous, but is still driven by the Ti⁴⁺/Ti³⁺ redox couple. Importantly, TiO₂(B) has pseudocapacitive electrochemical behavior during de-/sodiation based on a quantitative analysis of the cyclic voltammetry data. The results obtained in this study complement existing insights into the sodium storage mechanisms of TiO₂(B) and provide useful knowledge for further improving its anode performance for SIBs application. Full article

With their considerable capacity and structurally favorable characteristics, layered transition metal oxides have become strong contenders for cathode use in sodium-ion batteries (SIBs). Nevertheless, their practical deployment is challenged by pronounced capacity loss, predominantly induced by unstable cathode–electrolyte interphase (CEI) at elevated voltages. In this study, difluoroethylene carbonate (DFEC) is introduced as a functional electrolyte additive to engineer a robust and uniform CEI. The fluorine-enriched CEI effectively suppresses parasitic reactions, mitigates continuous electrolyte decomposition, and facilitates stable Na⁺ transport. Consequently, Na/NaNi_1/3Fe_1/3Mn_1/3O₂ (Na/NFM) cells with 2 wt.% DFEC retain 78.36% of their initial capacity after 200 cycles at 1 C and 4.2 V, demonstrating excellent long-term stability. Density functional theory (DFT) calculations confirm the higher oxidative stability of DFEC compared to conventional solvents, further supporting its interfacial protection role. This work offers valuable insights into electrolyte additive design for high-voltage SIBs and provides a practical route to significantly improve long-term electrochemical performance. Full article

Sodium metal batteries (SMBs) with ceramic solid electrolytes offer a promising route to improve the energy density of conventional Na-ion batteries (SIBs). Silicate-based ceramics have recently gained attention for their favourable properties, including better ionic conduction and wider stability windows. In this study, 10% Pr³⁺ and Nd³⁺ were doped into sodium gadolinium silicate ceramics to examine the effects on phase purity, ionic conductivity, and interfacial compatibility with sodium metal anodes. The materials were synthesized via solid-state methods and sintered at 950–1075 °C to study the impact of sintering temperature on densification and microstructure. Na₅Gd_0.9Pr_0.1Si₄O₁₂ (NGPS) and Na₅Gd_0.9Nd_0.1Si₄O₁₂ (NGNS) sintered at 1075 °C showed the highest room temperature total ionic conductivities of 1.64 and 1.74 mS cm⁻¹, respectively. The highest critical current density of 0.5 mA cm⁻² is achieved with a low interfacial area-specific resistance of 29.47 Ω cm² for NGPS and 22.88 Ω cm² for NGNS after Na plating/stripping experiments. These results highlight how doping enhances phase purity, ionic conductivity, and interfacial stability of silicates with Na metal anodes. Full article