Sb2O3 nanoparticles anchored on N-doped graphene nanoribbons as improved anode for sodium-ion batteries

Sodium-ion batteries (SIBs) are emerging as a promising alternative to conventional lithium-ion technology, due to the abundance of sodium resources. Still, major drawbacks for the commercial application of SIBs lie in the slow kinetic processes and poor cycling performance of the devices. In this work, a hybrid nanocomposite of Sb₂O₃ nanoparticles anchored on N-doped graphene nanoribbons (GNR) is implemented as anode material in SIBs. The obtained Sb₂O₃/N-GNR anode delivers a reversible specific capacity of 642 mA h g⁻¹ after 100 cycles at 0.1 A g⁻¹ and exhibits a good rate capability. Even after 500 cycles at 5 A g⁻¹, the specific capacity is maintained at about 405 mA h g⁻¹. Such good Na storage performance is mainly ascribed to the beneficial effect of N doping for charge transfer and to the improved microstructure that facilitates the Na⁺ diffusion through the overall electrode.

A hybrid nanocomposite of Sb₂O₃ nanoparticles anchored on N-doped graphene nanoribbons is used as anode in SIBs. These hybrid electrodes demonstrate a high charge transfer and improved microstructure, facilitating the Na⁺ diffusion in the electrode.     

3D hierarchical rose-like Ni2P@rGO assembled from interconnected nanoflakes as anode for lithium ion batteries

In recent years, anode materials of transition metal phosphates (TMPs) for lithium ion batteries (LIBs) have drawn a vast amount of attention from researchers, due to their high theoretical capacity and comparatively low intercalation potentials vs. Li/Li⁺. However, in practice, their application remains constrained by poor electrical conductivity, and dramatic volume expansion and severe agglomeration during the lithium process, which leads to questionable kinetic issues and a prompt decline in capacity during cycling. Herein, through an elaborate design, we developed a novel three-dimensional (3D) hierarchical rose-like architecture self-assembled from two-dimensional (2D) Ni₂P nanoflakes immobilized on reduced graphene oxide (rGO) via a combination of a hydrothermal process and phosphating treatment. Such a design provides unique superiority for Ni₂P-based anode materials for LIBs. Paraphrasing, the 3D hierarchical structure of Ni₂P distributes the stress on the anode material while cycling and provides more lithium storage space. The rGO not only enhances the conductivity of materials, but also serves as a flexible framework which immobilizes Ni₂P so that it prevents it from pulverization. Therefore, the synergistic effect between them guarantees the integrity of the material structure after a long-term cycling Li⁺ intercalation and deintercalation process. When it acted as anode material for LIBs, the as-obtained 3D rose-like Ni₂P@rGO electrode exhibited a noticeable electrochemical performance, which delivers a discharge capacity of 330.5 mA h g⁻¹ at a current density of 100 mA g⁻¹ after 100 cycles and retains 200.5 mA h g⁻¹ at 1000 mA g⁻¹.

In recent years, anode materials of transition metal phosphates (TMPs) for lithium ion batteries have drawn a vast amount of attention, due to their high theoretical capacity and comparatively low intercalation potentials vs. Li/Li⁺.     

Sonochemistry-enabled uniform coupling of SnO2 nanocrystals with graphene sheets as anode materials for lithium-ion batteries

SnO₂/graphene nanocomposite was successfully synthesized by a facile sonochemical method from SnCl₂ and graphene oxide (GO) precursors. In the sonochemical process, the Sn²⁺ is firstly dispersed homogeneously on the GO surface, then in situ oxidized to SnO₂ nanoparticles on both sides of the graphene nanosheets (RGO) obtained by the reduction of GO under continuous ultrasonication. Graphene not only provides a mechanical support to alleviate the volume changes of the SnO₂ anode and prevent nanoparticle agglomeration, but also serves as a conductive network to facilitate charge transfer and Li⁺ diffusion. When used as a lithium ion battery (LIB) anode, the SnO₂/graphene nanocomposite exhibits significantly improved specific capacity (1610 mA h g⁻¹ at 100 mA g⁻¹), good cycling stability (retaining 87% after 100 cycles), and competitive rate performance (273 mA h g⁻¹ at 500 mA g⁻¹) compared to those of bare SnO₂. This sonochemical method can be also applied to the synthesis of other metal-oxide/graphene composites and this work provides a large-scale preparation route for the practical application of SnO₂ in lithium ion batteries.

SnO₂/graphene nanocomposite was successfully synthesized by a facile sonochemical method from SnCl₂ and graphene oxide (GO) precursors.     

A stable TiO2–graphene nanocomposite anode with high rate capability for lithium-ion batteries

A rapid microwave hydrothermal process is adopted for the synthesis of titanium dioxide and reduced graphene oxide nanocomposites as high-performance anode materials for Li-ion batteries. With the assistance of hydrazine hydrate as a reducing agent, graphene oxide was reduced while TiO₂ nanoparticles were grown in situ on the nanosheets to obtain the nanocomposite material. The morphology of the nanocomposite obtained consisted of TiO₂ particles with a size of ∼100 nm, uniformly distributed on the reduced graphene oxide nanosheets. The as-prepared TiO₂–graphene nanocomposite was able to deliver a capacity of 250 mA h g⁻¹ ± 5% at 0.2C for more than 200 cycles with remarkably stable cycle life during the Li⁺ insertion/extraction process. In terms of high rate capability performance, the nanocomposite delivered discharge capacity of ca. 100 mA h g⁻¹ with >99% coulombic efficiency at C-rates of up to 20C. The enhanced electrochemical performance of the material in terms of high rate capability and cycling stability indicates that the as-developed TiO₂–rGO nanocomposites are promising electrode materials for future Li-ion batteries.

A rapid microwave hydrothermal process is adopted for the synthesis of titanium dioxide and reduced graphene oxide nanocomposites as high-performance anode materials for Li-ion batteries.     

Enhanced electrochemical properties of cellular CoPS@C nanocomposites for HER,OER and Li-ion batteries

Cellular CoPS@C nanocomposites were successfully synthesized via a facile two-steps route. The performances of the CoPS@C electrode as a non-noble metal electrocatalyst for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) show good activity. On the other hand, the electrochemical investigation of CoPS systems for lithium ion batteries (LIBs) is reported for the first time. The CoPS@C nanocomposite as a novel anode can maintain a capacity of about 713 mA h g⁻¹ after 50 cycles at a current density of 0.2 A g⁻¹, indicating its potential applications in lithium storage. Test results also demonstrate that the CoPS@C nanocomposite exhibit more excellent HER, OER and Li storage performances compared to the bulk CoPS sample.

A novel porous CoPS@C nanocomposite show excellent electrochemical properties for HER, OER, Li-storage.     

Bipolar fluorinated covalent triazine framework cathode with high lithium storage and long cycling capability

Organic materials with adjustable structures and wide sources are expected to become potential candidates for commercial cathodes of lithium-ion batteries (LIBs). However, most organic materials have unstable structures, poor conductivity, and are easily soluble in electrolytes, resulting in unsatisfactory lithium storage performance. Covalent–organic frameworks have attracted extensive attention due to their stable frame structures, adjustable pore structures and functionalized official groups. Herein, a fluorinated covalent triazine framework (FCTF) is synthesized by a simple ion-thermal method. Compared with the fluorine-free covalent triazine frameworks (CTFs), the introduction of fluorine improves the lithium storage performance of CTF. When used as a cathode for lithium ion batteries, FCTF can retain a reversible capacity of 125.6 mA h g⁻¹ after 200 cycles at a current density of 100 mA g⁻¹. Besides, it also delivers 106.3 mA h g⁻¹ after 400 cycles at a current density of 200 mA g⁻¹ with 0.03% decrease per cycle (from 40 to 400 cycles).

A bipolar fluorinated covalent triazine framework (FCTF) was successfully synthesized by the self-polymerization of tetrafluoroterephthalonitrile and exhibited high reversible capacities, long cyclability as a cathode for lithium ion batteries.     

Preparation of cobalt sulfide@reduced graphene oxide nanocomposites with outstanding electrochemical behavior for lithium-ion batteries

Cobalt sulfide@reduced graphene oxide composites were prepared through a simple solvothermal method. The cobalt sulfide@reduced graphene oxide composites are composed of cobalt sulfide nanoparticles uniformly attached on both sides of reduced graphene oxide. Some favorable electrochemical performances in specific capacity, cycling performance, and rate capability are achieved using the porous nanocomposites as an anode for lithium-ion batteries. In a half-cell, it exhibits a high specific capacity of 1253.9 mA h g⁻¹ at 500 mA g⁻¹ after 100 cycles. A full cell consists of the cobalt sulfide@reduced graphene oxide nanocomposite anode and a commercial LiCoO₂ cathode, and is able to hold a high capacity of 574.7 mA h g⁻¹ at 200 mA g⁻¹ after 200 cycles. The reduced graphene oxide plays a key role in enhancing the electrical conductivity of the electrode materials; and it effectively prevents the cobalt sulfide nanoparticles from dropping off the electrode and buffers the volume variation during the discharge–charge process. The cobalt sulfide@reduced graphene oxide nanocomposites present great potential to be a promising anode material for lithium-ion batteries.

Cobalt sulfide@reduced graphene oxide nanocomposites obtained through a dipping and hydrothermal process, exhibit ascendant lithium-ion storage properties.     

In situ production of a two-dimensional molybdenum disulfide/graphene hybrid nanosheet anode for lithium-ion batteries

A solvent-free, low-cost, high-yield and scalable single-step ball milling process is developed to construct 2D MoS₂/graphene hybrid electrodes for lithium-ion batteries. Electron microscopy investigation reveals that the obtained hybrid electrodes consist of numerous nanosheets of MoS₂ and graphene which are randomly distributed. The MoS₂/graphene hybrid anodes exhibit excellent cycling stability with high reversible capacities (442 mA h g⁻¹ for MoS₂/graphene (40 h); 553 mA h g⁻¹ for MoS₂/graphene (20 h); 342 mA h g⁻¹ for MoS₂/graphene (10 h)) at a high current rate of 250 mA g⁻¹ after 100 cycles, whereas the pristine MoS₂ electrode shows huge capacity fading with a retention of 37 mA h g⁻¹ at 250 mA g⁻¹ current after 100 cycles. The incorporation of graphene into MoS₂ has an extraordinary effect on its electrochemical performance. This work emphasises the importance of the construction of the 2D MoS₂/graphene hybrid structure to prevent capacity fading issues with the MoS₂ anode in lithium-ion batteries.

A solvent-free, low-cost, high-yield and scalable single-step ball milling process is developed to construct 2D MoS₂/graphene hybrid electrodes for lithium-ion batteries.     

Surface phosphation of 3D mesoporous NiCo2O4 nanowire arrays as bifunctional anodes for lithium and sodium ion batteries

A novel surface phosphate strategy was adopted to dramatically improve the charge transport, ion diffusion, electroactive sites, and cycle stability of mesoporous NiCo₂O₄ nanowire arrays (NWAs), drastically boosting their electrochemical properties. Consequently, the as-prepared phosphated NiCo₂O₄ NWA (P-NiCo₂O₄ NWA) electrode achieved excellent energy storage performance as a bifunctional anode material for both lithium ion batteries (LIBs) and sodium ion batteries (SIBs). When evaluated as an anode for LIBs, this P-NiCo₂O₄ NWA electrode showed a high reversible capacity up to 1156 mA h g⁻¹ for 1500 cycles at 200 mA g⁻¹ without appreciable capacity attenuation, while in SIBs, the electrode could also deliver an admirable initial capacity as high as 687 mA h g⁻¹ and maintained 83.5% of this after 500 cycles at the same current density. Most important, when the current density increased from 100 to 1000 mA g⁻¹, the capacity retention was about 63% in LIBs and 54% in SIBs. This work may shed light on the engineering of efficient electrodes for multifunctional flexible energy storage device applications.

A novel surface phosphate strategy was adopted to dramatically improve the charge transport, ion diffusion, electroactive sites, and cycle stability of mesoporous NiCo₂O₄ nanowire arrays (NWAs), drastically boosting their electrochemical properties.     

Electrochemical performance of CoSe2 with mixed phases decorated with N-doped rGO in potassium-ion batteries

Potassium-ion batteries (PIBs) have received much attention as next-generation energy storage systems because of their abundance, low cost, and slightly lower standard redox potential than lithium-ion batteries (LIBs). Nevertheless, they still face great challenges in the design of the best electrode materials for applications. Herein, we have successfully synthesized nano-sized CoSe₂ encapsulated by N-doped reduced graphene oxide (denoted as CoSe₂@N-rGO) by a direct one-step hydrothermal method, including both orthorhombic and cubic CoSe₂ phases. The CoSe₂@N-rGO anodes exhibit a high reversible capacity of 599.3 mA h g⁻¹ at 0.05 A g⁻¹ in the initial cycle, and in particular, they also exhibit a cycling stability of 421 mA h g⁻¹ after 100 cycles at 0.2 A g⁻¹. Density functional theory (DFT) calculations show that CoSe₂ with N-doped carbon can greatly accelerate electron transfer and enhance the rate performance. In addition, the intrinsic causes of the higher electrochemical performance of orthorhombic CoSe₂ than that of cubic CoSe₂ are also discussed.

Potassium-ion batteries (PIBs) have received much attention as next-generation energy storage systems because of their abundance, low cost, and slightly lower standard redox potential than lithium-ion batteries (LIBs).     

A germanium and zinc chalcogenide as an anode for a high-capacity and long cycle life lithium battery

High-performance lithium ion batteries are ideal energy storage devices for both grid-scale and large-scale applications. Germanium, possessing a high theoretical capacity, is a promising anode material for lithium ion batteries, but still faces poor cyclability due to huge volume changes during the lithium alloying/dealloying process. Herein, we synthesized an amorphous germanium and zinc chalcogenide (GZC) with a hierarchically porous structure via a solvothermal reaction. As an anode material in a lithium ion battery, the GZC electrode exhibits a high reversible capacity of 747 mA h g⁻¹ after 350 cycles at a current density of 100 mA g⁻¹ and a stable capacity of 370 mA h g⁻¹ after 500 cycles at a current density of 1000 mA g⁻¹ along with 92% capacity retention. All of these outstanding electrochemical properties are attributed to the hierarchically porous structure of the electrode that has a large surface area, fast ion conductivity and superior structural stability, which buffers the volumetric variation during charge/discharge processes and also makes it easier for the electrolyte to soak in, affording more electrochemically active sites.

High-performance lithium ion batteries are ideal energy storage devices for both grid-scale and large-scale applications.     

Carbon-coated SnO2 riveted on a reduced graphene oxide composite (C@SnO2/RGO) as an anode material for lithium-ion batteries

The research on graphene-based anode materials for high-performance lithium-ion batteries (LIBs) has been prevalent in recent years. In the present work, carbon-coated SnO₂ riveted on a reduced graphene oxide sheet composite (C@SnO₂/RGO) was fabricated using GO solution, SnCl₄, and glucose via a hydrothermal method after heat treatment. When the composite was exploited as an anode material for LIBs, the electrodes were found to exhibit a stable reversible discharge capacity of 843 mA h g⁻¹ at 100 mA g⁻¹ after 100 cycles with 99.5% coulombic efficiency (CE), and a specific capacity of 485 mA h g⁻¹ at 1000 mA g⁻¹ after 200 cycles; these values were higher than those for a sample without glucose (SnO₂/RGO) and a pure SnO₂ sample. The favourable electrochemical performances of the C@SnO₂/RGO electrodes may be attributed to the special double-carbon structure of the composite, which can effectively suppress the volume expansion of SnO₂ nanoparticles and facilitate the transfer rates of Li⁺ and electrons during the charge/discharge process.

The combined action of GO and glucose makes the SnO₂ dispersed uniformly. The synergistic effect of the unique double-carbon structure can effectively improve the electrical conductivity of the SnO₂ and strengthen lithium storage capability.     

Synthesis and electrochemical performance of NaV3O8 nanobelts for Li/Na-ion batteries and aqueous zinc-ion batteries

NaV₃O₈ nanobelts were successfully synthesized for Li/Na-ion batteries and rechargeable aqueous zinc-ion batteries (ZIBs) by a facile hydrothermal reaction and subsequent thermal transformation. Compared to the electrochemical performance of LIBs and NIBs, NaV₃O₈ nanobelt cathode materials in ZIBs have shown excellent electrochemical performance, including high specific capacity of 421 mA h g⁻¹ at 100 mA g⁻¹ and good cycle stability with a capacity retention of 94% over 500 cycles at 5 A g⁻¹. The good diffusion coefficients and high surface capacity of NaV₃O₈ nanobelts in ZIBs were in favor of fast Zn²⁺ intercalation and long-term cycle stability.

Compared to the electrochemical performance for LIBs and NIBs, NaV₃O₈ nanobelts electrode for ZIBs shows excellent electrochemical performance, including high specific capacity of 421 mA h g⁻¹ at 100 mA g⁻¹, good rate performance and cycle performance.     

FeNb2O6/reduced graphene oxide composites with intercalation pseudo-capacitance enabling ultrahigh energy density for lithium-ion capacitors

Lithium-ion capacitors (LICs), which combine the characteristics of lithium-ion batteries and supercapacitors, have been well studied recently. Extensive efforts are devoted to developing fast Li⁺ insertion/deintercalation anode materials to overcome the discrepancy in kinetics between battery-type anodes and capacitive cathodes. Herein, we design a FeNb₂O₆/reduced graphene oxide (FNO/rGO) hybrid material as a fast-charge anode that provides a solution to the aforementioned issue. The synergetic combination of FeNb₂O₆, whose unique structure promotes fast electron transport, and highly conductive graphene shortens the Li⁺ diffusion pathways and enhances structural stability, leading to excellent electrochemical performance of the FNO/rGO anode, including a high capacity (770 mA h g⁻¹ at 0.05 A g⁻¹) and long cycle stability (95.3% capacitance retention after 500 cycles). Furthermore, the FNO/rGO//ACs LIC achieves an ultrahigh energy density of 135.6 W h kg⁻¹ (at 2000 W kg⁻¹) with a wide working potential window from 0.01 to 4 V and remarkable cycling performance (88.5% capacity retention after 5000 cycles at 2 A g⁻¹).

FeNb₂O₆/reduced graphene oxide (FNO/rGO) hybrid material as a fast charge anode for LICs that provides a solution to overcome the discrepancy in kinetics between battery-type anodes and capacitive cathodes.     

Three-dimensional clusters of peony-shaped CuO nanosheets as a high-rate anode for Li-ion batteries

Copper oxide (CuO) has emerged as a promising anode material for lithium-ion batteries (LIBs) due to its high theoretical capacity, low cost and low toxicity to the natural environment. However, the low electronic/ionic conductivity and the imponderable volume expansion problem during the charge and discharge process hinder its practical applications. Herein, we introduced three-dimensional clusters of peony-shaped CuO nanosheets (TCP-CuO) to tackle these problems by increasing the surface of the active material. The unique three-dimensional peony-liked structure not only alleviates the volume expansion problem, but also enhances the electron/ion conductivity. As a result, the TCP-CuO electrode possesses a reversible high capacity of 641.1 mA h g⁻¹ at 0.1 A g⁻¹ after 80 cycles as well as an outstanding rate performance of 531.6 mA h g⁻¹ at a rate of 5C (1C = 674 mA g⁻¹) and excellent cycling durability of 441.1 mA h g⁻¹ at 1 A g⁻¹ after 100 cycles. This work demonstrated a novel strategy for the construction of a well-designed structure for other advanced energy-storage technologies.

TCP-CuO possesses a unique three-dimensional peony-liked architecture which not only alleviates volume expansion problem, but also enhances electron/ion conductivity. As an anode in LIBs, TCP-CuO delivers excellent electrochemical performances.     

The study of zirconium vanadate as a cathode material for lithium ion batteries

The electrochemical properties of ZrV₂O₇ (ZVO) and ZVO@C were investigated in lithium ion batteries. The first charge (or discharge) specific capacity of ZVO and ZVO@C are 279 mA h g⁻¹, 392 mA h g⁻¹, 208 mA h g⁻¹ and 180 mA h g⁻¹ for 0%, 3%, 5% and 9% of carbon, respectively. The capacity retention rates (with 0% 3%, 5% and 9% carbon content) are 33.0%, 52.5%, 56.4% and 76.1% after ten cycles, respectively. The low inner resistance relates to the good contact of the electrode rather than the high content of carbon, and the specific capacity retention rate increases with the increase of the carbon content.

The carbon content in the electrode is not the only factor that determines the internal resistance. The high capacity of lithium ion batteries is related to high conductivity. The lattice is stable (expect for shrinkage) when Li ions insert into ZVO.     

Design and synthesis of graphene/SnO2/polyacrylamide nanocomposites as anode material for lithium-ion batteries

Tin dioxide (SnO₂) is a promising anode material for lithium-ion batteries owing to its large theoretical capacity (1494 mA h g⁻¹). However, its practical application is hindered by these problems: the low conductivity, which restricts rate performance of the electrode, and the drastic volume change (400%). In this study, we designed a novel polyacrylamide/SnO₂ nanocrystals/graphene gel (PAAm@SnO₂NC@GG) structure, in which SnO₂ nanocrystals anchored in three-dimensional graphene gel network and the polyacrylamide layers could effectively prevent the agglomeration of SnO₂ nanocrystals, presenting excellent cyclability and rate performance. A capacity retention of over 90% after 300 cycles of 376 mA h g⁻¹ was achieved at a current density of 5 A g⁻¹. In addition, a stable capacity of about 989 mA h g⁻¹ at lower current density of 0.2 A g⁻¹ was achieved.

Tin dioxide (SnO₂) is a promising anode material for lithium-ion batteries owing to its large theoretical capacity (1494 mA h g⁻¹).     

Sodium insertion/extraction investigations into zinc ferrite nanospheres as a high performance anode material

Electrode materials with high fast charging and high capacity are urgently required for the realization of sodium-ion batteries (SIBs). In this work, zinc ferrite (ZnFe₂O₄) nanospheres have been prepared by the simple hydrothermal route and the structural analysis of ZnFe₂O₄ was evaluated by using X-ray diffraction. The morphology and microstructural characterizations are obtained using scanning electron microscopy and transmission electron microscopy. The results indicate that a single phase material was obtained with uniform sphere-like morphology and high crystallinity. The Brunauer–Emmett–Teller method was employed to determine the specific surface area of the ZnFe₂O₄ nanospheres which has been calculated to be 32 m² g⁻¹. The electrochemical results indicate that the composite possesses high sodium storage capability (478 mA h g⁻¹), and good cycling stability (284 mA h g⁻¹ at 100^th cycle) and rate capability (78 mA h g⁻¹ at 2 A g⁻¹). The high sodium storage performance of the ZnFe₂O₄ electrode is ascribed to the mesoporous nature of the ZnFe₂O₄ nanospheres. Further, sodium kinetics and the reaction mechanism in ZnFe₂O₄ nanospheres have been elucidated using electrochemical impedance spectroscopy, galvanostatic intermittent titration technique, ex situ TEM, and XAS. The acquired results indicate sluggish kinetics, reversibility of the material, and the stable structure of ZnFe₂O₄. Therefore, such a structure can be considered to be an attractive contender as a low cost anode for SIBs.

Electrode materials with high fast charging and high capacity are urgently required for the realization of sodium-ion batteries (SIBs).     

The influence of different Si : C ratios on the electrochemical performance of silicon/carbon layered film anodes for lithium-ion batteries

With a high specific capacity (4200 mA h g⁻¹), silicon based materials have become the most promising anode materials in lithium-ions batteries. However, the large volume expansion makes the capacity reduce rapidly. In this work, a periodic silicon/carbon (Si/C) multilayer thin film was synthesized by magnetron sputtering method on copper foil. The titanium (Ti) film (about 20 nm) as the transition layer was deposited on the copper foil prior to the deposition of the multilayer film. Superior electrochemical lithium storage performance was obtained by the multilayer thin film. The initial discharge and charge specific capacity of the Si (15 nm)/C (5 nm) multilayer film anode are 2640 mA h g⁻¹ and 2560 mA h g⁻¹ with an initial coulombic efficiency of ∼97%. The retention specific capacity is about 2300 mA h g⁻¹ and there is ∼87% capacity retention after 200 cycles.

With a high specific capacity (4200 mA h g⁻¹), silicon based materials have become the most promising anode materials in lithium-ions batteries.     

Double-layer carbon protected CoS2 nanoparticles as an advanced anode for sodium-ion batteries

Cobalt disulfides with high theoretical capacity are regarded as appropriate anode materials for sodium ion batteries (SIBs), but their intrinsically low conductivity and large volume expansion lead to a poor electrochemical performance. In this work, graphitic carbon coated CoS₂ nanoparticles are encapsulated in bamboo-like carbon nanotubes by pyrolysis and sulfidation process. Graphitic carbon can improve the electrical conductivity and prevent the agglomeration of CoS₂ nanoparticles. Meanwhile, bamboo-like carbon nanotubes can serve as conductive skeleton frames to provide rapid and constant transport pathways for electrons and offer void space to buffer the volume change of CoS₂ nanoparticles. The advanced anode material exhibits a long-term capacity of 432.6 mA h g⁻¹ at 5 A g⁻¹ after 900 cycles and a rate capability of 419.6 mA h g⁻¹ even at 10 A g⁻¹ in the carbonate ester-based electrolyte. This avenue can be applicable for preparing other metal sulfide/carbon anode materials for sodium-ion batteries.

The outstanding electrochemical performance is ascribed to the novel structure design of CoS₂@GC@B-CNT.