Investigation of Cu doped flake-NiO as an anode material for lithium ion batteries

Cu foil is widely used in commercial lithium ion batteries as the current collector of anode materials with excellent conductivity and stability. In this research, commercial Cu foil was chosen as the current collector and substrate for the synthesis of Cu doped flake-NiO via a traditional hydrothermal method. The effect of the ratio of Cu and the calcination temperature on the electrochemical performance of NiO was investigated. The structure and phase composition of the Cu doped flake-NiO electrode were studied through X-ray diffraction (XRD), scanning electron microscopy (SEM), Energy dispersive X-ray analysis (EDAX), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and inductive coupled plasma emission spectrometry (ICP). The electrochemical properties of the Cu doped flake-NiO electrode were studied through cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS) and a galvanostatic charge–discharge cycling technique. According to the results, the Cu-doped NiO electrode, calcined at 400 °C with a molar ratio of Cu : Ni = 1 : 8, exhibited a high reversible charge capacity. The good cycling stability and rate performance indicate that the as-prepared electrode can be applied as a potential anode for lithium ion batteries.

Cu doped flake-NiO shows excellent electrochemical performance as anode materials for lithium ion batteries.     

Ultrafine MoO2 nanoparticles encapsulated in a hierarchically porous carbon nanofiber film as a high-performance binder-free anode in lithium ion batteries

Flexible free-standing hierarchically porous carbon nanofibers embedded with ultrafine (∼3.5 nm) MoO₂ nanoparticles (denoted as MoO₂@HPCNFs) have been synthesized by electrospinning and subsequent heat treatment. When evaluated as a binder-free anode in Li-ion batteries, the as-obtained MoO₂@HPCNFs film exhibits excellent capacity retention with high reversible capacity (≥1055 mA h g⁻¹ at 100 mA g⁻¹) and good rate capability (425 mA h g⁻¹ at 2000 mA g⁻¹), which is much superior to most of the previously reported MoO₂-based materials. The synergistic effect of uniformly dispersed ultrasmall MoO₂ nanoparticles and a three-dimensionally hierarchical porous conductive network constructed by HPCNFs effectively improve the utilization rate of active materials, enhance the transport of both electrons and Li⁺ ions, facilitate the electrolyte penetration, and promote the Li⁺ storage kinetics and stability, thus leading to a greatly enhanced electrochemical performance.

A novel binder-free LIB anode made of ultrafine MoO₂ nanoparticles encapsulated in hierarchically porous carbon nanofibers exhibits high Li-storage performance.     

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⁺.     

Rheological phase reaction synthesis and electrochemical performance of rufigallol anode for lithium ion batteries

1,2,3,5,6,7-hexahydroxy-anthraquinone (rufigallol) and its metal–organic complex (rufigallol-Li/Ni, R-LN) were both synthesized. The electrochemical performance investigation of rufigallol and R-LN as anodes for lithium ion batteries indicates that pure rufigallol delivers high initial capacity but poor cycling stability, by contrast, the R-LN complex exhibits high initial capacity and excellent cycling stability.

Rufigallol was synthesized by rheological phase method with high yield and investigated as anode for lithium ion batteries.

Lithium ion batteries (LIBs) have proven to be clean and efficient energy-storage technologies to meet the growing demand for green and sustainable electric power storage. Considering the sustainability, low cost, abundant natural sources, structural design with tolerance for variable functional groups, fast reaction kinetics and high power density, organic electrode materials have been the most competitive alternative to traditional inorganic materials.^1–6 Quinone organic materials with carbonyl functional group have received great concern for their high theoretical capacities and reaction reversibility. While, the dissolution of small molecule quinones in the organic electrolyte and the resulting capacity attenuation have restricted their application. Therefore, it is urgently demanded to design new organic electrode materials with high energy efficiency and good cycling stability. Among small molecule quinones, 1,2,3,5,6,7-hexahydroxy-anthraquinone (rufigallol) as a critical component has been widely used in dye industry, drug synthesis, and organic materials.^7–10 Rufigallol was firstly synthesized in 1836.¹¹ Since then, very little efficient method for the preparation of rufigallol has been reported. Recently, Bisoyi and Kumar''s research indicates that the rufigallol can be achieved by self-condensation of gallic acid in the presence of sulfuric acid under microwave-assisted, and the yield reached 86%.¹² Also, as far as we know, there is no correlative literature exists about rufigallol being used as electrode materials for lithium ion batteries.It is well-known that the dissolution of organic molecule in the electrolyte can be effectively suppressed via salt formation. Therefore, constructing the metal–organic complex is an efficient way to obtain a stable and flexible framework as well as a better cycling stability.^13–19 In our previous study,^20,21 we have successfully realized the improvement of cycling stability for 3,4,9,10-perylene-tetracarboxylic acid-dianhydride (NTCDA) through the introducing of Li/Ni or Co/Mn to the matrix material. The obtained metal–organic complex, namely, Li/Ni-1,4,5,8-naphthalenetetracarboxylate or Co/Mn-1,4,5,8-naphthalenetetracarboxylate, showed a high specific capacity and a good cycling stability.Herein, we developed a simple, economical and effective rheological phase method²² to synthesize the rufigallol with high yield and investigated its electrochemical application in lithium ion batteries. In view of the easily connecting of hydroxyl groups in aromatic carbonyl compound for rufigallol with metal ions, in order to modify the cycling stability of pure rufigallol, we synthesized rufigallol-Li/Ni complex (R-LN) through the introducing of lithium and nickel by a hydrothermal method. When used as the LIBs anode, rufigallol shows initial discharge and charge capacities of 977 mA h g⁻¹ and 460 mA h g⁻¹, respectively, which is far higher than that of traditional graphite anode. The R-LN complex delivers initial a charge capacity of 560 mA h g⁻¹ and still remain at about 500 mA h g⁻¹ after 100 cycles, indicating a good electrochemical performance. Our work presents a new quinone-based organic materials with high capacity and competitive cycling stability, which enriches the organic electrode materials.     

Electroless plating of a Sn–Ni/graphite sheet composite with improved cyclability as an anode material for lithium ion batteries

A Sn–Ni/graphite sheet composite is synthesized by a simple electroless plating method as an anode material for lithium ion batteries (LIBs). The microstructure and electrochemical properties of the composite are characterized by field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), cyclic voltammetry (CV), and AC impedance spectroscopy. The results show that the as-prepared composite has Sn–Ni nanoparticles around 100 nm in size, where metallic Ni acts as an “anchor” to fix metallic Sn. The reunion phenomenon of Sn is alleviated by adding metallic Ni between the metallic Sn and graphite sheets. The Sn–Ni/graphite sheet electrode exhibits a good rate performance with a capability of 637.4, 586.3, 466.7, 371.5, 273.6, 165.3 and 97.3 mA h g⁻¹ at a current density of 0.1, 0.2, 0.5, 1.0, 2.0, 5.0 and 10 A g⁻¹, respectively. The good electrical conductivity of Ni, high specific capacity of Sn and excellent cycling capability of the graphite sheets have a synergistic effect and are the main reasons behind the superior electrochemical performance. Furthermore, the as-prepared composite exhibits excellent lithium storage capacity and the reversible capacity increased as the cycle number increased.

A Sn–Ni/graphite sheet composite is synthesized by a simple electroless plating method as an anode material for lithium ion batteries (LIBs).     

Application of soot discharged from the combustion of marine gas oil as an anode material for lithium ion batteries

Many studies have recently investigated the characteristics of combustion products emitted from ships and onshore plant facilities for use as energy sources. Most combustion products that have been reported until now are from heavy oils, however, no studies on those from light oils have been published. This study attempted to use the combustion products from the light oils from naval ships as anode materials for lithium ion batteries (LIBs). These products have a carbon black morphology and were transformed into highly crystalline carbon structures through a simple heat treatment. These new structured materials showed reversible capacities of 544, 538, 510, 485, 451 and 395 mA h g⁻¹ at C-rates of 0.1, 0.2, 0.5, 1.0, 2.0 and 5.0C, respectively, and excellent rate performance. These findings were the result of a combination hierarchical pores ranging from the meso- to macroscale and the high capacitive charge storage behavior of the soot. The results of this study prove that annealed soot with a unique multilayer graphite structure shows promising electrochemical performance suitable for the production of low-cost, high-performance LIB anode materials.

Many studies have recently investigated the characteristics of combustion products emitted from ships and onshore plant facilities for use as energy sources.     

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.     

Stabilization of lithium anode with ceramic-rich interlayer for all solid-state batteries

The deposition of thin layers of polymer/ceramic on a lithium surface to produce a strong barrier against dendrites was demonstrated. Different forms (needle, sphere, rod) and types of ceramic (Al₂O₃, Mg₂B₂O₅) were tested and polymer/ceramic interlayers of a few micrometers (4 μm minimum) between the lithium and the PEO-based solid polymer electrolyte (SPE) were deposited. Interlayers with high amounts of ceramic up to 85 wt% were successfully coated on the surface of lithium foil. Compact “polymer in ceramic” layers were observed when Al₂O₃ spheres were used for instance, providing a strong barrier against the progression of dendrites as well as a buffer layer to alleviate the lithium deformation during stripping/plating cycles. The electrochemical performance of the lithium anodes was assessed in symmetrical Li/SPE/Li cells and in full all-solid-state LiFePO₄ (LFP)/SPE/Li batteries. It was observed for all the cells that the charge transfer resistance was significantly reduced after the deposition of the polymer/ceramic layers on the lithium surface. In addition, the symmetrical cells were able to cycle at higher C-rates and the durability at C/4 was even improved by a factor of 8. Microscopic observations of Li/SPE/Li stacks after cycling revealed that the polymer/ceramic interlayer reduces the deformation of lithium upon cycling and avoids the formation of dendrites. Finally, LFP/SPE/Li batteries were cycled and better coulombic efficiencies as well as capacity retentions were obtained with the modified lithium electrodes. This work is patent-pending (WO2021/159209A1).

Significant electrochemical performance improvement of symmetric Li/Li polymer cells at C/4 by using ceramic-rich coated lithium anodes.     

Three-dimensional thiophene-diketopyrrolopyrrole-based molecules/graphene aerogel as high-performance anode material for lithium-ion batteries

Herein, 3,6-di(thiophen-2-yl)-2,5-dihydropyrrolo[3,4-c]pyrrole-1,4-dione (TDPP) and di-tert-butyl 2,2′-(1,4-dioxo-3,6-di(thiophen-2-yl)pyrrolo[3,4-c]pyrrole-2,5(1H,4H)-diyl)diacetate (TDPPA) were synthesized, which were then loaded in graphene aerogels. The as-prepared thiophene-diketopyrrolopyrrole-based molecules/reduced graphene oxide composites for lithium-ion battery (LIB) anode composites consist of DPPs nanorods on a graphene network. In relation to the DPPs part, embedding DPPs nanorods into graphene aerogels can effectively reduce the dissolution of DPPs in the electrolyte. It can serve to prevent electrode rupture and improve electron transport and lithium-ion diffusion rate, by partially connecting DPPs nanorods through graphene. The composite not only has a high reversible capacity, but also shows excellent cycling stability and performance, due to the densely distributed graphene nanosheets forming a three-dimensional conductive network. The TDPP₆₀ electrode exhibits high reversible capacity and excellent performance, showing an initial discharge capacity of 835 mA h g⁻¹ at a current density of 100 mA g⁻¹. Even at a current density of 1000 mA g⁻¹, after 500 cycles, it still demonstrates a discharge capacity of 303 mA h g⁻¹ with a capacity retention of 80.7%.

Herein, TDPP and TDPPA were synthesized and then loaded on graphene by hydrothermal method to obtain TDPP/RGO and TDPPA/RGO aerogel, which were applied as anode for LiBs.     

Structure and conductivity enhanced treble-shelled porous silicon as an anode for high-performance lithium-ion batteries

Silicon is regarded as the next generation anode material for lithium-ion batteries because of its high specific capacity, low intercalation potential and abundant reserves. However, huge volume changes during the lithiation and delithiation processes and low electrical conductivity obstruct the practical applications of silicon anodes. In this study, a treble-shelled porous silicon (TS-P-Si) structure was synthesized via a three-step approach. The TS-P-Si anode delivered a capacity of 858.94 mA h g⁻¹ and a capacity retention of 87.8% (753.99 mA h g⁻¹) after being subjected to 400 cycles at a current density of 400 mA g⁻¹. The good cycling performance was due to the unique structure of the inner silicon oxide layer, middle silver nano-particle layer and outer carbon layer, leading to a good conductivity and a decreased volume change of this silicon-based anode.

In this paper, a treble-shelled porous silicon structure is synthesized through three-step approach to enhance the structural stability and conductivity.     

A porous silicon anode prepared by dealloying a Sr-modified Al–Si eutectic alloy for lithium ion batteries

Silicon has been considered to be one of the most promising anode materials for next generation lithium ion batteries due to its high theoretical specific capacity. However, its huge volume expansion during the lithiation/delithiation process that can result in rapid capacity fading and low conductivity present significant challenges for application. In this study, the morphology of Si in an Al–Si eutectic alloy was modified by Sr, and porous Si was then produced by dealloying the precursor. Profiting from the unique structure, the Si anode exhibits an excellent reversible capacity of 405 mA h g⁻¹ at 0.5 A g⁻¹ after 100 cycles and a fantastic first cycle coulombic efficiency of 83.74%. Furthermore, the porous silicon modified by Sr delivers a stable capacity of 594.8 mA h g⁻¹ even at a high current density of 2 A g⁻¹ after 50 cycles, suggesting a good rate capability.

With a porous coralloid structure, the silicon anode prepared by dealloying the Sr-modified Al–Si eutectic alloy exhibits excellent cycle and rate performances.     

Synthesis of hierarchical Sn/SnO nanosheets assembled by carbon-coated hollow nanospheres as anode materials for lithium/sodium ion batteries

Tin-based anode materials have aroused interest due to their high capacities. Nevertheless, the volume expansion problem during lithium insertion/extraction processes has severely hindered their practical application. In particular, nano–micro hierarchical structure is attractive with the integrated advantages of nano-effect and high thermal stability of the microstructure. Herein, hierarchical Sn/SnO nanosheets assembled by carbon-coated hollow nanospheres were successfully synthesized by a facile glucose-assisted hydrothermal method, in which the glucose served as both morphology-control agent and carbon source. The hierarchical Sn/SnO nanosheets exhibit excellent electrochemical performances owing to the unique configuration and carbon coating. Specifically, a reversible high capacity of 2072.2 mA h g⁻¹ was observed at 100 mA g⁻¹. Further, 964.1 mA h g⁻¹ after 100 cycles at 100 mA g⁻¹ and 820.4 mA h g⁻¹ at 1000 mA g⁻¹ after 300 cycles could be obtained. Encouragingly, the Sn/SnO also presents certain sodium ion storage properties. This facile synthetic strategy may provide new insight into fabricating high-performance Sn-based anode materials combining the advantages of both structure and carbon coating.

Hierarchical Sn/SnO nanosheets assembled by carbon-coated hollow nanospheres with promising lithium and sodium storage performances.     

Li2ZnTi3O8/graphene nanocomposite as a high-performance anode material for lithium-ion batteries

An Li₂ZnTi₃O₈/graphene (LZTO/G) anode is successfully synthesized by a two-step reaction. The results show that LZTO particles can be well dispersed into the graphene conductive network. The conductive structure greatly improves the electrochemical performance of LZTO/G. When cycled for 400 cycles, 76.4% of the capacity for the 2nd cycle is maintained at 1 A g⁻¹. Also, 174.8 and 156.5 mA h g⁻¹ are still delivered at the 100th cycle for 5 and 6 A g⁻¹, respectively. The excellent cyclic performance and the large specific capacities at high current densities are due to the good conductive network of the LZTO active particles, large pore volume, small particle size, low charge-transfer resistance and high lithium diffusion coefficient.

The structure of G modifying LZTO is beneficial for the diffusion of Li⁺ ions and transportation of electrons.     

Controllable synthesis of nanostructured ZnCo2O4 as high-performance anode materials for lithium-ion batteries

Nanostructured ZnCo₂O₄ anode materials for lithium-ion batteries (LIBs) have been successfully prepared by a two-step process, combining facile and concise electrospinning and simple post-treatment techniques. Three different structured ZnCo₂O₄ anodes (nanoparticles, nanotubes and nanowires) can be prepared by simply adjusting the ratio of metallic salt and PVP in the precursor solutions. Charge–discharge tests and cyclic voltammetry (CV) have been conducted to evaluate the lithium storage performances of ZnCo₂O₄ anodes, particularly for ZnCo₂O₄ nanotubes obtained from a weight ratio 2 : 4 of metallic salt and PVP polymer in the precursor solution. Remarkably, ZnCo₂O₄ nanotubes exhibit high specific capacity, good rate property, and long cycling stability. Reversible capacity is still maintained at 1180.8 mA h g⁻¹ after 275 cycles at a current density of 200 mA g⁻¹. In case of rate capability, even after cycling at the 2000 mA g⁻¹ current density, the capacity could recover to 684 mA h g⁻¹. The brilliant electrochemical properties of the ZnCo₂O₄ anodes make them promising anodes for LIBs and other energy storage applications.

ZnCo₂O₄ nanoparticles, nanotubes, and nanofibers can be controllably prepared by simply tuning the weight ratios of metallic salts and PVP polymer in the precursor solution.     

Porous hydrogen substituted graphyne as a promising anode for lithium-ion batteries

Porous hydrogen substituted graphyne (HsGY) has been considered as a promising candidate for anode material due to its excellent electrochemical properties. In this work, we found that monolayer and bilayer HsGY are good electrodes for high charge capacity lithium-ion batteries based on density functional theory calculations. Mechanical tests reveal that monolayer and bilayer HsGY exhibit excellent mechanical properties, including large critical strains (>25%) and high in-plane stiffness (>200 N m⁻¹). The bilayer HsGY displays ultrahigh stiffness (400.27 N m⁻¹). Li adsorption on bilayer HsGY is stronger than that on the monolayer HsGY. Moreover, Li diffusion on the surfaces of monolayer and bilayer HsGY has low energy barriers (<0.5 eV). Our calculation results suggest that HsGY may contain the highest theoretical charge capacity among two-dimensional (2D) materials studied so far, with ultrahigh Li capacities of 3378 and 2895 mA h g⁻¹ for monolayer and bilayer HsGY, respectively. Given these advantages, including large critical strain, high mechanical stiffness, strong adsorption, low diffusive energy barrier, and high charge capacity, we conclude that both monolayer and bilayer HsGY could be promising anode materials for lithium-ion batteries.

Porous hydrogen substituted graphyne (HsGY) has been considered as a promising candidate for anode material due to its excellent electrochemical properties.     

A nanostructured SnO2/Ni/CNT composite as an anode for Li ion batteries

A SnO₂/Ni/CNT nanocomposite was synthesized using a simple one-step hydrothermal method followed by calcination. A structural study via XRD shows that the tetragonal rutile structure of SnO₂ is maintained. Further, X-ray photoelectron spectroscopy (XPS) and Raman studies confirm the existence of SnO₂ along with CNTs and Ni nanoparticles. The electrochemical performance was investigated via cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and galvanostatic charge–discharge measurements. The nanocomposite has been used as an anode material for lithium-ion batteries. The SnO₂/Ni/CNT nanocomposite exhibited an initial discharge capacity of 5312 mA h g⁻¹ and a corresponding charge capacity of 2267 mA h g⁻¹ during the first cycle at 50 mA g⁻¹. Pristine SnO₂ showed a discharge/charge capacity of 1445/636 mA h g⁻¹ during the first cycle at 50 mA g⁻¹. This clearly shows the effects of the optimum concentrations of CNTs and Ni. Further, the nanocomposite (SnNiCn) shows a discharge capacity as high as 919 mA h g⁻¹ after 210 cycles at a current density of 400 mA g⁻¹ in a Li-ion battery set-up. Thus, the obtained capacity from the nanocomposite is much higher compared to pristine SnO₂. The higher capacity in the nanoheterostructure is due to the well-dispersed nanosized Ni-decorated stabilized SnO₂ along with the CNTs, avoiding pulverization as a result of the volumetric change of the nanoparticles being minimized. The material accommodates huge volume expansion and avoids the agglomeration of nanoparticles during the lithiation and delithiation processes. The Ni nanoparticles can successfully inhibit Sn coarsening during cycling, resulting in the enhancement of stability during reversible conversion reactions. They ultimately enhance the capacity, giving stability to the nanocomposite and improving performance. Additionally, the material exhibits a lower Warburg coefficient and higher Li ion diffusion coefficient, which in turn accelerate the interfacial charge transfer process; this is also responsible for the enhanced stable electrochemical performance. A detailed mechanism is expressed and elaborated on to provide a better understanding of the enhanced electrochemical performance.

SnO₂/Ni/CNT nanocomposite approach has been demonstrated which confers shielding against volume expansion due to the use of optimum % of Ni & CNT exhibiting superior cycling stability and rate capabilities of the stable electrode structure.     

Hard carbon spheres prepared by a modified Stöber method as anode material for high-performance potassium-ion batteries

The Stöber method is a highly efficient synthesis strategy for homogeneous monodisperse polymer colloidal spheres and carbon spheres. This work delivers an extended Stöber method and investigates the synthesis process. By calcining the precursor under appropriate conditions, solid secondary particles of amorphous carbon (SSAC) and hollow secondary particles of graphitized carbon (HSGC) can be directly synthesized. The two materials have a nano-primary particle structure and a closely-packed sub-micron secondary particle structure, which can be used in energy storage. We find that SSAC and HSGC have high potassium-ion storage capacity with reversible capacities of 274 mA h g⁻¹ and 283 mA h g⁻¹ at 20 mA g⁻¹ respectively. Significantly, SSAC has better rate performance with a specific capacity of 107 mA h g⁻¹ at 1 A g⁻¹.

A modified Stöber method synthesizes resorcinol-formaldehyde resin-based secondary particle hard carbon spheres as anode material for high-performance potassium-ion batteries.     

High ion conductivity based on a polyurethane composite solid electrolyte for all-solid-state lithium batteries

Solid polymer electrolytes (SPE) are considered a key material in all-solid Li-ion batteries (SLIBs). However, the poor ion conductivity at room temperature limits its practical applications. In this work, a new composite polymer solid electrolyte based on polyurethane (PU)/LiTFSI–Al₂O₃–LiOH materials is proposed. By adding a few inert fillers (Al₂O₃) and active agents (LiOH) into the PU/LiTFSI system, the ion conductivity of the SPE reaches 2 × 10⁻³ S cm⁻¹ at room temperature. Exploiting LiFePO₄ (LFP)‖Li as electrodes, the PU-based composite lithium battery is prepared. The experimental result shows that the LFP|SPE|Li displays high specific discharge capacity. The first specific discharge capacities at 0.2C, 0.5C, 1C and 3C are 159.6, 126, 110 and 90.1 mA h g⁻¹ respectively, and the Coulomb efficiency is found to be stable in the region of 92–99% which also shows a desirable cyclic stability after 150 cycles.

Adding inert filler to reduce the coupling effect of functional groups to Li⁺ and modifying the functional groups to reduce the adsorption of Li⁺ can lead to high ionic conductivity.     

Synthesis of interconnected mesoporous ZnCo2O4 nanosheets on a 3D graphene foam as a binder-free anode for high-performance Li-ion batteries

Interconnected mesoporous sheet-like ZnCo₂O₄ nanomaterials directly grown on a three-dimensional (3D) graphene film (GF) coated on Ni foam (NF) have been successfully synthesized via an effective chemical vapor deposition (CVD) method combined with a subsequent hydrothermal route. When the ZnCo₂O₄@3DGF@NF composite material with a high surface area of 46.06 m² g⁻¹ is evaluated as a binder-free anode material for lithium ion batteries, it exhibits a superior electrochemical performance with a high discharge capacity (1223 mA h g⁻¹ at a current density of 500 mA g⁻¹ after 240 cycles), and an excellent reversibility (coulombic efficiency of 97–99%). Such an outstanding electrochemical performance may be attributed to its unique mesoporous sheet-like nanostructure with a 3DGF supporting, which can facilitate the electrolyte penetration and accelerate the ion/electron transport, as well as buffer the volume variation during charge/discharge processes.

Mesoporous ZnCo₂O₄ nanomaterials grown on a three-dimensional (3D) graphene film (GF) coated on Ni foam (NF) have been synthesized via an effective chemical vapor deposition (CVD) method combined with a subsequent hydrothermal route.     

Three-dimensional hierarchical ZnCo2O4@C3N4-B nanoflowers as high-performance anode materials for lithium-ion batteries

ZnCo₂O₄ has become one of the most widely used anode materials due to its good specific capacity, cost-efficiency, high thermal stability and environmental benignity. However, its poor conductivity and cycle stability have limited its practical application in lithium-ion batteries. To overcome these issues, we constructed a 3D nanoflower composite material (ZnCo₂O₄@C₃N₄-B) by combining ZnCo₂O₄ as a framework and B-doped g-C₃N₄ (g-C₃N₄-B) as a new carbon source material via a simple hydrothermal method. ZnCo₂O₄@C₃N₄-B exhibited exceptional specific capacitance of 919.76 mA h g⁻¹ after 500 cycles at 0.2 A g⁻¹ and a long-term capacity retention of 97.8% after 1000 cycles at 2 A g⁻¹. The high reversible capacity, long cycling life and good rate performance could be attributed to the 3D interconnected architecture and doping of g-C₃N₄-B. This work provides a simple and general strategy to design high-performance anode materials for lithium-ion batteries to meet the needs of practical applications.

ZnCo₂O₄ has become one of the most widely used anode materials due to its good specific capacity, cost-efficiency, high thermal stability and environmental benignity.