Graphene-wrapped yolk-shell of silica-cobalt oxide as high-performing anode for lithium-ion batteries.

Silica (SiO2) shows promise as anode material for lithium-ion batteries due to its low cost, comparable lithium storage discharge potential and high theoretical capacity (approximately 1961 mA h g-1). However, it is plagued by issues of low electrochemical activity, low conductivity and severe volume expansion. To address these challenges, we initially coat SiO2 with CoO, followed by introducing SiO2@CoO into graphene sheets to fabricate an anode composite material (SiO2@CoO/GS) with uniformly dispersed particles and a 3D graphene wrapped yolk-shell structure. The coating of CoO on SiO2 converted the negative surface charge of SiO2 to positive, enabling effective electrostatic interactions between SiO2@CoO and graphene oxide sheets, which provided essential prerequisites for synthesizing composite materials with uniformly dispersed particles and good coating effects. Furthermore, the Co-metal formed during the charge-discharge process can act as a catalyst and electron transfer medium, activating the lithium storage activity of SiO2 and enhancing the conductivity of the electrode, conclusively achieving a higher lithium storage capacity. Ultimately, due to the activation of SiO2 by Co-metal during cycling and the excellent synergistic effect between SiO2@CoO and graphene, SiO2@CoO/GS delivers a high reversible capacity of 738 mA h g-1 after 500 cycles at 200 mA g-1. The product also demonstrates excellent rate performance with a reversible capacity of 206 mA h g-1 at a high specific current of 12.8 A g-1. The outstanding rate performance of SiO2@CoO/GS may be ascribed to the pseudo-capacitive contribution at high specific current upon cycling.

Prilling and Coating Strategy to Synthesize High-Performance Spherical NaNi0.4Fe0.2Mn0.4O2 Cathode Materials for Sodium Ion Batteries.

Low-cost sodium ion batteries are of great significance in large-scale energy storage applications. With its high energy density and simple synthesis process, layered transition-metal oxides have become one of the most likely sodium ion battery cathode materials to replace lithium ion batteries in the energy storage market. Here, we report a prilling and MoS2 coating strategy to prepare the spherical cathode material. The spherical micronano particles shorten the diffusion path of Na+, restrain the complexity phase transitions, and enhance the tap density of the materials. In addition, the MoS2 coating improves the electrical conductivity of the material and the structural stability of the cathode material in air. The initial specific discharge capacity is 148.4 mA h g-1 at 0.1 C, which can be maintained at 128.9 mA h g-1 after exposure to air for 10 days. This method dramatically improves the energy density and structural stability of the cathode material, which provides a new scheme for preparing high-performance sodium ion batteries.

High-Entropy Configuration Strategy to Build High Performance Na-Ion Layered Oxide Cathodes Derived from Simple Techniques.

Layered transition metal oxides are commonly used as the cathode materials in sodium-ion batteries due to their low cost and easy manufacturing. However, the application is hindered by poor rate performance and complex phase transitions. To address these challenges, a new seven-component high-entropy layered oxide cathode material, O3-NaNi0.25Fe0.15Mn0.3Ti0.1Sn0.05Co0.05Li0.1O2 (HEO) has been developed. The entropy stabilization effect plays a crucial role in improving the performance of electrochemical systems and the stability of structures. The HEO exhibits a specific discharge capacity of 154.1 mA h g-1 at 0.1 C and 94.5 mA h g-1 at 7 C. In-situ and ex-situ XRD results demonstrate that the HEO effectively retards complex phase transitions. This work provides a high-entropy design for the storage materials with a high energy density. Meanwhile, it eliminates industry doubts about the performance of sodium ion layered oxide cathode materials.

Preoxidation and Prilling Combined with Doping Strategy to Build High-Performance Recycling Spent LiFePO4 Materials.

Direct regeneration has gained much attention in LiFePO4 battery recycling due to its simplicity, ecofriendliness, and cost savings. However, the excess carbon residues from binder decomposition, conductive carbon, and coated carbon in spent LiFePO4 impair electrochemical performance of direct regenerated LiFePO4. Herein, we report a preoxidation and prilling collaborative doping strategy to restore spent LiFePO4 by direct regeneration. The excess carbon is effectively removed by preoxidation. At the same time, prilling not only reduces the size of the primary particles and shortens the diffusion distance of Li+ but also improves the tap density of the regenerated materials. Besides, the Li+ transmission of the regenerated LiFePO4 is further improved by Ti4+ doping. Compared with commercial LiFePO4, it has excellent low-temperature performance. The collaborative strategy provides a new insight into regenerating high-performance spent LiFePO4.

Construction of a Preoxidation and Cation Doping Regeneration Strategy to Improve Rate Performance Recycling Spent LiFePO4 Materials.

Efficient recycling of spent lithium-ion batteries (LIBs) is significant for solving environmental problems and promoting resource conservation. Economical recycling of LiFePO4 (LFP) batteries is extremely challenging due to the inexpensive production of LFP. Herein, we report a preoxidation combine with cation doping regeneration strategy to regenerate spent LiFePO4 (SLFP) with severely deteriorated. The binder, conductive agent, and residual carbon in SLFP are effectively removed through preoxidation treatment, which lays the foundation for the uniform and stable regeneration of LFP. Mg2+ doping is adopted to promote the diffusion efficiency of lithium ions, reduces the charge-transfer impedance, and further improves the electrochemical performance of the regenerated LFP. The discharge capacity of SLFP with severe deterioration recovers successfully from 43.2 to 136.9 mA h g-1 at 0.5 C. Compared with traditional methods, this technology is simple, economical, and environment-friendly. It provided an efficient way for recycling SLFP materials.

Simple synthesis of a hierarchical LiMn0.8Fe0.2PO4/C cathode by investigation of iron sources for lithium-ion batteries.

Iron (Fe) substitution is an effective strategy for improving the electrochemical performance of LiMnPO4 which has poor conductivity. Herein, we focus on investigating the effect of substitution of Mn with different iron sources, on the structure and electrochemical performances of the LiMnPO4 materials. The Fe-substituted LiMnPO4/C composites were synthesized via a simple and rational solid-state method, and will be of benefit for engineering applications. The characterization of the materials shows an obvious influence of the iron sources on structure and morphology. The N-LMFP material prepared using soluble FeNO3 as iron sources exhibits an excellent rate capacity of 122 mA h g-1 at 5C, and superior cyclability with a capacity retention of 98.9% after 400 cycles at 2C. The enhanced rate capability and cycling stability of N-LMFP are the result of the lowered electron/ion resistance and the improved reversibility of the reaction, that originates from the homogeneous fine particles and hierarchical structure with large mesopores. This research provides significant guidelines for designing an LiMnPO4 cathode with a high performance.

Tuning Electrochemical Performance of Li-Rich Layered Cathode Materials with a Solid Phase Fusion Strategy.

Li-rich layered cathode materials (LRMs) have attracted extensive attention because of their high theoretical specific capacity. However, their practical application is limited by the severe depreciation of capacity and voltage during cycling. Herein, high electrical conductivity MoS2 is constructed on Li1.2Ni0.2Mn0.6O2 (LLNM) surface through solid phase fusion technology (SFT). Extraordinarily, the MoS2 modified layer lessens the interface side reaction and stabilizes the surface structure of LLNM. Meanwhile, the strong electron conductivity of MoS2 speeds up electron transit at the surface. The results demonstrate that LLNM-M10 exhibits a remarkable electrochemical performance as it retains 183.3 mA h g-1 at 1 C after 250 cycles. More crucially, the modified electrode exhibits an exceptional low-temperature performance of 120.3 mA h g-1 at 0.1 C and -10 °C. Therefore, this presented strategy may provide a new method for further application of Li-rich layered cathode materials.

Composite Nanoarchitectonics with CoS2 Nanoparticles Embedded in Graphene Sheets for an Anode for Lithium-Ion Batteries.

Cobalt sulfides are attractive as intriguing candidates for anodes in Lithium-ion batteries (LIBs) due to their unique chemical and physical properties. In this work, CoS2@rGO (CSG) was synthesized by a hydrothermal method. TEM showed that CoS2 nanoparticles have an average particle size of 40 nm and were uniformly embedded in the surface of rGO. The battery electrode was prepared with this nanocomposite material and the charge and discharge performance was tested. The specific capacity, rate, and cycle stability of the battery were systematically analyzed. In situ XRD was used to study the electrochemical transformation mechanism of the material. The test results shows that the first discharge specific capacity of this nanocomposite reaches 1176.1 mAhg-1, and the specific capacity retention rate is 61.5% after 100 cycles, which was 47.5% higher than that of the pure CoS2 nanomaterial. When the rate changes from 5.0 C to 0.2 C, the charge-discharge specific capacity of the nanocomposite material can almost be restored to the initial capacity. The above results show that the CSG nanocomposites as a lithium-ion battery anode electrode has a high reversible specific capacity, better rate performance, and excellent cycle performance.

Fluorophosphorus derivative forms a beneficial film on both electrodes of high voltage lithium-ion batteries.

Layered lithium-rich oxides, as a series of highly promising cathode material for lithium-ion batteries, attract extensive attention due to their high specific capacity and high working potential (4.6 V vs Li/Li+). However, the poor interface stability of the cathode and electrolyte seriously restricts their practical application. In this article, theoretical calculations, linear sweep voltammetry and cyclic voltammetry results indicate that tris (pentafluorophenyl) phosphine (TPFPP) is a potential dual-functional electrolyte additive to solve interface problems. The TPFPP additive can decompose preferentially on the surface of both electrodes and form uniform and stable protective films, which effectively inhibit the continuous decomposition of the electrolyte and significantly alleviate the dissolution of transition metal ions during cycling. Owing to the above effects, the capacity retention and coulombic efficiency of Li1.17Ni0.25Mn0.58O2 (LLO)/graphite (Gr) cells are improved from 62.6% and 97.7% to 90.6% and 99.8% after 200 cycles at 0.3 C (1 C = 300 mA g-1), respectively. This study provides a wide prospect for the application of lithium-rich materials in the future.

Investigation of the structure and performance of Li[Li0.13Ni0.305Mn0.565]O2 Li-rich cathode materials derived from eco-friendly and simple coating techniques.

Constructing uniform nanoceramic coating layers is a well-known challenge in the field of coating materials. Herein, Al2O3-coated Li[Li0.13Ni0.305Mn0.565]O2 (LLNM) Li-rich cathode materials are successfully prepared through a dry prilling coating (DPC) method. The structures and electrochemical performances of the Al2O3-coated products are systematically examined. Typically, the cycling stability is enhanced and voltage degradation upon cycling is reduced, benefiting from the unique and controllable nano-sized Al2O3 coating layer. Moreover, metal ion dissolution is avoided when using the DPC method, which is eco-friendly and suitable for large scale production.

Improved High Temperature Performance of a Spinel LiNi0.5Mn1.5O4 Cathode for High-Voltage Lithium-Ion Batteries by Surface Modification of a Flexible Conductive Nanolayer.

The composite cathode material of the conductive polymer polyaniline (PANI)-coated spinel structural LiNi0.5Mn1.5O4 (LNMO) for high-voltage lithium-ion batteries has been successfully synthesized by an in situ chemical oxidation polymerization method. The electrode of the LNMO-PANI composite material shows superior rate capability and excellent cycling stability. A capacity of 123.4 mAh g-1 with the capacity retention of 99.7% can be maintained at 0.5C after 200 cycles in the voltage range of 3.0-4.95 V (vs Li/Li+) at room temperature. Even with cycling at 5C, a capacity of 65.5 mAh g-1 can still be achieved. The PANI coating layer can not only reduce the dissolution of Ni and Mn from the LNMO cubic framework into the electrolyte during cycling, but also significantly improve the undesirable interfacial reactions between the cathode and electrolyte, and markedly increase the electrical conductivity of the electrode. At 55 °C, the LNMO-PANI composite material exhibits more superior cyclic performance than pristine, that is, the capacity retention of 94.5% at 0.5C after 100 cycles vs that of 13.0%. This study offers an effective strategy for suppressing the decomposition of an electrolyte under the highly oxidizing (>4.5 V) and elevated temperature conditions.

Bio-Inspired Synthesis of an Ordered N/P Dual-Doped Porous Carbon and Application as an Anode for Sodium-Ion Batteries.

Carbonaceous materials are one of the most promising anode materials for sodium-ion batteries, because of their abundance, stability, and safe usage. However, the practical application of carbon materials is hindered by poor specific capacity and low initial Coulombic efficiency. The design of porous structure and doping with heteroatoms are two simple and effective methods to promote the sodium storage performance. Herein, the N, P co-doped porous carbon materials are fabricated using renewable and biodegradable gelatin as carbon and nitrogen resource, phosphoric acid as phosphorus precursor and polystyrene nanospheres as a template. The product can deliver a reversible capacity of 230 mA h g-1 at a current density of 0.2 A g-1 , and even a high capacity of 113 mA h g-1 at 10 Ag-1 . The enhanced sodium storage performance is attributed to the synergistic effect of the porosity and the dual-doping of nitrogen and phosphorus.