Synthesis and Electrochemical Performance of Electrostatic Self-Assembled Nano-Silicon@N-Doped Reduced Graphene Oxide/Carbon Nanofibers Composite as Anode Material for Lithium-Ion Batteries

To improve the performance of PtRu/nitrogen-doped graphene composite carbon nanofibers, the composite carbon nanofibers were thermally compensated by deep cryogenic treatment (DCT), which realized the morphology reconstruction of composite carbon nanofibers. The effects of different DCT times were compared: 12 h, 18 h, and 24 h. The morphology reconstruction mechanism was explored by combining the change of inner chain structure and material group. The results showed that the fibers treated for 12 h had better physical and chemical properties, where the diameter is evenly distributed between 500 and 800 nm. Combined with Fourier infrared analysis, the longer the cryogenic time, the more easily the water vapor and nitrogen enter polymerization reaction, causing changes of chain structure and degradation performance. With great performance of carbonization and group transformation, the PtRu/nitrogen-doped graphene composite carbon nanofibers can be used as an efficient direct alcohol fuel cell catalyst and promote its commercialization.

Research on the Morphology Reconstruction of Deep Cryogenic Treatment on PtRu/nitrogen-Doped Graphene Composite Carbon Nanofibers

Zhu²,

Wang

et al. 2022

Strategies for Controlling or Releasing the Influence Due to the Volume Expansion of Silicon inside Si−C Composite Anode for High-Performance Lithium-Ion Batteries

Zhang

Weng

et al. 2022

Currently, silicon is considered among the foremost promising anode materials, due to its high capacity, abundant reserves, environmental friendliness, and low working potential. However, the huge volume changes in silicon anode materials can pulverize the material particles and result in the shedding of active materials and the continual rupturing of the solid electrolyte interface film, leading to a short cycle life and rapid capacity decay. Therefore, the practical application of silicon anode materials is hindered. However, carbon recombination may remedy this defect. In silicon/carbon composite anode materials, silicon provides ultra-high capacity, and carbon is used as a buffer, to relieve the volume expansion of silicon; thus, increasing the use of silicon-based anode materials. To ensure the future utilization of silicon as an anode material in lithium-ion batteries, this review considers the dampening effect on the volume expansion of silicon particles by the formation of carbon layers, cavities, and chemical bonds. Silicon-carbon composites are classified herein as coated core-shell structure, hollow core-shell structure, porous structure, and embedded structure. The above structures can adequately accommodate the Si volume expansion, buffer the mechanical stress, and ameliorate the interface/surface stability, with the potential for performance enhancement. Finally, a perspective on future studies on Si−C anodes is suggested. In the future, the rational design of high-capacity Si−C anodes for better lithium-ion batteries will narrow the gap between theoretical research and practical applications.

Nano-Silicon@Exfoliated Graphite/Pyrolytic Polyaniline Composite of a High-Performance Cathode for Lithium Storage

Zhu

Duan

et al. 2023

In this paper, a Si@EG composite was prepared by liquid phase mixing and the elevated temperature solid phase method, while polyaniline was synthesized by the in situ chemical polymerization of aniline monomer to coat the surface of nano-silicon and exfoliated graphite composites (Si@EG). Pyrolytic polyaniline (p-PANI) coating prevents the agglomeration of silicon nanoparticles, forming a good conductive network that effectively alleviates the volume expansion effect of silicon electrodes. SEM, TEM, XRD, Raman, TGA and BET were used to observe the morphology and analyze the structure of the samples. The electrochemical properties of the materials were tested by the constant current charge discharge and cyclic voltammetry (CV) methods. The results show that Si@EG@p-PANI not only inhibits the agglomeration between silicon nanoparticles and forms a good conductive network but also uses the outermost layer of p-PANI carbon coating to effectively alleviate the volume expansion of silicon nanoparticles during cycling. Si@EG@p-PANI had a high initial specific capacity of 1491 mAh g−1 and still maintains 752 mAh g−1 after 100 cycles at 100 mA g−1, which shows that it possesses excellent electrochemical stability and reversibility.