Self-assembled GeOX/Ti3C2TX Composites as Promising Anode Materials for Lithium Ion Batteries.

High-capacity germanium-based anode materials are alternative materials for outstanding electrochemical performance lithium-ion batteries (LIBs), but severe volume variation and pulverization problems during charging-discharging processes can seriously affect their electrochemical performance. In addressing this challenge, a simple strategy was used to prepare the self-assembled GeOX/Ti3C2TX composite in which the GeOX nanoparticles can grow directly on Ti3C2TX layers. Nanoscale GeOX uniformly renucleates on the surface and interlayers of Ti3C2TX, forming the stable multiphase structure, which guarantees its excellent electrochemical performance. Electrochemical evaluation has shown that the rate capability and reversibility of GeOX/Ti3C2TX are both greatly improved, which delivers a reversible discharge specific capacity of above 1400 mAh g-1 (at 100 mA g-1) and a reversible specific capacity of 900 mAh g-1 after 50 cycles while it still maintains a stable specific capacity of 725 mAh g-1 at 5000 mA g-1. Furthermore, the composite exhibits an exceptionally superior rate capability, making it a good electrochemical performance anode for LIBs.

Ultrahigh-Rate Behavior Anode Materials of MoSe2 Nanosheets Anchored on Dual-Heteroatoms Functionalized Graphene for Sodium-Ion Batteries.

MoSe2 is a prospective anode material for Na-ion batteries because of its layered structure and high theoretical capacity, while the unsatisfied electrochemical performance limits its further development. Herein, we report MoSe2 nanosheets anchored on dual-heteroatoms functionalized graphene by a solvothermal method. The heteroatoms and carbon matrix coexist in the form of graphitic-N/pyridinic-N/pyrrolic-N and P-C/P═O bonds, which result in excellent electronic conductivity of the materials and provide abundant active sites for electrochemical process. Results indicated that organic intercalation increased the layer spacing of the materials to facilitate sodium-ion diffusion, and the in situ formed carbon networks improved the conductivity among the layers of the materials and alleviated volume expansion during the continued charge and discharge process. As an anode of Na-ion batteries, the nanosheets materials exhibited ultrahigh rate performance and deliver capacities of approximately 200 mAh g-1 at the current density of 10 A g-1. The ultrahigh-rate performance can be attributed to its unique nanosheets structure, the dual-heteroatoms functionalized graphene, and the considerable pseudocapacitive quality of the material.

Multiple Linkage Modification of Lithium-Rich Layered Oxide Li1.2Mn0.54Ni0.13Co0.13O2 for Lithium Ion Battery.

A multiple linkage modification (MLM) method was investigated to comprehensively improve the properties of lithium-rich layered oxides. MLM Li1.2Mn0.54Ni0.13Co0.13O2 was successfully synthesized via continuous and appropriate heat treatment. The synthesized Li1.2Mn0.54Ni0.13Co0.13O2 particles were coated with a Li2ZrO3 layer and doped with Zr4+ by using a Zr compound as the MLM reagent. The Li2ZrO3 coating layer could protect materials from the corrosion of hydrogen fluoride, and the structure of the base materials was stabilized due to Zr4+ doping. In addition, the formation of Li2ZrO3 captured inactive residual lithium on the surface and absorbed lithium of host materials, thereby leading to the reduction in the Li/M ratio of materials and promoting the first-cycle Coulombic efficiency. The MLM material delivered the highest initial cycle Coulombic efficiency (∼85%), the best cycle and rate performance among bare and ZrO2-coated particles. These results indicate that MLM is an important technique for improving the performance of electrode materials.