Anchoring Carbon Spheres on Titanium Dioxide Modified Commercial Polyethylene (PE) Separator to Suppress Lithium Dendrites for Lithium Metal Batteries.

Lithium dendrites are easily generated for excessively-solved lithium ions (Li+) inside the lithium metal batteries, which will lead serious safety issues. In this experiment, carbon spheres (CS) are successfully anchored on TiO2 (CS@TiO2) in the hydrothermal polymerization, which is filtrated on the commercial PE separator (CS@TiO2@PE). The negative charge in CS can suppress random diffusion of anions through electrostatic interactions. Density functional theory (DFT) calculations show that CS contributes to the desolvation of Li+, thereby increasing the migration rate of Li+. Furthermore, TiO2 exhibits high affinity to liquid electrolytes and acts as a physical barrier to lithium dendrite formation. CS@TiO2 is a combination of the advantages of CS and TiO2. As results, the Li+ transference number of the CS@TiO2@PE separator can be promoted to 0.63. The Li||Li cell with the CS@TiO2@PE separator exhibits a stable cycle performance for more than 600 h and lower polarization voltage (17 mV) at 1 mA cm-2. The coulombic efficiency (CE) of the Li||Cu cells employe the CS@TiO2@PE separator is 81.63% over 130 cycles. The discharge capacity of LiFePO4||Li cells based on the CS@TiO2@PE separator is 1.73 mAh (capacity retention = 91.53% after 260 cycles). Thus, the CS@TiO2 layer inhibits lithium dendrite formation.

Lithiophilic Interface Layer Induced Uniform Deposition for Dendrite-free Lithium Metal Anodes in a 3D Polyethersulfone Frame.

Lithium metal anodes possess ultrahigh theoretical specific capacity for next-generation lithium metal batteries, but the infinite volume expansion and the growth of lithium dendrites remain a huge obstacle to their commercialization. Therefore, here, we construct a CuO-loaded 3D polyethersulfone (PES) nanofiber frame onto a lithiophilic Cu2O/Cu substrate to promote the lithium storage performance of the composite anode, and the 3D frame can effectively alleviate the volume expansion of lithium (Li) metal anodes. Meanwhile, lithium reacts with CuO in the composite nanofiber and Cu2O of the substrate to generate Li2O, which can strengthen the solid electrolyte interface (SEI) layer and achieve the uniform deposition of lithium. In addition, the combination of the heat treatment method and electrospinning technology solves the problem of poor adhesion between the fiber film and the substrate. As a result, the PES/CuO-Cu2O (PCC) composite current collector still maintains a smooth and flat lithium-depositing layer at 5 mA cm-2. The PCC-assembled Li||Cu half-cell can operate stably for 320 cycles at 0.5 mA cm-2, which is about 4 times that of bare Cu. Furthermore, symmetrical batteries with PCC@Li can maintain excellent cycle stability for 1770 h. Accordingly, this work provides a low-cost and highly effective strategy for stabilizing the lithium metal anode.

High-stability core-shell structured PAN/PVDF nanofiber separator with excellent lithium-ion transport property for lithium-based battery.

The ion transport channel constructed by the separator is crucial for the practical performance of Li-ion batteries, including cycling stability and high rate capability under high current. Traditional polyolefin separator is the storage of electrolyte, which guarantees the internal ion transport process. However, its weak interaction with electrolyte and low cationic transport capacity limit the application of lithium ion battery in large current. In this study, a kind of core-shell structured polyacrylonitrile (PAN)/polyvinylidene fluoride (PVDF) nanofiber separator composed of PAN core and PVDF shell was prepared by coaxial electrospinning technique. As a result, the mechanical strength of PAN/PVDF nanofiber separator is increased from 0.6 MPa of PVDF to 3.6 MPa for PAN core. Furthermore, PAN/PVDF nanofiber separator exhibits an improved lithium-ion transference number (0.66), which is resulted from F functional groups of PVDF shell. It is believed that the interactions between the lithium ion and F functional group could construct a fast ion transport channel. The LiCoO2/Li half-cells assembled with PAN/PVDF exhibited higher discharge capacity (5C) than those cells using pristine PVDF, PAN separators and polyethylene (PE) separator. It is worth mentioning that the cells with PAN/PVDF separator also have excellent cycle stability. This study provides a new idea about separator-design strategy for high-performance lithium-based battery.