High-Voltage Solid-State Lithium Metal Batteries with Stable Anodic and Cathodic Interfaces by a Laminated Solid Polymer Electrolyte.

Solid polymer electrolyte (SPE) is quite an attractive candidate for constructing high-voltage Li metal batteries (LMBs) with high energy density and excellent safety. However, sim ultaneous achievement of high-voltage stability against the cathode and good compatibility with the Li anode remains challenging for the current SPE technology. Herein, a dual-layered solid electrolyte (DLSE) consisting of an oxidation-resistant poly(acrylonitrile) (PAN) layer facing a high-potential cathode and a reduction-compatible poly(vinylidene fluoride) (PVDF) layer incorporated by Li6.4La3Zr1.4Ta0.6O12 (LLZTO) nanoparticles and an ionic liquid plasticizer in contact with a Li anode was fabricated. The uniquely designed DLSE holds favorable overall properties in ionic conductivity, Li+ transference number, and mechanical strength. Moreover, the combined advantages of two polymer electrolyte layers greatly address the interface issues on both the cathode and anode. Consequently, the high-voltage LMBs employing the DLSE exhibit excellent room-temperature performances including high rate capacity and long cycle life.

Preparation and Optimization of New High-Power Nanoscale Li4Ti5O12 Full-Cell System.

Lithium ion batteries with graphite negative electrodes have been developed to date due to their low power density, which limits their application in many cases, however. Nanoscale Li4Ti5O12 has higher power density than conventional graphite anode materials. In order to ensure that the full-cell system has high power and high energy, cathode materials are very important. In this paper, three different cathode materials, LiNi0.8Co0.15Al0.05O2 (NCA), LiNi0.6Co0.2Mn0.2O2 (NCM622), and LiCoO2 (LCO), were used to conduct a comprehensive study, and optimal NCA-Li4Ti5O12(LTO) full battery system was selected under high power conditions. On the basis, in order to further increase battery power density, and in combination with the mechanism of the supercapacitor non-Faradic energy storage, polyaniline activated carbon material (PANI-AC) with excellent capacitance characteristics was prepared. In the end, we proposed a new type of hybrid battery capacitor system with high power and high energy.

Hydrothermal synthesis of Bi2WO6 with a new tungsten source and enhanced photocatalytic activity of Bi2WO6 hybridized with C3N4.

Bi2WO6 nanosheets were synthesized by a hydrothermal method with H2WO4 for the first time. The band structure of Bi2WO6 was investigated on the basis of density functional theory calculations. Bi2WO6 photocatalysts showed photocatalytic activity for the degradation of methylene blue under visible light irradiation. Kinetic studies using radical scavenger technologies suggested that holes were the dominant photo-oxidants. After hybridization with C3N4, the photocatalytic activity of Bi2WO6 was obviously enhanced. The enhanced photocatalytic activity of the C3N4/Bi2WO6 photocatalysts could be attributed to the effective separation of photogenerated e-/h+ pairs. The photogenerated holes on the valence band of Bi2WO6 can transfer to the highest occupied molecular orbital of C3N4via the well-developed interface, causing a reduction in the probability of e-/h+ recombination; consequently, large numbers of photogenerated holes led to the enhancement of the photocatalytic activity.