In Situ Molecular Engineering Strategy to Construct Hierarchical MoS2 Double-Layer Nanotubes for Ultralong Lifespan "Rocking-Chair" Aqueous Zinc-Ion Batteries.

Rechargeable aqueous zinc ion batteries (AZIBs) have gained considerable attention owing to their low cost and high safety, but dendrite growth, low plating/stripping efficiency, surface passivation, and self-erosion of the Zn metal anode are hindering their application. Herein, a one-step in situ molecular engineering strategy for the simultaneous construction of hierarchical MoS2 double-layer nanotubes (MoS2-DLTs) with expanded layer-spacing, oxygen doping, structural defects, and an abundant 1T-phase is proposed, which are designed as an intercalation-type anode for "rocking-chair" AZIBs, avoiding the Zn anode issues and therefore displaying a long cycling life. Benefiting from the structural optimization and molecular engineering, the Zn2+ diffusion efficiency and interface reaction kinetics of MoS2-DLTs are enhanced. When coupled with a homemade ZnMn2O4 cathode, the assembled MoS2-DLTs//ZnMn2O4 full battery exhibited impressive cycling stability with a capacity retention of 86.6% over 10 000 cycles under 1 A g-1anode, outperforming most of the reported "rocking-chair" AZIBs. The Zn2+/H+ cointercalation mechanism of MoS2-DLTs is investigated by synchrotron in situ powder X-ray diffraction and multiple ex situ characterizations. This research demonstrates the feasibility of MoS2 for Zn-storage anodes that can be used to construct reliable aqueous full batteries.

Alkali etching zinc and manganese silicates derived from natural green algaes for supercapacitors with enhanced electrochemical properties.

A facile novel method of alkali etching was proposed to enhance the application of metal-silicates in supercapacitors. First, 3D N, S, P-doped C-zinc-silicate (C-ZnSi), and C-manganese-silicate (C-MnSi) were derived from calcined green algaes (GAs) in a N2 atmosphere. Second, the synthesized products were soaked in a 3.0 M NaOH aqueous solution for alkali etching (soaked for 6, 12 and 24 h) to obtain the etching metal silicates (e-C-ZnSi and e-C-MnSi). This method can yield a higher specific surface area and more pores, and this in turn can improve the electrochemical performance. In the three-electrode system, e-C-ZnSi and e-C-MnSi, which were soaked in NaOH solution for 12 h, exhibited the highest specific capacitances and cycling performance. Solid-state hybrid supercapacitor (HSC) devices were manufactured using C-MSi, e-C-MSi (M = Zn and Mn), and activated carbon (AC) (denoted as C-MSi//AC and e-C-MSi//AC). In the two-electrode system, the e-C-MSi//AC HSC devices exhibited higher areal specific capacitances and energy densities and better cycle performance than those of C-MSi//AC, especially e-C-MSi//AC-12 h HSC devices, which exhibited the best electrochemical properties. This study demonstrated that the naturally polluted GAs can be used as a reusable silica source for the synthesis of supercapacitors. Furthermore, alkali etching can enhance the electrochemical performance of metal silicates and can be used to prepare electrode materials applied for high-performance supercapacitors.

Biphase-Interface Enhanced Sodium Storage and Accelerated Charge Transfer: Flower-Like Anatase/Bronze TiO2/C as an Advanced Anode Material for Na-Ion Batteries.

Flower-like assembly of ultrathin nanosheets composed of anatase and bronze TiO2 embedded in carbon is successfully synthesized by a simple solvothermal reaction, followed with a high-temperature annealing. As an anode material in sodium-ion batteries, this composite exhibits outstanding electrochemical performances. It delivers a reversible capacity of 120 mA h g-1 over 6000 cycles at 10 C. Even at 100 C, there is still a capacity of 104 mA h g-1. Besides carbon matrix and hierarchical structure, abundant interfaces between anatase and bronze greatly enhance the performance by offering additional sites for reversible Na+ storage and improving the charge-transfer kinetics. The interface enhancements are confirmed by discharge/charge profiles, rate performances, electrochemical impedance spectra, and first-principle calculations. These results offer a new pathway to upgrade the performances of anode materials in sodium-ion batteries.

FeFe(CN)6 Nanocubes as a Bipolar Electrode Material in Aqueous Symmetric Sodium-Ion Batteries.

Bipolar materials, which work as both the cathode and anode material in aqueous sodium-ion batteries, have advantages over aqueous electrolytes such as the low cost of sodium and high convenience of the material processing. However, the available materials are greatly limited. Herein, Prussian blue FeFe(CN)6 nanocubes were successfully synthesized by using a modified co-precipitation method. Owing to the well-separated redox reactions, fair cycling stability and rate capability of FeFe(CN)6 , it could be developed as a bipolar material in an aqueous sodium-ion battery. The as-obtained full battery exhibits good cycling stability and rate capability. It was able to deliver a capacity of 32 mA h g-1 at 20 C, 76 % of the capacity at 2 C. After 200 cycles at 2 C, 97 % of the initial capacity was maintained for this battery, which suggests good cycling stability.