Aqueous rechargeable zinc‐metal‐based batteries are an attractive alternative to lithium‐ion batteries for grid‐scale energy‐storage systems because of their high specific capacity, low cost, eco‐friendliness, and nonflammability. However, uncontrollable zinc dendrite growth limits the cycle life by piercing the separator, resulting in low zinc utilization in both alkaline and mild/neutral electrolytes. Herein, a polyacrylonitrile coating layer on a zinc anode produced by a simple drop coating approach to address the dendrite issue is reported. The coating layer not only improves the hydrophilicity of the zinc anode but also regulates zinc‐ion transport, consequently facilitating the uniform deposition of zinc ions to avoid dendrite formation. A symmetrical cell with the polymer‐coating‐layer‐modified Zn anode displays dendrite‐free plating/stripping with a long cycle lifespan (>1100 h), much better than that of the bare Zn anode. The modified zinc anode coupled with a Mn‐doped V2O5 cathode forms a stable rechargeable full battery. This method is a facile and feasible way to solve the zinc dendrite problem for rechargeable aqueous zinc‐metal batteries, providing a solid basis for application of aqueous rechargeable Zn batteries.

Transition-metal oxides are a prospective anode material for lithium ion battery because of their high theoretical specific capacity. However, the insulating nature of these oxides causes sluggish electron transport, hindering them from reaching theoretical capacity. Herein, we prepared NiCo 2 O 4 nanowires (NiCo 2 O 4 NWs) on carbon papers (CPs) by a hydrothermal method. The structural characterization shows that a large number of NiCo 2 O 4 NWs were aligned on the CPs, forming an interconnected network. This unique architecture could enhance electrical conductivity and accommodate NiCo 2 O 4 expansion during lithiation. Thus, the NiCo 2 O 4 NWs/CPs composite electrode exhibits outstanding capacity and ideal cycling performance. The reversible capacity of the first cycle is 1024.9 mAh g −1 and remains to be 1016.7 mAh g −1 after 200 cycles at 100 mA g −1 . Our work provided a high performance anode for lithium ion batteries.

Silicon/carbon nanotube (Si/CNTs) nanocomposite is a promising anode material for lithium ion batteries (LIBs). Challenges related to the tricky synthesis process, as well as the weak interaction between Si and CNTs, hinder practical applications. To address these issues, a facile, one-step method to synthesize Si/CNTs nanocomposite by using silica (SiO2) as a reactant via a magnesium reduction process was developed. In this synthesis, the heat released enables the as-obtained Si to react with CNTs in the interfacial region to form silicon carbide (SiC). By virtue of the unique structure composed of Si nanoparticles strongly anchored to conductive CNTs network with stable Si–C chemical bonding, the Si/SiC/CNT nanocomposite delivers a stable capacity of ~1100 mAh g−1 and a capacity retention of about 83.8% after 200 cycles at a current density of 100 mA g−1. Our studies may provide a convenient strategy for the preparation of the Si/C anode of LIBs.

Silicon/carbon (Si/C) composite has been proven to be an effective method of enhancing the electrochemical performance of Si-based anodes for lithium-ion batteries (LIBs). However, the practical application of Si/C materials in LIBs is difficult because of the weak interaction between Si and C. In this study, we applied two-step diazotization reactions to modify graphite nanosheets (GNs) and Si nanoparticles (Si NPs), yielding a stable Si–Ar–GNs composite. Owing to aryl (Ar) group bonding, Si NPs were dispersed well on the GNs. The as-prepared Si–Ar–GNs composite delivered an initial reversible capacity of 1174.7 mAh·g−1 at a current density of 100 mAh·g−1. Moreover, capacity remained at 727.3 mAh·g−1 after 100 cycles, showing improved cycling performance. This synthesis strategy can be extended to prepare other Si/C anode materials of LIBs.