Aqueous Zn batteries have drawn tremendous attention for their several advantages. However, the challenges of Zn anodes such as the corrosion and ZnO densification have compromised their application in rechargeable Zn‐based batteries. In this paper, a straightforward strategy is employed to facilitate the uniform Zn stripping/plating of the Zn anode through using a ZrO2 coating layer, which contributes to the controllable nucleation sites for Zn2+ and fast Zn2+ transportation through the favorable Maxwell–Wagner polarization. As a result, the low polarization (24 mV at 0.25 mA cm−2), high Coulombic efficiency (99.36% at 20 mA cm−2), and long cycle life (over 3800 h at 0.25 mA cm−2) can be obtained for the ZrO2‐coated Zn anode. It is believed that the ZrO2 coating layer can also act as an inert physical barrier to decrease the contact of the anode and electrolyte, thus reducing both the Zn corrosion and formation of ZnO densification, and then improve the reversibility of Zn anode. The results demonstrated in this work provide an appealing strategy for the future development of rechargeable Zn‐based batteries.

Aqueous rechargeable zinc ion batteries (ZIBs) have been deemed to be possible candidates for large‐scale energy storage due to their ecoefficiency, substantial reserve, safety, and low cost. However, the challenges inherent in aqueous electrolytes, such as water splitting reactions, water evaporation, and liquid leakage, have greatly hindered their development in energy storage. Fortunately, polymer electrolytes would be able to overcome the abovementioned challenges. Moreover, the flexible properties of polymer electrolytes can facilitate their future application in wearable electronics. Recently, increasing attention has been attracted to the polymer electrolyte‐based zinc ion batteries. However, the development of polymer electrolytes for ZIBs is still in the early stages due to numerous challenges. Therefore, substantial research effort is required to overcome the challenges of polymer electrolyte‐based ZIBs. In this review, the current progress in developing polymer electrolytes, including solid polymer electrolytes, gel polymer electrolytes, and hybrid polymer electrolytes, as well as the interactions between electrodes and polymer electrolytes for ZIBs is comprehensively reviewed, analyzed, and discussed in terms of their synthesis, characterization, and performance validation. To facilitate further research and development of polymer electrolytes for ZIBs, the relevant challenges are summarized and analyzed, and some underlying approaches to overcome these challenges are also proposed.

A comprehensive understanding of the challenges in zinc-electrode materials and fabrication that limit the continuous development of rechargeable zinc–air batteries.

Lithium‐metal batteries (LMBs) with high energy densities are highly desirable for energy storage, but generally suffer from dendrite growth and side reactions in liquid electrolytes; thus the need for solid electrolytes with high mechanical strength, ionic conductivity, and compatible interface arises. Herein, a thiol‐branched solid polymer electrolyte (SPE) is introduced featuring high Li+ conductivity (2.26 × 10−4 S cm−1 at room temperature) and good mechanical strength (9.4 MPa)/toughness (≈500%), thus unblocking the tradeoff between ionic conductivity and mechanical robustness in polymer electrolytes. The SPE (denoted as M‐S‐PEGDA) is fabricated by covalently cross‐linking metal–organic frameworks (MOFs), tetrakis (3‐mercaptopropionic acid) pentaerythritol (PETMP), and poly(ethylene glycol) diacrylate (PEGDA) via multiple CSC bonds. The SPE also exhibits a high electrochemical window (>5.4 V), low interfacial impedance (<550 Ω), and impressive Li+ transference number (tLi+ = 0.44). As a result, Li||Li symmetrical cells with the thiol‐branched SPE displayed a high stability in a >1300 h cycling test. Moreover, a Li|M‐S‐PEGDA|LiFePO4 full cell demonstrates discharge capacity of 143.7 mAh g−1 and maintains 85.6% after 500 cycles at 0.5 C, displaying one of the most outstanding performances for SPEs to date.

Figure 15. a) Schematicdiagramoft he zinc/electrospun PCIn fiber battery. b) SEMa nd TEM images of the electrospun PCIn fibers. c) Electrochemicalperformances of the Zn/electrospun PCIn fiber battery.R eproducedw ith permission. [19]