锌
材料科学
电解质
沉积(地质)
金属
复合数
化学工程
聚合物
冶金
电极
电镀
镍
聚合物电解质
作者
Fu Zhou,Hongbo Wei,Mengyu Shuai,Zhang Wen,Ao Li,C Wang,Qi Liu
标识
DOI:10.1021/acsaem.6c00287
摘要
The development of polymer electrolytes for zinc metal batteries (ZMBs) is fundamentally constrained by the intrinsic trade-off between low ionic transport efficiency and poor interfacial stability. Herein, we present a high-flux composite polymer electrolyte (CPE) that is dendrite-free via an integrated strategy of 3D porous structure-organic/inorganic synergistic modification. Specifically, the 3D interconnected porous network, constructed through solvent casting, enables a liquid-phase assisted transport mechanism within mixed poly(vinylidene fluoride- co -hexafluoropropylene) (PVDF-HFP)/PVDF polymers. Additionally, layered organo-montmorillonite (OMMT) optimizes ion transport kinetics, attributed from the Lewis acidic sites (Al–OH), significant nanosheet barriers, and as well as interfacial polarization. Consequently, the as-prepared CPEs achieve improved transference number of 0.38 and recorded critical current density of 6.7 mA·cm –2 . Electrochemical tests show that the Zn||Zn symmetric cell delivers an ultralong cycling life of 5000 h at 0.1 mA·cm –2 (cumulative deposition capacity: 2.5 Ah·cm –2 ), and the Zn||Cu asymmetric cell maintains stable cycling over 6000 cycles at 0.5 mA·cm –2 . In a practical demonstration, the Zn||I 2 full battery retains 92.4% capacity after 1000 cycles at 0.5 A g –1 . This work offers a rational design strategy for high-performance CPEs in ZMBs.
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