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Enhancing the Kinetics of Zinc Ion Deposition by Catalytic Ion in Polymer Electrolytes for Advanced Zn–MnO_2 Batteries

机译:通过催化离子增强先进Zn–MnO_2电池聚合物电解质中锌离子沉积的动力学

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摘要

The practicality of zinc-ion batteries (ZIBs) is compromise seriously becauseof the mutual restrictions of hydrogen evolution, by-product formation andzincdendrite growth. Herein, anhydrous gel polymer electrolytes (GPEs)with catalytic ions and in situdomain-constrained zinc ions are designed.Innovatively, copper ions are confined in the network structure of the gel foraccelerating the deposition and migration kinetics of zinc ions. Not only doesthis anhydrous GPEs exhibit strong mechanicaland thermal properties, butit also presents a high ionic conductivity (24.32 mS cm~(?1)) and a high zinc iontransference number (0.42). Consequently, the anhydrous GPEs is capable ofstable cycling of symmetrical Zn cells at 1 mA cm~(?2) with acumulative capacityof 1000 mAh cm~(?2) and maintaines a high discharge specific capacity of124.6 mAh g~(?1) after 1000 long-term cycles of the Zn-MnO_2 battery (ZMB) at1 C. The synergistic catalytic strategy of composite gel opens new opportunitiesfor a promising pathway to facilitate the large-scale application of ZIBswith hydrogel electrolytes.
机译:锌离子电池(ZIBs)的实用性受到析氢、副产物形成和锌枝晶生长的相互限制,严重受到损害。本文设计了具有催化离子和原位域约束锌离子的无水凝胶聚合物电解质(GPE)。创新性地将铜离子限制在凝胶的网络结构中,以加速锌离子的沉积和迁移动力学。这种无水GPEs不仅具有很强的机械性能和热性能,而且具有高离子电导率(24.32 mS cm~(?1))和高锌离子转移数(0.42)。因此,无水GPEs能够在1 mA cm~(?2)下稳定循环对称Zn电池,累积容量为1000 mAh cm~(?2),并在Zn-MnO_2电池(ZMB)在1 C下长期循环1000次后仍能保持124.6 mAh g~(?1)的高放电比容量。复合凝胶的协同催化策略为促进ZIBs与水凝胶电解质的大规模应用开辟了新的途径。

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