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Building High Rate Capability and Ultrastable Dendrite‐Free Organic Anode for Rechargeable Aqueous Zinc Batteries

机译:构建高速率能力和超稳定的无枝晶有机阳极用于可充电水性锌电池

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摘要

Aqueous zinc‐ion batteries (ZIBs) are an alternative energy storage system for large‐scale grid applications compared with lithium‐ion batteries, when the low cost, safety, and durability are taken into consideration. However, the reliability of the battery systems always suffers from the serious challenge of the large Zn dendrite formation and “dead Zn,” thus bringing out the inferior cycling stability, and even cell shorting. Herein, a dendrite‐free organic anode, perylene‐3,4,9,10‐tetracarboxylic diimide (PTCDI) polymerized on the surface of reduced graphene oxide (PTCDI/rGO) utilized in ZIBs is reported. Moreover, the theoretical calculations prove the reason for the low redox potential. Due to the protons and zinc ions coparticipant phase transfer mechanism and the high charge transfer capability, the PTCDI/rGO electrode provides superior rate capability (121 mA h g at 5000 mA g , retaining the 95% capacity of that compared with 50 mA g ) and a long cycling life span (96% capacity retention after 1500 cycles at 3000 mA g ). In addition, the proton coparticipation energy storage mechanism of active materials is elucidated by various ex‐situ methods.
机译:考虑到低成本,安全性和耐用性,与锂离子电池相比,水溶锌离子电池(ZIBs)是大型电网应用的替代储能系统。然而,电池系统的可靠性始终受到严重的挑战,即形成大量的锌枝晶和“锌的死”,从而导致较差的循环稳定性,甚至电池短路。本文报道了在ZIBs中使用的无树枝状有机阳极per 3,4,9,10-四羧酸二酰亚胺(PTCDI)聚合在还原氧化石墨烯(PTCDI / rGO)的表面上。而且,理论计算证明了氧化还原电势低的原因。由于质子和锌离子的参与相转移机制和高电荷转移能力,PTCDI / rGO电极具有出色的倍率能力(在5000 mA g时为121 mA hg,与50 mA g相比保留了95%的容量)和循环寿命长(在3000 mA g下进行1500次循环后,容量保持96%)。此外,通过各种异位方法阐明了活性物质的质子参与能量存储机理。

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