阳极
锌
水溶液
铜
电化学
电解质
电池(电)
化学
普鲁士蓝
无机化学
X射线光电子能谱
材料科学
电极
化学工程
阴极
有机化学
物理化学
功率(物理)
工程类
物理
量子力学
作者
Tanya Gupta,Andrew Kim,Satyajit Phadke,Shaurjo Biswas,Thao- Han Luong,Benjamin Hertzberg,Mylad Chamoun,K. Evans‐Lutterodt,Daniel A. Steingart
标识
DOI:10.1016/j.jpowsour.2015.11.065
摘要
Prussian Blue Analogue (PBA)-Zn aqueous batteries are attractive because of the high potential of PBA against Zn (∼1.7 V), relative safety of the system, and high rate capability. But, despite the long cycle life of PBA half-cells, full PBA-Zn battery systems studied thus far have typically reported only up to 100 cycles and suffer significant capacity fade beyond that. In this work we demonstrate that the loss in capacity retention and cycle life is a combined effect of Zn2+ ion poisoning at the PBA cathode, as well as dendrite formation in the zinc anode. We address both these issues via the use of a dual ion (Na+ as the primary charge carrier) electrolyte and hyper-dendritic Zinc (HD Zn) as the anode. The copper hexacyanoferrate (CuHcf) vs. HD Zn system with Na+ ion electrolyte demonstrated herein exhibits 90% (83%) capacity retention after 300 (500) cycles at a 5C rate and a 3% reduction in usable capacity from 1C to 5C. Detailed characterization is done using in situ synchrotron energy-dispersive XRD (EDXRD), conventional XRD, XPS, SEM, TEM, and electrochemical techniques.
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