材料科学
聚烯烃
阳极
内阻
电池(电)
分离器(采油)
复合材料
光电子学
电极
化学
功率(物理)
量子力学
热力学
物理
物理化学
图层(电子)
作者
Matthew Gonzalez,Qizhang Yan,John Holoubek,Mingqian Li,Zhaohui Wu,Hongyao Zhou,Sean Kim,Haodong Liu,Bum-Young Jung,Suk-woo Lee,Zheng Chen
标识
DOI:10.1002/adfm.202102198
摘要
Abstract Battery separators are a critical component that greatly determine cell calendar life and safety. Generally, these separators are passive with no ability to reversibly change their properties in order to optimize battery performance. Here, an iongate separator is demonstrated, which allows ion transport while in the oxidized “on” state but limits ion transport when switched to the reduced “off” state. This is achieved by depositing a dense 300 nm thin film of polypyrrole:polydopamine (PPy:PDA) on a conventional polyolefin separator. By using this iongate separator as a third electrode, a rapid and reversible order of magnitude increase of iongate resistance is achievable. The iongate battery shows similar cycling performance to a normal battery while in the “on” state, but cycling can be reversibly shut‐off when the iongate separator is reduced to the “off” state. During elevated temperature storage with the iongate separator in the “off” state, battery capacity loss is decreased by 37% and transition metal crossover is greatly suppressed when compared to a normal battery without the iongate. Additionally, rapid shut‐off during discharge is demonstrated by directly shorting the iongate separator to the anode.
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