材料科学
插层(化学)
离子
石墨
水溶液
无机化学
对偶(语法数字)
化学工程
有机化学
冶金
化学
文学类
工程类
艺术
作者
Ying Zheng,Xiaolin Xie,Hiroshi Ueno,Ting Deng,Weitao Zheng
标识
DOI:10.1002/aenm.202401914
摘要
Abstract Anion intercalation in graphite is deemed as a promising electrode chemistry in aqueous energy storage systems due to its high onset potential. Given the limited space in graphite, multivalent anions are favorable to achieve high specific capacity. However, relevant studies are scarce so that fundamental understandings of multivalent anion intercalation remain unclear. Herein, the intercalation behaviors of ClO 4 − , SO 4 2− , and PO 4 3− in graphite are systematically investigated. High capacity and interaction between anion and graphite are proved to be contradictory as the electric charge increases. As a result, ClO 4 − and SO 4 2− intercalation exhibits promising performance in primitive graphite, while PO 4 3− intercalation is much restricted due to the intensified electronic interaction. Two Zn–graphite dual‐ion batteries based on ClO 4 − and SO 4 2− intercalations display high voltages of 1.85 V, and specific energies of 106 and 112 Wh kg −1 . This work provides fundamental understandings of multivalent anion intercalation and guidance to fabricate aqueous batteries (ABs) with high energy density.
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