材料科学
阴极
水溶液
锌
电子转移
胺气处理
氧化还原
桥接(联网)
亚胺
化学工程
无机化学
有机自由基电池
电化学
光谱学
阳极
X射线光电子能谱
金属有机骨架
三元运算
储能
自行车
红外光谱学
电极
作者
Libin Zhang,Yan Zhang,Xiangyu Wang,Xin Wang,Qing Wang,Jiajun Li,Zongyang Li,Kun Ding,Yiting Peng,Haimei Liu,Yonggang Wang
标识
DOI:10.1002/adfm.202513189
摘要
Abstract Organic materials have attracted considerable attention as high‐performance cathodes for aqueous zinc‐ion batteries (AZIBs) owing to their structural tunability and molecular diversity. However, their capacities are typically limited (≤350 mAh g −1 ), primarily due to redox reactions involving the transfer of only a few electrons (≤4 electrons) per molecule. Here, the study designs and synthesizes a six‐electron‐transfer organic cathode material, 5,12‐dihydro‐1,5,7,8,12,14‐hexaazapentacene (DHHAP), by bridging water‐soluble pyridinediamine and hydroxybenzoquinone units. First‐principles calculations and in situ ATR‐FTIR spectroscopy confirm that four imine (C═N) groups and two amine (─NH─) groups serve as redox‐active sites, affording a high theoretical capacity of 562 mAh g −1 . Electrochemical tests reveal that DHHAP delivers a remarkable discharge capacity of 507 mAh g −1 at 50 mA g −1 —approaching the theoretical limit—and exhibits excellent cycling stability over 10 000 cycles at 10 A g −1 . Moreover, it maintains outstanding rate capability and long‐term cycling performance even at high mass loadings (3–10 mg cm −2 ), underscoring its promise for practical applications in aqueous zinc‐ion batteries.
科研通智能强力驱动
Strongly Powered by AbleSci AI