共轭体系
氧化还原
阴极
离域电子
聚合物
锂(药物)
有机自由基电池
化学
材料科学
光化学
高分子化学
组合化学
无机化学
电化学
有机化学
电极
物理化学
内分泌学
医学
作者
Xiang Zhao,Xue Qiu,Haodong Xue,Si Liu,Dingli Liang,Chuan Yan,Weinan Chen,Yonggang Wang,Gang Zhou
标识
DOI:10.1002/anie.202216713
摘要
Organic p-type cathode materials have recently attracted increasing attention due to their higher redox potentials and rate capabilities in comparison to n-type cathodes. However, most of the p-type cathodes based on one-electron redox still suffer from limited stability and low specific capacity (<150 mAh g-1 ). Herein, two polymers, conjugated poly(diethyldihydrophenazine vinylene) (CPP) and non-conjugated poly(diethyldihydrophenazine ethylidene) (NCPP) containing two-electron redox dihydrophenazine, have been developed as p-type cathode materials. It is experimentally and theoretically found that the conjugated linkage among the redox centers in polymer CPP is more favorable for the effective charge delocalization on the conjugated polymer backbone and the sufficient oxidation in the higher potential region (3.3-4.2 V vs. Li/Li+ ). Consequently, the CPP cathode displays a higher reversible specific capacity of 184 mAh g-1 with excellent cycling stability.
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