阴极
水溶液
电解质
聚合物
材料科学
储能
化学工程
能量密度
离子
锌
纳米技术
化学
工程物理
复合材料
物理化学
电极
有机化学
热力学
物理
冶金
工程类
功率(物理)
作者
Yiyang Dai,Yao Yao,Liang Feng,Z. Q. Qiu,Min Deng,Qiang Peng
标识
DOI:10.1002/advs.202503156
摘要
Abstract Recently, research on aqueous zinc‐ion batteries (AZIBs) has always focused on improving the energy storage performance by increasing the number of active sites, particularly in designing organic/polymer materials with a high density of active sites. However, does a higher density of active sites necessarily induce enhanced energy storage performance? To verify this issue, we have designed two linear polymers, where TAPT‐DHBQ contains an additional pair of active sites (carbonyl groups) compared to TABQ‐DHBQ, with theoretical specific capacities of 545.26 and 379.14 mAh g −1 , respectively. Interestingly, the experimental results have deviated with the specific capacities of these polymers being comparable, measuring to be 325 mAh g −1 (TABQ‐DHBQ) and 280 mAh g −1 (TAPT‐DHBQ). This is attributed to the competition effect between neighboring active sites, which leads to decreased utilization of active sites. As a result, the Zn//TABQ‐DHBQ batteries with ZnI 2 electrolyte additive have exhibited high specific capacities of 618 and 360 mAh g −1 at the current densities of 1 and 10 A g −1 , along with a high energy density of 678.6 Wh kg −1 (1 A g −1 ). The finding underscores the importance of uniform electron cloud distribution in cathode materials for achieving efficient AZIBs.
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