材料科学
电化学
介孔材料
阴极
水溶液
多孔性
碳纤维
电池(电)
化学工程
电导率
纳米
三元运算
纳米技术
复合材料
电极
化学
复合数
功率(物理)
有机化学
催化作用
工程类
量子力学
物理化学
物理
计算机科学
程序设计语言
作者
Dong Guo,Wenqi Zhao,Fuping Pan,Guoliang Liu
标识
DOI:10.1002/batt.202100380
摘要
Abstract Rechargeable aqueous Zn−MnO 2 batteries are promising for stationary energy storage because of their high energy density, safety, environmental benignity, and low cost. Conventional gravel MnO 2 cathodes have low electrical conductivity, slow ion (de‐)insertion, and poor cycle stability, resulting in poor recharging performance and severe capacity fading. To improve the rechargeability of MnO 2 , strategies have been devised such as depositing micrometer‐thick MnO 2 on carbon cloth and blending nanostructured MnO 2 with additives and binders. The low electrical conductivity of binders and sluggish ion (de‐)insertion in micrometer‐thick MnO 2 , however, still limit the fast‐charging performance. Herein, we have prepared porous carbon fiber (PCF) supported MnO 2 cathodes (PCF@MnO 2 ), comprised of nanometer‐thick MnO 2 uniformly deposited on electrospun block copolymer‐derived PCF that have abundant uniform mesopores. The high electrical conductivity of PCF, fast electrochemical reactions in nanometer‐thick MnO 2, and fast ion transport through porous nonwoven fibers contribute to a high rate capability at high loadings. PCF@MnO 2 , at a MnO 2 loading of 59.1 wt %, achieves a MnO 2 ‐based specific capacity of 326 and 184 mAh g −1 at a current density of 0.1 and 1.0 A g −1 , respectively. Our approach of block copolymer‐based PCF as a support for zinc‐ion cathode inspires future designs of fast‐charging electrodes with other active materials.
科研通智能强力驱动
Strongly Powered by AbleSci AI