电化学
阴极
材料科学
过渡金属
兴奋剂
透射电子显微镜
动力学
水溶液
电极
衍射
金属
相(物质)
化学工程
分析化学(期刊)
无机化学
化学
纳米技术
冶金
物理化学
光电子学
催化作用
色谱法
有机化学
工程类
物理
光学
量子力学
作者
Hong Li,Zhenxiong Huang,Bohong Chen,Yu Jiang,Chuanhua Li,Wei Xiao,Xuemin Yan
标识
DOI:10.1016/j.jpowsour.2022.231198
摘要
MnO2-based cathodes for aqueous Zn-ion batteries (AZIBs) suffer from the sluggish kinetics of Zn2+ migration and chemical instability during cycling, severely impeding its practical application. The group Ⅷ metal (Fe, Co and Ni) doping in MnO2 is an intriguing idea to improve the electrochemical performance of MnO2-based electrodes for AZIBs due to its special electronic structure of d shell. According to density functional theory calculation results, the doping-element facilitates the increase in kinetics of Zn2+ migration and increase chemical stability during cycling. When tested in AZIBs, a Fe-doping MnO2 (FMO) electrode exhibits a superior cycling stability (a high specific capacity of 338.2 mAh g−1 at 1 A g−1 with a capacity retention of 86.3% after 200 cycles), as same as that of Co and Ni-doping MnO2 electrode. In combination of in-situ X-ray diffraction and ex-situ transmission electron microscope studies reveal that layered-FMO undergoes a structural transition to ZnxMnO2, Mn3O4 and ZnMn2O4, accompanying with the formation of ZnSO4(OH)6·5H2O during discharging process, while those phases revert back to the parent phase during the subsequent Zn extraction. This study might build a solid foundation for developing powerful cathode in AZIBs.
科研通智能强力驱动
Strongly Powered by AbleSci AI