尖晶石
电化学
机制(生物学)
相变
锌
材料科学
离子
相(物质)
冶金
化学
电极
凝聚态物理
物理化学
物理
有机化学
量子力学
作者
Chunyu Zhao,Mengqi Wu,Wencheng Lu,Yingjie Cheng,Xiaoya Zhang,Ruqian Lian,Yizhan Wang,Yingjin Wei
摘要
Phase transitions of Mn-based cathode materials associated with the charge and discharge process play a crucial role on the rate capability and cycle life of zinc ion batteries. Herein, a microscopic electrochemical failure mechanism of Zn-MnO2 batteries during the phase transitions from δ-MnO2 to λ-ZnMn2O4 is presented via systematic first-principle investigation. The initial insertion of Zn2+ intensifies the rearrangement of Mn. This is completed by the electrostatic repulsion and co-migration between guest and host ions, leading to the formation of λ-ZnMn2O4. The Mn relocation barrier for the λ-ZnMn2O4 formation path with 1.09 eV is significantly lower than the δ-MnO2 re-formation path with 2.14 eV, indicating the irreversibility of the layered-to-spinel transition. Together with the phase transition, the rearrangement of Mn elevates the Zn2+ migration barrier from 0.31 eV to 2.28 eV, resulting in poor rate performance. With the increase of charge-discharge cycles, irreversible and inactive λ-ZnMn2O4 products accumulate on the electrode, causing continuous capacity decay of the Zn-MnO2 battery.
科研通智能强力驱动
Strongly Powered by AbleSci AI