Electrochemical Failure Mechanism of δ‐MnO2 in Zinc Ion Batteries Induced by Irreversible Layered to Spinel Phase Transition

Author:

Zhao Chunyu1,Wu Mengqi2,Lu Wencheng3,Cheng Yingjie1,Zhang Xiaoya1,Saadoune Ismael4,Lian Ruqian2,Wang Yizhan15,Wei Yingjin15ORCID

Affiliation:

1. Key Laboratory of Physics and Technology for Advanced Batteries (Ministry of Education) College of Physics Jilin University Changchun 130012 P. R. China

2. Key Laboratory of Optic‐Electronic Information and Materials of Hebei Province National‐Local Joint Engineering Laboratory of New Energy Photoelectric Devices College of Physics Science and Technology Hebei University Baoding 071002 P. R. China

3. Key Laboratory of Material Simulation Methods and Software of Ministry of Education College of Physics Jilin University Changchun 130012 P. R. China

4. Applied Chemistry and Engineering Research Centre of Excellence Mohammed VI Polytechnic University Ben Guerir 43150 Morocco

5. Chongqing Research Institute Jilin University Chongqing 401123 P. R. China

Abstract

AbstractPhase 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 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.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Chongqing Municipality

Publisher

Wiley

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