Chemical Modulation of Local Transition Metal Environment Enables Reversible Oxygen Redox in Mn-Based Layered Cathodes
Muhammad Mominur Rahman, Scott McGuigan, Shaofeng Li, Lina Gao, Dong Hou, Zhijie Yang, Zhengrui Xu, Sang‐Jun Lee, Cheng‐Jun Sun, Jue Liu, Xiaojing Huang, Xianghui Xiao, Yong S. Chu, Sami Sainio, Dennis Nordlund, Xueqian Kong, Yijin Liu, Feng Lin
Abstract
Oxygen redox plays a prominent role in enhancing the energy density of Mn-based layered cathodes. However, understanding the factors affecting the reversibility of oxygen redox is nontrivial due to complicated structural and chemical transformations. Herein, we show that local Mn–O symmetry induced structural/chemical evolutions majorly dictate the reversibility of oxygen redox of NaxLiyMn1–yO2 in Na cells. NaxLiyMn1–yO2 with Jahn–Teller distorted MnO6 octahedra undergoes severe Mn dissolution during cycling, which destabilizes the transition metal layer resulting in poor Li retention and irreversible oxygen redox. Jahn–Teller distortion of MnO6 octahedra can be suppressed by modulating the local charge of Mn and Mn–O distance through Mg/Ti dual doping. This leads to reduced Mn dissolution and more reversible oxygen redox. Such stabilization significantly improves the electrochemical performance of Mg/Ti dual doped NaxLiyMn1–yO2. Through this work, we show that local structural stabilization through local chemical environment modification can promote reversible oxygen redox in layered cathodes.