氧化还原
阴极
硒
材料科学
无机化学
锰
氧气
X射线光电子能谱
半反应
离子
化学
化学工程
物理化学
有机化学
工程类
冶金
作者
Zhichen Xue,Neha Bothra,Dechao Meng,Guangxia Feng,Yuqi Li,Tony Cui,Hongchang Hao,Sang‐Jun Lee,Yijin Liu,Michal Bajdich,Jagjit Nanda,Xueli Zheng
标识
DOI:10.1002/adfm.202417758
摘要
Abstract Utilizing anion redox reaction is crucial for developing the next generation of high‐energy density, low‐cost sodium‐ion batteries. However, the irreversible oxygen redox reaction in Na‐ion layered cathodes, which leads to voltage fading and reduced overall lifespan, has hindered their practical application. In this study, selenium is incorporated as a synergistic redox active center of oxygen to improve the stability of Na‐ion cathodes. The redesigned cathode maintains stable voltage by demonstrating reversible oxygen redox while significantly suppressing the redox activity of manganese. The anionic redox contribution capacity of the selenium‐doped Na 0.6 Li 0.2 Mn 0.8 O 2 cathode remains as high as 84% after 50 cycles, while the pristine Na 0.6 Li 0.2 Mn 0.8 O 2 cathode experiences a reduction to 39% of its initial capacity. The X‐ray photoelectron spectroscopy data and computational analysis further revealed that selenium doping participates in redox as Se +4/5 which stabilizes the charged state and increases the energy step for O─O dimerization, thus improving the stability and lifespan of Na 0.6 Li 0.2 Mn 0.8 O 2 cathodes. The findings highlight the potential of redox coupling design to address the issue of voltage fade caused by irreversible anionic redox.
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