材料科学
阴极
化学物理
离子
储能
扩散
纳米技术
相(物质)
锂(药物)
化学工程
相变
结构稳定性
热力学
功率(物理)
物理化学
化学
医学
物理
有机化学
结构工程
工程类
内分泌学
作者
Mengting Liu,Bin Wu,Duo Si,Haojie Dong,Kai Chen,Lu Zheng,Xiulin Fan,Lianzheng Yu,Bing Xiao,Shulei Chou,Yao Xiao,Pengfei Wang
标识
DOI:10.1021/acsami.3c14951
摘要
Fierce phase transformation and limited sodium ion diffusion dynamics are critical obstacles that hinder the practical energy storage applications of P2-type layered sodium transition metal oxides (NaxTMO2). Herein, a synergistic strategy of electronic state tailoring and pillar effect was carefully implemented by substituting divalent Mg2+ into Na0.67Ni0.33Mn0.67O2 material with unique oriented hollow rodlike structures. Mg2+substitution can not only facilitate the anionic oxygen redox reactions and electronic conductivity through increasing the electronic states at Femi energy but also act as pillars within TMO2 layers to alleviate the severe phase transformation to improve structure stability. Moreover, the oriented hollow structure incorporating sufficient buffer spaces and rationally exposed electrochemically active facets effectively alleviates the stresses induced by low volume changes of 8% and provides more open channels for Na+ ion diffusion without crossing multiple grain boundaries. Hence, the Na0.67Mg0.08Ni0.25Mn0.67O2 cathode showed a superior rate capability with high energy density and cycling stability for sodium-ion storage. The underlying mechanisms of these achievements were deciphered through diversified dynamic analysis and the first principle calculations, providing new insights into P2-type NaxTMO2 cathodes for the infinite prospect as an alternative to lithium-ion batteries.
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