材料科学
X射线吸收精细结构
锰
镍
过渡金属
分析化学(期刊)
无机化学
相(物质)
光谱学
冶金
化学
催化作用
有机化学
物理
量子力学
生物化学
色谱法
作者
Xuehang Wu,Gui‐Liang Xu,Guiming Zhong,Zhengliang Gong,Matthew J. McDonald,Shiyao Zheng,Riqiang Fu,Zonghai Chen,Khalil Amine,Yong Yang
标识
DOI:10.1021/acsami.6b06701
摘要
P2-type sodium nickel manganese oxide-based cathode materials with higher energy densities are prime candidates for applications in rechargeable sodium ion batteries. A systematic study combining in situ high energy X-ray diffraction (HEXRD), ex situ X-ray absorption fine spectroscopy (XAFS), transmission electron microscopy (TEM), and solid-state nuclear magnetic resonance (SS-NMR) techniques was carried out to gain a deep insight into the structural evolution of P2–Na0.66Ni0.33–xZnxMn0.67O2 (x = 0, 0.07) during cycling. In situ HEXRD and ex situ TEM measurements indicate that an irreversible phase transition occurs upon sodium insertion-extraction of Na0.66Ni0.33Mn0.67O2. Zinc doping of this system results in a high structural reversibility. XAFS measurements indicate that both materials are almost completely dependent on the Ni4+/Ni3+/Ni2+ redox couple to provide charge/discharge capacity. SS-NMR measurements indicate that both reversible and irreversible migration of transition metal ions into the sodium layer occurs in the material at the fully charged state. The irreversible migration of transition metal ions triggers a structural distortion, leading to the observed capacity and voltage fading. Our results allow a new understanding of the importance of improving the stability of transition metal layers.
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