材料科学
兴奋剂
阴极
氧化物
钠
格子(音乐)
电压
无机化学
化学工程
光电子学
电气工程
冶金
化学
物理
声学
工程类
作者
Mingjian Li,Lei Chen,Zhiguo Liu,Lu Tang,D. A. Podgorny,Haohong Xian,Xiaobin Niu,Rui Wu,Jun Song Chen
标识
DOI:10.1021/acsami.5c13407
摘要
P2–Na0.67Ni0.33Mn0.67O2 represents an attractive cathode candidate for sodium-ion batteries. This material benefits from environmental sustainability, relative ease of synthesis, a high specific capacity, and operation at elevated voltages. However, its practical implementation is hindered by accelerated performance degradation and detrimental structural changes when charged beyond 4.2 V. Herein, we propose a strategic zinc-doping approach to address these limitations. Combined in situ XRD and DEMS, the Zn-doped P2–Na0.67Ni0.32Mn0.67Zn0.01O2 demonstrates remarkable suppression of lattice distortion (volume change <4%) and oxygen evolution even during high-voltage operation. Ex situ XPS confirms that Zn doping effectively mitigates Mn3+ induced Jahn–Teller distortion during cycling. The optimized cathode exhibits exceptional rate capability, delivering 99.1 mAh g–1 and 84.9 mAh g–1 at 5 and 10 C, respectively, within 1.5–4.3 V (vs Na/Na+). Furthermore, it demonstrates exceptional cycling stability at 10 C, retaining 92.9% of its capacity after 300 cycles. Complementing these findings, theoretical calculations reveal that NMNZ exhibits reduced volume changes, lowers the energy band center of O 2p orbitals, and enhances the stability of lattice oxygen.
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