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分级介孔/大孔共掺杂氧化镍纳米片阵列作为可充电锂氧电池的独立电极材料

Hierarchical Mesoporous/Macroporous Co-Doped NiO Nanosheet Arrays as Free-Standing Electrode Materials for Rechargeable Li-O Batteries.

作者信息

Wang Hui, Wang Hongjiao, Huang Jiasheng, Zhou Xuelong, Wu Qixing, Luo Zhongkuan, Wang Fang

机构信息

College of Chemistry and Environmental Engineering, Shenzhen University, Shenzhen 518060, Guangdong, China.

出版信息

ACS Appl Mater Interfaces. 2019 Nov 27;11(47):44556-44565. doi: 10.1021/acsami.9b13329. Epub 2019 Nov 12.

Abstract

Lithium-oxygen (Li-O) batteries have been widely recognized as appealing power systems for their extremely high energy density versus common Li-ion batteries. However, there are still lots of issues that need to be addressed toward the practical application. Here, free-standing Co-doped NiO three-dimensional nanosheets were prepared by a hydrothermal synthesis method and directly employed as the air-breathing cathode of the Li-O battery. The morphological phenomenon and electrochemical performance of the as-prepared cathode material were characterized by high-resolution scanning electron microscopy, X-ray diffraction, cyclic voltammetry, galvanostatic charge-discharge tests, and electrochemical impedance spectroscopy measurements. The Co-doped NiO electrode delivered a maximum discharge capacity of around 12 857 mA h g with a low overpotential (0.82 V) at 200 mA g. Under upper-limit specific capacities of 500 mA h g at 400 mA g, the Li-O batteries exhibited a long cycle life of 165 cycles. Compared with the undoped NiO electrode, the Li-O battery based on the Co-doped NiO cathode showed significantly higher oxygen reduction reaction and oxygen evolution reaction activities. This superior electrochemical performance is because of the partial substitution of Ni in the NiO matrix by Co to improve the p-type electronic conductivity of NiO. In addition, the morphology and specific surface area of NiO are affected by Co doping, which can expand the electrode-electrolyte contact area and lead to sufficient space for LiO deposition. This approach harnesses the great potential of Co-doped NiO nanosheets for practical applications as advanced electrodes for rechargeable Li-O batteries.

摘要

锂氧(Li-O)电池因其相对于普通锂离子电池极高的能量密度而被广泛认为是有吸引力的电源系统。然而,在实际应用方面仍有许多问题需要解决。在此,通过水热合成法制备了自支撑的Co掺杂NiO三维纳米片,并将其直接用作Li-O电池的空气呼吸阴极。通过高分辨率扫描电子显微镜、X射线衍射、循环伏安法、恒电流充放电测试和电化学阻抗谱测量对所制备的阴极材料的形态现象和电化学性能进行了表征。Co掺杂NiO电极在200 mA g时具有约12857 mA h g的最大放电容量和低过电位(0.82 V)。在400 mA g的500 mA h g上限比容量下,Li-O电池表现出165次循环的长循环寿命。与未掺杂的NiO电极相比,基于Co掺杂NiO阴极的Li-O电池显示出明显更高的氧还原反应和析氧反应活性。这种优异的电化学性能是由于Co在NiO基体中部分取代了Ni,从而提高了NiO的p型电子导电性。此外,Co掺杂影响了NiO的形态和比表面积,这可以扩大电极-电解质接触面积并为LiO沉积提供足够的空间。这种方法利用了Co掺杂NiO纳米片作为可充电Li-O电池的先进电极在实际应用中的巨大潜力。

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