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层状P2型Na(2/3)Ni(1/3)Mn(2/3)O2作为钠离子电池阴极材料的电化学与结构研究

Electrochemical and structural study of layered P2-type Na(2/3)Ni(1/3)Mn(2/3)O2 as cathode material for sodium-ion battery.

作者信息

Wen Yanfen, Wang Bei, Zeng Guang, Nogita Kazuhiro, Ye Delai, Wang Lianzhou

机构信息

Nanomaterials Center, School of Chemical Engineering, The University of Queensland, Queensland, 4072 (Australia).

出版信息

Chem Asian J. 2015 Mar;10(3):661-6. doi: 10.1002/asia.201403134. Epub 2015 Jan 14.

Abstract

P2-type Na(2/3)Ni(1/3)Mn(2/3)O2 was synthesized by a controlled co-precipitation method followed by a high-temperature solid-state reaction and was used as a cathode material for a sodium-ion battery (SIB). The electrochemical behavior of this layered material was studied and an initial discharge capacity of 151.8 mA h g(-1) was achieved in the voltage range of 1.5-3.75 V versus Na(+)/Na. The retained discharge capacity was found to be 123.5 mA h g(-1) after charging/discharging 50 cycles, approximately 81.4% of the initial discharge capacity. In situ X-ray diffraction analysis was used to investigate the sodium insertion and extraction mechanism and clearly revealed the reversible structural changes of the P2-Na(2/3)Ni(1/3)Mn(2/3)O2 and no emergence of the O2-Ni(1/3)Mn(2/3)O2 phase during the cycling test, which is important for designing stable and high-performance SIB cathode materials.

摘要

通过可控共沉淀法结合高温固态反应合成了P2型Na(2/3)Ni(1/3)Mn(2/3)O2,并将其用作钠离子电池(SIB)的正极材料。研究了这种层状材料的电化学行为,在相对于Na(+)/Na为1.5 - 3.75 V的电压范围内,初始放电容量达到151.8 mA h g(-1)。在充放电50次循环后,保留的放电容量为123.5 mA h g(-1),约为初始放电容量的81.4%。采用原位X射线衍射分析研究了钠嵌入和脱出机制,清楚地揭示了P2-Na(2/3)Ni(1/3)Mn(2/3)O2的可逆结构变化,并且在循环测试过程中未出现O2-Ni(1/3)Mn(2/3)O2相,这对于设计稳定且高性能的SIB正极材料很重要。

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