Wen Yanfen, Wang Bei, Zeng Guang, Nogita Kazuhiro, Ye Delai, Wang Lianzhou
Nanomaterials Center, School of Chemical Engineering, The University of Queensland, Queensland, 4072 (Australia).
Chem Asian J. 2015 Mar;10(3):661-6. doi: 10.1002/asia.201403134. Epub 2015 Jan 14.
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.
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。