scholarly journals Electrochemical performances discharged to lower potential for LiNi0.5Mn1.5O4 cathode material synthesized by PAA-assisted co-precipitation method

Author(s):  
Zhen Wang ◽  
Weiquan Shao ◽  
Shaou Chen ◽  
Lizhu He ◽  
Hongliang Li ◽  
...  
2010 ◽  
Vol 105-106 ◽  
pp. 664-667
Author(s):  
Sheng Wen Zhong ◽  
Wei Hu ◽  
Qian Zhang

The precursor of Mn0.75Ni0.25CO3 is prepared by carbonate co-precipitation method. And the cathode material 0.5Li2MnO3•0.5LiMn0.5Ni0.5O2 is synthesized with two stages calcining temperatures T1 and T2. T1 represents 400°C, 500°C, 600°C and T2 is selected at 750°C, 850°C, 950°C respectively. XRD Patterns shows that the cathode material has the integrated structures of Li2MnO3 and LiMO2, and it has better crystallization during the rise of calcined temperature at 950°C. The electrochemical performances tests indicates that the initial discharge specific capacity are greater than 220mAh/g at the current density 0.2 mA/cm2 in 2.5-4.6V at room temperature. When cathode material is calcined at 750°C, its discharge specific capacity even reach to 248mAh/g, but the cathode material has more perfect general electrochemical properties during calcined temperature at 950°C.


2015 ◽  
Vol 627 ◽  
pp. 206-210 ◽  
Author(s):  
Ruirui Zhao ◽  
Zilian Yang ◽  
JinCan Chen ◽  
Zhanjun Chen ◽  
Jiaxing Liang ◽  
...  

2019 ◽  
Vol 807 ◽  
pp. 50-56
Author(s):  
Yun Long Zhou ◽  
Zhi Biao Hu ◽  
Li Mei Wu ◽  
Jiao Hao Wu

Using hydrated manganese sulfate and general type graphene (GR) as raw materials, Mn3O4/GR composite has been successfully prepared by the liquid phase chemical co-precipitation method at room temperature. X-ray diffraction (XRD) was used to investigate the phase structure of Mn3O4powder and Mn3O4/GR composite; The electrochemical performances of the samples were elucidated by cyclic voltammetry and galvanostatic charge-discharge test in 0.5 mol/L Na2SO4electrolyte. The results show that the Mn3O4/GR composite possesses graphene phase and good reversibility; the composite also displays a specific capacitance of 318.8 F/g at a current density of 1 A/g.


2006 ◽  
Vol 972 ◽  
Author(s):  
Chiara Abate ◽  
Keith Duncan ◽  
Enrico Traversa ◽  
Eric Wachsman

AbstractNanocrystalline powders of Y2-xPrxRu2O7 were prepared by a co-precipitation method, and were tested as electrode on ESB and GDC electrolytes by electrochemical impedance spectroscopy in the 300-750°C temperatures range. The electrode polarization was studied as a function of the amount of praseodymium in the cathode material. Both systems, Y2-xPrxRu2O7/ESB and Y2-xPrxRu2O7/GDC, showed a similar variation of the electrode area specific resistance (ASR). Y1.5Pr0.5Ru2O7 cathode material presented the best performance, with ASR value of 0.19 Ωcm2 on ESB and 4.23 Ωcm2 on GDC at 700°C. Furthermore, the change in ASR with the oxygen partial pressure suggested that the rate limiting step is the surface diffusion of the adsorbed oxygen at the electrode surface to the triple-phase boundary. Thus, the low value of resistivity of the Y1.5Pr0.5Ru2O7 in contact with ESB results from a much lower charge transfer resistance compared to the Y2-xPrxRu2O7/GDC system, and a partial solid diffusion at the interface electrode/electrolyte that increases the effective triple phase boundary length. This suggests that Y2-xPrxRu2O7 is a promising material for cathode application in ESB-based electrolyte for intermediate temperature solid oxide fuel cells (IT-SOFCs).


2014 ◽  
Vol 07 (06) ◽  
pp. 1440013 ◽  
Author(s):  
Xiangjun Li ◽  
Hongxing Xin ◽  
Xiaoying Qin ◽  
Xueqin Yuan ◽  
Di Li ◽  
...  

Lithium and Mn rich solid solution materials Li [ Li 0.26 Ni 0.07 Co 0.07 Mn 0.56] O 2 were synthesized by a carbonate co-precipitation method and modified with a layer of graphene. The graphene-modified cathodes exhibit improved rate capability and cycling performance as compared to the bare cathodes. Electrochemical impedance spectroscopy (EIS) analyses reveal that the improved electrochemical performances are due to acceleration kinetics of lithium-ion diffusion and the charge transfer reaction of the graphene-modified cathodes.


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