Details

Autor(en) / Beteiligte

• Kiziltas-Yavuz, Nilüfer
• Bhaskar, Aiswarya
• Dixon, Ditty
• Yavuz, Murat
• Nikolowski, Kristian
• Lu, Li
• Eichel, Rüdiger-A.
• Ehrenberg, Helmut

Titel

Improving the rate capability of high voltage lithium-ion battery cathode material LiNi0.5Mn1.5O4 by ruthenium doping

Ist Teil von

• Journal of power sources, 2014-12, Vol.267, p.533-541

Ort / Verlag

Amsterdam: Elsevier B.V

Erscheinungsjahr

2014

Link zum Volltext

Quelle

Elsevier ScienceDirect Journals Complete

Beschreibungen/Notizen

• The citric acid-assisted sol–gel method was used to produce the high-voltage cathodes LiNi0.5Mn1.5O4 and LiNi0.4Ru0.05Mn1.5O4 at 800 °C and 1000 °C final calcination temperatures. High resolution powder diffraction using synchrotron radiation, inductively coupled plasma – optical emission spectroscopy and scanning electron microscopy analyses were carried out to characterize the structure, chemical composition and morphology. X-ray absorption spectroscopy studies were conducted to confirm Ru doping inside the spinel as well as to compare the oxidation states of transition metals. The formation of an impurity LixNi1−xO in LiNi0.5Mn1.5O4 powders annealed at high temperatures (T ≥ 800 °C) can be suppressed by partial substitution of Ni2+ by Ru4+ ion. The LiNi0.4Ru0.05Mn1.5O4 powder synthesized at 1000 °C shows the highest performance regarding the rate capability and cycling stability. It has an initial capacity of ∼139 mAh g−1 and capacity retention of 84% after 300 cycles at C/2 charging–discharging rate between 3.5 and 5.0 V. The achievable discharge capacity at 20 C for a charging rate of C/2 is ∼136 mAh g−1 (∼98% of the capacity delivered at C/2). Since the electrode preparation plays a crucial role on parameters like the rate capability, the influence of the mass loading of active materials in the cathode mixture is discussed. •LixNi1−xO was suppressed by Ru-doping as revealed by the presence of such an impurity phase in LiNi0.5Mn1.5O4.•LiNi0.4Ru0.05Mn1.5O4-1000 °C exhibits excellent electrochemical performances even at high C-rates.•The mass loadings of the cathodes significantly affect the delivered capacities especially at high C-rate.