Aluminum and Gallium Substitution into 0.5Li2MnO3·0.5Li(Ni0.375Mn0.375Co0.25)O2 Layered Composite and the Voltage Fade Effect. Issue 3 (1st January 2015)

• Record Type: Journal Article
• Authors: Lee, Eungje; Koritala, Rachel; Miller, Dean J.; Johnson, Christopher S.
• Is Part Of: Journal of the Electrochemical Society. Volume 162:Issue 3(2015)
• Page Start: A322
• Page End: A329
• Publication Date: 2015-01-01
• Subjects: Electrochemistry -- Periodicals; 541.3705
• DOI: 10.1149/2.0321503jes
• Languages: English
• ISSNs: 0013-4651

Abstract

Abstract : Lithium- and manganese-rich layered composite cathodes in the general form (Li2 MnO3 LiMO2 ; M = transition metals), suffer from voltage profile suppression during cycling in Li-ion cells leading to overall gradual energy losses in the system. The suppression in cathode voltage which is called 'voltage fade' is a general phenomenon for these class of materials which needs to be understood and mitigated for enabling this chemistry in advanced Li-ion cells. Synthetic manipulation of the composition in 0.5Li2 MnO3 0.5LiNi0.375 Mn0.375 Co0.25 O2 (= Li1.2 Ni0.15 Mn0.55 Co0.1 O2 in layered notation) cathode material via aluminum and gallium substitution (max. 10%) via sol-gel reaction was completed and the voltage fade percentage was measured following a prescribed electrochemical testing protocol. While the specific capacities (∼ 250 mAh/g) are unaffected by the Al and Ga substitution (up to 5%), ∼3 to 4% of the impedance-corrected average voltage is still lost (first 25 cycles) which is comparable to what the pristine material experiences. This result suggests that the path of structural change that occurs in the material during Li cycling is unaltered by synthetic manipulation of octahedral and/or tetrahedral sites though the use of Al and Ga non-redox active cations.