Electrochemical Performance of LiMnPO[subscript 4] Synthesized with Off-Stoichiometry
Name
Ceder_Electrochemical performance.pdf
Size
822.44 KB
Format
Adobe PDF
Checksum (MD5)
22f187cfe388567558c766d83529045f
Author(s) •
Kang, Byoungwoo
Ceder, Gerbrand
Date Issued
May 2010
Journal
Journal of The Electrochemical Society
Publisher
The Electrochemical Society
Citation
Kang, Byoungwoo, and Gerbrand Ceder. Electrochemical Performance of LiMnPO[sub 4] Synthesized with Off-Stoichiometry. Journal of The Electrochemical Society 157, no. 7 (2010): A808. © 2010 ECS - The Electrochemical Society
Version
Final published version
Abstract
LiMnPO[subscript 4] was synthesized from an off-stoichiometric mix of starting materials with nominal composition LiMn[subscript 0.9]P[subscript 0.95]O[subscript 4−δ]. Stoichiometric LiMnPO[subscript 4] with particle size <50 nm was found with X-ray diffraction even with the large overall deviation from stoichiometry in the sample, indicating that other noncrystalline compounds are present. The off-stoichiometric sample had a discharge capacity of 145 mAh/g at C/10 and ∼100mAh/g at 2C after a constant current constant voltage charge. Capacity retention was excellent without a significant capacity loss at 1C. The performance of LiMn[subscript 0.9]P[subscript 0.95]O[subscript 4−δ] could not be significantly improved by diluting the electrode with more carbon, indicating a more intrinsic kinetic limitation of the material for LiMnPO[subscript 4] in contrast to LiFePO[subscript 4] [Nature (London), 458, 190 (2009)]. This is further corroborated by the difference in the overpotential between the two materials. Although LiMnPO[subscript 4] has a sloping voltage profile, LiFePO[subscript 4] tends to have a constant overpotential at high rate.
MIT Department
Massachusetts Institute of Technology. Department of Materials Science and Engineering
Terms of Use
Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.
Persistent DSpace Link
DOI of Published Version
https://doi.org/10.1149/1.3428454