Lithium Ion Cell Performance Enhancement Using Aqueous LiFePO4Cathode Dispersions and Polyethyleneimine Dispersant
Author(s) -
Jianlin Li,
Beth L. Armstrong,
Jim Kiggans,
Claus Daniel,
David L. Wood
Publication year - 2012
Publication title -
journal of the electrochemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.258
H-Index - 271
eISSN - 1945-7111
pISSN - 0013-4651
DOI - 10.1149/2.037302jes
Subject(s) - dispersant , cathode , chemical engineering , materials science , electrochemistry , agglomerate , aqueous solution , electrode , dispersion (optics) , economies of agglomeration , wetting , composite number , particle (ecology) , diffusion , lithium (medication) , composite material , chemistry , organic chemistry , medicine , physics , endocrinology , optics , engineering , oceanography , geology , thermodynamics
Switching manufacturing of composite battery electrodes from an organic system to an aqueous system provides both economic and environmental advantages. However, particle agglomeration of the electrode components and poor wetting of electrode dispersions to the current collectors are inherently introduced. Particle agglomeration can be mitigated by selection of appropriate dispersants. This research examines the effect of dispersant, poly(ethyleneimine) (PEI), on the associated morphology and electrochemical performance of LiFePO4. The addition of PEI reduces the agglomerate size and contributes to a more homogeneous distribution of cathode constituents, which results in a smoother, more uniform cathode surface. The LiFePO4 cathodes with PEI demonstrated a higher Li+ diffusion coefficient (1 × 10−14 cm2 s−1), better initial capacity (>142 mAh g−1), greater capacity retention (∼100%), and superior rate performance compared to the cathodes without PEI. When PEI concentration was varied, the LiFePO4 cathode with 2 wt% PEI exhibited the best performance at 167 mAh g−1 capacity (98% of the theoretical capacity) and 100% retention after 50 cycles when discharged at 0.2C at 25◦C in a half cell. © 2012 The Electrochemical Society. [DOI: 10.1149/2.037302jes] All rights reserved.
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