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E. Peled (1979)
The Electrochemical Behavior of Alkali and Alkaline Earth Metals in Nonaqueous Battery Systems—The Solid Electrolyte Interphase ModelJournal of The Electrochemical Society, 126
Yuan Gao, J. Dahn (1996)
Synthesis and Characterization of Li1 + x Mn2 − x O 4 for Li‐Ion Battery ApplicationsJournal of The Electrochemical Society, 143
K. Takei, N. Terada, Kazuma Kumai, T. Iwahori, Toshiharu Uwai, T. Miura (1995)
Effects of the macroscopic structure of carbon black on its behaviour as the anode in a lithium secondary cellJournal of Power Sources, 55
J. Dahn, A. Sleigh, H. Shi, J. Reimers, Q. Zhong, B. Way (1993)
Dependence of the electrochemical intercalation of lithium in carbons on the crystal structure of the carbonElectrochimica Acta, 38
M. Kikuchi, Y. Ikezawa, T. Takamura (1995)
Surface modification of pitch-based carbon fibre for the improvement of electrochemical lithium intercalationJournal of Electroanalytical Chemistry, 396
S. Megahed, W. Ebner (1995)
Lithium-ion battery for electronic applicationsJournal of Power Sources, 54
T. Tran, J. Feikert, X. Song, K. Kinoshita (1995)
Commercial Carbonaceous Materials as Lithium Intercalation AnodesJournal of The Electrochemical Society, 142
M. Winter, P. Novák, A. Monnier (1998)
Graphites for lithium-ion cells : The correlation of the first-cycle charge loss with the Brunauer-Emmett-Teller surface areaJournal of The Electrochemical Society, 145
J. Besenhard, M. Winter, Jun Yang, W. Biberacher (1995)
Filming mechanism of lithium-carbon anodes in organic and inorganic electrolytesJournal of Power Sources, 54
Rosamaría Fong, U. Sacken, J. Dahn (1990)
Studies of Lithium Intercalation into Carbons Using Nonaqueous Electrochemical CellsJournal of The Electrochemical Society, 137
J. Besenhard, H. Fritz (1974)
Cathodic reduction of graphite in organic solutions of alkali and NR4+ saltsJournal of Electroanalytical Chemistry, 53
W. Xing, J. Dahn (1997)
Study of Irreversible Capacities for Li Insertion in Hard and Graphitic CarbonsJournal of The Electrochemical Society, 144
The aim of this work is to examine the performance and in particular the irreversible capacity of synthetic graphites. Our analysis is based on the evaluation and study of the differential capacity (dx/dV), computed by numerical differentiation of the galvanostatic curve. The dx/dV curve shows a series of peaks that correspond to potential plateaus. The area under each peak results in the charge related to the particular process, and by peak de-convolution analysis we can determine the charge consumed by or released from each process. This approach enables us to identify the processes involved (formation of SEI, solvated Li co-intercalation, cell self discharge, etc.).
Ionics – Springer Journals
Published: Mar 21, 2006
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