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Operando Tracking of Solution-Phase Concentration Profiles in Li-Ion Battery Positive Electrodes Using X-ray Fluorescence
Author(s) -
Jeremy I. G. Dawkins,
Mohammadreza Zamanzad Ghavidel,
Danny Chhin,
Isabelle Beaulieu,
Md. Sazzad Hossain,
Renfei Feng,
Janine Mauzeroll,
Steen B. Schougaard
Publication year - 2020
Publication title -
analytical chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.117
H-Index - 332
eISSN - 1520-6882
pISSN - 0003-2700
DOI - 10.1021/acs.analchem.0c02086
Subject(s) - chemistry , electrolyte , ethylene carbonate , battery (electricity) , electrode , analytical chemistry (journal) , ion , phase (matter) , synchrotron , cathode , chromatography , power (physics) , thermodynamics , physics , organic chemistry , nuclear physics
The trade-off between energy density and power capabilities is a challenge for Li-ion battery design as it highly depends on the complex porous structures that holds the liquid electrolyte. Specifically, mass-transport limitations lead to large concentration gradients in the solution-phase and subsequently to crippling overpotentials. The direct study of these solution-phase concentration profiles in Li-ion battery positive electrodes has been elusive, in part because they are shielded by an opaque and paramagnetic matrix. Herein we present a new methodology employing synchrotron hard X-ray fluorescence to observe the concentration gradient formation within Li-ion battery electrodes in operando . This methodology is substantiated with data collected on a model LiFePO 4 /Li cell using a 1 M LiAsF 6 in 1:1 ethylene carbonate/dimethyl carbonate (EC/DMC) electrolyte under galvanostatic and intermittent charge profiles. As such, the technique holds great promise for optimization of new composite electrodes and for numerical model validation.

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