Lithium-Ion Cell Performance and Transport Effects of Electrolyte Flow in a Convection Cell
Lithium-Ion Cell Performance and Transport Effects of Electrolyte Flow in a Convection Cell
Abstract
Lithium-ion batteries (LIBs) are pivotal for decarbonizing transportation and enabling
renewable energy storage. However, their broader adoption is constrained by internal
transport limitations affecting power density, energy density, and thermal management.
Commonly, Li-ion cells, packs, and systems suffer from overheating and from
polarization effects of uneven Li-ion salt concentration, especially under high-rate
operation. To address these challenges, we explore the concept of a Li-ion convection
cell with active flow of electrolyte across the cell.
Through pseudo 2D macrohomogeneous electrochemical modeling, we predict that
convection in a Li-ion cell could simultaneously mitigate bulk mass and thermal
transport limitations and heat generation. For a single cell under discharge, even
minimal electrolyte flow rates (~μm/s) enhance runtime by promoting Li + concentration
uniformity, thereby lowering charge-transfer, ohmic, and concentration overpotentials.
Furthermore, the reduction in heat generation and flow-induced heat removal help
maintain a cell within temperature cutoff limits and can enable dynamic thermal
regulation. We examine reactive and proactive electrolyte flow strategies, where flow is
initiated based on temperature thresholds or discharge rate shifts, respectively. Both
approaches suggest effective suppression of overheating and improved utilization at
high rates.
Additionally, simulations are extended to compare the effect of electrolyte convection for
cells with different cathode materials (LCO, LFP, NCA, NMC, LMO) and impacts beyond
the cell level. The benefits to internal cell behavior persist to varying degrees across
such cathode chemistries. Including pumping losses across a single cell, the net energy
benefit of flow becomes substantial under high-rate operation. However, the incremental
cost, volume, and weight of onboard flow infrastructure and excess electrolyte need to
be explored further.
Speaker
Javit Drake, PhD, Associate Professor, Massachusetts Institute of Technology
Javit Drake, PhD, is presently an Associate Professor in the Department of Chemical
Engineering at the Massachusetts Institute of Technology (MIT). His interests are 1) the
modeling of transport effects in systems using porous electrodes, such as batteries, 2)
coupling of chemical transport and solid mechanics, and 3) using technical and user
insights for product innovation. Javit Drake completed a bachelor’s degree in chemical
engineering and a minor in music at MIT in 1994, and a PhD in chemical engineering at
the University of California, Berkeley in 2000. His graduate research in gas-liquid
electrochemical flow cells was conducted with advisers Prof. John Newman and Prof.
Clayton Radke. Upon earning his doctorate, Drake worked two years at Agilent
Technologies. He then embarked on a nearly 20-year career at Duracell and parent
company, Procter & Gamble. During this time, Drake distinguished himself as a
technical innovator, leading programs and developing and applying models of porous
electrodes in electrochemical cells, multi-component diffusion, and solid and fluid
mechanics for new and enhanced products. His discoveries, inventions, and expertise
have led to 14 U.S. Patents, accelerated R&D initiatives by years, and helped enable
successful in-market products used by millions of consumers and totaling $B’s in
revenue.