SYSYApr 17

Scaling and Analytical Approximation of Porous Electrode Theory for Reaction-limited Batteries

arXiv:2604.166276.9h-index: 7
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This work provides an interpretable, physics-based framework for accelerating battery design and state estimation, unifying modeling across various electrochemical systems.

The authors developed a simplified 'lean model' of porous electrode theory using scaling analysis and analytical approximations, validated against numerical simulations of an NMC half-cell with excellent agreement at negligible computational cost.

Porous electrode theory (PET) provides essential insights into electrochemical states, but its computational complexity hinders real-time control and obscures scaling relations. To bridge the gap between high-fidelity simulations and reduced-order models, we present a framework of scaling analysis and analytical approximations. By assuming high-performance electrodes minimize transport limitations and overpotentials, we derive a simplified "lean model" governed by four dimensionless numbers: (i) a traditional Damk"ohler number, Da, scaling the characteristic reaction rate to the diffusion rate in the electrolyte-filled pores; (ii) the "process Damk"ohler number," Da_p, scaling the reaction rate to the applied capacity utilization rate (C-rate); (iii) the "wiring Damk"ohler number," Da_w, scaling the reaction rate to an effective electromigration rate for ions in the pores in series with electrons in the conducting matrix; and (iv) the "capacitive Damk"ohler number," Da_c, comparing the rates of Faradaic reactions and double-layer charging. For batteries, we derive analytical solutions for standard protocols, including galvanostatic discharge, chronoamperometry, and electrochemical impedance spectroscopy. Validated against numerical simulations of a practical NMC half-cell, our formulae show excellent agreement at negligible computational cost. This interpretable, physics-based framework accelerates battery design and state estimation while unifying the modeling of batteries, supercapacitors, fuel cells, and other porous electrode systems.

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