Issue 24, 2018

Guidelines for optimizing the architecture of battery insertion electrodes based on the concept of wiring lengths

Abstract

The kinetics of storing mass in a battery electrode are typically limited by slow diffusion in storage particles. The diffusion timescale can be made faster by decreasing the size of the particles, but then it becomes more difficult to efficiently contact each particle with ionic and electronic current collectors, e.g., electrolyte and carbon. To achieve an optimal balance, the dimensions of the various phases in the electrode architecture should be tuned to the transport properties of the storage phase. Here we quantify this strategy by modeling the kinetics of galvanostatic charging for several particle geometries using the Nernst–Planck formalism and assuming mass storage via a solid solution. We show that when ions and electrons are inserted at separate contact surfaces, in general the storage kinetics depend on two length scales – the ionic and electronic wiring lengths – that characterize the transport distances within the storage material to the respective current collectors. Quantitative guidelines for the optimal wiring lengths are derived for two model geometries, and the dependence on transport parameters, particle shape, and contact geometry is discussed. These results can guide the optimization of various aspects of the architecture of a battery electrode, including the size and shape of individual particles and the configuration of the electrolyte and current collector networks.

Graphical abstract: Guidelines for optimizing the architecture of battery insertion electrodes based on the concept of wiring lengths

Article information

Article type
Paper
Submitted
26 Mar 2018
Accepted
23 May 2018
First published
07 Jun 2018
This article is Open Access
Creative Commons BY license

Phys. Chem. Chem. Phys., 2018,20, 16449-16462

Guidelines for optimizing the architecture of battery insertion electrodes based on the concept of wiring lengths

R. E. Usiskin and J. Maier, Phys. Chem. Chem. Phys., 2018, 20, 16449 DOI: 10.1039/C8CP01946K

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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