Chemical staining for fundamental studies and optimization of binders in Li-ion battery negative electrodes

The spatial distribution of binders in Li-ion battery electrodes is critical to electrode performance, yet remains challenging to visualise, limiting binder optimisation efforts to chemical modifications rather than spatial control. Here, we show an accessible approach to staining carboxymethyl cellulose and styrene butadiene rubber binders in graphitic and Si-based Li-ion electrodes with silver and bromine, enabling detailed electron imaging and precise spectroscopic quantification of the binder domain. Leveraging these methods, we perform binder-informed optimisation of electrode manufacturing, achieving a 14% reduction in electronic resistivity, suppression of binder migration during high-temperature electrode drying, and a 40% decrease in electrode ionic resistance. Furthermore, staining enables electrode-scale, high-resolution backscattered electron imaging of complex binder hierarchies, revealing multiple types of agglomerates and elusive nanoscale binder films. These films completely coat graphitic surfaces in pristine electrodes but shatter into highly inhomogeneous fragments after calendering in both research-grade and commercial electrodes, presenting new perspectives on interpreting common cycling stability and electrode performance issues. We show how binder staining can advance fundamental understanding, quality control and manufacturing optimisation of Li-ion electrodes, particularly those based on widely used water-processable binders.

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Publication Details

Journal
Nature Communications
Published
2026-02-17
DOI
https://doi.org/10.1038/s41467-026-69002-1
Primary Topic
Advancements in Battery Materials
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article
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article

Chemical staining for fundamental studies and optimization of binders in Li-ion battery negative electrodes

Stanislaw P. Zankowski, Patrick S. Grant, Michael Metzler, Samuel Wheeler et al.
Nature Communications
Advancements in Battery Materials
article

Chemical staining for fundamental studies and optimization of binders in Li-ion battery negative electrodes

Stanislaw P. Zankowski, Patrick S. Grant, Michael Metzler, Samuel Wheeler, Thomas Barthelay, Wai Man Chan
article en

Abstract

The spatial distribution of binders in Li-ion battery electrodes is critical to electrode performance, yet remains challenging to visualise, limiting binder optimisation efforts to chemical modifications rather than spatial control. Here, we show an accessible approach to staining carboxymethyl cellulose and styrene butadiene rubber binders in graphitic and Si-based Li-ion electrodes with silver and bromine, enabling detailed electron imaging and precise spectroscopic quantification of the binder domain. Leveraging these methods, we perform binder-informed optimisation of electrode manufacturing, achieving a 14% reduction in electronic resistivity, suppression of binder migration during high-temperature electrode drying, and a 40% decrease in electrode ionic resistance. Furthermore, staining enables electrode-scale, high-resolution backscattered electron imaging of complex binder hierarchies, revealing multiple types of agglomerates and elusive nanoscale binder films. These films completely coat graphitic surfaces in pristine electrodes but shatter into highly inhomogeneous fragments after calendering in both research-grade and commercial electrodes, presenting new perspectives on interpreting common cycling stability and electrode performance issues. We show how binder staining can advance fundamental understanding, quality control and manufacturing optimisation of Li-ion electrodes, particularly those based on widely used water-processable binders.

Nature CommunicationsVol. 17(1)
University of Oxford (GB), The Faraday Institution (GB)
Openalex Percentile: Top 53%
Advancements in Battery Materials
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Chemical staining for fundamental studies and optimization of binders in Li-ion battery negative electrodes — Stanislaw P. Zankowski, Patrick S. Grant, et al. · Nature Communications (2026) | TGRS Research Map | TGRS