journal article·2025-04-11Open access

Operando Optical Microscopy for Visualization of Dendrite Growth in an Argyrodite LPSCl–Polymer Composite Electrolyte

Xiuyu Jin, Di Huang, Qiusu Miao, Ziting Zhu, Wei Tong, Alvaro Videla, Gao Liu

ACS Energy Letters· Volume 10· Issue 4

Abstract

Herein, we demonstrate the utility of optical microscopy as an accessible technique for the in situ visualization of dendrite growth within polymer-sulfide composite solid-state electrolytes. The composite electrolyte features in situ polymerization and cross-linking of the polymer between ceramic particles, which opens up extensive opportunities for accelerated materials discovery, given the vast array of acrylate/methacrylate monomers available. Specifically, the cross-linked polymer poly(triethylene glycol dimethacrylate) (poly(TEGDMA)) was observed to effectively fill pores and inhibit dendrite growth at the lithium metal interface, attributed to its glassy state at room temperature. This work represents the first application of optical microscopy to illustrate that the incorporation of glassy, undoped polymers such as poly(TEGDMA) can serve as a viable strategy for dendrite suppression in solid-state composite electrolytes.
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Research context

OpenAlex topics: Advanced Battery Materials and Technologies · Advancements in Battery Materials · Advanced battery technologies research

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Affiliations

The Energy Storage and Distributed Resources Division (ESDR)

Lawrence Berkeley National Laboratory

College of Chemistry

University of California

Departamento de Ingeniería de Minería, Pontificia Universidad Católica de Chile, Av. Vicuña Mackenna 4860, Macul, Santiago 7820436, Chile

Funding

Basic Energy Sciences · Laboratory Directed Research and Development · Vehicle Technologies Office

References (15)

Show source-provided references
1. 10.1038/nnano.2017.1610.1038/nnano.2017.16 ↗
2. 10.1021/acs.chemrev.0c0010110.1021/acs.chemrev.0c00101 ↗
3. 10.1021/acsenergylett.8b0199710.1021/acsenergylett.8b01997 ↗
4. 10.1016/j.ensm.2023.10286910.1016/j.ensm.2023.102869 ↗
5. 10.1016/j.ssi.2017.07.00510.1016/j.ssi.2017.07.005 ↗
6. 10.1002/aenm.20240360210.1002/aenm.202403602 ↗
7. 10.1002/adma.20190113110.1002/adma.201901131 ↗
8. 10.1002/advs.20190308810.1002/advs.201903088 ↗
9. 10.1039/D1EE03466A10.1039/D1EE03466A ↗
10. 10.1002/anie.20221568010.1002/anie.202215680 ↗
11. 10.1016/j.jpowsour.2020.22813510.1016/j.jpowsour.2020.228135 ↗
12. 10.1016/j.ensm.2021.07.02310.1016/j.ensm.2021.07.023 ↗
13. 10.1016/j.joule.2022.10.01110.1016/j.joule.2022.10.011 ↗
14. 10.1021/acsaem.3c0285810.1021/acsaem.3c02858 ↗
15. 10.1016/j.ensm.2018.05.01210.1016/j.ensm.2018.05.012 ↗