4.6 Article

Chemical Heterogeneity in PAN/LLZTO Composite Electrolytes by Synchrotron Imaging

Journal

JOURNAL OF THE ELECTROCHEMICAL SOCIETY
Volume 168, Issue 11, Pages -

Publisher

ELECTROCHEMICAL SOC INC
DOI: 10.1149/1945-7111/ac352a

Keywords

Chemical Inhomogeneity; Composite Electrolytes; X-ray Fluorescence Imaging; Transmission X-ray Microscope; Garnet

Funding

  1. AFOSR of the National Synchrotron Light Source II, a U.S. Department of Energy (DOE) Office of Science User Facility by Brookhaven National Laboratory [FA9550-20-1-0233, DE-SC0012704]

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Solid polymer/ceramic composite electrolytes show promising potential for batteries due to their thermal stability and mechanical properties. Chemical heterogeneity in these materials, such as inhomogeneity in ceramic phases and salt distribution at interfaces, plays a crucial role in their performance. Through advanced imaging techniques, this study reveals nanoscale chemical heterogeneity in composite electrolytes and highlights the need for further research to understand the relationship between chemical heterogeneity and ionic transport pathways.
Solid polymer/ceramic composite electrolytes are promising for batteries due to their attractive thermal stability and mechanical properties. Chemical heterogeneity in solid composite electrolytes, such as the inhomogeneity in the ceramic phase and salt distribution at the polymer/ceramic interface, is critical to the performance of solid composite electrolytes. However, such heterogeneity has not been well understood yet. In this work, we use Synchrotron-based X-ray fluorescence imaging (XRF) and Transmission X-ray Microscope (TXM) to image nanoscale chemical heterogeneity in polyacrylamide/Li7+xLa3Zr2-xTaxO12 (LLZTO) composite electrolytes and investigate the effects of lithium salt, salt concentration, and plasticizer. We find that LLZTO particles show strong inter- and intra-particles chemical heterogeneities, and the off-stoichiometry of Zr in an LLZTO particle is unlikely to be only balanced by Ta substitution. Moreover, statistical analysis suggests that LiI tends to accumulate at the ceramic/polymer interface at a low concentration of 5 wt%, but no such tendency was observed in samples with 10 wt% LiI. However, composite electrolytes with LiTFSI show interfacial accumulation at both 5 wt% and 10 wt%. This report provides insight into element distributions in solid composite electrolytes, and we hope further researches can shed light on the connections between chemical heterogeneity and ionic transport pathway inside.

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