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Related Concept Videos

Trends in Lattice Energy: Ion Size and Charge02:54

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An ionic compound is stable because of the electrostatic attraction between its positive and negative ions. The lattice energy of a compound is a measure of the strength of this attraction. The lattice energy (ΔHlattice) of an ionic compound is defined as the energy required to separate one mole of the solid into its component gaseous ions. For the ionic solid sodium chloride, the lattice energy is the enthalpy change of the process:
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Updated: Jan 12, 2026

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Space Charge Layer Evolution in All-Solid-State Batteries Probed via Operando Kelvin Probe Force Microscopy and

Chao Zhu1, Shigeru Kobayashi2, Yuki Sugisawa3

  • 1Max Planck Institute for Polymer Research, Ackermannweg 10, 55128 Mainz, Germany.

ACS Nano
|November 5, 2025
PubMed
Summary

Controversial space charge layers in solid-state batteries (ASSBs) were clarified using advanced microscopy and analysis. The study found these layers have a minor impact on interfacial resistance, paving the way for improved ASSB development.

Keywords:
Kelvin probeall-solid-state batteriesnondestructivenuclear reaction analysisscanning force microscopespace charge layer

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Area of Science:

  • Materials Science
  • Electrochemistry
  • Solid-State Ionics

Background:

  • Space charge layers at solid-solid interfaces are critical but poorly understood in solid-state batteries (ASSBs).
  • Existing controversies hinder the development of improved interfaces and overall ASSB performance.

Purpose of the Study:

  • To investigate the role and characteristics of space charge layers in ASSBs.
  • To quantitatively determine the interfacial resistance contribution of space charge layers.

Main Methods:

  • Utilized operando heterodyne Kelvin probe force microscopy (KPFM) and operando nuclear reaction analysis (NRA).
  • Studied a model thin-film ASSB: lithium (Li)|Li3PO4 (LPO)|LiCoO2 (LCO).
  • Operated the battery within a voltage range of 3.0 to 4.3 V vs Li/Li+.

Main Results:

  • Identified a space charge layer (<50 nm width) primarily at the LPO|LCO interface, caused by Li-ion redistribution.
  • Quantitatively determined the interfacial space charge layer resistance, with a maximum of 18.4–19.1 Ω cm² at 4.3 V vs Li/Li+.
  • Demonstrated that space charge layer resistance is significantly smaller than bulk solid electrolyte resistance in the studied ASSB.

Conclusions:

  • Resolved controversies regarding the role of space charge layers in ASSBs.
  • Advanced understanding of space charge layer evolution at solid electrolyte-electrode interfaces using KPFM and NRA.
  • The findings suggest space charge layers have a limited impact on overall interfacial resistance in optimized ASSBs.