4.8 Article

Variable-Energy Hard X-ray Photoemission Spectroscopy: A Nondestructive Tool to Analyze the Cathode-Solid-State Electrolyte Interface

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 12, Issue 2, Pages 2293-2298

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.9b16343

Keywords

solid-state battery; interface; ALD; X-ray photoemission spectroscopy; HRTEM

Funding

  1. China Automotive Battery Research Institute, Beijing
  2. Nature Science and Engineering Research Council of Canada (NSERC)
  3. Canada Research Chair Program (CRC)
  4. Canada Foundation for Innovation (CFI)
  5. Canadian Light Sources (CLS)
  6. University of Western Ontario
  7. CLS Postdoctoral Student Travel Support Program
  8. MITACS Elevate postdoctoral program
  9. State Key Lab of Advanced Metals and Materials, University of Science and Technology Beijing, Beijing, China

Ask authors/readers for more resources

All-solid-state batteries are expected to be promising next-generation energy storage systems with increased energy density compared to the state-of-the-art Li-ion batteries. Nonetheless, the electrochemical performances of the all-solid-state batteries are currently limited by the high interfacial resistance between active electrode materials and solid-state electrolytes. In particular, elemental interdiffusion and the formation of interlayers with low ionic conductivity are known to restrict the battery performance. Herein, we apply a nondestructive variable-energy hard X-ray photoemission spectroscopy to detect the elemental chemical states at the interface between the cathode and the solid-state electrolyte, in comparison to the widely used angle-resolved (variable-angle) X-ray photoemission spectroscopy/X-ray absorption spectroscopy methods. The accuracy of variable-energy hard X-ray photoemission spectroscopy is also verified with a focused ion beam and high-resolution transmission electron microscopy. We also show the significant suppression of interdiffusion by building an artificial layer via atomic layer deposition at this interface.

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