4.8 Article

In situ atomic-scale imaging of electrochemical lithiation in silicon

Journal

NATURE NANOTECHNOLOGY
Volume 7, Issue 11, Pages 749-756

Publisher

NATURE PORTFOLIO
DOI: 10.1038/NNANO.2012.170

Keywords

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Funding

  1. Laboratory Directed Research and Development (LDRD) project at Sandia National Laboratories (SNL)
  2. Nanostructures for Electrical Energy Storage (NEES), an Energy Frontier Research Center (EFRC)
  3. US Department of Energy, Office of Science, Office of Basic Energy Sciences [DESC0001160]
  4. US Department of Energy's National Nuclear Security Administration [DE-AC04-94AL85000]
  5. NSF [CMMI-0758554, 1100205, DMR-1008104, DMR-1120901, CMMI-0900692]
  6. AFOSR [FA9550-08-1-0325]
  7. Direct For Mathematical & Physical Scien
  8. Division Of Materials Research [1120901] Funding Source: National Science Foundation
  9. Div Of Civil, Mechanical, & Manufact Inn
  10. Directorate For Engineering [1100205] Funding Source: National Science Foundation

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In lithium-ion batteries, the electrochemical reaction between the electrodes and lithium is a critical process that controls the capacity, cyclability and reliability of the battery. Despite intensive study, the atomistic mechanism of the electrochemical reactions occurring in these solid-state electrodes remains unclear. Here, we show that in situ transmission electron microscopy can be used to study the dynamic lithiation process of single-crystal silicon with atomic resolution. We observe a sharp interface (similar to 1 nm thick) between the crystalline silicon and an amorphous LixSi alloy. The lithiation kinetics are controlled by the migration of the interface, which occurs through a ledge mechanism involving the lateral movement of ledges on the close-packed {111} atomic planes. Such ledge flow processes produce the amorphous LixSi alloy through layer-by-layer peeling of the {111} atomic facets, resulting in the orientation-dependent mobility of the interfaces.

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