4.8 Article

Enhanced Lithiation Cycle Stability of ALD-Coated Confined a-Si Microstructures Determined Using In Situ AFM

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 8, Issue 1, Pages 530-537

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.5b09544

Keywords

silicon; lithium ion; atomic force microscopy; in situ; battery

Funding

  1. US Army Research Lab
  2. Nanoscience Institute at the US Naval Research Lab

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Microfabricated amorphous silicon (alpha-Si) pits similar to 4 mu m in diameter and 100 nm thick were fabricated to be partially confined in a nickel (Ni) current collector. Corresponding unconfined pillars were also fabricated. The samples were coated with 1.5, 3, or 6 nm of Al2O3 ALD. These samples were tested in electrolytes of 3:7 by weight ethylene carbonate:ethyl methyl carbonate (EC:EMC) with 1.2 M LiPF6 salt with and without 2% fluoroethylene carbonate (FEC) and in a pure FEC electrolyte with 10 wt % LiPF6. The samples were imaged with an atomic force microscope during electrochemical cycling to evaluate morphology evolution and solid electrolyte interphase (SEI) formation. The partially confined alpha-Si structures had superior cycle efficiency relative to the unconfined alpha-Si pillars. Additionally, samples with 3 nm of ALD achieved higher charge capacity and enhanced cycle life compared to samples without ALD, demonstrated thinner SEI formation, and after 10 cycles at a 1 C rate remained mostly intact and had actually decreased in diameter. Finally, the samples with 3 nm of ALD had better capacity retention in the baseline 3:7 EC:EMC than in either of the FEC containing electrolytes.

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