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We report the molecular beam epitaxy of Bi1−xSbx thin films (0 ≤ x ≤ 1) on sapphire (0001) substrates using a thin (Bi,Sb)2Te3 buffer layer. The characterization of the films using reflection high energy diffraction, x-ray diffraction, atomic force microscopy, and scanning transmission electron microscopy reveals the epitaxial growth of films of reasonable structural quality. This is further confirmed via x-ray diffraction pole figures that determine the epitaxial registry between the thin film and the substrate. We further investigate the microscopic structure of thin films via Raman spectroscopy, demonstrating how the vibrational modes vary as the composition changes and discussing the implications for the crystal structure. We also characterize the samples using electrical transport measurements.
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Electrodeposited thin-film Cu x Sb anodes for Li-ion batteries: enhancement of cycle life via tuning of film composition and engineering of the film-substrate interface
Electrodeposited Cu–Sb thin films on Cu and Ni substrates are investigated as alloy anodes for Li-ion batteries to elucidate the effects of both the film composition and substrate interactions on anode cycling stability and lifetime. Thin films of composition Cu x Sb (0 < x < 2) exhibit the longest cycle lifetimes nearest x = 1. Additionally, the Cu–Sb films exhibit shorter cycle lifetimes when electrodeposited onto Cu substrates when compared to equivalent films on Ni substrates. Ex situ characterization and differential capacity analysis of the anodes reveal that significant interdiffusion occurs during cycling between pure Sb films and Cu substrates. The great extent of interdiffusion results in mechanical weakening of the film–substrate interface that exacerbates film delamination and decreases cycle lifetimes of Cu–Sb films on Cu substrates regardless of the film's composition. The results presented here demonstrate that the composition of the anode alone is not the most important predictor of long term cycle stability; the composition coupled with the identity of the substrate is key. These interactions are critical to understand in the design of high capacity, large volume change materials fabricated without the need for additional binders.
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- Award ID(s):
- 1710672
- PAR ID:
- 10064323
- Date Published:
- Journal Name:
- Journal of Materials Chemistry A
- Volume:
- 6
- Issue:
- 26
- ISSN:
- 2050-7488
- Page Range / eLocation ID:
- 12708 to 12717
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1039/c8ta01798k
