Study of the solid electrolyte interphase of Li-O2 battery electrolyte by analytical transmission electron microscopy

Microscopy ◽  
2020 ◽  
Vol 69 (4) ◽  
pp. 227-233 ◽  
Author(s):  
Mitsunori Kitta ◽  
Hikaru Sano

Abstract Investigation of solid electrolyte interphases (SEIs) on negative electrode surfaces is essential to improve the stable charge-discharge performance of rechargeable lithium-air batteries (Li-O2 batteries). In this study, a direct investigation of SEI films is conducted using analytical transmission electron microscopy (TEM). A thin Cu specimen is prefabricated for TEM observation and is utilised as a model substrate for SEI formation. The electrochemical cell constructed using dissolved oxygen in the electrolyte exhibits a greater electrochemical overpotential during the Li-metal deposition process than that constructed with a pristine electrolyte. This suggests that different electrochemical passivation features occur in each different electrochemical cell. TEM observation confirms that the surface film formed by O2 dissolute electrolyte is a polycrystalline Li2O film with a thickness of ~5 nm, whereas the film formed by the pristine electrolyte is organic-based, amorphous-like and 20–50 nm thick. The dissolved oxygen molecules are more easily reduced than the components of the electrolyte, leading to the formation of Li2O as a stable passivation SEI film, which is expected to exhibit good charge-discharge features during the operation of the Li-O2 battery.

Author(s):  
R.A. Ploc

Samples of low-nickel Zircaloy-2 (material MLI-788-see(1)), when anodically polarized in neutral 5 wt% NaCl solutions, were found to be susceptible to pitting and stress corrosion cracking. The SEM revealed that pitting of stressed samples was occurring below a 2000Å thick surface film which behaved differently from normal zirconium dioxide in that it did not display interference colours. Since the initial film thickness was approximately 65Å, attempts were made to examine the product film by transmission electron microscopy to deduce composition and how the corrosion environment could penetrate the continuous layer.


Author(s):  
George Guthrie ◽  
David Veblen

The nature of a geologic fluid can often be inferred from fluid-filled cavities (generally <100 μm in size) that are trapped during the growth of a mineral. A variety of techniques enables the fluids and daughter crystals (any solid precipitated from the trapped fluid) to be identified from cavities greater than a few micrometers. Many minerals, however, contain fluid inclusions smaller than a micrometer. Though inclusions this small are difficult or impossible to study by conventional techniques, they are ideally suited for study by analytical/ transmission electron microscopy (A/TEM) and electron diffraction. We have used this technique to study fluid inclusions and daughter crystals in diamond and feldspar.Inclusion-rich samples of diamond and feldspar were ion-thinned to electron transparency and examined with a Philips 420T electron microscope (120 keV) equipped with an EDAX beryllium-windowed energy dispersive spectrometer. Thin edges of the sample were perforated in areas that appeared in light microscopy to be populated densely with inclusions. In a few cases, the perforations were bound polygonal sides to which crystals (structurally and compositionally different from the host mineral) were attached (Figure 1).


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Bing Han ◽  
Yucheng Zou ◽  
Zhen Zhang ◽  
Xuming Yang ◽  
Xiaobo Shi ◽  
...  

AbstractCryogenic transmission electron microscopy (cryo-TEM) is a valuable tool recently proposed to investigate battery electrodes. Despite being employed for Li-based battery materials, cryo-TEM measurements for Na-based electrochemical energy storage systems are not commonly reported. In particular, elucidating the chemical and morphological behavior of the Na-metal electrode in contact with a non-aqueous liquid electrolyte solution could provide useful insights that may lead to a better understanding of metal cells during operation. Here, using cryo-TEM, we investigate the effect of fluoroethylene carbonate (FEC) additive on the solid electrolyte interphase (SEI) structure of a Na-metal electrode. Without FEC, the NaPF6-containing carbonate-based electrolyte reacts with the metal electrode to produce an unstable SEI, rich in Na2CO3 and Na3PO4, which constantly consumes the sodium reservoir of the cell during cycling. When FEC is used, the Na-metal electrode forms a multilayer SEI structure comprising an outer NaF-rich amorphous phase and an inner Na3PO4 phase. This layered structure stabilizes the SEI and prevents further reactions between the electrolyte and the Na metal.


Sign in / Sign up

Export Citation Format

Share Document