Skip to Main Content
 

Global Search Box

 
 
 
 

Files

File List


Masters thesis.pdf (3.7 MB)

ETD Abstract Container

Abstract Header

In-situ scanning tunneling microscopy studies of the SEI formation on graphite anodes in propylene carbonate

Dehiwala Liyanage, Chamathka H
http://rave.ohiolink.edu/etdc/view?acc_num=osu1574502965210263

Abstract Details

2019, Master of Science, Ohio State University, Chemistry.
Since its discovery in 1979, the solid electrolyte interface (SEI) has drawn attention due to its importance for efficient battery performance. Despite its significance, there is still some ambiguity with regards to how certain electrolytes form a protective interface to aid Li+ intercalation whilst others irreversibly degrade the anode structure. One of the most debated examples is the “EC-PC disparity” towards the graphite anode, where ethylene carbonate (EC) results in protective SEI formation whilst propylene carbonate (PC) leads to destructive graphite exfoliation. This study focuses on the correlation between the concentration of the Li+ salt, LiPF6 dissolved in PC and the growth of SEI on graphite. In-situ and in-operando electrochemical scanning tunneling microscope (STM) observation of the basal plane of highly oriented pyrolytic graphite (HOPG) is performed in 1 M, 2.5 M and 3 M LiPF6 dissolved in propylene carbonate (PC) in sequence to cyclic voltammetry (CV) and potential hold experiments. This technique allows the study of the topographic evolution of the basal plane and edge sites on HOPG with changes in the potential, as a result of solvent co-intercalation, reduction, graphite exfoliation and SEI formation. STM images obtained whilst holding the potential at selected values, gives an insight into the nature of SEI formation, in connection to the extent of regeneration of the graphite surface. It is found that below 0.9 V vs Li, solvent decomposition, followed by extensive graphite exfoliation takes place in the 1 M and to a lesser degree in 2.5 M LiPF6 electrolyte solutions. However, in the 3 M salt solution, graphite exfoliation is scarce and SEI formation is observed at potentials as high as 1.1 V vs Li, which clearly indicates a concentration dependent SEI formation on graphite. CV experiments conducted in parallel to EC-STM, provide further confirmation. The HOPG is cycled between 3 to 0.005 V vs Li in all three salt concentrations within Swagelok® type cells. A comparison of the initial cycle for the three concentrations reveals a shift in the onset potential for solvent reduction towards higher values, specifically, 1.2, 1.4 and 2.0 V for 1 M, 2.5 M and 3 M LiPF6 in PC. Previous studies have attributed the difference in SEI formation to the competition between the fluoride-containing anion and solvent towards the solvation of Li+.
Anne Co, Dr. (Advisor)
Zachary Schultz, Dr. (Committee Member)
72 p.
Chemistry
Lithium-ion batteries; Graphite anodes; Solid electrolyte interface; SEI; Propylene carbonate; PC; Electrochemical scanning tunneling microscopy; STM; Cyclic voltammetry

Recommended Citations

Citations

  • Dehiwala Liyanage, C. H. (2019). In-situ scanning tunneling microscopy studies of the SEI formation on graphite anodes in propylene carbonate [Master's thesis, Ohio State University]. OhioLINK Electronic Theses and Dissertations Center. http://rave.ohiolink.edu/etdc/view?acc_num=osu1574502965210263

    APA Style (7th edition)

  • Dehiwala Liyanage, Chamathka. In-situ scanning tunneling microscopy studies of the SEI formation on graphite anodes in propylene carbonate. 2019. Ohio State University, Master's thesis. OhioLINK Electronic Theses and Dissertations Center, http://rave.ohiolink.edu/etdc/view?acc_num=osu1574502965210263.

    MLA Style (8th edition)

  • Dehiwala Liyanage, Chamathka. "In-situ scanning tunneling microscopy studies of the SEI formation on graphite anodes in propylene carbonate." Master's thesis, Ohio State University, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1574502965210263

    Chicago Manual of Style (17th edition)

osu1574502965210263
266
© 2019, all rights reserved.
This open access ETD is published by The Ohio State University and OhioLINK.