journal article·2021-01Open access

Electrolyte‐Free Spectroscopy and Imaging of Graphite Intercalation

Madeline S. Stark, Judy Cheng, Hailey Kim, Kaci L. Kuntz, Scott C. Warren

Small· Volume 17· Issue 1

Abstract

Abstract Engineering electrode materials for optoelectronic and energy storage applications requires a fundamental understanding of intercalation using spatially‐resolved techniques. However, spectroscopic methods can have limited spatial resolution and low intensity since the signal passes through electrolyte. Here, a device geometry is presented in which the electrolyte is laterally separated from the area probed spectroscopically, so that the signal does not pass through the electrolyte. This geometry enables us to visualize ion transport with optical microscopy and monitor charge transfer with Raman and visible reflectance spectroscopies. In addition, vibrational changes are probed in the mid‐IR, a region previously difficult to access due to electrolyte absorption. This geometry will allow many layered electrodes to be probed in situ using time‐ and spatially‐resolved techniques, including photon and electron spectroscopies.
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Research context

OpenAlex topics: Advancements in Battery Materials · Graphene research and applications · Electrochemical Analysis and Applications

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Affiliations

Department of Chemistry and Department of Applied Physical Sciences University of North Carolina at Chapel Hill Chapel Hill North Carolina 27599 USA

Funding

National Science Foundation · U.S. Department of Energy · Office of Science · Basic Energy Sciences

References (26)

Show source-provided references
1. Köhler V. · Phys. Sci. Rev. · 2018 · 4 · 20170154
2. 10.1038/s41467-017-01787-810.1038/s41467-017-01787-8 ↗
3. 10.1038/ncomms522410.1038/ncomms5224 ↗
4. 10.1002/adma.20180809110.1002/adma.201808091 ↗
5. 10.1080/0001873011011364410.1080/00018730110113644 ↗
6. 10.1002/adma.20180821310.1002/adma.201808213 ↗
7. Hennig G. · Prog. Inorg. Chem. · 1959 · 1 · 126
8. 10.1063/1.169690510.1063/1.1696905 ↗
9. 10.1021/nn400207e10.1021/nn400207e ↗
10. 10.1021/acs.jpcc.9b0672610.1021/acs.jpcc.9b06726 ↗
11. Daumas N. · C.R. Hebd. Seances Acad. Sci., Ser. C · 1969 · 268 · 373
12. 10.1016/0379-6779(89)90402-510.1016/0379-6779(89)90402-5 ↗
13. 10.1016/0379-6779(81)90049-710.1016/0379-6779(81)90049-7 ↗
14. 10.1002/aenm.20140174210.1002/aenm.201401742 ↗
15. 10.1016/0379-6779(81)90009-610.1016/0379-6779(81)90009-6 ↗
16. Eklund P. C. · 1986 · 33710.1007/978-1-4757-5556-5_28 ↗
17. 10.1515/zpch-1940-450410.1515/zpch-1940-4504 ↗
18. 10.1016/0008-6223(71)90004-210.1016/0008-6223(71)90004-2 ↗
19. 10.1021/ac00038a00610.1021/ac00038a006 ↗
20. 10.1021/jp011454110.1021/jp0114541 ↗
21. 10.1021/jz100188d10.1021/jz100188d ↗
22. 10.1063/1.174964710.1063/1.1749647 ↗
23. Anders H. · 1967
24. 10.1039/a904544i10.1039/a904544i ↗
25. 10.1016/0022-0728(89)87079-210.1016/0022-0728(89)87079-2 ↗
26. 10.1016/0022-0728(89)85170-810.1016/0022-0728(89)85170-8 ↗