journal article·2023-08-23

Hydrogen-Type Binding Sites in Carbonaceous Electrodes for Rapid Lithium Insertion

Devin McGlamery, Charles McDaniel, Wei Xu, Nicholas P. Stadie

ACS Applied Materials & Interfaces· Volume 15· Issue 33
Publisher page

Abstract

Direct pyrolysis of coronene at 800 °C produces low-surface-area, nanocrystalline graphitic carbon containing a uniquely high content of a class of lithium binding sites referred to herein as “hydrogen-type” sites. Correspondingly, this material exhibits a distinct redox couple under electrochemical lithiation that is characterized as intermediate-strength, capacitive lithium binding, centered at ∼0.5 V vs Li/Li + . Lithiation of hydrogen-type sites is reversible and electrochemically distinct from capacitive lithium adsorption and from intercalation-type binding between graphitic layers. Hydrogen-type site lithiation can be fully retained even up to ultrafast current rates (e.g., 15 A g –1, ∼40 C) where intercalation is severely hampered by ion desolvation kinetics; at the same time, the bulk nature of these sites does not require a large surface area, and only minimal electrolyte decomposition occurs during the first charge/discharge cycle, making coronene-derived carbon an exceptional candidate for high-energy-density battery applications.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Advancements in Battery Materials · Advanced Battery Materials and Technologies · Supercapacitor Materials and Fabrication

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Chemistry & Biochemistry, Montana State University, Bozeman, Montana 59717, United States

Funding

Army Research Laboratory

References (35)

Show source-provided references
1. Yoshio M. · 200910.1007/978-0-387-34445-4 ↗
2. 10.1002/anie.20110500610.1002/anie.201105006 ↗
3. Nelson P. A. · 201910.2172/1503280 ↗
4. 10.1016/S0378-7753(02)00349-X10.1016/S0378-7753(02)00349-X ↗
5. 10.1016/j.jpowsour.2016.12.03210.1016/j.jpowsour.2016.12.032 ↗
6. 10.1016/j.jpowsour.2019.03.02710.1016/j.jpowsour.2019.03.027 ↗
7. 10.1021/cr030203g10.1021/cr030203g ↗
8. 10.1021/jz100188d10.1021/jz100188d ↗
9. 10.1149/2.1221802jes10.1149/2.1221802jes ↗
10. 10.3390/ma1416468310.3390/ma14164683 ↗
11. 10.1002/aenm.20210112610.1002/aenm.202101126 ↗
12. 10.1149/1945-7111/ac4b8710.1149/1945-7111/ac4b87 ↗
13. 10.1002/batt.20200025310.1002/batt.202000253 ↗
14. 10.1149/1.194898710.1149/1.1948987 ↗
15. 10.1016/S0378-7753(02)00585-210.1016/S0378-7753(02)00585-2 ↗
16. 10.1016/j.ceja.2020.10001410.1016/j.ceja.2020.100014 ↗
17. 10.1002/cssc.20140349010.1002/cssc.201403490 ↗
18. 10.1126/science.270.5236.59010.1126/science.270.5236.590 ↗
19. 10.1149/1.183724110.1149/1.1837241 ↗
20. 10.1016/S0008-6223(96)00098-X10.1016/S0008-6223(96)00098-X ↗
21. 10.1002/aenm.20190200710.1002/aenm.201902007 ↗
22. 10.1557/JMR.1990.043510.1557/JMR.1990.0435 ↗
23. 10.1149/1.205005710.1149/1.2050057 ↗
24. 10.1039/C8CC01932K10.1039/C8CC01932K ↗
25. 10.1021/acs.chemmater.0c0053510.1021/acs.chemmater.0c00535 ↗
26. 10.1038/nnano.2013.4610.1038/nnano.2013.46 ↗
27. 10.1021/acs.jpcc.0c0691810.1021/acs.jpcc.0c06918 ↗
28. 10.1007/s10853-020-05392-x10.1007/s10853-020-05392-x ↗
29. 10.1016/S0022-0728(96)04832-210.1016/S0022-0728(96)04832-2 ↗
30. 10.1039/C9TA13862E10.1039/C9TA13862E ↗
31. 10.1038/nmat360110.1038/nmat3601 ↗
32. 10.1021/acsnano.8b0191410.1021/acsnano.8b01914 ↗
33. 10.1021/acs.chemrev.0c0017010.1021/acs.chemrev.0c00170 ↗
34. 10.1126/science.124962510.1126/science.1249625 ↗
35. 10.1002/anie.20230139610.1002/anie.202301396 ↗