Intercalation Compounds from LiH and Graphite: Relative Stability of Metastable Stages and Thermodynamic Stability of Dilute Stage Id
Source abstract
Abstract
High Resolution Image Download MS PowerPoint Slide The intercalation of lithium into graphite was studied at temperatures between 400 and 550 °C by heating mixtures of LiH and graphite powders with molar ratios 4:1, 1:1, and 1:6 under dynamic vacuum for periods between 1 and 72 h. These conditions probe the formation and thermal stability of metastable staged Li–graphite intercalation compounds (Li-GICs) close to the competing formation of the thermodynamically stable carbide Li 2 C 2 . Li-GICs of stages I (LiC 6, Aα), II a (Li 0.5 C 6, AαA), II b (Li ∼0.33 C 6, AαABβB), III (Li ∼0.22 C 6, AαAB), IV (Li ∼0.167 C 6 ), and dilute stage lithium I d have been identified and characterized by powder X-ray diffraction and Raman spectroscopy. The rate and extent of intercalation (i.e., the achieved stage of Li-GIC) depends on LiH activity and temperature. Stage I was only observed for temperatures above 500 °C. At 400 °C, the highest intercalation corresponded to stage II b, which was obtained after 2 and 24 h for 4:1 and 1:1 reaction mixtures, respectively. Lower-staged Li-GICs attained at temperatures below 500 °C deintercalate upon prolonged dwelling with the exception of stage II a, which can be maintained for very long periods (several days) in the presence of LiH. At temperatures above 500 °C, the kinetically controlled formation of Li-GICs is followed by Li 2 C 2 carbide formation. It is shown that the Li-GIC I d coexists with Li 2 C 2 at temperatures up to 800 °C and that the Li content of I d (solubility of Li in graphite) increases between 550 and 800 °C. Consequently, I d with a temperature-dependent homogeneity range should be added as a stable phase in the Li–C phase diagram. A sketch of a revised Li–C phase diagram is provided.
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Research context
OpenAlex topics: Advancements in Battery Materials · Graphite, nuclear technology, radiation studies · Aluminum Alloys Composites Properties
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Materials and Environmental Chemistry, Stockholm University, SE-10691 Stockholm, Sweden
Funding
Vetenskapsr?det
References (43)
Show source-provided references
1. Dresselhaus M. S. · Adv. Phys. · 1981 · 30 · 13910.1080/00018738100101367 ↗
2. Noel M. · J. Power Sources · 2002 · 111 · 19310.1016/S0378-7753(02)00308-7 ↗
3. Enoki T. · 200310.1093/oso/9780195128277.001.0001 ↗
4. Ozawa K. · 200910.1002/9783527629022 ↗
5. Dahn J. R. · Phys. Rev. B · 1991 · 44 · 917010.1103/PhysRevB.44.9170 ↗
6. Ohzuku T. · J. Electrochem. Soc. · 1993 · 140 · 249010.1149/1.2220849 ↗
7. Billaud D. · Mater. Res. Bull. · 1993 · 28 · 47710.1016/0025-5408(93)90130-6 ↗
8. Billaud D. · J. Phys. Chem. Solids · 1996 · 57 · 77510.1016/0022-3697(95)00348-7 ↗
9. Billaud D. · Solid State Commun. · 2002 · 124 · 29910.1016/S0038-1098(02)00469-6 ↗
10. Wang X.-L. · Sci. Rep. · 2012 · 2 · 74710.1038/srep00747 ↗
11. Senyshyn A. · J. Electrochem. Soc. · 2013 · 160 · A319810.1149/2.031305jes ↗
12. He H. · Electrochim. Acta · 2013 · 92 · 14810.1016/j.electacta.2012.12.135 ↗
13. Herold A. · Bull. Soc. Chim. Fr. · 1955 · 999
14. Juza R. · Naturwissenschaften · 1965 · 52 · 56010.1007/BF00631568 ↗
15. Guerard D. · Carbon · 1975 · 13 · 33710.1016/0008-6223(75)90040-8 ↗
16. Pfluger P. · Synth. Met. · 1981 · 3 · 2710.1016/0379-6779(81)90038-2 ↗
17. Herold A. · Mater. Sci. Eng. · 1977 · 31 · 2510.1016/0025-5416(77)90006-4 ↗
18. Basu S. · Mater. Sci. Eng. · 1979 · 38 · 27510.1016/0025-5416(79)90132-0 ↗
19. Billaud D. · Synth. Met. · 1981 · 3 · 2110.1016/0379-6779(81)90037-0 ↗
20. Janot R. · Prog. Mater. Sci. · 2005 · 50 · 110.1016/S0079-6425(03)00050-1 ↗
21. Sacci R. L. · J. Electrochem. Soc. · 2014 · 161 · A61410.1149/2.082404jes ↗
22. Avdeev V. V. · J. Phys. Chem. Solids · 1996 · 57 · 94710.1016/0022-3697(95)00380-0 ↗
23. Reynier Y. · J. Power Sources · 2003 · 119 · 85010.1016/S0378-7753(03)00285-4 ↗
24. Imai Y. · J. Alloys Compd. · 2007 · 439 · 25810.1016/j.jallcom.2006.08.061 ↗
25. Persson K. · Phys. Rev. B · 2010 · 82 · 12541610.1103/PhysRevB.82.125416 ↗
26. Wang Z. · RSC Adv. · 2014 · 4 · 4069
27. Andersson A. M. · J. Power Sources · 1999 · 81 · 810.1016/S0378-7753(99)00185-8 ↗
28. Drüe M. · J. Alloys Compd. · 2013 · 575 · 40310.1016/j.jallcom.2013.06.001 ↗
29. Kozlov A. · Int. J. Mater. Res. · 2013 · 104 · 106610.3139/146.110960 ↗
30. Sangster J. · J. Phase Equilib. Diffus. · 2007 · 28 · 56110.1007/s11669-007-9193-8 ↗
31. Okamoto H. · Bull. Alloy Phase Diagrams · 1989 · 10 · 6910.1007/BF02882178 ↗
32. Ma X. · Dalton Trans. · 2009 · 1025010.1039/b913320h ↗
33. Ma X. · J. Solid State Chem. · 2008 · 181 · 162810.1016/j.jssc.2008.06.018 ↗
34. Yi T. · J. Mater. Chem. · 2012 · 22 · 2480510.1039/c2jm35257e ↗
35. Corbett J. · Inorg. Synth. · 1983 · 22 · 1510.1002/9780470132531.ch3 ↗
36. Rodriguez-Carvajal, J.Abstracts of the Satellite Meeting on Powder Diffraction of the XV Congress of the IUCr,Toulouse, France, 1990; p127.
37. Dollase W. A. · J. Appl. Crystallogr. · 1986 · 19 · 26710.1107/S0021889886089458 ↗
38. Woo K. C. · Phys. Rev. Lett. · 1983 · 50 · 18210.1103/PhysRevLett.50.182 ↗
39. Yazami, R.InLithium Ion Rechargeable Batteries;Ozawa, K., Ed.Wiley-VCH:Weinheim, Germany, 2009; pp67–102.10.1002/9783527629022.ch5 ↗
40. Doll G. L. · Phys. Rev. B · 1987 · 36 · 494010.1103/PhysRevB.36.4940 ↗
41. Inaba M. · J. Electrochem. Soc. · 1995 · 142 · 2010.1149/1.2043869 ↗
42. Reynier Y. F. · J. Electrochem. Soc. · 2004 · 151 · A42210.1149/1.1646152 ↗
43. Trucano P. · Nature · 1975 · 258 · 13610.1038/258136a0 ↗