Graczyk-Zajac, Magdalena ; Wimmer, Maximilian ; Xu, Yeping ; Buntkowsky, Gerd ; Neumann, Christian ; Riedel, Ralf (2017)
Lithium intercalation into disordered carbon/SiCN composite. Part 2: Raman spectroscopy and 7Li MAS NMR investigation of lithium storage sites.
In: Journal of Solid State Electrochemistry, 21 (1)
doi: 10.1007/s10008-016-3337-x
Artikel, Bibliographie
Kurzbeschreibung (Abstract)
Within this work, we analyze the lithium storage sites within carbon/silicon carbonitride (SiCN) composites. Commercial carbons, HD3 (hard carbon) and LD1N and LD2N (soft carbons), of varying porosity are impregnated with polysilazane (HTT 1800) and pyrolysed at 1100 °C. It is found in the first part of this study (Graczyk-Zajac et al. J Solid State Electrochem 19:2763–2769, 2015) that the initial porosity of the carbon phase plays an important role in determining the lithium insertion capacity and rate capability of the composite material. By applying Raman spectroscopy and solid-state 7Li MAS NMR on pristine, lithiated, and delithiated samples, we investigate the lithium storage sites within the composite materials. By means of Raman spectroscopy, it has been found that lithium storage in hard carbon-derived composites occurs in a significant extent via adsorption-like process within unorganized carbon, whereas for the soft carbon composites, storage in turbostratic carbon is identified. 7Li solid-state NMR confirms these findings revealing that more than 33 % of lithium stored in HD3/SiCN is adsorbed in ionic form at the surface and in pores of the composite, while around 38 % is stored between carbon layers. LD1N and LD2N composites store more than 50 % of lithium in the intercalation-type sites.
Typ des Eintrags: | Artikel |
---|---|
Erschienen: | 2017 |
Autor(en): | Graczyk-Zajac, Magdalena ; Wimmer, Maximilian ; Xu, Yeping ; Buntkowsky, Gerd ; Neumann, Christian ; Riedel, Ralf |
Art des Eintrags: | Bibliographie |
Titel: | Lithium intercalation into disordered carbon/SiCN composite. Part 2: Raman spectroscopy and 7Li MAS NMR investigation of lithium storage sites |
Sprache: | Englisch |
Publikationsjahr: | 2017 |
Verlag: | Springer |
Titel der Zeitschrift, Zeitung oder Schriftenreihe: | Journal of Solid State Electrochemistry |
Jahrgang/Volume einer Zeitschrift: | 21 |
(Heft-)Nummer: | 1 |
DOI: | 10.1007/s10008-016-3337-x |
Kurzbeschreibung (Abstract): | Within this work, we analyze the lithium storage sites within carbon/silicon carbonitride (SiCN) composites. Commercial carbons, HD3 (hard carbon) and LD1N and LD2N (soft carbons), of varying porosity are impregnated with polysilazane (HTT 1800) and pyrolysed at 1100 °C. It is found in the first part of this study (Graczyk-Zajac et al. J Solid State Electrochem 19:2763–2769, 2015) that the initial porosity of the carbon phase plays an important role in determining the lithium insertion capacity and rate capability of the composite material. By applying Raman spectroscopy and solid-state 7Li MAS NMR on pristine, lithiated, and delithiated samples, we investigate the lithium storage sites within the composite materials. By means of Raman spectroscopy, it has been found that lithium storage in hard carbon-derived composites occurs in a significant extent via adsorption-like process within unorganized carbon, whereas for the soft carbon composites, storage in turbostratic carbon is identified. 7Li solid-state NMR confirms these findings revealing that more than 33 % of lithium stored in HD3/SiCN is adsorbed in ionic form at the surface and in pores of the composite, while around 38 % is stored between carbon layers. LD1N and LD2N composites store more than 50 % of lithium in the intercalation-type sites. |
Fachbereich(e)/-gebiet(e): | 11 Fachbereich Material- und Geowissenschaften 11 Fachbereich Material- und Geowissenschaften > Materialwissenschaft 11 Fachbereich Material- und Geowissenschaften > Materialwissenschaft > Fachgebiet Disperse Feststoffe 07 Fachbereich Chemie |
Hinterlegungsdatum: | 14 Jun 2017 09:31 |
Letzte Änderung: | 29 Jan 2019 07:21 |
PPN: | |
Sponsoren: | We gratefully acknowledge the financial support of the German Research Foundation (DFG) SFB 595/A4 and SFB 595/B9 as well as SPP1473/J8. |
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