This work aims to study the insertion of (Formula presented.) anion in the crystalline structure of oriented pyrolytic graphite (PG) at the point of view of the anion itself. The electronic and atomic structures of the anion at different intercalation stages are studied. In particular double-edge (bicolor) X-ray absorption spectroscopy at the Al and Cl K-edges is carried out, highlighting a contraction of the anion bonding at the highest intercalation degree obtained electrochemically (stage 3), while the electronic population changes for both the edges upon cycle.
The Behavior of the Intercalant AlCl4 Anion during the Formation of Graphite Intercalation Compound: An X‐ray Absorption Fine Structure Study / Greco, Giorgia; Elia, Giuseppe Antonio; Kayser, Yves; Beckhoff, Burkhard; Perestjuk, Marko; Raoux, Simone; Hahn, Rober. - In: PHYSICA STATUS SOLIDI. A, APPLICATIONS AND MATERIALS SCIENCE. - ISSN 1862-6319. - 221:7(2024). [10.1002/pssa.202300776]
The Behavior of the Intercalant AlCl4 Anion during the Formation of Graphite Intercalation Compound: An X‐ray Absorption Fine Structure Study
Elia, Giuseppe Antonio;
2024
Abstract
This work aims to study the insertion of (Formula presented.) anion in the crystalline structure of oriented pyrolytic graphite (PG) at the point of view of the anion itself. The electronic and atomic structures of the anion at different intercalation stages are studied. In particular double-edge (bicolor) X-ray absorption spectroscopy at the Al and Cl K-edges is carried out, highlighting a contraction of the anion bonding at the highest intercalation degree obtained electrochemically (stage 3), while the electronic population changes for both the edges upon cycle.File | Dimensione | Formato | |
---|---|---|---|
Physica Status Solidi a - 2024 - Greco - The Behavior of the Intercalant AlCl4 Anion during the Formation of Graphite.pdf
accesso aperto
Tipologia:
2a Post-print versione editoriale / Version of Record
Licenza:
Creative commons
Dimensione
1.4 MB
Formato
Adobe PDF
|
1.4 MB | Adobe PDF | Visualizza/Apri |
Pubblicazioni consigliate
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
https://hdl.handle.net/11583/2995487