In the recent framework of the studies of Sn-doped MAX phase materials for potential applications as negative electrode materials in alkaline-ion batteries, this work explores the potentiality of the pure 211 MAX phase Ti2Al(1–y)Sny compound through solid-state synthesis and subsequent thermal oxidation. A complete structural investigation through neutron diffraction and thermal operando synchrotron X-ray diffraction elucidates the phase evolution during oxidation. In coin cell tests against lithium, both samples demonstrate initial anodic capacities attributed to irreversible conversion reactions, followed by reversible alloying/dealloying mechanisms. Similarly, tests against sodium show comparable electrochemical behavior, albeit with lower capacities due to sodium's lower reactivity with Sn oxide. The capacity retention after cycling can be associated to the structural stability of the electrodes. Overall, this study has a place in the broader framework of the Sn-doped MAX phases investigation, and once more it underscores the importance of optimizing Sn oxide formation for enhanced electrochemical performance in both Li-ion and Na-ion batteries, with implications for future active materials design.
Vallana, N., Ostroman, I., Marchionna, S., Palladini, C., Gentile, A., Perego, O., et al. (2025). The Oxidized Ti2(Al/Sn)C Behavior as Anode for Lithium- and Sodium-Ion Batteries: The Role of the MAX Phase Order. CHEMELECTROCHEM [10.1002/celc.202400712].
The Oxidized Ti2(Al/Sn)C Behavior as Anode for Lithium- and Sodium-Ion Batteries: The Role of the MAX Phase Order
Vallana N.;Ostroman I.;Palladini C.;Ferrara C.
;Ruffo R.
2025
Abstract
In the recent framework of the studies of Sn-doped MAX phase materials for potential applications as negative electrode materials in alkaline-ion batteries, this work explores the potentiality of the pure 211 MAX phase Ti2Al(1–y)Sny compound through solid-state synthesis and subsequent thermal oxidation. A complete structural investigation through neutron diffraction and thermal operando synchrotron X-ray diffraction elucidates the phase evolution during oxidation. In coin cell tests against lithium, both samples demonstrate initial anodic capacities attributed to irreversible conversion reactions, followed by reversible alloying/dealloying mechanisms. Similarly, tests against sodium show comparable electrochemical behavior, albeit with lower capacities due to sodium's lower reactivity with Sn oxide. The capacity retention after cycling can be associated to the structural stability of the electrodes. Overall, this study has a place in the broader framework of the Sn-doped MAX phases investigation, and once more it underscores the importance of optimizing Sn oxide formation for enhanced electrochemical performance in both Li-ion and Na-ion batteries, with implications for future active materials design.File | Dimensione | Formato | |
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