TY - JOUR
T1 - A First-Principles Investigation of Lithium and Sodium Ion Diffusion in C60 Molecular Solids
AU - Gorelik, Rachel
AU - Asaduzzaman, Abu
AU - Manga, Venkateswara Rao
AU - Thakur, Abhishek
AU - Muralidharan, Krishna
N1 - Funding Information: This work was performed at the High Performing Computing (HPC) center at the University of Arizona. A.A. acknowledges the support of Penn State’s EAGER grant. Publisher Copyright: © 2022 American Chemical Society.
PY - 2022/3/10
Y1 - 2022/3/10
N2 - C60-based molecular solids have shown promise as important constituents in electrode materials as well as for providing interfacial stability for solid state electrolytes in alkali ion batteries. At room temperature, the solid state C60 crystal is characterized by a face-centered cubic (FCC) structure, with large interstitial voids, which can accommodate and promote ion transport. In this regard, using density functional theory (DFT), we examined the diffusion of lithium and sodium ions within the FCC C60 lattice. The underlying diffusion mechanism for both ions consisted of motion between interstitial tetrahedral and octahedral voids within the C60 lattice. Multiple energy minimum sites were located within each interstitial void, and the diffusion of the ions involved jumps within voids as well as between voids. The rate-limiting step for ion diffusion corresponded to the motion between the tetrahedral and octahedral voids, and the respective activation barriers were determined to be 0.34 eV for lithium and 0.28 eV for sodium. Importantly, the evaluated activation barriers compare favorably with those of currently used solid state electrolytes and electrode materials in alkali ion batteries. These calculations provide insights into the diffusion mechanisms of alkali ions in C60 lattices and should enable utilizing C60 as important components for alkali-ion batteries.
AB - C60-based molecular solids have shown promise as important constituents in electrode materials as well as for providing interfacial stability for solid state electrolytes in alkali ion batteries. At room temperature, the solid state C60 crystal is characterized by a face-centered cubic (FCC) structure, with large interstitial voids, which can accommodate and promote ion transport. In this regard, using density functional theory (DFT), we examined the diffusion of lithium and sodium ions within the FCC C60 lattice. The underlying diffusion mechanism for both ions consisted of motion between interstitial tetrahedral and octahedral voids within the C60 lattice. Multiple energy minimum sites were located within each interstitial void, and the diffusion of the ions involved jumps within voids as well as between voids. The rate-limiting step for ion diffusion corresponded to the motion between the tetrahedral and octahedral voids, and the respective activation barriers were determined to be 0.34 eV for lithium and 0.28 eV for sodium. Importantly, the evaluated activation barriers compare favorably with those of currently used solid state electrolytes and electrode materials in alkali ion batteries. These calculations provide insights into the diffusion mechanisms of alkali ions in C60 lattices and should enable utilizing C60 as important components for alkali-ion batteries.
UR - http://www.scopus.com/inward/record.url?scp=85126093294&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85126093294&partnerID=8YFLogxK
U2 - 10.1021/acs.jpcc.1c09269
DO - 10.1021/acs.jpcc.1c09269
M3 - Article
SN - 1932-7447
VL - 126
SP - 4259
EP - 4266
JO - Journal of Physical Chemistry C
JF - Journal of Physical Chemistry C
IS - 9
ER -