Terahertz spectroscopy study of the confining potential for methane in the endofullerene CH4@C60

T Tanzeeha Jafari (National Institute of Chemical Physics and Biophysics 1 , Tallinn 12618,) A Anna Shugai (National Institute of Chemical Physics and Biophysics 1 , Tallinn 12618,) U Urmas Nagel (National Institute of Chemical Physics and Biophysics 1 , Tallinn 12618,) E Elizabeth S. Marsden (School of Chemistry and Chemical Engineering, University of Southampton 2 , Southampton SO17 1BJ,) S Sally Bloodworth (School of Chemistry and Chemical Engineering, University of Southampton 2 , Southampton SO17 1BJ,) G Gabriela Hoffman (School of Chemistry and Chemical Engineering, University of Southampton 2 , Southampton SO17 1BJ,) G George R. Bacanu (School of Chemistry and Chemical Engineering, University of Southampton 2 , Southampton SO17 1BJ,) M Mark C. Walkey (School of Chemistry and Chemical Engineering, University of Southampton 2 , Southampton SO17 1BJ,) M Malcolm H. Levitt (School of Chemistry, University of Southampton , Southampton SO17 1BJ,) R Richard J. Whitby (School of Chemistry and Chemical Engineering, University of Southampton 2 , Southampton SO17 1BJ,) T Toomas Rõõm (National Institute of Chemical Physics and Biophysics 1 , Tallinn 12618,)

Abstract

We used terahertz spectroscopy to study the non-covalent interaction between CH4 and the confining fullerene cage in endofullerene CH4@C60. The temperature dependence of the THz absorption spectra of powdered CH4@C60 was measured between 5 and 300 K. At temperatures below 50 K, the THz spectrum of CH4 shows a single line centered at 214 cm−1, which broadens and shifts to a higher energy as the temperature increases. These effects are explained by the anharmonicity of the CH4–C60 interaction potential function. The model involves the center-of-mass motion of CH4 in a spherically symmetric potential well. Line intensities are modeled by invoking an electric dipole moment induced by the translational displacement of CH4 from the center of the cage C60. The potential function and the dipole moment parameters were derived from the temperature dependence of the THz absorption spectra and compared with the parameters of previously studied endofullerenes. The quantum chemistry calculations reproduce the CH4 translation motion frequency and the potential function remarkably well.

Article Details

Volume / Issue Vol. 163, Issue 8
Published August 28, 2025
ISSN 0021-9606
Publisher American Institute of Physics

Journal Info

The Journal of Chemical Physics

American Institute of Physics

ISSN: 0021-9606 Physical Sciences

Authors (11)

T

Tanzeeha Jafari

National Institute of Chemical Physics and Biophysics 1 , Tallinn 12618,

A

Anna Shugai

National Institute of Chemical Physics and Biophysics 1 , Tallinn 12618,

U

Urmas Nagel

National Institute of Chemical Physics and Biophysics 1 , Tallinn 12618,

E

Elizabeth S. Marsden

School of Chemistry and Chemical Engineering, University of Southampton 2 , Southampton SO17 1BJ,

S

Sally Bloodworth

School of Chemistry and Chemical Engineering, University of Southampton 2 , Southampton SO17 1BJ,

G

Gabriela Hoffman

School of Chemistry and Chemical Engineering, University of Southampton 2 , Southampton SO17 1BJ,

G

George R. Bacanu

School of Chemistry and Chemical Engineering, University of Southampton 2 , Southampton SO17 1BJ,

M

Mark C. Walkey

School of Chemistry and Chemical Engineering, University of Southampton 2 , Southampton SO17 1BJ,

M

Malcolm H. Levitt

School of Chemistry, University of Southampton , Southampton SO17 1BJ,

R

Richard J. Whitby

School of Chemistry and Chemical Engineering, University of Southampton 2 , Southampton SO17 1BJ,

T

Toomas Rõõm

National Institute of Chemical Physics and Biophysics 1 , Tallinn 12618,