Atomic deuterium adsorption on multi-walled carbon nanotubes (MWCNTs) has been achieved with a high deuteration level (≃70% of deuterated carbon atoms), and studied using complementary spectroscopic techniques, namely, photoelectron spectroscopy and Raman spectroscopy. As a consequence of the deuterium (D) adsorption on the MWCNTs, the sp2 bonds of the C atoms are distorted toward an sp3 configuration, and the π plasmon excitation of the metallic MWCNTs is quenched, suggesting the transition to a semiconducting phase. Such a controlled deuteration in ultra-high vacuum conditions induces the opening of an energy gap in the metallic MWCNTs, with the valence band maximum at about ∼3.1 eV below the Fermi level. The bond distortion and the strain induced by the D uptake is evidenced by the modification of the Raman response. This work shows that the molecular cracking of D2 in ultra-high vacuum is an efficient way to obtain stable, homogeneous, and high uptake of deuterium atoms with minimal presence of defects.

Atomic deuterium bonding to multi-walled carbon nano tubes / Tayyab, Sammar; Apponi, Alice; Betti, Maria Grazia; Blundo, Elena; Castellano, Orlando; Cavoto, Gianluca; Pandolfi, Francesco; Polimeni, Antonio; Rago, Ilaria; Ruocco, Alessandro; Yadav, Ravi Prakash; Mariani, Carlo. - In: THE JOURNAL OF CHEMICAL PHYSICS. - ISSN 0021-9606. - 162:19(2025), pp. 1-8. [10.1063/5.0250642]

Atomic deuterium bonding to multi-walled carbon nano tubes

Tayyab, Sammar
;
Apponi, Alice;Betti, Maria Grazia
;
Blundo, Elena;Castellano, Orlando;Cavoto, Gianluca;Polimeni, Antonio;Rago, Ilaria;Yadav, Ravi Prakash;Mariani, Carlo
2025

Abstract

Atomic deuterium adsorption on multi-walled carbon nanotubes (MWCNTs) has been achieved with a high deuteration level (≃70% of deuterated carbon atoms), and studied using complementary spectroscopic techniques, namely, photoelectron spectroscopy and Raman spectroscopy. As a consequence of the deuterium (D) adsorption on the MWCNTs, the sp2 bonds of the C atoms are distorted toward an sp3 configuration, and the π plasmon excitation of the metallic MWCNTs is quenched, suggesting the transition to a semiconducting phase. Such a controlled deuteration in ultra-high vacuum conditions induces the opening of an energy gap in the metallic MWCNTs, with the valence band maximum at about ∼3.1 eV below the Fermi level. The bond distortion and the strain induced by the D uptake is evidenced by the modification of the Raman response. This work shows that the molecular cracking of D2 in ultra-high vacuum is an efficient way to obtain stable, homogeneous, and high uptake of deuterium atoms with minimal presence of defects.
2025
multi wall carbon nano tubes; deuterium; X-ray photoelectron spectroscopy; UV photoelectron spectroscopy, Raman spectroscopy
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Atomic deuterium bonding to multi-walled carbon nano tubes / Tayyab, Sammar; Apponi, Alice; Betti, Maria Grazia; Blundo, Elena; Castellano, Orlando; Cavoto, Gianluca; Pandolfi, Francesco; Polimeni, Antonio; Rago, Ilaria; Ruocco, Alessandro; Yadav, Ravi Prakash; Mariani, Carlo. - In: THE JOURNAL OF CHEMICAL PHYSICS. - ISSN 0021-9606. - 162:19(2025), pp. 1-8. [10.1063/5.0250642]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1738647
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