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Electronic structures and quantum capacitance of single-walled carbon nanotubes doped by 3d transition-metals: A first principles study.

Authors :
Yang, Jiancheng
Yang, Mingtao
Liu, Xiaori
Zhang, Mingkai
Gao, Mengkai
Chen, Long
Su, Jiachun
Huang, Yuan
Zhang, Yiqing
Shen, Boxiong
Source :
Electrochimica Acta. Jan2023, Vol. 439, pN.PAG-N.PAG. 1p.
Publication Year :
2023

Abstract

• Systematic study of 3d transition metal-doped CNTs. • V(Cr, Mn, Co)-doped CNTs show spin-polarization effects. • The 3d transition metal doping makes a big difference to the energy band. • 3d transition metal doping increases the quantum capacitance. • Ni-CNT has the largest quantum capacitance near zero potential. Supercapacitors are valued as one of the new green energy storage devices, but the low energy density limits the wide application of supercapacitors. In this paper, the effects of 3d transition metal doped on electronic structure and quantum capacitance of carbon nanotubes are investigated using DFT. The calculations show that elemental doping has caused the break-up of two degenerate states near the Fermi level, quasi-local state changes in the energy band, and the creation of new energy bands. The doping of V(Cr, Mn, Co) causes spin polarization in the energy band. The change in energy band affects the density of states near the Fermi level, effectively increasing the quantum capacitance and surface charge density of the carbon nanotube electrode. The quantum capacitance of Ni-doped carbon nanotubes is the largest, at 59.74 µF/cm2. In the range of water stability, Ti(V, Gr, Mn, Co)-CNT are suitable for use as electrode materials in symmetrical double layer supercapacitors. Sc(Fe, Cu, Zn)-CNT is suitable for use as anode materials in asymmetric double layer supercapacitors. Ni-CNT is suitable for use as a cathode material for asymmetric double layer supercapacitors. This study verifies the feasibility of 3d transition metal doping to improve the quantum capacitance of carbon nanotube electrodes. [Display omitted] [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00134686
Volume :
439
Database :
Academic Search Index
Journal :
Electrochimica Acta
Publication Type :
Academic Journal
Accession number :
161141477
Full Text :
https://doi.org/10.1016/j.electacta.2022.141666