skip to main content
US FlagAn official website of the United States government
dot gov icon
Official websites use .gov
A .gov website belongs to an official government organization in the United States.
https lock icon
Secure .gov websites use HTTPS
A lock ( lock ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.


Title: Length reduction kinetics of multiwalled carbon nanotubes correlated to planetary ball mill impact energy
Four commercial multiwalled carbon nanotubes with distinct lengths and diameters were subject to planetary ball milling to induce length reduction. The Burgio-Rojac energy model was employed to calculate the single impact energy and cumulative energy dissipated to the carbon nanotubes during milling. The ratio of sample mass to bead mass and the nanotube bulk density did not affect length reduction during grinding. The minimum impact energy barrier for carbon nanotube length reduction appeared directly proportional to nanotube diameter for parallel wall morphologies, although a nanotube sample with a cup-stacked wall morphology showed a much lower energy barrier. A normalized exponential equation relating carbon nanotube length and cumulative impact energy collapsed all data to a single exponential master curve described by the same scaling parameters, namely a pre-exponential term that includes the initial nanotube length and a scaling energy in the exponent.  more » « less
Award ID(s):
2022297
PAR ID:
10541042
Author(s) / Creator(s):
; ; ; ;
Publisher / Repository:
https://www.tandfonline.com/doi/abs/10.1080/1536383X.2023.2260028
Date Published:
Journal Name:
Fullerenes, Nanotubes and Carbon Nanostructures
Volume:
32
Issue:
1
ISSN:
1536-383X
Page Range / eLocation ID:
8 to 21
Subject(s) / Keyword(s):
carbon nanotubes ball milling Burgio-Rojac model
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. We report the synthesis and structure of single-walled aluminosilicate nanotubes with microporous zeolitic walls. This quasi-one-dimensional zeolite is assembled by a bolaform structure-directing agent (SDA) containing a central biphenyl group connected by C 10 alkyl chains to quinuclidinium end groups. High-resolution electron microscopy and diffraction, along with other supporting methods, revealed a unique wall structure that is a hybrid of characteristic building layers from two zeolite structure types, beta and MFI. This hybrid structure arises from minimization of strain energy during the formation of a curved nanotube wall. Nanotube formation involves the early appearance of a mesostructure due to self-assembly of the SDA molecules. The biphenyl core groups of the SDA molecules show evidence of π stacking, whereas the peripheral quinuclidinium groups direct the microporous wall structure. 
    more » « less
  2. Achieving the co-assembly of more than one component represents an important challenge in the drive to create functional self-assembled nanomaterials. Multicomponent nanomaterials comprised of several discrete, spatially sorted domains of components with high degrees of internal order are particularly important for applications such as optoelectronics. In this work, single-walled carbon nanotubes (SWNTs) were threaded through the inner channel of nanotubes formed by the bolaamphiphilic self-assembly of a naphthalenediimide-lysine (NDI-Bola) monomer. The self-assembly process was driven by electrostatic interactions, as indicated by ζ -potential measurements, and cation–π interactions between the surface of the SWNT and the positively charged, NDI-Bola nanotube interior. To increase the threading efficiency, the NDI-Bola nanotubes were fragmented into shortened segments with lengths of <100 nm via sonication-induced shear, prior to co-assembly with the SWNTs. The threading process created an initial composite nanostructure in which the SWNTs were threaded by multiple, shortened segments of the NDI-Bola nanotube that progressively re-elongated along the SWNT surface into a continuous radial coating around the SWNT. The resultant composite structure displayed NDI-Bola wall thicknesses twice that of the parent nanotube, reflecting a bilayer wall structure, as compared to the monolayer structure of the parent NDI-Bola nanotube. As a final, co-axial outer layer, poly( p -phenyleneethynylene) (PPE-SO 3 Na, M W = 5.76 × 10 4 , PDI – 1.11) was wrapped around the SWNT/NDI-Bola composite resulting in a three-component (SWNT/NDI-Bola/PPE-SO 3 Na) composite nanostructure. 
    more » « less
  3. Strategically introduced defects can be used to modify carbon nanotubes for new properties and functions. For example, chemical defects can act as atomic traps for electrons, holes, electron-hole pairs, and even molecules and ions ( 1 ). The ability to control the placement of these defects on carbon nanotubes could enable a plethora of fundamental studies and potential applications in imaging, sensing, disease diagnostics, and quantum information science ( 2 – 4 ). However, there is yet no effective way to do this with atomic precision ( 5 – 7 ). On page 535 of this issue, Lin et al. ( 8 ) report the creation of ordered defect arrays by programming DNA strands to wrap around and traverse the entire length of a single-walled carbon nanotube. 
    more » « less
  4. Abstract We use time-dependent density functional theory to investigate the possibility of hosting organic color centers in (6, 6) armchair single-walled carbon nanotubes, which are known to be metallic. Our calculations show that in short segments of (6, 6) nanotubes ∼ 5 nm in length there is a dipole-allowed singlet transition related to the quantum confinement of charge carriers in the smaller segments. The introduction of s p 3 defects to the surface of (6, 6) nanotubes results in new dipole-allowed excited states. Some of these states are redshifted from the native confinement state of the defect-free (6, 6) segments; this is similar behavior to what is observed with s p 3 defects to exciton transitions in semiconducting carbon nanotubes. This result suggests the possibility of electrically wiring organic color centers directly through armchair carbon nanotube hosts. 
    more » « less
  5. We present a semi-analytical expression for the dielectric response function of quasi-2D ultrathin films of periodically aligned single-walled carbon nanotubes. We derive the response function in terms of the individual nanotube conductivity, plasma frequency, and the volume fraction of carbon nanotubes in the film. The real part of the dielectric response function is negative for a sufficiently wide range of the incident photon energy, indicating that the film behaves as a hyperbolic metamaterial. Inhomogeneous broadening increases the effect. 
    more » « less