Browsing by Author "Hároz, Erik H."

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    Asymmetric excitation profiles in the resonance Raman response of armchair carbon nanotubes
    (American Physical Society, 2015) Hároz, Erik H.; Duque, Juan G.; Barros, Eduardo B.; Telg, Hagen; Simpson, Jeffrey R.; Walker, Angela R. Hight; Khripin, Constantine Y.; Fagan, Jeffrey A.; Tu, Xiaomin; Zheng, Ming; Kono, Junichiro; Doorn, Stephen K.
    We performed tunable resonance Raman spectroscopy on samples highly enriched in the (5,5), (6,6), (7,7), and (8,8) armchair structures of metallic single-wall carbon nanotubes. We present Raman excitation profiles (REPs) for both the radial breathing mode and G-band phonons of these species. G-band excitation profiles are shown to resolve the expected incoming and outgoing resonances of the scattering process. Notably, the profiles are highly asymmetric, with the higher-energy outgoing resonance weaker than the incoming resonance. These results are comparable to the asymmetric excitation profiles observed previously in semiconducting nanotubes, introduce a different electronic type, and broaden the structural range over which the asymmetry is found to exist. Modeling of the behavior with a third-order quantum model that accounts for the k dependence in energies and matrix elements, without including excitonic effects, is found to be insufficient for reproducing the observed asymmetry. We introduce an alternative fifth-order model in which the REP asymmetry arises from quantum interference introduced by phonon-mediated state mixing between the EM11 and K-momentum excitons. Such state mixing effectively introduces a nuclear coordinate dependence in the transition dipole moment and thus may be viewed as a non-Condon effect from a molecular perspective. This result unifies a molecularlike picture of nanotube transitions (introduced by their excitonic nature) with a condensed matter approach for describing their behavior.
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    Diameter dependence of TO phonon frequencies and the Kohn anomaly in armchair single-wall carbon nanotubes
    (American Physical Society, 2014) Telg, Hagen; Hároz, Erik H.; Duque, Juan G.; Tu, Xiaomin; Khripin, Constantine Y.; Fagan, Jeffrey A.; Zheng, Ming; Kono, Junichiro; Doorn, Stephen K.
    We present resonant Raman scattering experiments on nanotube samples enriched in metallic armchair single-wall carbon nanotubes (SWCNTs). We establish the transverse optical (ATO) phonon frequency for the (5,5) through (10,10) armchair species, ranging in diameter from 0.68 to 1.36 nm. The frequencies show a strong diameter dependence similar to that previously observed in semiconducting nanotubes. We show that the ATO frequencies in armchair SWCNTs are dramatically upshifted from those of semiconducting SWCNTs. Furthermore, using electrochemical doping, we demonstrated that the ATO frequencies in armchair SWCNTs are independent of the position of the Fermi level. These results suggest that the upshift is a result of a Kohn anomaly involving a forward-scattering mechanism of electrons close to the Fermi level. This is in contrast to the well-known Kohn anomaly that dominates the downshift of the ALO and E2g phonons in nonarmchair metallic SWCNTs and graphene, respectively.
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    Wafer-scale monodomain films of spontaneously aligned single-walled carbon nanotubes
    (Springer Nature, 2016) He, Xiaowei; Gao, Weilu; Xie, Lijuan; Li, Bo; Zhang, Qi; Lei, Sidong; Robinson, John M.; Hároz, Erik H.; Doorn, Stephen K.; Wang, Weipeng; Vajtai, Robert; Ajayan, Pulickel M.; Adams, W. Wade; Hauge, Robert H.; Kono, Junichiro
    The one-dimensional character of electrons, phonons and excitons in individual single-walled carbon nanotubes leads to extremely anisotropic electronic, thermal and optical properties. However, despite significant efforts to develop ways to produce large-scale architectures of aligned nanotubes, macroscopic manifestations of such properties remain limited. Here, we show that large (>cm2) monodomain films of aligned single-walled carbon nanotubes can be prepared using slow vacuum filtration. The produced films are globally aligned within ±1.5° (a nematic order parameter of ∼1) and are highly packed, containing 1 × 106 nanotubes in a cross-sectional area of 1 μm2. The method works for nanotubes synthesized by various methods, and film thickness is controllable from a few nanometres to ∼100 nm. We use the approach to create ideal polarizers in the terahertz frequency range and, by combining the method with recently developed sorting techniques, highly aligned and chirality-enriched nanotube thin-film devices. Semiconductor-enriched devices exhibit polarized light emission and polarization-dependent photocurrent, as well as anisotropic conductivities and transistor action with high on/off ratios.