Roth AM, Schierl C, Ferrer-Ruiz A, Minameyer M, Rodriguez-Perez L, Villegas C, Angeles Herranz M, Martin N, Guldi DM (2017)
Publication Type: Journal article
Publication year: 2017
Book Volume: 3
Pages Range: 164-173
Journal Issue: 1
DOI: 10.1016/j.chempr.2017.05.003
At the focal point of our studies are mutual interactions between an anionic heptamethine cyanine and individualized single-walled carbon nanotubes (SWCNTs) or exfoliated nanographene (NG). Here, we report the distinct near-infrared absorption of the heptamethine cyanine, which assists in visualizing the electronic interactions in the ground state with ease and precision. In statistical Raman assays, we conclude from downshifted 2D- and G-modes for SWCNTs, as well as upshifted 2D- and downshifted G-modes for NG, that these electronic interactions result in stable n-doping of SWCNTs and NG. Key to this shift of charge density is the electron-donating character of the heptamethine cyanine. In the excited state, a complete but metastable transfer of charges is accompanied by a radical-ion-pair state that lives for several nanoseconds. Such a time domain has not yet been realized, for example, in NG to date.
APA:
Roth, A.M., Schierl, C., Ferrer-Ruiz, A., Minameyer, M., Rodriguez-Perez, L., Villegas, C.,... Guldi, D.M. (2017). Low-Dimensional Carbon Allotropes: Ground- and Excited-State Charge Transfer with NIR-Absorbing Heptamethine Cyanine. Chem, 3(1), 164-173. https://doi.org/10.1016/j.chempr.2017.05.003
MLA:
Roth, Alexandra Marina, et al. "Low-Dimensional Carbon Allotropes: Ground- and Excited-State Charge Transfer with NIR-Absorbing Heptamethine Cyanine." Chem 3.1 (2017): 164-173.
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