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Solvent- and Wavelength-Dependent Photoluminescence Relaxation Dynamics of Carbon Nanotube sp3 Defect States.

Publication ,  Journal Article
He, X; Velizhanin, KA; Bullard, G; Bai, Y; Olivier, J-H; Hartmann, NF; Gifford, BJ; Kilina, S; Tretiak, S; Htoon, H; Therien, MJ; Doorn, SK
Published in: ACS nano
August 2018

Photoluminescent sp3 defect states introduced to single wall carbon nanotubes (SWCNTs) through low-level covalent functionalization create new photophysical behaviors and functionality as a result of defect sites acting as exciton traps. Evaluation of relaxation dynamics in varying dielectric environments can aid in advancing a more complete description of defect-state relaxation pathways and electronic structure. Here, we exploit helical wrapping polymers as a route to suspending (6,5) SWCNTs covalently functionalized with 4-methoxybenzene in solvent systems including H2O, D2O, methanol, dimethylformamide, tetrahydrofuran, and toluene, spanning a range of dielectric constants from 80 to 3. Defect-state photoluminescence decays were measured as a function of emission wavelength and solvent environment. Emission decays are biexponential, with short lifetime components on the order of 65 ps and long components ranging from around 100 to 350 ps. Both short and long decay components increase as emission wavelength increases, while only the long lifetime component shows a solvent dependence. We demonstrate that the wavelength dependence is a consequence of thermal detrapping of defect-state excitons to produce mobile E11 excitons, providing an important mechanism for loss of defect-state population. Deeper trap states (i.e., those emitting at longer wavelengths) result in a decreased rate for thermal loss. The solvent-independent behavior of the short lifetime component is consistent with its assignment as the characteristic time for redistribution of exciton population between bright and dark defect states. The solvent dependence of the long lifetime component is shown to be consistent with relaxation via an electronic to vibrational energy transfer mechanism, in which energy is resonantly lost to solvent vibrations in a complementary mechanism to multiphonon decay processes.

Duke Scholars

Published In

ACS nano

DOI

EISSN

1936-086X

ISSN

1936-0851

Publication Date

August 2018

Volume

12

Issue

8

Start / End Page

8060 / 8070

Related Subject Headings

  • Nanoscience & Nanotechnology
 

Citation

APA
Chicago
ICMJE
MLA
NLM
He, X., Velizhanin, K. A., Bullard, G., Bai, Y., Olivier, J.-H., Hartmann, N. F., … Doorn, S. K. (2018). Solvent- and Wavelength-Dependent Photoluminescence Relaxation Dynamics of Carbon Nanotube sp3 Defect States. ACS Nano, 12(8), 8060–8070. https://doi.org/10.1021/acsnano.8b02909
He, Xiaowei, Kirill A. Velizhanin, George Bullard, Yusong Bai, Jean-Hubert Olivier, Nicolai F. Hartmann, Brendan J. Gifford, et al. “Solvent- and Wavelength-Dependent Photoluminescence Relaxation Dynamics of Carbon Nanotube sp3 Defect States.ACS Nano 12, no. 8 (August 2018): 8060–70. https://doi.org/10.1021/acsnano.8b02909.
He X, Velizhanin KA, Bullard G, Bai Y, Olivier J-H, Hartmann NF, et al. Solvent- and Wavelength-Dependent Photoluminescence Relaxation Dynamics of Carbon Nanotube sp3 Defect States. ACS nano. 2018 Aug;12(8):8060–70.
He, Xiaowei, et al. “Solvent- and Wavelength-Dependent Photoluminescence Relaxation Dynamics of Carbon Nanotube sp3 Defect States.ACS Nano, vol. 12, no. 8, Aug. 2018, pp. 8060–70. Epmc, doi:10.1021/acsnano.8b02909.
He X, Velizhanin KA, Bullard G, Bai Y, Olivier J-H, Hartmann NF, Gifford BJ, Kilina S, Tretiak S, Htoon H, Therien MJ, Doorn SK. Solvent- and Wavelength-Dependent Photoluminescence Relaxation Dynamics of Carbon Nanotube sp3 Defect States. ACS nano. 2018 Aug;12(8):8060–8070.
Journal cover image

Published In

ACS nano

DOI

EISSN

1936-086X

ISSN

1936-0851

Publication Date

August 2018

Volume

12

Issue

8

Start / End Page

8060 / 8070

Related Subject Headings

  • Nanoscience & Nanotechnology