Standard

Electronically Excited States in Model Complexes of Noble Metal Clusters with Carbon Nanodots. / Pomogaev, V. A.; Lee, H. J.; Goh, E.; Tchaikovskaya, O. N.; Kononov, A. I.; Avramov, P. V.

In: Russian Physics Journal, Vol. 64, No. 11, 01.03.2022, p. 2076-2081.

Research output: Contribution to journal › Article › peer-review

Harvard

Pomogaev, VA, Lee, HJ, Goh, E, Tchaikovskaya, ON, Kononov, AI & Avramov, PV 2022, 'Electronically Excited States in Model Complexes of Noble Metal Clusters with Carbon Nanodots', Russian Physics Journal, vol. 64, no. 11, pp. 2076-2081. https://doi.org/10.1007/s11182-022-02558-9

APA

Pomogaev, V. A., Lee, H. J., Goh, E., Tchaikovskaya, O. N., Kononov, A. I., & Avramov, P. V. (2022). Electronically Excited States in Model Complexes of Noble Metal Clusters with Carbon Nanodots. Russian Physics Journal, 64(11), 2076-2081. https://doi.org/10.1007/s11182-022-02558-9

Vancouver

Pomogaev VA, Lee HJ, Goh E, Tchaikovskaya ON, Kononov AI, Avramov PV. Electronically Excited States in Model Complexes of Noble Metal Clusters with Carbon Nanodots. Russian Physics Journal. 2022 Mar 1;64(11):2076-2081. https://doi.org/10.1007/s11182-022-02558-9

Author

Pomogaev, V. A. ; Lee, H. J. ; Goh, E. ; Tchaikovskaya, O. N. ; Kononov, A. I. ; Avramov, P. V. / Electronically Excited States in Model Complexes of Noble Metal Clusters with Carbon Nanodots. In: Russian Physics Journal. 2022 ; Vol. 64, No. 11. pp. 2076-2081.

BibTeX

@article{758b9cb6f0bf415883cf54a859a91081,
title = "Electronically Excited States in Model Complexes of Noble Metal Clusters with Carbon Nanodots",
abstract = "Theoretical calculations of excited states in the complexes of gold and silver three-atom nanoclusters with carbon quantum nanodots are performed using the M062X functional and the def2SVP {H}/def2TZVP/def2TZVPP{Ag, Au} hybrid basis set. A subsequent calculation of the excited states is performed in an approximation of the time-dependent density functional theory implemented in Gaussian09. The chromophore centers of the nanodots are modeled by heterocyclic molecules of isoquino-diazaanthracene and benzopyrano-diazanaphthalene. The clusters are attached to the nanodots using ethyl mercaptan and methoxyethane bridges of various lengths. The energy transfer channels are considered depending on the mutual arrangement of energy levels of clusters and heterocycles.",
keywords = "carbon nanodots, excitation energy transfer, metal clusters, photophysical processes",
author = "Pomogaev, {V. A.} and Lee, {H. J.} and E. Goh and Tchaikovskaya, {O. N.} and Kononov, {A. I.} and Avramov, {P. V.}",
year = "2022",
month = mar,
day = "1",
doi = "10.1007/s11182-022-02558-9",
language = "English",
volume = "64",
pages = "2076--2081",
journal = "Russian Physics Journal",
issn = "1064-8887",
publisher = "Springer Nature",
number = "11",

}

RIS

TY - JOUR

T1 - Electronically Excited States in Model Complexes of Noble Metal Clusters with Carbon Nanodots

AU - Pomogaev, V. A.

AU - Lee, H. J.

AU - Goh, E.

AU - Tchaikovskaya, O. N.

AU - Kononov, A. I.

AU - Avramov, P. V.

PY - 2022/3/1

Y1 - 2022/3/1

N2 - Theoretical calculations of excited states in the complexes of gold and silver three-atom nanoclusters with carbon quantum nanodots are performed using the M062X functional and the def2SVP {H}/def2TZVP/def2TZVPP{Ag, Au} hybrid basis set. A subsequent calculation of the excited states is performed in an approximation of the time-dependent density functional theory implemented in Gaussian09. The chromophore centers of the nanodots are modeled by heterocyclic molecules of isoquino-diazaanthracene and benzopyrano-diazanaphthalene. The clusters are attached to the nanodots using ethyl mercaptan and methoxyethane bridges of various lengths. The energy transfer channels are considered depending on the mutual arrangement of energy levels of clusters and heterocycles.

AB - Theoretical calculations of excited states in the complexes of gold and silver three-atom nanoclusters with carbon quantum nanodots are performed using the M062X functional and the def2SVP {H}/def2TZVP/def2TZVPP{Ag, Au} hybrid basis set. A subsequent calculation of the excited states is performed in an approximation of the time-dependent density functional theory implemented in Gaussian09. The chromophore centers of the nanodots are modeled by heterocyclic molecules of isoquino-diazaanthracene and benzopyrano-diazanaphthalene. The clusters are attached to the nanodots using ethyl mercaptan and methoxyethane bridges of various lengths. The energy transfer channels are considered depending on the mutual arrangement of energy levels of clusters and heterocycles.

KW - carbon nanodots

KW - excitation energy transfer

KW - metal clusters

KW - photophysical processes

UR - http://www.scopus.com/inward/record.url?scp=85127147723&partnerID=8YFLogxK

U2 - 10.1007/s11182-022-02558-9

DO - 10.1007/s11182-022-02558-9

M3 - Article

AN - SCOPUS:85127147723

VL - 64

SP - 2076

EP - 2081

JO - Russian Physics Journal

JF - Russian Physics Journal

SN - 1064-8887

IS - 11

ER -

ID: 121234712