STUDY OF PHOTOINDUCED PROCESSES OF A DYAD BDP-C60 UNDER EXCITED BOTH ITS DONOR AND ACCEPTOR MOIETIES | Trang | TNU Journal of Science and Technology

STUDY OF PHOTOINDUCED PROCESSES OF A DYAD BDP-C60 UNDER EXCITED BOTH ITS DONOR AND ACCEPTOR MOIETIES

About this article

Received: 31/01/23                Revised: 20/04/23                Published: 20/04/23

Authors

Tran Thu Trang Email to author, TNU - University of Sciences

Abstract


In this paper, A BODIPY-C60 Dyad system composed of a BDP donor and a Fullerene acceptor has been studied photoinduced processes using ultrafast transient absorption spectroscopies. Under excitation at 380 nm, both donor (BDP) and acceptor (C60) were excited. The existence of three conformers of BDP-C60 structures was indicated as a result of different photoinduced processes under excitation wavelength at 380 nm, including both electron transfer and energy transfer. The ultrafast - Femtosecond transient absorption spectra deciphered the charge transfer and energy transfer between two parts of the dyad systems. The shortest donor-acceptor distance conformer (8.8 ), which is noted as conformer 1, was designated as the cause of two fast and ultrafast electron transfers from the Frank-Condon region and singlet excited state of BDP to C60.The rates of two-electron transfer processes were estimated at about 2.5 ×1012 and 1.7 × 1011 s-1. Likewise, the longer donor-acceptor distance conformers (17.5 and 20.5 ) were responsible for two energy transfer processes in the BDP-C60 dyad system.

Keywords


BODIPY; Fullerene; Transient absorption spectroscopies; Electron transfer; Energy transfer

Full Text:

PDF

References


[1] S.-S. Sun and N. S. Sariciftci, Organic photovoltaics: mechanisms, materials, and devices. CRC press, 2017.

[2] X. Liu, H. Chen, and S. Tan, "Overview of high-efficiency organic photovoltaic materials and devices," Renewable and sustainable energy reviews, vol. 52, pp. 1527-1538, 2015.

[3] M. H. Lee, B. D. Dunietz, and E. Geva, "Donor-to-donor vs donor-to-acceptor interfacial charge transfer states in the phthalocyanine–fullerene organic photovoltaic system," The Journal of Physical Chemistry Letters, vol. 5, no. 21, pp. 3810-3816, 2014.

[4] D. Xia, F. Yang, J. Li, C. Li, and W. Li, "Conjugated molecular dyads with diketopyrrolopyrrole-based conjugated backbones for single-component organic solar cells," Materials Chemistry Frontiers, vol. 3, no. 8, pp. 1565-1573, 2019.

[5] H. Fang, D. Xia, C. Zhao, S. Zhou, R. Wang, Y. Zang, C. Xiao, and W. Li, "Perylene bisimides-based molecular dyads with different alkyl linkers for single-component organic solar cells," Dyes and Pigments, vol. 203, 2022, Art. no. 110355.

[6] M. Poddar and R. Misra, "Recent advances of BODIPY based derivatives for optoelectronic applications," Coordination Chemistry Reviews, vol. 421, 2020, Art. no. 213462.

[7] M. A. Filatov, "Heavy-atom-free BODIPY photosensitizers with intersystem crossing mediated by intramolecular photoinduced electron transfer," Organic & Biomolecular Chemistry, vol. 18, no. 1, pp. 10-27, 2020.

[8] H. Imahori, K. Tamaki, D.M. Guldi, C. Luo, M. Fujitsuka, O. Ito, Y. Sakata, and S. Fukuzumi, "Modulating charge separation and charge recombination dynamics in porphyrin− fullerene linked dyads and triads: Marcus-Normal versus inverted region," Journal of the American Chemical Society, vol. 123, no. 11, pp. 2607-2617, 2001.

[9] H. Imahori, K. Tamaki, Y. Araki, Y. Sekiguchi, O. Ito, Y. Sakata, and S. Fukuzumi, "Stepwise Charge Separation and Charge Recombination in Ferrocene-m eso, m eso-Linked Porphyrin Dimer− Fullerene Triad," Journal of the American Chemical Society, vol. 124, no. 18, pp. 5165-5174, 2002.

[10] M. Rudolf, S. Kirner, and D. Guldi, "A multicomponent molecular approach to artificial photosynthesis–the role of fullerenes and endohedral metallofullerenes," Chemical Society Reviews, vol. 45, no. 3, pp. 612-630, 2016.

[11] S. Wang, N. Wattanatorn, N. Chiang, Y. Zhao, M. Kim, H. Ma, A. K. -Y. Jen, and P. S. Weiss, "Photoinduced charge transfer in single-molecule p–n junctions," The Journal of Physical Chemistry Letters, vol. 10, no. 9, pp. 2175-2181, 2019.

[12] K.-S. Kim, M.-S. Kang, H. Ma, and A. K.-Y. Jen, "Highly efficient photocurrent generation from a self-assembled monolayer film of a novel c60-tethered 2, 5-dithienylpyrrole triad," Chemistry of materials, vol. 16, no. 24, pp. 5058-5062, 2004.

[13] T. T. Tran, J. Rabah, M. H. Ha-Thi, E. Allard, S. Nizinski, G. Burdzinski, S. Aloise, H. Fensterbank, K. Baczko, H. Nasrallah, A. Vallee, G. Clavier, F. Miomandre, T. Pino, and R. Meallet-Renault, "Photoinduced Electron Transfer and Energy Transfer Processes in a Flexible BODIPY-C60 Dyad," J. Phys. Chem. B, vol. 124, no. 42, pp. 9396-9410, Oct. 22 2020, doi: 10.1021/acs.jpcb.0c05187.

[14] D. M. Guldi and M. Prato, "Excited-state properties of C60 fullerene derivatives," Accounts of chemical research, vol. 33, no. 10, pp. 695-703, 2000.

[15] F. Zhang and X. Zhang, "Solvent-induced optical properties of C60," Journal of Luminescence, vol. 130, no. 5, pp. 787-791, 2010, doi: 10.1016/j.jlumin.2009.11.033.

[16] A. A. Iagatti, L. Cupellini, G. Biagiotti, S. Caprasecca, S. Fedeli, A. Lapini, E. Ussano, S. Cicchi, P. Foggi, and M. Marcaccio, "Efficient photoinduced charge separation in a BODIPY–C60 dyad," The Journal of Physical Chemistry C, vol. 120, no. 30, pp. 16526-16536, 2016.

[17] Bandi, H. B. Gobeze, V. Lakshmi, M. Ravikanth, and F. D’Souza, "Vectorial charge separation and selective triplet-state formation during charge recombination in a pyrrolyl-bridged BODIPY–fullerene dyad," The Journal of Physical Chemistry C, vol. 119, no. 15, pp. 8095-8102, 2015.

[18] S. Leach, M. Vervloet, A. Després, E. Bréheret, J. P. Hare, T. J. Dennis, H. W. Kroto, R. Taylor, and D. R. Walton, "Electronic spectra and transitions of the fullerene C60," Chemical Physics, vol. 160, no. 3, pp. 451-466, 1992.

[19] C. A. Wijesinghe, M. E. El-Khouly, J. D. Blakemore, M. E. Zandler, S. Fukuzumi, and F. D'Souza, "Charge stabilization in a closely spaced ferrocene–boron dipyrrin–fullerene triad," Chemical Communications, vol. 46, no. 19, pp. 3301-3303, 2010.

[20] C. A. Wijesinghe, M. E. El‐Khouly, N. K. Subbaiyan, M. Supur, M. E. Zandler, K. Ohkubo, S. Fukuzumi, and F. D'Souza, "Photochemical Charge Separation in Closely Positioned Donor–Boron Dipyrrin–Fullerene Triads," Chemistry–A European Journal, vol. 17, no. 11, pp. 3147-3156, 2011.

"Times New Roman",serif;mso-fareast-font-family:Calibri;color:blue;mso-ansi-language:

PT-BR;mso-fareast-language:EN-US;mso-bidi-language:AR-SA'>

style='mso-element:field-end'>




DOI: https://doi.org/10.34238/tnu-jst.7259

Refbacks

  • There are currently no refbacks.
TNU Journal of Science and Technology
Rooms 408, 409 - Administration Building - Thai Nguyen University
Tan Thinh Ward - Thai Nguyen City
Phone: (+84) 208 3840 288 - E-mail: jst@tnu.edu.vn
Based on Open Journal Systems
©2018 All Rights Reserved