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Year 2025, Volume: 43 Issue: 1, 340 - 345, 28.02.2025

Abstract

References

  • REFERENCES
  • [1] Kılıçarslan FA, Erden İbrahim İ. Investigation of the effect of a nitro group as an anchor group in dye-sensitized solar cells. J Chem Res 2023;1:1–6.
  • [2] Yoosuf M, Pradhana SC, Soman S, Gopidas KR. Triple bond rigidified anthracene-triphenylamine sensitizers for dyesensitized solar cells. Sol Energy 2019;188:55–65. [CrossRef]
  • [3] Freitag M, Teuscher J, Saygili Y, Zhang X, Giordano F, Liska P, et al. Dye-sensitized solar cells for efficient power generation under ambient lighting. Nat Photonics 2017;11:372–378. [CrossRef]
  • [4] Giribabu L, Duvva N, Singh SP, Han L, Bedja IM, Gupta RK, et al. Stable and charge recombination minimized π extended thioalkyl substituted tetrathiafulvalene dye-sensitized solar cells. Mater Chem Front 2017;1:460–467. [CrossRef]
  • [5] Ludin NA, Mustafa NI, Hanafiah MM, Ibrahim MA, Teridi MAM, Sepeai S, et al. Prospects of life cycle assessment of renewable energy from solar photovoltaic technologies: a review. Renew Sustain Energ Rev 2018;96:11–28. [CrossRef]
  • [6] Tingare YS, Vinh NS, Chou HH, Liu YC, Long YS, Wu TC, et al. New Acetylene-Bridged 9,10- Conjugated anthracene sensitizers: application in outdoor and indoor dye-sensitized solar cells. Adv Energy Mater 2017;7:1700032. [CrossRef]
  • [7] Hagfeldt A, Boschloo G, Sun L, Kloo L, Pettersson H. Dye-Sensitized Solar Cells. Chem Rev 2010;110:6595–6663. [CrossRef]
  • [8] Abdullah MI, Janjua MRSA, Mahmood A, Ali S, Ali M. Quantum chemical designing of efficient sensitizers for dye sensitized solar cells. Bull Korean Chem Soc 2013;34:2093–2098. [CrossRef]
  • [9] Mahmood A. Triphenylamine based dyes for dye sensitized solar cells: A review. Sol Energy 2016;123:127–144. [CrossRef]
  • [10] Qu SY, Li, HJ, He T. New D-π-A dyes for efficient dye-sensitized solar cells. Sci China Chem 2012;55:677–697. [CrossRef]
  • [11] Liu XC, Liang JF, You J, Ying L, Xiao Y, Wang SR, et al. Small molecular hole-transporting and emitting materials for hole-only green organic light-emitting devices. Dyes Pigments 2016;131:41–48. [CrossRef]
  • [12] Shirota Y, Kageyama H. Charge carrier transporting molecular materials and their applications in devices. Chem Rev 2007;107:953–1010. [CrossRef]
  • [13] Zhang F, Wang Z, Zhu H, Pellte N, Luo J, Yi C, et al. Over 20% PCE perovskite solar cells with superior stability achieved by novel and low-cost hole-transporting materials. Nano Energy 2017;41:469–475. [CrossRef]
  • [14] Li W, Yang MD, Wang LK, Zhu WJ, Ye LN, Wu JY, et al. Aza-crown ether derivatives based on stilbene: Two-photon absorption and bioimaging. Dyes Pigments 2014;107:133–139. [CrossRef]
  • [15] Zhang L, Cole JM. Anchoring Groups for Dye- Sensitized Solar Cells. ACS Appl Mater Interfaces 2015;7:3427–3455. [CrossRef]
  • [16] Li Q, Wang Z, Ma H, Dong J, Huang Z, Quan Y. Effect of electron donor and acceptor in dithienopyrrolobenzothiadiazole- based organic dyes for efficient quasi-solid-state dye-sensitized solar cells. Dyes Pigments 2020;173:107999. [CrossRef]
  • [17] Duan L, Chen Y, Zong X, Liu R, Sun Z, Liang M, et al. Facile synthesis of triphenylamine-based hole-transporting materials for planar perovskite solar cells. J Power Sources 2019;435:226767. [CrossRef]
  • [18] Sun H, Li P, Liu D, Wang T, Li W, Hu W, et al. Tuning photophysical properties via alkoxyl groups in charge-separated triphenylamine sensitizers for dye-sensitized solar cells. J Photochem Photobiol A Chem 2019;368:233–241. [CrossRef]
  • [19] Wazzan N, Irfan A. Theoretical study of triphenylamine- based organic dyes with mono-, di-, and tri-anchoring groups for dye-sensitized solar cells. Organic Electron 2018;63:328–342. [CrossRef]
  • [20] Irfan A. Comparison of mono- and di-substituted triphenylamine and carbazole based sensitizers @ (TiO2)38 cluster for dye-sensitized solar cells applications. Comput Theor Chem 2019;1159:1–6. [CrossRef]
  • [21] Pati PB, Yang W, Zade SS. New dyes for DSSC containing triphenylamine based extended donor: Synthesis, photophysical properties and device performance. Spectrochim Acta Part A Molecular Biomolecular Spectroscopy 2017;178:106–113. [CrossRef]
  • [22] Chen S, Pei J, Pang Z, Wu W, Yu X, Zhang C. Axial-symmetric conjugated group promoting intramolecular charge transfer performances of triphenylamine sensitizers for dye-sensitized solar cells. Dyes Pigments 2020;174:108029. [CrossRef]
  • [23] Erden I, Kilicarslan FA, Karadoğan B. Synthesis of phthalocyanines with donor-acceptor properties and their applications to dye‑sensitized solar cell. Chem Pap 2019;1:1–6.

Synthesis of sensitizer containing triphenylamine as donor group and investigation of solar cell applicability

Year 2025, Volume: 43 Issue: 1, 340 - 345, 28.02.2025

Abstract

Developing technology and the increase in the world population increase the need for energy day by day. Renewable energy sources provide an affordable, eco-friendly way to meet this need. Solar energy, which is a renewable energy source, has sufficient capacity to obtain more affordable and clean energy compared to other sources. Researchers are interested in triphenylamine and its derivatives because of their numerous uses in solar cells, electronics, and medicine. This study, solar cell applicability was investigated by synthesizing an organic dye, in which the dye contains triphenylamine as the donor group and the hydroxyl group as the acceptor group that provides binding to TiO2. FTIR, MS, NMR, and UV-Vis spectroscopy are used to identify the compound’s (srl-2) structure. With srl-2-based DSSC and AM (amplitude modulation) irradiation (100 mW/cm2), a PCE (photoelectric conversion efficiency) value of 0.01% was attained.

References

  • REFERENCES
  • [1] Kılıçarslan FA, Erden İbrahim İ. Investigation of the effect of a nitro group as an anchor group in dye-sensitized solar cells. J Chem Res 2023;1:1–6.
  • [2] Yoosuf M, Pradhana SC, Soman S, Gopidas KR. Triple bond rigidified anthracene-triphenylamine sensitizers for dyesensitized solar cells. Sol Energy 2019;188:55–65. [CrossRef]
  • [3] Freitag M, Teuscher J, Saygili Y, Zhang X, Giordano F, Liska P, et al. Dye-sensitized solar cells for efficient power generation under ambient lighting. Nat Photonics 2017;11:372–378. [CrossRef]
  • [4] Giribabu L, Duvva N, Singh SP, Han L, Bedja IM, Gupta RK, et al. Stable and charge recombination minimized π extended thioalkyl substituted tetrathiafulvalene dye-sensitized solar cells. Mater Chem Front 2017;1:460–467. [CrossRef]
  • [5] Ludin NA, Mustafa NI, Hanafiah MM, Ibrahim MA, Teridi MAM, Sepeai S, et al. Prospects of life cycle assessment of renewable energy from solar photovoltaic technologies: a review. Renew Sustain Energ Rev 2018;96:11–28. [CrossRef]
  • [6] Tingare YS, Vinh NS, Chou HH, Liu YC, Long YS, Wu TC, et al. New Acetylene-Bridged 9,10- Conjugated anthracene sensitizers: application in outdoor and indoor dye-sensitized solar cells. Adv Energy Mater 2017;7:1700032. [CrossRef]
  • [7] Hagfeldt A, Boschloo G, Sun L, Kloo L, Pettersson H. Dye-Sensitized Solar Cells. Chem Rev 2010;110:6595–6663. [CrossRef]
  • [8] Abdullah MI, Janjua MRSA, Mahmood A, Ali S, Ali M. Quantum chemical designing of efficient sensitizers for dye sensitized solar cells. Bull Korean Chem Soc 2013;34:2093–2098. [CrossRef]
  • [9] Mahmood A. Triphenylamine based dyes for dye sensitized solar cells: A review. Sol Energy 2016;123:127–144. [CrossRef]
  • [10] Qu SY, Li, HJ, He T. New D-π-A dyes for efficient dye-sensitized solar cells. Sci China Chem 2012;55:677–697. [CrossRef]
  • [11] Liu XC, Liang JF, You J, Ying L, Xiao Y, Wang SR, et al. Small molecular hole-transporting and emitting materials for hole-only green organic light-emitting devices. Dyes Pigments 2016;131:41–48. [CrossRef]
  • [12] Shirota Y, Kageyama H. Charge carrier transporting molecular materials and their applications in devices. Chem Rev 2007;107:953–1010. [CrossRef]
  • [13] Zhang F, Wang Z, Zhu H, Pellte N, Luo J, Yi C, et al. Over 20% PCE perovskite solar cells with superior stability achieved by novel and low-cost hole-transporting materials. Nano Energy 2017;41:469–475. [CrossRef]
  • [14] Li W, Yang MD, Wang LK, Zhu WJ, Ye LN, Wu JY, et al. Aza-crown ether derivatives based on stilbene: Two-photon absorption and bioimaging. Dyes Pigments 2014;107:133–139. [CrossRef]
  • [15] Zhang L, Cole JM. Anchoring Groups for Dye- Sensitized Solar Cells. ACS Appl Mater Interfaces 2015;7:3427–3455. [CrossRef]
  • [16] Li Q, Wang Z, Ma H, Dong J, Huang Z, Quan Y. Effect of electron donor and acceptor in dithienopyrrolobenzothiadiazole- based organic dyes for efficient quasi-solid-state dye-sensitized solar cells. Dyes Pigments 2020;173:107999. [CrossRef]
  • [17] Duan L, Chen Y, Zong X, Liu R, Sun Z, Liang M, et al. Facile synthesis of triphenylamine-based hole-transporting materials for planar perovskite solar cells. J Power Sources 2019;435:226767. [CrossRef]
  • [18] Sun H, Li P, Liu D, Wang T, Li W, Hu W, et al. Tuning photophysical properties via alkoxyl groups in charge-separated triphenylamine sensitizers for dye-sensitized solar cells. J Photochem Photobiol A Chem 2019;368:233–241. [CrossRef]
  • [19] Wazzan N, Irfan A. Theoretical study of triphenylamine- based organic dyes with mono-, di-, and tri-anchoring groups for dye-sensitized solar cells. Organic Electron 2018;63:328–342. [CrossRef]
  • [20] Irfan A. Comparison of mono- and di-substituted triphenylamine and carbazole based sensitizers @ (TiO2)38 cluster for dye-sensitized solar cells applications. Comput Theor Chem 2019;1159:1–6. [CrossRef]
  • [21] Pati PB, Yang W, Zade SS. New dyes for DSSC containing triphenylamine based extended donor: Synthesis, photophysical properties and device performance. Spectrochim Acta Part A Molecular Biomolecular Spectroscopy 2017;178:106–113. [CrossRef]
  • [22] Chen S, Pei J, Pang Z, Wu W, Yu X, Zhang C. Axial-symmetric conjugated group promoting intramolecular charge transfer performances of triphenylamine sensitizers for dye-sensitized solar cells. Dyes Pigments 2020;174:108029. [CrossRef]
  • [23] Erden I, Kilicarslan FA, Karadoğan B. Synthesis of phthalocyanines with donor-acceptor properties and their applications to dye‑sensitized solar cell. Chem Pap 2019;1:1–6.
There are 24 citations in total.

Details

Primary Language English
Subjects Building Technology
Journal Section Research Articles
Authors

Fatma Aytan Kılıçarslan 0000-0002-4623-3067

Publication Date February 28, 2025
Submission Date October 16, 2023
Acceptance Date January 19, 2024
Published in Issue Year 2025 Volume: 43 Issue: 1

Cite

Vancouver Aytan Kılıçarslan F. Synthesis of sensitizer containing triphenylamine as donor group and investigation of solar cell applicability. SIGMA. 2025;43(1):340-5.

IMPORTANT NOTE: JOURNAL SUBMISSION LINK https://eds.yildiz.edu.tr/sigma/