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Theoretical study of YD2-o-C8-based derivatives as promising sensitizers for dye-sensitized solar cells

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Abstract

To screen efficient sensitizers for dye-sensitized solar cells (DSSCs), two series of porphyrin sensitizers have been reengineered based on one of the best sensitizers YD2-o-C8 by introducing different heterocycles into acceptor part to form stronger acceptors. The electronic structures and optical properties of these sensitizers have been investigated using density functional theory and its time-dependent density functional theory version. The computational results suggest that the stronger acceptor can result in a narrower HOMO–LUMO energy gap, an obvious red-shift and stronger absorption in long-wavelength region compared with YD2-o-C8. Meanwhile, the analyses of electron density difference plots suggest that all designed sensitizers possess longer electron transfer distance, larger fraction of electron exchange, and smaller overlap between the zones of density depletion and increment than these of YD2-o-C8, indicating enhanced electron transfer ability from donor to acceptor groups. Moreover, the designed dyes exhibit good performance in terms of the electron injection ability, the excited state lifetime, and the strength of the interaction between dye and the TiO2 surface. As a whole, all the designed dyes, especially P4 and P6 may act as excellent sensitizers for high-efficiency DSSCs.

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References

  1. O’regan B, Grfitzeli M (1991) A low-cost, high-efficiency solar cell based on dye-sensitized. Nature 353(6346):737–740

    Article  Google Scholar 

  2. Yu G, Gao J, Hummelen JC, Wudl F, Heeger AJ (1995) Polymer photovoltiac cells: enhanced efficiencies via a network of internal donor–acceptor heterojunctions. Science 270(5243):1789

    Article  Google Scholar 

  3. Lee MM, Teuscher J, Miyasaka T, Murakami TN, Snaith HJ (2012) Efficient hybrid solar cells based on meso-superstructured organometal halide perovskites. Science 338(6107):643–647

    Article  Google Scholar 

  4. Jung J, Pang X, Feng C, Lin Z (2013) Semiconducting conjugated polymer-inorganic tetrapod nanocomposites. Langmuir 29(25):8086–8092

    Article  Google Scholar 

  5. Pang X, Zhao L, Feng C, Lin Z (2011) Novel amphiphilic multiarm, starlike coil-rod diblock copolymers via a combination of click chemistry with living polymerization. Macromolecules 44(18):7176–7183

    Article  Google Scholar 

  6. Yella A, Lee H-W, Tsao HN, Yi C, Chandiran AK, Nazeeruddin MK, Diau EW-G, Yeh C-Y, Zakeeruddin SM, Grätzel M (2011) Porphyrin-sensitized solar cells with cobalt(II/III)-based redox electrolyte exceed 12 % efficiency. Science 334(6056):629–634

    Article  Google Scholar 

  7. Mathew S, Yella A, Gao P, Humphry-Baker R, Curchod BF, Ashari-Astani N, Tavernelli I, Rothlisberger U, Nazeeruddin MK, Grätzel M (2014) Dye-sensitized solar cells with 13 % efficiency achieved through the molecular engineering of porphyrin sensitizers. Nat Chem 6(3):242–247

    Article  Google Scholar 

  8. Li L-L, Diau EW-G (2013) Porphyrin-sensitized solar cells. Chem Soc Rev 42(1):291–304

    Article  Google Scholar 

  9. Wang C-L, Chang Y-C, Lan C-M, Lo C-F, Diau EW-G, Lin C-Y (2011) Enhanced light harvesting with π-conjugated cyclic aromatic hydrocarbons for porphyrin-sensitized solar cells. Energy Environ Sci 4(5):1788–1795

    Article  Google Scholar 

  10. Luo J, Xu M, Li R, Huang K-W, Jiang C, Qi Q, Zeng W, Zhang J, Chi C, Wang P (2013) N-annulated perylene as an efficient electron donor for porphyrin-based dyes: enhanced light-harvesting ability and high-efficiency Co(II/III)-based dye-sensitized solar cells. J Am Chem Soc 136(1):265–272

    Article  Google Scholar 

  11. Wang S-W, Wu K-L, Ghadiri E, Lobello MG, Ho S-T, Chi Y, Moser J-E, De Angelis F, Grätzel M, Nazeeruddin MK (2013) Engineering of thiocyanate-free Ru(II) sensitizers for high efficiency dye-sensitized solar cells. Chem Sci 4(6):2423–2433

    Article  Google Scholar 

  12. Cao K, Lu J, Cui J, Shen Y, Chen W, Alemu G, Wang Z, Yuan H, Xu J, Wang M (2014) Highly efficient light harvesting ruthenium sensitizers for dye-sensitized solar cells featuring triphenylamine donor antennas. J Mater Chem A 2(14):4945–4953

    Article  Google Scholar 

  13. Wang P, Klein C, Humphry-Baker R, Zakeeruddin SM, Grätzel M (2005) A high molar extinction coefficient sensitizer for stable dye-sensitized solar cells. J Am Chem Soc 127(3):808–809

    Article  Google Scholar 

  14. El-Shafei A, Hussain M, Islam A, Han L (2014) Structure–property relationship of hetero-aromatic-electron-donor antennas of polypyridyl Ru(II) complexes for high efficiency dye-sensitized solar cells. Prog Photovoltaics Res Appl 22(9):958–969

    Article  Google Scholar 

  15. Reynal A, Palomares E (2011) Ruthenium polypyridyl sensitisers in dye solar cells based on mesoporous TiO2. Eur J Inorg Chem 29:4509–4526

    Article  Google Scholar 

  16. Reynal A, Forneli A, Palomares E (2010) Dye structure–charge transfer process relationship in efficient ruthenium-dye based dye sensitized solar cells. Energy Environ Sci 3(6):805–812

    Article  Google Scholar 

  17. Chiba Y, Islam A, Watanabe Y, Komiya R, Koide N, Han L (2006) Dye-sensitized solar cells with conversion efficiency of 11.1 %. Jpn J Appl Phys 45(7L):L638

    Article  Google Scholar 

  18. Wang Q, Campbell WM, Bonfantani EE, Jolley KW, Officer DL, Walsh PJ, Gordon K, Humphry-Baker R, Nazeeruddin MK, Grätzel M (2005) Efficient light harvesting by using green Zn-porphyrin-sensitized nanocrystalline TiO2 films. J Phys Chem B 109(32):15397–15409

    Article  Google Scholar 

  19. Campbell WM, Jolley KW, Wagner P, Wagner K, Walsh PJ, Gordon KC, Schmidt-Mende L, Nazeeruddin MK, Wang Q, Grätzel M (2007) Highly efficient porphyrin sensitizers for dye-sensitized solar cells. J Phys Chem C 111(32):11760–11762

    Article  Google Scholar 

  20. Bessho T, Zakeeruddin SM, Yeh CY, Diau EWG, Grätzel M (2010) Highly efficient mesoscopic dye-sensitized solar cells based on donor–acceptor-substituted porphyrins. Angew Chem Int Ed 49(37):6646–6649

    Article  Google Scholar 

  21. Yella A, Mai CL, Zakeeruddin SM, Chang SN, Hsieh CH, Yeh CY, Grätzel M (2014) Molecular engineering of push-pull porphyrin dyes for highly efficient dye-sensitized solar cells: the role of benzene spacers. Angew Chem 126(11):3017–3021

    Article  Google Scholar 

  22. Yasin A, Jose R, Yusoff MM (2015) Predicting larger absorption cross-section in porphyrin dyes using DFT calculations. J Porphyrins Phthalocyanines 19(12):1270–1278

    Article  Google Scholar 

  23. Biroli AO, Tessore F, Vece V, Di Carlo G, Mussini P, Trifiletti V, De Marco L, Giannuzzi R, Manca M, Pizzotti M (2015) Highly improved performance of Zn II tetraarylporphyrinates in DSSCs by the presence of octyloxy chains in the aryl rings. J Mater Chem A 3(6):2954–2959

    Article  Google Scholar 

  24. Magnano G, Marinotto D, Cipolla M, Trifiletti V, Listorti A, Mussini P, Di Carlo G, Tessore F, Manca M, Biroli AO (2016) Influence of alkoxy chain envelopes on the interfacial photoinduced processes in tetraarylporphyrin-sensitized solar cells. Phys Chem Chem Phys 18(14):9577–9585

    Article  Google Scholar 

  25. Jacquemin D, Wathelet V, Perpete EA, Adamo C (2009) Extensive TD-DFT benchmark: singlet-excited states of organic molecules. J Chem Theory Comput 5(9):2420–2435

    Article  Google Scholar 

  26. Sánchez-de-Armas R, San-Miguel MA, Oviedo J, Sanz JF (2012) Molecular modification of coumarin dyes for more efficient dye sensitized solar cells. J Chem Phys 136(19):194702

    Article  Google Scholar 

  27. Martsinovich N, Troisi A (2011) High-throughput computational screening of chromophores for dye-sensitized solar cells. J Phys Chem C 115(23):11781–11792

    Article  Google Scholar 

  28. Labat F, Le Bahers T, Ciofini I, Adamo C (2012) First-principles modeling of dye-sensitized solar cells: challenges and perspectives. Acc Chem Res 45(8):1268–1277

    Article  Google Scholar 

  29. McNamara WR, Snoeberger Iii RC, Li G, Schleicher JM, Cady CW, Poyatos M, Schmuttenmaer CA, Crabtree RH, Brudvig GW, Batista VS (2008) Acetylacetonate anchors for robust functionalization of TiO2 nanoparticles with Mn(II)–terpyridine complexes. J Am Chem Soc 130(43):14329–14338

    Article  Google Scholar 

  30. Gu X, Zhou L, Li Y, Sun Q, Jena P (2012) Design of new metal-free dyes for dye-sensitized solar cells: a first-principles study. Phys Lett A 376(38):2595–2599

    Article  Google Scholar 

  31. Frisch M, Trucks G, Schlegel HB, Scuseria G, Robb M, Cheeseman J, Scalmani G, Barone V, Mennucci B, Ge Petersson (2009) Gaussian 09. Gaussian, Inc., Wallingford

    Google Scholar 

  32. Hay PJ, Wadt WR (1985) Ab initio effective core potentials for molecular calculations. Potentials for K to Au including the outermost core orbitals. J Chem Phys 82(1):299–310

    Article  Google Scholar 

  33. Zhao Y, Truhlar DG (2008) The M06 suite of density functionals for main group thermochemistry, thermochemical kinetics, noncovalent interactions, excited states, and transition elements: two new functionals and systematic testing of four M06-class functionals and 12 other functionals. Theoret Chem Acc 120(1–3):215–241

    Article  Google Scholar 

  34. Barone V, Cossi M (1998) Quantum calculation of molecular energies and energy gradients in solution by a conductor solvent model. J Phys Chem A 102(11):1995–2001

    Article  Google Scholar 

  35. Karthikeyan S, Lee JY (2013) Zinc-porphyrin based dyes for dye-sensitized solar cells. J Phys Chem A 117(42):10973–10979

    Article  Google Scholar 

  36. Balanay MP, Kim DH (2008) DFT/TD-DFT molecular design of porphyrin analogues for use in dye-sensitized solar cells. Phys Chem Chem Phys 10(33):5121–5127

    Article  Google Scholar 

  37. Lu T, Chen F (2012) Multiwfn: a multifunctional wavefunction analyzer. J Comput Chem 33(5):580–592

    Article  Google Scholar 

  38. Ciofini I, Le Bahers T, Adamo C, Odobel F, Jacquemin D (2012) Through-space charge transfer in rod-like molecules: lessons from theory. J Phys Chem C 116(22):11946–11955

    Article  Google Scholar 

  39. De Angelis F (2010) Direct vs. indirect injection mechanisms in perylene dye-sensitized solar cells: A DFT/TDDFT investigation. Chem Phys Lett 493(4):323–327

    Article  Google Scholar 

  40. Delley B (2000) From molecules to solids with the DMol3 approach. J Chem Phys 113(18):7756–7764

    Article  Google Scholar 

  41. Zeng W, Liu T, Wang Z, Tsukimoto S, Saito M, Ikuhara Y (2010) Oxygen adsorption on anatase TiO2 (101) and (001) surfaces from first principles. Mater Trans 51(1):171–175

    Article  Google Scholar 

  42. Liu D-S, Ding W-L, Zhu K-L, Geng Z-Y, Wang D-M, Zhao X-L (2014) The master factors influencing the efficiency of D–A–π–A configurated organic sensitizers in dye-sensitized solar cell via theoretically characterization: design and verification. Dyes Pigm 105:192–201

    Article  Google Scholar 

  43. Ding W-L, Wang D-M, Geng Z-Y, Zhao X-L, Xu W-B (2013) Density functional theory characterization and verification of high-performance indoline dyes with D–A–π–A architecture for dye-sensitized solar cells. Dyes Pigm 98(1):125–135

    Article  Google Scholar 

  44. Fitri A, Benjelloun AT, Benzakour M, Mcharfi M, Hamidi M, Bouachrine M (2014) Theoretical investigation of new thiazolothiazole-based D–π–A organic dyes for efficient dye-sensitized solar cell. Spectrochim Acta Part A Mol Biomol Spectrosc 124:646–654

    Article  Google Scholar 

  45. Yu P, Zhang F, Li M, He R (2015) Influence of position of auxiliary acceptor in D–A–π–A photosensitizes on photovoltaic performances of dye-sensitized solar cells. J Mater Sci 50(22):7333–7342. doi:10.1007/s10853-015-9290-8

    Article  Google Scholar 

  46. Guo M, He R, Dai Y, Shen W, Li M, Zhu C, Lin SH (2012) Electron-deficient pyrimidine adopted in porphyrin sensitizers: a theoretical interpretation of π-spacers leading to highly efficient photo-to-electric conversion performances in dye-sensitized solar cells. J Phys Chem C 116(16):9166–9179

    Article  Google Scholar 

  47. Yang L-N, Sun Z-Z, Chen S-L, Li Z-S (2013) The effects of various anchoring groups on optical and electronic properties of dyes in dye-sensitized solar cells. Dyes Pigm 99(1):29–35

    Article  Google Scholar 

  48. Chen S-L, Yang L-N, Li Z-S (2013) How to design more efficient organic dyes for dye-sensitized solar cells? Adding more sp 2-hybridized nitrogen in the triphenylamine donor. J Power Sources 223:86–93

    Article  Google Scholar 

  49. Li M, Kou L, Diao L, Zhang Q, Li Z, Wu Q, Lu W, Pan D, Wei Z (2015) Theoretical study of WS-9-based organic sensitizers for unusual vis/NIR absorption and highly efficient dye-sensitized solar cells. J Phys Chem C 119(18):9782–9790

    Article  Google Scholar 

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Acknowledgements

We acknowledge the generous financial support from Natural Science Foundation of China (21173169, 20803059), and Chongqing Municipal Natural Science Foundation (cstc2013jcyjA90015).

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Correspondence to Rongxing He.

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Weixia Hu and Pei Yu contributed equally to this work.

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Hu, W., Yu, P., Zhang, Z. et al. Theoretical study of YD2-o-C8-based derivatives as promising sensitizers for dye-sensitized solar cells. J Mater Sci 52, 1235–1245 (2017). https://doi.org/10.1007/s10853-016-0364-z

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