Atypical organic dyes used as sensitizers for efficient dye-sensitized solar cells

Yue Hu, Neil Robertson

PDF(784 KB)
PDF(784 KB)
Front. Optoelectron. ›› 2016, Vol. 9 ›› Issue (1) : 38-43. DOI: 10.1007/s12200-016-0568-5
REVIEW ARTICLE
REVIEW ARTICLE

Atypical organic dyes used as sensitizers for efficient dye-sensitized solar cells

Author information +
History +

Abstract

Since their invention, dye-sensitized solar cells (DSSCs) have received enormous research attention from scientists with different background due to the possibility of low-cost production and fabrication on flexible substrates. One of the most important components in DSSCs is the sensitizing dye, including metal-complexes and metal-free organic dyes. The donor-π bridge-acceptor (D-π-A) structure is the mainstream in the design of organic sensitizers because it facilitates efficient charge-transfer toward the TiO2 upon excitation. However, some sensitizers that do not follow this structure, or have some modification upon this structure, also present good efficiency when applied in DSSC devices. This review summarizes these atypical dyes in order to inspire more diverse designs toward highly efficient DSSCs.

Keywords

donor- acceptor-π bridge-acceptor (D-A-π-A) / donor-free / di-anchoring

Cite this article

Download citation ▾
Yue Hu, Neil Robertson. Atypical organic dyes used as sensitizers for efficient dye-sensitized solar cells. Front. Optoelectron., 2016, 9(1): 38‒43 https://doi.org/10.1007/s12200-016-0568-5

References

[1]
Kakiage K, Aoyama Y, Yano T, Oya K, Fujisawa J, Hanaya M. Highly-efficient dye-sensitized solar cells with collaborative sensitization by silyl-anchor and carboxy-anchor dyes. Chemical Communications, 2015, 51(88): 15894–15897
CrossRef Pubmed Google scholar
[2]
Gabrielsson E, Ellis H, Feldt S, Tian H, Boschloo G, Hagfeldt A, Sun L. Convergent/divergent synthesis of a linker-varied series of dyes for dye-sensitized solar cells based on the D35 donor. Advanced Energy Materials, 2013, 3(12): 1647–1656
CrossRef Google scholar
[3]
Yang J, Ganesan P, Teuscher J, Moehl T, Kim Y J, Yi C, Comte P, Pei K, Holcombe T W, Nazeeruddin M K, Hua J, Zakeeruddin S M, Tian H, Grätzel M. Influence of the donor size in D-p-A organic dyes for dye-sensitized solar cells. Journal of the American Chemical Society, 2014, 136(15): 5722–5730
CrossRef Pubmed Google scholar
[4]
Hagfeldt A, Boschloo G, Sun L, Kloo L, Pettersson H. Dye-sensitized solar cells. Chemical Reviews, 2010, 110(11): 6595–6663
CrossRef Pubmed Google scholar
[5]
Wang Z S, Cui Y, Hara K, Dan-oh Y, Kasada C, Shinpo A. A high-light-harvesting-efficiency coumarin dye for stable dye-sensitized solar cells. Advanced Materials, 2007, 19(8): 1138–1141
CrossRef Google scholar
[6]
Liang M, Xu W, Cai F, Chen P, Peng B, Chen J, Li Z. New triphenylamine-based organic dyes for efficient dye-sensitized solar cells. Journal of Physical Chemistry C, 2007, 111(11): 4465–4472
CrossRef Google scholar
[7]
Ooyama Y, Harima Y. Photophysical and electrochemical properties, and molecular structures of organic dyes for dye-sensitized solar cells. ChemPhysChem, 2012, 13(18): 4032–4080
CrossRef Pubmed Google scholar
[8]
Wu Y, Zhu W. Organic sensitizers from D-p-A to D-A-p-A: effect of the internal electron-withdrawing units on molecular absorption, energy levels and photovoltaic performances. Chemical Society Reviews, 2013, 42(5): 2039–2058
CrossRef Pubmed Google scholar
[9]
Qu S Y, Wu W, Hua J, Kong C, Long Y, Tian H. New diketopyrrolopyrrole (DPP) dyes for efficient dye-sensitized solar cells. Journal of Physical Chemistry C, 2010, 114(2): 1343–1349
CrossRef Google scholar
[10]
Qu S Y, Wang B, Guo F, Li J, Wu W, Kong C, Long Y, Hua J. New diketo-pyrrolo-pyrrole (DPP) sensitizer containing a furan moiety for efficient and stable dye-sensitized solar cells. Dyes and Pigments, 2012, 92(3): 1384–1393
CrossRef Google scholar
[11]
Qu S, Qin C, Islam A, Wu Y, Zhu W, Hua J, Tian H, Han L. A novel D-A-p-A organic sensitizer containing a diketopyrrolopyrrole unit with a branched alkyl chain for highly efficient and stable dye-sensitized solar cells. Chemical Communications, 2012, 48(55): 6972–6974
CrossRef Pubmed Google scholar
[12]
Guo F L, Qu S, Wu W, Li J, Ying W, Hua J. Synthesis and photovoltaic performance of new diketopyrrolopyrrole (DPP) dyes for dye-sensitized solar cells. Synthetic Metals, 2010, 160(15–16): 1767–1773
CrossRef Google scholar
[13]
Velusamy M, Justin Thomas K R, Lin J T, Hsu Y C, Ho K C. Organic dyes incorporating low-band-gap chromophores for dye-sensitized solar cells. Organic Letters, 2005, 7(10): 1899–1902
CrossRef Pubmed Google scholar
[14]
Zhu W H, Wu Y, Wang S, Li W, Li X, Chen J, Wang Z, Tian H. Organic D-A-p-A solar cell sensitizers with improved stability and spectral response. Advanced Functional Materials, 2011, 21(4): 756–763
CrossRef Google scholar
[15]
Wu Y Z, Zhang X, Li W, Wang Z S, Tian H, Zhu W. Hexylthiophene-featured D-A-p-A structural indoline chromophores for coadsorbent-free and panchromatic dye-sensitized solar cells. Advanced Energy Materials, 2012, 2(1): 149–156
CrossRef Google scholar
[16]
Cui Y, Wu Y, Lu X, Zhang X, Zhou G, Miapeh F B, Zhu W, Wang Z S. Incorporating benzotriazole moiety to construct D-A-π-A organic sensitizers for solar cells: significant enhancement of open-circuit photovoltage with long alkyl group. Chemistry of Materials, 2011, 23(19): 4394–4401
CrossRef Google scholar
[17]
Mao J, Guo F, Ying W, Wu W, Li J, Hua J. Benzotriazole-bridged sensitizers containing a furan moiety for dye-sensitized solar cells with high open-circuit voltage performance. Chemistry, an Asian Journal, 2012, 7(5): 982–991
CrossRef Pubmed Google scholar
[18]
Li H, Wu Y, Geng Z, Liu J, Xu D, Zhu W. Co-sensitization of benzoxadiazole based D-A-p-A featured sensitizers: compensating light-harvesting and retarding charge recombination. Journal of Materials Chemistry A, Materials for Energy and Sustainability, 2014, 2(35): 14649–14657
CrossRef Google scholar
[19]
Zhu H B, Wu Y, Liu J, Zhang W, Wu W, Zhu W H. D-A-p-A featured sensitizers containing an auxiliary acceptor of benzoxadiazole: molecular engineering and co-sensitization. Journal of Materials Chemistry A, Materials for Energy and Sustainability, 2015, 3(19): 10603–10609
CrossRef Google scholar
[20]
Pei K, Wu Y, Wu W, Zhang Q, Chen B, Tian H, Zhu W. Constructing organic D-A-p-A-featured sensitizers with a quinoxaline unit for high-efficiency solar cells: the effect of an auxiliary acceptor on the absorption and the energy level alignment. Chemistry-a European Journal, 2012, 18(26): 8190–8200 doi:10.1002/chem.201103542
Pubmed
[21]
Shi J, Chen J, Chai Z, Wang H, Tang R, Fan K, Wu M, Han H, Qin J, Peng T, Li Q, Li Z. High performance organic sensitizers based on 11,12-bis(hexyloxy) dibenzo [a,c]phenazine for dye-sensitized solar cells. Journal of Materials Chemistry, 2012, 22(36): 18830–18838
CrossRef Google scholar
[22]
Li W, Wu Y, Zhang Q, Tian H, Zhu W. D-A-p-A featured sensitizers bearing phthalimide and benzotriazole as auxiliary acceptor: effect on absorption and charge recombination dynamics in dye-sensitized solar cells. ACS Applied Materials & Interfaces, 2012, 4(3): 1822–1830
CrossRef Pubmed Google scholar
[23]
Li X, Zheng Z, Jiang W, Wu W, Wang Z, Tian H. New D-A-p-A organic sensitizers for efficient dye-sensitized solar cells. Chemical Communications, 2015, 51(17): 3590–3592
CrossRef Pubmed Google scholar
[24]
Yum J H, Holcombe T W, Kim Y, Rakstys K, Moehl T, Teuscher J, Delcamp J H, Nazeeruddin M K, Grätzel M. Blue-coloured highly efficient dye-sensitized solar cells by implementing the diketopyrrolopyrrole chromophore. Scientific Reports, 2013,3: 2446
CrossRef Pubmed Google scholar
[25]
Feldt S M, Gibson E A, Gabrielsson E, Sun L, Boschloo G, Hagfeldt A. Design of organic dyes and cobalt polypyridine redox mediators for high-efficiency dye-sensitized solar cells. Journal of the American Chemical Society, 2010, 132(46): 16714–16724
CrossRef Pubmed Google scholar
[26]
Abate A, Planells M, Hollman D J, Stranks S D, Petrozza A, Kandada A R S, Vaynzof Y, Pathak S K, Robertson N, Snaith H J. An organic “donor-free” dye with enhanced open-circuit voltage in solid-state sensitized solar cells. Advanced Energy Materials, 2014, 4(13): 1400166
CrossRef Google scholar
[27]
Hu Y, manuscripts in preparation
[28]
Abbotto A, Manfredi N, Marinzi C, De Angelis F, Mosconi E, Yum J H, Xianxi Z, Nazeeruddin M K, Grätzel M. Di-branched di-anchoring organic dyes for dye-sensitized solar cells. Energy & Environmental Science, 2009, 2(10): 1094–1101
CrossRef Google scholar
[29]
Cao D, Peng J, Hong Y, Fang X, Wang L, Meier H. Enhanced performance of the dye-sensitized solar cells with phenothiazine-based dyes containing double D-A branches. Organic Letters, 2011, 13(7): 1610–1613
CrossRef Pubmed Google scholar
[30]
Hong Y, Liao J Y, Cao D, Zang X, Kuang D B, Wang L, Meier H, Su C Y. Organic dye bearing asymmetric double donor-p-acceptor chains for dye-sensitized solar cells. Journal of Organic Chemistry, 2011, 76(19): 8015–8021
CrossRef Pubmed Google scholar
[31]
Abbotto A, Leandri V, Manfredi N, De Angelis F, Pastore M, Yum J H, Nazeeruddin M K, Grätzel M. Bis-donor-bis-acceptor tribranched organic sensitizers for dye-sensitized solar cells. European Journal of Organic Chemistry, 2011, 2011(31): 6195–6205
CrossRef Google scholar
[32]
Leandri V, Ruffo R, Trifiletti V, Abbotto A. Asymmetric tribranched dyes: an intramolecular cosensitization approach for dye-sensitized solar cells. European Journal of Organic Chemistry, 2013, 2013(30): 6793–6801
CrossRef Google scholar
[33]
Pramjit S, Eiamprasert U, Surawatanawong P, Lertturongchai P, Kiatisevi S. Carbazole-bridged double D-A dye for efficient dye-sensitized solar cell. Journal of Photochemistry and Photobiology A: Chemistry, 2015, 296(1): 1–10

Acknowledgements

We thank China Scholarship Council and the University of Edinburgh for financial support.

RIGHTS & PERMISSIONS

2014 Higher Education Press and Springer-Verlag Berlin Heidelberg
AI Summary AI Mindmap
PDF(784 KB)

Accesses

Citations

Detail

Sections
Recommended

/