journal article·2014-08-27Open access

Highly Stable Dye-Sensitized Solar Cells Based on Novel 1,2,3-Triazolium Ionic Liquids

Genevieve P. S. Lau, Hoi Nok Tsao, Shaik M. Zakeeruddin, Michael Grätzel, Paul J. Dyson

Abstract

We describe the design and synthesis of novel low viscosity bicyclic 1,2,3-triazolium ionic liquids. These new salts are applied as nonvolatile electrolytes in dye-sensitized solar cells, affording efficiencies up to 7.07% at low light intensities, and 6.00% when illuminated at 100 mW cm(-2). The devices are highly stable, retaining ca. 90% of their initial performance even after 1000 h of sun testing at 60 °C. The results obtained with these new ionic liquids compare very favorably to benchmark ionic liquid-based devices and illustrate the potential of the triazolium family of salts to compete with their imidazolium counterparts.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: TiO2 Photocatalysis and Solar Cells · Advanced Nanomaterials in Catalysis · Conducting polymers and applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Institut des Sciences et Ingénierie Chimiques, École Polytechnique Fédérale de Lausanne (EPFL), CH-1015 Lausanne, Switzerland

Funding

École Polytechnique Fédérale de Lausanne · Swiss National Science Foundation

References (26)

Show source-provided references
1. O’Regan B. · Nature · 1991 · 335 · 73710.1038/353737a0 ↗
2. Yella A. · Science · 2011 · 334 · 62910.1126/science.1209688 ↗
3. Mathew S. · Nat. Chem. · 2014 · 6 · 24210.1038/nchem.1861 ↗
4. Gonçalves L. M. · Energy Environ. Sci. · 2008 · 1 · 65510.1039/b807236a ↗
5. Zhang S. · Energy Environ. Sci. · 2013 · 6 · 144310.1039/c3ee24453a ↗
6. Kalowekamo J. · Sol. Energy · 2009 · 83 · 122410.1016/j.solener.2009.02.003 ↗
7. Wang P. · Nat. Mater. · 2003 · 2 · 40210.1038/nmat904 ↗
8. Jeon N. J. · J. Am. Chem. Soc. · 2013 · 135 · 1908710.1021/ja410659k ↗
9. Bai Y. · Nat. Mater. · 2008 · 7 · 62610.1038/nmat2224 ↗
10. Heo J. H. · Nat. Photonics · 2013 · 7 · 48610.1038/nphoton.2013.80 ↗
11. McGehee M. D. · Nature · 2013 · 501 · 32310.1038/nature12557 ↗
12. Fei Z. · Chem.—Eur. J. · 2006 · 12 · 212210.1002/chem.200500581 ↗
13. Zhang S. J. · J. Phys. Chem. Ref. Data · 2006 · 35 · 147510.1063/1.2204959 ↗
14. Wang P. · Chem. Mater. · 2004 · 16 · 269410.1021/cm049916l ↗
15. MacFarlane D. R. · Energy Environ. Sci. · 2014 · 7 · 23210.1039/C3EE42099J ↗
16. Fei Z. · Inorg. Chem. · 2006 · 45 · 1040710.1021/ic061232n ↗
17. Papageorgiou N. · J. Electrochem. Soc. · 1996 · 10 · 309910.1149/1.1837171 ↗
18. Marszalek M. · Inorg. Chem. · 2011 · 50 · 1156110.1021/ic201513m ↗
19. Armel V. · Chem. Commun. · 2010 · 46 · 314610.1039/b926087k ↗
20. Paulsson H. · J. Phys. Chem. B · 2003 · 107 · 1366510.1021/jp036859v ↗
21. Dyson P. J. · Chem. Commun. · 2004 · 220410.1039/b407217k ↗
22. Dyson P. J. · Chem. Commun. · 2003 · 50810.1039/b211669c ↗
23. Matsumoto H. · Chem. Lett. · 2001 · 30 · 2610.1246/cl.2001.26 ↗
24. Tseng M.-C. · Org. Lett. · 2011 · 13 · 443410.1021/ol201793v ↗
25. Schlichthörl G. · J. Phys. Chem. B · 1997 · 101 · 814110.1021/jp9714126 ↗
26. Sauvage F. · J. Am. Chem. Soc. · 2011 · 133 · 1310310.1021/ja203480w ↗