journal article·2018-08-27

Anisotropic One-Dimensional Aqueous Polymer Gel Electrolyte for Photoelectrochemical Devices: Improvement in Hydrophobic TiO2–Dye/Electrolyte Interface

Keval K. Sonigara, Jayraj V. Vaghasiya, Hiren K. Machhi, Jyoti Prasad, Alain Gibaud, Saurabh S. Soni

ACS Applied Energy Materials· Volume 1· Issue 8
Publisher page

Abstract

Aqueous photoelectrochemical devices have emerged recently as promising area because of their economic and ecological friendliness. In the present work, we have expedited surface active amphiphilic quasi-solid aqueous polymer gel electrolyte (PGE) with hydrophobic sensitizer SK3 in water-based dye sensitized solar cell (DSSC). PGE was prepared from amphiphilic block copolymer (PEO)–(PPO)–(PEO) with iodide–triiodide couple in pure aqueous media without any organic solvent. This block copolymer, with iodide-triiodide salt exhibits 1D-lamellar microcrystalline phase which shows stability in the temperature range of 25–50 °C. Parallel (||al) and perpendicular (⊥ar) alignment of anisotropic lamellar microcrystalline phase pertaining by PGE were characterized and applied in quasi-solid DSSC. Temperature dependency of ionic conductivity, triiodide diffusion, differential scanning calorimetry, viscosity, and 1-D lamellar anisotropic behavior were studied. Surface active effect of PGE at the hydrophobic dye sensitized photoanode was investigated and compared with liquid water based electrolyte. Because of the amphiphilic nature and thermoreversible sol–gel transition of PGE at a lower temperature (0 to −2 °C) allowing PGE to penetrate efficiently inside the hydrophobic surface of dye–TiO2 and resulted in a fused contact between dye–TiO2/PGE interface. This aqueous PGE successfully enhances the performance of DSSCs over liquid water based devices by improving their Voc and stability. Under 0.5 sun illumination, DSSC with 1-D lamellar perpendicularly align PGE shows an efficiency of 2.8% and stability up to 1000 h at 50 °C.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: TiO2 Photocatalysis and Solar Cells · Advanced Photocatalysis Techniques · Perovskite Materials and Applications

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

Affiliations

Department of Chemistry, Sardar Patel University, Vallabh Vidhyanagar, 388120, Gujarat India

Institut des Molécules et Matériaux du Mans, Universite du Maine, Le Mans 72000, France

Funding

University Grants Commission · Science and Engineering Research Board

References (47)

Show source-provided references
1. 10.1038/353737a010.1038/353737a0 ↗
2. 10.1039/C5CC06759F10.1039/C5CC06759F ↗
3. 10.1021/acsaem.7b0023010.1021/acsaem.7b00230 ↗
4. 10.1021/acsaem.7b0019610.1021/acsaem.7b00196 ↗
5. 10.1039/C4TA02529F10.1039/C4TA02529F ↗
6. 10.1021/am501523x10.1021/am501523x ↗
7. 10.1021/sc500448810.1021/sc5004488 ↗
8. 10.1016/j.jcis.2014.03.04710.1016/j.jcis.2014.03.047 ↗
9. 10.1039/C6SC01145D10.1039/C6SC01145D ↗
10. 10.1039/C6GC02625G10.1039/C6GC02625G ↗
11. 10.1002/ente.20160028510.1002/ente.201600285 ↗
12. 10.1002/adma.20100170310.1002/adma.201001703 ↗
13. 10.1021/nn400126910.1021/nn4001269 ↗
14. 10.1016/j.solener.2018.02.00910.1016/j.solener.2018.02.009 ↗
15. 10.3390/en905038410.3390/en9050384 ↗
16. 10.3303/CET144103610.3303/CET1441036 ↗
17. 10.1016/j.electacta.2014.09.01410.1016/j.electacta.2014.09.014 ↗
18. 10.1039/c2jm35245a10.1039/c2jm35245a ↗
19. 10.1039/C2EE23317G10.1039/C2EE23317G ↗
20. 10.1002/adma.20110483710.1002/adma.201104837 ↗
21. 10.1039/c2ee23263d10.1039/c2ee23263d ↗
22. 10.1039/C3TA14571A10.1039/C3TA14571A ↗
23. 10.1039/C4CS00456F10.1039/C4CS00456F ↗
24. 10.1021/la202670v10.1021/la202670v ↗
25. 10.1002/anie.20170437310.1002/anie.201704373 ↗
26. 10.1002/adma.20160223910.1002/adma.201602239 ↗
27. 10.1002/anie.20171084110.1002/anie.201710841 ↗
28. 10.1016/j.ensm.2018.03.01610.1016/j.ensm.2018.03.016 ↗
29. 10.1016/j.nantod.2016.10.00210.1016/j.nantod.2016.10.002 ↗
30. 10.1039/C5TA06414G10.1039/C5TA06414G ↗
31. 10.1039/C5NR06888F10.1039/C5NR06888F ↗
32. 10.1039/C7NR06128E10.1039/C7NR06128E ↗
33. 10.1039/C5TA06548H10.1039/C5TA06548H ↗
34. 10.1016/j.tsf.2007.05.09010.1016/j.tsf.2007.05.090 ↗
35. 10.1039/C6TA09777D10.1039/C6TA09777D ↗
36. Zistler M. · Int. J. Electrochem. Sci. · 2008 · 3 · 23610.1016/S1452-3981(23)15449-6 ↗
37. 10.1016/j.molliq.2010.04.02110.1016/j.molliq.2010.04.021 ↗
38. 10.1021/jp003000u10.1021/jp003000u ↗
39. 10.1016/j.jcis.2004.01.01210.1016/j.jcis.2004.01.012 ↗
40. 10.1021/cr00033a00310.1021/cr00033a003 ↗
41. 10.1039/c2cp43220j10.1039/c2cp43220j ↗
42. 10.1021/jp060372f10.1021/jp060372f ↗
43. 10.1016/j.electacta.2006.10.01410.1016/j.electacta.2006.10.014 ↗
44. 10.1021/acsomega.6b0001010.1021/acsomega.6b00010 ↗
45. 10.1016/j.jpowsour.2009.12.10710.1016/j.jpowsour.2009.12.107 ↗
46. 10.1021/am302925s10.1021/am302925s ↗
47. 10.1016/j.jphotochem.2003.11.01510.1016/j.jphotochem.2003.11.015 ↗