Photophysics of Voltage Increase by Photoinduced Dipole Layers in Sensitized Solar Cells
Source abstract
Abstract
Significant overpotentials between the sensitizer and both the electron and hole conductors hamper the performance of sensitized solar cells, leading to a reduced photovoltage. We show that by using properly designed type-II quantum dots (QDs) between the sensitizer and the hole conductor in thin absorber cells, it is possible to increase the open circuit voltage (Voc) by more than 100 mV. This increase is due to the formation of a photoinduced dipole (PID) layer. Photogenerated holes in the type-II QDs are retained in the core for a relatively long time, allowing for the accumulation of a positively charged layer. Negative charges are, in turn, injected and accumulated in the TiO2 anode, creating a dipole moment, which negatively shifts the TiO2 conduction band relative to the electrolyte. We study this phenomenon using a unique TiO2/CdSe/(ZnSe:Te/CdS)/polysulfide system, where the formation of a PID depends on the color of the illumination. The PID concept thus introduces a new design strategy, where the operating parameters of the solar cell can be manipulated separately.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Perovskite Materials and Applications · Quantum Dots Synthesis And Properties · Advanced Photocatalysis Techniques
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Physics of Complex Systems, Weizmann Institute of Science, Rehovot 76100, Israel
Department of Chemistry, Bar Ilan University, Ramat-Gan 52900, Israel
Funding
Leona M. and Harry B. Helmsley Charitable Trust · Israel Strategic Alternative Energy Foundation
References (26)
Show source-provided references
1. Robel I. · J. Am. Chem. Soc. · 2007 · 129 · 413610.1021/ja070099a ↗
2. Visoly-Fisher I. · ChemPhysChem · 2005 · 6 · 27710.1002/cphc.200400392 ↗
3. Goh C. · J. Appl. Phys. · 2007 · 101 · 11450310.1063/1.2737977 ↗
4. Barea E. M. · J. Am. Chem. Soc. · 2010 · 132 · 683410.1021/ja101752d ↗
5. Hod I. · Phys. Chem. Chem. Phys. · 2013 · 15 · 633910.1039/c3cp50242b ↗
6. Lee Y.-L. · Chem. Mater. · 2010 · 22 · 92210.1021/cm901762h ↗
7. Chi C.-F. · Appl. Phys. Lett. · 2011 · 98 · 01210110.1063/1.3533642 ↗
8. Rühle S. · J. Phys. Chem. B · 2005 · 109 · 1890710.1021/jp0514123 ↗
9. Shalom M. · J. Am. Chem. Soc. · 2009 · 131 · 987610.1021/ja902770k ↗
10. Buhbut S. · Nano Lett. · 2013 · 13 · 445610.1021/nl402360f ↗
11. Itzhakov S. · J. Phys. Chem. C · 2013 · 117 · 2220310.1021/jp312190x ↗
12. Wang J. · J. Am. Chem. Soc. · 2013 · 135 · 1591310.1021/ja4079804 ↗
13. Zhang L. · ACS Nano · 2012 · 6 · 832510.1021/nn303060r ↗
14. Sonawane K. G. · Nanotechnology · 2011 · 22 · 30570210.1088/0957-4484/22/30/305702 ↗
15. Avidan A. · Phys. Rev. B · 2010 · 82 · 16533210.1103/PhysRevB.82.165332 ↗
16. Tachan Z. · J. Phys. Chem. C · 2011 · 115 · 616210.1021/jp112010m ↗
17. Markus T. Z. · J. Phys. Chem. C · 2011 · 1323610.1021/jp2035955 ↗
18. Zewdu T. · Energy Environ. Sci. · 2011 · 4 · 463310.1039/c1ee02088a ↗
19. Montanari I. · J. Phys. Chem. B · 2002 · 106 · 1220310.1021/jp025824c ↗
20. McDonald S. a · Nat. Mater. · 2005 · 4 · 13810.1038/nmat1299 ↗
21. Pattantyus-abraham A. G. · ACS Nano · 2010 · 4 · 337410.1021/nn100335g ↗
22. Yu P. · J. Phys. Chem. B · 2006 · 110 · 2545110.1021/jp064817b ↗
23. Kim H. S. · Sci. Rep. · 2012 · 2 · 1
24. Burschka J. · Nature · 2013 · 499 · 31610.1038/nature12340 ↗
25. Liu M. · Nature · 2013 · 501 · 39510.1038/nature12509 ↗
26. Edri E. · J. Phys. Chem. Lett. · 2014 · 5 · 42910.1021/jz402706q ↗