journal article·2011-09-28Open access

Design and Development of Novel Linker for PbS Quantum Dots/TiO2 Mesoscopic Solar cell

Lioz Etgar, JinHyung Park, Claudia Barolo, Md. K. Nazeeruddin, Guido Viscardi, Michael Graetzel

Abstract

A novel bifunctional linker molecule, bis(4-mercaptophenyl)phosphinic acid, is designed to be used in a QDs solar cells. The linker anchors to TiO(2) mesoporous film through the phosphinic acid functional group and to the PbS QDs through the two thiol groups. The way of attachment of this new linker molecule in a photovoltaic PbS QDs/TiO(2) mesoporous device was studied by FTIR measurements. The photovoltaic performance of this new linker in a heterojunction PbS QDs solar cell show high V(oc) relative to QDs based solar cells, which will allow to receive high power conversion efficiency using this novel designed linker. This novel bifunctional linker molecule should pave the way for enhancing binding strength, and efficiency of QDs solar cells compared to the state-of-the-art linkers.
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Research context

OpenAlex topics: Quantum Dots Synthesis And Properties · Chalcogenide Semiconductor Thin Films · Molecular Junctions and Nanostructures

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

Affiliations

Laboratoire de Photonique et Interfaces, Institut des Sciences et Ingénierie Chimiques, Ecole Polytechnique Fédérale de Lausanne (EPFL), Station 6, CH-1015 Lausanne, Switzerland

Dipartimento di Chimica Generale e Chimica Organica, NIS Centre of Excellence, Università di Torino, Corso Massimo D’Azeglio 48, I-10125 Torino, Italy

References (22)

Show source-provided references
1. Reiko Y. O. · Appl. Phys. Lett. · 2009 · 94 · 07330810.1063/1.3086891 ↗
2. Kamat P. V. · J. Phys. Chem. C · 2008 · 112 · 1873710.1021/jp806791s ↗
3. Huynh W. U. · Science · 2002 · 295 · 242510.1126/science.1069156 ↗
4. Gur I. · Science · 2005 · 310 · 46210.1126/science.1117908 ↗
5. Jonhston K. W. · Appl. Phys. Lett. · 2008 · 92 · 15111510.1063/1.2912340 ↗
6. Luther J. M. · Nano lett. · 2008 · 8 · 348810.1021/nl802476m ↗
7. Ma W. · Nano Lett. · 2009 · 9 · 169910.1021/nl900388a ↗
8. Lee H. · Adv. Funct. Mater. · 2009 · 19 · 273510.1002/adfm.200900081 ↗
9. Zhang S. · Appl. Phys. Lett. · 2005 · 87 · 23310110.1063/1.2137895 ↗
10. Seo J. · Nanotechnology · 2009 · 20 · 9520210.1088/0957-4484/20/9/095202 ↗
11. Menny S. · J. Am. Chem. Soc. · 2009 · 131 · 987610.1021/ja902770k ↗
12. Mora-Sero I. · Nanotechnology · 2008 · 19 · 42400710.1088/0957-4484/19/42/424007 ↗
13. Robel I. · J .Am. Chem. Soc. · 2006 · 128 · 238510.1021/ja056494n ↗
14. Driver T. G. · J. Am. Chem. Soc. · 2007 · 129 · 383610.1021/ja070482f ↗
15. Watson D. A. · Organometallics · 2006 · 25 · 473110.1021/om0606791 ↗
16. Pinehart A. · Tetrahedron Lett. · 1999 · 40 · 547910.1016/S0040-4039(99)01052-7 ↗
17. Gallardo-Godoyyatt A. · Bioorg. Med. Chem. · 2007 · 15 · 30510.1016/j.bmc.2006.09.058 ↗
18. Wyatt P. · Org. Biomol. Chem. · 2004 · 2 · 152810.1039/b315491b ↗
19. Jing Y. · Tetraheron Lett. · 2004 · 45 · 461510.1016/j.tetlet.2004.04.116 ↗
20. Hyun B.-R. · ACS Nano · 2008 · 2 · 220610.1021/nn800336b ↗
21. 10.1002/adma.20110106510.1002/adma.201101065 ↗
22. Guerrero G. · Chem. Mater. · 2001 · 13 · 436710.1021/cm001253u ↗