Integration of Type II Nanorod Heterostructures into Photovoltaics
Source abstract
Abstract
High-quality epitaxial interfaces and delicate control over shape anisotropy make nanorod heterostructures (NRHs) with staggered band offsets efficient in separating and directing photogenerated carriers. Combined with versatile and scalable wet chemical means of synthesis, these salient features of NRHs are useful for improving both the performance and the cost-effectiveness of photovoltaics (PVs). However, inefficient carrier transport and extraction have imposed severe limitations, outweighing the benefits of enhanced charge separation. Hence integration of type II NRHs into PVs has thus far been unfruitful. Here, we demonstrate PVs that utilize NRHs as an extremely thin absorber between electron and hole transporting layers. In the limit approaching monolayer thickness, PVs incorporating NRHs have up to three times the short circuit current and conversion efficiency over devices made from their single-component counterparts. Comparisons between linear and curved NRHs are also made, revealing the importance of internal geometry and heterointerfacial area for enhanced contribution of charge-separated state absorption to photocurrent and in contacting charge transport layers.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Quantum Dots Synthesis And Properties · Chalcogenide Semiconductor Thin Films · ZnO doping and properties
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Materials Science and Engineering, University of Illinois, Urbana, Illinois 61801, United States,
Department of Electrical and Computer Engineering, University of Illinois, Urbana, Illinois 61801, United States
References (32)
Show source-provided references
1. Pattantyus A. G. · ACS Nano · 2010 · 4 · 337410.1021/nn100335g ↗
2. Sambur J. B. · Science · 2010 · 330 · 6310.1126/science.1191462 ↗
3. Gur I. · Science · 2005 · 310 · 46210.1126/science.1117908 ↗
4. Dooley C. J. · J. Phys. Chem. C Lett. · 2008 · 112 · 1207410.1021/jp804040r ↗
5. Chuang C. · J. Phys. Chem. Lett. · 2010 · 1 · 253010.1021/jz1008399 ↗
6. Lee D. C. · J. Am. Chem. Soc. · 2010 · 132 · 996010.1021/ja102716p ↗
7. Bang J. · Chem. Mater. · 2010 · 22 · 23310.1021/cm9027995 ↗
8. Shieh F. · J. Phys. Chem. B Lett. · 2005 · 109 · 853810.1021/jp0509008 ↗
9. Halpert J. E. · J. Am. Chem. Soc. · 2006 · 128 · 1259010.1021/ja0616534 ↗
10. Kumar S. · Small · 2007 · 3 · 163310.1002/smll.200700155 ↗
11. Smith A. M. · Nat. Nanotechnol. · 2008 · 4 · 5610.1038/nnano.2008.360 ↗
12. McDaniel H. · J. Am. Chem. Soc. · 2010 · 132 · 328610.1021/ja910233a ↗
13. Zhong H. · J. Phys. Chem. C · 2007 · 111 · 653810.1021/jp0709407 ↗
14. Li B. Y. · Adv. Mater. · 2009 · 21 · 446110.1002/adma.200901338 ↗
15. Rivest J. B. · ACS Nano · 2011 · 5 · 381110.1021/nn2001454 ↗
16. Geyer S. · Phys Rev. B · 2010 · 82 · 1552011
17. Bang J. H. · ACS Nano · 2009 · 3 · 146710.1021/nn900324q ↗
18. Sun B. · Nano Lett. · 2009 · 9 · 1234
19. Yu D. · Science · 2003 · 300 · 127710.1126/science.1084424 ↗
20. Vanmaekelbergh D. · Chem. Soc. Rev. · 2005 · 34 · 29910.1039/b314945p ↗
21. Liu Y. · Nano Lett. · 2010 · 10 · 196010.1021/nl101284k ↗
22. Shim M. · J. Chem. Phys. · 1999 · 111 · 695510.1063/1.479988 ↗
23. Huynh W. U. · Science · 2002 · 295 · 242510.1126/science.1069156 ↗
24. Luther J. M. · Nano Lett. · 2008 · 8 · 348810.1021/nl802476m ↗
25. Talapin D. · Science · 2005 · 310 · 8610.1126/science.1116703 ↗
26. Konstantatos G. · Nature · 2006 · 442 · 18010.1038/nature04855 ↗
27. Murphy J. E. · J. Phys. Chem. B · 2006 · 110 · 2545510.1021/jp0646123 ↗
28. Lee J.-S. · Nat. Nanotechnol. · 2011 · 6 · 34810.1038/nnano.2011.46 ↗
29. Wehrenberg B. L. · J. Phys. Chem. B · 2005 · 109 · 2019210.1021/jp053621t ↗
30. Kaiser I. · Sol. Energy Mater. Sol. Cells · 2001 · 67 · 8910.1016/S0927-0248(00)00267-1 ↗
31. Yu W. W. · Chem. Mater. · 2003 · 15 · 285410.1021/cm034081k ↗
32. Robel I. · J. Am. Chem. Soc. · 2007 · 129 · 413610.1021/ja070099a ↗