Why Surface Chemistry Matters for QD–QD Resonance Energy Transfer
Source abstract
Abstract
High Resolution Image Download MS PowerPoint Slide Resonance energy transfer (RET) has been shown to occur in films of semiconductor quantum dots (QDs) with variation in QD composition and size. When coupled with charge carrier transfer, RET could provide a complementary strategy for light harvesting in QD based solid state photovoltaic devices. Due to a direct dependence on the optical properties of the donor and acceptor, QD surface chemistry plays a drastic role in determining the efficiency of RET. Here, the impact of QD surface chemistry on RET in QD films was investigated using a pair of different sized CdSe QDs spin-cast onto a glass substrate. The effects of QD surface passivation on RET were studied by removing surface ligands through QD washing and adding an insulating ZnS shell. In addition, QD films were subjected to solid state ligand exchanges with thiolated ligands in order to mimic a layer-by-layer deposition method commonly used in the construction of QD photovoltaics. These solid state ligand exchanges exhibit drastic quenching of RET in the films. These experiments highlight the importance of understanding surface chemistry when designing photovoltaics that utilize RET.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Quantum Dots Synthesis And Properties · Chalcogenide Semiconductor Thin Films · Perovskite Materials and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Radiation Laboratory, ‡Department of Chemistry & Biochemistry, and §Department of Chemical and Biomolecular Engineering, University of Notre Dame, Notre Dame, Indiana 46556, United States
Funding
Army Research Office · Basic Energy Sciences
References (46)
Show source-provided references
1. 10.1021/jp806791s10.1021/jp806791s ↗
2. 10.1016/S1386-9477(02)00374-010.1016/S1386-9477(02)00374-0 ↗
3. 10.1021/jz402016210.1021/jz4020162 ↗
4. 10.1021/jz300290d10.1021/jz300290d ↗
5. 10.1021/cr900356p10.1021/cr900356p ↗
6. 10.1021/acs.chemrev.5b0006310.1021/acs.chemrev.5b00063 ↗
7. 10.1021/cr900137k10.1021/cr900137k ↗
8. 10.1021/acsenergylett.6b0042910.1021/acsenergylett.6b00429 ↗
9. 10.1021/jp953550610.1021/jp9535506 ↗
10. 10.1021/cr030063a10.1021/cr030063a ↗
11. 10.1039/b310853h10.1039/b310853h ↗
12. 10.1021/cm034081k10.1021/cm034081k ↗
13. 10.1126/science.120984510.1126/science.1209845 ↗
14. 10.1021/ar800112v10.1021/ar800112v ↗
15. 10.1103/PhysRevLett.76.151710.1103/PhysRevLett.76.1517 ↗
16. 10.1103/PhysRevB.54.863310.1103/PhysRevB.54.8633 ↗
17. 10.1039/B812884G10.1039/B812884G ↗
18. 10.1021/jp909972b10.1021/jp909972b ↗
19. 10.1021/nn403872x10.1021/nn403872x ↗
20. 10.1021/acsenergylett.6b0056910.1021/acsenergylett.6b00569 ↗
21. 10.1021/jp506757a10.1021/jp506757a ↗
22. 10.1021/nn301982e10.1021/nn301982e ↗
23. 10.1021/nn100021b10.1021/nn100021b ↗
24. 10.1002/cphc.20130060510.1002/cphc.201300605 ↗
25. 10.1038/nphoton.2009.9610.1038/nphoton.2009.96 ↗
26. 10.1021/nl100415q10.1021/nl100415q ↗
27. 10.1021/ja310737m10.1021/ja310737m ↗
28. 10.1021/nl049322h10.1021/nl049322h ↗
29. 10.1021/nn203728t10.1021/nn203728t ↗
30. Lakowicz J. R. · 200610.1007/978-0-387-46312-4 ↗
31. Turro N. J. · 2010
32. 10.1021/la100580g10.1021/la100580g ↗
33. 10.1021/nn303150j10.1021/nn303150j ↗
34. 10.1021/jp404031s10.1021/jp404031s ↗
35. 10.1021/nn401383t10.1021/nn401383t ↗
36. 10.1103/PhysRevB.87.08120110.1103/PhysRevB.87.081201 ↗
37. 10.1146/annurev-physchem-040513-10364910.1146/annurev-physchem-040513-103649 ↗
38. 10.1021/ja071457c10.1021/ja071457c ↗
39. 10.1038/nature1147610.1038/nature11476 ↗
40. 10.1021/jp504240u10.1021/jp504240u ↗
41. 10.1021/la104542n10.1021/la104542n ↗
42. 10.1021/ja411127w10.1021/ja411127w ↗
43. 10.1021/jp906827m10.1021/jp906827m ↗
44. 10.1021/acs.chemrev.6b0003010.1021/acs.chemrev.6b00030 ↗
45. 10.1103/PhysRevE.81.05130310.1103/PhysRevE.81.051303 ↗
46. 10.1021/jp502123n10.1021/jp502123n ↗