Long-Range Charge Transport via Redox Ligands in Quantum Dot Assemblies
Source abstract
Abstract
We present a strategy to actively engineer long-range charge transport in colloidal quantum dot assemblies by using ligand functionalities that introduce electronic states and provide a path for carrier transfer. This is a shift away from the use of inactive spacers to modulate charge transport through the lowering of the tunneling barrier for interparticle carrier transfer. This is accomplished with the use of electronically coupled redox ligands by which a self-exchange chain reaction takes place and long-range charge transport is enabled across the film. We identified the different modes of charge transport in these quantum dot/redox ligand assemblies, their energetic position and kinetics, and explain how to rationally manipulate them through modulation of the Fermi level and redox ligand coverage.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Quantum Dots Synthesis And Properties · Molecular Junctions and Nanostructures · Electrochemical Analysis and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Optoelectronic Materials Section, Faculty of Applied Sciences, Delft University of Technology, Van der Maasweg 9, 2629 HZDelft, The Netherlands
Funding
Schweizerischer Nationalfonds zur F?rderung der Wissenschaftlichen Forschung
References (30)
Show source-provided references
1. 10.1126/science.aaz854110.1126/science.aaz8541 ↗
2. 10.1039/D0CS01336F10.1039/D0CS01336F ↗
3. 10.1038/s41570-018-0024-810.1038/s41570-018-0024-8 ↗
4. 10.3390/s9090726610.3390/s90907266 ↗
5. 10.1021/cr900137k10.1021/cr900137k ↗
6. 10.1038/nnano.2015.24710.1038/nnano.2015.247 ↗
7. 10.1126/science.aac552310.1126/science.aac5523 ↗
8. 10.1038/s41467-020-16560-710.1038/s41467-020-16560-7 ↗
9. 10.1038/s41565-018-0189-910.1038/s41565-018-0189-9 ↗
10. 10.1021/nl101284k10.1021/nl101284k ↗
11. 10.1021/nn302971610.1021/nn3029716 ↗
12. 10.1038/nnano.2011.4610.1038/nnano.2011.46 ↗
13. 10.1021/acsenergylett.0c0009310.1021/acsenergylett.0c00093 ↗
14. 10.1021/acs.analchem.9b0033610.1021/acs.analchem.9b00336 ↗
15. 10.1038/s41467-017-02091-110.1038/s41467-017-02091-1 ↗
16. 10.1021/am507334m10.1021/am507334m ↗
17. 10.1021/jacs.8b0134710.1021/jacs.8b01347 ↗
18. 10.1021/cm303361s10.1021/cm303361s ↗
19. 10.1021/nn500897c10.1021/nn500897c ↗
20. Faulkner L. R. · 2001
21. 10.1021/ja500936n10.1021/ja500936n ↗
22. Stauffer D. · 201810.1201/9781315274386 ↗
23. 10.1016/S0022-0728(83)80601-910.1016/S0022-0728(83)80601-9 ↗
24. 10.1021/acs.jpcc.8b1094810.1021/acs.jpcc.8b10948 ↗
25. 10.1016/S0022-0728(80)80058-110.1016/S0022-0728(80)80058-1 ↗
26. 10.1016/S0022-0728(80)80002-710.1016/S0022-0728(80)80002-7 ↗
27. 10.1016/0022-0728(89)85097-110.1016/0022-0728(89)85097-1 ↗
28. 10.1021/j100323a06210.1021/j100323a062 ↗
29. 10.1103/RevModPhys.15.110.1103/RevModPhys.15.1 ↗
30. 10.1021/j100342a08610.1021/j100342a086 ↗