journal article·2018-08-01

Energy Level Alignment of Molybdenum Oxide on Colloidal Lead Sulfide (PbS) Thin Films for Optoelectronic Devices

Diogenes Placencia, Paul Lee, Joseph G. Tischler, Erin L. Ratcliff

ACS Applied Materials & Interfaces· Volume 10· Issue 30
Publisher page

Abstract

Interfacial charge transport in optoelectronic devices is dependent on energetic alignment that occurs via a number of physical and chemical mechanisms. Herein, we directly connect device performance with measured thickness-dependent energy-level offsets and interfacial chemistry of 1,2-ethanedithiol-treated lead sulfide (PbS) quantum dots and molybdenum oxide. We show that interfacial energetic alignment results from partial charge transfer, quantified via the chemical ratios of Mo5+ relative to Mo6+. The combined effect mitigates leakage current in both the dark and the light, relative to a metal contact, with an overall improvement in open circuit voltage, fill factor, and short circuit current.
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

U.S. Naval Research Laboratory, 4555 Overlook Avenue Southwest, Washington, D.C. 20375, United States

Department of Chemistry & Biochemistry, University of Arizona, 1306 East University Boulevard, Tucson, Arizona 85721, United States

Department of Materials Science & Engineering, University of Arizona, 1235 East James E. Rogers Way, Tucson, Arizona 85721, United States

Funding

Office of Naval Research

References (34)

Show source-provided references
1. 10.1038/nphoton.2015.28010.1038/nphoton.2015.280 ↗
2. 10.1038/natrevmats.2016.10010.1038/natrevmats.2016.100 ↗
3. 10.1038/srep0222510.1038/srep02225 ↗
4. 10.1021/acs.chemmater.6b0293910.1021/acs.chemmater.6b02939 ↗
5. 10.1038/nnano.2012.6310.1038/nnano.2012.63 ↗
6. 10.1002/adma.20170327910.1002/adma.201703279 ↗
7. 10.1039/c2nr11836j10.1039/c2nr11836j ↗
8. 10.1002/adma.20030539510.1002/adma.200305395 ↗
9. 10.1021/cr900137k10.1021/cr900137k ↗
10. 10.1021/acs.chemrev.6b0010210.1021/acs.chemrev.6b00102 ↗
11. 10.1126/science.111670310.1126/science.1116703 ↗
12. 10.1038/nmat400710.1038/nmat4007 ↗
13. 10.1021/nn500897c10.1021/nn500897c ↗
14. 10.1021/ja206303g10.1021/ja206303g ↗
15. 10.1002/adma.20140328110.1002/adma.201403281 ↗
16. 10.1038/s41598-017-00669-910.1038/s41598-017-00669-9 ↗
17. 10.1038/nmat398410.1038/nmat3984 ↗
18. 10.1038/nmat381610.1038/nmat3816 ↗
19. 10.1016/j.nanoen.2017.06.04010.1016/j.nanoen.2017.06.040 ↗
20. 10.1021/acsami.7b0856810.1021/acsami.7b08568 ↗
21. 10.1021/acsami.6b0101810.1021/acsami.6b01018 ↗
22. 10.1002/adma.20140125010.1002/adma.201401250 ↗
23. 10.1039/C7TA07014D10.1039/C7TA07014D ↗
24. 10.1021/acs.jpclett.7b0068310.1021/acs.jpclett.7b00683 ↗
25. 10.1021/nl201472u10.1021/nl201472u ↗
26. 10.1021/nl201572910.1021/nl2015729 ↗
27. 10.1002/adma.20120163010.1002/adma.201201630 ↗
28. 10.1021/acs.jpcc.7b0404510.1021/acs.jpcc.7b04045 ↗
29. 10.1002/aenm.20140054910.1002/aenm.201400549 ↗
30. 10.1038/srep0538010.1038/srep05380 ↗
31. 10.1021/acsnano.5b0683310.1021/acsnano.5b06833 ↗
32. 10.1039/c2jm14911g10.1039/c2jm14911g ↗
33. 10.1021/acs.jpclett.5b0044410.1021/acs.jpclett.5b00444 ↗
34. 10.1038/srep4076110.1038/srep40761 ↗