journal article·2021-01-12Open access

S-Rich PbS Quantum Dots: A Promising p-Type Material for Optoelectronic Devices

Dmytro Bederak, Dmitry N. Dirin, Nataliia Sukharevska, Jamo Momand, Maksym V. Kovalenko, Maria A. Loi

Chemistry of Materials· Volume 33· Issue 1

Abstract

PbS colloidal quantum dots (CQDs) are versatile building blocks for bottom-up fabrication of various optoelectronic devices. The transport properties of thin films of this class of materials depend on the size of the CQDs, their surface ligands, and stoichiometry. The most common synthetic methods yield PbS CQDs with an excess of Pb atoms, which induces n-type transport properties in CQD films. In this work, we developed a new synthesis, which offers S-rich PbS CQDs. Thanks to their sufficient colloidal stability in nonpolar solvents, we established a protocol for the integration of these CQDs into thin field-effect transistors and found strong hole-dominated transport with a hole mobility of about 1 x 10(-2) cm(2)/Vs. Moreover, we were able to enhance the electron mobility for almost two orders of magnitude while keeping the hole mobility nearly the same. This approach allows us to obtain reliably p-doped PbS CQDs, which can be used for the fabrication of various electronic and optoelectronic devices.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Quantum Dots Synthesis And Properties · Chalcogenide Semiconductor Thin Films · Copper-based nanomaterials and applications

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

Affiliations

Zernike Institute for Advanced Materials, University of Groningen, Nijenborgh 4, 9747AG Groningen, The Netherlands

Department of Chemistry and Applied Biosciences, ETH Zürich, Vladimir Prelog Weg 1, Zürich 8093, Switzerland

Empa-Swiss Federal Laboratories for Materials Science and Technology, Uberlandstrasse 129, Dübendorf 8600, Switzerland

References (35)

Show source-provided references
1. 10.1021/nn506223h10.1021/nn506223h ↗
2. 10.1002/solr.20160002110.1002/solr.201600021 ↗
3. 10.1016/j.joule.2020.05.01110.1016/j.joule.2020.05.011 ↗
4. 10.1002/adma.20030539510.1002/adma.200305395 ↗
5. 10.1021/ja063166u10.1021/ja063166u ↗
6. 10.1126/science.aaa295110.1126/science.aaa2951 ↗
7. 10.1038/nmat466110.1038/nmat4661 ↗
8. 10.1103/PhysRevLett.110.19680210.1103/PhysRevLett.110.196802 ↗
9. 10.1039/C6EE01577H10.1039/C6EE01577H ↗
10. 10.1002/aelm.20150046710.1002/aelm.201500467 ↗
11. 10.1063/1.486921610.1063/1.4869216 ↗
12. 10.1038/nmat398410.1038/nmat3984 ↗
13. 10.1038/nmat480010.1038/nmat4800 ↗
14. 10.1002/adma.20170757210.1002/adma.201707572 ↗
15. 10.1039/C8EE00278A10.1039/C8EE00278A ↗
16. 10.1002/adma.20180166110.1002/adma.201801661 ↗
17. 10.1063/1.497844410.1063/1.4978444 ↗
18. 10.1021/nl404818z10.1021/nl404818z ↗
19. 10.1021/nn305735610.1021/nn3057356 ↗
20. 10.1021/acs.jpcc.6b0585810.1021/acs.jpcc.6b05858 ↗
21. 10.1126/sciadv.aao155810.1126/sciadv.aao1558 ↗
22. 10.1021/acsanm.8b0169610.1021/acsanm.8b01696 ↗
23. 10.1016/0168-583X(86)90291-010.1016/0168-583X(86)90291-0 ↗
24. 10.1021/ja110999710.1021/ja1109997 ↗
25. 10.1039/c1ra00279a10.1039/c1ra00279a ↗
26. 10.1039/c4py00073k10.1039/c4py00073k ↗
27. 10.1002/pssa.20160054310.1002/pssa.201600543 ↗
28. 10.1016/j.apsusc.2018.06.15210.1016/j.apsusc.2018.06.152 ↗
29. 10.1021/nn900863a10.1021/nn900863a ↗
30. 10.1021/acsenergylett.8b0003510.1021/acsenergylett.8b00035 ↗
31. 10.1002/adma.20180008210.1002/adma.201800082 ↗
32. 10.1021/ja500628810.1021/ja5006288 ↗
33. 10.1039/cs973020023310.1039/cs9730200233 ↗
34. 10.1021/ic50116a04710.1021/ic50116a047 ↗
35. 10.1016/S0022-0728(97)00192-710.1016/S0022-0728(97)00192-7 ↗