journal article·2017-10-11Open access

Work Function Control of Germanium through Carborane-Carboxylic Acid Surface Passivation

Andrew C. Serino, Mary E. Anderson, Liban M. A. Saleh, Rafal M. Dziedzic, Harrison Mills, Liv K. Heidenreich, Alexander M. Spokoyny, Paul S. Weiss

Abstract

Self-assembled monolayers (SAMs) of carborane isomers with different dipole moments passivate germanium to modulate surface work function while maintaining chemical environment and surface energy. To identify head groups capable of monolayer formation on germanium surfaces, we studied thiol-, hydroxyl-, and carboxyl-terminated carboranes. These films were successfully formed with carboxylic acid head groups instead of the archetypal thiol, suggesting that the carborane cluster significantly affects headgroup reactivity. Film characterization included X-ray and ultraviolet photoelectron spectroscopies as well as contact angle goniometry. Using these carboranes, the germanium surface work function was tailored over 0.4 eV without significant changes to wetting properties.
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Research context

OpenAlex topics: Molecular Junctions and Nanostructures · Nanowire Synthesis and Applications · Semiconductor materials and devices

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Affiliations

Department of Chemistry and Biochemistry, Hope College, Holland, Michigan 49423, United States

Funding

Division of Chemistry · Basic Energy Sciences · University of California, Los Angeles · U.S. Department of Defense · American Chemical Society Petroleum Research Fund · 3M · National Defense Science and Engineering Graduate Fellowship

References (30)

Show source-provided references
1. 10.1038/nmat315910.1038/nmat3159 ↗
2. 10.1021/ja076878910.1021/ja0768789 ↗
3. 10.1021/acs.jpcc.5b0117710.1021/acs.jpcc.5b01177 ↗
4. 10.1143/APEX.1.05140610.1143/APEX.1.051406 ↗
5. 10.1103/PhysRevB.83.24531510.1103/PhysRevB.83.245315 ↗
6. 10.1016/j.sse.2010.06.01210.1016/j.sse.2010.06.012 ↗
7. 10.1021/jp710893k10.1021/jp710893k ↗
8. 10.1126/science.121882910.1126/science.1218829 ↗
9. 10.1021/am508764810.1021/am5087648 ↗
10. 10.1021/nl501081q10.1021/nl501081q ↗
11. 10.1021/nn800673d10.1021/nn800673d ↗
12. Grimes R. N. · 2016
13. 10.1021/acsnano.5b0132910.1021/acsnano.5b01329 ↗
14. 10.1021/jacs.6b0202610.1021/jacs.6b02026 ↗
15. 10.1038/nmat482310.1038/nmat4823 ↗
16. 10.1039/c1sc00115a10.1039/c1sc00115a ↗
17. 10.1021/ja993816c10.1021/ja993816c ↗
18. 10.1021/la803468e10.1021/la803468e ↗
19. 10.1146/annurev.physchem.56.092503.14130710.1146/annurev.physchem.56.092503.141307 ↗
20. 10.1021/la904864c10.1021/la904864c ↗
21. 10.1021/ja808066t10.1021/ja808066t ↗
22. 10.1021/jp308990x10.1021/jp308990x ↗
23. 10.1021/ja054950210.1021/ja0549502 ↗
24. 10.1021/jp063264210.1021/jp0632642 ↗
25. 10.1021/acs.jpcc.6b0481610.1021/acs.jpcc.6b04816 ↗
26. 10.1021/la051122d10.1021/la051122d ↗
27. 10.1016/S0039-6028(03)00958-010.1016/S0039-6028(03)00958-0 ↗
28. 10.1016/j.apsusc.2014.07.12710.1016/j.apsusc.2014.07.127 ↗
29. 10.1002/adma.20080326710.1002/adma.200803267 ↗
30. 10.1021/cr00010a00210.1021/cr00010a002 ↗