Tapered Cross Section Photoelectron Spectroscopy Provides Insights into the Buried Interfaces of III‐V Semiconductor Devices
Source abstract
Abstract
Abstract Interfaces are key elements that define electronic properties of the final device. Inevitably, most of the active interfaces of III–V semiconductor devices are buried and it is therefore not straightforward to characterize them. The Tapered Cross Section Photoelectron Spectroscopy (TCS‐PES) approach is promising to address such a challenge. That the TCS‐PES can be used to study the relevant heterojunction in epitaxial III–V architectures prepared by metalorganic chemical vapor deposition is demonstrated here. A MULTIPREP polishing system that enables controlling the angle between the sample holder and the polishing plate has been employed to improve the reproducibility of the polishing procedure. With this procedure, that preparing the TCS of III–V semiconductor devices with tapering angles lower than 0.02° is possible is demonstrated. The PES provides then information about the buried interfaces of Ge|GaInP and GaAs|GaInP layer stacks. Both, chemical and electronic properties have been measured by PES. It evidences that the preparation of the TCSs under an uncontrolled atmosphere modifies the pristine properties of the critical buried heterointerfaces. Surface states and reaction layers are created on the TCS surface, which restrict unambiguous conclusions on buried interface energetics.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Chalcogenide Semiconductor Thin Films · Semiconductor materials and devices · Quantum Dots Synthesis And Properties
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Surface Science Laboratory Department of Materials and Earth Sciences Technical University of Darmstadt Otto‐Berndt‐Strasse 3 64287 Darmstadt Germany
Fundamentals of Energy Materials Institute of Physics Ilmenau University of Technology Gustav‐Kirchhoff‐Strasse 5 98693 Ilmenau Germany
Funding
Deutsche Forschungsgemeinschaft
References (36)
Show source-provided references
1. 10.1002/pip.247510.1002/pip.2475 ↗
2. 10.1038/s41560-020-0598-510.1038/s41560-020-0598-5 ↗
3. 10.1002/aenm.20200287410.1002/aenm.202002874 ↗
4. 10.1038/ncomms928610.1038/ncomms9286 ↗
5. 10.1021/acsami.2c0184510.1021/acsami.2c01845 ↗
6. 10.1021/acsami.1c1893810.1021/acsami.1c18938 ↗
7. Bett A. W. · 2013 · 1
8. 10.1002/admi.20160111810.1002/admi.201601118 ↗
9. 10.1021/acs.chemrev.8b0055810.1021/acs.chemrev.8b00558 ↗
10. 10.1002/9783527636839.ch1510.1002/9783527636839.ch15 ↗
11. 10.1002/pssb.20200046310.1002/pssb.202000463 ↗
12. 10.1002/pssb.20210046210.1002/pssb.202100462 ↗
13. 10.1002/admi.20180195110.1002/admi.201801951 ↗
14. 10.1063/1.512404910.1063/1.5124049 ↗
15. 10.1021/acs.nanolett.0c0454410.1021/acs.nanolett.0c04544 ↗
16. 10.1063/1.290282810.1063/1.2902828 ↗
17. 10.1063/1.497358710.1063/1.4973587 ↗
18. 10.1016/j.jcrysgro.2004.12.10110.1016/j.jcrysgro.2004.12.101 ↗
19. 10.1016/j.apsusc.2015.10.09810.1016/j.apsusc.2015.10.098 ↗
20. 10.1016/j.apsusc.2022.15463010.1016/j.apsusc.2022.154630 ↗
21. 10.1149/2162-8777/abb75010.1149/2162-8777/abb750 ↗
22. 10.1016/j.apsusc.2020.14590310.1016/j.apsusc.2020.145903 ↗
23. 10.1002/adfm.20191067910.1002/adfm.201910679 ↗
24. 10.1021/acsami.0c1148410.1021/acsami.0c11484 ↗
25. 10.1002/solr.20210029810.1002/solr.202100298 ↗
26. 10.1002/sia.74001010310.1002/sia.740010103 ↗
27. 10.1380/ejssnt.2006.17410.1380/ejssnt.2006.174 ↗
28. 10.1063/1.486809110.1063/1.4868091 ↗
29. 10.1063/1.147157710.1063/1.1471577 ↗
30. 10.1063/1.274035910.1063/1.2740359 ↗
31. 10.1016/S0368-2048(96)80117-410.1016/S0368-2048(96)80117-4 ↗
32. 10.1063/1.34624210.1063/1.346242 ↗
33. 10.1116/1.310026610.1116/1.3100266 ↗
34. 10.1016/j.apsusc.2021.15051310.1016/j.apsusc.2021.150513 ↗
35. 10.1021/acs.jpclett.0c0077810.1021/acs.jpclett.0c00778 ↗
36. 10.1016/j.apsadv.2021.10011210.1016/j.apsadv.2021.100112 ↗