Solution Monolayer Epitaxy for Tunable Atomically Sharp Oxide Interfaces
Source abstract
Abstract
Abstract Interfaces play an important role in a variety of devices including transistors, solar cells, and memory components. Atomically sharp interfaces are essential to avoid charge traps that hamper efficient device operation. Sharp interfaces usually require thin‐film fabrication techniques involving ultrahigh vacuum and high substrate temperatures. A new self‐limiting wet chemical process for deposition of epitaxial layers from alkoxide precursors is presented. This method is fast, cheap, and yields perfect interfaces as validated by various analysis techniques. It allows the growth of heterostructures with half‐unit‐cell resolution. The method is demonstrated by designing a hole‐type oxide interface SrTiO3/BaO/LaAlO3. It is shown that transport through this interface exhibits properties of mixed electron–hole contributions with hole mobility exceeding that of electrons.
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Research context
OpenAlex topics: Electronic and Structural Properties of Oxides · Semiconductor materials and devices · Chemical and Physical Properties of Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Raymond and Beverly Sackler School of Physics Tel Aviv University Tel Aviv 6997801 Israel
Raymond and Beverly Sackler School of Chemistry Tel Aviv University Tel Aviv 6997801 Israel
Ernst Ruska Centre for Microscopy and Spectroscopy with Electrons Research Centre Jülich 52425 Jülich Germany
Funding
Israel Science Foundation · Ministry of Science and Technology, Israel · United States-Israel Binational Science Foundation · National Science Foundation · U.S. Department of Energy
References (34)
Show source-provided references
1. 10.1364/AO.4.00014710.1364/AO.4.000147 ↗
2. 10.1109/ASMC.2008.452901410.1109/ASMC.2008.4529014 ↗
3. 10.1021/acs.nanolett.5b0142410.1021/acs.nanolett.5b01424 ↗
4. 10.1126/science.114600610.1126/science.1146006 ↗
5. 10.1038/nature0757610.1038/nature07576 ↗
6. 10.1103/PhysRevB.80.14040310.1103/PhysRevB.80.140403 ↗
7. 10.1038/nphys207910.1038/nphys2079 ↗
8. 10.1103/PhysRevLett.107.05680210.1103/PhysRevLett.107.056802 ↗
9. 10.1103/PhysRevLett.109.25720710.1103/PhysRevLett.109.257207 ↗
10. 10.1038/nmat367410.1038/nmat3674 ↗
11. 10.1103/PhysRevLett.113.21680110.1103/PhysRevLett.113.216801 ↗
12. 10.1103/PhysRevLett.104.12680210.1103/PhysRevLett.104.126802 ↗
13. 10.1103/PhysRevLett.104.12680310.1103/PhysRevLett.104.126803 ↗
14. 10.1126/science.113743010.1126/science.1137430 ↗
15. 10.1103/PhysRevLett.112.13680110.1103/PhysRevLett.112.136801 ↗
16. 10.1038/nature1439810.1038/nature14398 ↗
17. 10.1103/PhysRevB.94.04512010.1103/PhysRevB.94.045120 ↗
18. 10.1038/nature0230810.1038/nature02308 ↗
19. 10.1038/nature0245010.1038/nature02450 ↗
20. 10.1103/PhysRevLett.102.10760210.1103/PhysRevLett.102.107602 ↗
21. Liu Z. Q. · Phys. Rev. X · 2013 · 3 · 021010
22. 10.1103/PhysRevLett.101.25680110.1103/PhysRevLett.101.256801 ↗
23. 10.1007/s10005001004510.1007/s100050010045 ↗
24. 10.1080/14786435.2010.51898310.1080/14786435.2010.518983 ↗
25. 10.1103/PhysRevLett.103.22680210.1103/PhysRevLett.103.226802 ↗
26. 10.1126/science.110289610.1126/science.1102896 ↗
27. 10.1103/PhysRevB.92.07530910.1103/PhysRevB.92.075309 ↗
28. 10.1103/PhysRevB.75.12140410.1103/PhysRevB.75.121404 ↗
29. 10.1103/PhysRevLett.99.15550210.1103/PhysRevLett.99.155502 ↗
30. 10.1038/ncomms611810.1038/ncomms6118 ↗
31. 10.1002/admi.20130000110.1002/admi.201300001 ↗
32. 10.1038/ncomms923910.1038/ncomms9239 ↗
33. 10.17815/jlsrf-2-10610.17815/jlsrf-2-106 ↗
34. 10.17815/jlsrf-2-6710.17815/jlsrf-2-67 ↗