journal article·2017-10Open access

Electrostatically tuned dimensional crossover in LaAlO3/SrTiO3 heterostructures

Michelle Tomczyk, Rongpu Zhou, Hyungwoo Lee, Jung-Woo Lee, Guanglei Cheng, Mengchen Huang, Patrick Irvin, Chang-Beom Eom, Jeremy Levy

APL Materials· Volume 5· Issue 10

Abstract

We report a gate-tunable dimensional crossover in sub-micrometer-scale channels created at the LaAlO3/SrTiO3 interface. Conducting channels of widths 10 nm and 200 nm are created using conducting atomic force microscope lithography. Under sufficient negative back-gate tuning, the orbital magnetoconductance of the 200 nm channel is strongly quenched, and residual signatures of low-field weak-antilocalization become strikingly similar to that of the 10 nm channel. The dimensional crossover for the 200 nm channel takes place near the conductance quantum G = 2e2/h. The ability to tune the dimensionality of narrow LaAlO3/SrTiO3 channels has implications for interpreting transport in a variety of gate-tunable oxide-heterostructure devices.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Electronic and Structural Properties of Oxides · Magnetic and transport properties of perovskites and related materials · Advanced Condensed Matter Physics

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

Affiliations

Department of Physics and Astronomy, University of Pittsburgh, Pittsburgh, Pennsylvania 15260, USA

Pittsburgh Quantum Institute, Pittsburgh, Pennsylvania 15260, USA

Department of Materials Science and Engineering, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA

Funding

Office of Naval Research Vannevar Bush Faculty Fellowship · U.S. Department of Energy

References (28)

Show source-provided references
1. 10.1126/science.114600610.1126/science.1146006 ↗
2. 10.1103/physrevlett.104.12680310.1103/physrevlett.104.126803 ↗
3. 10.1038/nmat193110.1038/nmat1931 ↗
4. 10.1038/nature0230810.1038/nature02308 ↗
5. 10.1146/annurev-matsci-070813-11343710.1146/annurev-matsci-070813-113437 ↗
6. 10.1038/nmat375310.1038/nmat3753 ↗
7. 10.1038/nmat381010.1038/nmat3810 ↗
8. 10.1063/1.235442210.1063/1.2354422 ↗
9. 10.1103/physrevlett.112.13680110.1103/physrevlett.112.136801 ↗
10. 10.1063/1.476893610.1063/1.4768936 ↗
11. 10.7567/apex.6.08520110.7567/apex.6.085201 ↗
12. 10.1021/acs.nanolett.5b0021610.1021/acs.nanolett.5b00216 ↗
13. 10.1038/nmat213610.1038/nmat2136 ↗
14. 10.1063/1.350650910.1063/1.3506509 ↗
15. 10.1038/ncomms1068110.1038/ncomms10681 ↗
16. 10.1126/science.116829410.1126/science.1168294 ↗
17. 10.1038/nnano.2011.5610.1038/nnano.2011.56 ↗
18. 10.1038/nature1439810.1038/nature14398 ↗
19. 10.1103/physrevlett.117.09680110.1103/physrevlett.117.096801 ↗
20. 10.1038/ncomms109610.1038/ncomms1096 ↗
21. 10.1073/pnas.101484910810.1073/pnas.1014849108 ↗
22. 10.1021/nl300108810.1021/nl3001088 ↗
23. 10.1021/acs.nanolett.6b0042110.1021/acs.nanolett.6b00421 ↗
24. 10.1103/physrevx.3.01102110.1103/physrevx.3.011021 ↗
25. 10.1103/physrevb.83.07540210.1103/physrevb.83.075402 ↗
26. 10.1103/physrevlett.60.156610.1103/physrevlett.60.1566 ↗
27. 10.1021/nl303372910.1021/nl3033729 ↗
28. 10.1063/1.483185510.1063/1.4831855 ↗