Disorder Control in Crystalline GeSb2Te4 and its Impact on Characteristic Length Scales
Source abstract
Abstract
Crystalline GeSb2Te4 (GST) is a remarkable material, as it allows to continuously tune the electrical resistance by orders of magnitude without involving a structural phase transition or stoichiometric changes. While well‐ordered specimen are metallic, increasing amounts of disorder eventually lead to an insulating state with vanishing conductivity in the 0 K limit, but a similar number of charge carriers. Hence, GST provides ideal grounds to explore the impact of disorder on transport properties. Here, a sputter‐deposition process is employed that enables growing biaxially textured GST films with large grain sizes on mica substrates. The resulting films exhibit a systematic variation between metallic and truly insulating specimen upon varying deposition temperature. Transport measurements reveal that their electron mean free path can be altered by a factor of 20, while always remaining more than an order of magnitude smaller than the lateral grain size. This proves unequivocally that grain boundaries play a negligible role for electron scattering, while intra‐grain scattering, presumably by disordered vacancies, dominates. These findings underline that the insulating state and the system's evolution toward metallic conductivity are intrinsic properties of the material.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Advanced Thermoelectric Materials and Devices · Phase-change materials and chalcogenides · Chalcogenide Semiconductor Thin Films
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Physikalisches Institut (IA), RWTH Aachen University 52056 Aachen Germany
Peter Grünberg Institut PGI 10, Forschungszentrum Jülich 52428 Jülich Germany
Funding
Deutsche Forschungsgemeinschaft · Seventh Framework Programme
References (30)
Show source-provided references
1. 10.1021/cr900040x10.1021/cr900040x ↗
2. 10.1038/nmat200910.1038/nmat2009 ↗
3. 10.1002/adma.20170673510.1002/adma.201706735 ↗
4. 10.1002/adma.20180377710.1002/adma.201803777 ↗
5. 10.1103/PhysRevB.81.08120410.1103/PhysRevB.81.081204 ↗
6. 10.1088/0034-4885/78/1/01300110.1088/0034-4885/78/1/013001 ↗
7. 10.1103/PhysRevB.78.22411110.1103/PhysRevB.78.224111 ↗
8. 10.1021/ic051677w10.1021/ic051677w ↗
9. 10.1038/nmat180710.1038/nmat1807 ↗
10. 10.1103/PhysRevB.73.04521010.1103/PhysRevB.73.045210 ↗
11. 10.1038/nmat293410.1038/nmat2934 ↗
12. 10.1002/adfm.20150083010.1002/adfm.201500830 ↗
13. 10.1021/acs.chemmater.7b0159510.1021/acs.chemmater.7b01595 ↗
14. 10.1038/nmat345610.1038/nmat3456 ↗
15. 10.1002/adfm.20170590110.1002/adfm.201705901 ↗
16. 10.1038/srep2384310.1038/srep23843 ↗
17. 10.1088/1361-6528/28/6/06570610.1088/1361-6528/28/6/065706 ↗
18. 10.1038/s41598-017-02710-310.1038/s41598-017-02710-3 ↗
19. 10.1116/1.57362810.1116/1.573628 ↗
20. 10.1016/j.surfrep.2016.03.00110.1016/j.surfrep.2016.03.001 ↗
21. Altshuler B. L. · Sov. Phys. JETP · 1979 · 50 · 968
22. 10.1103/PhysRevB.27.389710.1103/PhysRevB.27.3897 ↗
23. 10.1103/RevModPhys.57.28710.1103/RevModPhys.57.287 ↗
24. 10.1103/PhysRevB.60.1420910.1103/PhysRevB.60.14209 ↗
25. Möbius A. · Crit. Rev. Solid State Mater. Sci · 2018 · 1370575
26. 10.1103/PhysRevB.86.20530210.1103/PhysRevB.86.205302 ↗
27. Hikami S. · Prog. Theor. Phys · 1980 · 63 · 2
28. 10.1088/0022-3719/15/36/01810.1088/0022-3719/15/36/018 ↗
29. 10.1063/1.500050210.1063/1.5000502 ↗
30. F. R. L.Lange Dissertation Aachen Germany2016.