Reversible Amorphous–Crystalline Phase Transformation in an Ultrathin van der Waals FeTe System
Source abstract
Abstract
Searching for new phase-change materials for memory and neuromorphic device applications and further understanding the phase transformation mechanism are attracting wide attention. Phase transformation from the amorphous phase to the crystal phase has been unraveled in iron telluride (FeTe) bulk film deposited by pulsed laser deposition, recently. However, the van der Waals-layered feature of FeTe in the crystal form was not noted, which will benefit the scaling of the memory devices and shine light on phase-change heterostructures or interfacial phase-change materials. Moreover, the demonstration of advanced memory or neuromorphic device applications is lacking. Here, we investigate the phase transformation of FeTe starting from mechanically exfoliated van der Waals layers from a bulk single crystal. Surficial amorphization is revealed at the surface layers of FeTe flakes after exfoliation under ambient conditions, which could be transformed back to the crystalline phase with laser irradiation or heating. The conductance drop of the flake devices near 400 K verifies the phase transformation electrically. Memristor behavior of the amorphous surface in FeTe has been further demonstrated, proving the reversibility of the phase transformation and shining light on the possible applications of neuromorphic devices.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Phase-change materials and chalcogenides · Quantum Dots Synthesis And Properties · Chalcogenide Semiconductor Thin Films
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
College of Advanced Interdisciplinary Studies & Hunan Provincial Key Laboratory of Novel Nano-Optoelectronic Information Materials and Devices, National University of Defense Technology, Changsha 410073, China
Nanhu Laser Laboratory, National University of Defense Technology, Changsha 410073, China
School of Physics, Beijing Institute of Technology, Beijing 100081, China
Funding
National Natural Science Foundation of China
References (35)
Show source-provided references
1. 10.1038/nmat200910.1038/nmat2009 ↗
2. 10.1038/nmat233010.1038/nmat2330 ↗
3. Pearson A. D. · Adv. Glass Technol. · 1962 · 2 · 357
4. 10.1038/s41578-018-0076-x10.1038/s41578-018-0076-x ↗
5. 10.1126/science.aao321210.1126/science.aao3212 ↗
6. 10.1126/science.abi633210.1126/science.abi6332 ↗
7. 10.1039/C8NR06567E10.1039/C8NR06567E ↗
8. 10.1021/acsomega.7b0081210.1021/acsomega.7b00812 ↗
9. 10.1021/cm200835a10.1021/cm200835a ↗
10. 10.1039/C9NR02112D10.1039/C9NR02112D ↗
11. 10.3390/ma1008086210.3390/ma10080862 ↗
12. 10.1126/science.aay029110.1126/science.aay0291 ↗
13. 10.1002/adma.20170356810.1002/adma.201703568 ↗
14. 10.1073/pnas.080732510510.1073/pnas.0807325105 ↗
15. 10.1016/0038-1098(70)90619-810.1016/0038-1098(70)90619-8 ↗
16. 10.1103/PhysRevLett.96.13610110.1103/PhysRevLett.96.136101 ↗
17. 10.1016/j.physc.2015.02.02010.1016/j.physc.2015.02.020 ↗
18. 10.1038/s41467-020-17253-x10.1038/s41467-020-17253-x ↗
19. 10.1021/acsnano.1c0573810.1021/acsnano.1c05738 ↗
20. 10.1016/j.mattod.2020.11.02210.1016/j.mattod.2020.11.022 ↗
21. 10.1016/j.actamat.2016.04.01710.1016/j.actamat.2016.04.017 ↗
22. 10.1063/1.471907410.1063/1.4719074 ↗
23. 10.1016/j.scib.2022.06.02210.1016/j.scib.2022.06.022 ↗
24. 10.1016/j.physc.2018.02.04210.1016/j.physc.2018.02.042 ↗
25. 10.1103/PhysRevB.83.03510310.1103/PhysRevB.83.035103 ↗
26. 10.1088/2053-1591/aafea610.1088/2053-1591/aafea6 ↗
27. 10.1103/PhysRevLett.25.22210.1103/PhysRevLett.25.222 ↗
28. 10.1126/science.125168210.1126/science.1251682 ↗
29. 10.1103/PhysRevB.78.13451410.1103/PhysRevB.78.134514 ↗
30. 10.1126/science.aab317510.1126/science.aab3175 ↗
31. 10.1103/PhysRevB.79.14051010.1103/PhysRevB.79.140510 ↗
32. 10.1109/jetcas.2016.254771810.1109/jetcas.2016.2547718 ↗
33. 10.1021/acsnano.2c0035010.1021/acsnano.2c00350 ↗
34. 10.1021/acs.nanolett.8b0099410.1021/acs.nanolett.8b00994 ↗
35. 10.1002/advs.20190296410.1002/advs.201902964 ↗