journal article·2022-03-08

Direct Growth of Magnetic Non-van der Waals Cr2X3(X = S, Se, and Te) on SiO2/Si Substrates through the Promotion of KOH

Song Luo, Xukun Zhu, Hang Liu, Shixin Song, Yang Chen, Chen Liu, Wenzhe Zhou, Caisheng Tang, Gonglei Shao, Yuanyuan Jin, Jie Guan, Vincent C. Tung, Huimin Li, Xuli Chen, Fangping Ouyang, Song Liu

Chemistry of Materials· Volume 34· Issue 5
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Abstract

Two-dimensional (2D) magnetic materials can be used to construct multifunctional electronic and spintronic devices attributed to their unique 2D restricted magnetic properties. However, some magnetic materials are non-van der Waals materials, and the substrate used in chemical vapor deposition (CVD) is usually a van der Waals substrate like mica. This kind of substrate can cause transfer problems and increase the complexity of equipment fabrication or magnetic measurement. It is meaningful to further optimize the current production process for realizing good repeatability and simple fabrication. Growing materials on SiO2/Si can directly make electronic devices and measure magnetic properties. Herein, we use potassium hydroxide to modify a SiO2/Si substrate and succeed in growing Cr2X3 (X = S, Se, and Te) directly on the SiO2/Si surface by a CVD method. OH– is attached to the surface of SiO2/Si, thereby inhibiting the growth of thin layered Cr2X3 along the [001] zone axis. Through density function theory calculation, it is verified that the formation energy of Cr2S3 and SiO2/Si heterojunction can be enlarged by introducing OH–, which is beneficial to the growth of Cr2X3 on the SiO2/Si surface. At the same time, we have also achieved Cr2S3 and Cr2Se3 with controlled size and thickness. The thinnest thickness of the three materials on SiO2/Si can be close to 1 unit cell. Cr2S3, Cr2Se3, and Cr2Te3 nanosheets exhibit ferrimagnetic, spin glass, and ferromagnetic behavior, respectively. This work can provide a new method for the growth of non-van der Waals 2D materials on SiO2/Si, and it is of great significance to the fabrication of spintronic devices.
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Research context

OpenAlex topics: 2D Materials and Applications · MXene and MAX Phase Materials · Graphene research and applications

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

Affiliations

Institute of Chemical Biology and Nanomedicine (ICBN), State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha 410082, P. R. China

Powder Metallurgy Research Institute and State Key Laboratory of Powder Metallurgy, Central South University, Changsha 410083, P. R. China

Physical Sciences and Engineering Division, KAUST Solar Centre, King Abdullah University of Science and Technology (KAUST), Thuwal 23955, Kingdom of Saudi Arabia

School of Physics, Southeast University, Nanjing 211189, P. R. China

College of Materials Science and Engineering, Hunan University, Changsha 410082, P. R. China

Powder Metallurgy Research Institute and State Key Laboratory of Powder Metallurgy, School of Physics and Electronics, Institute of Super-Microstructure and Ultrafast Process in Advanced Materials, Central South University, Changsha 410083, P. R. China

Funding

National Natural Science Foundation of China

References (44)

Show source-provided references
1. 10.1002/inf2.1204810.1002/inf2.12048 ↗
2. 10.1038/nphys139910.1038/nphys1399 ↗
3. 10.1021/acs.nanolett.8b0305710.1021/acs.nanolett.8b03057 ↗
4. 10.1103/PhysRevB.101.12540110.1103/PhysRevB.101.125401 ↗
5. 10.1038/nature2206010.1038/nature22060 ↗
6. 10.1038/s41563-018-0149-710.1038/s41563-018-0149-7 ↗
7. 10.1021/acs.nanolett.8b0068310.1021/acs.nanolett.8b00683 ↗
8. 10.1038/s41467-020-17253-x10.1038/s41467-020-17253-x ↗
9. 10.1038/nature2239110.1038/nature22391 ↗
10. 10.1038/s41565-018-0063-910.1038/s41565-018-0063-9 ↗
11. 10.1038/s41586-018-0626-910.1038/s41586-018-0626-9 ↗
12. 10.1038/s41565-018-0121-310.1038/s41565-018-0121-3 ↗
13. 10.1038/ncomms887310.1038/ncomms8873 ↗
14. 10.1088/2053-1583/ab1bc010.1088/2053-1583/ab1bc0 ↗
15. Xie L. · Adv. Electron. Mat. · 2020 · 7 · 200096210.1002/aelm.202000962 ↗
16. 10.1021/acsanm.1c0039110.1021/acsanm.1c00391 ↗
17. 10.1021/acsanm.9b0117910.1021/acsanm.9b01179 ↗
18. 10.1021/acsnano.0c0553410.1021/acsnano.0c05534 ↗
19. 10.1021/acs.nanolett.9b0038610.1021/acs.nanolett.9b00386 ↗
20. 10.1021/acs.nanolett.9b0512810.1021/acs.nanolett.9b05128 ↗
21. 10.1002/adma.20190589610.1002/adma.201905896 ↗
22. 10.1002/adma.20190005610.1002/adma.201900056 ↗
23. 10.1038/s41563-021-00927-210.1038/s41563-021-00927-2 ↗
24. 10.1038/s41467-021-21072-z10.1038/s41467-021-21072-z ↗
25. 10.1021/acs.chemmater.1c0122210.1021/acs.chemmater.1c01222 ↗
26. 10.1039/D0NR04108D10.1039/D0NR04108D ↗
27. 10.1002/adfm.20180588010.1002/adfm.201805880 ↗
28. 10.1021/jacs.8b0780610.1021/jacs.8b07806 ↗
29. 10.1007/s12274-020-3020-510.1007/s12274-020-3020-5 ↗
30. 10.1021/nn300726r10.1021/nn300726r ↗
31. 10.1021/acsnano.9b0364810.1021/acsnano.9b03648 ↗
32. 10.1021/acsami.9b2239710.1021/acsami.9b22397 ↗
33. 10.1021/acs.chemmater.0c0108910.1021/acs.chemmater.0c01089 ↗
34. 10.1021/acs.chemmater.1c0114710.1021/acs.chemmater.1c01147 ↗
35. 10.1021/jacs.9b1349210.1021/jacs.9b13492 ↗
36. 10.1021/acs.chemmater.9b0441610.1021/acs.chemmater.9b04416 ↗
37. 10.1103/PhysRevB.54.1116910.1103/PhysRevB.54.11169 ↗
38. 10.1103/PhysRevB.47.55810.1103/PhysRevB.47.558 ↗
39. 10.1103/PhysRevB.49.1425110.1103/PhysRevB.49.14251 ↗
40. 10.1103/PhysRevB.13.518810.1103/PhysRevB.13.5188 ↗
41. 10.1103/PhysRevB.59.175810.1103/PhysRevB.59.1758 ↗
42. 10.1103/PhysRevLett.77.386510.1103/PhysRevLett.77.3865 ↗
43. 10.1002/jcc.2049510.1002/jcc.20495 ↗
44. 10.6028/jres.049.04410.6028/jres.049.044 ↗