journal article·2015-10-27

Predicting Two-Dimensional Silicon Carbide Monolayers

Zhiming Shi, Zhuhua Zhang, Alex Kutana, Boris I. Yakobson

ACS Nano· Volume 9· Issue 10
Publisher page

Abstract

Intrinsic semimetallicity of graphene and silicene largely limits their applications in functional devices. Mixing carbon and silicon atoms to form two-dimensional (2D) silicon carbide (SixC1-x) sheets is promising to overcome this issue. Using first-principles calculations combined with the cluster expansion method, we perform a comprehensive study on the thermodynamic stability and electronic properties of 2D SixC1-x monolayers with 0 ≤ x ≤ 1. Upon varying the silicon concentration, the 2D SixC1-x presents two distinct structural phases, a homogeneous phase with well dispersed Si (or C) atoms and an in-plane hybrid phase rich in SiC domains. While the in-plane hybrid structure shows uniform semiconducting properties with widely tunable band gap from 0 to 2.87 eV due to quantum confinement effect imposed by the SiC domains, the homogeneous structures can be semiconducting or remain semimetallic depending on a superlattice vector which dictates whether the sublattice symmetry is topologically broken. Moreover, we reveal a universal rule for describing the electronic properties of the homogeneous SixC1-x structures. These findings suggest that the 2D SixC1-x monolayers may present a new "family" of 2D materials, with a rich variety of properties for applications in electronics and optoelectronics.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Graphene research and applications · Boron and Carbon Nanomaterials Research · Topological Materials and Phenomena

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

Affiliations

Institute of Theoretical Chemistry, Jilin University, Changchun 130023, People’s Republic of China

Department of Materials Science and NanoEngineering, Department of Chemistry, and the Smalley Institute for Nanoscale Science and Technology, Rice University, Houston, Texas 77005, United States

Funding

Army Research Office · Office of Naval Research

References (45)

Show source-provided references
1. 10.1038/nature0423310.1038/nature04233 ↗
2. 10.1126/science.112592510.1126/science.1125925 ↗
3. 10.1038/nature0423510.1038/nature04235 ↗
4. 10.1103/PhysRevB.50.1491610.1103/PhysRevB.50.14916 ↗
5. 10.1103/PhysRevB.61.999410.1103/PhysRevB.61.9994 ↗
6. 10.1103/PhysRevB.76.07513110.1103/PhysRevB.76.075131 ↗
7. 10.1103/PhysRevLett.102.23680410.1103/PhysRevLett.102.236804 ↗
8. 10.1063/1.352421510.1063/1.3524215 ↗
9. 10.1103/PhysRevLett.108.15550110.1103/PhysRevLett.108.155501 ↗
10. 10.1021/nl301047g10.1021/nl301047g ↗
11. 10.1103/PhysRevLett.109.05680410.1103/PhysRevLett.109.056804 ↗
12. 10.1021/nl304347w10.1021/nl304347w ↗
13. 10.1103/PhysRevLett.108.24550110.1103/PhysRevLett.108.245501 ↗
14. 10.1103/PhysRevLett.99.18680110.1103/PhysRevLett.99.186801 ↗
15. 10.1021/nl203065e10.1021/nl203065e ↗
16. 10.1103/PhysRevB.80.15545310.1103/PhysRevB.80.155453 ↗
17. 10.1126/science.119497510.1126/science.1194975 ↗
18. 10.1103/PhysRevB.77.07540310.1103/PhysRevB.77.075403 ↗
19. 10.1021/jp210536m10.1021/jp210536m ↗
20. 10.1016/j.diamond.2006.01.01310.1016/j.diamond.2006.01.013 ↗
21. 10.1002/adma.20040126310.1002/adma.200401263 ↗
22. 10.1002/anie.20110600410.1002/anie.201106004 ↗
23. 10.1021/nl403010s10.1021/nl403010s ↗
24. 10.1021/ja107711m10.1021/ja107711m ↗
25. 10.1021/jp412633y10.1021/jp412633y ↗
26. 10.1021/ja405359a10.1021/ja405359a ↗
27. 10.1021/jz502093c10.1021/jz502093c ↗
28. 10.1039/C4NR00177J10.1039/C4NR00177J ↗
29. 10.1103/PhysRevLett.111.14550210.1103/PhysRevLett.111.145502 ↗
30. 10.1103/PhysRevLett.110.08550110.1103/PhysRevLett.110.085501 ↗
31. 10.1063/1.300643110.1063/1.3006431 ↗
32. 10.1039/C4NR03247K10.1039/C4NR03247K ↗
33. 10.1063/1.476973110.1063/1.4769731 ↗
34. 10.1103/PhysRevLett.97.21680310.1103/PhysRevLett.97.216803 ↗
35. 10.1063/1.357128210.1063/1.3571282 ↗
36. 10.1103/PhysRevB.46.180410.1103/PhysRevB.46.1804 ↗
37. 10.1002/smll.20120298810.1002/smll.201202988 ↗
38. 10.1103/PhysRevLett.71.438910.1103/PhysRevLett.71.4389 ↗
39. 10.1016/0378-4371(84)90096-710.1016/0378-4371(84)90096-7 ↗
40. 10.1016/S0364-5916(02)80006-210.1016/S0364-5916(02)80006-2 ↗
41. 10.1103/PhysRevLett.80.89110.1103/PhysRevLett.80.891 ↗
42. 10.1103/PhysRevB.50.1795310.1103/PhysRevB.50.17953 ↗
43. 10.1103/PhysRevB.59.175810.1103/PhysRevB.59.1758 ↗
44. 10.1103/PhysRevB.54.1116910.1103/PhysRevB.54.11169 ↗
45. 10.1103/PhysRevB.70.24130310.1103/PhysRevB.70.241303 ↗