journal article·2011-07-22

Amorphous and Crystalline GeTe Nanocrystals

Indika U. Arachchige, Ronald Soriano, Christos D. Malliakas, Sergei A. Ivanov, Mercouri G. Kanatzidis

Advanced Functional Materials· Volume 21· Issue 14
Publisher page

Abstract

Abstract A facile method for the synthesis of crystalline and amorphous GeTe nanoparticles (NPs) using bis((trimethylsilyl)amido)germanium(II), Ge[N(SiMe3)2]2, and elemental tellurium dispersed in tri‐n‐octylphosphine (TOP) is reported. As synthesized, crystalline particles exhibit narrow dispersity at smaller sizes and tend to grow into anisotropic shapes with increasing reaction time (growth). Furthermore, crystalline GeTe NPs possess rhombohedral symmetry with absorption band energies in near IR region (0.76–0.86 eV). Amorphous GeTe particles prepared at low temperatures are nearly spherical in morphology and display amorphous‐to‐crystalline phase transition at 209–237 °C depending on their primary particle size. Detailed investigation of the local structure of the amorphous GeTe using pair distribution function (PDF) method reveals that it is closely related to that of the pressure‐ and temperature‐stabilized orthorhombic GeTe.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Phase-change materials and chalcogenides · Chalcogenide Semiconductor Thin Films · Quantum Dots Synthesis And Properties

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

References (33)

Show source-provided references
1. 10.1021/cr900040x10.1021/cr900040x ↗
2. 10.1063/1.34862010.1063/1.348620 ↗
3. 10.1038/nmat135010.1038/nmat1350 ↗
4. 10.1126/science.256.5062.142510.1126/science.256.5062.1425 ↗
5. 10.1021/cm100448310.1021/cm1004483 ↗
6. 10.1021/cg800200410.1021/cg8002004 ↗
7. 10.1021/ja062507110.1021/ja0625071 ↗
8. 10.1021/nl061102b10.1021/nl061102b ↗
9. 10.1021/ja108309s10.1021/ja108309s ↗
10. 10.1039/B917024C10.1039/B917024C ↗
11. 10.1021/cm101596510.1021/cm1015965 ↗
12. 10.1021/ja107520b10.1021/ja107520b ↗
13. Kovalenko M. V. · J. Am. Chem. Soc. · 2007 · 129 · 1354
14. 10.1039/b416066e10.1039/b416066e ↗
15. 10.1063/1.235271110.1063/1.2352711 ↗
16. 10.1002/smll.20060052910.1002/smll.200600529 ↗
17. 10.1021/ic00018a00510.1021/ic00018a005 ↗
18. 10.1063/1.172723110.1063/1.1727231 ↗
19. 10.1021/la047718310.1021/la0477183 ↗
20. 10.1103/PhysRevB.38.1326310.1103/PhysRevB.38.13263 ↗
21. 10.1063/1.165918910.1063/1.1659189 ↗
22. 10.1007/BF0054984210.1007/BF00549842 ↗
23. 10.1143/JPSJ.56.15810.1143/JPSJ.56.158 ↗
24. 10.1103/PhysRevB.36.422210.1103/PhysRevB.36.4222 ↗
25. Warren B. E. · 1990
26. 10.1021/ic50161a05610.1021/ic50161a056 ↗
27. 10.1002/pssb.1970038013610.1002/pssb.19700380136 ↗
28. 10.1021/cm00034a02910.1021/cm00034a029 ↗
29. 10.1021/ic00063a04210.1021/ic00063a042 ↗
30. 10.1021/cm00032a00410.1021/cm00032a004 ↗
31. 10.1107/S002188980301756410.1107/S0021889803017564 ↗
32. 10.1080/0895795960820140810.1080/08957959608201408 ↗
33. 10.1088/0953-8984/19/33/33521910.1088/0953-8984/19/33/335219 ↗