Pressure-induced amorphization and an amorphous-amorphous transition in densified porous silicon
Contribuinte(s) |
Institute of Mathematics & Physics (ADT) Materials Research |
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Data(s) |
09/12/2008
09/12/2008
29/11/2001
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Resumo |
Deb, S. K., Wilding, M. C., Somayazulu, M., McMillan, P. F. (2001). Pressure-induced amorphization and an amorphous-amorphous transition in densified porous silicon. Nature, 414, 528-530. RAE2008 Crystalline and amorphous forms of silicon are the principal materials used for solid-state electronics and photovoltaics technologies. Silicon is therefore a well-studied material, although new structures and properties are still being discovered1, 2, 3, 4. Compression of bulk silicon, which is tetrahedrally coordinated at atmospheric pressure, results in a transition to octahedrally coordinated metallic phases5. In compressed nanocrystalline Si particles, the initial diamond structure persists to higher pressure than for bulk material, before transforming to high-density crystals6. Here we report compression experiments on films of porous Si, which contains nanometre-sized domains of diamond-structured material7, 8, 9. At pressures larger than 10 GPa we observed pressure-induced amorphization10, 11. Furthermore, we find from Raman spectroscopy measurements that the high-density amorphous form obtained by this process transforms to low-density amorphous silicon upon decompression. This amorphous?amorphous transition is remarkably similar to that reported previously for water12, 13, which suggests an underlying transition between a high-density and a low-density liquid phase in supercooled Si (refs 10, 14, 15). The Si melting temperature decreases with increasing pressure, and the crystalline semiconductor melts to a metallic liquid with average coordination 5 (ref. 16). Peer reviewed |
Formato |
3 |
Identificador |
Deb , S K , Wilding , M C , Somayazulu , M & McMillan , P F 2001 , ' Pressure-induced amorphization and an amorphous-amorphous transition in densified porous silicon ' Nature , vol 414 , pp. 528-530 . DOI: 10.1038/35107036 1476-4687 PURE: 89657 PURE UUID: 13121924-e18a-4098-b08b-c7b24842fc52 dspace: 2160/1494 |
Idioma(s) |
eng |
Relação |
Nature |
Tipo |
/dk/atira/pure/researchoutput/researchoutputtypes/contributiontojournal/article |
Direitos |