Pulse deposition of Au on graphite
Samo za registrovane korisnike
1996
Članak u časopisu (Objavljena verzija)
Metapodaci
Prikaz svih podataka o dokumentuApstrakt
In this paper we present pulse deposition as a new method to favor the self-assembly of nanostructured materials. Nucleation and growth of gold thin layers deposited on highly oriented pyrolytic graphite substrate have been studied using scanning tunneling microscopy in air. Depositions were performed in a pulsed regime and, for comparison, continuously in time. Much higher cluster density and better arrangement of clusters are obtained for pulse deposition than for gold deposited continuously. The formation of the channel structure of the deposited layer is favored and achieved earlier. The results indicate that the number of surface defect sites increases with subsequent pulses, behavior attributed to the previously formed clusters taking on the role of surface defect sites.
Ključne reči:
deposition process / nucleation / physical vapour deposition / scanning tunnelling microscopyIzvor:
Thin Solid Films, 1996, 288, 1-2, 212-216Izdavač:
- Elsevier
DOI: 10.1016/S0040-6090(96)08827-X
ISSN: 0040-6090
WoS: A1996VZ20500040
Scopus: 2-s2.0-0030285134
Institucija/grupa
IHTMTY - JOUR AU - Rakočević, Zlatko Lj. AU - Štrbac, Svetlana AU - Peruško, Davor AU - Bibić, Nataša M. AU - Nenadović, T. PY - 1996 UR - https://cer.ihtm.bg.ac.rs/handle/123456789/4266 AB - In this paper we present pulse deposition as a new method to favor the self-assembly of nanostructured materials. Nucleation and growth of gold thin layers deposited on highly oriented pyrolytic graphite substrate have been studied using scanning tunneling microscopy in air. Depositions were performed in a pulsed regime and, for comparison, continuously in time. Much higher cluster density and better arrangement of clusters are obtained for pulse deposition than for gold deposited continuously. The formation of the channel structure of the deposited layer is favored and achieved earlier. The results indicate that the number of surface defect sites increases with subsequent pulses, behavior attributed to the previously formed clusters taking on the role of surface defect sites. PB - Elsevier T2 - Thin Solid Films T1 - Pulse deposition of Au on graphite VL - 288 IS - 1-2 SP - 212 EP - 216 DO - 10.1016/S0040-6090(96)08827-X ER -
@article{ author = "Rakočević, Zlatko Lj. and Štrbac, Svetlana and Peruško, Davor and Bibić, Nataša M. and Nenadović, T.", year = "1996", abstract = "In this paper we present pulse deposition as a new method to favor the self-assembly of nanostructured materials. Nucleation and growth of gold thin layers deposited on highly oriented pyrolytic graphite substrate have been studied using scanning tunneling microscopy in air. Depositions were performed in a pulsed regime and, for comparison, continuously in time. Much higher cluster density and better arrangement of clusters are obtained for pulse deposition than for gold deposited continuously. The formation of the channel structure of the deposited layer is favored and achieved earlier. The results indicate that the number of surface defect sites increases with subsequent pulses, behavior attributed to the previously formed clusters taking on the role of surface defect sites.", publisher = "Elsevier", journal = "Thin Solid Films", title = "Pulse deposition of Au on graphite", volume = "288", number = "1-2", pages = "212-216", doi = "10.1016/S0040-6090(96)08827-X" }
Rakočević, Z. Lj., Štrbac, S., Peruško, D., Bibić, N. M.,& Nenadović, T.. (1996). Pulse deposition of Au on graphite. in Thin Solid Films Elsevier., 288(1-2), 212-216. https://doi.org/10.1016/S0040-6090(96)08827-X
Rakočević ZL, Štrbac S, Peruško D, Bibić NM, Nenadović T. Pulse deposition of Au on graphite. in Thin Solid Films. 1996;288(1-2):212-216. doi:10.1016/S0040-6090(96)08827-X .
Rakočević, Zlatko Lj., Štrbac, Svetlana, Peruško, Davor, Bibić, Nataša M., Nenadović, T., "Pulse deposition of Au on graphite" in Thin Solid Films, 288, no. 1-2 (1996):212-216, https://doi.org/10.1016/S0040-6090(96)08827-X . .