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Nanostructural characterization of amorphous diamondlike carbon films
Author(s) -
Michael P. Siegal,
D. R. Tallant,
J. C. Barbour,
Regina L. Simpson,
D. L. Overmyer
Publication year - 2000
Publication title -
physical review. b, condensed matter
Language(s) - English
Resource type - Journals
eISSN - 1095-3795
pISSN - 0163-1829
DOI - 10.1103/physrevb.61.10451
Subject(s) - materials science , carbon film , amorphous solid , pulsed laser deposition , raman spectroscopy , amorphous carbon , carbon fibers , thin film , substrate (aquarium) , characterization (materials science) , silicon , atom (system on chip) , nanotechnology , topology (electrical circuits) , crystallography , optoelectronics , optics , composite material , composite number , chemistry , mathematics , combinatorics , geology , computer science , physics , oceanography , embedded system
Nanostructural characterization of amorphous diamondlike carbon (a-C) films grown on silicon using pulsed-laser deposition (PLD) is correlated to both growth energetic and film thickness. Raman spectroscopy and x-ray reflectivity probe both the topological nature of 3- and 4-fold coordinated carbon atom bonding and the topographical clustering of their distributions within a given film. In general, increasing the energetic of PLD growth results in films becoming more ``diamondlike'', i.e. increasing mass density and decreasing optical absorbance. However, these same properties decrease appreciably with thickness. The topology of carbon atom bonding is different for material near the substrate interface compared to material within the bulk portion of an a-C film. A simple model balancing the energy of residual stress and the free energies of resulting carbon topologies is proposed to provide an explanation of the evolution of topographical bonding clusters in a growing a-C film

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