Networks of ultra-fine Ag nanocrystals in a Teflon AF® matrix by vapour phase e-beam-assisted deposition

被引:17
作者
Biswas, A. [1 ]
Bayer, I. S.
Marken, B.
Pounds, T. D.
Norton, M. G.
机构
[1] Univ Alaska, Nanocomposite Res Lab, Off Elect Minatruizat, Fairbanks, AK 99775 USA
[2] Washington State Univ, Sch Mech & Mat Engn, Pullman, WA 99164 USA
关键词
D O I
10.1088/0957-4484/18/30/305602
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
We have fabricated nanocomposite thin films comprising silver (Ag) nanoparticles dispersed in a Teflon AF (R) polymer matrix using electron-beam-assisted physical vapour deposition. Four different Ag nanoparticle volume fillings (20%, 35%, 70% and 75%) were achieved by varying the relative metal-polymer evaporation rates with the formation of highly crystalline Ag nanoparticles regardless of the filling ratio. The present fabrication technique allowed full control over dispersion uniformity of nanoparticles in the polymer network. At 20% and 35% metal volume fillings, the nanocomposite film morphology consists of a uniformly dispersed assembly of equiaxed isolated Ag nanoparticles. At higher metal volume fractions the nanocomposite structures displayed two different and unique Ag nanoparticle arrangements within the polymer matrix. In particular, at 70% metal filling, the formation of irregularly shaped clusters of individually assembled nanocrystals was observed. At a slightly higher volume filling (75%), larger irregularly shaped Ag nanocrystals that appeared to be the result of coalescence and grain growth were observed. Finally, a composite theory developed by Tandon and Weng was used to estimate various elastic properties of the nanocomposite films. At high metal filling, the reinforcing effect of the Ag nanoparticles was reflected as approximately a sixfold increase in the elastic modulus compared to the virgin polymer film. Possible applications of such ultra-fine metal nanoparticles networks are discussed.
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页数:6
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