SYNTHESIS OF BUCKMINSTERFULLERENE IN THE WAKE OF ENERGETIC IONS

Citation
Lt. Chadderton et al., SYNTHESIS OF BUCKMINSTERFULLERENE IN THE WAKE OF ENERGETIC IONS, Nuclear instruments & methods in physics research. Section B, Beam interactions with materials and atoms, 91(1-4), 1994, pp. 71-77
Citations number
23
Categorie Soggetti
Physics, Nuclear","Nuclear Sciences & Tecnology","Instument & Instrumentation
ISSN journal
0168583X
Volume
91
Issue
1-4
Year of publication
1994
Pages
71 - 77
Database
ISI
SICI code
0168-583X(1994)91:1-4<71:SOBITW>2.0.ZU;2-5
Abstract
Experiments are described in which polymide Was irradiated with 4 x 10 (14) lithium ions/cm2 (at MeV energies), and pyrolityic graphite with 10(12) dysprosium ionS/cm2 (at GeV energies). Chromotographic analysis of the irradiated samples revealed small but definite quantities of f ullerene in every case, whilst none was detected in either the corresp onding unirradiated material or the virgin solvent. The C60 molecule ( fullerene) has been previously macroscopically synthesized in flames, sparks, arcs, ablating laser beams, and under high dose-rate electron irradiation. A common feature is the high transient energy density, fo llowed by a rapid ''quench''. The new method described here is essenti ally microscopic, based on latent particle-track formation in condense d matter.A simple theoretical model for efficient fullerene genesis co nsists of a short (approximately 2 nm long) core of highly ionized car bon only approximately 0.6 nm in diameter, wrapped about the energetic projectile ion. The lifetime of this is short (approximately 10(-15) s) relative to that of the energy deposition Process (approximately 10 (-12) s) over the long (approximately 200 mum) particle trajectory, so that primary excited electrons have very quickly lost their energy an d remanent energy is vested in excited atoms. This core is the dense p rimaeval ''gas'' which most probably gives rise, in the absence of inh omogeneities and impurities, to homogeneous ''nucleation and growth'' of fullerene molecules (from C, C2* etc). Fullerene formation most li kely begins first at the outer track wall, and proceeds inwardly as pa rt of the ''quench''. This model for fullerene genesis is equally appr opriate for earlier methods of experimental production. In each case a high energy density is required for a high volume density of excited carbon, and there is probably a critical lower threshold energy. The a bility to transform graphite, and probably both diamond and amorphous carbon, to the new allotrope of carbon, also means that we are dealing with a phase transition of the first order - a ''reconstructive trans formation''.