Double wall carbon nanotubes (DWCNTs) have proven to have a very good structural stability when exposed to high static pressures. We report here on the study of DWCNTs after application of shock wave (dynamic) compression up to 36 GPa in a recovery assembly. TEM images of so‐treated samples reveal a threshold between 19 and 26 GPa of shock wave compression above which significant structural damage is induced whereas only minor damage can be detected below. The threshold detected with TEM coincides well with the collapse pressure of DWCNTs previously reported [You et al., High Press. Res. 31, 186 (2011); Aguiar et al., Phys. Chem. C 115, 5378 (2011)]. Raman data demonstrate a gradual accumulation of structural defects via an increase in D‐band to G‐band intensity ratio (ID/IG‐ratio) from ∼0.2 to ∼0.8 in going from the source CNT material to the nanotubes after compression to 36 GPa. Despite severe damage; the DWCNTs exposed to 36 GPa of shock wave compression survived which is evidenced by Raman spectra. The DWCNTs demonstrate a higher susceptibility to structural damage under dynamic than static pressure.
Équipe 104 : NanomatériauxInternational audienceWe report on a first study of single walled carbon nanotubes (SWCNTs) after application of dynamic (shock) compression. The experiments were conducted at 19 GPa and 36 GPa in a recovery assembly. For comparison, an experiment at a static pressure of 36 GPa was performed on the material from the same batch in a diamond anvil cell (DAC). After the high pressure treatment the samples were characterized by Raman spectroscopy and transmission electron microscopy (TEM). After exposure to 19 GPa of shock compression the CNT material exhibited substantial structural damage such as CNT wall disruption, opening of the tube along its axis (unzipping) and tube shortening (cutting). Dynamic compression to 36 GPa resulted in essentially complete CNT destruction whereas at least a fraction of the nanotubes was recovered after 36 GPa of static compression though severely damaged. The results of these shock wave experiments underline the prospect of using SWCNTs as reinforcing units in material WILEY-VCH Verlag GmbH &Co. KGaA, Weinheim
1074, Web: www.ltu.seWe have studied the thermal and chemical stability of HiPCOproduced single-walled carbon nanotube bundles to high laser power in air and argon. The samples were exposed to 110 kW/ cm 2 during 8 h with a 1.96 eV laser and the temperature was monitored via downshift of G þ -Raman peak. The structural changes in the carbon nanotubes (CNTs) caused by laser heating were monitored by recording their Raman spectra at ambient T (reference conditions) to ensure unaltered resonance conditions. The initial temperature was estimated to be 550 8C and 870 8C in air and argon, respectively. The Raman signal intensity from the CNTs radial breathing mode (RBM) increased rapidly at the beginning of the laser heating both under air and argon due to desorption of impurities for all but the smallest diameter CNTs. The temperature dropped by 30% under argon and 60% under air due to destruction of the absorbers -CNTs in resonance with incident radiation. The final RBM spectra exhibited intensity loss only for the smallest diameter CNTs in argon atmosphere and for all but the largest diameter CNTs in air. Our results demonstrate the importance of (i) impurity desorption from exterior and interior of CNTs; (ii) different temperature thresholds for the CNT destruction due to oxidation and overheating; (iii) the role of photon absorbers on the thermal stability of the sample. The small diameter CNTs are more easily destroyed than large diameter ones. The metallic nanotubes also tend to have lower thermal stability.
Theory predicts that tetragonal polymeric C 60 will undergo a phase transition into a metallic phase at pressures around 20 GPa. Raman and structural experiments at high pressures confirmed formation of a new phase above 20 GPa although the question about its electrical properties was still open. We report on the first simultaneous in situ study of vibrational and electrical properties of two-dimensional (2D) tetragonal C 60 polymer at pressures up to 30 GPa in a diamond anvil cell (DAC) specially designed for this purpose. Our results reveal an anomaly in Raman spectra and a drop in electrical resistance of the sample at 20-25 GPa. We tentatively associate this anomalous behaviour with a phase transition into the conductive phase although its metallic character is yet to be proven. At high pressures the Raman spectra exhibit a high degree of disorder. Upon pressure release the order was partially restored and, more importantly, a significant amount of the initial 2D polymeric phase was recovered.
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