The high-pressure behavior of LuFe2O4 is characterized based on synchrotron X-ray diffraction and neutron diffraction, resistivity measurements, X-ray absorption spectroscopy and infrared spectroscopy studies. The results obtained enabled us to propose a P-T phase diagram. In this study, the low pressure charge-ordering melting could be detected by synchrotron XRD in the P-T space. In addition to the ambient pressure monoclinic C2/m and rhombohedral R(3) over bar m phases, the possible P (1) over bar triclinic phase, the monoclinic high pressure form Pm and metastable modulated monoclinic phases were observed; the latter modulated monoclinic phases were not observed in the present neutron diffraction data. Furthermore, the transition to the Pm phase which was already characterized by strong kinetics is found to be favored at high temperature (373 K). Based on X-ray absorption spectroscopy data the Pm phase, which could be recovered at atmospheric pressure, can be explained by a change in the Fe-local environment from a five-fold coordination to a distorted 5 + 1 one.

Double-walled carbon nanotubes (DWNTs), consisting of two coaxial and weakly van der Waals coupled single-walled carbon nanotubes (SWNTs), are one of the most ideal and fundamental systems to study the effects of inter-tube coupling on the physical properties in one-dimensional structures.On this poster, we report on the investigations of individual, spatially isolated and suspended double-walled carbon nanotubes (DWNTs) by combination of high-resolution electron microscopy, electron diffraction, Rayleigh spectroscopy and Raman spectroscopy (Figure 1) [1,2]. We first present an overview of the effect of the diameters, inter-tube distance and nature (metallic or semiconducting) on the Raman signature (Radial Breathing Like [1,3,4] and Tangential Modes [4-6]) of DWNTs. We then examine the features of tangential modes and find a clear frequency shift of the inner-layer G modes as a function of the inter-tube distance with respect to the corresponding G modes in equivalent single-walled carbon nanotubes (SWNT).[4-6] These results are understood by considering the effects of the relaxation of the layers and the interaction between the relaxed structures.[7] Finally, we study the experimental excitation dependence of the G modes intensity of the constituent inner and outer SWNTs. In particular, we discuss the effects of the quantum interference between different electronic transitions on the observed behaviors.[8]References[1] D.I. Levshov et al., Carbon, 114, 141 (2017). [2] D.I. Levshov et al., Phys Rev. B 96 (2017), 195410.[3] D.I. Levshov et al., Nano Lett. 11(11) (2011), 4800. [4] H.-N. Tran et al., Adv. Nat. Sci. Nanosci. Nanotechnol. (2017), 8, 15018.[5] D. Levshov et al., J. Phys. Chem. C 119(40) (2015), 23196.[6] D.I. Levshov et al., Phys. Status Solidi B 254(11) (2017), 1700251.[7] V.N. Popov et al., Phys. Rev. B 97 (2018), 165417.[8] H.-N. Tran et al., Phys. Rev. B 95 (2017), 95 (20), 205411

We report the direct and unambiguous evidence of the existence of inner semiconducting tube (iSCT) photoluminescence (PL) from measurements performed on four individual free-standing index-identified double-walled carbon nanotubes (DWNTs). Based on thorough Rayleigh scattering, Raman scattering and PL experiments, we are able to demonstrate that the iSCT PL is observed with a quantum yield estimated as a few 10-6 independently of the semiconducting or metallic nature of the outer tube. This result is mainly attributed to ultrafast exciton transfer from inner to outer tube. Furthermore, by carrying out PL excitation experiments on the (14,1)@(15,12) DWNT, we show that the iSCT PL can be detected through the optical excitation of the outer tube (Figure 1) indicating that the exciton transfer can also occur in the opposite way.References[1] D.I. Levshov et al., Phys Rev. B 96 (2017), pp. 195410

Middle infrared response on a carbon nanotube is very weak because this homonuclear allotrope of carbon does not bear permanent dipoles. Nevertheless, a significant number of infrared phonons are predicted by the group theory. Encapsulating molecules inside nanotubes (called hybrid nanotubes in the following) is a common strategy to add new functionalities. The one-dimensional nature of single-walled carbon nanotubes (SWCNT) internal channels has been exploited here to induce a molecular order and specific interactions which are dependent of the size of the nano container.Here we report the discovery of a strong dependence on the infrared response of the hybrid nanotube due to confinement effect when dimethylquaterthiophenes are encapsulated inside SWCNTs. Results are compared to experiments performed on nanotubes where dyes are π-stacked at the outer surface. Surprisingly, the confinement properties lead to an exaltation of the infrared absorption response in the carbon nanotubes from dye molecule interactions. Thanks to the comparison between the experimental investigations and DFT calculations, we elucidate the origin of the large enhancement of this infrared absorption and demonstrate that interactions between conjugated oligomers and nanotubes can be probed.

Middle infrared response on a carbon nanotube is very weak because this homonuclear allotrope of carbon does not bear permanent dipoles. Nevertheless, a significant number of infrared phonons are predicted by the group theory. Encapsulating molecules inside nanotubes (called hybrid nanotubes in the following) is a common strategy to add new functionalities. The one-dimensional nature of single-walled carbon nanotubes (SWCNT) internal channels has been exploited here to induce a molecular order and specific interactions which are dependent of the size of the nano container (figure).Here we report the discovery of a strong dependence on the infrared response of the hybrid nanotube due to confinement effect when dimethylquaterthiophenes are encapsulated inside SWCNTs1. Results are compared to experiments performed on nanotubes where dyes are π-stacked at the outer surface. Surprisingly, the confinement properties lead to an exaltation of the infrared absorption response in the carbon nanotubes from dye molecule interactions. Thanks to the comparison between the experimental investigations and DFT calculations, we elucidate the origin of the large enhancement of this infrared absorption and demonstrate that interactions between conjugated oligomers and nanotubes can be probed.

Results and questions aboutStructural properties of molecules inside carbon nanotubes

Infrared spectrscopy : theory and applications