Liquid crystals have found wide applications in many fields ranging from detergents to information displays and they are also increasingly being used in the ‘bottom-up' self-assembly approach of material nano-structuration. Moreover, liquid-crystalline organizations are frequently observed by biologists. Here we show that one of the four major lyotropic liquid-crystal phases, the columnar one, is much more stable on dilution than reported so far in literature. Indeed, aqueous suspensions of imogolite nanotubes, at low ionic strength, display the columnar liquid-crystal phase at volume fractions as low as ∼0.2%. Consequently, due to its low visco-elasticity, this columnar phase is easily aligned in an alternating current electric field, in contrast with usual columnar liquid-crystal phases. These findings should have important implications for the statistical physics of the suspensions of charged rods and could also be exploited in materials science to prepare ordered nanocomposites and in biophysics to better understand solutions of rod-like biopolymers.

Micron-long germanium-based double-walled imogolite nanotubes were synthesized at high concentrations, as evidenced by cryo-TEM, AFM, SAXS and IR characterization methods. In addition, the spontaneous formation of a liquid-crystalline phase was observed. The novel synthesis route made it possible for the first time to obtain both long and concentrated germanium-based imogolite-like nanotubes in a single step.

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Inorganic nanotubes represent an emerging class of nanobuilding blocks. Among them, imogolites are alumino-silicate or alumino-germanate nanotubes with well controlled diameter and helicity. As such, they constitute a model platform for the study of molecular interactions and confinement at the nanoscale, complementing the one constituted by carbon nanotubes. We focus here on double-walled alumino-germanate nanotubes, discovered very recently [1]. They are formed of two concentric tubes (figure inset), with respective internal diameters of 1.6 and 3.1nm and up to 1 micron in length [2]. We report the first experimental study, using wide angle x-ray scattering, performed on films of oriented nanotubes (figure). Structural changes of the nanotubes and behavior of the confined water under heating are investigated in-situ. The study of oriented samples gives new information that is not available with powder diffraction. Above all, the contribution to the scattering signal of internal and external tubes can be separated as well as the translational/rotational correlations. The use of wide image plate detectors allows one to access large area of the reciprocal space in a single image. Simulations of the two-dimensionnal scattering diagrams will be presented. A key question, the correlation between internal and external tube, which is of great interest for understanding friction properties at the nanoscale, will be discussed.

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