arXiv subjects

G. Diamantopoulos

Publications and source records attributed to G. Diamantopoulos.

3 recordsLinked to original sources

arXiv2020

The Peculiar Size and Temperature Dependence of Water Diffusion in Carbon Nanotubes studied with 2D NMR Diffusion-Relaxation D-T2eff Spectroscopy

It is well known that water inside hydrophobic nano-channels diffuses faster than bulk water. Recent theoretical studies have shown that this enhancement depends on the size of the hydrophobic nanochannels. However, experimental evidence of this dependence is lacking. Here, by combining two-dimensional Nuclear Magnetic Resonance (NMR) diffusion-relaxation D-T2eff spectroscopy in the stray field of a superconducting magnet, and Molecular Dynamics (MD) simulations, we analyze the size dependence of water dynamics inside carbon nanotubes (CNTs) of different diameters (1.1 nm to 6.0 nm), in the temperature range of 265K to 305K. Depending on the CNTs diameter, the nanotube water is shown to resolve in two or more tubular components acquiring different self-diffusion coefficients. Most notable, a favourable CNTs diameter range 3.0-4.5 nm is experimentally verified for the first time, in which water molecule dynamics at the centre of the CNTs exhibit distinctly non-Arrhenius behaviour, characterized by ultrafast diffusion and extraordinary fragility, a result of significant importance in the efforts to understand water behaviour in hydrophobic nanochannels.

physics.chem-ph↗

arXiv2017

Ultrafast stratified diffusion of water inside carbon nanotubes. Direct experimental evidence with 2D (D-T2) NMR spectroscopy

Water, when confined at the nanoscale acquires extraordinary transport properties. And yet there is no direct experimental evidence of these properties at nanoscale resolution. Here, by using 2D NMR diffusion-relaxation (D-T2) and spin-lattice - spin-spin relaxation (T1-T2) spectroscopy, we succeeded to resolve at the nanoscale water diffusion in single and double-walled carbon nanotubes (SWCNT/DWCNT). In SWCNTs, spectra display the characteristic shape of uniform water diffusion restricted in one dimension. Remarkably, in DWCNTs water is shown to split into two axial components with the inner one acquiring unusual flow properties: high fragility, ultrafast self-diffusion coefficient, and "rigid" molecular environment, revealing a stratified cooperative motion mechanism to underlie fast diffusion in water saturated CNTs.

cond-mat.mes-hall↗

arXiv2009

Spin order and lattice frustration in optimally doped manganites. A high temperature NMR study.

The physics underlying the complex glassy phenomena, which accompany the formation of polarons in optimally doped manganites (ODM) is a cumbersome issue with many unexplained aspects. In this article we present $^{139}$La and $^{55}$Mn NMR in the temperature range 80K - 900K of ODM La$_{0.67}$Ca$_{0.33}$MnO$_3$. We show that local lattice distortions, established in the Paramagnetic (PM) phase for $T<700$K, induce a genuine spin-glass state, which for $T<T_c$ consolidates with the Ferromagnetic (FM) state into a single thermodynamic phase. Comparative NMR experiments on La$_{0.77}$Ca$_{0.23}$MnO$_3$, La$_{0.59}$Ca$_{0.41}$MnO$_3$, and La$_{0.70}$Sr$_{0.30}$MnO$_3$ demonstrate the dominant role of lattice distortions, which appear to control (i) the stability of the spin glass phase component and (ii) the kind (1st or 2nd order) of the PM-FM phase transition. The experimental results are in agreement with the predictions of the compressible random bond - random field Ising model, where consideration of a strain field induced by lattice distortions, is shown to invoke at $T_c$ a discontinuous (1st order like) change of both the FM and the "glassy" Edwards-Anderson (EA) order parameters.

cond-mat.str-el↗