Thermodynamic and Dynamic Transitions and Interaction Aspects in Reorientation Dynamics of Molecular Probe in Organic Compounds: A Series of 1-alkanols with TEMPO.

The spectral and dynamic properties of 2,2,6,6-tetramethyl-1-piperidinyloxy (TEMPO) in a series of 1-alkanols ranging from methanol to 1-decanol over a temperature range 100-300 K were investigated by electron spin resonance (ESR). The main characteristic ESR temperatures connected with slow to fast motion regime transition; T50G 's and TX1fast 's are situated above the corresponding glass temperatures, Tg, and for the shorter members, the T50G 's lie above or close to melting point, Tm, while the longer ones the T50G < Tm relationship indicates that the TEMPO molecules are in the local disordered regions of the crystalline media. The T50G 's and especially TX1fast 's are compared with the dynamic crossover temperatures, TXVISC = 8.72M0.66, as obtained by fitting the viscosity data in the liquid n-alkanols with the empirical power law. In particular, for NC > 6, the TX1fast 's lie rather close to the TXVISC resembling apolar n-alkanes [PCCP 2018,20,11145-11151], while for NC < 6, they are situated in the vicinity of Tm. The absence of a coincidence for lower1-alkanols indicates that the T50G is significantly influenced by the mutual interaction between the polar TEMPO and the protic polar medium due to the increased polarity and proticity destroyed by the larger-scale melting transition.

A Combined Atomic and Molecular Probe Characterization of Aromatic Hydrocarbons via PALS and ESR: Methylbenzene.

A combined study of one of the simplest aromatic hydrocarbons, i.e., methylbenzene (toluene) (TOL), via the annihilation of an ortho-positronium (o-Ps) probe via positron annihilation lifetime spectroscopy (PALS) and the rotation dynamics of nitroxide spin probe 2,2,6,6-tetramethyl-piperidinyl-1-oxy (TEMPO) using electron spin resonance (ESR) over a wide temperature range, 10-300 K, is reported. The o-Ps lifetime, τ3, and the relative o-Ps intensity, I3, as a function of temperature exhibit changes defining several characteristic PALS temperatures in the slowly and rapidly cooled samples. Similarly, the spectral parameter of TEMPO mobility in TOL, 2Azz', and its correlation time, τc, reveal several effects at a set of the characteristic ESR temperatures, which were determined and compared with the PALS results. Finally, the physical origins of the changes in free volume expansion and spin probe mobility are revealed. They are reflected in a series of the mutual coincidences between the characteristic PALS and ESR temperatures and appropriate complementary thermodynamic and dynamic techniques.

On the Mutual Relationships between Molecular Probe Mobility and Free Volume and Polymer Dynamics in Organic Glass Formers: cis-1,4-poly(isoprene).

We report on the reorientation dynamics of small spin probe 2,2,6,6-tetramethylpiperidinyl-1-oxyl (TEMPO) in cis-1,4-poly(isoprene) (cis-1,4-PIP10k) from electron spin resonance (ESR) and the free volume of cis-1,4-PIP10k from positron annihilation lifetime spectroscopy (PALS) in relation to the high-frequency relaxations of cis-1,4-PIP10k using light scattering (LS) as well as to the slow and fast processes from broadband dielectric spectroscopy (BDS) and neutron scattering (NS). The hyperfine coupling constant, 2Azz '(T), and the correlation times, τ c(T), of cis-1,4-PIP10k/TEMPO system as a function of temperature exhibit several regions of the distinct spin probe TEMPO dynamics over a wide temperature range from 100 K up to 350 K. The characteristic ESR temperatures of changes in the spin probe dynamics in cis-1,4-PIP10k/TEMPO system are closely related to the characteristic PALS ones reflecting changes in the free volume expansion from PALS measurement. Finally, the time scales of the slow and fast dynamics of TEMPO in cis-1,4-PIP10k are compared with all of the six known slow and fast relaxation modes from BDS, LS and NS techniques with the aim to discuss the controlling factors of the spin probe reorientation mobility in polymer, oligomer and small molecular organic glass-formers.

Dynamics of Confined Short-Chain alkanol in MCM-41 by Dielectric Spectroscopy: Effects of matrix and system Treatments and Filling Factor.

The dynamics of n-propanol confined in regular MCM-41 matrix with the pore size Dpore = 40 Å, under various matrix conditioning and sample confining conditions, using broadband dielectric spectroscopy (BDS), is reported. First, various drying procedures with the capacitor filling under air or N2 influence the BDS spectra of the empty MCM-41 and the confined n-PrOH/MCM-41 systems, but have a little effect on the maximum relaxation time of the main process. Finally, various filling factors of n-PrOH medium in the optimally treated MCM-41 system lead to unimodal or bimodal spectra interpreted in terms of the two distinct dynamic phases in the confined states.

Molecular probe dynamics and free volume heterogeneities in n-propanol confined in a regular MCM-41 matrix by ESR and PALS.

A combined investigation of the spin probe TEMPO mobility and the free volume holes in n-propanol (n-PrOH) confined in a regular virgin MCM-41 matrix by means of ESR or PALS techniques, respectively, is reported. Dynamics of spin probe TEMPO alters at several characteristic ESR temperatures which are close to the characteristic PALS ones reflecting the changes in o-Ps annihilation and the related free volume. Correlations between these characteristic ESR and PALS temperatures indicate the common physical origins of the respective changes in the free volume expansion and the TEMPO mobility in the confined liquid n-PrOH. The significant difference in dynamic heterogeneity of TEMPO after confinement and free volume dispersion reflect the strongly altered structural-dynamic relationships in the confined n-PrOH medium with respect to the bulk situation.

ESR evidence of the dynamic crossover in the supercooled liquid states of a series of solid n-alkanes.

A study of the rotation dynamics of the spin probe TEMPO by electron spin resonance (ESR) spectroscopy in a series of six short- and medium-sized n-alkanes is presented. In addition to the usual crossover effects connected with solid-liquid phase transitions at temperature Tm and the solid-solid transition at Tss, we find a strong correlation between the change in reorientation at the characteristic ESR temperature TfastX1 < Tss and/or Tm with the ratio TfastX1/Tm = 0.76 ± 0.03 and the characteristic dynamic temperature, TX, obtained from the viscosity data. This indicates the presence of local disordered regions in the crystalline structure which is indeed sensitive to dynamic change at the crossover temperature TX ≅ TfastX1.

The free-volume structure of a polymer melt, poly(vinyl methylether) from molecular dynamics simulations and cavity analysis.

In this work we analyze and compare the free volume of a polymer system poly(vinyl methylether) (PVME) at 300 K obtained by the two direct but different approaches: Positron annihilation lifetime spectroscopy (PALS) and computer simulations. The free volume is calculated from the simulated cells of PVME by means of numerical methods based on grid scanning and probing the structure with a probe of a given radius R(P). The free-volume structure was found to be percolated for small probes at R(P)=0.53 A. As the probe radius increases, the cavity structure breaks into isolated cavities, reaching a maximum of the cavity number at R(P)=0.78 A. We further develop methods for a geometrical analysis of the free-volume cavities by considering their shape. The geometrical computations show that the cavities have elongated shape with side-to-length ratio corresponding to approximately 1:0.55 and with an average length of 6 A. Based on the overlap between the computed cavities and simplified geometrical representations, the best match of the cavity shape is obtained for the approximation to the ellipsoidal shape (overlap on 84.4%). A match with other examined shapes follows the sequence: ellipsoid>cylinder>bar>sphere>cube. Finally, the computed geometrical parameters are used as input parameters into the quantum-mechanical models for the orthopositronium (o-Ps) lifetime in various free-volume hole geometries. Comparison with the experimental data gives support for two ideas about the existence of an o-Ps particle in the polymeric matrix: (i) the positronium cannot localize in a portion of very small cavities; (ii) and in the case of the percolated cavities, several o-Ps particles occupy some subcavities in the same cavity. Additionally, radial distribution functions of the free volume indicate the existence of two kinds of free volume, a structured one, corresponding to interstitial spaces along the polymer chain, and the so-called "bulk free volume," distributed randomly in the structure. PALS measurements seem to be mainly related with this bulk free volume. The cavities represented by the idealized geometries are visualized in three-dimensional space providing a unique representation on the free-volume structures.