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1. A “hump” in the third-order dielectric response of a highly polar liquid: Now you see it, now you don’t

   https://doi.org/10.1063/5.0248963  

   Thoms, Erik; Richert, Ranko (March 2025, The Journal of Chemical Physics)

   We have measured the linear and nonlinear dielectric responses of S-methoxypropylene carbonate, a highly polar glass-former, for which it has been reported that the “hump,” which is typical of third harmonic susceptibilities, disappears across a 5 K temperature change. To understand this unusual feature, we have measured the responses to high amplitude ac and dc electric fields at the fundamental frequency. The static limits of these results are entered into a model aimed at reproducing nonlinear dielectric susceptibility spectra using the concept of a fictive electric field. This model reproduces the “hump” in the third-harmonic response and its seeming disappearance. It is revealed that the “hump” is predominantly the result of reduced time constants, a consequence of the energy the sample absorbs from the electric field. At elevated temperatures, the “hump” only appears to vanish because its reduced amplitude submerges below the extraordinarily high level of polarization saturation of this liquid. 

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2. AC versus DC field effects on the crystallization behavior of a molecular liquid, vinyl ethylene carbonate (VEC)

   https://doi.org/10.1039/d0cp05290f  

   Duarte, Daniel M.; Richert, Ranko; Adrjanowicz, Karolina (January 2021, Physical Chemistry Chemical Physics)

   null (Ed.)

   Using electric fields to control crystallization processes shows a strong potential for improving pharmaceuticals, but these field effects are not yet fully explored nor understood. This study investigates how the application of alternating high electric fields can influence the crystallization kinetics as well as the final crystal product, with a focus on the possible difference between alternating (ac) and static (dc) type fields applied to vinyl ethylene carbonate (VEC), a molecular system with field-induced polymorphism. Relative to ac fields, static electric fields lead to more severe accumulation of impurity ions near the electrodes, possibly affecting the crystallization behavior. By tuning the amplitude and frequency of the electric field, the crystallization rate can be modified, and the crystallization outcome can be guided to form one or the other polymorph with high purity, analogous to the findings derived from dc field experiments. Additionally, it is found that low-frequency ac fields reduce the induction time, promote nucleation near T g , and affect crystallization rates as in the dc case. Consistency is also observed for the Avrami parameters n derived from ac and dc field experiments. Therefore, it appears safe to conclude that ac fields can replicate the effects seen using dc fields, which is advantageous for samples with mobile charges and the resulting conductivity. 

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3. The effect of imprint on remanent piezoelectric properties and ferroelectric aging of PbZr _0.52 Ti _0.48 O ₃ thin films

   https://doi.org/10.1111/jace.16367  

   Akkopru‐Akgun, Betul; Zhu, Wanlin; Lanagan, Michael T.; Trolier‐McKinstry, Susan (March 2019, Journal of the American Ceramic Society)

   Abstract Ferroelectric films suffer from both aging and degradation under high ac‐field drive conditions due to loss of polarization with time. In this study, the roles of defect chemistry and internal electric fields on the long‐term stability of the properties of piezoelectric films were explored. For this purpose, lead zirconate titanate (PZT) films with a Zr/Ti ratio of 52/48 doped with Mn‐ (PMZT) or Nb‐ (PNZT) were deposited on Pt coated Si substrates by the sol‐gel method. It was demonstrated that the magnitude of the internal field is much higher in PMZT films compared to PNZT films after poling in the temperature range of 25‐200°C under an electric field of −240 kV/cm. The development of the internal field is thermally activated, with activation energies from 0.5 ± 0.06 to 0.8 ± 0.1 eV in Mn doped films and from 0.8 ± 0.1 to 1.2 ± 0.2 eV in Nb doped films. The different activation energies for imprint suggests that the physical mechanism underlying the evolution of the internal field in PMZT and PNZT films differs; the enhanced internal field upon poling is attributed to (a) alignment of oxygen vacancy—acceptor ion defect dipoles (,) in PMZT films, and (b) thermionic injection of electron charges and charge trapping in PNZT films. In either case, the internal field reduces back switching, enhances the remanent piezoelectric properties, and dramatically improves the aging behavior. PMZT films exhibited the greatest enhancement, with reduced high temperature (180°C) aging rates of 2%‐3%/decade due to improved stability of the poled state. In contrast, PNZT films showed significantly larger high temperature aging rates (15.5%/decade) in the piezoelectric coefficient, demonstrating that the fully poled state was not retained with time. 

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4. One experiment makes a direct comparison of structural recovery with equilibrium relaxation

   https://doi.org/10.1063/5.0131342  

   Richert, Ranko (December 2022, The Journal of Chemical Physics)

   For a molecular glass-former, propylene glycol, we directly compare the equilibrium fluctuations, measured as “structural” relaxation in the regime of linear response, with structural recovery, i.e., field induced physical aging in the limit of a small perturbation. The two distinct correlation functions are derived from a single experiment. Because the relaxation time changes only 2% during structural recovery, no aging model is needed to analyze the results. Although being conceptually different processes, dielectric relaxation and recovery dynamics are observed to be identical for propylene glycol, whereas single-particle dynamics as seen by photon correlation spectroscopy are significantly faster. This confirms the notion that structural recovery and aging are governed by all modes observed by dielectric spectroscopy, i.e., including cross correlations, not only by single-particle dynamics. A comparison with analogous results for other materials suggests that the relation between relaxation and recovery time scales may be material specific rather than universal. 

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5. Dynamic permittivity of confined water under a static background field

   https://doi.org/10.1063/5.0233894  

   Bratko, D; Mulpuri, N (October 2024, The Journal of Chemical Physics)

   Molecular and collective reorientations in interfacial water are by-and-large decelerated near surfaces subjected to outgoing electric fields (pointing from surface to liquid, i.e., when the surface carries positive charge). In incoming fields at negatively charged surfaces, these rates show a nonmonotonic dependence on field strength where fastest reorientations are observed when the field alignment barely offsets the polarizing effects due to interfacial hydrogen bonding. This extremum coincides with a peak of local static permittivity. We use molecular dynamics simulations to explore the impact of background static field on high frequency AC permittivity in hydration water under an electric field mimicking the conditions inside a capacitor where one of the confinement walls is subject to an outgoing field and the other one to an incoming field. At strong static fields, the absorption peak undergoes a monotonic blue shift upon increasing field strength in both hydration layers. At intermediate fields, however, the hydration region at the wall under an incoming field (the negative capacitor plate) features a red shift coinciding with maximal static-permittivity and reorientation-rate. The shift is mostly determined by the variation of the inverse static dielectric constant as proposed for mono-exponentially decaying polarization correlations. Conversely, hydration water at the opposite (positively charged) surface features a monotonic blue shift consistent with conventional saturation. The sensitivity of absorption peaks on the field suggests that surface charge densities could be deduced from sub-THz dielectric spectroscopy experiments in porous materials when interfaces accommodate a major fraction of water contained in the system. 

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