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- ItemAnion and ether group influence in protic guanidinium ionic liquids(Cambridge : RSC Publ., 2023) Rauber, Daniel; Philippi, Frederik; Becker, Julian; Zapp, Josef; Morgenstern, Bernd; Kuttich, Björn; Kraus, Tobias; Hempelmann, Rolf; Hunt, Patricia; Welton, Tom; Kay, Christopher W. M.Ionic liquids are attractive liquid materials for many advanced applications. For targeted design, in-depth knowledge about their structure-property-relations is urgently needed. We prepared a set of novel protic ionic liquids (PILs) with a guanidinium cation with either an ether or alkyl side chain and different anions. While being a promising cation class, the available data is insufficient to guide design. We measured thermal and transport properties, nuclear magnetic resonance (NMR) spectra as well as liquid and crystalline structures supported by ab initio computations and were able to obtain a detailed insight into the influence of the anion and the ether substitution on the physical and spectroscopic properties. For the PILs, hydrogen bonding is the main interaction between cation and anion and the H-bond strength is inversely related to the proton affinity of the constituting acid and correlated to the increase of 1H and 15N chemical shifts. Using anions from acids with lower proton affinity leads to proton localization on the cation as evident from NMR spectra and self-diffusion coefficients. In contrast, proton exchange was evident in ionic liquids with triflate and trifluoroacetate anions. Using imide-type anions and ether side groups decreases glass transitions as well as fragility, and accelerated dynamics significantly. In case of the ether guanidinium ionic liquids, the conformation of the side chain adopts a curled structure as the result of dispersion interactions, while the alkyl chains prefer a linear arrangement.
- ItemRejuvenation through plastic deformation of a La-based metallic glass measured by fast-scanning calorimetry(Amsterdam : Elsevier B.V., 2020) Meylan, C.M.; Orava, J.; Greer, A.L.We explore the glassy states achievable after a metallic glass is formed on liquid quenching. Samples of La55Al25Ni20 (at.%) metallic glass (rod and ribbon) are studied. The extent of structural relaxation at room temperature is characterized for this low-glass-transition temperature glass. Plastic deformation (uniaxial compression) rejuvenates the glass to states of higher enthalpy characteristic of glass formation at high cooling rate. Deformation increases the heterogeneity of the glass, widening the spectrum of relaxation times. The extent of rejuvenation in samples of low aspect ratio is compared with that under conditions of high constraint in notched samples. The deformation-induced rejuvenation is particularly susceptible to reduction on subsequent ageing. Fast-scanning calorimetry is useful in characterizing the dynamics of structural relaxation. The shadow glass transition is more evident on fast heating, and is observed in this glass for the first time. A new excess exothermic effect is observed before the glass transition.
- ItemPentacene in 1,3,5-Tri(1-naphtyl)benzene: A Novel Standard for Transient EPR Spectroscopy at Room Temperature(Wien [u.a.] : Springer, 2021) Schröder, Mirjam; Rauber, Daniel; Matt, Clemens; Kay, Christopher W. M.Testing and calibrating an experimental setup with standard samples is an essential aspect of scientific research. Single crystals of pentacene in p-terphenyl are widely used for this purpose in transient electron paramagnetic resonance (EPR) spectroscopy. However, this sample is not without downsides: the crystals need to be grown and the EPR transitions only appear at particular orientations of the crystal with respect to the external magnetic field. An alternative host for pentacene is the glass-forming 1,3,5-tri(1-naphtyl)benzene (TNB). Due to the high glass transition point of TNB, an amorphous glass containing randomly oriented pentacene molecules is obtained at room temperature. Here we demonstrate that pentacene dissolved in TNB gives a typical “powder-like” transient EPR spectrum of the triplet state following pulsed laser excitation. From the two-dimensional data set, it is straightforward to obtain the zero-field splitting parameters and relative populations by spectral simulation as well as the B1 field in the microwave resonator. Due to the simplicity of preparation, handling and stability, this system is ideal for adjusting the laser beam with respect to the microwave resonator and for introducing students to transient EPR spectroscopy. © 2021, The Author(s).
- ItemA phase space approach to supercooled liquids and a universal collapse of their viscosity(Lausanne : Frontiers Media, 2016) Weingartner, Nicholas B.; Pueblo, Chris; Nogueira, Flavio S.; Kelton, K. F.; Nussinov, ZoharA broad fundamental understanding of the mechanisms underlying the phenomenology of supercooled liquids has remained elusive, despite decades of intense exploration. When supercooled beneath its characteristic melting temperature, a liquid sees a sharp rise in its viscosity over a narrow temperature range, eventually becoming frozen on laboratory timescales. Explaining this immense increase in viscosity is one of the principle goals of condensed matter physicists. To that end, numerous theoretical frameworks have been proposed, which explain and reproduce the temperature dependence of the viscosity of supercooled liquids. Each of these frameworks appears only applicable to specific classes of glassformers, and each possesses a number of variable parameters. Here, we describe a classical framework for explaining the dynamical behavior of supercooled liquids based on statistical mechanical considerations, and possessing only a single variable parameter. This parameter varies weakly from liquid to liquid. Furthermore, as predicted by this new classical theory and its earlier quantum counterpart, we find with the aid of a small dimensionless constant that varies in size from ∼0.05 to 0.12, a universal (16 decades) collapse of the viscosity data as a function of temperature. The collapse appears in all known types of glass-forming supercooled liquids (silicates, metallic alloys, organic systems, chalcogenide, sugars, and water).
- ItemThermomechanical characterization and modeling of cold-drawing of poly(ethylene Terephthalate)(Basel : MDPI, 2019) Oberer, Jürgen; Schneider, Konrad; Majschak, Jens-PeterThe tensile testing of amorphous polyethylene terephthalate is observed until failure by IR thermography and optical strain measurement. The deformation can be subdivided in six deformation phases: elastic deformation, neck formation with a localized sharp temperature rise, neck propagation, which is also known as cold-drawing, with heat generation in a transition zone, crack initialization with local heating, crack growth, and rupture. These deformation phases are showing different mechanical and thermal reactions to the deformation. The initial and drawn samples are studied with differential scanning calorimetry. Alongside heating due to the dissipation of mechanical energy, latent heat due to strain-induced crystallization was detected. While the material is cold-drawn, a high dependence on the crosshead speed is found for the heat generation as well as the draw ratio, mechanical response, and morphological changes due to orientation and crystallization. For cold-drawing, a thermomechanical model is introduced, which is based on the first law of thermodynamics and reproduces the temperature distribution along the sample.
- ItemGlassy dynamics of poly(2-vinyl-pyridine) brushes with varying grafting density(London : Royal Soc. of Chemistry, 2015) Neubauer, Nils; Winkler, René; Tress, Martin; Uhlmann, Petra; Reiche, Martin; Kipnusu, Wycliffe Kiprop; Kremer, FriedrichThe molecular dynamics of poly(2-vinyl-pyridine) (P2VP) brushes is measured by Broadband Dielectric Spectroscopy (BDS) in a wide temperature (250 K to 440 K) and broad spectral (0.1 Hz to 1 MHz) range. This is realized using nanostructured, highly conductive silicon electrodes being separated by silica spacers as small as 35 nm. A “grafting-to”-method is applied to prepare the P2VP-brushes with five different grafting densities (0.030 nm−2 to 0.117 nm−2), covering the “true-brush” regime with highly stretched coils and the “mushroom-to-brush” transition regime. The film thickness ranges between 1.8 to 7.1 (±0.2) nm. Two relaxations are observed, an Arrhenius-like process being attributed to fluctuations in the poly(glycidyl-methacrylate) (PGMA) linker used for the grafting reaction and the segmental dynamics (dynamic glass transition) of the P2VP brushes. The latter is characterized by a Vogel–Fulcher–Tammann dependence similar to bulk P2VP. The results can be comprehended considering the length scale on which the dynamic glass transition (≤1 nm) takes place.