scholarly journals Application of microimaging to diffusion studies in nanoporous materials

Adsorption ◽  
2020 ◽  
Author(s):  
Christian Chmelik ◽  
Roger Gläser ◽  
Jürgen Haase ◽  
Seungtaik Hwang ◽  
Jörg Kärger

AbstractMicroimaging on the basis of, respectively, interference microscopy and IR microscopy permit the observation of the distribution of guest molecules in nanoporous solids and their variation with time. Thus attainable knowledge of both concentration gradients and diffusion fluxes provides direct access to the underlying diffusion phenomena. This includes, in particular, the measurement of transport diffusion under transient, i. e. under non-equilibrium conditions, and of self- or tracer diffusion on considering the rate of tracer exchange. Correlating the difference in guest concentration close to the external surface to its equilibrium value with the influx into the nanoporous solid, microimaging does as well allow the direct determination of surface resistances. Examples illustrating the variety of information thus attainable include the comparison of mass transfer under equilibrium and non-equilibrium conditions, single- and multicomponent diffusion and chemical reactions. They, finally, introduce into the potentials of microimaging for an in-depth study of mass transfer in mixed-matrix membranes. This tutorial review may serve as first introduction into the topic. Further references are linked for the interested reader.

Author(s):  
A. A. Kalinnikov ◽  
S. A. Grigoriev ◽  
D. G. Bessarabov

The paper considers a non-equilibrium poroelectroelastic theory of a polymer electrolyte under the conditions of water electrolysis with the purpose of further use for a theoretical description of mass transfer processes in l ayers of a membrane-electrode assembly. Moreover, this paper carries out the review and analysis of the models of electro- chemical and mass-exchange processes in the electrolyzers, and analyzes the problems of their physicochemical description. We make a conclusion about the need to use models of water sorption and scaling of polymer electrolyte and analyze the models of water sorption and swelling of the polymer electrolyte. It is concluded that the existing poroelectroelastic theory is the most suitable for its modification for use in non-equilibrium conditions during elec- trolysis. The basic equation of the balance of pressures of the classical equilibrium poroelectroelastic theory for polymer electrolyte is considered. A modification of the poroelectroelastic theory has been carried out in order to its use in non-equilibrium conditions of water electrolysis for the purpose of further modeling of mass transfer processes. Based on experimental data available in open sources, the paper makes an analysis of the properties and features of elastic forces in the polymer electrolyte, and then refines the dependencies of the elastic forces in the polymer electro- lyte from the swelling and temperature. Taking into account the existing experimental data on the permeability of gases in a polymer electrolyte and the feature of swelling of the polymer electrolyte in a contact with liquid water, parameters of the non-equilibrium poroelectroelastic theory have been obtained for the water electrolysis conditions.


2018 ◽  
Vol 19 ◽  
pp. 96-124
Author(s):  
Jörg Kärger ◽  
Rustem Valiullin

Nanoporous materials find widespread application in material upgrading by separation (“molecular sieving”) and catalytic conversion. Mass transfer in these materials is a key phenomenon deciding about their technological performance. This chapter deals with the application of measurement techniques which are able to follow the diffusive fluxes of the guest molecules in such materials over “microscopic” distances, including the pulsed field gradient (PFG) technique of Nuclear Magnetic Resonance (NMR) and the techniques of microimaging by interference microscopy (IFM) and by IR microscopy (IRM). Microscopic measurement is a prerequisite for attaining unbiased information about the elementary steps of mass transfer and about their role within the overall process of technological exploitation. We dedicate this treatise to the memory of our dear and highly esteemed colleague Nicolaas Augustinus Stolwijk, notably in recognition of his manifold activities in the field of diffusion, distinguished by their impressively high standard in connecting the message of various techniques of measurement and in combining them to comprehensive views on quite intricate subjects.


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Jan Ravnik ◽  
Michele Diego ◽  
Yaroslav Gerasimenko ◽  
Yevhenii Vaskivskyi ◽  
Igor Vaskivskyi ◽  
...  

AbstractMetastable self-organized electronic states in quantum materials are of fundamental importance, displaying emergent dynamical properties that may be used in new generations of sensors and memory devices. Such states are typically formed through phase transitions under non-equilibrium conditions and the final state is reached through processes that span a large range of timescales. Conventionally, phase diagrams of materials are thought of as static, without temporal evolution. However, many functional properties of materials arise as a result of complex temporal changes in the material occurring on different timescales. Hitherto, such properties were not considered within the context of a temporally-evolving phase diagram, even though, under non-equilibrium conditions, different phases typically evolve on different timescales. Here, by using time-resolved optical techniques and femtosecond-pulse-excited scanning tunneling microscopy (STM), we track the evolution of the metastable states in a material that has been of wide recent interest, the quasi-two-dimensional dichalcogenide 1T-TaS2. We map out its temporal phase diagram using the photon density and temperature as control parameters on timescales ranging from 10−12 to 103 s. The introduction of a time-domain axis in the phase diagram enables us to follow the evolution of metastable emergent states created by different phase transition mechanisms on different timescales, thus enabling comparison with theoretical predictions of the phase diagram, and opening the way to understanding of the complex ordering processes in metastable materials.


Author(s):  
Sumit Pal ◽  
Antara Reja ◽  
Subhajit Bal ◽  
Baishakhi Tikader ◽  
Dibyendu Das

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