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Water behavior studies were performed in porous ceramic media based on proton conducting yttrium-doped barium cerate BaCe0.85Y0.15O3-α (BCY15), which is a component of a new high-temperature dual membrane fuel cell (dmFC) design. Complex permittivity measurements were carried out on porous samples at room temperature. A new phenomenon was observed during wetting—a gigantic enhancement of the real component of the capacitance at lower frequencies. A possible explanation is the formation of semi-liquid layer with dipole structure on the pores walls, which is supposed to be organized also at operating temperatures. Since the electrochemically active volumetric layer facilitates the water formation, it should improve the operation of the dmFC by decreasing its resistance, which is experimentally confirmed. This phenomenon can be of importance also for classical proton conducting solid oxide fuel cells, as well as for operation in electrolyzer mode.

International audience; This paper reports impedance studies of a dual membrane fuel cell - an innovative design based on the idea for a junction between an oxygen ion conducting cathode/electrolyte part and proton conducting anode/electrolyte part through a mixed oxygen ion and proton conducting porous membrane. Thus oxygen, hydrogen and water are located in three independent chambers. This concept allows avoiding all the severe pitfalls connected to the presence of water at electrodes in both SOFC and PCFC. The performed measurements of the 3 compartments and the data analysis are improved by introducing some specialized approaches and techniques, which are discussed. The impedance contribution in the proof of the new concept is also presented.

This work presents results of a measurement setup which was constructed for understanding the performance contributions of the individual compartments and reactions taking place in the patented concept of IDEAL-Cell (described in detail in[1]). By inserting a third measurement point at the central membrane of an ideal cell it was possible to measure the cell in three different modes corresponding to hydrogen, oxygen compartment and the full cell. Recorded maximum power densities of (~4, ~7, 11, 16) mW/cm² at (600, 650, 700, 750) °C in H2-O2 atmosphere respectively were observed which were similar to the values of proof of concept ideal cell samples tested so far. Moreover in our setup it was possible to record higher maximum power densities for the hydrogen (proton conducting) compartment which was (~14, 22, 33*, ~38*) mW/cm² at (600, 650, 700, 750) °C.

In this study the technique of the Differential Impedance Analysis (DIA) is applied for distinction of two models which give similar impedance diagrams presented with slightly depressed semi-circles—two time-constants Voigt model with high degree of mixing and one time-constant model in which the capacitance is replaced with constant phase element (CPE). Those two models are often used for impedance investigations of solid state. The applicability of the recognition procedure is confirmed on synthetic models as well as on real samples of yttria-stabilized zirconia (YSZ) and Er-doped BaTiO 3 .

This work shows the enhanced capability of differential impedance analysis (DIA) for recognition of CPE behavior. It is based on the procedure of a secondary DIA, which analyses the frequency dependence of the local operating model parameters' estimates in the zones where there is no adequacy between the object and the local estimator. The new algorithm is successfully examined on synthetic models of CPE, Warburg, Randles, Randles with CPE modification, simple Faradaic reaction with CPE capacitance, as well as on real data obtained on yttrium iron garnet single crystals and yttria stabilized zirconia single crystals.

The purpose of this study is to compare the investigations of amorphous magnetic ribbons combining the usual structural methods with physical impedance spectroscopy (PIS) and X-ray photoelectron spectroscopy (XPS). The samples are commercially available rapidly quenched ribbons for torroidal transformers. Two types of ribbons were thermally treated below the temperature of amorphous–crystalline phase transition. Two binding energies of B 1 s electrons are determined by XPS in one of the as-quenched ribbons, which show impedance time constant spectra without dispersion. The other ribbon, possessing only one value of binding energy of the B 1 s electron (B I state) in a rapidly as-quenched state, undergoes transition to a still amorphous state but acquires high electromagnetic losses and show another value of the binding energy of the B 1 s electron (B II state) after the heat-treatment procedure. This latter type of ribbons show structural impedance spectra containing various time constant values.

The nanosized Co, B, H, particles synthesized by the ‘tea’ and ‘antigravity’ methods using a borohydride reduction process have been subjected to structure and composition studies by X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM) and selected area diffraction (SAD). The amounts of the elements Co, B, O2, H2 and C as mean volume values, and surface values for the as-prepared particles, as well as after Ar+ etching to a depth of about 15 nm and 30 nm from the initial particle surface, are determined. About 1.5 atoms of cobalt per atom of boron correspond to samples obtained by the ‘antigravity’ method. The binding energy (BE) of 1s electrons of boron atoms has only one value. These particles are angular and are in the typical nanocrystalline state. In the case of samples prepared by the ‘tea’ method, two atoms of cobalt per atom of boron are found. The presence of two kinds of BE (B1 and B11) of 1s electrons of boron atoms in the particles obtained by the ‘tea’ method is observed and almost equal amounts of these two states are established in the spectrum. The particles' shape and structure are typical of the amorphous state. The fact that there is one peak when the ‘antigravity’ method is applied, in contrast to the two peaks with the ‘tea’ method indicates the presence of a metal amorphous state in the latter case.

This paper presents results for the conductivity of BaCe0.85Y0.15O2-δ (BCY15) measured by electrochemical impedance spectroscopy in wet hydrogen and in Air, as well as test results from the application of the material in a new dual membrane fuel cell configuration (“IDEAL Cell”), in which the water is produced and evacuated through a separate chamber. The conductivity of dense BCY15 in wet hydrogen atmosphere at 700 °C is 2.0 10-2 S/cm. The measured values in air are of the same order. Preliminary tests of the material in the new cell design, where the three types of conductivity (protonic, oxide ion and mixed) are used in different cell compartments, are successfully performed.

Most electrochemical objects are intrinsically nonstationary or contain valuable evolving phenomena. This paper presents the essentials of the theory of Nonstationary Impedance Spectroscopy (NIS) including the ideas of nonstationary and instantaneous impedance, the new mathematical background and the main approach to the development of nonstationary impedance models. The practical issues for the application of the new techniques are discussed.

IDEAL-Cell is a new concept of a high temperature fuel cell operating in the range 600-700 °C. It is based on the junction between the anode part of a PCFC and the cathode part of a SOFC through a mixed H+ and O2- conducting porous ceramic membrane. This concept, extensively described in the present paper, aims at avoiding all the severe pitfalls connected with the presence of water at the electrodes in both SOFC and PCFC concepts. Spark Plasma Sintering samples were designed specifically for proving the IDEAL-Cell concept. The first electrochemical results obtained at 600 °C under hydrogen on millimeter thick samples show that IDEAL-Cell behaves like a high temperature fuel cell. It is estimated that the overall efficiency of this new concept should greatly surpass that of standard SOFCs and PCFCs and that the material constraints, especially in the case of interconnect materials, should significantly decrease.