AIR ELECTRODES OF SOLID OXIDE ELECTROCHEMICAL CELLS

FIELD

Disclosed are air electrode materials suitable for use in solid oxide electrochemical cells (SOCs). The disclosed cells can operate in a dual function modes, i.e., as a fuel cell and as an electrolysis cell. In both cases, chemical energy and electrical energy can be directly convert from one mode to the other; thereby providing a highly efficient energy conversion process that can be used as a sustainable energy source.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1A to 1C are the drawings of several kinds of solid oxide electrochemical cells (SOCs). FIG. 1A shows the drawing of solid oxide fuel cells (SOFCs). The oxygen reduction reaction (ORR) takes place at the air electrode (cathode), the hydrogen oxidation reaction (HOR) takes place at the fuel electrode (anode), and the oxygen ion transport through the electrolyte. FIG. 1B shows the drawing of protonic conducting fuel cells (PCFCs), in which proton transport through the electrolyte. FIG. 1C shows the drawing of protonic conducting electrolysis cells. The oxygen evolution reaction (OER) takes place at the air electrode (positive electrode), and the hydrogen evolution reaction takes place at the fuel electrode (negative electrode).

FIG. 2A shows the schematics of the PB9CN crystal structure. FIG. 2B is the X-Ray diffraction (XRD) pattern for PBCO (bottom), PB9CN (middle) and PB10CN (top). FIG. 2C to 2E are high resolution TEM images of the PB9CN lattice.

FIGS. 3A to 3C provide an electrochemical stability comparison of PB10CN and PBCO. FIG. 3A compares the change of interfacial polarization resistance (R_p) of both materials at 600° C. under the open circuit conditions (OCV). FIGS. 3B and 3C show the surface of PBCO and PB10CN electrodes after a stability test at 600° C.

FIGS. 4A to 4E show the suppression of Ba segregation by Nb doping. FIG. 4A shows the surface of a fresh PB sample. FIG. 4B shows the surface of a fresh PBCO sample. FIG. 4C shows the surface of an annealed PB10CN sample. FIG. 4D shows the surface of an annealed PBCO sample. FIG. 4E shows the elemental distribution at the precipitated particle on the surface of annealed PBCO.

FIGS. 5A to 5G display the atomic level function of Nb doping by density functional theory (DFT) based calculation. FIG. 5A represents the calculation model of PBCO. FIG. 5B represents the calculation model of Nb doped PBCO. FIG. 5C shows the charge density difference of PBCO. FIG. 5D shows the charge density difference of Nb doped PBCO. FIG. 5E shows the calculation model of the PBCO surface. FIG. 5F shows the calculation model of the PBCO surface with Ba segregation. FIG. 5G is a table comparing the cohesive energy (E_c), formation energy (E_f), Ba segregation energy (E_s) difference between PBCO and Nb-doped PBCO.

FIGS. 6A to 6D show the improvement in catalytic activity obtained by Ba deficiency. FIG. 6A shows the electrical conductivity of PB9CN and PB10CN. FIG. 6B shows the oxygen non-stoichiometry of PB9CN and PB10CN. FIG. 6C shows the surface kinetic coefficient (k) and chemical diffusion coefficient (D) of PB9CN and PB10CN. FIG. 6D shows the interfacial polarization resistance (R_p) of PB9CN and PB10CN.

FIG. 7A to 7E depict measurements of the electrochemical performance of PB9CN applied on an oxygen ion conducting electrolyte. FIG. 7A shows the comparison of interfacial polarization resistance (R_p) of PB9CN and other state-of-the-art air electrode materials under the dry air condition. FIG. 7B shows the durability of PB9CN under dry air and OCV conditions. FIG. 7C is a plot of the I-V-P curves of a fuel cell with a configuration of Ni-GDC|GDC|PB9CN. FIG. 7D is a graph of the comparison of peak power density of GDC-based single cells with PB9CN and other state-of-the-art air electrode materials. FIG. 7E demonstrates the durability of a single cell with a configuration of Ni-GDC|GDC|PB9CN at 500° C.

FIG. 8A to 8F depict the electrochemical performance of PB9CN applied on a proton conducting electrolyte. FIG. 8A is a plot of the I-V-P curves of a fuel cell with a configuration of Ni-BZCYYb|BZCYYb|PB9CN-BZCYYb. FIG. 8B shows the comparison of peak power density of BZCYYb-based single cells with PB9CN and other state-of-the-art air electrode materials. FIG. 8C shows the comparison of interfacial polarization resistance (R_p) of PB9CN and other state-of-the-art air electrode materials under the humidified air condition (˜3 vol % H₂O). FIG. 8D depicts the electrolysis performance of a single cell with a configuration of Ni-BZCYYb|BZCYYb|PB9CN-BZCYYb. FIG. 8E indicates the observed durability of PB9CN under humidified air (3 vol % H₂O) and OCV conditions. FIG. 8F shows the durability of an electrolysis cell with a configuration of Ni-BZCYYb|BZCYYb|PB9CN-BZCYYb at 600° C. FIG. 8G shows reversible operation between fuel cell mode and electrolysis cell mode of a single cell with a configuration of Ni-BZCYYb|BZCYYb|PB9CN-BZCYYb at 600° C.

DETAILED DESCRIPTION

The materials, compounds, compositions, articles, and methods described herein may be understood more readily by reference to the following detailed description of specific aspects of the disclosed subject matter and the Examples included therein.

Before present materials, compounds, compositions, and methods are disclosed and described, it is to be understood that the aspects described below are not limited to specific synthetic methods or specific reagents, as such may, of course, vary. It is also to be understood that the terminology used herein is for the purpose of describing particular aspects only and is not intended to be limiting.

All percentages, ratios and proportions herein are by weight, unless otherwise specified. All temperatures are in degrees Celsius (° C.) unless otherwise specified.

Also, throughout this specification, various publications are referenced. The disclosures of these publications in their entireties are hereby incorporated by reference into this application in order to more fully describe the state of the art to which the disclosed matter pertains. The references disclosed are also individually and specifically incorporated by reference herein for the material contained in them that is discussed in the sentence in which the reference is relied upon.

The terms “comprise” (and any form of comprise, such as “comprises” and “comprising”), “have” (and any form of have, such as “has” and “having”), “include” (and any form of include, such as “includes” and “including”) and “contain” (and any form of contain, such as “contains” and “containing”) are open-ended linking verbs. As a result, an apparatus that “comprises,” “has,” “includes” or “contains” one or more elements possesses those one or more elements, but is not limited to possessing only those elements. Likewise, a method that “comprises,” “has,” “includes” or “contains” one or more steps possesses those one or more steps, but is not limited to possessing only those one or more steps.

Ranges can be expressed herein as from “about” one particular value, and/or to “about” another particular value. When such a range is expressed, another aspect includes from the one particular value and/or to the other particular value. Similarly, when values are expressed as approximations, by use of the antecedent “about,” it will be understood that the particular value forms another aspect. It will be further understood that the endpoints of each of the ranges are significant both in relation to the other endpoint, and independently of the other endpoint. It is also understood that there are a number of values disclosed herein, and that each value is also herein disclosed as “about” that particular value in addition to the value itself. For example, if the value “10” is disclosed, then “about 10” is also disclosed. It is also understood that when a value is disclosed, then “less than or equal to” the value, “greater than or equal to the value,” and possible ranges between values are also disclosed, as appropriately understood by the skilled artisan. For example, if the value “10” is disclosed, then “less than or equal to 10” as well as “greater than or equal to 10” is also disclosed. It is also understood that throughout the application data are provided in a number of different formats and that this data represent endpoints and starting points and ranges for any combination of the data points. For example, if a particular data point “10” and a particular data point “15” are disclosed, it is understood that greater than, greater than or equal to, less than, less than or equal to, and equal to 10 and 15 are considered disclosed as well as between 10 and 15. It is also understood that each unit between two particular units are also disclosed. For example, if 10 and 15 are disclosed, then 11, 12, 13, and 14 are also disclosed.

The terms “a” and “an” are defined as one or more unless this disclosure explicitly requires otherwise. Ranges may be expressed herein as from “about” one particular value, and/or to “about” another particular value. When such a range is expressed, another aspect includes from the one particular value and/or to the other particular value. Similarly, when values are expressed as approximations, by use of the antecedent “about,” it will be understood that the particular value forms another aspect. It will be further understood that the endpoints of each of the ranges are significant both in relation to the other endpoint, and independently of the other endpoint.

Values expressed as “greater than” do not include the lower value. For example, when the “variable x” is defined as “greater than zero” expressed as “0<x” the value of x is any value, fractional or otherwise that is greater than zero. Similarly, values expressed as “less than” do not include the upper value. For example, when the “variable x” is defined as “less than 2” expressed as “x<2” the value of x is any value, fractional or otherwise that is less than 2.

“Optional” or “optionally” means that the subsequently described event or circumstance can or cannot occur, and that the description includes instances where the event or circumstance occurs and instances where it does not

Any embodiment of any of the apparatuses, systems, and methods can consist of or consist essentially of rather than comprise/include/contain/have any of the described steps, elements, and/or features. Thus, in any of the claims, the term “consisting of” or “consisting essentially of” can be substituted for any of the open-ended linking verbs recited above, in order to change the scope of a given claim from what it would otherwise be using the open-ended linking verb.

The feature or features of one embodiment may be applied to other embodiments, even though not described or illustrated, unless expressly prohibited by this disclosure or the nature of the embodiments.

Any embodiment of any of the apparatuses, systems, and methods can consist of or consist essentially of—rather than comprise/include/contain/have—any of the described steps, elements, and/or features. Thus, in any of the claims, the term “consisting of or “consisting essentially of can be substituted for any of the open-ended linking verbs recited above, in order to change the scope of a given claim from what it would otherwise be using the open-ended linking verb. The feature or features of one embodiment may be applied to other embodiments, even though not described or illustrated, unless expressly prohibited by this disclosure or the nature of the embodiments.

In the disclosure and appended Claims, the following nomenclature is provided: PrBa_0.9Co_1.96Nb_0.04O_5+δ is referred to as PB9CN, PrBaCo_1.96Nb_0.04O_5+δ is referred to as PB10CN and PrBaCo₂O_5+δ is referred to as PBCO.

One aspect of the disclosure relates to a multi-functional air electrode for solid oxide electrochemical cells, having the formula:

PrBa_0.9Co_1.96Nb_0.04O_5+δ.

Another aspect of the disclosure relates to Ba deficient, Nb doped multi-functional air electrode for solid oxide electrochemical cells, having the formula:

PrBa_1-xCo_1-yNb_yO_5+δ

wherein the index x is from about 0.1 to about 0.5, and the index y is from 0.01 to about 0.07. Non-limiting examples of this aspect includes:

PrBa_0.9Co_1.97Nb_0.03O_5+δ, PrBa_0.9Co_1.95Nb_0.05O_5+δ, PrBa_0.9Co_1.93Nb_0.07O_5+δ,

PrBa_0.9Co_1.92Nb_0.08O_5+δ, PrBa_0.85Co_1.96Nb_0.04O_5+δ, PrBa_0.85Co_1.95Nb_0.05O_5+δ,

PrBa_0.85Co_1.94Nb_0.06O_5+δ, PrBa_0.85Co_1.93Nb_0.07O_5+δ, PrBa_0.8Co_1.96Nb_0.04O_5+δ,

PrBa_0.8Co_1.95Nb_0.05O_5+δ, PrBa_0.8Co_1.94Nb_0.06O_5+δ, and PrBa_0.8Co_1.93Nb_0.07O_5+δ,

Example 1
Discovery and Application of Air Electrode

The disclosed electrode material PrBa_0.9Co_1.96Nb_0.04O_5+δ (PB9CN) when compared to a conventional electrode material PrBaCo₂O_5+δ (PBCO), which has increased oxygen transport properties and ORR activity. In order to suppress the Ba segregation of PBCO thereby enhancing the electrochemical stability, Nb is doped into the PBCO crystal structure to create PrBaCo_1.96Nb_0.04O_5+δ (PB10CN). In order to further improve the oxygen transport properties and electrochemical activity of PB10CN, Ba deficiency was introduced into PB10CN thereby forming PB9CN. As disclosed herein, PB9CN, shows desirable activity and stability, and can be seen as having applicability when applied to high-temperature electrochemical devices, for example, solid oxide fuel cells (SOFCs), protonic conducting fuel cells (PCFCs), protonic conducting electrolysis cells (PCECs), as well as low-temperature electrochemical devices, for example, proton exchange membrane fuel cells (PEMFCs), rechargeable metal-air batteries, and water splitting devices.

Synthesis of Air Electrode Powder

PrBa_0.9Co_1.96Nb_0.04O_5+δ (PB9CN), PrBaCo_1.96Nb_0.04O_5+δ (PB10CN) and PrBaCo₂O_5+δ (PBCO) powder were synthesized by the sol-gel method. A stoichiometric amount of metal nitrate was dissolved in deionized water with ethylenediaminetetraacetic acid (EDTA) and citric acid (CA). The molar ratio between metal ion, EDTA and CA was 1:1:1.5. Then ammonium hydroxide was used to adjust the pH to approximately 9. After evaporating the water, the gel was calcined at 250° C. for 10 hours. The primary powder was then grounded and calcined at 600° C. for 5 hours. Finally, the powder was fired at 1100° C. for 2 hours to get the desired phase, as confirmed by X-ray diffraction (XRD).

FIG. 2A shows a schematic view of the crystal structure of PB9CN. Compared to the PBCO crystal structure, Nb doped into the Co site for PB10CN. In addition, 10% Ba deficiency was created for PB9CN. PB9CN shows a double perovskite structure as confirmed by X-ray diffraction (XRD) in FIG. 2B and the high resolution-transmission electron microscopy (HR-TEM) images in FIG. 2C to FIG. 2E. The layered [Co(Nb)O₂]—[PrO]—[Co(Nb)O₂]—[BaO] structure and the Ba deficiency is vital to rapid transport of oxygen species^25-27. Introduction of less reducible cation is beneficial for the stability of air electrode materials²⁸. The content of Nb as the B-site ion was 2% as determined by Energy-dispersive X-ray spectroscopy (EDS).

Preparation of Symmetrical Cells and Single Cells

To fabricate symmetrical cells, Sm_0.2Ce_0.8O_1.9(SDC) and BaZr_0.1Ce_0.7Y_0.1Yb_0.1O_3−δ (BZCYYb) powder was mixed with a sufficient amount of of PVB then dry pressed and sintered at 1450° C. for 5 hours. PB9CN, PB10CN, and PBCO ink (air electrode powder mixed with V-006) were brush painted on both sides of the electrolyte followed by firing at 950° C. for 2 hours. To fabricate single cells, Ni—Gd_0.1Ce_0.9O_1.95(GDC) and Ni-BZCYYb half cells were prepared by tape casting and sintering at 1450° C. for 5 hours. The air electrode ink was brush painted on the GDC or BZCYYb electrolyte and fired at 950° C. for 2 hours. For all the symmetrical cells and single cells, the effective area is about 0.28 cm².

Electrochemical Measurements

For symmetrical cell measurement, two pieces of silver mesh were used as current collector. Impedance spectra were acquired using a Solartron 1255 HF frequency response analyzer interfaced with an EG&G PAR potentiostat model 273A with an AC amplitude of 10 mV in the frequency range from 100 kHz to 0.01 Hz. The stability test was performed at 600 and 550° C. under the OCV condition. For the evaluation of GDC based single cells, wet hydrogen (with 3 vol % H₂O) was used as fuel and ambient air (without flowing) as oxidant. For the evaluation of BZCYYb based single cells, wet hydrogen (with 3 vol % H₂O) was supplied to the fuel electrode and humidified air was supplied to the air electrode. The cell performance was monitored with an Arbin multi-channel electrochemical testing system.

Phase structure of air electrode powders were characterized by X-ray diffraction (Panalytical)(Pert PRO Alpha-1 XRD). The microstructure and morphology of the cells were examined by a scanning electron microscope (SEM, LEO 1530). The Nb content of PB9CN powder sample and the elemental distribution at the surface of PBCO sample were characterized by a scanning transmission electron microscope (STEM, Hitachi HD-2700). Surface kinetic coefficient (k) and chemical diffusion coefficient (D) were characterized by electrical conductivity relaxation (ECR) measurement. Oxygen non-stoichiometry was determined by combination of iodometric titration at room temperature and thermogravimetric analysis (TGA) at elevated temperatures.

The Vienna ab initio simulation package (VASP) is used for theoretical calculations. The interactions between the valence electrons and ion core is described by projector augmented wave (PAW) formalism of density functional theory²¹. The exchange correlation functional is depicted by the spin-polarized generalized gradient approximation proposed by Perdew, Burke, and Ernzerhof (PBE)²². The Gaussian smearing method was used²³, and the width of smearing was chosen as 0.05 eV. Our plane wave base uses a kinetic energy cutoff of 400 eV. The Monkhorst-Pack k-point grid is used for sampling the Brillouin region with a k-point mesh of 7×7×7 for the bulk calculation and 5×5×1 for the surface model²⁴. The bulk models are shown in FIGS. 5A and 5B, with the size of 8.00 Å×7.76 Å×7.63 Å, containing 4 Pr, 4 Ba, 8 Co, and 24 O atoms. After one Co atoms is replaced by Nb, the supercell size is 7.94 Å×7.83 Å×7.74 Å, with the volume slightly increased. The surface slab model is shown in FIGS. 5E and 5F, with seven atomic layers, and the lateral size is 8.00 Å×7.63 Å. For the geometry optimizations of bulk, we allow the volume of the supercell relaxed, as well as all the internal coordinates, until the force on each atom is less than 0.01 eV/Å. For the surface model, the bottom two atomic layer are fixed, and the other atoms are allowed to relax. The self-consistent convergence criterion for the calculation of the ground state energy is less than 10⁻⁵eV

FIG. 2A shows a schematic view of the crystal structure of PB9CN. Compared to the PBCO crystal structure, Nb doped into the Co site for PB10CN. In addition, 10% Ba deficiency was created for PB9CN. PB9CN shows a double perovskite structure as confirmed by X-ray diffraction (XRD) in FIG. 2B and the high resolution-transmission electron microscopy (HR-TEM) images in FIG. 2C to FIG. 2E. Without wishing to be limited by theory, the layered [Co(Nb)O₂]—[PrO]—[Co(Nb)O₂]—[BaO] structure and the Ba deficiency is directly relates to the rapid transport of oxygen species^25-27. Introduction of less reducible cation provides for the stability of air electrode materials²⁸. The content of Nb as the B-site ion was 2% as determined by Energy-dispersive X-ray spectroscopy (EDS).

Double perovskite material PrBaCo₂O_5+δ (PBCO) shows fast oxygen transport properties, which makes it a good candidate as air electrode materials for SOFCs²⁹. However, due to the segregation behavior, the stability of PBCO is questionable and not commonly reported^14,15,30. To suppress the surface segregation, less reducible cation, Nb, was doped into the PBCO crystal structure to create PrBaCo_1.96Nb_0.04O_5+δ (PB10CN), the XRD pattern of both PBCO and PB were shown in FIG. 2B²⁸.

The electrochemical stability of PBCO and PB10CN on SDC-based symmetrical cells was first evaluated. FIG. 3A compares the change of interfacial polarization resistance (R_p) of both materials at 600° C. under the OCV condition. Initially, PB10CN and PBCO show similar R_p. After about 200 hours' operation, the R_pof PBCO increased about 25%. However, the R_pof PBCN10 was relatively stable. FIGS. 3B and 3C show the surface of PBCO and PB10CN electrodes after the stability test at 600° C. Formation of particles took place on the surface of PBCO, however, the surface of PB10CN maintained clean.

In order to eliminate the complex microstructure of electrodes, PBCO and PB10CN dense samples were prepared. After polishing the surface, these samples were annealed at 600° C. for 20 hours. FIGS. 4A and 4B show the fresh clean surface of PBCO and PB after polishing. FIGS. 4C and 4D show the surface after annealing. After annealing, the surface of PB10CN didn't show an obvious change. However, the particle precipitated to the surface of the PBCO sample as compared in FIGS. 4C and 4D. The surface of PBCO was characterized by STEM. As shown in FIG. 4E, a linear scan of elemental distribution at the precipitated particle on the surface of PBCO illustrates that Ba segregation took place at the surface of PBCO during the annealing process, which is in accordance with previous studies^15,30. The bulk material maintains the double perovskite structure. With Nb doping, such segregation was successfully suppressed, thereby enhancing the electrochemical stability.

Theoretical Calculations

A theoretical calculation based on density functional theory (DFT) was conducted to develop a molecular-level understanding as it relates to the enhancement of stability by Nb doping. The cohesive energy and the formation energy of PBCO without (FIG. 5A) and with Nb doping (FIG. 5B). The cohesive energy is defined as

E
_c
=E
_T−Σ_in_iE_i

where E_Tis the total energy of the system, E_iis the energy of an isolated atom i, and n_iis the amount of atom i in the system. The formation energy is defined as

$E_{f} = E_{T} - \sum_{j} n_{j} E_{j}$

where E_Tis the total energy of the system, E_jis the energy of an atom j in its corresponding bulk, and n_jis the amount of atom j in the system. The cohesive energy and formation energy of the Nb doped model are 8.85 eV and 6.97 eV more stable than those of the undoped system, respectively, indicating that Nb doping significantly enhanced that structure stability of PBCO. As shown in FIGS. 5C and 5D, Nb doping can transfer more electrons from the metal atoms to oxygen atoms. As a result, the framework is enhanced, resulting in a more stable structure.

In addition, the surface segregation energy of Ba was calculated, which is defined as the energy difference between FIGS. 5E and 5F. Compared to the undoped system, Nb doping increases the Ba segregation energy by 0.30 eV. In addition, after Nb doping the segregation increases by 0.30 eV. These results are consistent with that Nb doping enhanced cohesive and formation energies, as well as the electronic structure analysis. All the calculated energy values are listed in FIG. 5G.

Without wishing to be limited by theory, creating cation deficiency is an effective method to improve the electrochemical performance of air electrode materials^27,31,32. By creating Ba deficiencies (V_Ba″), more electron holes (h′) and/or oxygen vacancies (Vo″) can be generated to compensate the charge neutrality. Higher concentration of electron holes can enhance the overall electrical conductivity and higher oxygen vacancies can improve the oxygen ion transport properties. Both cases can have beneficial effects on the overall ORR and OER activities^32-34.

As it relates to the effects of Ba deficiencies, the electrical conductivity of PrBa_0.9Co_1.96Nb_0.04O_5+δ (PB9CN) and PrBaCo_1.96Nb_0.04O_5+δ (PB10CN) were compared. As shown in FIG. 6A, both PB9CN and PB10CN showed adequate and comparable electrical conductivity at intermediate temperatures (˜800 S cm⁻¹at 600° C.). The similar electrical conductivity indicated that V_Ba″ did not have a noticeable influence on the concentration of electron holes. In other words, more Vo″ would be created by V_Ba″. The oxygen non-stoichiometry of PB9CN and PB10CN was characterized by iodometric titration and TGA. As compared in FIG. 6B, PB9CN has a higher concentration of oxygen vacancy than PB at temperatures up to 800° C. Two oxygen transport properties, i.e., surface kinetic coefficient (k) and chemical diffusion coefficient (D) were further measured by electrical conductivity relaxation (ECR) method. At intermediate temperatures, PB9CN exhibited better oxygen transport properties than PB as shown in FIG. 6C. Finally, the improved electrochemical properties were demonstrated on SDC based symmetrical cells. FIG. 6D provides a comparison of the R_pof PB9CN and PB10CN at 550-700° C. The R_pof PB9CN was lower than that of PB10CN. For example, at 550° C., the R_pof PB9CN was ˜0.25 Ωcm², which is comparable or better than other existing air electrode materials. These results proved that creating Ba deficiency dramatically improved the electrochemical performance by enhancing the oxygen transport properties.

The electrochemical performance of the PB9CN air electrode was determined on multiple types of SOCs. FIG. 7A compares the R_pof PB9CN with several state-of-the-art air electrode materials on SDC electrolyte supported symmetrical cells. Among all these materials, PB9CN shows the best performance. For example, at 650° C. R_pof PB9CN is only 0.068 Ωcm², lower than that of STFC-15 (˜0.089 Ωcm²)¹⁷, BSCF-GDC core shell fibre (˜0.105 Ωcm²)³⁵and PBCC (˜0.14 Ωcm²)¹⁸. The activation energy of PB9CN is 79.98 kJ mol⁻¹, which is similar to the activation energy of BCFZY (79.2 kJ mol⁻¹)¹⁹, the low activation energy guarantees the good ORR activity of PB9CN at even lower temperatures. A stable R_pat 600 and 550° C. for more than 1000 hours is shown in FIG. 7B. PB9CN was then applied on GDC based single cells. FIG. 7C shows the I-V-P curves of the single cell with a configuration of Ni-GDC|GDC|PB9CN at 600, 550, and 500° C. According to the comparison on peak power density of GDC or SDC based single cells in FIG. 7D, PB9CN air electrode outperforms most of the other air electrode materials or catalysts^36-40. Moreover, the single cell shows stable performance at 500° C. for over 200 hours without obvious performance degradation as shown in FIG. 7E.

Because the observed rapid and stable oxygen transport properties of PB9CN is beneficial for proton conduction as well⁸, the electrochemical performance of PB9CN on single cells based on proton conducting electrolytes, i.e. BaZr_0.1Ce_0.7Y_0.1Yb_0.1O_3−δ (BZCYYb) was tested. FIG. 8A shows the I-V-P curves of the BZCYYb-based single cell with PB9CN-BZCYYb (mass ratio 7:3) composite air electrode at 650, 600, 550, and 500° C. As shown in FIG. 8B, the single cell performance of PB9CN is enhanced when compared to other air electrode materials and is comparable to PrBa_0.5Sr_0.5Co_1.5Fe_0.5O_5+δ (PBSCF) with a PLD layer^{5,20,26,41,42}. The applicability of PB9CN to protonic ceramic electrolysis cells (PCECs) was also determined. Because water is necessary to supply to the air electrode during the electrolysis for PCECs, the R_pof PB9CN on BZCYYb based symmetrical cells with ˜3 vol % H₂O was tested. As shown in FIG. 8C, the R_pof PB9CN is comparable or lower than other air electrode materials for PCFCs^20,41,43,44. PB9CN was then applied to BZCYYb-based PCECs as an air electrode with humidified air (˜30 vol % H₂O) in the air electrode and humidified H₂(˜3 vol % H₂) in the fuel electrode. When the applied voltage was 1.3V, the electrolysis current densities were 2.75, 1.73, and 1.07 A cm⁻²at 650, 600, and 550° C. The stability of PB9CN against water was examined on both BZCYYb based symmetrical cells (FIG. 8E) and electrolysis single cells (FIG. 8F and FIG. 8G). Under both cases, a slight performance degradation was shown during the first tens of hours. However, the performance maintained stable for the following hundreds of hours. These outstanding electrochemical performance and stability confirms the applicability of PB9CN as an air electrode material for multiple kinds of solid oxide electrochemical cells.

The present disclosure provides a description of the structure and use of non-limiting illustrative embodiments. Although certain embodiments have been described with a certain degree of particularity, or with reference to one or more individual embodiments, those skilled in the art could make numerous alterations to the disclosed embodiments without departing from the scope of this invention. As such, the various illustrative embodiments of the devices are not intended to be limited to the particular forms disclosed. Rather, they include all modifications and alternatives falling within the scope of the claims, and embodiments other than the one shown may include some or all of the features of the depicted embodiment. For example, components may be omitted or combined as a unitary structure, and/or connections may be substituted. Further, where appropriate, aspects of any of the examples described above may be combined with aspects of any of the other examples described to form further examples having comparable or different properties and addressing the same or different problems. Similarly, it will be understood that the benefits and advantages described above may relate to one embodiment or may relate to several embodiments.

APPENDIX

1 Liu, M., Lynch, M. E., Blinn, K., Alamgir, F. M. & Choi, Y. Rational SOFC material design: new advances and tools. Materials Today 14, 534-546, doi:10.1016/s1369-7021(11)70279-6 (2011).

2 Park, S., Shao, Y., Liu, J. & Wang, Y. Oxygen electrocatalysts for water electrolyzers and reversible fuel cells: status and perspective. Energy & Environmental Science 5, doi:10.1039/c2ee22554a (2012).

3 Pellow, M. A., Emmott, C. J. M., Barnhart, C. J. & Benson, S. M. Hydrogen or batteries for grid storage? A net energy analysis. Energy & Environmental Science 8, 1938-1952, doi:10.1039/c4ee04041d (2015).

4 Chen, Y. et al. A robust fuel cell operated on nearly dry methane at 500° C. enabled by synergistic thermal catalysis and electrocatalysis. Nature Energy, doi:10.1038/s41560-018-0262-5 (2018).

5 Duan, C. et al. Highly durable, coking and sulfur tolerant, fuel-flexible protonic ceramic fuel cells. Nature 557, 217-222, doi:10.1038/s41586-018-0082-6 (2018).

6 Chuancheng Duan, R. K., Huayang Zhu, Neal Sullivan, Liangzhu Zhu, Liuzhen Bian, Dylan Jennings and Ryan O'Hayre. Highly efficient reversible protonic ceramic electrochemical cells for power generation and fuel production. nature Energy 4, 230-240, doi:10.1038/s41560-019-0333-2 (2019).

7 Vollestad, E. et al. Mixed proton and electron conducting double perovskite anodes for stable and efficient tubular proton ceramic electrolysers. Nat Mater, doi:10.1038/s41563-019-0388-2 (2019).

8 Ding, H. et al. Self-sustainable protonic ceramic electrochemical cells using a triple conducting electrode for hydrogen and power production. Nature Communications 11, doi:10.1038/s41467-020-15677-z (2020).

9 Ding, D., Li, X., Lai, S. Y., Gerdes, K. & Liu, M. Enhancing SOFC cathode performance by surface modification through infiltration. Energy & Environmental Science 7, doi:10.1039/c3ee42926a (2014).

10 Gao, Z., Mogni, L. V., Miller, E. C., Railsback, J. G. & Barnett, S. A. A perspective on low-temperature solid oxide fuel cells. Energy & Environmental Science 9, 1602-1644, doi:10.1039/c5ee03858h (2016).

11 Kim, J. et al. Proton conducting oxides: A review of materials and applications for renewable energy conversion and storage. Renewable and Sustainable Energy Reviews 109, 606-618, doi:10.1016/j.rser.2019.04.042 (2019).

12 Duan, C., Huang, J., Sullivan, N. & O'Hayre, R. Proton-conducting oxides for energy conversion and storage. Applied Physics Reviews 7, doi:10.1063/1.5135319 (2020).

13 Chen, Y. et al. A robust and active hybrid catalyst for facile oxygen reduction in solid oxide fuel cells. Energy & Environmental Science 10, 964-971, doi:10.1039/c6ee03656b (2017).

14 Téllez, H., Druce, J., Ju, Y.-W., Kilner, J. & Ishihara, T. Surface chemistry evolution in LnBaCo₂O₅+double perovskites for oxygen electrodes. International Journal of Hydrogen Energy 39, 20856-20863, doi:10.1016/j.ijhydene.2014.06.102 (2014).

15 Wei, B., Schroeder, M. & Martin, M. Surface Cation Segregation and Chromium Deposition on the Double-Perovskite Oxide PrBaCo₂O_5+δ. ACS Appl Mater Interfaces 10, 8621-8629, doi:10.1021/acsami.7b17881 (2018).

16 Kim, J.-H. & Manthiram, A. Layered LnBaCo2O5+δ perovskite cathodes for solid oxide fuel cells: an overview and perspective. Journal of Materials Chemistry A 3, 24195-24210, doi:10.1039/c5ta06212h (2015).

17 Zhang, S.-L. et al. Cobalt-substituted SrTi0.3Fe0.7O3−δ: a stable high-performance oxygen electrode material for intermediate-temperature solid oxide electrochemical cells. Energy & Environmental Science 11, 1870-1879, doi:10.1039/c8ee00449h (2018).

18 Chen, Y. et al. A highly active, CO2-tolerant electrode for the oxygen reduction reaction. Energy & Environmental Science 11, 2458-2466, doi:10.1039/c8ee01140k (2018).

19 Duan, C., Hook, D., Chen, Y., Tong, J. & O'Hayre, R. Zr and Y co-doped perovskite as a stable, high performance cathode for solid oxide fuel cells operating below 500° C. Energy & Environmental Science 10, 176-182, doi:10.1039/c6ee01915c (2017).

20 Song, Y. et al. Self-Assembled Triple-Conducting Nanocomposite as a Superior Protonic Ceramic Fuel Cell Cathode. Joule, doi:10.1016/j.joule.2019.07.004 (2019).

21 Kresse, G. Efficient iterative schemes for ab initio total-energy calculations using a plane-wave basis set. PHYSICAL REVIEW B 54, 11169-11186 (1996).

22 John P. Perdew, K. B., Matthias Ernzerhof. Generalized Gradient Approximation Made Simple. PHYSICAL REVIEW LETTERS 77, 3865-3868 (1996).

23 Methfessel, M. & Paxton, A. T. High-precision sampling for Brillouin-zone integration in metals. Phys Rev B Condens Matter 40, 3616-3621, doi:10.1103/physrevb.40.3616 (1989).

24 Monkhorst, H. J. & Pack, J. D. Special points for Brillouin-zone integrations. Physical Review B 13, 5188-5192, doi:10.1103/PhysRevB.13.5188 (1976).

25 Choi, S. et al. Highly efficient and robust cathode materials for low-temperature solid oxide fuel cells: PrBa_0.5Sr_0.5Co_(2-x)Fe_(x)O_(5+δ). Sci Rep 3, 2426, doi:10.1038/srep02426 (2013).

26 Kim, J. et al. Triple-conducting layered perovskites as cathode materials for proton-conducting solid oxide fuel cells. ChemSusChem 7, 2811-2815, doi:10.1002/cssc.201402351 (2014).

27 Feifei Dong, M. N., Yubo Chen, Dengjie Chen, Moses O. Tad and Zongping Shao. Structural and oxygen-transport studies of double perovskites PrBa1xCo₂O_5+δ (× ¼ 0.00, 0.05, and 0.10) toward their application as superior oxygen reduction electrodes. Journal of Materials Chemistry A 2, 20520, doi:10.1039/C4TA04372C (2014).

28 Tsvetkov, N., Lu, Q., Sun, L., Crumlin, E. J. & Yildiz, B. Improved chemical and electrochemical stability of perovskite oxides with less reducible cations at the surface. Nat Mater 15, 1010-1016, doi:10.1038/nmat4659 (2016).

29 Zhang, K., Ge, L., Ran, R., Shao, Z. & Liu, S. Synthesis, characterization and evaluation of cation-ordered LnBaCo₂O_5+δ as materials of oxygen permeation membranes and cathodes of SOFCs. Acta Materialia 56, 4876-4889, doi:10.1016/j.actamat.2008.06.004 (2008).

30 Druce, J. et al. Surface termination and subsurface restructuring of perovskite-based solid oxide electrode materials. Energy Environ. Sci. 7, 3593-3599, doi:10.1039/c4ee01497a (2014).

31 Ren, R. et al. Tuning the defects of the triple conducting oxide BaCo_0.4Fe_0.4Zr_0.1Y_0.1O_3−δperovskite toward enhanced cathode activity of protonic ceramic fuel cells. Journal of Materials Chemistry A 7, 18365-18372, doi:10.1039/c9ta04335g (2019).

31 Tang, W. et al. Understanding of A-site deficiency in layered perovskites: promotion of dual reaction kinetics for water oxidation and oxygen reduction in protonic ceramic electrochemical cells. Journal of Materials Chemistry A, doi:10.1039/dOta05137c (2020).

33 Zhao, B. et al. A tailored double perovskite nanofiber catalyst enables ultrafast oxygen evolution. Nat Commun 8, 14586, doi:10.1038/ncomms14586 (2017).

34 Jin Suntivich, K. J. M., Hubert A. Gasteiger, John B. Goodenough, Yang Shao-Horn. A Perovskite Oxide Optimized for Oxygen Evolution Catalysis from Molecular Orbital Principles. Science 334, 1383-1385 (2011).

35 Lee, J. G., Park, J. H. & Shul, Y. G. Tailoring gadolinium-doped ceria-based solid oxide fuel cells to achieve 2 W cm(-2) at 550 degrees C. Nat Commun 5, 4045, doi:10.1038/ncomms5045 (2014).

36 Chen, Y. et al. A Highly Efficient Multi-phase Catalyst Dramatically Enhances the Rate of Oxygen Reduction. Joule 2, 938-949, doi:10.1016/j.joule.2018.02.008 (2018).

37 Haile, Z. S. S. M. A high-performance cathode for the next generation of solid-oxide fuel cells. nature (2004).

38 Song, Y. et al. A Cobalt-Free Multi-Phase Nanocomposite as Near-Ideal Cathode of Intermediate-Temperature Solid Oxide Fuel Cells Developed by Smart Self-Assembly. Adv Mater, e1906979, doi:10.1002/adma.201906979 (2020).

39 Kuai, X. et al. Boosting the Activity of BaCo0.4Fe0.4Zr0.1Y0.1O3−δ Perovskite for Oxygen Reduction Reactions at Low-to-Intermediate Temperatures through Tuning B-Site Cation Deficiency. Advanced Energy Materials, doi:10.1002/aenm.201902384 (2019).

40 Ding, C. & Hashida, T. High performance anode-supported solid oxide fuel cell based on thin-film electrolyte and nanostructured cathode. Energy & Environmental Science 3, doi:10.1039/c0ee00255k (2010).

41 Chuancheng Duan, J. T., Meng Shang, Stefan Nikodemski, Michael Sanders, Sandrine Ricote, Ali Almansoori, Ryan O'Hayre. Readily processed protonic ceramic fuel cells with high performance at low temperatures. Science 349, 1321-1326 (2015).

42 Choi, S. et al. Exceptional power density and stability at intermediate temperatures in protonic ceramic fuel cells. Nature Energy 3, 202-210, doi:10.1038/s41560-017-0085-9 (2018).

43 Grimaud, A. et al. Hydration Properties and Rate Determining Steps of the Oxygen Reduction Reaction of Perovskite-Related Oxides as H+-SOFC Cathodes. Journal of The Electrochemical Society 159, B683-B694, doi:10.1149/2.101205jes (2012).

44 Lin, Y. et al. Evaluation of Ba_0.5Sr_0.5Co_0.8Fe_0.2O₃−δ as a potential cathode for an anode-supported proton-conducting solid-oxide fuel cell. Journal of Power Sources 180, 15-22, doi:10.1016/j.jpowsour.2008.02.044 (2008).

AIR ELECTRODES OF SOLID OXIDE ELECTROCHEMICAL CELLS

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