BACKGROUND OF THE INVENTION

1. Field of the Invention

[0001] This present invention relates to engineering methods for constructing rechargeable oxide-ion battery (ROB) cells and stacks. More specifically, the invention details the processing steps using a cell membrane assembly and a stainless steel housing structure.

2. Description of Related Art

[0002] Electrical energy storage is crucial for the effective proliferation of an electrical economy and for the implementation of many renewable energy

technologies. During the past two decades, the demand for the storage of electrical energy has increased significantly in the areas of portable, transportation, load- leveling and central backup applications. The present electrochemical energy storage systems are simply too costly to penetrate major new markets. Higher performance is required, and environmentally acceptable materials are preferred. Transformational changes in electrical energy storage science and technology are in great demand to allow higher and faster energy storage at lower costs and longer lifetimes necessary for major market enlargement. Most of these changes require new materials and/or innovative concepts, with demonstration of larger redox capacities that react more rapidly and reversibly with cations and/or anions.

[0003] Batteries are by far the most common form of storing electrical energy, ranging from: standard every day lead - acid cells, nickel-metal hydride (NiMH) batteries taught by Kitayama in U.S. Patent No. 6,399,247 Bl, metal-air cells taught by Isenberg in U.S. Patent No. 4,054,729, and to the lithium-ion battery taught by Ohata in U.S. Patent No. 7,396,612 B2. These latter metal-air, nickel-metal hydride and lithium-ion battery cells require liquid electrolyte systems.

[0004] Batteries range in size from button cells used in watches, to megawatt load leveling applications. They are, in general, efficient storage devices, with output energy typically exceeding 90% of input energy, except at the highest power densities. [0005] Rechargeable batteries have evolved over the years from lead-acid through nickel-cadmium and nickel-metal hydride (NiMH) to lithium-ion batteries. NiMH batteries were the initial workhorse for electronic devices such as computers and cell phones, but they have almost been completely displaced from that market by lithium- ion batteries because of the latter's higher energy storage capacity. Today, NiMH technology is the principal battery used in hybrid electric vehicles, but it is likely to be displaced by the higher power energy and now lower cost lithium batteries, if the latter's safety and lifetime can be improved. Of the advanced batteries, lithium-ion is the dominant power source for most rechargeable electronic devices.

[0006] What is needed is a dramatically new electrical energy storage device that can easily discharge and charge a high capacity of energy quickly and reversibly, as needed. What is also needed is a device that can operate for years without major maintenance. What is also needed is a device that does not need to operate on natural gas, hydrocarbon fuel or its reformed by-products such as H ₂ . One possibility is a rechargeable oxide-ion battery (ROB), as set out, for example, in Application Serial No. 12/695,386, filed on January 28, 2010 (now, U.S. Patent Publication No. US 2011/0033769) (ESCM 283139-01284), and Application Serial No. 12/876,391, filed on September 7, 2010 (ESCM 283139-01292).

[0007] A ROB comprises a metal electrode, an oxide-ion conductive electrolyte, and a cathode. The metal electrode undergoes reduction-oxidation cycles during charge and discharge processes for energy storage. The working principles of a rechargeable oxide-ion battery cell 10 are schematically shown in Fig. 1. In discharge mode, oxide-ion anions migrate from high partial pressure of the oxygen side (air electrode- 12) to low partial pressure of the oxygen side (metal electrode- 14) under the driving force of the gradient oxygen chemical potential. Electrolyte is shown as 16. There exist two possible reaction mechanisms to oxidize the metal. One of them, solid-state diffusion reaction as designated as Path 1 , is that oxide ion can directly

electrochemically oxidize metal to form metal oxide. The other, gas-phase transport reaction designated as Path 2, involves generation and consumption of gaseous phase oxygen. The oxide ion can be initially converted to a gaseous oxygen molecule on a metal electrode, and then further reacts with metal via solid-gas phase mechanism to form metal oxide. In charge mode, the oxygen species, released by reducing metal oxide to metal via electrochemical Path 1 or solid-gas mechanism Path 2, are transported from a metal electrode back to an air electrode.

[0008] During discharge/charge cycles metal redox reactions induce significant volume variation, for instance, if iron (Fe) metal is used, the volume change associated with the reaction of Fe+l/20 ₂ =FeO is 1.78 times. Therefore, the metal electrode must be appropriately designed so that the drastic volume variation can be properly accommodated. For energy storage application, oxide ion must be transported across the electrolyte between a metal electrode and a cathode to carry electrical charge. Therefore, the metal electrode must be hermetically sealed to prevent direct contact with an oxygen-containing environment (for example, air). Otherwise, oxygen in air will directly consume the metal without involving charge transfer between electrodes, which will lead to self discharge.

[0009] The cell voltage for each individual ROB cell is limited in most cases, for practical applications where certain voltage output is demanded, ROB cells must be connected together to form a stack to raise the voltage of a ROB device. Thus, there is a need of engineering methods to construct a ROB stack using single ROB cells. It is a main object of this invention to provide ROB cell and stack designs that supply the above needs by using cost-effective materials and processing techniques.

SUMMARY OF THE INVENTION

[0010] The above needs for producing a ROB cell and stack are supplied and object accomplished by utilizing a cell membrane assembly, stainless steel housing structure, seal(s), and electrical collector(s). The construction of the planar ROB cell and stack, has an oxidation resistant metal housing, such as nickel-based alloys, chromium-based alloys or iron-based alloys, preferably stainless steel. The planar design, compared with tubular designs, reduces cell Ohmic loss. Both electrolyte supported and skeleton supported cells can be accommodated in the planar design. The ROB cell of this invention uses brazing and welding seals to separate active metal components from air, and also has compliant cell-to-cell current collectors.

[0011] The above object is accomplished by providing a process for constructing a rechargeable oxide-ion battery (ROB) cell comprising the steps: a) forming a membrane assembly of a top air electrode, a bottom negative metal electrode and a middle contacting ceramic electrolyte which extends beyond the contacting electrode(s);

b) sealing the extending sides of the ceramic electrolyte surface of the membrane assembly to a surface of a metallic frame which surrounds the membrane assembly, to form a framed membrane assembly;

c) incorporating active metal components into hollow portions of a metal housing structure to form an active housing structure;

d) forming electrically conductive contact between the framed membrane assembly and the active housing structure; and

e) joining the framed membrane assembly and the active housing structure, using a process selected from brazing and welding or their combination to form an ROB cell.

[0012] The invention also includes a process for constructing multiple ROB cell stacks comprising the further steps of:

f) forming electrical contact between two cells by installing a cell to cell collector between the air electrode of a first ROB cell and the central section of the bottom surface of the active housing structure of a successive second ROB cell made as described above; and

g) forming an insulation seal between the top surface of the picture frame described above of the peripheral section of the first ROB cell and the bottom peripheral section of a second successive ROB cell made as described above.

[0013] Preferably, the bottom negative electrode is a metal electrode.

BRIEF DESCRIPTION OF THE DRAWINGS

[0014] For a better understanding of the invention, reference may be made to the preferred embodiments exemplary of this invention, shown in the accompanying drawings in which:

[0015] FIG. 1 illustrates the known working principals of a rechargeable oxide-ion battery (ROB) cell;

[0016] FIGS. 2A and 2B, which best describe the invention, are schematic illustrations of joining together a planar ROB cell of this invention, showing component arrangement (FIG. 2A), and a complete cell (FIG. 2B); [0017] FIG. 3 summarizes the exemplary processing steps of construction of a planar cell of this invention in a step by step detail;

[0018] FIG. 4 shows a three-dimensional schematic view of a tested proof-of- concept ROB cell;

[0019] FIG. 5 shows the discharge/charge curves of the proof-of-concept ROB cell of this invention at 785°C; and

[0020] FIG. 6 is a schematic illustration of a planar ROB battery stack of a plurality of electrically connected cells according to this invention.

DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0021] The requirements of a ROB cell include:

a) an air electrode for reversible conversion of oxygen into an oxide ion (O ^2" ) that carries/has two electrical charges;

b) an oxide-ion conductive electrolyte for transporting electrical charge in the form of O ^2" ;

c) a metal electrode where electrical charge associated with the oxide-ion is stored or released by an active metal component(s), and for accommodating the volume change associated with a metal redox reaction;

d) a reliable seal separating direct contact between air and active metal; and

e) cost effectiveness.

[0022] Referring now to FIGS. 2A and 2B, which show a schematic illustration of joining components (2A), and which show a finished planar ROB cell (2B). The top air electrode is shown as 20, while 22 shows a sandwiched ceramic middle electrolyte, and 24 shows the bottom metal electrode. Components 20, 22 and 24 together form a membrane assembly, generally shown as 40, best shown in FIG. 3. In FIGS. 2A and 2B, 26 shows a surrounding metallic frame, which is herein defined as a "picture frame." A seal 28 connects the membrane assembly 40 to the picture frame 26. A metal housing structure 30 is shown, where active material 32 will fill the metal housing pockets or holes 50. An electrical current collector 34 is shown between the metal housing structure 30 and the bottom metal electrode 24, best shown in FIG. 2B, while 36 shows the seal connecting the picture frame 26 and the metal housing structure 30. [0023] Referring now to FIG. 3, an exemplary ROB cell fabrication process is illustrated. In step 1, a membrane assembly 40 is formed having a top air electrode 20, a bottom metal electrode 24 and a middle ceramic electrolyte 22. These three components can be adhered together by classic materials processing techniques involving forming, tape casting, tape calendaring, screen printing, extrusion, and pressing followed by high-temperature sintering. Useful air electrodes include, for example, doped LaMn0 _3-z , LaCo0 _3-z , LaCo _x Fei _-x 03 _-z , SmySri _-y Co03 _-z , doped ceria, stabilized zirconia, doped/updoped LaaSri.aGabMgi.bCb-z, doped Bi ₂ 0 ₃ and their mixture, where x = 0 to 1, y = 0.2 to 0.7, z = 0.001 to 0.1, a = 0.5 to 1, and b = 0.6 to 1. Useful ceramic electrolytes include oxide ion conductive materials, for example, doped Ce0 ₂ , stabilized zirconia, doped/updoped LaaSri.aGabMgi.bCb-z, and their mixture.

[0024] Useful bottom metal electrodes include, for example, electronically conductive materials, such as electrically conductive ceramics, silver, gold, platinum, palladium, nickel, copper, stainless steel, and any of their mixtures.

[0025] Continuing with FIG. 3, a metallic frame 26, made of oxidation-resistant alloy, is configured to surround the membrane assembly 40 as a "picture frame," where the inside perimeter of the metallic frame 26 contains a seal 28 that contacts the inside of metallic frame 26 and top surface 42 and side ends 44 of the ceramic electrolyte 22. Useful seals include, for example, glass, ceramic, brazing alloys, or a combination of the two. Finally, the components are heat treated to provide a framed membrane assembly 46.

[0026] Additionally, a hollow oxidation-resistant metal alloy housing structure 30, having sides 48 and interior pockets/holes/pores 50 (refer to FIG. 2A) is provided.

Chromium-based alloy, Ni-based alloys or Fe-based alloys can be selected to fabricate the metal housing structure 30. Stainless steel is preferable, however, in this invention because of its low cost, resistance against oxidation, and its reasonable thermal expansion match with membrane assembly 40. Active material components 32 are comprised of any single-phase metal or metal oxide material selected from the group consisting of Ti, Ce, Cr, Mn, Fe, Co, Ni, Cu, Mo, and W, and of any two-phase material selected from the group consisting of Ti-Ti0 ₂ , Ce-Ce0 ₂ , Cr-Cr ₂ 0 ₃ , Mn-

Mn ₂ 0 ₃ , Mn-Mn ₃ 0 ₄ , Mn-MnO, Fe-FeO, Fe-Fe ₃ 0 ₄ , Fe-Fe ₂ 0 ₃ , Co-CoO, Co-Co ₃ 0 ₄ , Co-

Co ₂ 0 ₃ , Ni-NiO, Cu-Cu ₂ 0, Cu-CuO, Mo-Mo0 ₂ , Mo-Mo0 ₃ , and W-W0 ₃ , preferably Fe, Fe oxide and Fe alloyed with other elements including, for example, Cu, Mo, W and Mn. The active material 32 is incorporated into the interior pockets 50, to provide an active housing structure 52. The interior skeleton of the housing structure 30 can have, for example, a plurality of transverse members 54, as shown, slightly shorter to accommodate electrical current collectors 34.

[0027] Electrical current collectors 34 (also see FIGS. 2A and 2B) are also applied between the bottom surface 24' of the metal electrode 24 and the top surface 56 of the plurality of transverse members 54 of the metal housing structure. Useful current collectors 34 include metals, for example, Pt, Ag, Au, Ni, Cu, alloys, and electrically conductive ceramics such as doped/undoped Ce0 ₂ , stabilized zirconia,

doped/undoped La _x Sri _-x GayMgi _-y 03 _-z , doped LaCr0 _3-z , doped SrTi0 _3-z , doped LaV0 _3- z, Gd ₂ Ti _x Moi _-x 07, Sr ₂ Mgi _-x Mn _x Mo06 _-z , and any of their mixtures, where x = 0.5 to 1, y = 0.6 to 1 and z = 0.001 to 0.1. Then framed membrane assembly 46 and active housing structure 52 are then sealed together as shown by use of seal 36 which can include glass, welding, cement, ceramics, brazing, or combinations to form a planar rechargeable oxide-ion battery (ROB) cell supported by a metal housing structure.

[0028] Example: a proof-of-concept cell, similar in structure and materials most respects to FIG. 2B was made; using a stainless steel (430SS) housing structure. A commercial "Hionics®" electrolyte membrane was purchased from Fuel Cell Material and was nominally 150-μιη (micrometers) thick. A porous platinum air electrode and a porous platinum metal electrode were attached to the electrolyte membrane to form the cell membrane assembly 64. Then the assembly was sealed onto a stainless steel picture frame 68 using a ceramic adhesive sold commercially as Aremco

"ceramabond552®" 66. Iron sponge active material powder (Alfa Aesar) was loaded into the pocket of a metal housing structure made of stainless steel. A Pt current collector was established between the porous Pt metal electrode and the metal housing structure. The picture frame and the metal housing structure were then welded together to form a ROB cell, as shown in FIG. 4. To facilitate electrochemical testing, gas inlet 60 and outlet 62 were created by welding stainless steel tubes through the picture frame. The cell electrical performance was measured at 785°C during constant voltage discharge/charge. As shown in FIG. 5, the cell displayed a steady-state current density of about 30mA/cm ² during charging at 1.2V for 1800 seconds. The bottom negative value curve shows current density at discharge at 0.8V for 1800 seconds. Such steady performance based on these two curves validates the feasibility of the ROB cell of this invention.

[0029] Referring to FIG. 6, this invention also describes the processing steps for assembling a ROB stack; using the constructed cells including: e) installing cell-to- cell current collector 58 between the air electrode 20' of a first ROB cell 80, and the central section of the bottom surface 70 of the metal housing structure 30' of a second successive ROB cell 82; and f) forming insulation seal 72 between the top surface 74 of the picture frame of the first ROB cell and the bottom peripheral section 76 of the metal housing structure of the second successive ROB cell. Useful cell-to-cell current collectors include, for example, metal/alloy screen or a contact past made of metal or electrically conductive ceramic such as doped LaMn03 _-z , LaCo03 _-z , LaCo _x Fei _-x 03 _-z , Sm _y Sri _-y Co0 _3-z , where x is = 0 to 1, y = to 0.2 to 0.7 and z = 0.001 to 0.1. Useful insulation seals 72 includes, for example, Mica and/or glass.

[0030] While specific embodiments of the invention have been described in detail, it will be appreciated by those skilled in the art that various modifications and alternatives to those details could be developed in light of the overall teachings of the disclosure. Accordingly, the particular embodiments disclosed are meant to be illustrative only and not limiting as to the scope of the invention which is to be given the full breadth of the appended claims and any and all equivalents thereof.