The present disclosure relates to a reference electrode for on-board battery cell diagnostics and a method of fabricating the same.
High-energy density, electrochemical cells, such as lithium-ion batteries may be used in a variety of consumer products and vehicles, such as Hybrid Electric Vehicles (HEVs) and Electric Vehicles (EVs). Typical lithium-ion, lithium sulfur, and lithium-lithium symmetrical batteries include a first electrode, a second electrode, an electrolyte material, and a separator. One electrode serves as a positive electrode or cathode and another serves as a negative electrode or anode. A stack of battery cells may be electrically connected to increase overall output.
Rechargeable lithium-ion batteries operate by reversibly passing lithium-ions back and forth between the negative electrode and the positive electrode. A separator and an electrolyte are disposed between the negative and positive electrodes. The electrolyte is suitable for conducting lithium-ions and may be in solid (e.g., solid state diffusion) or liquid form. Lithium-ions move from a cathode (positive electrode) to an anode (negative electrode) during charging of the battery, and in the opposite direction when discharging the battery. It may be desirable to perform electrochemical analysis on batteries or certain components of batteries, such as the cathode and the anode.
For example, electrochemical analysis may produce calibrations for control systems in electric vehicles pertaining to fast charge, lithium plating, state of charge, and power estimation. The electrodes may be analyzed by providing a reference electrode in an electrochemical cell having positive and negative electrodes. The reference electrode enables monitoring of individual positive and negative electrode potentials as the cell is being cycled. Potentials may be monitored in a lab setting or during real-time use of a system including the electrochemical cell. For example, potentials may be detected during operation of a vehicle, as part of regular vehicle diagnostics. Detected potentials may be used in vehicle control algorithms to improve cell performance, such as by raising anode potential to decrease lithium plating.
A properly operating reference electrode is required to permit accurate and reproducible measurements for analysis of an electrochemical cell. Therefore, a reference electrode should have stable and reproducible potential. Reference electrodes used are preferably reversible type electrodes. In a reversible electrode a small cathodic current produces the reduction reaction, while a small anodic current produces the oxidation reaction. Generally, the three main requirements for a satisfactory reference electrode, are reversibility (non-polarizability), reproducibility, and stability.
A reference electrode assembly for an electrochemical cell includes a separator constructed from an electrically-insulating porous material. The reference electrode assembly also includes a current collector having a sputtered electrically-conducting porous layer arranged directly on the separator and a sputtered lithium iron phosphate (LFP) layer arranged directly on the electrically-conducting porous layer. The reference electrode assembly additionally includes an electrical contact connected to the current collector.
The electrical contact may include either a gold/graphite or a silver epoxy tab.
The separator may be either doped or coated with a ceramic material to minimize a likelihood of an electrical short circuit.
The electrically-conducting porous layer may include an aluminum layer having a thickness in a 50-500 nm range and arranged directly on the separator.
The electrically-conducting porous layer having the aluminum layer may additionally include a carbon layer having a thickness in a 5-50 nm range and arranged directly on the aluminum layer, such that the aluminum layer is sandwiched between the separator and the carbon layer.
The electrically-conducting porous layer may include a graphite-carbon layer having a thickness in a 50-500 nm range and arranged directly on the separator.
The electrically-conducting porous layer may include a nickel layer having a thickness in a 50-500 nm range and arranged directly on the separator.
The electrically-conducting porous layer may include a Tin layer having a thickness in a 50-500 nm range and arranged directly on the separator.
The LFP layer may have a thickness in a 70-500 nm range.
A particular method using successive vacuum deposition of individual layers onto the separator is employed in fabricating the reference electrode assembly.
Specifically, the method may include setting up the separator in the vacuum chamber with arranging the separator on a movable fixture. In the subject embodiment, the method may also include applying the current collector onto the separator with bombarding a stationary current collector target and a stationary LFP target to vacuum deposit the respective layers onto the current collector while transporting the movable fixture.
Alternatively, the method may include setting up in the vacuum chamber the separator with arranging the separator on a stationary fixture. In the subject embodiment, the method may also include setting up a current collector target and an LFP target on a movable fixture, such as a rotatable turret, and sequentially bombarding the respective current collector target and the LFP target while shifting the movable fixture to vacuum deposit the respective layers onto the current collector.
The above features and advantages, and other features and advantages of the present disclosure, will be readily apparent from the following detailed description of the embodiment(s) and best mode(s) for carrying out the described disclosure when taken in connection with the accompanying drawings and appended claims.
Those having ordinary skill in the art will recognize that terms such as “above,” “below,” “upward,” “downward,” “top,” “bottom,”, “left”, “right”, etc., are used descriptively for the figures, and do not represent limitations on the scope of the disclosure, as defined by the appended claims. Furthermore, the teachings may be described herein in terms of functional and/or logical block components and/or various processing steps. It should be realized that such block components may be comprised of a number of hardware, software, and/or firmware components configured to perform the specified functions.
Referring to
In Li-Ion batteries, lithium ions move from the anode 14 through the electrolyte 18 to the cathode 16 during discharge, and back when charging. Li-Ion batteries use a lithium compound as the material at the positive electrode and typically graphite at the negative electrode. Generally, the reactants in the electrochemical reactions in a Li-Ion cell 10 are materials of anode and cathode, both of which are compounds that may host lithium atoms. During discharge, an oxidation half-reaction at the anode 14 produces positively charged lithium ions and negatively charged electrons. The oxidation half-reaction may also produce uncharged material that remains at the anode 14. Lithium ions move through the electrolyte 18, electrons move through an external circuit (including a connection to the electrical load 12 or to a charging device), and then they recombine at the cathode (together with the cathode material) in a reduction half-reaction. The electrolyte 18 and the external circuit provide conductive media for lithium ions and electrons, respectively, but do not partake in the electrochemical reaction.
Generally, during discharge of an electrochemical battery cell, electrons flow from the anode 14 toward the cathode 16 through the external circuit. The reactions during discharge lower the chemical potential of the cell, so discharging transfers energy from the cell to wherever the electric current dissipates its energy, mostly in the external circuit. During charging, the described reactions and transports go in the opposite direction: electrons move from the positive electrode to the negative electrode through the external circuit. To charge the cell, the external circuit has to provide electric energy. This energy is then stored (with some loss) as chemical energy in the cell. In a Li-Ion cell, both the anode 14 and cathode 16 allow lithium ions to move in and out of their structures via a process called insertion (intercalation) or extraction (deintercalation), respectively. Typically, the anode 14 and the cathode 16 are associated with respective electrically conductive current collectors - an anode current collector 22 and a cathode current collector 24. Each current collector 22, 24 may include metal in the form of metal foil, a metal grid or screen, or expanded metal having suitable thickness to accommodate an increased amount of electrode material. Current collector materials may, for example, include copper, nickel, aluminum, and various electrically conductive alloys.
It may be desirable to perform electrochemical analysis on the anode 14 and cathode 16 electrodes to produce calibrations for control systems employing the electrochemical storage cell 10, such as in hybrid electric and electric vehicles, for example pertaining to fast charge, lithium plating, state of charge, and power estimation. The anode 14 and cathode 16 electrodes may be analyzed by providing a reference electrode assembly 26 (shown in
The reference electrode assembly 26 is disposed between the anode 14 and the separator diaphragm 20. The reference electrode assembly 26 includes a second separator 28. The second separator 28 is constructed from an electrically-insulating porous material providing increased surface area, compared to a non-porous material, for faster charging. The second separator 28 may be constructed from a polymer or a mixture of polymeric materials, such as polypropylene or polyethylene, or aramid fibers. Additionally, the second separator 28 may be either doped or coated with an insulating ceramic material 28A (shown in
The reference electrode assembly 26 also includes a reference current collector 30. The reference current collector 30 has an electrically-conducting porous layer 32 arranged on the second separator 28. Specifically, the reference current collector 30 is sputtered, in a vacuum chamber, directly onto the second separator 28. The electrically-conducting porous layer 32 may include an aluminum layer 32A arranged on the second separator 28 and may additionally include a carbon layer 32B arranged on the aluminum layer 32A (shown in
In a separate embodiment shown in
The reference electrode assembly 26 additionally includes a sputtered lithium iron phosphate (LFP) layer 34 arranged directly on the electrically-conducting porous layer 32 (shown in
With resumed reference to
A method 100 of fabricating the reference electrode assembly 26 for an electrochemical cell, such as the Li-Ion cell 10 described with respect to
After frame 104, the method advances to apply the current collector 30 onto the separator 28, starting in frame 106. In frame 106, the method includes, sputtering, in the vacuum chamber 200, the electrically-conducting porous layer 32 directly onto or over the separator 28. As described with respect to
After frame 106, the method advances to frame 108. In frame 108 the method includes sputtering, in the vacuum chamber 200, the lithium iron phosphate (LFP) layer 34 directly onto the sputtered electrically-conducting porous layer 32. The sputtered LFP layer 34 may have a thickness in the 70-500 nm range. As shown in
Alternatively, as shown in
From frame 108, method 100 may advance to frame 110, where the method includes generating the electrical contact 36 connected to the current collector 30. The electrical contact 36 may be fabricated by applying the epoxy tab 36A from either gold/graphite or silver to an extension of or a projection from the current collector 30. After frame 110, the method may proceed to frame 112. In frame 112 the method may include organizing, packaging, and/or queueing up the reference electrode assembly 26 for subsequent incorporation into an electrochemical cell, such as the Li-Ion cell 10 described above. The method may conclude in frame 114.
The detailed description and the drawings or figures are supportive and descriptive of the disclosure, but the scope of the disclosure is defined solely by the claims. While some of the best modes and other embodiments for carrying out the claimed disclosure have been described in detail, various alternative designs and embodiments exist for practicing the disclosure defined in the appended claims. Furthermore, the embodiments shown in the drawings or the characteristics of various embodiments mentioned in the present description are not necessarily to be understood as embodiments independent of each other. Rather, it is possible that each of the characteristics described in one of the examples of an embodiment may be combined with one or a plurality of other desired characteristics from other embodiments, resulting in other embodiments not described in words or by reference to the drawings. Accordingly, such other embodiments fall within the framework of the scope of the appended claims.