According to the present invention, techniques related to energy devices are provided. More particularly, embodiments of the present invention relate to methods to design, manufacture, and structure a multi-component energy device having a unified structure. The individual components can include electrochemical cells, photovoltaic cells, fuel-cells, capacitors, ultracapacitors, thermoelectric, piezoelectric, micro electromechanical turbines, or energy scavengers. The methods and systems described herein are also applicable to a variety of energy systems.
According to an embodiment of the present invention, a method for using an integrated battery and device structure is provided. The method includes using two or more stacked electrochemical cells integrated with each other formed overlying a surface of a substrate. The two or more stacked electrochemical cells include related two or more different electrochemistries with one or more devices formed using one or more sequential deposition processes. The one or more devices are integrated with the two or more stacked electrochemical cells to form the integrated battery and device structure as a unified structure overlying the surface of the substrate. The one or more stacked electrochemical cells and the one or more devices are integrated as the unified structure using the one or more sequential deposition processes. The integrated battery and device structure is configured such that the two or more stacked electrochemical cells and one or more devices are in electrical, chemical, and thermal conduction with each other.
Numerous benefits are achieved by way of the present invention over conventional techniques. For example, electrochemical cells described herein present multiple chemistries to accommodate a wider range of voltage and current compared to individual ones. Additionally, energy-scavenging elements are utilized to collect energy and replenish it to other components within the unified structure. Depending upon the embodiment, one or more of these benefits may be achieved. These and other benefits will be described in more detail throughout the present specification and more particularly below.
These and other objects and features of the present invention and the manner of obtaining them will become apparent to those skilled in the art, and the invention itself will be best understood by reference to the following detailed description read in conjunction with the accompanying drawings.
Preparing a stacked cell on the back surface of a silicon (Si) solar cell as shown in
After the back metal contact is created, a separation layer of electrically insulating and thermally conductive aluminum nitride (AlN), having a thickness of 3-5 μm, is fabricated onto the aluminum layer using PVD. This layer has the function of removing heat from the two elements and convey it to a heat sink.
After the cooling element is completed, the battery components are deposited sequentially and conformally by a physical vapor deposition (PVD) process: an aluminum (Al) current collector layer (1-3 μm thick), a lithium manganese oxide (LiMn2O4) cathode layer (3-5 μm thick), a lithium phosphorous oxynitride (UPON) ceramic electrolyte layer (1-3 μm thick), a lithium (Li) metal anode layer (3-5 μm thick), and a copper (Cu) current collector layer (1-3 μm thick), respectively.
Two stacked cells having different electrochemistries are fabricated onto each other by using physical vapor deposition as reported in
The first battery components are deposited using a PVD process onto an aluminum (Al) metal film used as cathode current collector: a lithium iron phosphate (LiFePO4) cathode layer (3-5 μm thick), a lithium phosphorous oxynitride (LIPON) ceramic electrolyte layer (1-3 μm thick), a lithium (Li) metal anode layer (3-5 μm thick) and a copper (Cu) current collector layer (1-3 μm thick), respectively.
After the copper (Cu) metal current collector is created, a separation layer of electrically insulating and thermally conductive aluminum nitride (AlN), having a thickness of 3-5 μm, is fabricated onto the copper layer using PVD. This layer has the function of removing heat from the two elements and convey it to a heat sink.
After the cooling element is completed, the second battery components are deposited sequentially and conformally by a PVD process: an aluminum (Al) current collector layer (1-3 μm thick), a lithium manganese oxide (LiMn2O4) cathode layer (3-5 μm thick), a lithium phosphorous oxynitride (LIPON) ceramic electrolyte layer (1-3 μm thick), a lithium (Li) metal anode layer (3-5 μm thick) and a copper (Cu) current collector layer (1-3 μm thick), respectively.
Preparing a stacked cell on the back surface of a proton-exchange membrane (PEM) fuel-cell as shown in
After assembly of the fuel-cell a separation layer of electrically insulating and thermally conductive aluminum nitride (AlN), having a thickness of 3-5 μm, is fabricated onto the fuel-cell current collector using PVD. This layer has the function of removing heat from the two elements and conveying it to a heat sink.
After the cooling element is completed, the battery components are deposited sequentially and conformally by a PVD process. Respectively an aluminum (Al) current collector layer (1-3 μm thick), a lithium manganese oxide (LiMn2O4) cathode layer (3-5 μm thick), a lithium phosphorous oxynitride (UPON) ceramic electrolyte layer (1-3 μm thick), a lithium (Li) metal anode layer (3-5 μm thick) and a copper (Cu) current collector layer (1-3 μm thick).
Preparing a stacked cell on the back surface of an electrochemical double layer capacitor (EDLC), which is also known as an ultra-capacitor) as shown in
EDLCs describe a class of energy-storage devices that incorporate active materials including high-surface-area carbons (activated carbons), electroactive polymers, transition metal oxides and nitrides. The separation materials include advanced dielectrics, conventional and advanced polymer electrolytes and ionic conducting materials. Electrodes arrangement can be symmetric or anti-symmetric. In
After assembly of the ultra-capacitor a separation layer of electrically insulating and thermally conductive aluminum nitride (AlN), having a thickness of 3-5 μm, is fabricated onto the dielectric material layer using PVD. This layer has the function of removing heat from the two elements and conveying it to a heat sink.
After the cooling element is completed, the battery components are deposited sequentially and conformally by a PVD process: an aluminum (Al) current collector layer (1-3 μm thick), a lithium manganese oxide (LiMn2O4) cathode layer (3-5 μm thick), a lithium phosphorous oxynitride (LIPON) ceramic electrolyte layer (1-3 μm thick), a lithium (Li) metal anode layer (3-5 μm thick) and a copper (Cu) current collector layer (1-3 μm thick), respectively.
It is also understood that the examples and embodiments described herein are for illustrative purposes only and that various modifications or changes in light thereof will be suggested to persons skilled in the art and are to be included within the spirit and purview of this application and scope of the appended claims.
This application is a continuation of U.S. patent application Ser. No. 14/060,387, filed Oct. 22, 2013, which is a continuation of U.S. patent application Ser. No. 13/465,243 filed May 7, 2012, now U.S. Pat. No. 8,597,722, which is a continuation of U.S. patent application Ser. No. 12/614,169 filed Nov. 6, 2009, now U.S. Pat. No. 8,192,789, which claims priority to U.S. Provisional Patent Application No. 61/112,707 filed Nov. 7, 2008, the entire contents of which are incorporated herein by reference.
Number | Name | Date | Kind |
---|---|---|---|
4740431 | Little | Apr 1988 | A |
5569520 | Bates | Oct 1996 | A |
6083637 | Walz et al. | Jul 2000 | A |
6650000 | Ballantine et al. | Nov 2003 | B2 |
6664786 | Kretschmann et al. | Dec 2003 | B2 |
7150931 | Jaffrey | Dec 2006 | B1 |
7862927 | Krasnov et al. | Jan 2011 | B2 |
8192789 | Albano et al. | Jun 2012 | B2 |
8334464 | Edwards et al. | Dec 2012 | B2 |
20020012846 | Skotheim | Jan 2002 | A1 |
20030044662 | Walsh | Mar 2003 | A1 |
20040185310 | Jenson et al. | Sep 2004 | A1 |
20050073314 | Bertness et al. | Apr 2005 | A1 |
20050079418 | Kelley et al. | Apr 2005 | A1 |
20050147877 | Tarnowski | Jul 2005 | A1 |
20050258801 | Johnson et al. | Nov 2005 | A9 |
20060038536 | LaFollette et al. | Feb 2006 | A1 |
20060055175 | Grinblat | Mar 2006 | A1 |
20070190418 | Chiang et al. | Aug 2007 | A1 |
20090288943 | Kwak | Nov 2009 | A1 |
20100196744 | Tucholski et al. | Aug 2010 | A1 |
Number | Date | Country |
---|---|---|
1619876 | May 2005 | CN |
0 108 492 | May 1984 | EP |
2 420 027 | May 2006 | GB |
9-171842 | Jun 1997 | JP |
2002-170975 | Jun 2002 | JP |
2005-056655 | Mar 2005 | JP |
2006-40636 | Feb 2006 | JP |
10-2008-0070828 | Jul 2008 | KR |
10-2008-0080900 | Sep 2008 | KR |
WO-2007061928 | May 2007 | WO |
WO-2008035258 | Mar 2008 | WO |
Entry |
---|
Machine translation of JP 2005-056655A, Kanbe Chicka, 2005 (Year: 2005). |
Office Action dated Sep. 27, 2012, directed to CN Application No. 2009/80144551.2; 23 pages. |
Extended European Search Reported dated Feb. 27, 2014, directed to EP Application No. 09825485.7; 8 pages. |
International Search Report and Written Opinion dated Dec. 29, 2009, directed to International Application No. PCT/US2009/063571; 8 pages. |
Albano et al., U.S. Office Action dated Dec. 2, 2010, directed to U.S. Appl. No. 12/614,169; 11 pages. |
Albano et al., U.S. Office Action dated Mar. 11, 2011, directed to U.S. Appl. No. 12/614,169; 15 pages. |
Albano et al., U.S. Office Action dated Oct. 27, 2011, directed to U.S. Appl. No. 12/614,169; 14 pages. |
Albano et al., U.S. Office Action dated Dec. 17, 2012, directed to U.S. Appl. No. 13/465,243; 7 pages. |
Albano et al., U.S. Office Action dated Apr. 4, 2016, directed to U.S. Appl. No. 14/060,387; 10 pages. |
Albano et al., U.S. Office Action dated Nov. 15, 2016, directed to U.S. Appl. No. 14/060,387; 10 pages. |
Number | Date | Country | |
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20170250441 A1 | Aug 2017 | US |
Number | Date | Country | |
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61112707 | Nov 2008 | US |
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Parent | 14060387 | Oct 2013 | US |
Child | 15595872 | US | |
Parent | 13465243 | May 2012 | US |
Child | 14060387 | US | |
Parent | 12614169 | Nov 2009 | US |
Child | 13465243 | US |