IP Library Granted Patent US 12,266,752
Granted Patent B2
US 12,266,752 · App. 16/855,676 · Granted Apr 1, 2025

Modification of lithium ion electrode materials via atomic layer deposition techniques

Inventors: Anil U. Mane (Naperville, IL); Jason R. Croy (Plainfield, IL); Jeffrey W. Elam (Elmhurst, IL); Arturo Gutierrez (Naperville, IL); Jihyeon Gim (Naperville, IL); Devika Choudhury (Naperville, IL); Eungje Lee (Naperville, IL); Hakim Iddir (Elmhurst, IL)
Assignee: UCHICAGO ARGONNE, LLC
H01M4/0428C23C16/45555H01M4/366H01M4/483H01M4/525H01M10/0525H01M2004/028
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 12,266,752
App. No.
16/855,676
Granted
Apr 1, 2025
Kind
B2
Abstract

A method for coating of lithium ion electrode materials via atomic layer deposition. The coated materials may be integrated in part as a dopant in the electrode itself via heat treatment forming a doped lithium electrode.

Claims (27)

1. A method of modifying a cathode comprising:

providing a lithium carbonate or lithium hydroxide cathode precursor in a reactor; and

depositing on the cathode precursor a first material by atomic layer deposition process including at least one cycle of:

pulsing a first metal precursor into the reactor for a first metal precursor pulse time;

exposing the cathode precursor to the first metal precursor for a first metal precursor exposure time and at a first partial pressure and binding the first metal precursor;

purging the reactor of the first metal precursor;

pulsing a co-reactant precursor into the reactor for a first co-reactant pulse time;

exposing the cathode precursor to the co-reactant precursor for a co-reactant precursor exposure time and at a second partial pressure, the co-reactant precursor reacting with the bound first metal precursor therein to form the first material; and

purging the reactor of the co-reactant precursor;

wherein the cathode precursor prior to deposition is non-calcinated and non-lithiated.

2. The method of claim 1 , further comprising calcinating the cathode precursor after depositing of the first material.

3. The method of claim 2 , wherein the calcinating is at a temperature in the range of 300° C. to 1000° C.

4. The method of claim 1 , wherein the cathode precursor comprises a metallic element with a first oxidation state.

5. The method of claim 4 , wherein the cathode precursor comprises LiCoO 2 or LiOH.

6. The method of claim 4 , wherein the first material comprises an ALD deposited metallic element having the first oxidation state.

7. The method of claim 5 , wherein the first material comprises aluminum.

8. The method of claim 1 , depositing a second material by atomic layer deposition process including at least one cycle of:

pulsing a second metal precursor into the reactor for a second metal precursor pulse time;

exposing the cathode precursor to the second metal precursor for a second metal precursor exposure time and at a second metal precursor partial pressure and binding the second metal precursor;

purging the reactor of the second metal precursor;

pulsing a second co-reactant precursor into the reactor for a second co-reactant pulse time;

exposing the cathode precursor to the second co-reactant precursor for a second co-reactant precursor exposure time and at a second partial pressure, the co-reactant precursor reacting with the bound first metal precursor therein to form the second material and

purging the reactor of the co-reactant precursor.

9. The method of claim 8 , wherein the second material comprises an ALD deposited metallic element having the second oxidation state that is different from the first oxidation state.

10. The method of claim 8 , wherein following calcination, the first material forms a first material dopant within the cathode precursor bulk and the second material is not a dopant.

11. The method of claim 1 , further comprising, following or during calcination, lithiation of the coated cathode precursor to form a modified cathode.

12. The method of claim 1 , wherein the cathode precursor comprises a manganese-rich layered-layered spinel carbonate, a nickel-rich hydroxide, or a mixture thereof.

Assignments (2)
CONFIRMATORY LICENSE Recorded Jan 22, 2021
From: UCHICAGO ARGONNE, LLC
To: UNITED STATES DEPARTMENT OF ENERGY
Reel/Frame 054998/0547 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 2, 2020
From: MANE, ANIL U.; ELAM, JEFFREY W.; CROY, JASON; GIM, JIHYEON; GUTIERREZ, ARTURO; LEE, EUNGJE; IDDIR, HAKIM H.; CHOUDHURY, DEVIKA
To: UCHICAGO ARGONNE, LLC
Reel/Frame 054511/0975 →
Continuity (1)
Related Publication 20210336240A1 · Oct 28, 2021
References Cited (26)
US 8906449B2 · Li et al. · 2014 [cited by applicant]
US 20120301778A1 · Trevey · 2012 [cited by examiner]
US 20140008568A1 · Fujdala et al. · 2014 [cited by applicant]
US 20160351973A1 · Albano et al. · 2016 [cited by applicant]
US 20170338522A1 · Hu et al. · 2017 [cited by applicant]
US 20190103231A1 · Chai et al. · 2019 [cited by applicant]
US 20200052326A1 · Hu et al. · 2020 [cited by applicant]
US 20200119342A1 · Watanabe · 2020 [cited by examiner]
US 20210234153A1 · Xiao · 2021 [cited by examiner]
EP 3026738A1 · 2016 [cited by examiner]
WO WO2016025866A1 · 2016 [cited by applicant]
WO WO2020257176A1 · 2020 [cited by applicant]
Croy, et al., “Prospects for spinel-stabilized, high-capacity lithium-ion battery cathodes,” Journal of Power Sources 334, pp. 213-220 (2016). [cited by applicant]
Long, et al., “Advances in Stabilizing ‘Layered-Layered’ xLi2MnO3 x (1-x)LiMO2 (M=Mn, Ni, Co) Electrodes with a Spinel Component,” Journal of the Electro Chemical Society 161(14), pp. A2160-A2167 (2014). [cited by applicant]
Wang, et al., “Synthesis of high capacity cathodes for lithium-ion batteries by morphology-tailored hydroxide co-precipitation,” Journal of Power Sources 274, pp. 451-457 (2015). [cited by applicant]
“Global EV Outlook 2021,” International Energy Agency, retrieved from https://www.iea.org/reports/global-ev-outlook-2021 on Nov. 15, 2022, 101 pages (2021). [cited by applicant]
Bi, et al., “Stability of Li2CO3 in cathode of lithium ion battery and its influence on electrochemical performance,” RSC Advances 6(23), pp. 19233-19237 (2016). [cited by applicant]
Buechel, et al., “Electrical vehicles (EV) battery supply chain: Country risks and lithium supply,” S&P Global Market Intelligence, retrieved from https://www.spglobal.com/marketintelligence/en/mi/research-analysis/elec… [cited by applicant]
Butler, et al., “Development Status of the Metal Oxide Regenerable CO2 Removal System for the NASA EMU,” SAE Technical Paper 972505, 10 pages (1997). [cited by applicant]
Chen, et al., “Mechanism for Al2O3 Atomic Layer Deposition on LiMn204 from In Situ Measurements and Ab Initio Calculations,” Chem 4(10), pp. 2418-2435 (2018). [cited by applicant]
Darapaneni, et al., “Elucidating the Redox Behavior during Atomic Layer Deposition on Lithium-Ion Battery Cathode Materials,” Chemistry of Materials 33(20), pp. 8079-8088 (2021). [cited by applicant]
Gutierrez, et al., “Multifunctional Films Deposited by Atomic Layer Deposition for Tailored Interfaces of Electrochemical Systems,” Journal of the Electrochemical Society 167(14):140541 (2020) (24 page accepted manuscri… [cited by applicant]
Han, et al., “Negating interfacial impedance in garnet-based solid-state Li metal batteries,” Nature Materials 16, pp. 572-579 (2017) (advanced online publication provided; 9 pages). [cited by applicant]
Kang, et al., “Modification of LiMn2O4 surfaces by controlling the Acid-Base surface chemistry of atomic layer deposition,” Applied Surface Science 599:153329 (2022) (45 page accepted manuscript provided). [cited by applicant]
Park, et al., “Ultrathin Lithium-Ion Conducting Coatings for Increased Interfacial Stability in High Voltage Lithium-Ion Batteries,” Chemistry of Materials 26(10), pp. 3128-3134 (2014). [cited by applicant]
Young, et al., “High-Rate Spinel LiMn204 (LMO) Following Carbonate Removal and Formation of Li-Rich Interface by ALD Treatment,” The Journal of Physical Chemistry C 123(39), 23783-23790 (2019). [cited by applicant]