IP Library › Granted Patent US 10,734,674
Granted Patent B2
US 10,734,674 · App. 16/101,602 · Granted Aug 4, 2020

Solid-state thin film hybrid electrochemical cell

Inventors: Vladimir Igorevich Meshcheryakov (Ozyory, RU); Arnoux Rossouw (Dubna, RU); Anton Mikhailovich Manakhov (Ivanovo, RU); Nikolay Anatolievich Pogorelov (Ulyanovsk, RU); Elana Viktorovna Kolesnikova (Aleksandrov, RU); Vladimir Aleksandrovich Chugunov (Ulyanovsk, RU)
Assignee: Thinika, LLC
H01M10/0562H01G11/06H01G11/46H01G11/56H01G11/68H01G11/84H01M4/36H01M4/485H01M4/661H01M6/40H01M10/058H01M10/0525H01M10/0585
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Quick Facts
Patent No.
US 10,734,674
App. No.
16/101,602
Granted
Aug 4, 2020
Kind
B2
Abstract

Thin film all-solid-state power sources, including pseudocapacitors having solid inorganic Li + -ion conductive electrolyte, for IoT, microsensors, MEMS, RFID TAGs, medical devices, elements of microfluidic chips Micro Electro Harvesting and ultra-light energy storage. An electrochemical power source includes a substrate; a first current collector layer on the substrate; a first buffer/cache layer on the first current collector layer; a solid-state electrolyte layer on the first buffer/cache layer; a second buffer/cache layer on the solid-state electrolyte layer; a second current collector layer on the second buffer/cache layer. Each buffer/cache layer is formed of Li X M Y O 3 , where M is Nb, Ta, Ti, V, X is 0.8-1.4, and Y is 1.2-0.6. The buffer/cache layer is 15-1000 nm. At least one Faradaic layer is between the first collector layer and the first buffer layer and/or between the second collector layer and the second buffer layer.

Claims (69)

1. An electrochemical power source comprising:

a substrate;

a first current collector layer on the substrate;

a first buffer/cache layer on the first current collector layer, wherein the first buffer/cache layer accumulates energy;

a solid-state electrolyte layer on the first buffer/cache layer;

a second buffer/cache layer on the solid-state electrolyte layer, wherein the second buffer/cache layer accumulates energy;

a second current collector layer on the second buffer/cache layer,

wherein each of the buffer/cache layers is formed of Li X M Y O 3 ,

wherein

M is any of Nb, Ta, Ti, V,

X is in a range of 0.8 to 1.4, and

Y is in a range of 1.2 to 0.6.

2. The power source of claim 1 , further comprising an outer protective layer above the second collector layer.

3. The power source of claim 1 , wherein a thickness of each of the buffer/cache layers is in a range of 15 to 1000 nm.

4. The power source of claim 1 , wherein each layer is a thin film.

5. The power source of claim 1 , wherein the solid-state electrolyte layer is an all-solid-state electrolyte layer.

6. The power source of claim 1 , further comprising at least one Faradaic layer between the first current collector layer and the first buffer/cache layer and/or between the second current collector layer and the second buffer/cache layer.

7. The power source of claim 6 , wherein the Faradaic layer is formed of WO 2.4-2.9 :M1:M2:E1:E2:E3,

wherein

M1 is a dopant element selected from Mo, Ti, Ni, V, Cr, Al, Nb, Ta, Co, Mn,

M2 is a dopant element selected from Mo, Ti, Ni, V, Cr, Al, Nb, Ta, Co, Mn,

E1 is a dopant element selected from H, N, C, Si, Ge, P, B,

E2 is a dopant element selected from H, N, C, Si, Ge, P, B,

E3 is a dopant element selected from H, N, C, Si, Ge, P, B, and

M1 differs from M2 and E1, E2, E3 differ from each other.

8. The power source of claim 6 , wherein the Faradaic layer is formed of MoO 2.4-2.9 :M1:M2:E1:E2:E3,

wherein

M1 is a dopant element selected from Ti, Ni, V, Cr, Al, Nb, Ta, Co, Mn,

M2 is a dopant element selected from Ti, Ni, V, Cr, Al, Nb, Ta, Co, Mn,

E1 is a dopant element selected from H, N, C, Si, Ge, P, B,

E2 is a dopant element selected from H, N, C, Si, Ge, P, B,

E3 is a dopant element selected from H, N, C, Si, Ge, P, B, and

M1 differs from M2 and E1, E2, E3 differ from each other.

9. The power source of claim 6 , wherein a thickness of the Faradaic layer is in a range of 100 to 1000 nm.

10. The power source of claim 1 , wherein the first buffer/cache layer and/or the second buffer/cache layer provides protection against overcharging and/or discharging below a cut-off voltage.

11. A method of manufacturing an electrochemical power source, the method comprising:

forming a first current collector layer on a substrate;

forming a first buffer/cache layer on the first current collector layer, wherein the first buffer/cache layer accumulates energy;

forming a solid-state electrolyte layer on the first buffer/cache layer;

forming a second buffer/cache layer on the solid-state electrolyte layer, wherein the second buffer/cache layer accumulates energy;

forming a second current collector layer on the second buffer/cache layer,

wherein each of the two buffer/cache layers is formed of Li X M Y O 3 ,

wherein

M is any of Nb, Ta, Ti, V,

X is in a range of 0.8 to 1.4, and

Y is in a range of 1.2 to 0.6.

12. The method of claim 11 , wherein the first buffer/cache layer and/or the second buffer/cache layer provides protection against overcharging and/or discharging below a cut-off voltage.

13. The method of claim 12 , further including forming an outer protective layer above the second collector layer.

14. The method claim 12 , wherein a thickness of each of the buffer/cache layers is in the range of 15 to 1000 nm.

15. The method of claim 11 , wherein each layer is a thin film.

16. The method of manufacturing an electrochemical power source of claim 11 , wherein the solid-state electrolyte layer is an all-solid-state electrolyte layer.

17. The method of claim 11 , further including forming at least one Faradaic layer between the first current collector layer and the first buffer/cache layer and/or between the second current collector layer and the second buffer/cache layer.

18. The method of claim 17 , wherein the Faradaic layer is formed of WO 2.4-2.9 :M1:M2:E1:E2:E3,

wherein

M1 is a dopant element selected from Mo, Ti, Ni, V, Cr, Al, Nb, Ta, Co, Mn,

M2 is a dopant element selected from Mo, Ti, Ni, V, Cr, Al, Nb, Ta, Co, Mn,

E1 is a dopant element selected from H, N, C, Si, Ge, P, B,

E2 is a dopant element selected from H, N, C, Si, Ge, P, B,

E3 is a dopant element selected from H, N, C, Si, Ge, P, B, and

M1 differs from M2 and E1, E2, E3 differ from each other.

19. The method of claim 17 , wherein the Faradaic layer is formed of MoO 2.4-2.9 :M1:M2:E1:E2:E3,

wherein

M1 is a dopant element selected from Ti, Ni, V, Cr, Al, Nb, Ta, Co, Mn,

M2 is a dopant element selected from Ti, Ni, V, Cr, Al, Nb, Ta, Co, Mn,

E1 is a dopant element selected from H, N, C, Si, Ge, P, B,

E2 is a dopant element selected from H, N, C, Si, Ge, P, B,

E3 is a dopant element selected from H, N, C, Si, Ge, P, B, and

M1 differs from M2 and E1, E2, E3 differ from each other.

20. The method of claim 17 , wherein a thickness of the Faradaic layer is in a range of 100 to 1000 nm.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 13, 2018
From: MESHCHERYAKOV, VLADIMIR IGOREVICH; ROSSOUW, ARNOUX; MANAKHOV, ANTON MIKHAILOVICH; POGORELOV, NIKOLAY ANATOLIEVICH; KOLESNIKOVA, ELENA VIKTOROVNA; CHUGUNOV, VLADIMIR ALEKSANDROVICH
To: THINIKA, LLC
Reel/Frame 046623/0611 →
Continuity (2)
Provisional Application 62544998 · Aug 14, 2017
Related Publication 20190051936A1 · Feb 14, 2019
Cited By (5)
US 12,224,611 US 12,296,717 US 12,441,212 US 12,533,968 US 12,539,773