IP Library Granted Patent US 10,333,181
Granted Patent B2
US 10,333,181 · App. 15/100,107 · Granted Jun 25, 2019

Transparent autophotorechargeable electrochemical device

Inventors: Frederic Sauvage (Digeon, FR); Christian Andriamiadamanana (Rivery, FR); Christel Laberty (Paris, FR)
Assignees: CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE; UNIVERSITE DE PICARDIE JULES VERNE; SORBONNE UNIVERSITE
H01M10/465H01G9/2004H01G9/2022H01G9/2031H01M4/483H01M4/485H01M4/505H01M4/5825H01M10/0525H01M14/005H01L2924/0002H01M4/502H01M4/523Y02E10/542Y02E60/122Y02T10/7011Y02T10/7022
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Quick Facts
Patent No.
US 10,333,181
App. No.
15/100,107
Granted
Jun 25, 2019
Kind
B2
Abstract

A transparent photorechargeable electrochemical device is provided. An n-type semiconductor may be used as a positive-electrode active material in the transparent photorechargeable electrochemical device. A method for photorecharging the device is also provided.

Claims (33)

1. A method for photorecharging a transparent photorechargeable electrochemical device which is sealed under inert atmosphere the transparent photorechargeable electrochemical device comprising:

a positive electrode having a transparent conductive carrier on which a positive-electrode film is deposited,

said positive-electrode film comprising titanium dioxide by way of positive-electrode active material,

said titanium dioxide being capable of intercalating and deintercalating ions of an alkali metal M 1 ;

a negative electrode comprising an element chosen from said alkali metal M 1 , an alloy of said alkali metal M 1 , and an intermetallic compound of said alkali metal M 1 ; and

a non-aqueous liquid electrolyte comprising a salt of said alkali metal M 1 and an organic solvent,

said positive and negative electrodes respectively having electrode potentials E 1 and E 2 where E 1 >E 2 , E 1 and E 2 being calculated versus the electrode potential of the M 1 + /M 1 0 couple, the titanium dioxide and the negative electrode being directly in contact with the electrolyte,

said method comprising:

exposing said device, to a source of light waves for at least 30 minutes in order to obtain said recharged device.

2. The method according to claim 1 , wherein the device is exposed on the side of the positive electrode to a source of light waves.

3. The method according to claim 1 , wherein the alkali metal M 1 is choosen from lithium, sodium and potassium.

4. The method according to claim 1 , wherein the titanium dioxide has a specific surface area measured by the B.E.T method ranging from 20 m 2 /g to 500 m 2 /g.

5. The method according to claim 1 , wherein the positive electrode film has a porous structure comprising at least mesopores.

6. The method according to claim 1 , wherein the positive electrode film furthermore comprises at least one dye and/or at least one reflector of light.

7. The method according to claim 1 , wherein the transparent conductive carrier is a transparent conductive glass of FTO, of ITO or of ZITO.

8. The method according to claim 1 , wherein the positive electrode film has a thickness ranging from 0.1 to 25 μm.

9. A method for photorecharging a transparent photorechargeable electrochemical device which is sealed under inert atomosphere comprising:

a positive electrode having a transparent conductive carrier on which a positive-electrode film is deposited,

said positive-electrode film comprising titanium dioxide by way of positive-electrode active material,

said titanium dioxide being capable of intercalating and deintercalating ions of an alkali metal M 1 ;

a negative electrode comprising an element chosen from said alkali metal M 1 , an alloy of said alkali metal M 1 , and an intermetallic compound of said alkali metal M 1 ; and

a non-aqueous liquid electrolyte comprising a salt of said alkali metal M 1 and an organic solvent,

said positive and negative electrodes respectively having electrode potentials E 1 and E 2 where E 1 >E 2 , E 1 and E 2 being calculated versus the electrode potential of the M 1 + /M 1 0 couple,the titanium dioxide and the negative electrode being directly in contact with the electrolyte, said method comprising the step of:

i′) exposing said device, to a source of light waves for at least 10 hours;

ii') using the device of step i′) to power an electrical apparatus; and

iii') letting the device of step ii') relax in open circuit in the dark for at least 6 hours, in order to obtain said recharged device.

10. The method according to claim 9 , wherein the device is exposed on the side of the positive electrode to a source of light waves.

11. The method according to claim 9 , wherein the alkali metal M 1 is chosen from lithium, sodium and potassium.

12. The method according to claim 9 , wherein the titanium dioxide has a specific surface area measured by the B.E.T method ranging from 20 m 2 /g to 500 m 2 /g.

13. The method according to claim 9 , wherein the positive electrode film has a porous structure comprising at least mesopores.

14. The method according to claim 9 , wherein the positive electrode film furthermore comprises at least one dye and/or at least one reflector of light.

15. The method according to claim 9 , wherein the transparent conductive carrier is a transparent conductive glass of FTO, of ITO or of ZITO.

16. The method according to claim 9 , wherein the positive electrode film has a thickness ranging from 0.1 to 25 μm.

Assignments (2)
MERGER AND CHANGE OF NAME Recorded Mar 20, 2019
From: UNIVERSITE PIERRE ET MARIE CURIE (PARIS 6); UNIVERSITE PARIS SORBONNE PARIS IV; SORBONNE UNIVERSITE
To: SORBONNE UNIVERSITE
Reel/Frame 048648/0863 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 17, 2017
From: SAUVAGE, FRÉDÉRIC; ANDRIAMIADAMANANA, CHRISTIAN; LABERTY, CHRISTEL
To: CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE; UNIVERSITE DE PICARDIE JULES VERNE; UNIVERSITE PIERRE ET MARIE CURIE (PARIS 6)
Reel/Frame 043884/0317 →
Priority Claims (1)
FR 13 61775 · Nov 28, 2013 · national
Continuity (1)
Related Publication 20180175463A1 · Jun 21, 2018