Copolymer for photoelectrocatalytic water splitting

Patent metadata

Field	Value
Publication number	US-10882948-B2
Application number	US-201815955768-A
Country	US
Kind code	B2
Filing date	Apr 18, 2018
Priority date	Apr 18, 2018
Publication date	Jan 5, 2021
Grant date	Jan 5, 2021

Abstract

A copolymer containing carbazole- and cyanovinylene-based moieties, a photoelectrode comprising a metal oxide substrate and the copolymer as a photoelectrocatalyst component to the photoelectrode, as well as a photoelectrochemical cell including the photoelectrode. Methods of producing the copolymers, and methods of using the photoelectrochemical cell to produce hydrogen gas and oxygen gas through water splitting are also provided.

First claim

The invention claimed is:

1. A copolymer of formula (I)

or a salt thereof, a solvate thereof, a tautomer thereof, a stereoisomer thereof, or a mixture thereof;
wherein:
R 1 is selected from the group consisting of a hydrogen, an optionally substituted alkyl, an optionally substituted cycloalkyl, an optionally substituted arylalkyl, an optionally substituted aryl, an optionally substituted alkanoyl, and an optionally substituted aroyl;
each R 2 is independently selected from the group consisting of an optionally substituted alkyl, an optionally substituted cycloalkyl, an optionally substituted arylalkyl, and an optionally substituted aryl;
each R 3 is independently selected from the group consisting of a hydrogen, an optionally substituted alkyl, an optionally substituted cycloalkyl, an optionally substituted arylalkyl, an optionally substituted aryl, an optionally substituted alkoxy, an optionally substituted alkanoyl, an optionally substituted aroyl, a halogen, a nitro, and a cyano;
each R 4 is independently selected from the group consisting of a hydrogen, an optionally substituted alkyl, an optionally substituted cycloalkyl, an optionally substituted arylalkyl, an optionally substituted aryl, an optionally substituted alkoxy, an optionally substituted alkanoyl, and an optionally substituted aroyl;
each R 5 is independently selected from the group consisting of a hydrogen, an optionally substituted alkyl, an optionally substituted cycloalkyl, an optionally substituted arylalkyl, an optionally substituted aryl, an optionally substituted alkoxy, an optionally substituted alkanoyl, an optionally substituted aroyl, a halogen, a nitro, and a cyano; and
n is a positive integer in a range of 2-10,000.

2. The copolymer of claim 1 ,
wherein each R 3 , R 4 and R 5 are a hydrogen;
R 1 is a hydrogen or an optionally substituted alkyl; and
each R 2 is independently an optionally substituted alkyl.

3. The copolymer of claim 2 ,
wherein R 1 is 2 -ethylhexyl; and
each R 2 is independently 2-ethylhexyl or dodecyl.

4. The copolymer of claim 1 , which has a formula selected from the group consisting of

wherein n is a positive integer in the range of 2-10000 for each of formulae (P1) and (P2).

5. The copolymer of claim 1 , which is in the form of microspheres having a diameter of 0.5-5 μm.

6. The copolymer of claim 1 , which has a BET surface area of 30-120 m 2 /g, and a pore size of 8-25 Å.

7. The copolymer of claim 1 , which has a band gap energy of 2.3-3.0 eV.

8. The copolymer of claim 1 , which has a fluorescence emission peak of 510-570 nm upon excitation at a wavelength of 380-400 nm.

9. A method of producing the copolymer of claim 1 , the method comprising:
reacting a dialdehyde of formula (II)

or a salt, solvate, tautomer or stereoisomer thereof, with a dinitrile of formula (III)

or a salt, solvate, tautomer or stereoisomer thereof in the presence of a base to form the copolymer, wherein:
R 1 is selected from the group consisting of a hydrogen, an optionally substituted alkyl, an optionally substituted cycloalkyl, an optionally substituted arylalkyl, an optionally substituted aryl, an optionally substituted alkanoyl, and an optionally substituted aroyl;
each R 2 is independently selected from the group consisting of an optionally substituted alkyl, an optionally substituted cycloalkyl, an optionally substituted arylalkyl, and an optionally substituted aryl;
each R 3 is independently selected from the group consisting of a hydrogen, an optionally substituted alkyl, an optionally substituted cycloalkyl, an optionally substituted arylalkyl, an optionally substituted aryl, an optionally substituted alkoxy, an optionally substituted alkanoyl, an optionally substituted aroyl, a halogen, a nitro, and a cyano;
each R 4 is independently selected from the group consisting of a hydrogen, an optionally substituted alkyl, an optionally substituted cycloalkyl, an optionally substituted arylalkyl, an optionally substituted aryl, an optionally substituted alkoxy, an optionally substituted alkanoyl, and an optionally substituted aroyl; and
each R 5 is independently selected from the group consisting of a hydrogen, an optionally substituted alkyl, an optionally substituted cycloalkyl, an optionally substituted arylalkyl, an optionally substituted aryl, an optionally substituted alkoxy, an optionally substituted alkanoyl, an optionally substituted aroyl, a halogen, a nitro, and a cyano.

10. The method of claim 9 , wherein a molar ratio of the dialdehyde of formula (II) to the dinitrile of formula (III) is in a range of 1:2 to 2:1.

11. A photoelectrode, comprising:
a metal oxide conducting substrate; and
a layer comprising the copolymer of formula (I) of claim 1 deposited over the metal oxide conducting substrate;
wherein the layer has a thickness in a range of 5-500 nm.

12. The photoelectrode of claim 11 , wherein the metal oxide conducting substrate is fluorine doped tin oxide.

13. The photoelectrode of claim 11 , which has an ultraviolet visible absorption with an onset absorption edge in a range of 450-550 nm.

14. A photoelectrochemical cell, comprising:
the photoelectrode of claim 11 ;
a counter electrode; and
an electrolyte solution comprising water and an inorganic salt in contact with both electrodes.

15. The photoelectrochemical cell of claim 14 , wherein the electrolyte solution has an inorganic salt concentration of 0.05-1 M, and a pH in a range of 5-9.

16. The photoelectrochemical cell of claim 14 , wherein the photoelectrode has a photo-current density in a range of 0.2-0.5 μA/cm 2 when the electrodes are subjected to a potential of 0.25 to 0.75 V under visible light irradiation.

17. The photoelectrochemical cell of claim 14 , wherein the photoelectrode has a photo-current density in a range of 0.01-0.5 mA/cm 2 when the electrodes are subjected to a potential of 0.8 to 2.0 V under visible light irradiation.

18. The photoelectrochemical cell of claim 14 , further comprising a reference electrode in contact with the electrolyte solution.

19. The photoelectrochemical cell of claim 16 , wherein the photo-current density decreases by less than 25% after subjecting the electrodes to a potential of 0.25 to 0.75 V under visible light irradiation for 2-8 hours, relative to that measured immediately after the subjecting commences.

20. A method of splitting water into hydrogen gas and oxygen gas, the method comprising:
subjecting the electrodes of the photoelectrochemical cell of claim 14 to a potential of 0.25 to 2.0 V; and
concurrently irradiating the photoelectrochemical cell with visible light, thereby forming hydrogen gas and oxygen gas.

Assignees

• Univ King Fahd Pet & Minerals

Inventors

• Ullah Nisar
• MANSHA Muhammad
• Khan Ibrahim
• Sohail Manzar
• Qurashi Ahsanulhaq

Classifications

• C25B11/087

  Photocatalytic compound · CPC title

• C25B1/04

  by electrolysis of water · CPC title

• C25B1/55 Primary

  Photoelectrolysis · CPC title

• C08G61/124 Primary

  with a five-membered ring containing one nitrogen atom in the ring · CPC title

• C08G2261/5222

  electrofluorescent · CPC title