Organic solar cell and photodetector materials and devices

Patent metadata

Field	Value
Publication number	US-2020328357-A1
Application number	US-202016792000-A
Country	US
Kind code	A1
Filing date	Feb 14, 2020
Priority date	Feb 15, 2019
Publication date	Oct 15, 2020
Grant date	—

Abstract

Narrow bandgap n-type small molecules are attracting attention in the near-infrared organic optoelectronics field, due to their easy tunable energy band with a molecular design flexibility. However, only a few reports demonstrate narrow bandgap non-fullerene acceptors (NFAs) that perform well in organic solar cells (OSCs), and the corresponding benefits of NFA photodiodes have not been well investigated in organic photodetectors (OPDs). Here, the ultra-narrow bandgap NFAs CO1-4F, CO1-4Cl and o-IO1 were designed and synthesized for the achieved efficient near-infrared organic photodiodes such as solar cells and photodetectors. Designing an asymmetrical CO1-4F by introducing two different π-bridges including alkylthienyl and alkoxythienyl units ultimately provides an asymmetric A-D′-D-D″-A molecular configuration. This enables a delicate modulation in energy band structure as well as maintains an intense intramolecular charge transfer characteristic of the excited state.

First claim

What is claimed is:

1 . A composition of matter, comprising:
one or more organic semiconducting molecules having the structure (and isomers thereof):

wherein:
each Ar is independently a substituted or non-substituted aromatic functional group, or each Ar is independently nothing and the valence of its respective thiophene ring is completed with hydrogen;
X is C, Si, Ge, N or P; Y is O, S, Se or N—R 6 ;
Z is O, S, Se, or N—R 6 ;
each R, R 1 , R 2 , R 3 , R 4 , R 5 and R 6 is independently hydrogen or a substituted or non-substituted alkyl, aryl or alkoxy chain but R 3 is different from Z—R 2 ;
R 4 is either a hydrogen or the same as Z—R 2 ;
R 5 is either a hydrogen or the same as R 3 ; and
A′ is an acceptor moiety.

2 . The composition of matter of claim 1 , wherein A′ has the structure (and isomers thereof):

where

wherein EWG is any electron withdrawing group.

3 . The composition of matter of claim 2 , wherein Ar′ is one of the following:

4 . The composition of matter of claim 1 , wherein each of the one or more organic semiconducting molecules have the structure (and isomers thereof):

wherein X is C, Si, Ge, N or P; Z is O, Y is S, R 4 is hydrogen, R 5 is hydrogen, each R 1 , R 2 and R 3 is independently hydrogen or a substituted or non-substituted alkyl, aryl or alkoxy chain, and R 3 is different from OR 2 .

5 . The composition of matter of claim 4 , wherein each of the one or more organic semiconducting molecules have the structure (and isomers thereof):

where:
X is F or Cl, and
R 1 , R 2 , R 3 , R 4 are independently hydrogen or a substituted or non-substituted alkyl, aryl or alkoxy chain.

6 . The composition of matter of claim 1 , wherein the dithiophene has the side chains R 1 soluble in a solvent used to solution process a device comprising the composition of matter.

7 . A device comprising an active region including the composition of matter of claim 1 , wherein each of the organic semiconducting molecules are an electron acceptor.

8 . The device of claim 7 , wherein:
the active region comprises each of the electron acceptors forming a heterojunction with an electron donor comprising a second organic semiconducting molecule, and the active region has a thickness of at least 300 nanometers or in a range of 200 nm to 1 micrometer.

9 . The device of claim 8 , further comprising:
a cathode; an anode; and the active region between the cathode and the anode; and wherein: holes and electrons are generated in the active region in response to electromagnetic radiation incident on the active region, the electrons are collected in the electron acceptor and are transmitted through to the cathode, and the holes are collected in the electron donor and transmitted through to the anode.

10 . The device of claim 9 , further comprising:
a hole blocking layer between the cathode and the active region, and an electron blocking layer between the anode and the active region.

11 . The device of claim 8 , wherein the device is an organic solar cell outputting current in response to sunlight absorbed in the active region.

12 . The device of claim 8 , wherein the device is a photodetector outputting current in response to infrared electromagnetic radiation absorbed in the active region.

13 . The device of claim 8 , wherein the device is a solar cell or photodetector having an external quantum efficiency (EQE) above 60% in the wavelength range of 600-950 nm.

14 . The device of claim 7 , wherein each of the electron donors comprise at least one compound selected from PTB7-Th, another BDT based polymer, a CPDT based polymer, a DPP based polymer, or a DTP based polymer.

15 . The composition of matter of claim 1 , comprising a plurality of the electron donors and a plurality of the organic semiconducting molecules that are phase separated, wherein the organic semiconducting molecules are disposed in a hierarchical network and the electron donors comprising the second organic semiconducting molecules occupy spaces in the hierarchical network.

16 . The composition of matter of claim 15 , wherein the hierarchical network comprises larger mid rib shaped regions connected by smaller or thinner regions.

17 . The composition of matter of claim 15 , wherein the composition of matter is solution processed with an additive that promotes formation of the hierarchical network.

18 . A method of making a device, comprising:
solution processing a composition of matter including electron donor molecules and electron acceptor molecules of the structure (and isomers thereof):

wherein:
each Ar is independently a substituted or non-substituted aromatic functional group, or each Ar is independently nothing and the valence of its respective thiophene ring is completed with hydrogen;
X is C, Si, Ge, N or P; Y is O, S, Se or N—R 6 ;
Z is O, S, Se, or N—R 6 ;
each R, R 1 , R 2 , R 3 , R 4 , R 5 and R 6 is independently hydrogen or a substituted or non-substituted alkyl, aryl or alkoxy chain but R 3 is different from Z—R 2 ;
R 4 is either a hydrogen or the same as Z—R 2 ;
R 5 is either a hydrogen or the same as R 3 ; and
A′ is an acceptor moiety, wherein the electron acceptor is solution process in an active region of a solar cell, photodetector, or transistor; and
combining the composition of matter with an additive so that:
the plurality of the electron donor molecules and the plurality of electron acceptor molecules are phase separated,
the electron acceptor molecules are disposed in a hierarchical network and
the electron donor molecules occupy spaces in the hierarchical network.

19 . A composition of matter, comprising:
an organic semiconducting molecule having an A-D′-D-D″-A structure, wherein: D′ is a first donor moiety, D is a second donor moiety different from D′, D″ is a third donor moiety different from D and D′, and A is an acceptor moiety.

20 . The composition of matter of claim 19 , wherein:
D′ is a donor moiety comprising an alkoxythienyl, D is a donor moiety comprising a dithiophene, and D″ is a donor moiety comprising an alkylthienyl, and A is an acceptor moiety comprising (3-oxo-2,3-dihydro-1H-inden-1-ylidene)malononitrile (IC).

21 . The composition of matter of claim 19 , wherein the organic semiconducting molecule has a HOMO in a range of −5.0 eV to −5.5 eV, a LUMO in a range of −3.8 eV to −4.3 eV, and a bandgap in a range of 1.0 eV to 1.4 eV.

Assignees

• Univ California

Inventors

• Lee Jaewon
• Ko Soe-Jin
• Huang Jianfei
• Seifrid Martin
• Wang Hengbin
• Nguyen Thuc-Quyen
• Bazan Guillermo C

Classifications

• H10K30/50

  Photovoltaic [PV] devices · CPC title

• H10K85/6576

  comprising only sulfur in the heteroaromatic polycondensed ring system, e.g. benzothiophene · CPC title

• C07D495/04 Primary

  Ortho-condensed systems · CPC title

• Y02E10/549

  Organic PV cells · CPC title

• H01L51/0068

  Electricity · mapped topic