Light-emitting electrochemical cells with band-edge enhanced light emission due to chiral liquid crystalline structure

Abstract

To provide light-emitting electrochemical cell devices comprising chiral liquid crystalline materials.SOLUTION: The chiral liquid crystalline material mixtures of the devices function as both electrolytes and as light-emitting materials. The chiral liquid crystalline material mixtures form photonic crystal structures creating a photonic stop band. The presence of the photonic stop band enables the light-emitting electrochemical cell devices to emit light with improved energy efficiency.SELECTED DRAWING: Figure 2

Description

[Technical field]

[0001] CROSS-REFERENCE TO RELATED APPLICATIONS This application claims the benefit under 35 U.S.C. §119(e) of U.S. Provisional Application No. 62 / 691,865, filed June 29, 2018, the disclosure of which is incorporated herein by reference. [Background technology]

[0002] A light-emitting electrochemical cell (LEC) is a light-emitting device that uses electroluminescence from organic or organometallic materials. Both LECs and organic light-emitting diodes (OLEDs) consist of one or more layers of organic materials sandwiched between two electrodes. The difference between the two is that in OLEDs, electron and hole charge carriers are generated outside the device and injected into the organic materials through the cathode or anode, whereas in LECs, ionic charge carriers are generated at the electrodes by reaction with or loss of electrons, and then the ionic charge carriers move within the device. The first LECs fabricated had organic layers made of polymeric light-emitting materials (which are generally very similar to those used in OLEDs) and solid electrolytes (QB Pei, et al., Science 269, 1086-1088 (1995)). [Brief description of the drawings]

[0003] [Figure 1] FIG. 1 is a diagram of a prior art ionic transition metal complex that acts as both a light emitting material and an electrolyte. [Diagram 2] FIG. 1 is a diagram of a light-emitting electrochemical cell of the present invention. [Diagram 3] 1 is a general chemical structure of a Ruthenium II-containing ionic transition metal complex that functions as an electrolyte and a light-emitting material. [Figure 4] FIG. 4 shows a more detailed structure of the ruthenium II complex of FIG. Summary of the Invention

[0004] The embodiments according to this disclosure include an organic layer with a chiral nematic liquid crystal structure, and the mixture of large amounts of electrolytes used in the liquid crystal polymer matrix is ​​believed to be unsuitable for the purpose. Since in LECs there is only a single layer of organic material or a mixture of organic materials between the electrodes, the use of IMTC alone introduces the concept of an organic light-emitting device containing a single organic material, greatly simplifying OLEDs. Since IMTC is a triplet emitter (phosphorescent material) in contrast to singlet light-emitting polymers, IMTC-based devices may also be more energy efficient than earlier polymer-based LECs. Even with the use of IMTC, LECs fabricated at this time are limited both in light output and in the energy efficiency of their fabrication. This is in large part because the excitons generated by the interaction of ions in the center of the organic phase have sufficient mobility to encounter polarons or other species and are then quenched.

[0005] The structure of a light emitting electrochemical cell (LEC) 200 is shown in FIG. 2. The LEC includes a first electrode 202, which may be formed from either a light transmissive or light reflective material. If the first electrode 202 is light transmissive, it may be formed from indium tin oxide, tin oxide, graphene, or any other suitable light transmissive material. If the first electrode 202 is light reflective, it may be formed from aluminum, magnesium / aluminum alloy, or any other suitable light reflective material. The LEC 200 of the present invention further includes a conductive liquid crystal alignment layer 204 formed on a surface of the first electrode 202. This layer 204 conducts charge carriers from the first electrode to the chiral liquid crystal organic material layer 208. This layer 204 further has the property that when a liquid crystalline fluid material layer is formed on its upper surface 206, the rod-shaped molecules of the liquid crystalline fluid material adjacent the surface of the layer 204 are uniformly aligned with their long axes all pointing in the same direction (as far as random thermal vibrations in the liquid crystal phase will permit) and with their long axes parallel to the surface 206 of the liquid crystal alignment layer 204. The conductive liquid crystal alignment layer 204 may be a rubbed layer of poly(3,4-ethylenedioxythiophene) polystyrenesulfonate (PEDOT:PSS), a conductive liquid crystal photoalignment layer such as that described in U.S. Pat. No. 9,508,942, or other conductive liquid crystal alignment layer as known in the art. The LEC 200 of the present invention further comprises a layer 208 of chiral liquid crystalline organic material. This layer has a chiral liquid crystalline structure in which the rod-shaped molecules within the layer are oriented with their long axes parallel to the surface 206, and the direction of their long axes is twisted in a helical manner as they pass upward through the layer 208. This arrangement is illustrated diagrammatically (but greatly enlarged) by the arrangement of rod-shaped objects 212. This arrangement is preferably obtained from the material of the layer 208 having a chiral nematic (also called cholesteric) liquid crystalline order. The material of the layer 208 may be a liquid crystalline fluid, but preferably the material is a solid. If the material is solid, it may be a chiral liquid crystalline glass, but more preferably the material is a polymer formed by polymerizing a layer containing a chiral liquid crystalline fluid precursor monomer material into a polymer in which the chiral liquid crystalline structure is fixed in place by molecular crosslinking. Polymerization of the precursor monomer is preferably achieved by exposure to radiation, more preferably ultraviolet radiation. The LEC 200 further includes a second electrode 210. The second electrode 210 may be formed from either an optically transparent or optically reflective material. However, if the first electrode 204 is formed from an optically reflective material, then the second electrode 210 must be formed from an optically transparent material. If the second electrode 210 is optically transparent, it may be formed from indium tin oxide, tin oxide, graphene, or any other suitable optically transparent material. If the second electrode 210 is optically reflective, it may be formed from aluminum, magnesium / aluminum alloy, or any other suitable optically reflective material.

[0006] When a bias voltage creates a potential across the LEC, one of the electrodes 202 and 210 acts as an anode and one acts as a cathode relative to the other of the two electrodes. Either the first or second electrode can act as an anode or a cathode (in the example shown in FIG. 2, electrode 202 is considered the anode and electrode 210 is considered the cathode). The material of the chiral liquid crystal organic material layer 208 acts as an electrolyte. Molecular species in the layer 208 are oxidized to cations at the anode 202 and reduced to anions at the cathode 210. The material in the region 218 adjacent to the cathode 210 acts as if it is negatively doped. The material in the region 214 adjacent to the anode acts as if it is positively doped. As the potential difference across the layer 208 increases, this "doped" layer grows inward from the electrodes toward the center of the layer 208. The doped regions act like electrodes in an OLED, injecting holes (from the "doped" material region 218 closer to the cathode 210) and electrons (from the "doped" material region 214 closer to the anode 202) into the "undoped" material in region 216 in the center of the chiral liquid crystal organic material layer 208.

[0007] The material in chiral liquid crystal organic material layer 208 not only acts as an electrolyte but also as an electroluminescent material. When electrons and holes are injected from regions 218 and 214, respectively, into region 216, they recombine to form excitons on the electroluminescent molecules of the chiral liquid crystal organic material in layer 208 in the center of region 216. These excitons decay and emit light. As described above, the chiral liquid crystal organic material layer 208 contains rod-like molecules that spontaneously align into helical structures due to their liquid crystal order. The liquid crystal material of layer 208 is optically anisotropic, having a refractive index (n e ) is the refractive index for light whose associated electric vector is oriented in one of the directions perpendicular to the long axis of the rod-like molecule (n o ) is higher than that of the helical structure of layer 208. Light emitted in the center of zone 216 encounters the helical structure of layer 208 and is decomposed into two circularly polarized components (right-handed and left-handed). For example, if the helical structure of layer 208 is a right-handed helix, it will be emitted perpendicular to the plane of layer 208 and have a wavelength of λ=nP where λ is the wavelength of the emission n=(n o +n e ) / 2, P is the pitch of the helical structure of layer 208) The electric vector of right-handed circularly polarized light, given by e and o This medium acts as a photonic crystal for left-handed circularly polarized light. The properties of such a photonic crystal are that the luminescent material within the photonic crystal has a spectral width Δλ = λΔn / n (where Δn = n o -n e) wavelength band (the "stop band") where no solution exists for the wave equation for light propagation. However, light can be emitted at the edges of the band with an intensity higher than in a vacuum. Furthermore, light emitted at the band edges can be trapped or trapped in the photonic crystal, leading to an increase in the photon density in the center of the photonic crystal.

[0008] From the above description of the effect of the photonic crystal structure in the device 200, it is believed that when the light-emitting molecules in the center of the region 216 emit light by electroluminescence at the band edge of the stop band formed by the chiral liquid crystal structure, a high density of photons will accumulate in the center of the region 216. The photons interact with the excitons formed in the region 216 to induce more left-handed circularly polarized light (or right-handed circularly polarized light if the helical structure in the chiral liquid crystal organic material layer 208 spontaneously forms a left-handed helix). The stimulated emission of left-handed circularly polarized light accumulates until all the emission is left-handed polarized and stimulated. All the emission is also in a small cone with an angle nearly perpendicular to the plane of the surface 206. This nearly eliminates the loss of light due to internal reflection at the layer interfaces (e.g., between the electrodes 202 and 210 and the layer 208) in the device 200.

[0009] One problem with the use of organometallic electrolytes similar to 100 in FIG. 1 is that they are triplet emitters. In nearly all electroluminescent materials, light emission occurs when an electron occupying an excited state molecular orbital returns to a ground state molecular orbital already occupied by an unpaired electron that remains unexcited. If the excited state electron has the opposite spin state as the electron in the ground state molecular orbital, the excited state is called a singlet state and the light emission is called singlet emission. If the excited state electron is in the same spin state as the unpaired electron in the ground state, the excited state is called a triplet state and the light emission is called triplet emission. Triplet state electrons are quantum mechanically forbidden from returning to the ground energy state. As a result, in most electroluminescent materials, only singlet emission occurs. Triplet excited state electrons in these materials slowly return to the ground state by a mechanism that does not involve light emission. Since triplet state excitations are three times more abundant than singlet excitations, it is highly advantageous for emissive molecules to emit both singlet and triplet light. Heavy metal atom-containing luminescent materials, such as tris(2,2'bipyridyl)ruthenium(II) hexafluorophosphate in Figure 1, act as combined triplet and singlet emitters because the presence of the heavy metal atom induces spin-orbit interactions that perturb the triplet excited state molecular orbitals and induce emission from the triplet excitation in a shorter time. There are several competing mechanisms that involve the exciton donating its energy to an excited state electron that returns to the ground energy state. If emission from the exciton does not occur in a short enough time, one of the non-radiative (non-radiative) processes will dominate. Although the presence of the heavy metal atom reduces the time required for triplet emission, there is still enough time for the triplet exciton to undergo non-radiative interactions with the ionic charge carriers and polarons formed in the LEC. These non-radiative interactions severely limit the energy efficiency of light emission in IMTC-type LECs. Due to the very high photon density in the helical chiral structure of these OLEDs, the emission stimulated by photon-exciton interactions occurs much faster than the spontaneous singlet exciton emission. Thus, stimulated emission quickly "short-circuits" the heavy-metal-induced spontaneous emission that harvests triplet excitons, greatly limiting the light loss through non-radiative mechanisms. LECs utilizing the chiral band edge effect are much more energy efficient than conventional LECs.

[0010] An example of a chiral liquid crystalline organic material for use in layer 208 uses a Ruthenium II-containing electrolyte and a light emitting material having the general structure 300 of Figure 3, where A is a rigid, rod-like or strip-like aromatic moiety, S is a flexible spacer, C is a crosslinking group (preferably a photocrosslinking group), and X is a - is a negatively charged counterion. Ionic materials of this type can act as both electrolytes and triplet emitters in LEC devices. The inclusion of rod-like structures A and flexible spacers S in the overall structure 300 of the material means that high percentages of material 300 can be incorporated into chiral liquid crystal material formulations for use in layer 208 without unduly reducing the stability of the chiral liquid crystal phase of the material formulation. A more specific example of a Ruthenium II-containing ionic material is shown in structure 400 in Figure 4, where n is any integer from 1 to 12, possibly varying at each position in the structure, m is an integer from 3 to 14, and Y may be selected from a methacryl group, a vinyl ether group, a maleimide group, a fumarate group, a maleate group, or other suitable photocrosslinking group.

[0011] Materials having structures as shown in Figures 3 and 4 are highly unlikely to have a stable chiral liquid crystal phase in the usable temperature range when used in chiral liquid crystal organic material layer 208 as pure materials for constructing the material. Furthermore, the materials shown in Figures 3 and 4 are believed to be less useful than chiral additives for inducing a helical structure with the appropriate pitch in layer 208 as required. For this reason, the material composition of layer 208 may be supplemented with additional liquid crystal materials, such as those having the general structure described in U.S. Pat. No. 6,867,243: BSASB where A is a chromophore, S is a flexible spacer, and B is an end group susceptible to photopolymerization. Particularly useful materials for this application are those having the molecular structure BSASB, as described in U.S. Patent Application Publication No. 2017 / 033290, where the chromophore A is rod- or strip-shaped and the structural unit [ka] where n=2-10 and the dotted bond lines connect the structural unit to the remainder of the molecule. Other particularly useful materials for this application are those having the molecular structure BSASB as described in WO 2018 / 06578, where the chromophore A is rod- or strip-shaped and the structural unit [ka] In this case, n=2 to 10, and "the X moiety is hydrogen, linear or branched C 1 ~C 8 Alkyl, linear or branched C 1 ~C 8 alkoxy and halogen," and dashed bond lines connect the structural units to the rest of the molecule. It should be noted that the materials used in layer 208 have a molecular orbital structure that does not contain any unoccupied molecular orbitals (energy levels such that energy from the excitons that are intended to emit light is transferred to vacant molecular orbitals, resulting in quenching).

[0012] The materials used in the chiral liquid crystal organic material layer 208 may also contain a chiral dopant. A particularly useful chiral dopant is one having the structure BSASB as described above and in U.S. Pat. No. 6,867,243 or U.S. Patent Publication No. 2017 / 033290 or WO 2018 / 065786, or a combination of structures from one or more of the above patent documents, wherein one or both of the flexible spacers contain an optically active center.

[0013] Unless otherwise noted, all patents, patent applications, articles and other publications discussed or mentioned herein are incorporated by reference as if set forth in their entirety herein. The above description of the disclosed embodiments is provided to enable any person skilled in the art to make or use the present invention. Various modifications of the above embodiments will be readily apparent to those skilled in the art, and the general principles described herein may be applied to other embodiments without departing from the spirit or scope of the present invention. Accordingly, the description and drawings set forth herein represent presently preferred embodiments of the present invention, and are therefore representative of the broadly contemplated subject matter of the present invention. It is further understood that the scope of the present invention encompasses other embodiments that may become apparent to those skilled in the art, and that the scope of the present invention is limited only by the appended claims.

Claims

1. 1. A light-emitting electrochemical cell comprising two electrodes and a layer comprising a material, the layer is disposed between the two electrodes; the material of the layer contains an electrolyte and exhibits a chiral liquid crystal phase; Light-emitting electrochemical cell.

2. 10. The light-emitting electrochemical cell of claim 1, wherein the material comprises one or more of an organic material or an organometallic material.

3. 3. The light-emitting electrochemical cell of claim 2, wherein the material comprises one or more organometallic materials that are ionic.

4. 10. The light-emitting electrochemical cell of claim 1, wherein the chiral liquid crystal phase is a chiral nematic liquid crystal phase.

5. The light-emitting electrochemical cell of claim 1 , wherein the material comprises a polymeric material.

6. 6. The light-emitting electrochemical cell of claim 5, wherein the polymeric material is photopolymerized.

7. 10. The light-emitting electrochemical cell of claim 1, wherein the material comprises a glass phase.

8. 10. The light-emitting electrochemical cell of claim 1, wherein at least one of the two electrodes is transparent.

9. 10. The light-emitting electrochemical cell of claim 1, wherein one of the electrodes is light-reflective.

10. 10. The light-emitting electrochemical cell of claim 1, wherein the material comprises one or more electroluminescent materials.

11. The light-emitting electrochemical cell of claim 1 , wherein the material acts as a one-dimensional photonic crystal.

12. 10. The light-emitting electrochemical cell of claim 1, wherein the material exhibits a photonic stop band in the emission spectrum of any light-emitting material located within the layer.

13. 13. The light-emitting electrochemical cell of claim 12, wherein the luminescent material in said layer emits light at a wavelength at the edge of said photonic stop band.

14. 10. The light-emitting electrochemical cell of claim 1, wherein the material emits light by stimulated emission.

15. The material has the structure: where A is a rigid, rod-like or strip-like aromatic moiety, S is a flexible spacer, C is a bridging group, and X - is a negatively charged counterion, 10. The light-emitting electrochemical cell of claim 1.

16. 16. The light-emitting electrochemical cell of claim 15, wherein the crosslinking group is a photonic crosslinking group.

17. The material has the structure:

10. The light-emitting electrochemical cell of claim 1, comprising a molecule having the formula: where A is a chromophore, S is a flexible spacer, and B is an end group susceptible to photopolymerization.

18. 20. The light-emitting electrochemical cell of claim 17, wherein the material comprises a liquid crystal structure.

19. 18. The light-emitting electrochemical cell of claim 17, wherein one or both of the flexible spacers S comprises an optically active center.

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