MOLECULAR BUILDING BLOCK METHODS FOR PRODUCING HIGH-EFFICIENCY ORGANIC SOLAR CELLS AND DEVICES AND SYSTEMS PRODUCED THEREFROM

Abstract

Disclosed is a fabrication method for constructing low-cost, morphologically stable, highly ordered, and crystalized layered organic solar cells. The method implements self-assembled molecular monolayers as building blocks (a bottom up strategy) to fabricate a device. This approach enables the creation of a layered material with desired morphology in a controlled way. In such geometry, optoelectronic and transport properties can be controlled by metal atom inclusions into the molecular monolayers, which presents a range of options in creating photo-sensitive molecular building blocks to cover a wide range of the solar spectra from IR to visible to UV.

Claims

1. A method for fabricating an active material for solar cells, the method comprising: providing a substrate; immersing the substrate in a first solution comprising first molecules capable of self-assembly to form a first stacked self-assembled molecular monolayer on top of the substrate; and depositing a first metallic layer on top of the first stacked self-assembled molecular monolayer.

2. The method of claim 1, wherein the substrate includes any type of a metallic substrate, such as, Gold, Silver, Aluminum, or Copper.

3. The method of claim 2 comprising annealing the metallic substrate in a butane/propane flame with intermediate cooling under N.sub.2.

4. The method of claim 1, wherein the first solution comprising first molecules capable of self-assembly comprises n-hexane containing dithiol-group molecules.

5. The method of claim 1, wherein the dithiol-group molecules comprise bipyridine dithiol molecules.

6. The method of claim 1, wherein depositing the first metallic layer (metallic: atoms or nanoparticles or aggregates) on top of the first stacked self-assembled molecular monolayer comprises immersing the substrate with the first stacked self-assembled molecular monolayer in a solution with metal atom precursors.

7. The method of claim 6 further comprising immersing the substrate in a second solution comprising second molecules capable of self-assembly to form a second stacked self-assembled molecular monolayer on top of the first metallic layer.

8. The method of claim 7 further comprising depositing a second metallic layer (metallic: atoms or nanoparticles or aggregates) on top of the second stacked self-assembled molecular monolayer.

9. An active material for solar cells comprising: a substrate; a first stacked self-assembled molecular monolayer on top of the substrate; and a first metallic layer on top of the first stacked self-assembled molecular monolayer.

10. The active material of claim 9, wherein the substrate includes any type of a metallic substrate, such as Gold, Silver, Aluminum, or Copper.

11. The active material of claim 9, wherein the first stacked self-assembled molecular monolayer comprise dithiol-group molecules.

12. The active material of claim 11, wherein the dithiol-group molecules comprise bipyridine dithiol molecules.

13. The active material of claim 9 further comprising a second stacked self-assembled molecular monolayer on top of the first metallic layer.

14. The active material of claim 13 further comprising a second metallic layer on top of the second stacked self-assembled molecular monolayer.

15. The active material of claim 14 further comprising a third stacked self-assembled molecular monolayer on top of the second metallic layer.

16. A solar cell comprising an active layer comprising the active material of claim 9, a cathode layer, and an anode layer.

17. The solar cell of claim 12, wherein the substrate is any type of a metallic substrate such as Gold, Silver, Aluminum, or Copper.

18. The solar cell of claim 16, wherein the first stacked self-assembled molecular monolayer comprise dithiol-group molecules or molecules with end group have affinity to bond to a metallic substrate.

19. The solar cell of claim 16, wherein the active material further comprises a second stacked self-assembled molecular monolayer on top of the first metallic layer.

20. The solar cell of claim 19, wherein the active material further comprises a second metallic layer on top of the second stacked self-assembled molecular monolayer.

Description

BRIEF DESCRIPTION OF THE DRAWING

[0012] The patent or application file contains at least one drawing executed in color. Copies of this patent or patent application publication with color drawing(s) will be provided by the Office upon request and payment of the necessary fee.

[0013] Features and advantages of the present disclosure including disclosed methods and devices produced therefrom and described herein may be better understood by reference to the accompanying drawings in which:

[0014] FIGS. 1(a)-1(b) are the schematics of creating SAM of dithiol-group molecules on a gold substrate, according to an aspect of the present disclosure.

[0015] FIGS. 2(a)-2(b) are the schematics of creating a metallic layer on top of SAM of dithiol-group molecules after immersing the sample into the solution with metal atom precursors, according to an aspect of the present disclosure.

[0016] FIGS. 3(a)-3(d) are the schematics of creating SAMs with metal atom inclusions separated by metallic layers, according to an aspect of the present disclosure.

[0017] FIGS. 4(a)-4(d) are the schematic diagram of the molecular building-block fabrication process for the layered organic solar absorbers and the deposition of the top electrode, according to an aspect of the present disclosure.

[0018] FIGS. 5(a)-(d) show the density-functional theory results: (a, b) optimized structures of cross-linked 5,5-bis(mercaptomethyl)-2,2-bipyridine (BPD) molecules without (a) and with (b) metal atom inclusions; (c) electron affinity of the system for different metal ions; and (d) absorption spectra of the BPD self-assembly for different metal ions.

[0019] FIG. 6 is a cross section side view illustrating an embodiment of a solar cell device.

[0020] The reader will appreciate the foregoing details, as well as others, upon considering the following detailed description of certain non-limiting embodiments including the disclosed method and devices and systems produced therefrom according to the present disclosure. The reader may also comprehend certain of such additional details upon using the disclosed method and devices and systems described herein.

DETAILED DESCRIPTION

[0021] The present disclosure is related to fabricating high-performance, operationally stable organic solar cells using a molecular building-block method. In the proposed architecture, the stability is ensured by cross-linking of the molecules whereas the metal atom inclusion increases the functionality of the devices. This method also extends the applicability of the proposed devices to optoelectronic applications (e.g., light-emitting diodes).

[0022] For example, the following are some advantages of the proposed organic photovoltaics over conventional organic and inorganic solar cells: [0023] Low cost, safe and environmentally friendly fabrication methods; [0024] The first SAM can replace expensive and unstable organic hole transport material (e.g. spiro-OMeTAD); [0025] Synthesis of SAMs with well-controlled electronic and optical properties for absorbing different spectrum of the radiation (i.e, tandem cells); [0026] The organic solar cells of the present disclosure are mechanically and operationally more stable, are more durable, and have higher solar conversion efficiency than the conventional organic solar cells; and [0027] The organic solar cells of the present disclosure are cost effective as compared to the conventional organic solar cells based on polymer heterojunctions (P3HT/PCBM).

[0028] The disclosed method can create stable organic layered materials with optoelectronic and transport properties suitable for solar energy harvesting and electronics applications implementing a molecular building block strategy.

[0029] The synthesis of the layered materials based on molecular building blocks can include the following stages according to an embodiment of the present disclosure.

[0030] Stage 1

[0031] In the first step (see FIG. 1 (a)), self-assembly of dithiol-group molecular monolayers 1 can be performed on a metallic (e.g., gold) surface 2, which may play the role of bottom electrode. For example, this step can be performed using the molecular self-assembly processing approach presented in Hamoudi et al. (H. Hamoudi, Z. Guo, M. Prato, C. Dablemont, W. Q. Zheng, B. Bourguignon, M. Canepad and V. A. Esaulov, On the self assembly of short chain alkanedithiols, Phys. Chem. Chem. Phys. 10, 6836-6841 (2008)). The gold substrate 2 can be first annealed in a butane/propane flame with intermediate cooling under N.sub.2.

[0032] Absolute ethanol can be used for the final rinsing before drying under N.sub.2. The resulting gold support can be immersed into n-hexane containing the dithiol-group molecules (see FIG. 1 (a)). In the absence of ambient light, highly ordered SAMs can be obtained with free standing thiol groups 1, as depicted in FIG. 1 (b). The dithiol-end molecules can be chosen in such a way that they represent the hole transport layer (HTM) for creating solar cells. The self-assembled monolayer approach can be used as a tool to create new materials and devices.

[0033] Stage 2

[0034] In the second stage, metallic atoms or nanoparticles 3 can be deposited on top of the SAM produced in the previous state. This can be done by immersing the sample into a solution with desired metal atom precursors or nanoparticles, as depicted in FIGS. 2(a)-2(b). This step can create a good contact between the different SAMs. This metallic layer 3 can also serve as a transport channel for the photogenerated charge carriers minimizing their travel distance.

[0035] Stage 3

[0036] In the next stage, different molecular monolayers (e.g., 4,5) can be self-assembled on top of the first SAM (FIGS. 3(a)-3(d)) to adsorb the different range of the solar spectra (IR, visible, and UV). For example, this step can use the bottom-up fabrication method presented in Hamoudi (H. Hamoudi, Bottom-up nanoarchitectonics of two-dimensional freestanding metal doped carbon nanosheet, RSC Adv. 4, 22035 (2014)). First, the suitable molecules for creating SAMs can be chosen. For example, bipyridine dithiol molecules can be a good candidate. Next, the metal substrate with the HTM molecular layer can be immersed in a solution containing active bipyridine dithiol molecules and metal atom precursors 6 (see FIG. 3(a)). This can result in the formation of SAM with metal atom inclusions (FIG. 3(b)), which can determine the optoelectronic properties of the layer. The metal atoms can be chosen in such a way that the resulting layer can absorb a certain frequency or certain frequencies of the spectrum. To broaden the spectrum of the absorbed light, other molecular layers with different metal ions can be created using the same process. For that purpose, the resulting samples can be immersed in solutions 7 again (FIG. 3(c)). A separating metallic layer 3 can be inserted between each SAM as described above (see FIG. 2(b)). Different organometallics and Dye-sensitized molecules can be used in this layer.

[0037] The difference between these layers and the first SAM is that the properties of these monolayers, such as electron affinity, ionization potential and localization of electronic states (i.e., HOMO-LUMO states), can be well-controlled by including different redox-active metal atoms, which are trapped between the pyridine rings of the SAMs. This approach can enable the shifting of the active-layer absorption spectrum to the infrared region for the development of the transparent solar cell technology.

[0038] To test the effect of metal atom inclusions on the optoelectronic properties of the proposed SAMs, first principles density functional theory calculations can be conducted. For example, cross-linked 5,5-bis(mercaptomethyl)-2,2-bipyridine (BPD) molecules are considered. FIGS. 5(a) and 5(b) show the optimized structure of these molecules without (FIG. 5(a)) and with (FIG. 5(b)) Ni-atom inclusions. FIG. 5(c) shows the electron affinity of the SAM for different metal ions. Electron affinity, which determines the charge carrier transport in the system, is strongly affected by the presence of the metal ions. Optical properties of the considered system are also affected by the metal atoms. This is shown in FIG. 5(d), where the absorption coefficient is plotted as a function of photon energy for different metal ions.

[0039] Stage 4

[0040] In the next stage, ultraviolet or electron beams can be used to cross-link the molecular layer, thus increasing their stability, for example, as presented in Hamoudi (H. Hamoudi, Bottom-up nanoarchitectonics of two-dimensional freestanding metal doped carbon nanosheet, RSC Adv. 4, 22035 (2014)).

[0041] Stage 5

[0042] In following stage, a top electrode 8 can be deposited to complete the solar cell (FIG. 4(d)). The electrode material can be selected in such way that the transparency of the whole device remains preserved. FIGS. 4(a)-4(d) summarize the fabrication processes of the device according to an embodiment of the present disclosure.

[0043] In the present technology, the solar radiation can be absorbed directly on the SAMs, and the charge collection can also take place through the molecular chains. In some non-limiting examples, the present technology can be composed of metal substrate, highly-ordered self-assembled hole transport material, followed by multilayer of SAMs of light absorbers to utilize solar radiation in a broad range of spectrum from IR to UV. Each SAM can be separated by atomic-thick metallic layers which contribute to a fast collection of photogenerated charge carriers. The molecular SAMs in the building-block devices of the present technology have much more structural stability, especially after electron beam cross-linking of the organic molecules.

[0044] FIG. 6 illustrates one implementation of the structure and operating principle of a solar cell device 100 made of the molecular layered materials according to an embodiment of the present disclosure. As shown in FIG. 6, the solar cell device 100 may include a cathode layer 101, an anode layer 103, and an active layer 102 disposed between the cathode layer 101 and the anode layer 103 using the building blocks (bottom up) method. The active layer 102 can include the SAMs according to an embodiment of the present disclosure. The cathode layer 101 functions as a cathode electrode. The anode layer 103 can include an anode electrode.

[0045] In some embodiments, the cathode layer 101 can include an Al layer and/or a Ag layer that functions as a cathode, and the anode layer 103 can include an indium-tin oxide (ITO) layer that functions as an anode. In other specific embodiments, the cathode layer 101 can include an indium-tin oxide (ITO) layer that functions as a cathode, and the anode layer 103 can include an aluminum layer that functions as an anode. Other materials may also be used to form the cathode layer 101, such as calcium, magnesium, lithium, sodium, potassium, strontium, cesium, barium, iron, cobalt, nickel, copper, silver, zinc, tin, samarium, ytterbium, chromium, gold, graphene, an alkali metal fluoride, an alkaline-earth metal fluoride, an alkali metal chloride, an alkaline-earth metal chloride, an alkali metal oxide, an alkaline-earth metal oxide, a metal carbonate, a metal acetate, and/or a combination of two or more of the above materials. Further, other materials may be used to form the anode layer 103 (or a transparent electrode), such as fluorine-doped tin oxide (FTO), aluminum-doped zinc oxide (AZO), antimony-tin mixed oxide (ATO), a conductive polymer, a network of metal nanowire, a network of carbon nanowire, nanotube, nanosheet, nanorod, carbon nanotube, silver nanowire, or graphene.

[0046] It should be understood that various changes and modifications to the presently preferred embodiments described herein will be apparent to those skilled in the art. Such changes and modifications can be made without departing from the spirit and scope of the present subject matter and without diminishing its intended advantages. It is therefore intended that such changes and modifications be covered by the appended claims.