Patent Application
20070295395
This disclosure is related to photovoltaic materials and devices. More specifically, this disclosure is related to a photovoltaic device for conversion of an incident wavelength of electromagnetic radiation to electricity comprising a trimetasphere.
In the discussion of the state of the art that follows, reference is made to certain structures and/or methods. However, the following references should not be construed as an admission that these structures and/or methods constitute prior art. Applicants expressly reserve the right to demonstrate that such structures and/or methods do not qualify as prior art against the present invention.
Organic thin film photovoltaic devices are usually composed of a photoactive polymer (such as poly(phenylene vinylene) or PPV) that generates an electron/hole pair (known as an exciton) upon absorption of a photon. In order to generate a photocurrent, the electrons and holes must be removed from each other to opposite electrodes. If these charges are not separated, recombination of the charges occurs, resulting in heat or radiation or other detrimental event.
A material with high electron affinity (such as Alcian blue) can accept the electronic charge to prevent this recombination and transfer it to an electrode to generate current. Classic fullerene materials, e.g., fullerene structures where the interior space is empty, and carbon nanotubes are known for their high electron affinity.
Despite their effectiveness in photovoltaic devices, the energy efficiency of classic fullerene materials has been poor compared with other photovoltaic technologies. Materials with improved electron affinity and mobility are required for improving overall solar energy conversion efficiency.
For example, classic fullerene materials and carbon nanotube materials are very non-polar and typically have poor miscibility with the photoactive polymers used in combination in the making of photovoltaic devices. One approach has been to form derivatives of these materials to promote higher compatibility. However, by derivatization the electronic properties of the materials, such as electron affinity, are compromised and the materials become less efficient as electron acceptors. PCBM (6,6)-phenyl-C61-butyric acid is a fullerene derivative with an organic group to improve solubility and miscibility with the host material (for example, see T. Munters et al., Thin Solid Filmis, 403-404 (2002), pp. 247-251).
In another example, C60 and other carbonaceous nanomaterials (classical fullerenes, classic metallofullerenes, e.g., a fullerene with one or more metal ions in an interior space (such as Gd+3@C60), and carbon nanotubes) can readily react with environmental contaminants such as oxygen to produce singlet oxygen. Singlet oxygen can form epoxides or hydroxyls on the fullerene surface which contributes in disrupting the electronic properties of the materials. In the presence of visible radiative energy of approximately 500 to 700 nm, classical fullerenes such as C60 may also under go internal dimerization (2+2 cycloaddition) reactions or polymerization reactions at elevated temperatures. In a photovoltaic cell, decreased efficiencies would result from the inevitable consumption of electron affinity material as described above.
An exemplary photovoltaic device for conversion of an incident wavelength of electromagnetic radiation to electricity comprises an absorber of the incident wavelength of electromagnetic radiation, a trimetasphere, the trimetasphere in electron transferring contact with the absorber, an anode in electrical contact with the trimetasphere, and a cathode in electrical contact with the absorber.
An exemplary electrical circuit comprises an absorber of incident electromagnetic radiation, a trimetasphere-containing material in electron transferring contact with the absorber, an anode, a cathode and a current path from the anode to the cathode.
A exemplary method of converting incident electromagnetic radiation to an electrical signal comprises absorbing the incident electromagnetic radiation by an absorber or a photoactive material to produce an electron-hole pair, transferring an electron in a Lowest Unoccupied Molecular Orbital (LUMO) of the absorber or the photoactive material across a band gap to a trimetasphere-containing material, injecting an electron from the trimetasphere-containing material into an anode, transferring a hole in a Highest Occupied Molecular Orbital (HOMO) of the absorber or the photoactive material to a cathode, and completing a circuit between the anode and the cathode.
The objects and advantages of the invention will become apparent from the following detailed description of preferred embodiments thereof in connection with the accompanying drawings in which like numerals designate like elements and in which:
Trimetaspheres are a unique class of materials having unique electronic structures conferring highly efficient electron transport properties, increased oxidative, thermal, and radiative stability. Trimetaspheres are carbon-cage structures encapsulating one or more metal atoms or ions complexed with a nitrogen or other non-carbon heteroatom or ion in the interior space of the cage. When used in energy transfer applications, such as dopants in photovoltaic cells, efficient energy conversions can result.
Generally, the trimetaspheres suitable for use in this application have the general formula A3-nXnN@Cm, where n ranges from 0 to 3, A and X may be trivalent metals and may be either a rare earth metal or a group IIIB metal, and m is between about 60 and about 200.
The size of the trimetasphere cage increases as the ionic radius for the metal increases. For example, to form a trimetasphere having a cage size at or below about 68, the metal atoms preferably have an ionic radius below about 0.090 nm (±0.005 nm). To form a trimetasphere metallofullerene having a cage size between about 68 carbon atoms and about 80 carbon atoms, the metal atoms are preferably trivalent and have an ionic radius below about 0.095 nm (±0.005 nm).
Preferably, the trimetasphere are selected from the A3-nXnN@C68, A3-nXnN@C78, or A3-nXnN@C80 families of endohedral fullerenes. Element A is selected from the group consisting of a rare earth element and a group IIIB element, preferably selected from the group consisting of Scandium, Yttrium, Lanthanum, Cerium, Praseodymium, Neodymium, Gadolinium, Terbium, Dysprosium, Holmium, Erbium, Thulium, and Ytterbium; and more preferably selected from the group consisting of Erbium, Holmium, Scandium and Yttrium. Preferably, Element X is selected from the group consisting of a rare earth element and a group IIIB element preferably selected from the group consisting of Scandium, Yttrium, Lanthanum, Cerium, Praseodymium, Neodymium, Gadolinium, Terbium, Dysprosium, Holmium, Erbium, Thulium, and Ytterbium, and more preferably is Scandium.
As used herein, “endohedral” refers to the encapsulation of atoms inside the carbon cage network. Accepted symbols for elements and subscripts to denote numbers of elements are used herein. Further, all elements to the right of an @ symbol are part of the carbon cage network, while all elements listed to the left are contained within the carbon cage network. Under this notation, Sc3N@C80 indicates that the Sc3N trimetallic nitride is situated within a C80 carbon cage.
The electronic structure of the trimetasphere distinguishes it from classical fullerenes and classic metallofullerenes due to the encapsulated metal-heteroatom/ion complex. The complex confers novel electronic properties resulting in superior electron accepting (ease of reduction) and electron transfer (high mobility) properties. The formal charge assignment in these materials suggests a charge disparity among the component materials. As an example,
Trimetasphere materials have significantly different physical properties and limitations as potential electron accepting materials for electro-optic devices. Trimetaspheres are more polar (polarizable) than classical carbonaceous nanomaterials, as demonstrated by their increased solubility in more polar solvents, and increased retention times on separation media that discriminates according to polarizability and compound polarity. As a result unanticipated advantages may be realized in system compatibility and miscibility with cell components, in the place of the less polar classical fullerenes and nanotubes. For example, the external fullerene cage in the trimetasphere material is relatively non-reactive in comparison to classical metallofullerene and has a much higher thermal stability than traditional fullerene materials.
Trimetasphere can be used in photovoltaic devices.
The absorber can be any photoactive material (polymer, molecular organic, inorganic, etc.) or combination of materials, which can absorb photons to generate an exciton; the trimetasphere can be any trimetasphere disclosed herein; and the anode (and cathodes) can be any electronically conductive material, such as a metal or semiconductor, with a work function that allows accepting or donating an electron from the bulk materials.
Differing electronic properties are to be expected for variations of trimetaspheres having alternative structures than those depicted in
Trimetaspheres can be incorporated into polymer based photovoltaic devices by any suitable means, including heterojunction devices and blended devices.
For example, trimetaspheres can be spin coated with conducting polymers, such as polythiophene and PPV, onto conductive or semiconductive substrates, such as indium-tin-oxide (ITO) coated glass or metal electrodes, e.g., aluminum, to form a surface contact between the trimetasphere and the absorber, e.g., a heterojunction. In another example, trimetaspheres have been vapor deposited at elevated temperatures in a reduced atmosphere onto conductive or semiconductive substrates. Optionally, to provide an electrical contact, metal electrodes can be deposited onto the trimetasphere material.
In another example, the trimetasphere/absorber mixture can be deposited by any method in which the two materials can be blended to form a blended junction. Examples of these methods include, but are not limited to: (a) dissolving both materials in a solvent and casting a film on a substrate (e.g. electrode) via spin coating, dip coating, etc.; (b) trimetasphere can be vapor deposited onto films of the absorber host; (c) trimetasphere and absorbers can be co-deposited by vapor deposition or similar process; and (d) alternate layers of trimetasphere/absorber can be deposited via molecular self assembly processes. Mixtures of the trimetasphere/absorber can be homogeneous, or deposited with a concentration gradient through the material.
Some of these example methods have been tested for photocurrent measurements with applied voltage bias while exposed to light and dark conditions.
In another exemplary embodiment, the outside of the carbon cage is derivatized with an organic group. These organic groups can affect the solubility of the trimetasphere, or make them compatible with one or more other components, such as the absorber. The derivatization changes both the ability of the trimetasphere to disperse into another material as well as the electronic properties of the structure of the trimetasphere.
Applications of these materials include applications and devices in which electron and energy transfer can be enabled or enhanced. For example: photovoltaic devices, thermo-electrics, light emitting diodes, capacitors, and transistors use the electronic principles discussed herein to operate. Each of these applications can be adapted to incorporate trimetaspheres.
Further details concerning trimetaspheres, their material characteristics and their uses may be found in U.S. Pat. No. 6,303,760, the entire disclosure of which is herein incorporated by reference.
Although the present invention has been described in connection with preferred embodiments thereof, it will be appreciated by those skilled in the art that additions, deletions, modifications, and substitutions not specifically described may be made without department from the spirit and scope of the invention as defined in the appended claims.
At least some aspects of this invention were made with Government support under the sponsorship of the Missile Defense Agency, Phase II SBIR contract no. DASG60-02-C-0043. The Government may have certain rights in this invention.
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/US05/10214 | 3/25/2005 | WO | 6/25/2007 |
| Number | Date | Country | |
|---|---|---|---|
| 60556435 | Mar 2004 | US |
