This invention is directed to a heteroisomeric semiconductor devices. More particularly, the present invention is directed to diodes and/or transistors constructed using different isomers of the same semiconducting compound, such as boron carbide, to form p-type and n-type regions.
Both p and n type semiconducting materials are a commonly used to form semiconducting devices. A p-n junction diode is a typical example of a device containing such a junction between a p and n type material. A p-n junction diode is a typical example of a device containing such a junction between a p and n type material. The diode can be constructed by forming an interface or junction between a semiconducting material having holes as the majority carrier (the “p” material) and a semiconducting material having electrons as the majority carrier (the “n” material). In addition to single junction devices, multiple junctions can be formed consecutively to form other devices, such as p-n-p or n-p-n transistors. Known semiconducting materials suitable for use in forming p-n junctions include silicon, germanium, gallium arsenide, and boron carbide.
Conventionally, p-n junction devices can be formed as either heterojunction devices or homojunction devices. In heterojunction devices, two semiconductor materials having a different stoichiometry are selected to form a p-n junction. Based on the selection of materials, devices with various bias voltages can be created. Strain can be created at interfaces of dissimilar materials, which can lead to structural defect failure. Different materials may also have diffusion across the interface or side reactions leading to an altogether different semiconductor, which can lead to eventual failure and increased recombination rates for electron-hole pairs.
In homojunction devices, the same bulk semiconductor material is used to form both halves of the p-n junction, but dopants are added to one or both sides of the junction in order to modify the majority carrier. Homojunction devices typically have little or no strain at the junction interface. Due to fabrication difficulties and interdiffusion effects, however, it is difficult to create a sharp transition between the p and n materials. Devices with non-abrupt transitions between the p and n materials typically suffer from increased recombination at the p-n junction. Additionally, doping of the semiconductor materials can lead to introduction of other impurities.
Heterojunction and homojunction devices are useful for a myriad of applications. One area of particular interest is the conversion of the kinetic energy of particles incident upon them to electric energy. This occurs, for example, in photovoltaic cells. A photovoltaic cell typically comprises a plurality of p-n hetero- or homojunction devices designed such that incident photons dislodge electron/hole pairs that may then move in a circuit to form an electric current. While reasonably effective photovoltaics are known, there is a need for devices that can convert other types of incident radiation, such as alpha particles, beta particles, and neutrons, to an electric current.
What is needed are p-n junction devices that are effective for conversion of incident particles into electrical current. The devices should be capable of withstanding a variety of operating environments. The devices should be constructed of materials with a high neutron capture cross-section, and significant capture cross-section for other incident particles of interest as well as stability against radiation damage.
The present invention utilizes different isomers of the same semiconducting compound to form p-type and n-type regions. For example, boron carbide, boron carbon phosphide, boron carbon nitride, and boron carbon arsenide are semi-conductors with one or more isomer possessing p-type characteristics and one or more isomer possessing n-type characteristics. Different isomers of such compounds may be used in adjoining regions to form the p-type and n-type regions of diodes or transistors.
a, 6b, and 6c depict various properties of devices according to an embodiment of the invention.
I. Heteroisomer Junctions of Semiconductor Materials
The present invention provides devices containing heteroisomeric junctions or interfaces of semiconductor materials. A heteroisomeric junction can be created by forming an interface between two semiconductor materials having the same stoichiometry but a different atomic arrangement.
One example of a semiconductor device in accordance with the present invention is a boron carbide diode formed from two boron carbide isomers that have the same stoichiometry and lattice structure but a different atomic arrangement. Because the two boron carbide structures have the same stoichiometry and lattice structure, there is little or no strain at the diode interface. However, the different atomic arrangement of the two boron carbide isomers results in differing electronic properties. This allows a p-n junction to be formed without having to incorporate dopants or other impurities into the boron carbide structures.
In an embodiment, the invention provides semiconducting devices having at least one heteroisomer junction or interface, such as diodes and transistors. In another embodiment, the invention provides methods for fabricating heteroisomer junction devices.
II. Fabrication of Boron Carbide Heteroisomer Junctions
A. Semiconductor and Substrate Materials
A boron carbide heteroisomer diode can be constructed by using two carborane isomers having the chemical composition C2B10H12 as precursors. In diodes formed according to embodiments of this invention, orthocarborane, or closo-1, 2-dicarbadodecaborane, can be used as a precursor to form a p-type material. Metacarborane, or closo-1, 7-dicarbadodecaborane, can be used as a precursor to form an n-type material.
In another embodiment, other materials may be used to construct a boron carbide diode. Paracarborane, or closo-1, 2-dicarbadodecaborane, can be used as a precursor to form an n-type material in a boron carbide diode. Phospha-carbadodecaborane can be used as a precursor to form a p-type material in a boron carbide diode.
In an embodiment, boron carbide heteroisomer devices can be formed by depositing two or more boron carbide isomer layers on a substrate. One technique for depositing a boron carbide film on a metal substrate is plasma-enhanced chemical vapor deposition (PECVD). In PECVD, the precursor molecule or molecules for forming a desired film, as well as one or more optional inert atoms or molecules, are exposed to an energy source (such as microwave energy) to form a plasma. In an embodiment, the plasma used for depositing a layer of a boron carbide diode is formed using a single precursor, such as orthocarborane or metacarborane. In addition to the precursors, the gas used to form the plasma can also contain one or more inert gases, such as argon.
B. Forming a Boron Carbide Device
In an embodiment, a PECVD technique can be used to form a boron carbide heteroisomer junction device.
In the embodiment shown in
A plasma, such as argon, is struck 225 in the PECVD chamber. The first precursor is introduced 230 into the chamber. The first precursor decomposes 235 in reaction to the plasma and is deposited 240 as decomposed as the first layer on the substrate. One skilled in the art will appreciate that the thickness of the layer deposited may be controlled by controlling the amount of the first precursor introduced into the chamber. To form p-n junction with the p-material residing on the substrate, orthocarborane can be selected as the first precursor. However, the metacarborane or paracarborane could be used as the first precursor so that an n-type layer is deposited on the substrate.
After forming the first layer on the substrate, a second layer is formed on top of the first layer. In an example where the first layer was a p-type layer formed using orthocarborane as a precursor, the second layer can be formed using a precursor suitable for forming an n-type layer, such as metacarborane or paracarborane. To deposit the second layer, the substrate may be remasked 245, if desired. A second precursor is introduced 250 into the processing chamber. The second precursor decomposes 255 in reaction to the plasma and is deposited 260 as decomposed on the first layer to form a second layer. One skilled in the art will appreciate that the thickness of the second layer may be controlled by controlling the amount of the second precursor introduced into the chamber. The second layer differs from the first layer in the physical configuration of its molecules, rather than the chemical formulation. After forming the second layer, the device may be returned to ambient temperature 270 and removed from the PECVD chamber.
While method 200 is directed to the use of PECVD, one skilled in the art will appreciate that other semiconductor fabrications techniques may be used. For example, the precursors may be deposited and the decomposed, for example using radiation, such as x-rays or electrons. After forming a heteroisomer junction device, one or more electrical connections, such as bonding pads, can be attached to the exposed surfaces of the semiconductor layers. One skilled in the art will appreciate that all or part of method 200 may be repeated to form other devices, such as transistors, by depositing additional layers of isomers. Likewise, further semiconductor techniques may be used before, during, or after method 200 to fabricate other circuit components for use in conjunction with the heteroisomeric device(s) created using method 200. The bonding pad can be composed of the same material as the substrate, or another suitable conductive material. The bonding pad allows a heteroisomer junction device to be electrically connected as a component in a electric circuit. In an embodiment where the heteroisomer junction device is a transistor, the electrical connection can be in either the form of a bonding pad (for the source or drain) or a gate bonding pad (for the gate of the transistor). In another embodiment, a heteroisomer junction device deposited on a conducting substrate can use the substrate for forming electrical connections.
C. Composition of Boron Carbide Layers
Method 200 shown in
Note that FIGS. 3 to 5 show only bonds 310 between boron and carbon atoms in the cage structure. In the precursor molecules, additional hydrogens would be attached to the cage to form a stable molecule. Boron carbide as illustrated in FIGS. 3 to 5 may exist stably in thin films, such as may be used to form semiconductor devices. In the semiconducting layers used in embodiments of this invention, the cage structures represent repeating units that are found in the boron carbide layers. However, the cage structures within a layer may be deformed to some degree due in order to form a layer.
III. Electrical and Photosensitive Properties of Boron Carbide Diodes
The boron carbide diodes according to various embodiments of the invention have a variety of beneficial properties.
c shows the behavior of the same example diode when in the presence of light. In
IV. Additional Boron Carbide Device Structures
In additional embodiments of the invention, a variety of heteroisomer junction devices can be constructed using heteroisomer p-n junctions. In addition to diodes, transistors can also be constructed, such as p-n-p or n-p-n transistors.
In the embodiment shown in
In another embodiment, a transistor can be formed using only a single p-n junction.
The principles and modes of operation of this invention have been described above with reference to various exemplary and preferred embodiments. As understood by those of skill in the art, the overall invention, as defined by the claims, encompasses other preferred embodiments not specifically enumerated herein.
This application claims priority under 35 U.S.C. § 119(e) from Provisional U.S. Patent Application 60/598,142, filed on Aug. 2, 2004, and Provisional U.S. Patent Application 60/604,727, filed on Aug. 24, 2004.
The Board of Regents of the University of Nebraska acknowledges that some funding for the research leading to this application was provided by the United States Government under Contract/Sponsor/Grant NSF #EPS-9901900 and NSF CHE-0346501.
Number | Date | Country | |
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60598142 | Aug 2004 | US | |
60604727 | Aug 2004 | US |