WO2019147602A1 - Amphoteric p-type and n-type doping of group iii-vi semiconductors with group-iv atoms - Google Patents
Amphoteric p-type and n-type doping of group iii-vi semiconductors with group-iv atoms Download PDFInfo
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Definitions
- (Al,In,Ga) 2 0 3 represents a newly developing III- VI family of semiconducting oxide materials. It holds great promise, but currently suffers from an inability to achieve effective p-type doping.
- the material is typically doped using silicon (Group-IV) to substitute for gallium (or aluminum or indium) to achieve a n-type material.
- silicon Group-IV
- Magnesium Group-II
- Magnesium has been used to substitute for the same gallium (or aluminum or indium) to achieve a p-type material.
- this requires the addition of a separate magnesium source.
- magnesium exhibits a large memory effect in metalorganic chemical vapor deposition (MOCVD) growth which means it is difficult to obtain p-n heterojunctions where the p-type material is grown first.
- MOCVD metalorganic chemical vapor deposition
- IV-doped III- VI semiconductors including p- type III- VI semiconductors doped with Si. Also provided are the IV-doped III- VI
- methods of forming a p-type IV-doped III- VI semiconductor comprise exposing a substrate to a vapor composition comprising a group III precursor comprising a group III element, a group VI precursor comprising a group VI element, and a group IV precursor comprising a group IV element, under conditions to form a p-type IV-doped III- VI semiconductor via metalorganic chemical vapor deposition (MOCVD) on the substrate.
- MOCVD metalorganic chemical vapor deposition
- Embodiments make use of a flow ratio defined as a flow rate of the group VI precursor to a flow rate of the group III precursor wherein the flow ratio is below an inversion flow ratio value for the IV-doped III- VI semiconductor.
- a p-type IV-doped III- VI semiconductor which comprises a group III element, a group VI element and a group IV element.
- FIG. 1A shows a plot of carrier concentration as a function of VI-III flow ratio for Ga 3 0 2 :Si formed according to an illustrative embodiment.
- FIG. 1B shows a plot of Hall mobility as a function of VI-III flow ratio for Ga 3 0 2 :Si formed according to an illustrative embodiment.
- FIG. 2A shows a cross-sectional view of a schematic of a field effect transistor (FET) with a fin structure fabricated using p-type Ga 3 0 2 :Si according to an illustrative embodiment.
- FIG. 2B shows a perspective view of the fin-FET.
- FET field effect transistor
- FIG. 3 A is a plot of the I-V curve and FIG. 3B is a plot of the transfer
- VDS 20 V of a p-type Ga 2 0 3 :Si 3 pm by 3 pm fin array fin-FET (shown in FIGs. 2 A and 2B).
- the fin-FET shows an on/off ratio of 10 6 and a breakdown voltage of over 150 V.
- FIG. 4A shows an XRD omega/2theta scan of - 150 nm thick Ga 2 0 3 :Si grown using a VEIII ratio of 150 (top), at a VEIII ratio of 100 (middle) and an XRD omega/2theta scan of a P-Ga 2 0 3 substrate (TAMURA Corp) (bottom).
- FIG. 4B shows a TEM image of typical morphology of the - 150 nm thick Ga 2 0 3 :Si on sapphire. The inset shows SAED patterns obtained along the [5-10] zone axis at the K-Ga 2 0 3 /Al 2 0 3 interface.
- FIG. 5 A shows the carrier concentration and resistivity of Ga 2 0 3 :Si on sapphire (0001) as a function of growth temperature at VEIII ratio of 150 and FIG. 5B shows the same at a VI/III ratio of 100.
- FIG. 5C shows the Hall mobility of Ga 2 0 3 :Si on sapphire (0001) as a function of growth temperature at VI/III ratio of 100 and 150.
- FIG. 7 A show schematic illustrations of 2D p- type Ga 2 C>3:Si channel microstrip array FETs with details of device scale
- FIG. 7B shows an optical micrograph of the fabricated device.
- the inset is an optical micrograph of the probing.
- FIG. 9 A shows a schematic illustration of the 2D Ga 2 C>3:Si channel microstrip array FETs.
- FIG. 9B shows a schematic illustration of three portions of the Ga 2 C> 3 channel.
- IV-doped III- VI semiconductors including p- type III- VI semiconductors doped with Si. Also provided are the IV-doped III- VI
- An embodiment of a method of forming an IV-doped III- VI semiconductor comprises a step of exposing a substrate to a vapor composition comprising a group III precursor comprising a group III element, a group VI precursor comprising a group VI element, and a group IV precursor comprising a group IV element. The exposure takes place under conditions sufficient to form a compound semiconductor from the group III, group VI, and group IV precursors via MOCVD.
- the group III, group VI, group IV precursors adsorb to the surface of substrate where they react to form the compound semiconductor, typically as a layer on the surface of the substrate.
- the method may include a predeposition step to form a wetting layer on the substrate prior to exposure to the vapor composition.
- the predeposition step may comprise exposing the substrate to the group III precursor (i.e., without the group VI precursor and without the group IV precursor).
- the group III precursors are metalorganic compounds comprising a group III element.
- the group III element is selected from Ga, Al, and In.
- a variety of group III precursors may be used, e.g., trimethylgallium, trimethylaluminum,
- a single group III precursor is used, e.g., a gallium-containing group III precursor to provide a Ga-group VI compound semiconductor. In embodiments, more than one group III precursor is used so as to facilitate alloying of the group III elements in the formation of the compound semiconductor.
- a gallium-containing group III precursor, an aluminum-containing group III precursor and an indium-containing group III precursor may be used to provide a GaAlln-group VI compound semiconductor.
- the ratios of Ga, Al, In may vary, depending upon the desired properties and application for the semiconductor.
- a gallium- containing group III precursor and an indium-containing group III precursor may be used to provide a Gain-group VI compound semiconductor. Again, in such a compound
- the ratios of Ga and In may vary.
- the group VI precursors are compounds comprising a group VI element.
- the group VI element is O.
- a variety of group VI precursors may be used, e.g., water, oxygen, N 2 0, and ozone.
- the group IV precursors are compounds comprising a group IV element.
- the group IV precursors are used as dopants, i.e., to provide an IV-doped III- VI.
- the group IV element is Si.
- a variety of group IV precursors may be used, e.g., SiH 4 , tetraethylorthosilicate, Si 2 I3 ⁇ 4, SiCU.
- the vapor composition may also comprise one or more such carrier gases.
- a carrier gas e.g., N 2 , Ar, H 2
- the vapor composition may also comprise one or more such carrier gases.
- conditions refers to the growth temperature, the pressure of the vapor composition, the flow ratio of the group VI precursor to the group III precursor, and the carrier gas.
- the present methods are based, at least in part, on the finding that certain of these conditions may be adjusted to tune the doping type of the compound semiconductor from n-type to p-type, even when using the same dopant, i.e., the same group IV precursor.
- certain of these conditions may be adjusted so that the group IV element of the group IV precursor substitutes for the group VI element in the forming compound semiconductor to provide a p-type IV-doped III- VI semiconductor or so that the group IV element substitutes for the group III element to provide an n-type IV- doped III- VI semiconductor.
- the flow ratio of the group VI precursor to the group III precursor may be adjusted to provide both an n-type IV-doped III- VI semiconductor (at certain flow ratios) and a p-type IV-doped III- VI semiconductor (at other flow ratios) even when using the same group IV precursor.
- an inversion flow ratio value has been found, below which value a p-type IV-doped III- VI semiconductor is formed and above which value a n-type IV-doped III- VI semiconductor is formed even when using the same group IV precursor.
- the inversion flow ratio value for a particular material system may be referenced at a particular growth temperature, pressure, and carrier gas being used in the method.
- the inversion flow ratio value for this material system is about 125. That is, for VI-III flow ratios below 125, the compound semiconductor formed is p-type (silicon substitutes for oxygen, taking up two extra electrons from the lattice, thus acting as a doubly ionized acceptor to achieve very effective p-type doping). For VI-III flow ratios above 125, the compound semiconductor formed is n-type (silicon substitutes for gallium). (See FIG. 1 A.) This inversion flow ratio value of 125 may be referenced, e.g., at a growth temperature of 1000 °C, a pressure of 50 mbar, and N 2 as the carrier gas.
- FIGs. 5A-5C further support the findings described above. Moreover, these figures show the growth temperature does not changing the nature of doping, only the ratio of the flows of the group III and VI precursors.
- the present methods may comprise carrying out the step of exposure to the vapor composition under conditions (e.g., VI-III flow ratio) selected to achieve a desired doping type (either p-type or n-type) for the IV-doped III- VI semiconductor being formed. Since both doping types may be achieved using the same group IV precursor, the methods may further comprise forming a second IV-doped III- VI semiconductor having the opposite doping type to provide a p-n heterojunction. For example, the method can be used to form an n-type IV-doped III- VI semiconductor on a p-type IV-doped III- VI semiconductor or vice versa.
- VI-III flow ratio e.g., VI-III flow ratio
- illustrative growth temperatures include those in the range of from about 500 °C to about 1500 °C, including from about 600 °C to about 1000 °C, or from about 700 °C to about 1000 °C.
- Illustrative pressures include those in the range of from about 10 mbar to about 100 mbar, including from about 50 mbar to about 150 mbar.
- substrates may be used in the present methods, e.g., sapphire (a-sapphire, m-sapphire, c-sapphire), AI2O3, silicon (Si(l l l), Si(l00)), native -Ga 2 0 3 , MgO, ZnO, etc.
- the IV-doped III- VI semiconductors formed using the present methods are also encompassed by the present disclosure.
- the IV-doped III- VI semiconductors may be characterized by their carrier concentrations.
- the IV-doped III- VI semiconductor is p-type having a carrier concentration in the range of from about 10 15 cm 3 to about 10 20 cm 3 , from about 10 16 cm 3 to about 10 20 cm 3 , from about 10 17 cm 3 to about 10 20 cm 3 or from about 10 18 cm 3 to about 10 20 cm 3 .
- the IV-doped III- VI semiconductor is n-type having a carrier concentration in any of the ranges disclosed above.
- the IV-doped III- VI semiconductors may be characterized by their Hall mobility.
- the Hall mobility may be in the range of from about 5 to about 300 cm 2 /Vs, about 10 to about 300 cm 2 /Vs, or from about 5 to about 150 cm 2 /Vs.
- Known techniques may be used to measure carrier concentration and Hall mobility.
- the IV-doped III- VI semiconductors may be characterized by the phase of the III-
- the phase of the material may be, e.g., b or K.
- p-n heterojunctions formed from any of the disclosed p-type IV-doped III- VI semiconductor and another n-type semiconductor or from any of the disclosed p-type IV-doped III- VI semiconductors and any of the disclosed n-type IV-doped III- VI semiconductors.
- Devices incorporating the IV-doped III- VI semiconductors are also encompassed by the present disclosure.
- Illustrative devices include photodetectors (including solar-blind UV photodetectors), field effect transistors (including fin structured transistors see FIGs. 2A- 2B and 7A-7B), light emitting diodes and combinations thereof.
- Other applications include use of the IV-doped III- VI semiconductors in high voltage direct current transmission lines, variable frequency drives and switch mode power supplies.
- a commercial horizontal-flow MOCVD reactor (AIXTRON 200/4 RF) was used to grow doped Ga 2 0 3 thin films on c-plane sapphire (0001) at a growth temperature of about 1000 °C using a conventional trimethylgallium (TMGa) bubbler and high purity deionized water loaded in a custom quartz bubbler as the gallium and oxygen precursors, respectively.
- Silane (SiH 4 ) was used as the silicon precursor.
- H 2 was used as the carrier gas.
- TMGa was flowed for 1 minute to predeposit gallium on the substrate before introducing the water.
- Doped Ga 2 0 3 thin films were investigated using VI / III flow ratios in the range of from 100 to 150.
- FIG. 1 A shows the carrier concentration as a function of the III- VI flow ratio.
- VI-III flow ratios below -125 the as-grown material is p-type (silicon substitutes for oxygen). At an VI- III flow ratio of -125 an inversion takes place and the material becomes
- FETs field effect transistors
- FIGs. 2A and 2B An insulated gate consisting of -100 nm of silicon dioxide was deposited over the semiconductor material (i.e., p-type Ga 3 0 2 ) and source, drain, and gate contacts were deposited.
- the epitaxial layer of Ga 2 0 3 was only -1.2 nm thick. Hall mobility measurements indicated the layer was p-type with a carrier concentration of 3.423 x 10 18 cm 3 .
- the source-drain spacing was 20 pm and the gate was just 5 pm wide.
- the fin-FET transistors were then experimentally characterized using an HP 4155C semiconductor parameter analyzer to measure the family of curves. The results are shown in FIGs. 3 A and 3B. The measured results show the excellent conductivity of the p- type layer achieved with the novel doping technique used in this Example.
- Ga?0 has emerged as a next generation semiconductor material for high power electronic devices. This is in great part due to its high breakdown electric field ( ⁇ 8 MV/cm), which largely surpasses that of competing materials systems such as SiC or GaN.
- K-Ga 2 0 (an orthorhombic polymorph which is normally considered to be transient) can be stabilized in heteroepitaxial growth on sapphire (0001) substrates by MOCVD.
- MOCVD Metal Organic Chemical Vapor Deposition
- high levels of shallow acceptor p- type conduction may be achieved in such layers using silicon impurity doping under Ga rich growth conditions.
- 2D layers of such p- type Ga 2 0 3 :Si are then processed into microstrip array ring FETs using conventional photolithography. The operational characteristics of the FETs proved to be consistent with p- type conduction.
- a phenomenological model coherent with a p- type channel is also presented.
- a commercial MOCVD reactor (AIXTRON 200/4 RF) was used to grow Ga 2 0 3 on sapphire (0001) substrates at growth temperatures ranging from 730 to 1000 °C.
- Trimethylgallium (TMGa), high purity deionized water and SiFE were adopted as the Ga, O and Si precursors, respectively.
- N 2 was used as the carrier gas.
- Total pressure was 50 mbar.
- VEIII ratio was either 100 (Ga-rich) or 150 (O-rich).
- the SiFE flow rate was fixed at 15 seem.
- FIGs. 5 A and 5B show the results as a function of growth temperature for both VEIII ratios.
- a VEIII ratio of 150 Ga 2 0 3 :Si grown at 730 °C shows «-type characteristics.
- the carrier concentration decreased linearly to - 4.4 x 10 17 cm 3 .
- FIG. 5B shows that the lower VEIII ratio (100) consistently gave p- type characteristics.
- the Si dopant acts as a shallow acceptor by substituting on the O-site of the Ga 2 0 3
- the VEIII ratio of 100 growth condition would generate a higher density of oxygen vacancies (Vo) by virtue of the Ga-rich nature of the growth which lets the Si substitute more readily at the O- sites.
- FIG. 2C shows the Hall mobility of the Ga 2 0 3 :Si as a function of growth temperature for VI/III ratios of 150 and 100.
- a VI/III ratio of 150 a ( «-type) mobility near 50 cm 2 /V s was observed for a growth temperature of 1000 °C.
- Ring type FETs were fabricated and evaluated for the characteristics of the FET device of - 150 nm thick p- type Ga 2 0 3 :Si with VEIII ratio of 100.
- FIG. 6 shows the I-V curves. It is observed that the drain current decreases with increasing gate voltage. However, it was not possible to achive pinch-off due to the gate electrode burning at gate voltages higher than 50 V. To avoid this issue the channel thickness was reduced to - 1.2 nm and the ring pattern FETs were patterned with microstrips. Ga 2 0 3 :Si channel layers were grown at 1000 °C with a VEIII ratio of 100.
- the channel thickness was estimated to be - 1.2 ⁇ 0.5 nm based on interferometric growth rate calibration and AFM step-edge profilometry. Hall measurements confirmed the p- type nature of the layers with a resistivity of - 0.007 Q cm, a carrier concentration of - 1.7 x 10 20 cm 3 and a mobility of - 5.7 cm 2 /V-s.
- Standard photolithography and lift-off were employed to deposit source and drain metal contacts. Before their deposition, 3 pm x 3 pm microstrip patterns were formed by electron cyclotron resonance-reactive ion etching (ECR-RIE) with CF 4 for 5 minutes.
- ECR-RIE electron cyclotron resonance-reactive ion etching
- the metal contacts were Ti (20 nm) / Au (150 nm) deposited by e-beam evaporation.
- Si0 2 of 100 nm thick gate dielectric material was formed by plasma-enhanced chemical vapor deposition (PECVD). After dielectric and passivation film deposition, the gate metal contact was formed with Pt(20 nm) / Ti(20 nm) / Au(l50 nm) on the Si0 2 film.
- FIG. 7A shows schematic illustrations of the device with top- and cross- sectional views illustrating the device scale.
- FIG. 7B shows an optical microscope image of the fabricated device.
- FIG. 8A shows the DC source-drain current versus source-drain voltage (IDS-VDS) output characteristics for the depletion-mode FETs measured by increasing gate-source voltage (VGS) stepwise from -50 to 100 V.
- the maximum IDS was 2.19 mA and it was effectively modulated by VGS from -50 to 100 V, which is consistent with a p- type channel.
- FIG. 8B displays a similar set of curves obtained from the simulation. It can be seen that the theoretical model is consistent with the experimental data in showing an output resistance increase with positive gate voltage, and IDS bunching with little variation of the output resistance for VGS ⁇ 0.
- FIG. 8C shows transfer characteristics at VDS of 10 to 40 V in a logarithmic scale.
- the device achieved an on/off ratio of - 10 8 by minimizing the thickness and width of the channel.
- a plot of the gate current as a function of drain-source voltage (not shown) showed that IG increases above a VGS of 50 V because of a gate leakage current. It is expected that the on/off ratio can be further improved through optimization of the dielectric layer.
- m is the hole mobility (cm 1 /Vs) and ⁇ ‘ is the channel length (cm).
- the channel is made of three portions with different conductances
- D is the thickness of the S1O2 barrier
- y is the vertical coordinate inside the Ga 2 0, layer
- l ⁇ is the Debye length in the Ga 2 0 3 layer fitted to reproduce the
- MOCVD showed consistent p- type Hall signal for layers grown with lower VI/I 11 ratios during growth.
- Room temperature mobilities were up to 7 cm 2 /Vs, resistivities were as low as 0.007 Q.cm and carrier concentrations were up to -10 20 cm 3 for thinner layers.
- Ring mesa FETs were fabricated based on -1.2 nm thick / Ga 2 0,:Si channels formed into a number of 3 pm wide microstrips. The devices achieved a maximum drain current density of 2.19 mA and an on/off ratio of - 10 8 and showed characteristics consistent with a p- type conduction in the channel.
- the p- type Ga?0 demonstrated in this Example represents a significant advance in the state of the art, which may herald the fabrication of a range of junction based devices. These may be smaller/thinner and bring both cost (more devices/wafer and less growth time) and operating speed advantages (due to miniaturisation) than current isotype FETs. Moreover the demonstration of the first functioning devices based on scaling down to 2D device channels in Ga 2 0 3 based FETs opens up the perspective of faster devices and improved heat evacuation.
Abstract
Methods of forming a p-type IV-doped III-VI semiconductor are provided which comprise exposing a substrate to a vapor composition comprising a group III precursor comprising a group III element, a group VI precursor comprising a group VI element, and a group IV precursor comprising a group IV element, under conditions to form a p-type IV-doped III-VI semiconductor via metalorganic chemical vapor deposition (MOCVD) on the substrate. Embodiments make use of a flow ratio defined as a flow rate of the group VI precursor to a flow rate of the group III precursor wherein the flow ratio is below an inversion flow ratio value for the IV-doped III-VI semiconductor.
Description
AMPHOTERIC P-TYPE AND N-TYPE DOPING OF GROUP III- VI
SEMICONDUCTORS WITH GROUP-IV ATOMS
CROSS-REFERENCE TO RELATED APPLICATIONS
[0001] The present application claims priority to U.S. Provisional Patent Application No. 62/623,183 that was filed January 29, 2018, the entire contents of which are hereby incorporated by reference.
REFERENCE TO GOVERNMENT RIGHTS
[0002] This invention was made with government support under ECCS-1748339 awarded by the National Science Foundation. The government has certain rights in the invention.
BACKGROUND
[0003] (Al,In,Ga)203 represents a newly developing III- VI family of semiconducting oxide materials. It holds great promise, but currently suffers from an inability to achieve effective p-type doping. The material is typically doped using silicon (Group-IV) to substitute for gallium (or aluminum or indium) to achieve a n-type material. Magnesium (Group-II) has been used to substitute for the same gallium (or aluminum or indium) to achieve a p-type material. However, this requires the addition of a separate magnesium source. In addition, magnesium exhibits a large memory effect in metalorganic chemical vapor deposition (MOCVD) growth which means it is difficult to obtain p-n heterojunctions where the p-type material is grown first.
SUMMARY
[0004] Provided are methods of forming IV-doped III- VI semiconductors, including p- type III- VI semiconductors doped with Si. Also provided are the IV-doped III- VI
semiconductors and devices incorporating the IV-doped III- VI semiconductors.
[0005] In an aspect, methods of forming a p-type IV-doped III- VI semiconductor are provided which comprise exposing a substrate to a vapor composition comprising a group III precursor comprising a group III element, a group VI precursor comprising a group VI element, and a group IV precursor comprising a group IV element, under conditions to form a p-type IV-doped III- VI semiconductor via metalorganic chemical vapor deposition
(MOCVD) on the substrate. Embodiments make use of a flow ratio defined as a flow rate of the group VI precursor to a flow rate of the group III precursor wherein the flow ratio is below an inversion flow ratio value for the IV-doped III- VI semiconductor.
[0006] In another aspect, a p-type IV-doped III- VI semiconductor is provided which comprises a group III element, a group VI element and a group IV element.
[0007] Other principal features and advantages of the disclosure will become apparent to those skilled in the art upon review of the following drawings, the detailed description, and the appended claims.
BRIEF DESCRIPTION OF THE DRAWINGS
[0008] Illustrative embodiments of the present disclosure will hereafter be described with reference to the accompanying drawings.
[0009] FIG. 1A shows a plot of carrier concentration as a function of VI-III flow ratio for Ga302:Si formed according to an illustrative embodiment. FIG. 1B shows a plot of Hall mobility as a function of VI-III flow ratio for Ga302:Si formed according to an illustrative embodiment.
[0010] FIG. 2A shows a cross-sectional view of a schematic of a field effect transistor (FET) with a fin structure fabricated using p-type Ga302:Si according to an illustrative embodiment. FIG. 2B shows a perspective view of the fin-FET.
[0011] FIG. 3 A is a plot of the I-V curve and FIG. 3B is a plot of the transfer
characteristics at VDS = 20 V of a p-type Ga203:Si 3 pm by 3 pm fin array fin-FET (shown in FIGs. 2 A and 2B). The fin-FET shows an on/off ratio of 106 and a breakdown voltage of over 150 V.
[0012] FIG. 4A shows an XRD omega/2theta scan of - 150 nm thick Ga203:Si grown using a VEIII ratio of 150 (top), at a VEIII ratio of 100 (middle) and an XRD omega/2theta scan of a P-Ga203 substrate (TAMURA Corp) (bottom). FIG. 4B shows a TEM image of typical morphology of the - 150 nm thick Ga203:Si on sapphire. The inset shows SAED patterns obtained along the [5-10] zone axis at the K-Ga203/Al203 interface.
[0013] FIG. 5 A shows the carrier concentration and resistivity of Ga203:Si on sapphire (0001) as a function of growth temperature at VEIII ratio of 150 and FIG. 5B shows the same
at a VI/III ratio of 100. FIG. 5C shows the Hall mobility of Ga203:Si on sapphire (0001) as a function of growth temperature at VI/III ratio of 100 and 150.
[0014] FIG. 6 shows I-V curves of - 150 nm thick p- type Ga203:Si on sapphire (0001) from VGS = -10 to 40 V and the inset is an optical microscope image of the fabricated device.
[0015] FIG. 7 A show schematic illustrations of 2D p- type Ga2C>3:Si channel microstrip array FETs with details of device scale FIG. 7B shows an optical micrograph of the fabricated device.
[0016] FIG. 8A shows I-V curves from VGS = -50 to 100 V. The inset is an optical micrograph of the probing. FIG. 8B shows simulation data of I-V curves from VGS = -40 to 40 V. FIG. 8C shows transfer characteristics at VDS = 10 to 40 V.
[0017] FIG. 9 A shows a schematic illustration of the 2D Ga2C>3:Si channel microstrip array FETs. FIG. 9B shows a schematic illustration of three portions of the Ga2C>3 channel.
DETAILED DESCRIPTION
[0018] Provided are methods of forming IV-doped III- VI semiconductors, including p- type III- VI semiconductors doped with Si. Also provided are the IV-doped III- VI
semiconductors and devices incorporating the IV-doped III- VI semiconductors.
[0019] The present methods are based on the technique of metalorganic chemical vapor deposition (MOCVD). As such, any reactor system suitable for carrying out MOCVD may be used to carry out the methods. An embodiment of a method of forming an IV-doped III- VI semiconductor comprises a step of exposing a substrate to a vapor composition comprising a group III precursor comprising a group III element, a group VI precursor comprising a group VI element, and a group IV precursor comprising a group IV element. The exposure takes place under conditions sufficient to form a compound semiconductor from the group III, group VI, and group IV precursors via MOCVD. That is, the group III, group VI, group IV precursors adsorb to the surface of substrate where they react to form the compound semiconductor, typically as a layer on the surface of the substrate. The method may include a predeposition step to form a wetting layer on the substrate prior to exposure to the vapor composition. The predeposition step may comprise exposing the substrate to the group III precursor (i.e., without the group VI precursor and without the group IV precursor).
[0020] The group III precursors are metalorganic compounds comprising a group III element. In embodiments, the group III element is selected from Ga, Al, and In. A variety of group III precursors may be used, e.g., trimethylgallium, trimethylaluminum,
trimethylindium, triethylgallium, triethylaluminum, triethylindium, triisopropylgallium, triisopropylaluminum, triisopropylindium, triisobutylgallium, and triisobutylaluminum. In embodiments, a single group III precursor is used, e.g., a gallium-containing group III precursor to provide a Ga-group VI compound semiconductor. In embodiments, more than one group III precursor is used so as to facilitate alloying of the group III elements in the formation of the compound semiconductor. By of illustration, a gallium-containing group III precursor, an aluminum-containing group III precursor and an indium-containing group III precursor may be used to provide a GaAlln-group VI compound semiconductor. In such a compound semiconductor, the ratios of Ga, Al, In may vary, depending upon the desired properties and application for the semiconductor. As another illustration, a gallium- containing group III precursor and an indium-containing group III precursor may be used to provide a Gain-group VI compound semiconductor. Again, in such a compound
semiconductor, the ratios of Ga and In may vary.
[0021] The group VI precursors are compounds comprising a group VI element. In embodiments, the group VI element is O. A variety of group VI precursors may be used, e.g., water, oxygen, N20, and ozone.
[0022] The group IV precursors are compounds comprising a group IV element. In the present methods, the group IV precursors are used as dopants, i.e., to provide an IV-doped III- VI. In embodiments, the group IV element is Si. A variety of group IV precursors may be used, e.g., SiH4, tetraethylorthosilicate, Si2I¾, SiCU.
[0023] Because one or more of the group III, group VI, and group IV precursors may be provided in a carrier gas (e.g., N2, Ar, H2), the vapor composition may also comprise one or more such carrier gases.
[0024] By“ conditions” as that term is used with respect to the present methods, refers to the growth temperature, the pressure of the vapor composition, the flow ratio of the group VI precursor to the group III precursor, and the carrier gas. The present methods are based, at least in part, on the finding that certain of these conditions may be adjusted to tune the doping type of the compound semiconductor from n-type to p-type, even when using the same dopant, i.e., the same group IV precursor. That is, certain of these conditions may be adjusted
so that the group IV element of the group IV precursor substitutes for the group VI element in the forming compound semiconductor to provide a p-type IV-doped III- VI semiconductor or so that the group IV element substitutes for the group III element to provide an n-type IV- doped III- VI semiconductor.
[0025] These findings are particularly surprising given the widely accepted challenges in the field for obtaining p-type III- VI semiconductors such as p-type Ga203. Specifically, for p- type Ga203 thin films, shallow donor level (due to oxygen vacancy) with low formation energy can influence the efficiency of doping and compensate for native acceptors. This requires high formation energy, which makes it difficult to grow the p-type material. See also Mastro et al. ,“Opportunities and Future Directions for Ga203,” ECS Journal of Solid-State Science and Technology , 6 (5) p. 356-359 (2017), which provides additional evidence of these challenges.
[0026] By way of illustration, it has been found that the flow ratio of the group VI precursor to the group III precursor may be adjusted to provide both an n-type IV-doped III- VI semiconductor (at certain flow ratios) and a p-type IV-doped III- VI semiconductor (at other flow ratios) even when using the same group IV precursor. Similarly, an inversion flow ratio value has been found, below which value a p-type IV-doped III- VI semiconductor is formed and above which value a n-type IV-doped III- VI semiconductor is formed even when using the same group IV precursor. The inversion flow ratio value for a particular material system may be referenced at a particular growth temperature, pressure, and carrier gas being used in the method.
[0027] These findings are demonstrated in the Examples below using trimethylgallium (group III precursor), water (group VI precursor) and silane (group IV precursor) to provide both n-type Ga302:Si and p-type Ga302:Si simply by adjusting the flow ratio of the O precursor to the Ga precursor. In other words, it has been found that Si acts as an amphoteric dopant for Ga302 via adjustments of the VI-III flow ratio. This vastly simplifies
manufacturability of doped Ga203, thereby enabling many applications of this important material. Moreover, it has been found that the inversion flow ratio value for this material system is about 125. That is, for VI-III flow ratios below 125, the compound semiconductor formed is p-type (silicon substitutes for oxygen, taking up two extra electrons from the lattice, thus acting as a doubly ionized acceptor to achieve very effective p-type doping). For VI-III flow ratios above 125, the compound semiconductor formed is n-type (silicon
substitutes for gallium). (See FIG. 1 A.) This inversion flow ratio value of 125 may be referenced, e.g., at a growth temperature of 1000 °C, a pressure of 50 mbar, and N2 as the carrier gas.
[0028] FIGs. 5A-5C further support the findings described above. Moreover, these figures show the growth temperature does not changing the nature of doping, only the ratio of the flows of the group III and VI precursors.
[0029] Thus, the present methods may comprise carrying out the step of exposure to the vapor composition under conditions (e.g., VI-III flow ratio) selected to achieve a desired doping type (either p-type or n-type) for the IV-doped III- VI semiconductor being formed. Since both doping types may be achieved using the same group IV precursor, the methods may further comprise forming a second IV-doped III- VI semiconductor having the opposite doping type to provide a p-n heterojunction. For example, the method can be used to form an n-type IV-doped III- VI semiconductor on a p-type IV-doped III- VI semiconductor or vice versa.
[0030] With reference back to the growth temperature and pressure described above, illustrative growth temperatures include those in the range of from about 500 °C to about 1500 °C, including from about 600 °C to about 1000 °C, or from about 700 °C to about 1000 °C. Illustrative pressures include those in the range of from about 10 mbar to about 100 mbar, including from about 50 mbar to about 150 mbar. A variety of substrates may be used in the present methods, e.g., sapphire (a-sapphire, m-sapphire, c-sapphire), AI2O3, silicon (Si(l l l), Si(l00)), native -Ga203, MgO, ZnO, etc.
[0031] The IV-doped III- VI semiconductors formed using the present methods are also encompassed by the present disclosure. The IV-doped III- VI semiconductors may be characterized by their carrier concentrations. In embodiments, the IV-doped III- VI semiconductor is p-type having a carrier concentration in the range of from about 1015 cm 3 to about 1020 cm 3, from about 1016 cm 3 to about 1020 cm 3, from about 1017 cm 3 to about 1020 cm 3 or from about 1018 cm 3 to about 1020 cm 3. In embodiments, the IV-doped III- VI semiconductor is n-type having a carrier concentration in any of the ranges disclosed above. The IV-doped III- VI semiconductors may be characterized by their Hall mobility. In embodiments, the Hall mobility may be in the range of from about 5 to about 300 cm2/Vs, about 10 to about 300 cm2/Vs, or from about 5 to about 150 cm2/Vs. Known techniques may be used to measure carrier concentration and Hall mobility.
[0032] The IV-doped III- VI semiconductors may be characterized by the phase of the III-
VI semiconductor. By way of illustration, for Ga302, the phase of the material may be, e.g., b or K.
[0033] Also encompassed by the present disclosure are p-n heterojunctions formed from any of the disclosed p-type IV-doped III- VI semiconductor and another n-type semiconductor or from any of the disclosed p-type IV-doped III- VI semiconductors and any of the disclosed n-type IV-doped III- VI semiconductors.
[0034] Devices incorporating the IV-doped III- VI semiconductors are also encompassed by the present disclosure. Illustrative devices include photodetectors (including solar-blind UV photodetectors), field effect transistors (including fin structured transistors see FIGs. 2A- 2B and 7A-7B), light emitting diodes and combinations thereof. Other applications include use of the IV-doped III- VI semiconductors in high voltage direct current transmission lines, variable frequency drives and switch mode power supplies.
[0035] Additional information regarding MOCVD, techniques for characterizing the IV- doped III- VI semiconductors, and devices in which the IV-doped III- VI semiconductors may be incorporated may be found in the Appendix I (entire document), Appendix II (especially Section 2.2 and Section 4), and Appendix III (entire document) included in U.S. Provisional Application No. 62/623,183, the entire contents of which are hereby incorporated by reference.
EXAMPLE
[0036] Example 1
[0037] A commercial horizontal-flow MOCVD reactor (AIXTRON 200/4 RF) was used to grow doped Ga203 thin films on c-plane sapphire (0001) at a growth temperature of about 1000 °C using a conventional trimethylgallium (TMGa) bubbler and high purity deionized water loaded in a custom quartz bubbler as the gallium and oxygen precursors, respectively. Silane (SiH4) was used as the silicon precursor. H2 was used as the carrier gas. First, TMGa was flowed for 1 minute to predeposit gallium on the substrate before introducing the water. Doped Ga203 thin films were investigated using VI / III flow ratios in the range of from 100 to 150.
[0038] FIG. 1 A shows the carrier concentration as a function of the III- VI flow ratio. For
VI-III flow ratios below -125 the as-grown material is p-type (silicon substitutes for oxygen).
At an VI- III flow ratio of -125 an inversion takes place and the material becomes
compensated. At an VI- III- flow ratio higher than -125 the material becomes n-type (silicon substitutes for gallium). The only aspect of the growth that was changed was the VI-III flow ratio. In all cases, the growth temperature was 1000 °C and the only variable changed was the ratio of the trimethylgallium and water flow rate being introduced into the reaction chamber. The Hall mobility of the as-grown material as a function of the VI-III flow ratio is plotted in FIG. 1B.
[0039] In order to verify that the as-grown material is indeed p-type at low VI-III flow ratios, a series of field effect transistors (FETs) with a fin structure were fabricated using the p-type material (see FIGs. 2A and 2B). An insulated gate consisting of -100 nm of silicon dioxide was deposited over the semiconductor material (i.e., p-type Ga302) and source, drain, and gate contacts were deposited. The epitaxial layer of Ga203 was only -1.2 nm thick. Hall mobility measurements indicated the layer was p-type with a carrier concentration of 3.423 x 1018 cm 3. The source-drain spacing was 20 pm and the gate was just 5 pm wide.
[0040] The fin-FET transistors were then experimentally characterized using an HP 4155C semiconductor parameter analyzer to measure the family of curves. The results are shown in FIGs. 3 A and 3B. The measured results show the excellent conductivity of the p- type layer achieved with the novel doping technique used in this Example.
[0041] Example 2
[0042] Ga?0, has emerged as a next generation semiconductor material for high power electronic devices. This is in great part due to its high breakdown electric field (~ 8 MV/cm), which largely surpasses that of competing materials systems such as SiC or GaN.
Furthermore, the emergence of «-type doping capacity and single crystal Ga?0, substrates has allowed the development of various unipolar electronic devices including metal oxide semiconductor field effect transistors (MOSFETs), Schottky diodes, metal semiconductor field effect transistors (MESFET).1-3 The vast majority of this work has focused on homoepitaxial growth of monoclinic -Ga203, which is the most stable of five common polymorphs (a, b g, d and e). A major drawback of Ga203 till present, however, has been lack of a method to obtain p- type conduction. This is a key limitation for its adoption in a whole range of semiconductor device applications. Moreover, the relatively low thermal
conductivity of Ga203 and the problem of Ga203 substrate cost being two orders of
magnitude higher than sapphire are both currently hindering the fuller development of Ga20, based power electronics.
[0043] K-Ga20, (an orthorhombic polymorph which is normally considered to be transient) can be stabilized in heteroepitaxial growth on sapphire (0001) substrates by MOCVD.4 In this Example, it is shown that high levels of shallow acceptor p- type conduction may be achieved in such layers using silicon impurity doping under Ga rich growth conditions. 2D layers of such p- type Ga203:Si are then processed into microstrip array ring FETs using conventional photolithography. The operational characteristics of the FETs proved to be consistent with p- type conduction. This is the first demonstration of both shallow acceptor doping of Ga202 and a p- type Ga202 channel FET. A phenomenological model coherent with a p- type channel is also presented.
[0044] A commercial MOCVD reactor (AIXTRON 200/4 RF) was used to grow Ga203 on sapphire (0001) substrates at growth temperatures ranging from 730 to 1000 °C.
Trimethylgallium (TMGa), high purity deionized water and SiFE were adopted as the Ga, O and Si precursors, respectively. N2 was used as the carrier gas. Total pressure was 50 mbar. VEIII ratio was either 100 (Ga-rich) or 150 (O-rich). The SiFE flow rate was fixed at 15 seem.
[0045] As shown in FIG. 4 A, XRD analysis was performed to analyze the phases of the grown - 150 nm thick Ga203:Si with different VI/III ratio 100 and 150 (top and middle). The XRD results show three peaks for each Ga203:Si layer. These three peaks were observed, similar to the results of the P-Ga203 substrate (bottom). However the TEM analysis in FIG.
4B showed the result of k-phase with the space group of Pna11 4 The k-phase Ga203:Si was grown in the (002) direction and the 6 rotated domains were observed in the - 150 nm thick Ga203:Si.
[0046] Electrical properties were measured using Van der Pauw Hall measurements. Ohmic contacts were obtained using a Ga/In eutectic. FIGs. 5 A and 5B show the results as a function of growth temperature for both VEIII ratios. At a VEIII ratio of 150, Ga203:Si grown at 730 °C shows «-type characteristics. As growth temperature was increased from 730 °C to 1000 °C, the carrier concentration decreased linearly to - 4.4 x 1017 cm 3. FIG. 5B shows that the lower VEIII ratio (100) consistently gave p- type characteristics. Assuming that the Si dopant acts as a shallow acceptor by substituting on the O-site of the Ga203, the VEIII ratio of 100 growth condition would generate a higher density of oxygen vacancies (Vo) by
virtue of the Ga-rich nature of the growth which lets the Si substitute more readily at the O- sites. This assumption is consistent with FIG. 2C which shows the Hall mobility of the Ga203:Si as a function of growth temperature for VI/III ratios of 150 and 100. For a VI/III ratio of 150, a («-type) mobility near 50 cm2/V s was observed for a growth temperature of 1000 °C. For a VI/III ratio of 100, a p- type mobility of ~ 3.3 cm2/Vs was observed. This demonstrates Si is acting as an amphoteric dopant in K-Ga203. Si impurity doping is generally incorporated so as to substitute for Ga where it acts as a shallow donor so as to create heavily doped «-type Ga2C>3. But as the density of Vo increases under Ga-rich growth conditions, the above results suggest that Si can act as a shallow acceptor by substituting on the O-sites in K-Ga203, and thus promote a transformation to predominantly p- type conduction. These p- type results were confirmed via multiple independent measurements.
[0047] Ring type FETs were fabricated and evaluated for the characteristics of the FET device of - 150 nm thick p- type Ga203:Si with VEIII ratio of 100. FIG. 6 shows the I-V curves. It is observed that the drain current decreases with increasing gate voltage. However, it was not possible to achive pinch-off due to the gate electrode burning at gate voltages higher than 50 V. To avoid this issue the channel thickness was reduced to - 1.2 nm and the ring pattern FETs were patterned with microstrips. Ga203:Si channel layers were grown at 1000 °C with a VEIII ratio of 100. The channel thickness was estimated to be - 1.2 ± 0.5 nm based on interferometric growth rate calibration and AFM step-edge profilometry. Hall measurements confirmed the p- type nature of the layers with a resistivity of - 0.007 Q cm, a carrier concentration of - 1.7 x 1020 cm 3 and a mobility of - 5.7 cm2/V-s.
[0048] Standard photolithography and lift-off were employed to deposit source and drain metal contacts. Before their deposition, 3 pm x 3 pm microstrip patterns were formed by electron cyclotron resonance-reactive ion etching (ECR-RIE) with CF4 for 5 minutes. The metal contacts were Ti (20 nm) / Au (150 nm) deposited by e-beam evaporation. Si02 of 100 nm thick gate dielectric material was formed by plasma-enhanced chemical vapor deposition (PECVD). After dielectric and passivation film deposition, the gate metal contact was formed with Pt(20 nm) / Ti(20 nm) / Au(l50 nm) on the Si02 film. The gate length, and the spacing between the source/drain and the inside source circular pad were 15, 20 and 100 pm, respectively. FIG. 7A shows schematic illustrations of the device with top- and cross- sectional views illustrating the device scale. FIG. 7B shows an optical microscope image of the fabricated device.
[0049] Next, the FETs were fabricated and tested using a semiconductor parameter analyzer and probe station. FIG. 8A shows the DC source-drain current versus source-drain voltage (IDS-VDS) output characteristics for the depletion-mode FETs measured by increasing gate-source voltage (VGS) stepwise from -50 to 100 V. The maximum IDS was 2.19 mA and it was effectively modulated by VGS from -50 to 100 V, which is consistent with a p- type channel. Because of the heavy /^-doping, the 2D microstrip channel is normally-on, and the channel off-state was observed for a gate bias of 50 V (IDS = 0.1 pA at VDS of 40 V). In addition, because of the high sheet resistance, even with a drain voltage as high as 40 V, the voltage drop in the FET channel is still lower than |VG-VT|, which is the condition for current saturation in long channel FETs. So the IDS-VDS characteristics remain linear. FIG. 8B displays a similar set of curves obtained from the simulation. It can be seen that the theoretical model is consistent with the experimental data in showing an output resistance increase with positive gate voltage, and IDS bunching with little variation of the output resistance for VGS<0. This is also consistent with a /i-type channel. FIG. 8C shows transfer characteristics at VDS of 10 to 40 V in a logarithmic scale. The device achieved an on/off ratio of - 108 by minimizing the thickness and width of the channel. A plot of the gate current as a function of drain-source voltage (not shown) showed that IG increases above a VGS of 50 V because of a gate leakage current. It is expected that the on/off ratio can be further improved through optimization of the dielectric layer.
[0050] A phenomenological model was developed based on the device configuration displayed in FIGs. 7A-7B. FIGs. 9A-9B show the schematic of the model device that consists of a linear array of d = 3 pm wide micro-strips separated from each other by d = 3 pm. They are covered by a disk-shaped source contact of 200 pm in diameter, and separated from a square shaped drain by a 30 pm wide circular channel. So, in each quadrant, the channel length, Li, varies between a minimum value when it is perpendicular to the disk and a maximum value when it is tangential to the disk. The position of the ith microstrip is identified by its distance, di, from the center of the source disk.
[0051] At EG = 0 V, the channel is uniform and the current between source and drain in the ith micro-strip channel is given by h = e sSVi (1)
[0052] where e is the electron charge (C), Ps is the 2D hole concentration (carriers/cm2), d the wire width (cm) and u, is the hole velocity in the ith channel (cm/s). In the absence of saturation velocity (long channel-low mobility),
[0053] where m is the hole mobility (cm 1 /Vs) and Ϊ‘ is the channel length (cm).
[0054] If di = 2 id with 0 < i < N, Equ.l becomes for top and bottom right quadrants
2.84 epspVDS (3)
[0055] Because of the relatively big gate pad on the left side of the source, channel lengths are longer for a sizeable portion of the FIN-microstrips, so it is estimated that the total current should be multiplied by a factor h~1.8-1.9<2. Finally,
[0057]
the channel potential induced by the gate bias, the expression for the current reads h(VG) = eps(VG = 0)dm VDS/(L + Ll 2exp(eVc/kT) + L ) (6) or after summation over all channels,
[0058] This equation shows that for Vc<0 (VG<0) the drain current decreases, whereas for Vc>0 (VG>0) the drain current increases in agreement with the experimental data. This is consistent with the channel being p- type. In quantitative terms, it shows that current decreases by several orders of magnitude under positive VG compared to a limiting increase by a factor 2 under negative VG. This asymmetry in the variation of the I-V characteristics for VG<0 and VG>0 is also consistent with the experimental data.
[0059] From the Poisson equation, one can derive an expression of Vc for intermediate gate bias:
[0060] where D is the thickness of the S1O2 barrier, y is the vertical coordinate inside the Ga20, layer, and lϋ is the Debye length in the Ga203 layer fitted to reproduce the
experimental I-V characteristics. FIG. 8B displays simulation data of I-V curves from VGS = -
40 to 40 V, for which a channel mobility m = 23 cm2/Vs and hole concentration ps = 2.35 x l012/cm2 was used.
[0061] In conclusion, K-Ga?0,:Si layers grown on sapphire (0001) substrates by
MOCVD showed consistent p- type Hall signal for layers grown with lower VI/I 11 ratios during growth. Room temperature mobilities were up to 7 cm2/Vs, resistivities were as low as 0.007 Q.cm and carrier concentrations were up to -1020 cm 3 for thinner layers. Ring mesa FETs were fabricated based on -1.2 nm thick / Ga20,:Si channels formed into a number of 3 pm wide microstrips. The devices achieved a maximum drain current density of 2.19 mA and an on/off ratio of - 108 and showed characteristics consistent with a p- type conduction in the channel.
[0062] The p- type Ga?0, demonstrated in this Example represents a significant advance in the state of the art, which may herald the fabrication of a range of
junction based devices. These may be smaller/thinner and bring both cost (more devices/wafer and less growth time) and operating speed advantages (due to miniaturisation) than current isotype FETs. Moreover the demonstration of the first functioning devices based on scaling down to 2D device channels in Ga203 based FETs opens up the perspective of faster devices and improved heat evacuation.
[0063] References for Example 2
1 M. Higashiwaki, K. Sasaki, T. Kamimura, M. Hoi Wong, D. Krishnamurthy, A. Kuramata, T. Masui, and S. Yamakoshi, Appl. Phys. Lett. 103, 123511 (2013).
2 K. Sasaki, M. Higashiwaki, A. Kuramata, T. Masui, and S. Yamakoshi, J. Cryst. Growth 378, 591 (2013).
3 K. Sasaki, DaikiWakimoto, Q.T. Thieu, Y. Koishikawa, A. Kuramata, M. Higashiwaki, and S. Yamakoshi, IEEE Electron Device Lett. 38, 783 (2017).
4 M. Razeghi, J.-H. Park, R. McClintockl, D. Pavlidis, F.H. Teherani, D.J. Rogers, B.A. Magill, G.A. Khodaparast, Y. Xu, J. Wu, and V.P. Dravid, Proc. SPIE 10533, 105330R (2018).
5 A. Munoz-Yague and S.Baceiredo, J. Electrochem. Soc. 129, 2108 (1982).
6 I. TERAMOTO, J. Phys. Chem. Solids 33, 2089 (1972).
7 H.P. Meier, R.F. Broom, P.W. Epperlein, E. van Giesen, C. Harder, and H. Jackel, J. Vac. Sci. Technol. B 6, 692 (1988).
8 K. Agawa, K. Hirakawa, N. Sakamoto, Y. Hashimoto, and T. Ikoma, Appl. Phys. Lett. 65, 1171 (1994).
9 A.A. Quivy, A.L. Sperandio, E.C.F. Silva, and J.R. Leite, J. Cryst. Growth 206, 171 (1999).
10 T. Oishi, Y. Koga, K. Harada, and M. Kasu, Appl. Phys. Express 8, 031101 (2015).
11 M. Baldini, M. Albrecht, A. Fiedler, K. Irmscher, R. Schewski, and G. Wagner, ECS J. Solid State Sci. Technol. 6, Q3040 (2017).
[0064] The word "illustrative" is used herein to mean serving as an example, instance, or illustration. Any aspect or design described herein as "illustrative" is not necessarily to be construed as preferred or advantageous over other aspects or designs. Further, for the purposes of this disclosure and unless otherwise specified, "a" or "an" means "one or more.”
[0065] The foregoing description of illustrative embodiments of the disclosure has been presented for purposes of illustration and of description. It is not intended to be exhaustive or to limit the disclosure to the precise form disclosed, and modifications and variations are possible in light of the above teachings or may be acquired from practice of the disclosure. The embodiments were chosen and described in order to explain the principles of the disclosure and as practical applications of the disclosure to enable one skilled in the art to utilize the disclosure in various embodiments and with various modifications as suited to the particular use contemplated. It is intended that the scope of the disclosure be defined by the claims appended hereto and their equivalents.
Claims
1. A method of forming a p-type IV-doped III- VI semiconductor, the method comprising:
exposing a substrate to a vapor composition comprising a group III precursor comprising a group III element, a group VI precursor comprising a group VI element, and a group IV precursor comprising a group IV element, under conditions to form a p-type IV- doped III- VI semiconductor via metalorganic chemical vapor deposition (MOCVD) on the substrate.
2. The method of claim 1, wherein the conditions comprise use of a flow ratio defined as a flow rate of the group VI precursor to a flow rate of the group III precursor and the flow ratio is below an inversion flow ratio value for the IV-doped III- VI semiconductor so as to provide the p-type IV-doped III- VI semiconductor.
3. The method of claim 1, further comprising exposing the substrate to the vapor composition under conditions to form an n-type IV-doped III- VI semiconductor via MOCVD from the vapor composition.
4. The method of claim 3, wherein the n-type IV-doped III- VI semiconductor is in contact with the p-type IV-doped III- VI semiconductor, thereby forming a p-n
heterojunction.
5. The method of claim 3, wherein the conditions comprise use of a flow ratio defined as a flow rate of the group VI precursor to a flow rate of the group III precursor and the flow ratio is above an inversion flow ratio value for the IV-doped III- VI semiconductor so as to provide the n-type IV-doped III- VI semiconductor.
6. The method of claim 1, wherein the conditions comprise use of a first flow ratio defined as a flow rate of the group VI precursor to a flow rate of the group III precursor to provide the p-type IV-doped III- VI semiconductor;
wherein the method further comprises exposing the substrate to the vapor composition under conditions to form an n-type IV-doped III- VI semiconductor via MOCVD from the vapor composition, wherein the conditions comprise use of a second, different flow ratio to provide the n-type IV-doped III- VI semiconductor.
7. The method of claim 6, wherein the n-type IV-doped III- VI semiconductor is in contact with the p-type IV-doped III- VI semiconductor, thereby forming a p-n
heterojunction.
8. The method of claim 1, wherein the group III precursors are selected from a Ga-containing group III precursor, an Al-containing group III precursor, an In-containing group III precursor and combinations thereof.
9. The method of claim 1, wherein the group III precursor is a Ga-containing group III precursor.
10. The method of claim 1, wherein the group VI precursor comprises O.
11. The method of claim 1, wherein the group IV precursor comprises Si.
12. The method of claim 1, wherein the carrier gas comprises N2, H2, Ar, or combinations thereof.
13. The method of claim 1, wherein the group III precursors are selected from a Ga-containing group III precursor, an Al-containing group III precursor, an In-containing group III precursor and combinations thereof; wherein the group VI precursor comprises O; and wherein the group IV precursor comprises Si.
14. The method of claim 13, wherein the p-type IV-doped III- VI semiconductor formed is p-type Si-doped Ga203.
15. The method of claim 13, wherein the p-type IV-doped III- VI semiconductor formed is p-type Si-doped (Ga,In)203.
16. The method of claim 13, wherein the carrier gas comprises N2, H2, Ar, or combinations thereof.
17. A p-type IV-doped III- VI semiconductor comprising a group III element, a group VI element and a group IV element.
18. A p-n heterojunction comprising a layer of an n-type semiconductor in contact with the p-type IV-doped III- VI semiconductor of claim 17.
19. The p-n heterojunction of claim 18, wherein the n-type semiconductor is an n- type IV-doped III- VI semiconductor comprising the group III element, the group VI element and the group IV element.
20. A device comprising the p-type IV-doped III- VI semiconductor of claim 17 and another material layer in contact with the p-type IV-doped III- VI semiconductor.
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Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11930719B2 (en) | 2019-01-31 | 2024-03-12 | Northwestern University | Magnetic memory device using doped semiconductor layer |
| US20240096618A1 (en) * | 2021-02-19 | 2024-03-21 | Northwestern University | Methods for forming k-phase gallium oxide materials |
| CN119730440A (en) * | 2024-11-18 | 2025-03-28 | 中山德华芯片技术有限公司 | Planar short wave infrared detector and preparation method and application thereof |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR3085535B1 (en) * | 2019-04-17 | 2021-02-12 | Hosseini Teherani Ferechteh | A method of manufacturing p-type gallium oxide by intrinsic doping, the resulting thin film of gallium oxide and its use |
| US12622008B2 (en) | 2021-09-14 | 2026-05-05 | Northwestern University | III-Nitride/gallium oxide based high electron mobility transistors |
| US20240229293A1 (en) * | 2023-01-11 | 2024-07-11 | University Of South Carolina | Phase stabilized growth of monoclinic-gallium oxide on thermally conducting materials |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20060027814A1 (en) * | 2002-11-18 | 2006-02-09 | Atsushi Watanabe | Semiconductor light-emitting element and method of manufacturingthe same |
| US20080092954A1 (en) * | 2005-01-12 | 2008-04-24 | In-Solar Tech. Co. Ltd. | Optical Absorber Layers For Solar Cell And Method Of Manufacturing The Same |
| US20110186856A1 (en) * | 2010-01-29 | 2011-08-04 | Advanced Optoelectronic Technology, Inc. | Light emitting element and method for manufacturing the same |
| US20170077330A1 (en) * | 2007-04-09 | 2017-03-16 | Taiwan Semiconductor Manufacturing Company, Ltd. | Photovoltaics on silicon |
| US20180287001A1 (en) * | 2017-04-03 | 2018-10-04 | International Business Machines Corporation | High voltage photovoltaics with stacked multi-junctions using wide bandgap materials |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3600240A (en) | 1968-12-12 | 1971-08-17 | Ibm | Epitaxial growth from solution with amphoteric dopant |
| NL161919C (en) | 1969-06-20 | 1980-03-17 | Sharp Kk | METHOD FOR MANUFACTURING A SEMICONDUCTOR DEVICE CONTAINING A P, N TRANSITION |
| FR2296264A1 (en) | 1974-12-24 | 1976-07-23 | Radiotechnique Compelec | PROCESS FOR REALIZING A HETEROJUNCTION SEMICONDUCTOR DEVICE |
| JPS58156598A (en) | 1982-03-09 | 1983-09-17 | Semiconductor Res Found | Method for crystal growth |
| US4583110A (en) | 1984-06-14 | 1986-04-15 | International Business Machines Corporation | Intermetallic semiconductor ohmic contact |
| US4939102A (en) | 1989-01-17 | 1990-07-03 | American Telephone And Telegraph Company | Method of growing III-V semiconductor layers with high effective hole concentration |
| US5268582A (en) | 1992-08-24 | 1993-12-07 | At&T Bell Laboratories | P-N junction devices with group IV element-doped group III-V compound semiconductors |
| FR2892231B1 (en) | 2005-10-14 | 2008-06-27 | Commissariat Energie Atomique | MAGNETIC DEVICE WITH MAGNETORESISTIVE TUNNEL JUNCTION AND MAGNETIC MEMORY WITH RANDOM ACCESS |
| US9205420B2 (en) * | 2011-04-22 | 2015-12-08 | President And Fellows Of Harvard College | Nanostructures, systems, and methods for photocatalysis |
| JP6758569B2 (en) * | 2015-03-20 | 2020-09-23 | 株式会社タムラ製作所 | High withstand voltage Schottky barrier diode |
| US9917137B1 (en) | 2017-01-11 | 2018-03-13 | International Business Machines Corporation | Integrated magnetic tunnel junction (MTJ) in back end of line (BEOL) interconnects |
| KR101883759B1 (en) * | 2017-04-25 | 2018-07-31 | 엘지전자 주식회사 | Compound semiconductor solar cell and method for manufacturing the same |
-
2019
- 2019-01-23 US US16/771,604 patent/US11417523B2/en active Active
- 2019-01-23 WO PCT/US2019/014650 patent/WO2019147602A1/en not_active Ceased
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20060027814A1 (en) * | 2002-11-18 | 2006-02-09 | Atsushi Watanabe | Semiconductor light-emitting element and method of manufacturingthe same |
| US20080092954A1 (en) * | 2005-01-12 | 2008-04-24 | In-Solar Tech. Co. Ltd. | Optical Absorber Layers For Solar Cell And Method Of Manufacturing The Same |
| US20170077330A1 (en) * | 2007-04-09 | 2017-03-16 | Taiwan Semiconductor Manufacturing Company, Ltd. | Photovoltaics on silicon |
| US20110186856A1 (en) * | 2010-01-29 | 2011-08-04 | Advanced Optoelectronic Technology, Inc. | Light emitting element and method for manufacturing the same |
| US20180287001A1 (en) * | 2017-04-03 | 2018-10-04 | International Business Machines Corporation | High voltage photovoltaics with stacked multi-junctions using wide bandgap materials |
Non-Patent Citations (1)
| Title |
|---|
| NIU: "Epitaxial systems and combining oxides and semiconductors", 2013, Retrieved from the Internet <URL:https://www.sciencedirect.com/topics/chemistry/metal-organic-chemical-vapor-deposition> * |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11930719B2 (en) | 2019-01-31 | 2024-03-12 | Northwestern University | Magnetic memory device using doped semiconductor layer |
| US20240096618A1 (en) * | 2021-02-19 | 2024-03-21 | Northwestern University | Methods for forming k-phase gallium oxide materials |
| CN119730440A (en) * | 2024-11-18 | 2025-03-28 | 中山德华芯片技术有限公司 | Planar short wave infrared detector and preparation method and application thereof |
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