Thin (40–150 nm), highly doped n+ (1019–1020 cm−3) Ga2O3 layers deposited using pulsed laser deposition (PLD) were incorporated into Ti/Au ohmic contacts on (001) and (010) β-Ga2O3 substrates with carrier concentrations between 2.5 and 5.1 × 1018 cm−3. Specific contact resistivity values were calculated for contact structures both without and with a PLD layer having different thicknesses up to 150 nm. With the exception of a 40 nm PLD layer on the (001) substrate, the specific contact resistivity values decreased with increasing PLD layer thickness: up to 8× on (001) Ga2O3 and up to 16× on (010) Ga2O3 compared with samples without a PLD layer. The lowest average specific contact resistivities were achieved with 150 nm PLD layers: 3.48 × 10−5 Ω cm2 on (001) Ga2O3 and 4.79 × 10−5 Ω cm2 on (010) Ga2O3. Cross-sectional transmission electron microscopy images revealed differences in the microstructure and morphology of the PLD layers on the different substrate orientations. This study describes a low-temperature process that could be used to reduce the contact resistance in Ga2O3 devices.
I. INTRODUCTION
Beta-gallium oxide (β-Ga2O3) is a wide bandgap (EG ∼ 4.8 eV) semiconductor that has attracted growing interest due to the availability of bulk crystals and a variety of shallow n-type dopants (Sn, Si, and Ge)1 covering a broad doping range. It is considered a promising candidate for next-generation power electronics,2,3 in part due to the fact that it has a higher theoretical breakdown field and power figure-of-merit than either GaN or SiC.4
For power devices, it is necessary to minimize the ohmic contact resistance, which contributes to the on-resistance of the device and increases the conduction losses in the circuit. Reducing the contact resistance is often achieved by doping the semiconductor surface heavily to decrease the depletion width, making it thin enough to allow carriers to the tunnel.5
The standard metallization for Ga2O3 ohmic contacts consists of annealed Ti/Au.6–9 Various processes have been reported to reduce the contact resistance of Ti/Au contacts to Ga2O3 (Table I). Values range from ∼10−3 to ∼10−7 Ω cm2 and depend on doping concentration and the type of process. Many processes incorporate a highly doped (n+), 100–180 nm-thick Ga2O3 layer produced using Si-ion implantation with high-temperature (925–975 °C) activation anneal.1–4 Several of the aforementioned processes also included reactive ion etching using BCl3/Ar.10–13 A specific contact resistance of 4.6 × 10−6 Ω cm2 was achieved using Si-ion implantation (implant dosage = 5 × 1019 cm−2) and a postimplant anneal at 950 °C.14 In a separate study, contacts on the (010) orientation without implantation were pseudo-ohmic with a specific contact resistivity of ; Si-ion implantation and RIE treatment (MBE)15,16 and metal organic vapor phase epitaxy (MOVPE) have also been used to create highly doped Ga2O3 layers for ohmic contacts.10,17,18 Low-resistance (8.3 × 10−7 Ω cm2) ohmic contacts were achieved on a Si-doped β-Ga2O3 (1.4 × 1020 cm−3) regrown MOVPE layer.10 The ∼100 nm-thick n+-Ga2O3 growth step was preceded by a heavy Si delta doping at the etched Ga2O3 surface in the contact region. The lowest specific contact resistance (1.62 × 10−7 Ω cm2) was achieved on heavily doped (3.23 × 1020 cm−3) MOVPE layers.19
Metallization . | Substrate orientation/doping concentration (cm−3) . | Epitaxial layer/doping concentration (cm−3) . | n+ processing conditions . | n+ thickness . | Doping of n + region (cm−3) . | . | Reference . |
---|---|---|---|---|---|---|---|
Ti/Au (20/80 nm) | (001) 1018 | … | … | … | … | 5 × 10−4 | 35 |
Ti/Au/Ni (20/150/50 nm) | (010) Fe-doped β-Ga2O3 | UID β-Ga2O3 buffer layer | MOVPE Si-doped Ga2O3 films, 600 °C | 170 nm | 3.23 × 1020 | 1.62 × 10−7 | 19 |
Ti/Au/Ni (20/100/30 nm) | (010) Fe-doped β-Ga2O3 | MOVPE β-Ga2O3 1.5 × 1017 | SF6/Ar RIE + Si delta doped then MOVPE regrow, 600 °C | 100 nm | 1.4 × 1020 | 8.3 × 10−7 | 10 |
Ti(50 nm)/Au (30 nm) | (010) Fe-doped β-Ga2O3 semi-insulating | MBE β-Ga2O3 1017 | Si-implantation, 950 °C activation for 30-min in N2, | 150 nm | 5 × 1019 | 4.6 × 10−6 | 14 |
Ti (20 nm)/Au (230 nm) | (010) Fe-doped β-Ga2O3 semi-insulating | MBE Sn-doped β-Ga2O3 7 × 1017 | Si-implantation, 925 °C activation for 30-min in N2, and BCl3/Ar RIE | 150 nm | 5 × 1019 | 8.1 × 10−6 | 11 |
Ti/Au (20/80 nm) | (010) Fe-doped β-Ga2O3 semi-insulating | UID β-Ga2O3 buffer layer 1017 and MBE Si-doped β-Ga2O3 1.8 × 1018 | … | … | … | 3.29 × 10−3 | 12 |
Ti/Au (20/80 nm) | (010) Fe-doped β-Ga2O3 semi-insulating | UID β-Ga2O3 buffer layer 1017 and MBE Si-doped β-Ga2O3 1.8 × 1018 | Si-implantation, 950 °C activation for 30-min in N2, and BCl3/Ar RIE | 180 nm | 3 × 1019 | 1.51 × 10−4 | 12 |
Ti/Au (20/80 nm) | (010) Fe-doped β-Ga2O3 semi-insulating | UID β-Ga2O3 buffer layer 1017 and MBE Si-doped β-Ga2O3 1.8 × 1018 | Si-implantation, 975 °C for 30-min in N2 + 975 °C activation for 30-min in N2, and BCl3/Ar RIE | 180 nm | 3 × 1019 | 3.93 × 10−5 | 12 |
Ti/Au (20/230 nm) | (010) Fe-doped β-Ga2O3 semi-insulating | MBE UID β-Ga2O3 buffer layer | Si-implantation, 950 °C activation for 30-min in N2 | 150 nm | 5 × 1019 | 7.5 × 10−6 | 13 |
Metallization . | Substrate orientation/doping concentration (cm−3) . | Epitaxial layer/doping concentration (cm−3) . | n+ processing conditions . | n+ thickness . | Doping of n + region (cm−3) . | . | Reference . |
---|---|---|---|---|---|---|---|
Ti/Au (20/80 nm) | (001) 1018 | … | … | … | … | 5 × 10−4 | 35 |
Ti/Au/Ni (20/150/50 nm) | (010) Fe-doped β-Ga2O3 | UID β-Ga2O3 buffer layer | MOVPE Si-doped Ga2O3 films, 600 °C | 170 nm | 3.23 × 1020 | 1.62 × 10−7 | 19 |
Ti/Au/Ni (20/100/30 nm) | (010) Fe-doped β-Ga2O3 | MOVPE β-Ga2O3 1.5 × 1017 | SF6/Ar RIE + Si delta doped then MOVPE regrow, 600 °C | 100 nm | 1.4 × 1020 | 8.3 × 10−7 | 10 |
Ti(50 nm)/Au (30 nm) | (010) Fe-doped β-Ga2O3 semi-insulating | MBE β-Ga2O3 1017 | Si-implantation, 950 °C activation for 30-min in N2, | 150 nm | 5 × 1019 | 4.6 × 10−6 | 14 |
Ti (20 nm)/Au (230 nm) | (010) Fe-doped β-Ga2O3 semi-insulating | MBE Sn-doped β-Ga2O3 7 × 1017 | Si-implantation, 925 °C activation for 30-min in N2, and BCl3/Ar RIE | 150 nm | 5 × 1019 | 8.1 × 10−6 | 11 |
Ti/Au (20/80 nm) | (010) Fe-doped β-Ga2O3 semi-insulating | UID β-Ga2O3 buffer layer 1017 and MBE Si-doped β-Ga2O3 1.8 × 1018 | … | … | … | 3.29 × 10−3 | 12 |
Ti/Au (20/80 nm) | (010) Fe-doped β-Ga2O3 semi-insulating | UID β-Ga2O3 buffer layer 1017 and MBE Si-doped β-Ga2O3 1.8 × 1018 | Si-implantation, 950 °C activation for 30-min in N2, and BCl3/Ar RIE | 180 nm | 3 × 1019 | 1.51 × 10−4 | 12 |
Ti/Au (20/80 nm) | (010) Fe-doped β-Ga2O3 semi-insulating | UID β-Ga2O3 buffer layer 1017 and MBE Si-doped β-Ga2O3 1.8 × 1018 | Si-implantation, 975 °C for 30-min in N2 + 975 °C activation for 30-min in N2, and BCl3/Ar RIE | 180 nm | 3 × 1019 | 3.93 × 10−5 | 12 |
Ti/Au (20/230 nm) | (010) Fe-doped β-Ga2O3 semi-insulating | MBE UID β-Ga2O3 buffer layer | Si-implantation, 950 °C activation for 30-min in N2 | 150 nm | 5 × 1019 | 7.5 × 10−6 | 13 |
In this study, we investigated the use of thin (∼40–150 nm), highly doped (n+) Ga2O3 layers deposited using pulsed laser deposition (PLD) as an approach to reduce the contact resistance of Ti/Au ohmic contacts on (001) and (010) β-Ga2O3 substrates. PLD has been demonstrated to readily produce highly conductive β-Ga2O3 films.20–24 The use of PLD could simplify processing and avoid the high temperatures (900–1000 °C) associated with Si-ion implantation.11–14
II. EXPERIMENT
A. β-Ga2O3 samples
Single-crystalline, Sn-doped (n-type) β-Ga2O3 wafers produced by the edge-defined film-growth (EFG) method were purchased from Novel Crystal Technology, Japan. Two orientations with slightly different doping concentrations were used: (001) with ND = 5.10 × 1018 cm−3 and (010) with ND = 4.80 × 1018 cm−3 or ND = 2.50 × 1018 cm−3. A commercial pulsed laser deposition system with a KrF excimer laser, located at the Air Force Research Laboratory, was used to deposit n+ layers from a Ga2O3–1 wt. % SiO2 target. The base pressure of the PLD chamber was 2.66 × 10−6 Pa, and deposition was performed in Ar at 13.3 Pa. The substrate temperature was 550 °C, and the laser was operated at a pulse rate of 10 Hz with an energy density of 3 J cm−2 measured at the target. The thicknesses of the PLD layers were 40, 80, and 150 ± 10 nm, based on a growth rate of 96 nm/h.20
B. Device fabrication
The substrates were ultrasonicated in acetone, isopropyl alcohol, and de-ionized (DI) water for 10 min each and blown dry in nitrogen after each step.6 Ti/Au (20 nm/80 nm) ohmic contact metal stacks were deposited onto the Ga2O3 substrates (with or without PLD layers) via electron-beam evaporation using a Kurt Lesker PVD 75 deposition system having a base pressure of ∼3.3 × 10−5 Pa. Circular transfer length method (CTLM) patterns for measuring contact resistance were fabricated using photolithography as described below. First, a negative resist was used to pattern the CTLM mask, followed by UV exposure and development to expose the desired areas. CTLM structures comprised contact spacings, d = 10, 20, 30, 40, 50, and 60 μm, and the inner circle radius was fixed at 100 μm [Fig. 1(b)]. The contacts were etched using a Commonwealth Scientific Ion Mill (base pressure = ∼10−5 Pa) with Ar ions at 30 A and 450 V. It is noted that the ion milling step can produce damage to the contact sidewalls and to the Ga2O3 surface area between the contacts but does not damage the Ga2O3 surface directly underneath the contacts since these regions are covered and, therefore, not exposed to the ions. To ensure that the Au/Ti/PLD layers were completely etched, each device was over-etched 25–33 ± 4 nm (no PLD, 40, and 80 nm samples) and 40–45 ± 5 nm (150 nm samples) into the substrate, as determined from multiple measurements for each sample using a KLA Tencor P-15 profilometer. To complete the ohmic contact processing, the samples were subjected to a rapid thermal anneal (RTA) at 470 °C for 1 min in N2.8 A schematic illustration of the fabrication steps and resulting cross-sectional structure is given in Fig. 1.
C. Electrical characterization
I–V characteristics of the fabricated CTLM devices were collected with an Agilent 4155C semiconductor parameter analyzer with a Signatone S-1160-4 N probe station. A voltage ranging from −1 to 1 V was applied between a probe placed on the inner metal circle and one on the outer metal area. Five to eight sets of CTLM structures were measured for each sample, and the specific contact resistivity value was taken from the average of these sets.
Hall measurements were conducted at room temperature using a Nanometrics HL5500 Hall System with a magnetic field strength of 0.5 T. Ti/Al/Ni/Au (20/100/50/50 nm) ohmic contacts were deposited via electron-beam deposition in a van der Pauw pattern followed by an RTA at 470 °C for 1 min in N2. Ohmic contacts were placed on bare (001) and (010) Sn-doped β-Ga2O3 substrates to obtain the carrier concentration of each substrate and on (001) and (010) Fe-doped β-Ga2O3 substrates coated with Si-doped β-Ga2O3 PLD layers to obtain the carrier concentrations of the PLD layers.
D. TEM sample prep and characterization
Selected samples were prepared for characterization using transmission electron microscopy (TEM). The samples were capped with platinum to prevent damage during the sample preparation process. Liftout and thinning were achieved using a FEI Helios 650 Nanolab focused ion beam (FIB) instrument. After liftout, the samples were attached to a Cu TEM grid and thinned to ∼65 nm. Scanning transmission electron microscopy (STEM), high-angle annular dark field (HAADF) imaging, and energy-dispersive x-ray (EDX) analysis were conducted using a Themis 200 TEM. High resolution TEM (HRTEM) images were obtained using a Tecnai F20 TEM.
III. RESULTS AND DISCUSSION
For contacts on semiconductor layers that are thicker than the contact spacing d, the current flows primarily in the topmost layer of the semiconductor. The thickness of this layer and its effective sheet resistance were calculated for a similar contact structure and similar doping concentration in the Ga2O3 substrate to be ∼40 μm and ∼5 Ω/sq, respectively.25 For these conditions, the CTLM equations should be valid for specific contact resistivity values > 10−6 Ω cm2.26
Hall measurement . | CTLM specific contact resistivity(Ω cm2) . | |||||
---|---|---|---|---|---|---|
Substrate orientation | Substrate carrier concentration (cm−3) | PLD layer carrier concentration (cm−3) | No PLD | 40 nm Si-doped PLD | 80 nm Si-doped PLD | 150 nm Si-doped PLD |
(001) | 5.10 × 1018 | 2.60 × 1019 | 2.64 × 10−4 | 5.88 × 10−4 | 6.41 × 10−5 | 3.48 × 10−5 |
(010) | 4.80 × 1018 | 2.00 × 1020 | 8.03 × 10−4 | 1.96 × 10−4 | 9.11 × 10−5 | … |
*(010) | 2.50 × 1018 | 2.80 × 1020 | … | … | … | 4.79 × 10−5 |
Hall measurement . | CTLM specific contact resistivity(Ω cm2) . | |||||
---|---|---|---|---|---|---|
Substrate orientation | Substrate carrier concentration (cm−3) | PLD layer carrier concentration (cm−3) | No PLD | 40 nm Si-doped PLD | 80 nm Si-doped PLD | 150 nm Si-doped PLD |
(001) | 5.10 × 1018 | 2.60 × 1019 | 2.64 × 10−4 | 5.88 × 10−4 | 6.41 × 10−5 | 3.48 × 10−5 |
(010) | 4.80 × 1018 | 2.00 × 1020 | 8.03 × 10−4 | 1.96 × 10−4 | 9.11 × 10−5 | … |
*(010) | 2.50 × 1018 | 2.80 × 1020 | … | … | … | 4.79 × 10−5 |
The quality of the linear fit is measured by the Pearson product (regression coefficient, R2). In the ideal situation, the Pearson product equals unity (R2 = 1). R-squared values for these data are typically, R2 = 0.99. However, in some cases, there was significant scatter, e.g., 40 nm PLD layer on the (001) substrate.
Table II and Fig. 4 show the specific contact resistivity values calculated from the data shown in Figs. 2 and 3. The average specific contact resistivities for contacts without a PLD layer were 2.64 × 10−4 and 8.03 × 10−4 Ω cm2, on the (001) and (010) substrates, respectively. The different values can be attributed to the anisotropic properties of different β-Ga2O3 surfaces and to the slightly higher doping concentration in the (001) substrate. Different thermal, optical, and electrical properties along different β-Ga2O3 crystal directions have been reported.29–32
β-Ga2O3 has two strong cleavage planes of (100) and (001) with low surface energies potentially susceptible to the growth of off-axis planes. Substrate orientations for the epitaxial growth of β-Ga2O3 films with high electrical quality are typically (010) or (100) with miscuts. Homoepitaxial growth on (001) by MBE revealed an additional reflection by x-ray diffraction and depositions in this work by PLD on (001) also indicated a minor contribution.33 The additional planes could possibly generate point defects in the lattice causing Ga vacancies, which are dominant acceptors. Lower carrier concentrations in films deposited on (001) substrates are, thus, attributed to elevated acceptor levels.
For the (010) substrate, the contact resistance values decreased as the PLD layer thickness increased. The lowest average value of 4.79 × 10−5 Ω cm2 on the (010) substrate was achieved for a PLD layer thickness of 150 nm. For the (001) substrate, the contact resistivity initially increased for contacts with a 40 nm PLD layer. This increase could be associated with the nonuniformity of the thin PLD layer (e.g., in terms of thickness, doping, and/or stoichiometry); as discussed above, the TEM results indicate that the PLD layers grow differently on different surface orientations. However, the contact resistivity decreased for (001) contacts with thicker (80 and 150 nm) PLD layers. The (001) substrate with the 150 nm PLD layer had the lowest average value of specific contact resistivity: . The lowest contact resistance values for both (010) and (001) substrates were achieved for contact structures that comprised PLD layers having a deposited thickness of 150 nm, which is in the range of thicknesses of reported n+ layers used to reduce the contact resistance in Ga2O3 ohmic contacts (see Table I). However, further investigation is required to precisely determine the optimal thickness of the n+ PLD layer.
We note here that the contact resistivity values were typically lower for the (001) substrate than the (010) substrate even though the carrier concentration was approximately an order of magnitude lower in the PLD layers grown on the (001) substrates. This is further evidence that the PLD layers in the gaps between contacts were completely etched during the ion milling step, indicating that the n+ PLD layers provide a low-resistance tunneling barrier for current transport into the β-Ga2O3 substrate.
Contact structures were characterized in the cross section using TEM to investigate the microstructure, morphology, and chemical compositions. The thickness of the as-deposited PLD layers in the samples selected for analysis was 80 nm. HAADF STEM images of annealed contact structures on (001) and (010) β-Ga2O3 substrates are shown in Figs. 5(a) and 6(a), respectively. It is apparent from the images that, after annealing, the thickness of the PLD layers was reduced by ∼20 nm. The PLD film grown on the (001) substrate appears to comprise multiple grains, whereas the film grown on the (010) substrate appears epitaxial such that the interface between the substrate and film is difficult to discern. Additional TEM images and FFT diffraction patterns are included in the supplementary material.34 The layers on both substrates, however, appear continuous and without voids. According to EDX analysis [Figs. 5(b), 5(c), 6(b), and 6(c)], a similar layered structure is present on both substrates after annealing. From bottom to top, the layers can be described as , intermixed Au–Ti, Au, intermixed Au–Ti, and another layer of .
IV. CONCLUSIONS
The results of this study show that thin n+ Ga2O3 PLD layers can be used to reduce the contact resistance of Ti/Au ohmic contacts on (001) and (010) β-Ga2O3 substrates. The specific contact resistance was reduced by up to 8× and 16× on (001) and (010) substrates, respectively. The results provide a point of reference for the further optimization of highly doped Ga2O3 PLD layers to minimize the contact resistance in Ga2O3 devices.
ACKNOWLEDGMENTS
This material is based upon work supported by the Air Force Office of Scientific Research under Award No. FA9550-21-1-0360 (Program Manager Ali Sayir) and Air Force Research Laboratory under Award No. FA807518D0015. The use of the Materials Characterization Facility at Carnegie Mellon University was supported by Grant No. MCF-677785.
AUTHOR DECLARATIONS
Conflict of Interest
The authors have no conflicts to disclose.
Author Contributions
Elizabeth V. Favela: Conceptualization (equal); Data curation (equal); Formal analysis (lead); Investigation (equal); Methodology (equal); Validation (equal); Visualization (lead); Writing – original draft (lead); Writing – review & editing (equal). Hyung Min Jeon: Conceptualization (equal); Funding acquisition (equal); Investigation (equal); Methodology (equal); Project administration (equal); Resources (equal); Supervision (equal); Writing – original draft (equal); Writing – review & editing (equal). Kevin D. Leedy: Conceptualization (equal); Funding acquisition (equal); Investigation (equal); Methodology (equal); Project administration (equal); Resources (equal); Supervision (equal); Writing – original draft (equal); Writing – review & editing (equal). Kun Zhang: Data curation (equal); Formal analysis (equal); Investigation (equal); Validation (equal); Writing – review & editing (equal). Szu-Wei Tung: Investigation (equal); Writing – review & editing (equal). Francelia Sanchez Escobar: Investigation (equal); Validation (equal); Writing – review & editing (equal). C. V. Ramana: Funding acquisition (equal); Supervision (equal); Writing – review & editing (equal). Lisa M. Porter: Conceptualization (equal); Funding acquisition (equal); Supervision (equal); Validation (equal); Writing – review & editing (equal).
DATA AVAILABILITY
The data that support the findings of this study are available within the article and its supplementary material.