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As gallium oxide-based heterojunction devices gain prominence, low-resistance contacts to aluminum gallium oxide material are of increasing importance for high performance and access to modulation doped layers. Here, the activation of ion-implanted silicon donors is investigated as a function of donor density from 5 × 1018 cm−3 to 1 × 1020 cm−3, activation anneal duration from 6 s to 600 s, and activation temperature from 900°C to 1140°C. Importantly, ohmic behavior was achievable across a reasonably wide process window at moderate to high doping concentrations. Specific contact resistance of 1 × 10−3 Ω cm2 and sheet resistance of 2.8 kΩ/□ were achieved for a 60 nm-deep 1 × 1020 cm−3 box implant after activation at 1000°C for 6 s with standard Ti/Au contacts. Under these conditions, an activation efficiency of 7% was observed with Hall mobility of ~32 cm2/Vs. Furthermore, we demonstrate a Schottky diode formed of implanted material with a rectification ratio > 106 and further confirm the Hall carrier density results using capacitance–voltage profiling analysis. Finally, we show the significant impact of anneal duration and the potential for deleterious over-annealing which reduces the active carrier density, mobility, and resultant material conductivity. [ABSTRACT FROM AUTHOR]

Activation of ion‐implanted p‐type dopants in gallium nitride has demonstrated great progress utilizing high pressures to enable novel and traditional device architectures; however, such conditions consistently exhibit anomalously enhanced diffusion up to several microns in very short periods of time for device relevant concentrations. Here, this diffusion is shown to be modulated by unintentional hydrogen content within the anneal ambient and thus controllable by inclusion of a high‐temperature hydrogen getter. Furthermore, diffusion is also shown to be greatly suppressed using co‐implanted oxygen at low concentrations while simultaneously maintaining characteristics of p‐type material in photoluminescence. Subsequently, after annealing at 1300 °C for 30 min in 3.8 kbar of nitrogen pressure, the magnesium concentration in the diffusion tail is suppressed by 28% at 1–1.5 μm in depth using a hydrogen getter alone, which reduces hydrogen uptake by 45% and fully suppressed at >1 μm in depth using co‐implantation alone and further reduced with concurrent use of a hydrogen getter. Co‐implantation alone reduces the in‐diffused magnesium dose by 60% compared to reference samples. [ABSTRACT FROM AUTHOR]

The low thermal conductivity of β-Ga2O3 is a significant concern for maximizing the potential of this ultra-wide bandgap semiconductor as a power switching device technology. Here, we report on the use of nanocrystalline diamond (NCD) deposited via microwave plasma enhanced chemical vapor deposition (MP-CVD) as a top-side, device-level thermal management solution on a lateral β-Ga2O3 transistor. NCD was grown via MP-CVD on β-(AlxGa1−x)2O3/β-Ga2O3 heterostructures prior to the gate formation of the field-effect transistor. A reduced growth temperature of 400 °C and a SiNx barrier layer were used to protect the oxide semiconductors from etching in the MP-CVD H2 plasma environment. Raman spectroscopy showed a highly sp3-bonded NCD film was obtained at 400 °C, with grain size of about 50–100 nm imaged via atomic force microscopy. The incorporation of the NCD heat-spreading layer resulted in a β-(AlxGa1−x)2O3/β-Ga2O3 heterostructure field-effect transistor showing a decrease in the total thermal resistance at the gate by 42%. The fabrication process, including the NCD etch in the gate region, will need to be improved to minimize the impact of these processes on important device characteristics (i.e., drain current, threshold voltage, and leakage current). [ABSTRACT FROM AUTHOR]

Conformal atomic layer deposition (ALD) inside macroscopic nanoporous solids with aspect ratios greater than 103 can require ALD reactant exposures on the order of 103 Torr-s or greater. For some ALD chemistries, such large exposures raise the concern of non-self-limiting deposition. In the case of ZnO ALD from diethylzinc (DEZ) and H2O, exposures in the 10–103 Torr-s range have resulted in metallic Zn deposition at typical temperatures used for ZnO ALD on wafers (e.g., ∼180 °C). This Zn deposition can be suppressed by lowering the deposition temperature, but this slows H2O desorption and, thus, can necessitate impractically long purge times. In this work, we use static-dose ALD with DEZ and H2O exposures >104 Torr-s to deposit ZnO inside Al2O3 nanoparticle compacts (NPCs) with 50.5 ± 0.3% porosity, 100 nm NP diameter, 1.55 ± 0.05 mm thickness, and an aspect ratio of 7800 ± 200 (based on the half-thickness), and we explore a novel approach to the deposition temperature, T: T is cycled between 160 °C (for H2O purges) and 120 °C (for all other steps). For comparison, we also deposit ZnO with T held constant at 120 or 160 °C. Whereas the T = 160 °C process results in Zn metal deposition and nonuniform infiltration, the temperature-cycled process yields apparently self-limiting ZnO deposition at a growth per cycle (GPC) of ∼2.1 Å/cyc, forming an electrically conductive ZnO network that is uniform throughout the thickness of the NPC, with the exception of some ZnO depletion near the NPC surfaces, possibly due to the (unoptimized) long DEZ purge time. The T = 120 °C process produces similar results, although the GPC is slightly elevated, indicating diminished removal of H2O and/or OH during purges. We employ scanning electron microscopy with energy-dispersive x-ray spectroscopy, x-ray diffractometry, electrical resistivity measurements, and ALD chamber pressure analysis in our comparison of the three ALD processes. [ABSTRACT FROM AUTHOR]

Codoping of gallium nitride for improved acceptor ionization has long been theorized; however, reduction to practice proves difficult via growth. Herein, implementation of codoping via ion implantation and symmetric multicycle rapid thermal annealing utilizing magnesium codoped with silicon or oxygen is demonstrated. Results show enhanced photoluminescence with both donor species but with an order of magnitude greater increase with concurrent p‐type hall for codoping with oxygen. Furthermore, the addition of nitrogen to balance stoichiometry suppresses defect photoluminescence signals. The incorporation of the donor and nitrogen demonstrates defect reduction beyond magnesium, only implants despite the additional implant dose and resultant damage with coimplantation. The enhanced hole concentrations evident with oxygen incorporation reveal important considerations for device design given unintentional doping during growth and future incorporation of ion implantation capabilities. [ABSTRACT FROM AUTHOR]

The first step of a multi-cycle rapid thermal annealing process was systematically studied. The surface, structure, and optical properties of Mg implanted GaN thin films annealed at temperatures ranging from 900 to 1200 °C were investigated by Raman spectroscopy, photoluminescence, UV-visible spectroscopy, atomic force microscopy, and Nomarski microscopy. The GaN thin films are capped with two layers of in-situ metal organic chemical vapor deposition -grown AlN and annealed in 24 bar of N2 overpressure to avoid GaN decomposition. The crystal quality of the GaN improves with increasing annealing temperature as confirmed by UV-visible spectroscopy and the full widths at half maximums of the E2 and A1 (LO) Raman modes. The crystal quality of films annealed above 1100 °C exceeds the quality of the as-grown films. At 1200 °C, Mg is optically activated, which is determined by photoluminescence measurements. However, at 1200 °C, the GaN begins to decompose as evidenced by pit formation on the surface of the samples. Therefore, it was determined that the optimal temperature for the first step in a multi-cycle rapid thermal anneal process should be conducted at 1150 °C due to crystal quality and surface morphology considerations. [ABSTRACT FROM AUTHOR]

Ion implantation of magnesium for p‐type GaN presents many opportunities; however, activation has proven difficult due to the decomposition of GaN at relevant annealing temperatures. Herein, testing the efficacy of multiple in situ and ex situ caps based on aluminum nitride and silicon nitride for GaN protection during annealing is presented. Photoluminescence shows better activation for in situ metal organic chemical vapor deposition (MOCVD)‐grown aluminum nitride caps compared with ex situ sputtered aluminum nitride and the best performance by ex situ plasma‐enhanced chemical vapor deposition (PECVD) silicon nitride. Furthermore, only samples annealed at the highest temperatures tested show preferential growth of UV luminescence to yellow‐green luminescence reinforcing the need for better capping solutions and higher temperature annealing. [ABSTRACT FROM AUTHOR]