Abstract:MgO has proven effective in the past as a surface passivation layer to minimize current collapse in AlGaN∕GaN high electron mobility transistors (HEMTs). However, MgO is not environmentally stable and more stable oxides need to be developed. MgCaO can be produced that is lattice matched to the GaN. Three samples were grown with 0%, 50% and 75% of Ca, which had respective lattice mismatches of −6.5% for MgO, −1% for Mg0.50Ca0.50O and +4% for Mg0.25Ca0.75O. Drain saturation current in HENTs had increases of 4.5%… Show more
“…The Sc 2 O 3 was deposited by radiofrequency (RF) plasma-activated molecular beam epitaxy (MBE) at 100°C using elemental Sc evaporated from a standard effusion all at 1130°C and O 2 derived from an Oxford RF plasma source. [22][23][24] For comparison, we also fabricated devices with just the native oxide present in the gate region and also with a UV-ozone-induced oxide. The latter was produced by exposing the sample to UVozone at room temperature for 5 min.…”
We report on a comparison of different gate oxides for AlGaN/GaN highelectron-mobility transistor (HEMT) pH sensors. The HEMTs show a linear increase in drain-source current as the pH of the electrolyte solutions introduced to the gate region is decreased. Three different gate oxides were examined, namely the native oxide on the AlGaN surface, a UV-ozone-induced oxide and an Sc 2 O 3 gate deposited by molecular beam epitaxy. The Sc 2 O 3 produced superior results in terms of resolution in measuring small changes in pH. The devices with Sc 2 O 3 in the gate region exhibited a linear change in current between pH 3 and 10 of 37 lA/pH with a resolution of <0.1 pH over the entire pH range. In contrast, the native oxide devices showed a larger change in current, $70 lA/pH, but with a degraded resolution of $0.4 pH. Results for the UV-ozone oxide were intermediate in resolution, 0.2 pH. These HEMTs have promise for detecting pH changes in biological samples and can be readily integrated into a standard package for wireless data transmission.
“…The Sc 2 O 3 was deposited by radiofrequency (RF) plasma-activated molecular beam epitaxy (MBE) at 100°C using elemental Sc evaporated from a standard effusion all at 1130°C and O 2 derived from an Oxford RF plasma source. [22][23][24] For comparison, we also fabricated devices with just the native oxide present in the gate region and also with a UV-ozone-induced oxide. The latter was produced by exposing the sample to UVozone at room temperature for 5 min.…”
We report on a comparison of different gate oxides for AlGaN/GaN highelectron-mobility transistor (HEMT) pH sensors. The HEMTs show a linear increase in drain-source current as the pH of the electrolyte solutions introduced to the gate region is decreased. Three different gate oxides were examined, namely the native oxide on the AlGaN surface, a UV-ozone-induced oxide and an Sc 2 O 3 gate deposited by molecular beam epitaxy. The Sc 2 O 3 produced superior results in terms of resolution in measuring small changes in pH. The devices with Sc 2 O 3 in the gate region exhibited a linear change in current between pH 3 and 10 of 37 lA/pH with a resolution of <0.1 pH over the entire pH range. In contrast, the native oxide devices showed a larger change in current, $70 lA/pH, but with a degraded resolution of $0.4 pH. Results for the UV-ozone oxide were intermediate in resolution, 0.2 pH. These HEMTs have promise for detecting pH changes in biological samples and can be readily integrated into a standard package for wireless data transmission.
“…Therefore, all of the binding energies are accurate on an absolute scale within 0.02-0.03 eV, over the binding energy range of 0-100 eV. 28 The bottom part of the figure shows a lattice image of the crystalline MgCaO. These types of films have shown excellent passivation properties on AlGaN/ GaN HEMTs.…”
Section: Methodsmentioning
confidence: 96%
“…These types of films have shown excellent passivation properties on AlGaN/ GaN HEMTs. 28 The digital samples all showed a uniform depth profile, as determined by Auger electron spectroscopy, especially near the surface, as shown in Fig. 2.…”
Section: Methodsmentioning
confidence: 99%
“…Crystalline films of Mg 0.5 Ca 0.5 O are lattice matched to GaN and produce superior surface passivation on HEMT structures than MgO. 28 The HEMTs passivated with Mg 0.5 Ca 0.5 O and Mg 0.25 Ca 0.75 O showed higher passivation effectiveness (90% of dc current) than the MgO passivated HEMTs (83% of dc current). This is due to the closer lattice matching of these calcium containing oxides and the reduction in interface traps associated with lattice mismatch.…”
Section: Introductionmentioning
confidence: 98%
“…This is due to the closer lattice matching of these calcium containing oxides and the reduction in interface traps associated with lattice mismatch. 28 In addition, while pure MgO degrades over time in atmosphere due to reaction with water vapor to form magnesium hydroxide, Mg(OH) 2 , uncapped MgCaO shows much less degradation and, when capped with 5 nm of Sc 2 O 3 , showed no detectable changes.…”
MgCaO offers promise as a gate dielectric for GaN-based metal-oxide-semiconductor (MOS) transistors, particularly in combination with environmentally stable capping layers such as Sc 2 O 3 . X-ray photoelectron spectroscopy (XPS) was used to measure the energy discontinuity in the valence band (DE v ) of Mg 0.5 Ca 0.5 O/GaN heterostructures in which the MgCaO was grown by rf plasma-assisted molecular beam epitaxy on top of thick GaN templates on sapphire substrates. A value of DE v = 0.65 eV ± 0.10 eV was obtained by using the Ga 3d energy level as a reference. Given the bandgap of 7.45 eV for the MgCaO, we infer a conduction band offset DE C of 3.36 eV in the Mg 0.5 Ca 0.5 O system.
We have prepared two new CaII amidinates, which comprise a new class of ALD precursors. The syntheses proceed by a direct reaction between Ca metal and the amidine ligands in the presence of ammonia. Bis(N,N′‐diisopropylformamidinato)calcium(II) (1) and bis(N,N′‐diisopropylacetamidinato)calcium(II) (2) adopt dimeric structures in solution and in the solid state. X‐ray crystallography revealed asymmetry in one of the bridging ligands to afford the structure [(η2‐L)Ca(μ‐η2:η2‐L)(μ‐η2:η1‐L)Ca(η2‐L)]. These amidinate complexes showed unprecedentedly high volatility as compared to the widely employed and commercially available CaII precursor, [Ca3(tmhd)6]. In CaS ALD with 1 and H2S, the ALD window was approximately two times wider and lower in temperature by about 150 °C than previously reported with [Ca3(tmhd)6] and H2S. Complexes 1 and 2, with their excellent volatility and thermal stability (up to at least 350 °C), are the first homoleptic CaII amidinates suitable for use as ALD precursors.
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