A Monolayer MoS2 FET with an EOT of 1.1 nm Achieved by the Direct Formation of a High-κ Er2O3 Insulator Through Thermal Evaporation

Achieving the direct growth of an ultrathin gate insulator with high uniformity and high quality on monolayer transition metal dichalcogenides (TMDCs) remains a challenge due to the chemically inert surface of TMDCs. Although the main solution for this challenge is utilizing buffer layers before oxide is deposited on the atomic layer, this method drastically degrades the total capacitance of the gate stack. In this work, we constructed a novel direct high-κ Er₂O₃ deposition system based on thermal evaporation in a differential-pressure-type chamber. A uniform Er₂O₃ layer with an equivalent oxide thickness of 1.1 nm was achieved as the gate insulator for top-gated MoS₂ field-effect transistors (FETs). The top gate Er₂O₃ insulator without the buffer layer on MoS₂ exhibited a high dielectric constant that reached 18.0, which is comparable to that of bulk Er₂O₃ and is the highest among thin insulators (< 10 nm) on TMDCs to date. Furthermore, the Er₂O₃/MoS₂ interface (D_it ≈ 6 × 10¹¹ cm⁻² eV⁻¹) is confirmed to be clean and is comparable with that of the h-BN/MoS₂ heterostructure. These results prove that high-quality dielectric properties with retained interface quality can be achieved by this novel deposition technique, facilitating the future development of 2D electronics.     

Attempt to extract features and classify subjective poor physical conditions in facial images using deep metric learning

Artificial Life and Robotics - With the spread of COVID-19, the need for remote detection of physical conditions is increasing, for example, there are several situations wherein the body...     

Numerical study of the correlation between fish school arrangement and propulsive performance

Artificial Life and Robotics - We focus on the distances in flow direction and its vertical direction on three fish school arrangements, and correlate the fish school in uniform flow with fluid...     

Optimization of train timetables and placement of charging facilities for battery-powered LRT

The energy consumption of a battery-powered train in an interstation depends on the running time and state of energy (SOE) at departure. In this paper, we develop an optimization method of train timetables to minimize energy consumption in line with several stations. The variables in this proposed optimization model are running, dwell, and charging times as real numbers and places of charging facilities as binaries. Additionally, we conducted a case study using the real-world light rail transit (LRT) route, vehicle, and onboard battery model to confirm the effectiveness. In the case study, the proposed method can optimize the timetable and placement of charging facilities by considering the track gradient and battery SOE.     

Acyltransferase Domain Exchange between Two Independent Type I Polyketide Synthases in the Same Producer Strain of Macrolide Antibiotics

Streptomyces graminofaciens A-8890 produces two macrolide antibiotics, FD-891 and virustomycin A, both of which show significant biological activity. In this study, we identified the virustomycin A biosynthetic gene cluster, which encodes type I polyketide synthases (PKSs), ethylmalonyl-CoA biosynthetic enzymes, methoxymalony-acyl carrier protein biosynthetic enzymes, and post-PKS modification enzymes. Next, we demonstrated that the acyltransferase domain can be exchanged between the Vsm PKSs and the PKSs involved in FD-891 biosynthesis (Gfs PKSs), without any supply problems of the unique extender units. We exchanged the malonyltransferase domain in the loading module of Gfs PKS with the ethylmalonyltransferase domain and the methoxymalonyltransferase domain of Vsm PKSs. Consequently, the expected two-carbon-elongated analog 26-ethyl-FD-891 was successfully produced with a titer comparable to FD-891 production by the wild type; however, exchange with the methoxymalonyltransferase domain did not produce any FD-891 analogs. Furthermore, 26-ethyl-FD-891 showed potent cytotoxic activity against HeLa cells, like natural FD-891.