7 research outputs found

    Enhanced Switchable Ferroelectric Photovoltaic Effects in Hexagonal Ferrite Thin Films via Strain Engineering

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    Ferroelectric photovoltaics (FPVs) are being extensively investigated by virtue of switchable photovoltaic responses and anomalously high photovoltages of ∼10<sup>4</sup> V. However, FPVs suffer from extremely low photocurrents due to their wide band gaps (<i>E</i><sub>g</sub>). Here, we present a promising FPV based on hexagonal YbFeO<sub>3</sub> (h-YbFO) thin-film heterostructure by exploiting its narrow <i>E</i><sub>g</sub>. More importantly, we demonstrate enhanced FPV effects by suitably exploiting the substrate-induced film strain in these h-YbFO-based photovoltaics. A compressive-strained h-YbFO/Pt/MgO heterojunction device shows ∼3 times enhanced photovoltaic efficiency than that of a tensile-strained h-YbFO/Pt/Al<sub>2</sub>O<sub>3</sub> device. We have shown that the enhanced photovoltaic efficiency mainly stems from the enhanced photon absorption over a wide range of the photon energy, coupled with the enhanced polarization under a compressive strain. Density functional theory studies indicate that the compressive strain reduces <i>E</i><sub>g</sub> substantially and enhances the strength of d–d transitions. This study will set a new standard for determining substrates toward thin-film photovoltaics and optoelectronic devices

    Photochemical Hydrogen Doping Induced Embedded Two-Dimensional Metallic Channel Formation in InGaZnO at Room Temperature

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    The photochemical tunability of the charge-transport mechanism in metal-oxide semiconductors is of great interest since it may offer a facile but effective semiconductor-to-metal transition, which results from photochemically modified electronic structures for various oxide-based device applications. This might provide a feasible hydrogen (H)-radical doping to realize the effectively H-doped metal oxides, which has not been achieved by thermal and ion-implantation technique in a reliable and controllable way. In this study, we report a photochemical conversion of InGaZnO (IGZO) semiconductor to a transparent conductor via hydrogen doping to the local nanocrystallites formed at the IGZO/glass interface at room temperature. In contrast to thermal or ionic hydrogen doping, ultraviolet exposure of the IGZO surface promotes a photochemical reaction with H radical incorporation to surface metal–OH layer formation and bulk H-doping which acts as a tunable and stable highly doped n-type doping channel and turns IGZO to a transparent conductor. This results in the total conversion of carrier conduction property to the level of metallic conduction with sheet resistance of ∼16 Ω/□, room temperature Hall mobility of 11.8 cm<sup>2</sup> V<sup>–1</sup> sec<sup>–1</sup>, the carrier concentration at ∼10<sup>20</sup> cm<sup>–3</sup> without any loss of optical transparency. We demonstrated successful applications of photochemically highly n-doped metal oxide via optical dose control to transparent conductor with excellent chemical and optical doping stability

    Selective Dissolution of Surface Nickel Close to Platinum in PtNi Nanocatalyst toward Oxygen Reduction Reaction

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    We report new insights in dissolution mechanisms of nickel in PtNi bimetallic nanoparticles (NPs) to develop active and durable oxygen reduction catalysts for fuel cells. Leaching out nickel by using acidic aqueous solution has been regarded as one of the most efficient chemical treatments to obtain a platinum-rich surface, which has shown both increased activity and stability during oxygen reduction reaction. In this work, we introduce a new approach using hydroquinone dissolved in ethanol to leach out nickel from PtNi NPs. The degree of alloying level is followed by X-ray photoelectron and absorption spectroscopies. Electrochemical measurements including potential cycling under oxygen reduction conditions allow us to investigate the dissolution behavior of nickel, depending on the chemical systems, and assess the relationship with electrochemical activity and stability. From comparative studies regarding the traditional acid treatment and the hydroquinone method introduced in this article, it is revealed that, while acid treatment preferentially removes oxidized Ni clusters, hydroquinone dissolves Ni atoms close to surface platinum. Electrochemical measurements help with the understanding of the different leaching mechanisms and highlight the influence of alloyed nickel on the activity of platinum and durability of the catalyst in the oxygen reduction reaction

    Effect of Nb Doping on Chemical Sensing Performance of Two-Dimensional Layered MoSe<sub>2</sub>

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    Here, we report that Nb doping of two-dimensional (2D) MoSe<sub>2</sub> layered nanomaterials is a promising approach to improve their gas sensing performance. In this study, Nb atoms were incorporated into a 2D MoSe<sub>2</sub> host matrix, and the Nb doping concentration could be precisely controlled by varying the number of Nb<sub>2</sub>O<sub>5</sub> deposition cycles in the plasma enhanced atomic layer deposition process. At relatively low Nb dopant concentrations, MoSe<sub>2</sub> showed enhanced device durability as well as NO<sub>2</sub> gas response, attributed to its small grains and stabilized grain boundaries. Meanwhile, an increase in the Nb doping concentration deteriorated the NO<sub>2</sub> gas response. This might be attributed to a considerable increase in the number of metallic NbSe<sub>2</sub> regions, which do not respond to gas molecules. This novel method of doping 2D transition metal dichalcogenide-based nanomaterials with metal atoms is a promising approach to improve the performance such as stability and gas response of 2D gas sensors

    Alloyed 2D Metal–Semiconductor Atomic Layer Junctions

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    Heterostructures of compositionally and electronically variant two-dimensional (2D) atomic layers are viable building blocks for ultrathin optoelectronic devices. We show that the composition of interfacial transition region between semiconducting WSe<sub>2</sub> atomic layer channels and metallic NbSe<sub>2</sub> contact layers can be engineered through interfacial doping with Nb atoms. W<sub><i>x</i></sub>Nb<sub>1–<i>x</i></sub>Se<sub>2</sub> interfacial regions considerably lower the potential barrier height of the junction, significantly improving the performance of the corresponding WSe<sub>2</sub>-based field-effect transistor devices. The creation of such alloyed 2D junctions between dissimilar atomic layer domains could be the most important factor in controlling the electronic properties of 2D junctions and the design and fabrication of 2D atomic layer devices

    Wafer-Scale Integration of Highly Uniform and Scalable MoS<sub>2</sub> Transistors

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    Molybdenum disulfide with atomic-scale flatness has application potential in high-speed and low-power logic devices owing to its scalability and intrinsic high mobility. However, to realize viable technologies based on two-dimensional materials, techniques that enable their large-area growth with high quality and uniformity on wafer cale is a prerequisite. Here, we provide a route toward highly uniform growth of a wafer-scale, four-layered MoS<sub>2</sub> film on a 2 in. substrate via a sequential process consisting of the deposition of a molybdenum trioxide precursor film by sputtering followed by postsulfurization using a chemical vapor deposition process. Spatial spectroscopic analyses by Raman and PL mapping validated that the as-synthesized MoS<sub>2</sub> thin films exhibit high uniformity on a 2 in. sapphire substrate. The highly uniform MoS<sub>2</sub> layers allow a successful integration of devices based on ∼1200 MoS<sub>2</sub> transistor arrays with a yield of 95% because of their extreme homogeneity on Si wafers. Moreover, a pulse electrical measurement technique enabled investigation of the inherent physical properties of the atomically thin MoS<sub>2</sub> layers by minimizing the charge-trapping effect. Such a facile synthesis method can be possibly applied to other 2D transition metal dichalcogenides to ultimately realize the chip integration of device architectures with all 2D-layered building blocks

    Alloyed 2D Metal–Semiconductor Heterojunctions: Origin of Interface States Reduction and Schottky Barrier Lowering

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    The long-term stability and superior device reliability through the use of delicately designed metal contacts with two-dimensional (2D) atomic-scale semiconductors are considered one of the critical issues related to practical 2D-based electronic components. Here, we investigate the origin of the improved contact properties of alloyed 2D metal–semiconductor heterojunctions. 2D WSe<sub>2</sub>-based transistors with mixed transition layers containing van der Waals (M–vdW, NbSe<sub>2</sub>/W<sub><i>x</i></sub>Nb<sub>1–<i>x</i></sub>Se<sub>2</sub>/WSe<sub>2</sub>) junctions realize atomically sharp interfaces, exhibiting long hot-carrier lifetimes of approximately 75,296 s (78 times longer than that of metal–semiconductor, Pd/WSe<sub>2</sub> junctions). Such dramatic lifetime enhancement in M–vdW-junctioned devices is attributed to the synergistic effects arising from the significant reduction in the number of defects and the Schottky barrier lowering at the interface. Formation of a controllable mixed-composition alloyed layer on the 2D active channel would be a breakthrough approach to maximize the electrical reliability of 2D nanomaterial-based electronic applications
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