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Hot Carrier Injection (HCI) Reliability of Fabricated Y-gate HEMT with Various Top Length

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ECS Journal of Solid State science and Technology 2023年第3期12卷 035001-035001页

作者： Chen, Yu-Lin Yeh, Wen-Kuan Chen, Ke-Horng Hsu, Heng-Tung Hsu, Chin-Tsai Godwin Raj, D. Chou, Hung-Ting Wu, Jui-Sheng Yu, Tien-Han Godfrey, D. Graduate Degree Program of College of Electrical and Computer Engineering National Yang Ming Chiao Tung University Hsinchu Taiwan International College of Semiconductor Technology National Yang Ming Chiao Tung University Hsinchu Taiwan National Applied Research Laboratories Hsinchu Taiwan Dept of ECE Amal Jyothi College of Engineering Kerala India National Chung Shan Institute of Science and Technology Taoyuan Taiwan Deparment of Materials Science and Engineering National Yang Ming Chiao Tung University Hsinchu Taiwan Dept of Electronics and Communication Engineering Dayananda Sagar University Bengaluru India

Device degradation due to hot carrier injection (HCI) in different Y-gate HEMT devices is thoroughly analyzed. To further understand the HCI reliability of the Y-gate HEMT devices, the device is fabricated with AlGaN/GaN structure with different top lengths (Ltop). An HCI stress time of 6000 s was conducted on these devices, while V t stability in other stress time domains, leakage current, and transconductance degradation are also discussed. In this work, we have demonstrated that increasing the LTop length could avoid the virtual gate effect and disperse the influence of the electric field under HCI stress. Furthermore, the effects of trapping in various locations, such as in the bulk SiN or AlGaN/GaN interface has been discussed. These trapping effects caused by the HCI stress might be the source of the Vth shift. Overall, The large Y-gate HEMT showed the lowest degradation of DC characteristics after the long HCI stress test. © 2023 The Electrochemical Society ("ECS"). Published on behalf of ECS by IOP Publishing Limited.

关键词： High electron mobility transistors

Preparation of a New Hybrid Mgalldh@Magnetite Activated Charcoal by Hydrothermal Method for Stability and Adsorption Mechanism of Congo Red

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SSRN 2024年

作者： Ahmad, Nur Kameda, Tomohito Rahman, Mir Tamzid Rahman, Farzana Lesbani, Aldes Graduate School of Mathematics and Natural Science FMIPA Universitas Sriwijaya Sumatera Selatan Palembang30139 Indonesia Research Center of Inorganic Materials and Complexes Universitas Sriwijaya Sumatera Selatan Palembang30139 Indonesia Graduate School of Environmental Studies Tohoku University 6-6-20 Aoba Aramaki Aobaku Sendai980-8579 Japan Department of Chemistry Jahangirnagar University Dhaka Savar1342 Bangladesh Department of Nutrition and Food Engineering Daffodil International University Birulia1216 Bangladesh Master Program of Material Science Graduate School of Universitas Sriwijaya Sumatera Selatan Palembang30139 Indonesia

Background The removal of hazardous dyes from water by magnetic adsorbents has received significant interest due to their low cost and ease of separation from the solution phase. This study explores the efficacy of a novel hybrid adsorbent, magnetite and activated charcoal-modified MgAl layered double hydroxide (MgAlLDH@MAC), for removing congo red (CR) from aqueous solutions. Methods MgAlLDH@MAC was successfully prepared via a co-precipitation to hydrothermal method and characterized using FE-SEM, FE-STEM, VSM, BET, XRD, FTIR, XPS, and HPLC analysis. Significant findings The incorporation of magnetite and activated charcoal was successful, resulting in excellent adsorption performance for CR and easy separation from the solution due to its magnetic properties. The adsorbent achieved a maximum adsorption capacity of 625 mg/g, which is in line with the Langmuir isotherm and pseudo-second-order kinetic model. Moreover, the adsorbent demonstrated excellent stability and reusability, retaining 91.78% efficiency after five adsorption-desorption. This study offers a fresh viewpoint on creating high-performance LDH adsorbents that remove dyes quickly and effectively using carbon and magnetite materials. © 2024, The Authors. All rights reserved.

关键词： Magnetite

Photoelectrochemical X-Ray Absorption Spectroscopy of Graphene/Si Heterojunction Platform with Multifunctional Atomic Bridging Layer for Efficient Solar-Powered Co2 Conversion

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SSRN 2025年

作者： Wu, Heng-Liang Wu, Po-Hsien Chen, Hsuan-Yu Yu, Sheng-Yu Chang, Chen Liu, Tsung-Hsin Song, Ruo-Nong Lin, Jr-Wen Cyue, Zih-Wei Chan, Kwun-Man Chen, Cheng-Ying Chan, Ting-Shan Chen, Jeng-Lung Pao, Chih Wen Chen, Chun-Wei Department of Materials Science and Engineering National Taiwan University Taipei106319 Taiwan Center for Condensed Matter Sciences National Taiwan University Taipei106319 Taiwan International Graduate Program of Molecular Science and Technology National Taiwan University Taipei106319 Taiwan Academia Sinica Taipei11529 Taiwan Department of Optoelectronics and Materials Technology National Taiwan Ocean University Keelung202301 Taiwan National Synchrotron Radiation Laboratory Research Center Hsinchu300092 Taiwan Center of Atomic Initiative for New Materials National Taiwan University Taipei10617 Taiwan Department of Chemistry National Taiwan University Taipei106319 Taiwan

The facile integration and stability of Si-based photoelectrode architectures are the remaining challenges in the photoelectrochemical (PEC) conversion of CO2 to fuels. In this work, the single-atomic-layer graphene is used as a functional bridging layer to integrate both Si photocathodes and photoanodes, which enable the direct electrodeposition of metal-based electrocatalysts (Cu, Ag and InSn alloys) and a semiconductor-based catalyst (NiFe-LDH) on the graphene/Si heterojunction electrodes for PEC CO2 reduction and O2 evolution reaction, respectively. Photoelectrochemical X-ray absorption spectroscopy results show that the electrodeposited catalysts on the graphene layer are active and leads to efficient transport of photogenerated electrons from Si junctions to electrocatalysts. We demonstrate a PEC device with a full-cell configuration consisting of InSn/graphene/Si heterojunction photocathode and NiFe-LDH/graphene/Si heterojunction photoanode, exhibiting a reduced photovoltage of ~1080 mV compared to the electrochemical counterparts. A self-powered overall PEC CO2 reduction with a promising solar-to-fuel conversion efficiency of 3.2% can be obtained by integrating the graphene/Si heterojunction photocathode and photoanode with a Si photovoltaic. By combining the inherent chemical inertness of graphene with its role as an atomic bridging layer, the facile integration of Si photoelectrodes with various catalysts presents a promising platform for stable and efficient solar-to-fuel conversion. © 2025, The Authors. All rights reserved.

关键词： X ray absorption spectroscopy

Pulsed Terahertz Time Domain Spectroscopy for Evaluating Treatment Efficacy: Initial Validation in Monitoring Pancreatic Ductal Adenocarcinoma

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Pulsed Terahertz Time Domain Spectroscopy for Evaluating Tre...

International Conference on Infrared and Millimeter Waves

作者： Debamitra Chakraborty Bradley N. Mills Jing Cheng Ivan Komissarov Scott A. Gerber Roman Sobolewski Materials Science Graduate Program University of Rochester Rochester New York USA Laboratory for Laser Energetics University of Rochester Rochester New York USA Department of Surgery University of Rochester Medical Center Rochester New York USA Department of Electrical and Computer Engineering University of Rochester Rochester New York USA

Pancreatic Ductal Adenocarcinoma (PDAC) is a highly invasive malignancy with limited curative effectiveness. Here, we report the viability of using pulsed Terahertz (THz) time domain spectroscopy (THz TDS) to monitor the efficacy of Stereotactic Body Radiation Therapy (SBRT) in treating PDAC in murine models. Our study shows that THz imaging can provide reliable and reproducible results to differentiate the changes in untreated and SBRT-treated PDAC tissue using THz refractive index and absorption coefficient as mapping parameters with statistical significance. Hence the study highlights that pulsed THz-TDS can be used as a technique to monitor tumor responses to immunotherapy, providing a comprehensive assessment of the tumor’s reaction to the treatment.

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Force-Trainable Liquid Crystal Elastomer Enabled by Mechanophore-Induced Radical Polymerization

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Angewandte Chemie 2025年

作者： Yiyi Xu Yinliang Huang Jinyu Wang Dr. Shuai Huang Prof. Hong Yang Prof. Quan Li Institute of Advanced Materials and School of Chemistry and Chemical Engineering Southeast University Nanjing 211189 China Materials Science Graduate Program Kent State University Kent OH 44242 USA

In nature, organisms adapt to environmental changes through training to learn new abilities, offering valuable insights for developing intelligent materials. However, replicating this “adaptive learning” in synthetic materials presents a significant challenge. This study introduces a feasible approach to train liquid crystal elastomers (LCEs) by integrating a mechanophore tetraarylsuccinonitrile into their main chain, addressing the challenge of enabling synthetic materials to exchange substances with their environment. Inspired by biological training, the LCEs can self-strengthen and acquire new functionalities through mechanical stress-induced radical polymerization. The research not only enhances the mechanical performance of LCEs, but also endows them with the ability to learn properties such as flexibility, light responsiveness, and fluorescence. These advancements are crucial for overcoming the limitations of current materials, paving the way for the creation of advanced intelligent soft materials with autonomous self-improvement, akin to the adaptive skills of living organisms.

关键词： force-induced chemical reaction mechanical stress-induced radical polymerization liquid crystal elastomer soft actuator smart material

Nernst-Ettingshausen effect in thin Pt and W films at low temperatures

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arXiv

arXiv 2023年

作者： Luo, Renjie Legvold, Tanner J. Chen, Liyang Natelson, Douglas Department of Physics and Astronomy Rice University HoustonTX77005 United States Applied Physics Graduate Program Smalley-Curl Institute Rice University HoustonTX77005 United States Department of Electrical and Computer Engineering Department of Materials Science and NanoEngineering Rice University HoustonTX77005 United States

As spin caloritronic measurements become increasingly common techniques for characterizing material properties, it is important to quantify potentially confounding effects. We report measurements of the Nernst-Ettingshausen response from room temperature to 5 K in thin film wires of Pt and W, metals commonly used as inverse spin Hall detectors in spin Seebeck characterization. Johnson-Nyquist noise thermometry is used to assess the temperature change of the metals with heater power at low temperatures, and the thermal path is analyzed via finite-element modeling. The Nernst-Ettingshausen response of W is found to be approximately temperature-independent, while the response of Pt increases at low temperatures. These results are discussed in the context of theoretical expectations and the possible role of magnetic impurities in Pt. Copyright © 2023, The Authors. All rights reserved.

关键词： Inverse problems

High Spatial Resolution Terahertz Time-Domain Imaging of Murine Pancreatic Ductal Adenocarcinoma Tissues

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High Spatial Resolution Terahertz Time-Domain Imaging of Mur...

Conference on Lasers and Electro-Optics (CLEO)

作者： Debamitra Chakraborty Bradley N. Mills Jing Cheng Ivan Komissarov Scott Gerber Roman Sobolewski Materials Science Graduate Program University of Rochester Rochester New York USA Laboratory for Laser Energetics University of Rochester Rochester New York USA Department of Surgery University of Rochester Medical Center Rochester New York USA Department of Electrical and Computer Engineering University of Rochester Rochester New York USA

We developed a terahertz time-domain spectroscopy system to generate high-resolution 2-dimensional images of paraffin-embedded murine pancreatic ductal adenocarcinoma tissues using the refractive index and absorption ... 详细信息

ISBN: (纸本)9781957171258

关键词： Absorption coefficient Biological imaging Refractive index Spatial resolution Terahertz spectroscopy Tissue

Chemical Structures and Stability of Amine Plasma Polymers Deposited on Porous Hydroxyapatite Artificial Bone with Bipolar Pulsed Discharges

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SSRN 2024年

作者： Harumningtyas, Anjar Anggraini Ito, Tomoko Michlíček, Miroslav Kodama, Joe Nečas, David Kita, Hidekazu Kaito, Takashi Zajíčková, Lenka Hamaguchi, Satoshi International Priority Graduate Program on Applied and Engineering Physics Division of Precision Engineering and Applied Physics Osaka University 2-1 Yamadaoka Suita Osaka565-0871 Japan Division of Materials and Manufacturing Science Graduate School of Engineering Osaka University 2-1 Yamadaoka Suita Osaka565-0871 Japan Jalan Babarsari Kotak Pos 6101 ykbb Yogyakarta55281 Indonesia Department of Condensed Matter Physics Faculty of Science Masaryk University Kotlarska 2 Brno61137 Czech Republic Department of Orthopaedic Surgery Osaka University Graduate School of Medicine Osaka565-0871 Japan CEITEC Central European Institute of Technology Brno University of Technology Purkyňova 123 Brno61200 Czech Republic

A recent in vivo study by Kodama et al. shows that porous artificial bones coated with aminecontaining polymers deposited in a plasma-enhanced chemical vapour deposition (PECVD) process with high-voltage, low-frequency bipolar pulsed discharges significantly enhanced bone regeneration. This article reports the chemical and physical properties of amine plasma polymers (PPs) formed under the same deposition conditions, including the film stability for up to two months, the effects of sterilization on the chemical compositions of the films, and the penetration of amine PPs into the inner surfaces of interconnected microscopic pores of the amine-PP-coated porous artificial bone. It was found that, immediately after the plasma polymerization process, approximately 15% of nitrogen atoms on the surface of the deposited amine PP formed primary amines but the number decreased to approximately 5% over one month if the sample was exposed to ambient air or sterilized by autoclaving or ethylene oxide gas. Nitriles ( –CN) were also detected in the deposited amine PPs. Molecular dynamics simulations of simplified deposition processes suggest that the observed nitriles were likely to be formed by the incorporation of gas-phase cyano radicals that were also observed in the experiments of this study. © 2024, The Authors. All rights reserved.

关键词： Hydroxyapatite

Mo-Terminated Edges in Mos2 for Site-Specific Hydrolysis and DNA Cleavage

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SSRN 2024年

作者： Wang, Cong Wu, Menghan Li, Muqing Zhao, Yingcan Zhao, Mingchuang Zhang, Yunhao Bai, Yichao Gao, Jianxiang Wang, Xiaoxia Tian, Xilin Zhang, Han Chang, Liang Zou, Xiaolong Liu, Bilu Kang, Feiyu Terrones, Mauricio Lei, Yu Institute of Materials Research Shenzhen Key Laboratory of Advanced Layered Materials for Value-added Applications Guangdong Provincial Key Laboratory of Thermal Management Engineering and Materials Center of Double Helix Tsinghua Shenzhen International Graduate School Tsinghua University Shenzhen518055 China Institute of Materials Research Shenzhen Geim Graphene Center Shenzhen Key Laboratory of Advanced Layered Materials for Value-added Applications Tsinghua-Berkeley Shenzhen Institute Tsinghua Shenzhen International Graduate School Tsinghua University Shenzhen518055 China Environmental Science Program Department of Life Sciences Beijing Normal University-Hong Kong Baptist University United International College Guangdong 519087 China Tsinghua Shenzhen International Graduate School Tsinghua University Shenzhen518055 China Department of Physics Department of Chemistry Department of Materials Sciences Center for 2-Dimensional and Layered Materials The Pennsylvania State University University Park PA16802 United States International Collaborative Laboratory of 2D Materials for Optoelectronics Science and Technology Ministry of Education Institute of Microscale Optoelectronics Shenzhen University Shenzhen518060 China Key Laboratory of Optoelectronic Devices and Systems China

The hydrolysis of DNA serves as the foundational principle for gene engineering that enable precise gene cleavage at the molecular level. This process typically occurs in biological nucleases, which exhibit nucleobase-selective and catalytic hydrolysis capabilities rarely replicated in abiotic nanomaterials. Here, we demonstrate that molybdenum-terminated (Mo-terminated) edges of molybdenum disulfide (MoS2) possess the unique ability to abstract a proton (H+) from water molecules, thereby facilitating catalytic hydrolysis reactions that cleave the phosphodiester bonds in DNA through the action of hydroxide ions. The enhanced proton absorption at Mo-terminated edges of MoS2 significantly reduces the activation energy required for the DNA hydrolysis reaction. Furthermore, the favorable interaction between the Mo-terminated edges and thymine nucleobases promotes both charge transfer and P-O bond cleavage, enabling targeted DNA hydrolysis at 'TTTTTTT' sequences under dark conditions. This discovery underscores the potential of MoS2 as a stable, efficient nanosystem for precise genetic editing, heralding advanced applications in the field of gene engineering. © 2024, The Authors. All rights reserved.

关键词： DNA sequences