《Performance Projection of Vacuum Gate Dielectric Doping-Free Carbon Nanoribbon/Nanotube Field-Effect Transistors for Radiation-Immune Nanoelectronics》

  • 来源专题:现代化工
  • 编译者: 武春亮
  • 发布时间:2024-06-05
  • In all nanodevices, zigzag carbon nanotubes (ZCNTs) and armchair-edge graphene nanoribbons (A-GNRs) serve as carbon-based channels for CNT- and GNR-based (T)FETs, as shown in left and right figures, respectively [
    41
    ,
    42
    ]. It is worth indicating that coaxial gate configurations (left figures) and double gate configurations (right figures) have been adopted for CNT- and GNR-based devices, respectively [
    39
    ,
    40
    ,
    41
    ,
    42
    ,
    43
    ,
    44
    ]. Note that our study encompasses FET and tunnel FET modes. Additionally, the DL-TFET is not a combination of the Schottky barrier and tunnel FETs because it lacks a Schottky junction between the electrically doped source and the CNT/GNR [
    46
    ].
    Figure 1
    a,b present lengthwise cut views of the conventional Gate-All-Around (GAA) CNT(T)FET and Double Gate (DG) GNR(T)FET, respectively. These devices feature SiO
    2
    gate dielectrics and n-i-n or p-i-n chemical doping profiles [
    45
    ,
    47
    ]. The control gate covers the intrinsic channel region for both devices.
    Figure 1
    c,d showcase the proposed vacuum gate dielectric doping-free CNT(T)FET and GNR(T)FET, respectively. As their names suggest, these devices operate under dielectric-less [
    27
    ,
    28
    ,
    29
    ] and doping-free [
    46
    ] paradigms. Electrostatic control is utilized to achieve the doping profile necessary for FET and TFET operation via electrical source and drain doping gates.
    Figure 1
    e,f offer lengthwise cut views of the two proposed vacuum devices, revealing the absence of a bulk dielectric material around the channel, which is entirely controlled electrostatically, while 2D dielectrics can conceptually be adopted to cover the carbon channels forming metal-vacuum-2D dielectric-carbon structure, which is beneficial than MOS structure for radiation hardness. Notably, the CNT- and GNR-based vacuum devices are fully reconfigurable and can operate as FETs, TFETs, or BTBT FETs depending on applied biasing conditions (doping and control).
    Figure 1
    g,h present cross-sectional views perpendicular to the carbon-based channel. In the case of the CNTFET, even the inner environment of the CNT is considered a vacuum, which offers benefits in terms of immunity against radiation effects.
    Table 1
    provides details of the proposed designs, encompassing configuration, structure, and physical, dimensional, and electrical parameters of the vacuum nanodevices. It is important to note that this information and parameters are nominal, and any changes for parametric investigation’s sake will be explicitly highlighted.
  • 原文来源:https://www.mdpi.com/2079-4991/14/11/962
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    • 来源专题:现代化工
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(2014 - 2018)Waves Random Media (1991 - 2004) Volume number: Issue number (if known): Article or page number: Nanotechnology Purpose-led Publishing is a coalition of three not-for-profit publishers in the field of physical sciences: AIP Publishing, the American Physical Society and IOP Publishing. Together, as publishers that will always put purpose above profit, we have defined a set of industry standards that underpin high-quality, ethical scholarly communications. We are proudly declaring that science is our only shareholder. ACCEPTED MANUSCRIPT ? The following article is Open access Ultrafast and highly sensitive detection of SARS-CoV-2 spike protein by field-effect transistor graphene-based biosensors Thiago Alonso Alonso Stephan Lacerda Sousa1, Nathalie Almeida2, Fabrício Santos2, Priscilla Filgueiras3, Camila Corsini3, Camila Lacerda4, Thais Silva4, Rafaella F. Q. Grenfell5 and Flavio Plentz2 Accepted Manuscript online 26 July 2024 ? © 2024 The Author(s). Published by IOP Publishing Ltd What is an Accepted Manuscript? DOI 10.1088/1361-6528/ad67e8 Download Accepted Manuscript PDF Figures Skip to each figure in the article Tables Skip to each table in the article References Citations Article data Skip to each data item in the article What is article data? Open science Article metrics 1 Total downloads Submit Submit to this Journal Share this article Article and author information Author e-mailsthiagostephan@gmail.com Author affiliations1 Physics, Technical University of Denmark, Fysikvej B309, Lyngby, Hovedstaden, 2800, DENMARK 2 Physics, Universidade Federal de Minas Gerais, Av. Pres. Ant?nio Carlos, 6627, Pampulha, Belo Horizonte, MG, 31270-901, BRAZIL 3 Funda??o Oswaldo Cruz Instituto René Rachou, Av. Augusto de Lima, 1715, Barro Preto, Belo Horizonte, Minas Gerais, 30190-002, BRAZIL 4 Physics, Universidade Federal de Minas Gerais, Av. Pres. Ant?nio Carlos, 6627, Pampulha, Belo Horizonte, 31270-901, BRAZIL 5 Funda??o Oswaldo Cruz Centro de Pesquisas René Rachou, Rua Professor José Vieira de Mendon?a, 1000, Belo Horizonte, Minas Gerais, 30190-002, BRAZIL ORCID iDsThiago Alonso Alonso Stephan Lacerda Sousa https://orcid.org/0000-0001-8838-3648 Dates Received 13 March 2024 Revised 16 July 2024 Accepted 26 July 2024 Accepted Manuscript online 26 July 2024 Peer review information Method: Single-anonymous Revisions: 1 Screened for originality? Yes Journal RSS Sign up for new issue notifications 10.1088/1361-6528/ad67e8 Abstract The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), etiological agent for the coronavirus disease 2019 (COVID-19), has resulted in over 775 million global infections. Early diagnosis remains pivotal for effective epidemiological surveillance despite the availability of vaccines. Antigen-based assays are advantageous for early COVID-19 detection due to their simplicity, cost-effectiveness, and suitability for point-of-care testing (PoCT). This study introduces a graphene field-effect transistor-based biosensor designed for high sensitivity and rapid response to the SARS-CoV-2 spike protein. By functionalizing graphene with monoclonal antibodies and applying short-duration gate voltage pulses, we achieve selective detection of the viral spike protein in human serum within 100 μs and at concentrations as low as 1 fg/mL, equivalent to 8 antigen molecules per μL of blood. Furthermore, the biosensor estimates spike protein concentrations in serum from COVID-19 patients. Our platform demonstrates potential for next-generation PoCT antigen assays, promising fast and sensitive diagnostics for COVID-19 and other infectious diseases. 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