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Using Single Atom Catalysts as Nanozymes in FET Sensors FET

Using Single Atom Catalysts as Nanozymes in FET Sensors FET

Amirreza Khodadadian (ORCID: 0000-0003-2374-0557)
  • Grant DOI 10.55776/P36520
  • Funding program Principal Investigator Projects
  • Status ongoing
  • Start June 1, 2023
  • End May 31, 2026
  • Funding amount € 475,713
  • Project website
  • dc

Disciplines

Chemistry (50%); Mathematics (20%); Nanotechnology (30%)

Keywords

    Single Atom Catalysts, Nanozymes, Field-Effect Transistor Sensors, Machine Learning, Mathematical Modeling

Abstract

The restrictions of enzymes necessitate looking for new materials to be used as their alternatives. Nanomaterials which can mimic enzymatic reactions are among the most promising materials. Single- atom catalysts (SACs) function at the extreme length scale of nanomaterial catalysts and show significant catalytic activity. The development of heterogeneous catalysts with cooperativity between metal centers, keeping all the salient features of SACs, can offer a platform for the development of the next generation of single-atom nanozymes (SANs). The catalytic interactions are generally dynamic and all known catalysts are based on electronic interactions. The application of in-situ surface techniques such as XAS, XPS, XRD, and TEM along with electrochemical methods, e.g., nano-FETs that bring the opportunity to follow bio-catalyst phenomena during the reaction time can be most convenient and useful. In this research, we will develop a method to examine the biocatalytic activity of SAN by the combination of nano-FETs and simulation data. We will synthesize the new SANs with special features, e.g. as enzyme comparable bio-catalytic activity and selectivity. We will optimize the biocatalytic activity/selectivity of SANs and examine the applicability of SANs in biological applications. We provide a framework to model the device and determine the experimental parameters. We present using SACs as biocatalysts in nano- FET systems. A broad family of various metals with the ability to be applied as heterogeneous SACs is selected to be converted to SANs functionalized by different carbon-based surrounding environments. We monitor their bio-catalytic behavior specifically for bio-catalytic reactions, e.g. peroxidase reaction, CO2 reduction, hydrogen or oxygen evolution reaction, and oxygen reduction. The SANs embedded inside the nano-FET semiconductor layer will eliminate the insulating membrane to enhance bioFET sensitivity. We investigate the capability of SANs as nanozymes in the biological enzyme-based reaction and examine the sensor performance using simulation and experimental data. We develop a self-consistent computational model, discuss its novel numerical methods, and use Bayesian inversion to estimate experimental important parameters. A machine learning setting based on rough neuralnetworks will be developed to predict the sensor behavior.

Research institution(s)
  • Universität Linz - 48%
  • Technische Universität Wien - 52%
Project participants
  • Clemens Heitzinger, Technische Universität Wien , national collaboration partner
  • Dirk Praetorius, Technische Universität Wien , national collaboration partner
  • Maryam Parvizi, Technische Universität Wien , national collaboration partner
  • Bernhard Jakoby, Universität Linz , national collaboration partner
  • Samaneh Mirsian, Universität Linz , national collaboration partner
  • Wolfgang Hilber, Universität Linz , associated research partner
International project participants
  • Michael Schöning, Fachhochschule Aachen / Standort Jülich - Germany
  • Sven Ingebrandt, RWTH Aachen - Germany
  • Maryam Parvizi, Technische Universität Wien - Germany
  • Thomas Wick, Universität Hannover - Germany
  • Mehdi Dehghan, Amirkabir University of Technology - Iran
  • Mohammad Teshnehlab, K. N. Toosi University of Technolog - Iran
  • Fatemeh Molaabasi, Motamed Cancer Institute - Iran
  • Luca Selmi, University of Modena and Reggio Emilia - Italy

Research Output

  • 34 Citations
  • 8 Publications

Discovering
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matters.

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