6 results on '"Thomas Quast"'
Search Results
2. Reduced‐Graphene‐Oxide‐Based Needle‐Type Field‐Effect Transistor for Dopamine Sensing
- Author
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Wolfgang Schuhmann, Erika Scavetta, Corina Andronescu, Thomas Quast, Federica Mariani, and T. Quast, F. Mariani, E. Scavetta, W. Schuhmann, C. Andronescu
- Subjects
Bioelectronics ,Materials science ,business.industry ,Graphene ,Chemie ,Oxide ,Needle type ,Catalysis ,law.invention ,spearhead field-effect transistors graphene oxide dopamine bioelectronics neurotransmitter ,chemistry.chemical_compound ,chemistry ,Dopamine ,law ,Electrochemistry ,medicine ,Optoelectronics ,Field-effect transistor ,business ,medicine.drug - Abstract
Owing to their intrinsic amplifying effect together with their temporal resolution, field-effect transistors (FETs) are gaining momentum for the detection of different biomolecules at ultralow concentration levels such as, for example, neurotransmitters, particularly if the concentration level of the analyte is below the detection limit of commonly used electrochemical sensing methods. We demonstrate the fabrication of a spearhead reduced graphene oxide (rGO)-based FET. The fabrication of the rGO-based FET by means of an electrochemical pulse deposition technique enables a controllable process including both the deposition and reduction of the deposited graphene oxide between two carbon nanoelectrodes to form the channel of the rGO-based FET. While using double-barrel carbon nanoelectrodes, the as-produced FETs offer new possibilities in terms of their applicability in very small volumes as well as the option of being positioned close to the desired measurement region. The fabrication process was evaluated and optimized to obtain rGO-based FETs with high performance. The as-fabricated devices were evaluated in terms of sensitivity and selectivity towards dopamine. The tested devices not only showed high sensitivity towards dopamine with a linear response ranging from 1 nM to 1μM, but also maintained a similar sensing performance in the presence of 500 μM ascorbic acid.
- Published
- 2020
- Full Text
- View/download PDF
3. Towards Reproducible Fabrication of Nanometre‐Sized Carbon Electrodes: Optimisation of Automated Nanoelectrode Fabrication by Means of Transmission Electron Microscopy
- Author
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Tsvetan Tarnev, Patrick Wilde, Alexander Botz, Stephan Feldhege, Corina Andronescu, Wolfgang Schuhmann, Miriam Marquitan, Armin Lindner, Thomas Quast, Harshitha Barike Aiyappa, and Yen-Ting Chen
- Subjects
Fabrication ,Materials science ,010405 organic chemistry ,chemistry.chemical_element ,Nanotechnology ,010402 general chemistry ,01 natural sciences ,Catalysis ,0104 chemical sciences ,law.invention ,Electrode fabrication ,chemistry ,law ,Transmission electron microscopy ,Electrode ,Electrochemistry ,Nanometre ,Electron microscope ,Carbon - Published
- 2018
- Full Text
- View/download PDF
4. Scrutinizing Intrinsic Oxygen Reduction Reaction Activity of a Fe−N−C Catalyst via Scanning Electrochemical Cell Microscopy
- Author
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Ndrina Limani, Emmanuel Batsa Tetteh, Moonjoo Kim, Thomas Quast, Emmanuel Scorsone, Bruno Jousselme, Wolfgang Schuhmann, Renaud Cornut, Laboratoire Innovation en Chimie des Surfaces et NanoSciences (LICSEN UMR 3685), Nanosciences et Innovation pour les Matériaux, la Biomédecine et l'Energie (ex SIS2M) (NIMBE UMR 3685), Institut Rayonnement Matière de Saclay (IRAMIS), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université Paris-Saclay-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université Paris-Saclay-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Institut Rayonnement Matière de Saclay (IRAMIS), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université Paris-Saclay-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université Paris-Saclay-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Ruhr University Bochum (RUB), Seoul National University [Seoul] (SNU), Laboratoire Capteurs Diamant (LCD-LIST), Département Métrologie Instrumentation & Information (DM2I), Laboratoire d'Intégration des Systèmes et des Technologies (LIST (CEA)), Direction de Recherche Technologique (CEA) (DRT (CEA)), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Direction de Recherche Technologique (CEA) (DRT (CEA)), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université Paris-Saclay-Laboratoire d'Intégration des Systèmes et des Technologies (LIST (CEA)), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université Paris-Saclay, and European Project: 812398,SENTINEL
- Subjects
diamond, instrumentation, nanodiamond, oxygen reduction reaction, sensor ,Electrochemistry ,[CHIM]Chemical Sciences ,[PHYS.PHYS.PHYS-INS-DET]Physics [physics]/Physics [physics]/Instrumentation and Detectors [physics.ins-det] ,Catalysis - Abstract
International audience; Carbon-based nanomaterials are renowned for their exceptional properties, making them propitious candidates for oxygen reduction reaction (ORR) electrocatalysis. However, their intrinsic activity is often challenging to investigate unambiguously with conventional methodologies due to the inherent complexities of such systems and the material itself. Zooming into the material and gaining electrochemical information with high resolution is a way to get rid of many experimental factors that influence the catalytic activity in macro-scale measurements. Herein, we employ nano-scale scanning electrochemical cell microscopy (SECCM) to investigate individual catalyst agglomerates with and without Nafion content. The intrinsic ORR activity of the catalyst was unravelled by using a unique approach of normalizing the data of all measured points by their distinctive electrochemical surface area (ECSA). When coupling with scanning electron microscopy (SEM), the structure and morphology of the catalytically active agglomerateswere visualized
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- View/download PDF
5. Nanoelectrochemical Platform for Elucidating the Reaction between a Solid Active Material and a Dissolved Redox Species for Mediated Redox‐Flow Batteries
- Author
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Dr. Carla Santana Santos, Dr. Thomas Quast, Prof. Edgar Ventosa, and Prof. Wolfgang Schuhmann
- Subjects
mediated redox flow battery ,solid active material ,redox targeting flow battery ,confined electrochemistry ,nanoelectrochemistry ,Industrial electrochemistry ,TP250-261 ,Chemistry ,QD1-999 - Abstract
Abstract Mediated processes using a solid material, often called “solid booster”, have been proposed to increase the energy density in redox flow batteries (RFB). The strategy alters the energy storage in the dissolved redox species to a solid active material placed in a compartment of the device. Understanding the reaction kinetics of the dissolved redox mediator and the solid booster is crucial for proposing feasible pairs of solid boosters and dissolved redox mediators. We demonstrate a nanoelectrochemical methodology to monitor the reaction between the dissolved species in solution and the solid active material electrodeposited in recessed carbon nanoelectrodes. Our strategy overcomes issues inherent to standard methodologies, such as mass transport limitation, and evaluation of the intrinsic reactivity of the solid material. As a proof of concept, Prussian blue was electrodeposited in a recessed carbon nanoelectrode and used as a confined‐solid material platform to evaluate the reaction between the reduced form of Prussian blue and triiodide, I3- . A high conversion rate of the solid booster was observed in the presence of μM concentrations of the dissolved redox species. The proposed nanoelectrode was successfully employed as a potentiometric sensor to monitor the evolution of the reaction with the dissolved active species.
- Published
- 2024
- Full Text
- View/download PDF
6. Scrutinizing Intrinsic Oxygen Reduction Reaction Activity of a Fe−N−C Catalyst via Scanning Electrochemical Cell Microscopy
- Author
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Dr. Ndrina Limani, Dr. Emmanuel Batsa Tetteh, Moonjoo Kim, Dr. Thomas Quast, Dr. Emmanuel Scorsone, Dr. Bruno Jousselme, Prof. Dr. Wolfgang Schuhmann, and Dr. Renaud Cornut
- Subjects
intrinsic activity ,multi-walled carbon nanotubes ,oxygen reduction reaction ,scanning electrochemical cell microscopy ,scanning electron microscopy ,Industrial electrochemistry ,TP250-261 ,Chemistry ,QD1-999 - Abstract
Abstract Carbon‐based nanomaterials are renowned for their exceptional properties, making them propitious candidates for oxygen reduction reaction (ORR) electrocatalysis. However, their intrinsic activity is often challenging to investigate unambiguously with conventional methodologies due to the inherent complexities of such systems and the material itself. Zooming into the material and gaining electrochemical information with high resolution is a way to get rid of many experimental factors that influence the catalytic activity in macro‐scale measurements. Herein, we employ nano‐scale scanning electrochemical cell microscopy (SECCM) to investigate individual catalyst agglomerates with and without Nafion content. The intrinsic ORR activity of the catalyst was unravelled by using a unique approach of normalizing the data of all measured points by their distinctive electrochemical surface area (ECSA). When coupling with scanning electron microscopy (SEM), the structure and morphology of the catalytically active agglomerates were visualized.
- Published
- 2023
- Full Text
- View/download PDF
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