Academic literature on the topic 'Non-Nernstian electron transfer'

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Journal articles on the topic "Non-Nernstian electron transfer"

1

Ardo, Shane, Darren Achey, Amanda J. Morris, Maria Abrahamsson, and Gerald J. Meyer. "Non-Nernstian Two-Electron Transfer Photocatalysis at Metalloporphyrin–TiO2Interfaces." Journal of the American Chemical Society 133, no. 41 (2011): 16572–80. http://dx.doi.org/10.1021/ja206139n.

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2

S., Thamizh Suganya, Balaganesan P., Visuvasam J., and Rajendran L. "An analytical expression of non-Nernstian catalytic mechanism at micro and macro electroduces at voltammetry." Asia Mathematika 5, no. 1 (2021): 1–10. https://doi.org/10.5281/zenodo.4723579.

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In this paper, the electrode surface concentration for non-Nernstian and Nernstian CT and the chemical thermodynamics is derived. This model represented a heat or partial differential equation and reconstructed changes over time in the Voltammetry chemical kinetics by using homotopy perturbation and Laplace transform method. In this closed form of analytical solutions of the concentration at electrode surface for non-Nernstian and Nernstian CT is derived. The non-Nernstian catalytic mechanism attains the steady-state and a general transient current-potential is expressed. The influence of Sum
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3

Gonzalez, Joaquin, Manuela Lopez-Tenes, and Angela Molina. "Non-Nernstian Two-Electron Transfer Reactions for Immobilized Molecules: A Theoretical Study in Cyclic Voltammetry." Journal of Physical Chemistry C 117, no. 10 (2013): 5208–20. http://dx.doi.org/10.1021/jp312621u.

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4

Molina, A., J. M. Gómez-Gil, J. Gonzalez, and E. Laborda. "Analytical theory for the voltammetry of the non-Nernstian catalytic mechanism at macro and microelectrodes: Interplay between the rates of mass transport, electron transfer and catalysis." Journal of Electroanalytical Chemistry 847 (August 2019): 113097. http://dx.doi.org/10.1016/j.jelechem.2019.04.057.

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5

Sanjay, Sooraj, Fahimul Islam Sakib, Mainul Hossain, and Navakanta Bhat. "(Invited, Digital Presentation) Super-Nernstian Isfet Combining Two-Dimensional WSe2/MoS2 Heterostructure with Negative Capacitance." ECS Meeting Abstracts MA2022-02, no. 15 (2022): 823. http://dx.doi.org/10.1149/ma2022-0215823mtgabs.

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Ion-sensitive field-effect transistors (ISFETs) are quite popular as compact, low-cost biosensors with fast response time and label-free detection1. They can be used as pH sensors or functionalized for complex biomolecule detection. The voltage sensitivity (Sv) in classical ISFETs is fundamentally limited to 59 mV/pH (Nernst limit). Surpassing the Nernst limit requires complex device architectures or novel transport phenomena. Sensitivity beyond the Nernst limit can be achieved using specific device architectures such as dual gate ISFETs2, negative capacitance ISFETs (NC-ISFET)3, tunnel ISFETs
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Markelova, Ekaterina, Christopher T. Parsons, Raoul-Marie Couture, et al. "Deconstructing the redox cascade: what role do microbial exudates (flavins) play?" Environmental Chemistry 14, no. 8 (2017): 515. http://dx.doi.org/10.1071/en17158.

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Environmental contextRedox potential is a controlling variable in aquatic chemistry. Through time series data, we show that microbial exudates released by bacteria may control trends in redox potential observed in natural waters. In particular, electron transfer between these exudates and the electrode could explain the values measured in the presence of abundant oxidants such as oxygen and nitrate. AbstractRedox electrodes are commonly used to measure redox potentials (EH) of natural waters. The recorded EH values are usually interpreted in terms of the dominant inorganic redox couples. To fu
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Sairaman, Saikrithika, and Saikrithika Sairaman. "(Digital Presentation) In-Situ Electro-Organic Synthesis and Functionalization of Catechol Derivative on Carbon Black and Its Interference-Free Voltammetric pH Sensing Application." ECS Meeting Abstracts MA2022-02, no. 56 (2022): 2159. http://dx.doi.org/10.1149/ma2022-02562159mtgabs.

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Catechol, 1,2-dihydroxybenzene (1,2-DHB), is a well-known organic redox molecule and a potent biological electron-transfer mediator widely used in electrocatalysis, bio-electrocatalysis, energy-storage and pH sensing applications. Functionalization of catechol (CA) over the carbon-electrode is an essential step to achieving the desired application. There are several studies reported for the chemical synthesis of functionalized CA derivatives following surface immobilization procedure [1-3]. Indeed, preparation of a simple and stable catechol functionalized electrochemically modified electrode
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