Determination of Activation Energy on Hydrogen Evolution Reaction for Nickel-Based Porous Electrodes during Alkaline Electrolysis

The aim of the present work is to evaluate the activation energy (Ea) at different cathodic overpotentials (η) by potentiodynamic tests which were carried out at different temperatures of Ni-based, NiCr-m, and NiCr-p porous electrodes, during the alkaline electrolysis processes. On the other hand, t...

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Main Authors: Melina Velasco-Plascencia, Octavio Vázquez-Gómez, Luis Olmos, Francisco Reyes-Calderón, Héctor J. Vergara-Hernández, Julio C. Villalobos
Format: Article
Language:English
Published: MDPI AG 2023-03-01
Series:Catalysts
Subjects:
Online Access:https://www.mdpi.com/2073-4344/13/3/517
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author Melina Velasco-Plascencia
Octavio Vázquez-Gómez
Luis Olmos
Francisco Reyes-Calderón
Héctor J. Vergara-Hernández
Julio C. Villalobos
author_facet Melina Velasco-Plascencia
Octavio Vázquez-Gómez
Luis Olmos
Francisco Reyes-Calderón
Héctor J. Vergara-Hernández
Julio C. Villalobos
author_sort Melina Velasco-Plascencia
collection DOAJ
description The aim of the present work is to evaluate the activation energy (Ea) at different cathodic overpotentials (η) by potentiodynamic tests which were carried out at different temperatures of Ni-based, NiCr-m, and NiCr-p porous electrodes, during the alkaline electrolysis processes. On the other hand, the electrochemical stability of the electrodes was evaluated by cyclic voltammetry after 1000 cycles of operation and by potentiostatic tests after 10 h at −1.5 V vs. SCE. The electrodes were sintered with a heating rate of 25 °C/min up to a temperature of 1000 °C (Ni-based and NiCr-m) and 1200 °C (NiCr-p) for 60 min. The results showed that the Ea value was lower for the Ni-based system at equilibrium; however, the NiCr-p electrode had a better performance due to higher negative apparent Ea values as a function of η (dEa/dη). The cyclic voltammetry tests suggest that the NiCr-p electrode improves its activity by about 71% in its long-term operation in comparison with Ni-based and NiCr-m. A similar behavior was observed in the potentiostatic test which showed a higher cathodic current density associated with a charge transfer process after 10 h. The higher stability of the NiCr-p is attributed to a homogeneous Cr distribution in the nickel matrix.
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spelling doaj.art-bcc97aa48fd14e42b1f785a18ab839002023-11-17T10:10:32ZengMDPI AGCatalysts2073-43442023-03-0113351710.3390/catal13030517Determination of Activation Energy on Hydrogen Evolution Reaction for Nickel-Based Porous Electrodes during Alkaline ElectrolysisMelina Velasco-Plascencia0Octavio Vázquez-Gómez1Luis Olmos2Francisco Reyes-Calderón3Héctor J. Vergara-Hernández4Julio C. Villalobos5Tecnológico Nacional de México/Instituto Tecnológico de Morelia, Avenida Tecnológico No. 1500, Lomas de Santiaguito, Morelia 58120, MexicoTecnológico Nacional de México/Instituto Tecnológico de Morelia, Avenida Tecnológico No. 1500, Lomas de Santiaguito, Morelia 58120, MexicoINICIT, Universidad Michoacana de San Nicolás de Hidalgo, Avenida Francisco J. Múgica S/N Ciudad Universitaria, Morelia 58040, MexicoTecnológico Nacional de México/Instituto Tecnológico de Morelia, Avenida Tecnológico No. 1500, Lomas de Santiaguito, Morelia 58120, MexicoTecnológico Nacional de México/Instituto Tecnológico de Morelia, Avenida Tecnológico No. 1500, Lomas de Santiaguito, Morelia 58120, MexicoTecnológico Nacional de México/Instituto Tecnológico de Morelia, Avenida Tecnológico No. 1500, Lomas de Santiaguito, Morelia 58120, MexicoThe aim of the present work is to evaluate the activation energy (Ea) at different cathodic overpotentials (η) by potentiodynamic tests which were carried out at different temperatures of Ni-based, NiCr-m, and NiCr-p porous electrodes, during the alkaline electrolysis processes. On the other hand, the electrochemical stability of the electrodes was evaluated by cyclic voltammetry after 1000 cycles of operation and by potentiostatic tests after 10 h at −1.5 V vs. SCE. The electrodes were sintered with a heating rate of 25 °C/min up to a temperature of 1000 °C (Ni-based and NiCr-m) and 1200 °C (NiCr-p) for 60 min. The results showed that the Ea value was lower for the Ni-based system at equilibrium; however, the NiCr-p electrode had a better performance due to higher negative apparent Ea values as a function of η (dEa/dη). The cyclic voltammetry tests suggest that the NiCr-p electrode improves its activity by about 71% in its long-term operation in comparison with Ni-based and NiCr-m. A similar behavior was observed in the potentiostatic test which showed a higher cathodic current density associated with a charge transfer process after 10 h. The higher stability of the NiCr-p is attributed to a homogeneous Cr distribution in the nickel matrix.https://www.mdpi.com/2073-4344/13/3/517Hydrogen evolution reactionNi-based electrodepowder metallurgy
spellingShingle Melina Velasco-Plascencia
Octavio Vázquez-Gómez
Luis Olmos
Francisco Reyes-Calderón
Héctor J. Vergara-Hernández
Julio C. Villalobos
Determination of Activation Energy on Hydrogen Evolution Reaction for Nickel-Based Porous Electrodes during Alkaline Electrolysis
Catalysts
Hydrogen evolution reaction
Ni-based electrode
powder metallurgy
title Determination of Activation Energy on Hydrogen Evolution Reaction for Nickel-Based Porous Electrodes during Alkaline Electrolysis
title_full Determination of Activation Energy on Hydrogen Evolution Reaction for Nickel-Based Porous Electrodes during Alkaline Electrolysis
title_fullStr Determination of Activation Energy on Hydrogen Evolution Reaction for Nickel-Based Porous Electrodes during Alkaline Electrolysis
title_full_unstemmed Determination of Activation Energy on Hydrogen Evolution Reaction for Nickel-Based Porous Electrodes during Alkaline Electrolysis
title_short Determination of Activation Energy on Hydrogen Evolution Reaction for Nickel-Based Porous Electrodes during Alkaline Electrolysis
title_sort determination of activation energy on hydrogen evolution reaction for nickel based porous electrodes during alkaline electrolysis
topic Hydrogen evolution reaction
Ni-based electrode
powder metallurgy
url https://www.mdpi.com/2073-4344/13/3/517
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