Oxygen evolution reaction electrocatalyst based on grafted cobalt and nickel doped carbon dots

• CoNi-CDs are synthesized via hydrothermal microwave method. • CoNi-CDs are diazotized and electro-grafted onto carbon surfaces. • Electro-grafting generates an ordered pattern distribution. • High oxygen evolution reaction (OER) electrocatalytic activity in a basic medium. • Electro-grafting significantly enhances OER electrocatalyst activity. Cobalt and nickel co-doped carbon dots (CoNi-CDs) have been synthesized using hydrothermal microwave assisted methodology. CoNi-CDs have been characterized, showing their ability to be diazotized and electro-grafted onto carbon surfaces, generating an ordered pattern distribution over carbon electrode surfaces. High electrocatalytic activity through oxygen evolution reaction (OER) in basic medium has been proved, showing that the electrocatalyst activity is enhanced when the CoNi-CDs are grafted onto the working electrode instead of just drop-casted. Grafted CoNi-CDs over carbon screen printed electrodes (grafted CoNi-CDs/CSPE) present lower overpotential for OER compared with RuO 2 reference material drop-casted over CSPE. Furthermore, the high turnover frequency of the electrocatalytic centers (cobalt and nickel ions) embedded into the carbon nanostructure enhances the OER electrocatalysis using a small amount of metal for the preparation of the electrocatalyst. In addition, good stability is shown for the modified electrodes used during OER electrocatalyst.

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Journal
Electrochimica Acta
Published
2026-01-21
DOI
https://doi.org/10.1016/j.electacta.2026.148285
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
0.00

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article

Oxygen evolution reaction electrocatalyst based on grafted cobalt and nickel doped carbon dots

Emiliano Martínez‐Periñán, Eva Mateo‐Martí, Cristina Gutiérrez-Sánchez, Encarnación Lorenzo et al.
Electrochimica Acta
Electrocatalysts for Energy Conversion
article

Oxygen evolution reaction electrocatalyst based on grafted cobalt and nickel doped carbon dots

Emiliano Martínez‐Periñán, Eva Mateo‐Martí, Cristina Gutiérrez-Sánchez, Encarnación Lorenzo, Julio Corrales Cristeto
article en

Abstract

• CoNi-CDs are synthesized via hydrothermal microwave method. • CoNi-CDs are diazotized and electro-grafted onto carbon surfaces. • Electro-grafting generates an ordered pattern distribution. • High oxygen evolution reaction (OER) electrocatalytic activity in a basic medium. • Electro-grafting significantly enhances OER electrocatalyst activity. Cobalt and nickel co-doped carbon dots (CoNi-CDs) have been synthesized using hydrothermal microwave assisted methodology. CoNi-CDs have been characterized, showing their ability to be diazotized and electro-grafted onto carbon surfaces, generating an ordered pattern distribution over carbon electrode surfaces. High electrocatalytic activity through oxygen evolution reaction (OER) in basic medium has been proved, showing that the electrocatalyst activity is enhanced when the CoNi-CDs are grafted onto the working electrode instead of just drop-casted. Grafted CoNi-CDs over carbon screen printed electrodes (grafted CoNi-CDs/CSPE) present lower overpotential for OER compared with RuO 2 reference material drop-casted over CSPE. Furthermore, the high turnover frequency of the electrocatalytic centers (cobalt and nickel ions) embedded into the carbon nanostructure enhances the OER electrocatalysis using a small amount of metal for the preparation of the electrocatalyst. In addition, good stability is shown for the modified electrodes used during OER electrocatalyst.

Electrochimica ActaVol. 553
IMDEA Nanoscience (ES), Centro de Astrobiología (ES), Universidad Autónoma de Madrid (ES)
Comunidad de Madrid, Ministerio de Ciencia e Innovación
Openalex Percentile: Top 83%
Electrocatalysts for Energy Conversion
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Oxygen evolution reaction electrocatalyst based on grafted cobalt and nickel doped carbon dots — Emiliano Martínez‐Periñán, Eva Mateo‐Martí, et al. · Electrochimica Acta (2026) | TGRS Research Map | TGRS