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Thermoplasmonic In Situ Fabrication of Nanohybrid Electrocatalysts over Gas Diffusion Electrodes for Enhanced H(2)O(2) Electrosynthesis
[Image: see text] Large-scale development of electrochemical cells is currently hindered by the lack of Earth-abundant electrocatalysts with high catalytic activity, product selectivity, and interfacial mass transfer. Herein, we developed an electrocatalyst fabrication approach which responds to the...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10407842/ https://www.ncbi.nlm.nih.gov/pubmed/37560189 http://dx.doi.org/10.1021/acscatal.3c01837 |
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author | Zhang, Yu Mascaretti, Luca Melchionna, Michele Henrotte, Olivier Kment, Štepan Fornasiero, Paolo Naldoni, Alberto |
author_facet | Zhang, Yu Mascaretti, Luca Melchionna, Michele Henrotte, Olivier Kment, Štepan Fornasiero, Paolo Naldoni, Alberto |
author_sort | Zhang, Yu |
collection | PubMed |
description | [Image: see text] Large-scale development of electrochemical cells is currently hindered by the lack of Earth-abundant electrocatalysts with high catalytic activity, product selectivity, and interfacial mass transfer. Herein, we developed an electrocatalyst fabrication approach which responds to these requirements by irradiating plasmonic titanium nitride (TiN) nanocubes self-assembled on a carbon gas diffusion layer in the presence of polymeric binders. The localized heating produced upon illumination creates unique conditions for the formation of TiN/F-doped carbon hybrids that show up to nearly 20 times the activity of the pristine electrodes. In alkaline conditions, they exhibit enhanced stability, a maximum H(2)O(2) selectivity of 90%, and achieve a H(2)O(2) productivity of 207 mmol g(TiN)(–1) h(–1) at 0.2 V vs RHE. A detailed electrochemical investigation with different electrode arrangements demonstrated the key role of nanocomposite formation to achieve high currents. In particular, an increased TiO(x)N(y) surface content promoted a higher H(2)O(2) selectivity, and fluorinated nanocarbons imparted good stability to the electrodes due to their superhydrophobic properties. |
format | Online Article Text |
id | pubmed-10407842 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-104078422023-08-09 Thermoplasmonic In Situ Fabrication of Nanohybrid Electrocatalysts over Gas Diffusion Electrodes for Enhanced H(2)O(2) Electrosynthesis Zhang, Yu Mascaretti, Luca Melchionna, Michele Henrotte, Olivier Kment, Štepan Fornasiero, Paolo Naldoni, Alberto ACS Catal [Image: see text] Large-scale development of electrochemical cells is currently hindered by the lack of Earth-abundant electrocatalysts with high catalytic activity, product selectivity, and interfacial mass transfer. Herein, we developed an electrocatalyst fabrication approach which responds to these requirements by irradiating plasmonic titanium nitride (TiN) nanocubes self-assembled on a carbon gas diffusion layer in the presence of polymeric binders. The localized heating produced upon illumination creates unique conditions for the formation of TiN/F-doped carbon hybrids that show up to nearly 20 times the activity of the pristine electrodes. In alkaline conditions, they exhibit enhanced stability, a maximum H(2)O(2) selectivity of 90%, and achieve a H(2)O(2) productivity of 207 mmol g(TiN)(–1) h(–1) at 0.2 V vs RHE. A detailed electrochemical investigation with different electrode arrangements demonstrated the key role of nanocomposite formation to achieve high currents. In particular, an increased TiO(x)N(y) surface content promoted a higher H(2)O(2) selectivity, and fluorinated nanocarbons imparted good stability to the electrodes due to their superhydrophobic properties. American Chemical Society 2023-07-20 /pmc/articles/PMC10407842/ /pubmed/37560189 http://dx.doi.org/10.1021/acscatal.3c01837 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Zhang, Yu Mascaretti, Luca Melchionna, Michele Henrotte, Olivier Kment, Štepan Fornasiero, Paolo Naldoni, Alberto Thermoplasmonic In Situ Fabrication of Nanohybrid Electrocatalysts over Gas Diffusion Electrodes for Enhanced H(2)O(2) Electrosynthesis |
title | Thermoplasmonic
In Situ Fabrication of Nanohybrid
Electrocatalysts over Gas Diffusion Electrodes for Enhanced H(2)O(2) Electrosynthesis |
title_full | Thermoplasmonic
In Situ Fabrication of Nanohybrid
Electrocatalysts over Gas Diffusion Electrodes for Enhanced H(2)O(2) Electrosynthesis |
title_fullStr | Thermoplasmonic
In Situ Fabrication of Nanohybrid
Electrocatalysts over Gas Diffusion Electrodes for Enhanced H(2)O(2) Electrosynthesis |
title_full_unstemmed | Thermoplasmonic
In Situ Fabrication of Nanohybrid
Electrocatalysts over Gas Diffusion Electrodes for Enhanced H(2)O(2) Electrosynthesis |
title_short | Thermoplasmonic
In Situ Fabrication of Nanohybrid
Electrocatalysts over Gas Diffusion Electrodes for Enhanced H(2)O(2) Electrosynthesis |
title_sort | thermoplasmonic
in situ fabrication of nanohybrid
electrocatalysts over gas diffusion electrodes for enhanced h(2)o(2) electrosynthesis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10407842/ https://www.ncbi.nlm.nih.gov/pubmed/37560189 http://dx.doi.org/10.1021/acscatal.3c01837 |
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