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Ultrasmall, Coating-Free, Pyramidal Platinum Nanoparticles for High Stability Fuel Cell Oxygen Reduction
[Image: see text] Ultrasmall (<5 nm diameter) noble metal nanoparticles with a high fraction of {111} surface domains are of fundamental and practical interest as electrocatalysts, especially in fuel cells; the nanomaterial surface structure dictates its catalytic properties, including kinetics a...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9975930/ https://www.ncbi.nlm.nih.gov/pubmed/35920442 http://dx.doi.org/10.1021/acsami.2c07738 |
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author | Mastronardi, Valentina Magliocca, Emanuele Gullon, José Solla Brescia, Rosaria Pompa, Pier Paolo Miller, Thomas S. Moglianetti, Mauro |
author_facet | Mastronardi, Valentina Magliocca, Emanuele Gullon, José Solla Brescia, Rosaria Pompa, Pier Paolo Miller, Thomas S. Moglianetti, Mauro |
author_sort | Mastronardi, Valentina |
collection | PubMed |
description | [Image: see text] Ultrasmall (<5 nm diameter) noble metal nanoparticles with a high fraction of {111} surface domains are of fundamental and practical interest as electrocatalysts, especially in fuel cells; the nanomaterial surface structure dictates its catalytic properties, including kinetics and stability. However, the synthesis of size-controlled, pure Pt-shaped nanocatalysts has remained a formidable chemical challenge. There is an urgent need for an industrially scalable method for their production. Here, a one-step approach is presented for the preparation of single-crystal pyramidal nanocatalysts with a high fraction of {111} surface domains and a diameter below 4 nm. This is achieved by harnessing the shape-directing effect of citrate molecules, together with the strict control of oxidative etching while avoiding polymers, surfactants, and organic solvents. These catalysts exhibit significantly enhanced durability while, providing equivalent current and power densities to highly optimized commercial Pt/C catalysts at the beginning of life (BOL). This is even the case when they are tested in full polymer electrolyte membrane fuel cells (PEMFCs), as opposed to rotating disk experiments that artificially enhance electrode kinetics and minimize degradation. This demonstrates that the {111} surface domains in pyramidal Pt nanoparticles (as opposed to spherical Pt nanoparticles) can improve aggregation/corrosion resistance in realistic fuel cell conditions, leading to a significant improvement in membrane electrode assembly (MEA) stability and lifetime. |
format | Online Article Text |
id | pubmed-9975930 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-99759302023-03-02 Ultrasmall, Coating-Free, Pyramidal Platinum Nanoparticles for High Stability Fuel Cell Oxygen Reduction Mastronardi, Valentina Magliocca, Emanuele Gullon, José Solla Brescia, Rosaria Pompa, Pier Paolo Miller, Thomas S. Moglianetti, Mauro ACS Appl Mater Interfaces [Image: see text] Ultrasmall (<5 nm diameter) noble metal nanoparticles with a high fraction of {111} surface domains are of fundamental and practical interest as electrocatalysts, especially in fuel cells; the nanomaterial surface structure dictates its catalytic properties, including kinetics and stability. However, the synthesis of size-controlled, pure Pt-shaped nanocatalysts has remained a formidable chemical challenge. There is an urgent need for an industrially scalable method for their production. Here, a one-step approach is presented for the preparation of single-crystal pyramidal nanocatalysts with a high fraction of {111} surface domains and a diameter below 4 nm. This is achieved by harnessing the shape-directing effect of citrate molecules, together with the strict control of oxidative etching while avoiding polymers, surfactants, and organic solvents. These catalysts exhibit significantly enhanced durability while, providing equivalent current and power densities to highly optimized commercial Pt/C catalysts at the beginning of life (BOL). This is even the case when they are tested in full polymer electrolyte membrane fuel cells (PEMFCs), as opposed to rotating disk experiments that artificially enhance electrode kinetics and minimize degradation. This demonstrates that the {111} surface domains in pyramidal Pt nanoparticles (as opposed to spherical Pt nanoparticles) can improve aggregation/corrosion resistance in realistic fuel cell conditions, leading to a significant improvement in membrane electrode assembly (MEA) stability and lifetime. American Chemical Society 2022-08-03 /pmc/articles/PMC9975930/ /pubmed/35920442 http://dx.doi.org/10.1021/acsami.2c07738 Text en © 2022 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 | Mastronardi, Valentina Magliocca, Emanuele Gullon, José Solla Brescia, Rosaria Pompa, Pier Paolo Miller, Thomas S. Moglianetti, Mauro Ultrasmall, Coating-Free, Pyramidal Platinum Nanoparticles for High Stability Fuel Cell Oxygen Reduction |
title | Ultrasmall, Coating-Free,
Pyramidal Platinum Nanoparticles
for High Stability Fuel Cell Oxygen Reduction |
title_full | Ultrasmall, Coating-Free,
Pyramidal Platinum Nanoparticles
for High Stability Fuel Cell Oxygen Reduction |
title_fullStr | Ultrasmall, Coating-Free,
Pyramidal Platinum Nanoparticles
for High Stability Fuel Cell Oxygen Reduction |
title_full_unstemmed | Ultrasmall, Coating-Free,
Pyramidal Platinum Nanoparticles
for High Stability Fuel Cell Oxygen Reduction |
title_short | Ultrasmall, Coating-Free,
Pyramidal Platinum Nanoparticles
for High Stability Fuel Cell Oxygen Reduction |
title_sort | ultrasmall, coating-free,
pyramidal platinum nanoparticles
for high stability fuel cell oxygen reduction |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9975930/ https://www.ncbi.nlm.nih.gov/pubmed/35920442 http://dx.doi.org/10.1021/acsami.2c07738 |
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