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Co Nanoparticle Catalysts Encapsulated by BaO–La(2)O(3) Nanofractions for Efficient Ammonia Synthesis Under Mild Reaction Conditions
[Image: see text] Ruthenium catalysts may allow for realization of renewable energy-based ammonia synthesis processes using mild reaction conditions (<400 °C, <10 MPa). However, ruthenium is relatively rare and therefore expensive. Here, we report a Co nanoparticle catalyst loaded on a basic B...
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/PMC9301956/ https://www.ncbi.nlm.nih.gov/pubmed/35874216 http://dx.doi.org/10.1021/acsomega.2c01973 |
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author | Miyahara, Shin-ichiro Sato, Katsutoshi Tsujimaru, Kotoko Wada, Yuichiro Ogura, Yuta Toriyama, Takaaki Yamamoto, Tomokazu Matsumura, Syo Inazu, Koji Nagaoka, Katsutoshi |
author_facet | Miyahara, Shin-ichiro Sato, Katsutoshi Tsujimaru, Kotoko Wada, Yuichiro Ogura, Yuta Toriyama, Takaaki Yamamoto, Tomokazu Matsumura, Syo Inazu, Koji Nagaoka, Katsutoshi |
author_sort | Miyahara, Shin-ichiro |
collection | PubMed |
description | [Image: see text] Ruthenium catalysts may allow for realization of renewable energy-based ammonia synthesis processes using mild reaction conditions (<400 °C, <10 MPa). However, ruthenium is relatively rare and therefore expensive. Here, we report a Co nanoparticle catalyst loaded on a basic Ba/La(2)O(3) support and prereduced at 700 °C (Co/Ba/La(2)O(3)_700red) that showed higher ammonia synthesis activity at 350 °C and 1.0–3.0 MPa than two benchmark Ru catalysts, Cs(+)/Ru/MgO and Ru/CeO(2). The synthesis rate of the catalyst at 350 °C and 1.0 MPa (19.3 mmol h(–1) g(–1)) was 8.0 times that of Co/Ba/La(2)O(3)_500red and 6.9 times that of Co/La(2)O(3)_700red. The catalyst showed ammonia synthesis activity at temperatures down to 200 °C. Reduction at the high temperature induced the formation of BaO–La(2)O(3) nanofractions around the Co nanoparticles by decomposition of BaCO(3), which increased turnover frequency, inhibited the sintering of Co nanoparticles, and suppressed ammonia poisoning. These strategies may also be applicable to other non-noble metal catalysts, such as nickel. |
format | Online Article Text |
id | pubmed-9301956 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-93019562022-07-22 Co Nanoparticle Catalysts Encapsulated by BaO–La(2)O(3) Nanofractions for Efficient Ammonia Synthesis Under Mild Reaction Conditions Miyahara, Shin-ichiro Sato, Katsutoshi Tsujimaru, Kotoko Wada, Yuichiro Ogura, Yuta Toriyama, Takaaki Yamamoto, Tomokazu Matsumura, Syo Inazu, Koji Nagaoka, Katsutoshi ACS Omega [Image: see text] Ruthenium catalysts may allow for realization of renewable energy-based ammonia synthesis processes using mild reaction conditions (<400 °C, <10 MPa). However, ruthenium is relatively rare and therefore expensive. Here, we report a Co nanoparticle catalyst loaded on a basic Ba/La(2)O(3) support and prereduced at 700 °C (Co/Ba/La(2)O(3)_700red) that showed higher ammonia synthesis activity at 350 °C and 1.0–3.0 MPa than two benchmark Ru catalysts, Cs(+)/Ru/MgO and Ru/CeO(2). The synthesis rate of the catalyst at 350 °C and 1.0 MPa (19.3 mmol h(–1) g(–1)) was 8.0 times that of Co/Ba/La(2)O(3)_500red and 6.9 times that of Co/La(2)O(3)_700red. The catalyst showed ammonia synthesis activity at temperatures down to 200 °C. Reduction at the high temperature induced the formation of BaO–La(2)O(3) nanofractions around the Co nanoparticles by decomposition of BaCO(3), which increased turnover frequency, inhibited the sintering of Co nanoparticles, and suppressed ammonia poisoning. These strategies may also be applicable to other non-noble metal catalysts, such as nickel. American Chemical Society 2022-07-11 /pmc/articles/PMC9301956/ /pubmed/35874216 http://dx.doi.org/10.1021/acsomega.2c01973 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Miyahara, Shin-ichiro Sato, Katsutoshi Tsujimaru, Kotoko Wada, Yuichiro Ogura, Yuta Toriyama, Takaaki Yamamoto, Tomokazu Matsumura, Syo Inazu, Koji Nagaoka, Katsutoshi Co Nanoparticle Catalysts Encapsulated by BaO–La(2)O(3) Nanofractions for Efficient Ammonia Synthesis Under Mild Reaction Conditions |
title | Co Nanoparticle
Catalysts Encapsulated by BaO–La(2)O(3) Nanofractions
for Efficient Ammonia Synthesis
Under Mild Reaction Conditions |
title_full | Co Nanoparticle
Catalysts Encapsulated by BaO–La(2)O(3) Nanofractions
for Efficient Ammonia Synthesis
Under Mild Reaction Conditions |
title_fullStr | Co Nanoparticle
Catalysts Encapsulated by BaO–La(2)O(3) Nanofractions
for Efficient Ammonia Synthesis
Under Mild Reaction Conditions |
title_full_unstemmed | Co Nanoparticle
Catalysts Encapsulated by BaO–La(2)O(3) Nanofractions
for Efficient Ammonia Synthesis
Under Mild Reaction Conditions |
title_short | Co Nanoparticle
Catalysts Encapsulated by BaO–La(2)O(3) Nanofractions
for Efficient Ammonia Synthesis
Under Mild Reaction Conditions |
title_sort | co nanoparticle
catalysts encapsulated by bao–la(2)o(3) nanofractions
for efficient ammonia synthesis
under mild reaction conditions |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9301956/ https://www.ncbi.nlm.nih.gov/pubmed/35874216 http://dx.doi.org/10.1021/acsomega.2c01973 |
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