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Title:Selective semi-hydrogenation of acetylene using asingle-atom cobalt on carbon nitride photocatalyst with water as a proton source
Authors:ID Fortunato, Anna (Author)
ID Perilli, Daniele (Author)
ID Dron, Alexandru (Author)
ID Celorrio, Verónica (Author)
ID Dražić, Goran (Author)
ID Ðorđević, Luka (Author)
ID Calvillo, Laura (Author)
ID Di Valentin, Cristiana (Author)
ID Arcudi, Francesca (Author)
Files:URL URL - Source URL, visit https://onlinelibrary.wiley.com/doi/10.1002/smtd.202500527
 
.pdf PDF - Presentation file, download (2,12 MB)
MD5: 75495678BAB82DD487F2038A3CD0C90F
 
Language:English
Typology:1.01 - Original Scientific Article
Organization:Logo KI - National Institute of Chemistry
Abstract:Light-powered strategies for the semi-hydrogenation of acetylene to ethylene are rapidly emerging as sustainable alternatives to the traditional thermochemical processes. The development of a robust, selective, as well as recyclable, non-noble catalyst that can be powered by visible light and uses water as proton source to accomplish this important reaction remains a key challenge. Here the first demonstration of a cobalt single-atom catalyst supported on carbon-nitride (Co−CN) as an all-in-one photocatalyst for the semi-hydrogenation of acetylene to ethylene is reported using water as the proton source, offering advantages over current hydrogenation technologies. Carbon nitride hosts the individual catalytic active sites of cobalt thus combining photosensitizer and cocatalyst in one unit, in line with first-principles modelling. Under visible light irradiation, Co−CN reduces acetylene to ethylene with stable activity for over 40 days of continuous operation, ≥99.9% selectivity, and provides means for coupling organic upgrading to produce valuable oxidation products. The heterogeneous Co−CN can be easily recovered and reused repeatedly without loss of catalytic activity and structural integrity. Thereby, the integrated and recyclable platform overcomes the need of coupling a separate photosensitizer to a catalyst, and using noble metal catalysts with an external H2 gas feed.
Publication status:Published
Publication version:Version of Record
Publication date:22.01.2026
Year of publishing:2026
Number of pages:str. 1-9
Numbering: iss. ǂ2, Vol. 10, [article no.] 2500527
PID:20.500.12556/DiRROS-27380 New window
UDC:544.3/.4
ISSN on article:2366-9608
DOI:10.1002/smtd.202500527 New window
COBISS.SI-ID:239134723 New window
Copyright:© 2025 The Author(s). Small Methods published by Wiley-VCH GmbH.
Note:Opis vira z dne 12. 6. 2025; Nasl. z nasl. zaslona;
Publication date in DiRROS:04.02.2026
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Downloads:13
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Record is a part of a journal

Title:Small methods
Publisher:Wiley-VCH
ISSN:2366-9608
COBISS.SI-ID:114598915 New window

Document is financed by a project

Funder:Italian Ministry of University and Research
Funding programme:Rita Levi Montalcini Program
Project number:PGR20E2KCG

Funder:Fondazione Cariparo
Funding programme:Starting Package Program

Funder:University of Padova
Project number:STARS@UNIPD 2023

Funder:EC - European Commission
Funding programme:HE
Project number:101077698
Name:Photocatalytic Reactions Under Light and Dark with Transient Supramolecular Assemblies
Acronym:PhotoDark

Funder:Italian Ministry of University and Research
Project number:CN00000013
Name:PNRR – M4C2I1.4 ICSC – Centro Nazionale di Ricerca in High Performance Computing, Big Data and Quantum Computing

Licences

License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.
Licensing start date:19.05.2025
Applies to:Version of Record valid from 2025-05-19 Text and Data Mining valid from 2025-05-19

Secondary language

Language:Slovenian
Keywords:kataliza, fotokatalizatorji, etilen, žlahtne snovi, vodik


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