Oxidative dehydrogenation of cyclohexene on atomically precise subnanometer Cu4−nPdn (0 ≤ n ≤ 4) tetramer clusters: the effect of cluster composition and support on performance. (10th October 2022)
- Record Type:
- Journal Article
- Title:
- Oxidative dehydrogenation of cyclohexene on atomically precise subnanometer Cu4−nPdn (0 ≤ n ≤ 4) tetramer clusters: the effect of cluster composition and support on performance. (10th October 2022)
- Main Title:
- Oxidative dehydrogenation of cyclohexene on atomically precise subnanometer Cu4−nPdn (0 ≤ n ≤ 4) tetramer clusters: the effect of cluster composition and support on performance
- Authors:
- Jašík, Juraj
Valtera, Stanislav
Vaidulych, Mykhailo
Bunian, Muntaseer
Lei, Yu
Halder, Avik
Tarábková, Hana
Jindra, Martin
Kavan, Ladislav
Frank, Otakar
Bartling, Stephan
Vajda, Štefan - Abstract:
- Abstract : High fidelity selectivity tuning of the oxidative dehydrogenation of cyclohexene was achieved through the control of the atomic composition of CuPd clusters and their interactions with the support. Abstract : The pronounced effects of the composition of four-atom monometallic Cu and Pd and bimetallic CuPd clusters and the support on the catalytic activity and selectivity in the oxidative dehydrogenation of cyclohexene are reported. The ultra-nanocrystalline diamond supported clusters are highly active and dominantly produce benzene; some of the mixed clusters also produce cyclohexadiene, which are all clusters with a much suppressed combustion channel. The also highly active TiO2 -supported tetramers solely produce benzene, without any combustion to CO2 . The selectivity of the zirconia-supported mixed CuPd clusters and the monometallic Cu cluster is entirely different; though they are less active in comparison to clusters with other supports, these clusters produce significant fractions of cyclohexadiene, with their selectivity towards cyclohexadiene gradually increasing with the increasing number of copper atoms in the cluster, reaching about 50% for Cu3 Pd1 . The zirconia-supported copper tetramer stands out from among all the other tetramers in this reaction, with a selectivity towards cyclohexadiene of 70%, which far exceeds those of all the other cluster–support combinations. The findings from this study indicate a positive effect of copper on the stabilityAbstract : High fidelity selectivity tuning of the oxidative dehydrogenation of cyclohexene was achieved through the control of the atomic composition of CuPd clusters and their interactions with the support. Abstract : The pronounced effects of the composition of four-atom monometallic Cu and Pd and bimetallic CuPd clusters and the support on the catalytic activity and selectivity in the oxidative dehydrogenation of cyclohexene are reported. The ultra-nanocrystalline diamond supported clusters are highly active and dominantly produce benzene; some of the mixed clusters also produce cyclohexadiene, which are all clusters with a much suppressed combustion channel. The also highly active TiO2 -supported tetramers solely produce benzene, without any combustion to CO2 . The selectivity of the zirconia-supported mixed CuPd clusters and the monometallic Cu cluster is entirely different; though they are less active in comparison to clusters with other supports, these clusters produce significant fractions of cyclohexadiene, with their selectivity towards cyclohexadiene gradually increasing with the increasing number of copper atoms in the cluster, reaching about 50% for Cu3 Pd1 . The zirconia-supported copper tetramer stands out from among all the other tetramers in this reaction, with a selectivity towards cyclohexadiene of 70%, which far exceeds those of all the other cluster–support combinations. The findings from this study indicate a positive effect of copper on the stability of the mixed tetramers and potential new ways of fine-tuning catalyst performance by controlling the composition of the active site and via cluster–support interactions in complex oxidative reactions under the suppression of the undesired combustion of the feed. … (more)
- Is Part Of:
- Faraday discussions. Volume 242(2023)
- Journal:
- Faraday discussions
- Issue:
- Volume 242(2023)
- Issue Display:
- Volume 242, Issue 2023 (2023)
- Year:
- 2023
- Volume:
- 242
- Issue:
- 2023
- Issue Sort Value:
- 2023-0242-2023-0000
- Page Start:
- 70
- Page End:
- 93
- Publication Date:
- 2022-10-10
- Subjects:
- Chemistry -- Periodicals
Metallurgy -- Periodicals
Electrochemistry -- Periodicals
540 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/fd#!issueid=fd016192&type=current&issnprint=1359-6640 ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d2fd00108j ↗
- Languages:
- English
- ISSNs:
- 1359-6640
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3866.900000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 26679.xml