Interfacial Electronic Effects in Co@N-Doped Carbon Shells Heterojunction Catalyst for Semi-Hydrogenation of Phenylacetylene
Metal-supported catalyst with high activity and relatively simple preparation method is given priority to industrial production. In this work, this study reported an easily accessible synthesis strategy to prepare Mott-Schottky-type N-doped carbon encapsulated metallic Co (Co@N<sub>p+g</sub...
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2021
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oai:doaj.org-article:0c35296493b844ac905a23334a9517a02021-11-25T18:29:44ZInterfacial Electronic Effects in Co@N-Doped Carbon Shells Heterojunction Catalyst for Semi-Hydrogenation of Phenylacetylene10.3390/nano111127762079-4991https://doaj.org/article/0c35296493b844ac905a23334a9517a02021-10-01T00:00:00Zhttps://www.mdpi.com/2079-4991/11/11/2776https://doaj.org/toc/2079-4991Metal-supported catalyst with high activity and relatively simple preparation method is given priority to industrial production. In this work, this study reported an easily accessible synthesis strategy to prepare Mott-Schottky-type N-doped carbon encapsulated metallic Co (Co@N<sub>p+g</sub>C) catalyst by high-temperature pyrolysis method in which carbon nitride (g-C<sub>3</sub>N<sub>4</sub>) and dopamine were used as support and nitrogen source. The prepared Co@N<sub>p+g</sub>C presented a Mott-Schottky effect; that is, a strong electronic interaction of metallic Co and N-doped carbon shell was constructed to lead to the generation of Mott-Schottky contact. The metallic Co, due to high work function as compared to that of N-doped carbon, transferred electrons to the N-doped outer shell, forming a new contact interface. In this interface area, the positive and negative charges were redistributed, and the catalytic hydrogenation mainly occurred in the area of active charges. The Co@N<sub>p+g</sub>C catalyst showed excellent catalytic activity in the hydrogenation of phenylacetylene to styrene, and the selectivity of styrene reached 82.4%, much higher than those of reference catalysts. The reason for the promoted semi-hydrogenation of phenylacetylene was attributed to the electron transfer of metallic Co, as it was caused by N doping on carbon.Yuan HuangHaoting YanChenyang ZhangYize WangQinhong WeiRenkun ZhangMDPI AGarticlecobalt catalystN-doped carbonMott-Schottky effectcatalytic hydrogenationphenylacetyleneChemistryQD1-999ENNanomaterials, Vol 11, Iss 2776, p 2776 (2021) |
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cobalt catalyst N-doped carbon Mott-Schottky effect catalytic hydrogenation phenylacetylene Chemistry QD1-999 |
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cobalt catalyst N-doped carbon Mott-Schottky effect catalytic hydrogenation phenylacetylene Chemistry QD1-999 Yuan Huang Haoting Yan Chenyang Zhang Yize Wang Qinhong Wei Renkun Zhang Interfacial Electronic Effects in Co@N-Doped Carbon Shells Heterojunction Catalyst for Semi-Hydrogenation of Phenylacetylene |
description |
Metal-supported catalyst with high activity and relatively simple preparation method is given priority to industrial production. In this work, this study reported an easily accessible synthesis strategy to prepare Mott-Schottky-type N-doped carbon encapsulated metallic Co (Co@N<sub>p+g</sub>C) catalyst by high-temperature pyrolysis method in which carbon nitride (g-C<sub>3</sub>N<sub>4</sub>) and dopamine were used as support and nitrogen source. The prepared Co@N<sub>p+g</sub>C presented a Mott-Schottky effect; that is, a strong electronic interaction of metallic Co and N-doped carbon shell was constructed to lead to the generation of Mott-Schottky contact. The metallic Co, due to high work function as compared to that of N-doped carbon, transferred electrons to the N-doped outer shell, forming a new contact interface. In this interface area, the positive and negative charges were redistributed, and the catalytic hydrogenation mainly occurred in the area of active charges. The Co@N<sub>p+g</sub>C catalyst showed excellent catalytic activity in the hydrogenation of phenylacetylene to styrene, and the selectivity of styrene reached 82.4%, much higher than those of reference catalysts. The reason for the promoted semi-hydrogenation of phenylacetylene was attributed to the electron transfer of metallic Co, as it was caused by N doping on carbon. |
format |
article |
author |
Yuan Huang Haoting Yan Chenyang Zhang Yize Wang Qinhong Wei Renkun Zhang |
author_facet |
Yuan Huang Haoting Yan Chenyang Zhang Yize Wang Qinhong Wei Renkun Zhang |
author_sort |
Yuan Huang |
title |
Interfacial Electronic Effects in Co@N-Doped Carbon Shells Heterojunction Catalyst for Semi-Hydrogenation of Phenylacetylene |
title_short |
Interfacial Electronic Effects in Co@N-Doped Carbon Shells Heterojunction Catalyst for Semi-Hydrogenation of Phenylacetylene |
title_full |
Interfacial Electronic Effects in Co@N-Doped Carbon Shells Heterojunction Catalyst for Semi-Hydrogenation of Phenylacetylene |
title_fullStr |
Interfacial Electronic Effects in Co@N-Doped Carbon Shells Heterojunction Catalyst for Semi-Hydrogenation of Phenylacetylene |
title_full_unstemmed |
Interfacial Electronic Effects in Co@N-Doped Carbon Shells Heterojunction Catalyst for Semi-Hydrogenation of Phenylacetylene |
title_sort |
interfacial electronic effects in co@n-doped carbon shells heterojunction catalyst for semi-hydrogenation of phenylacetylene |
publisher |
MDPI AG |
publishDate |
2021 |
url |
https://doaj.org/article/0c35296493b844ac905a23334a9517a0 |
work_keys_str_mv |
AT yuanhuang interfacialelectroniceffectsincondopedcarbonshellsheterojunctioncatalystforsemihydrogenationofphenylacetylene AT haotingyan interfacialelectroniceffectsincondopedcarbonshellsheterojunctioncatalystforsemihydrogenationofphenylacetylene AT chenyangzhang interfacialelectroniceffectsincondopedcarbonshellsheterojunctioncatalystforsemihydrogenationofphenylacetylene AT yizewang interfacialelectroniceffectsincondopedcarbonshellsheterojunctioncatalystforsemihydrogenationofphenylacetylene AT qinhongwei interfacialelectroniceffectsincondopedcarbonshellsheterojunctioncatalystforsemihydrogenationofphenylacetylene AT renkunzhang interfacialelectroniceffectsincondopedcarbonshellsheterojunctioncatalystforsemihydrogenationofphenylacetylene |
_version_ |
1718411057352933376 |