GIEC OpenIR
In-situ facile synthesis novel N-doped thin graphene layer encapsulated Pd@N/C catalyst for semi-hydrogenation of alkynes
Liu, Jianguo1; Lin, Shanshan2,3; Sun, Jiangming2,4; Ma, Longlong1
2022
Source PublicationJOURNAL OF CATALYSIS
ISSN0021-9517
Volume405Pages:553-560
Corresponding AuthorLiu, Jianguo(liujg@seu.edu.cn) ; Ma, Longlong(mall@seu.edu.cn)
AbstractTransition metal-catalyzed semi-hydrogenation of alkynes has become one of the most popular methods for alkene synthesis. Specifically, the noble metal Pd, Rh, and Ru-based heterogeneous catalysts have been widely studied and utilized in both academia and industry. But the supported noble metal catalysts are generally suffering from leaching or aggregation during harsh reaction conditions, which resulting low catalytic reactivity and stability. Herein, we reported the facile synthesis of nitrogen doped graphene encapsulated Pd catalyst and its application in the chemo-selective semi-hydrogenation of alkynes. The graphene layer served as "bulletproof" over the active Pd Nano metal species, which was confirmed by Xray and TEM analysis, enhanced the catalytic stability during the reaction conditions. The optimized prepared Pd@N/C catalyst showed excellent efficiency in semi-hydrogenation of phenylacetylene and other types of alkynes with un-functionalized or functionalized substituents, including the hydrogenation sensitive functional groups (NO2, ester, and halogen). (C) 2021 Elsevier Inc. All rights reserved.
KeywordN doped Graphene Pd@N/C Semi-hydrogenation Alkynes
DOI10.1016/j.jcat.2021.11.012
WOS KeywordETHENE-RICH STREAMS ; SELECTIVE HYDROGENATION ; PALLADIUM CATALYSTS ; CARBON SPHERES ; CORE-SHELL ; ACETYLENE ; NANOPARTICLES ; EFFICIENT ; REDUCTION ; ETHYLENE
Indexed BySCI
Language英语
Funding ProjectNational Key R&D Program of China[2018YFB1501500] ; National Natural Science Foundation of China[51976225]
WOS Research AreaChemistry ; Engineering
Funding OrganizationNational Key R&D Program of China ; National Natural Science Foundation of China
WOS SubjectChemistry, Physical ; Engineering, Chemical
WOS IDWOS:000784450000008
PublisherACADEMIC PRESS INC ELSEVIER SCIENCE
Citation statistics
Cited Times:6[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.giec.ac.cn/handle/344007/36243
Collection中国科学院广州能源研究所
Corresponding AuthorLiu, Jianguo; Ma, Longlong
Affiliation1.Southeast Univ, Sch Energy & Environm, Key Lab Energy Thermal Convers & Control, Minist Educ, Nanjing 210096, Peoples R China
2.Chinese Acad Sci, Guangzhou Inst Energy Convers, CAS Key Lab Renewable Energy, Guangdong Prov Key Lab New & Renewable Energy Res, Guangzhou 510640, Peoples R China
3.Univ Chinese Acad Sci, Beijing 100049, Peoples R China
4.Univ Sci & Technol China, Sch Energy Sci & Engn, Hefei 230026, Peoples R China
Recommended Citation
GB/T 7714
Liu, Jianguo,Lin, Shanshan,Sun, Jiangming,et al. In-situ facile synthesis novel N-doped thin graphene layer encapsulated Pd@N/C catalyst for semi-hydrogenation of alkynes[J]. JOURNAL OF CATALYSIS,2022,405:553-560.
APA Liu, Jianguo,Lin, Shanshan,Sun, Jiangming,&Ma, Longlong.(2022).In-situ facile synthesis novel N-doped thin graphene layer encapsulated Pd@N/C catalyst for semi-hydrogenation of alkynes.JOURNAL OF CATALYSIS,405,553-560.
MLA Liu, Jianguo,et al."In-situ facile synthesis novel N-doped thin graphene layer encapsulated Pd@N/C catalyst for semi-hydrogenation of alkynes".JOURNAL OF CATALYSIS 405(2022):553-560.
Files in This Item:
There are no files associated with this item.
Related Services
Recommend this item
Bookmark
Usage statistics
Export to Endnote
Google Scholar
Similar articles in Google Scholar
[Liu, Jianguo]'s Articles
[Lin, Shanshan]'s Articles
[Sun, Jiangming]'s Articles
Baidu academic
Similar articles in Baidu academic
[Liu, Jianguo]'s Articles
[Lin, Shanshan]'s Articles
[Sun, Jiangming]'s Articles
Bing Scholar
Similar articles in Bing Scholar
[Liu, Jianguo]'s Articles
[Lin, Shanshan]'s Articles
[Sun, Jiangming]'s Articles
Terms of Use
No data!
Social Bookmark/Share
All comments (0)
No comment.
 

Items in the repository are protected by copyright, with all rights reserved, unless otherwise indicated.