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Pd single-atom catalysts derived from strong metal-support interaction for selective hydrogenation of acetylene
Guo, Yalin1,2; Li, Yangyang1,2; Du, Xiaorui3; Li, Lin1; Jiang, Qike4; Qiao, Botao1
2022-05-19
Source PublicationNANO RESEARCH
ISSN1998-0124
Pages7
Corresponding AuthorJiang, Qike(qike@dicp.ac.cn) ; Qiao, Botao(bqiao@dicp.ac.cn)
AbstractSelective hydrogenation of acetylene in excess ethylene is an important reaction in both fundamental study and practical application. Pd-based catalysts with high intrinsic activity are commonly employed, but usually suffer from low selectivity. Pd single-atom catalysts (SACs) usually exhibit outstanding ethylene selectivity due to the weak pi-bonding ethylene adsorption. However, the preparation of high-loading and stable Pd SACs is still confronted with a great challenge. In this work, we report a simple strategy to fabricate Pd SACs by means of reducing conventional supported Pd catalysts at suitable temperatures to selectively encapsulate the co-existed Pd nanoparticles (NPs)/clusters. This is based on our new finding that single atoms only manifest strong metal-support interaction (SMSI) at higher reduction temperature than that of NPs/clusters. The derived Pd SACs (Pd-1/CeO2 and Pd-1/alpha-Fe2O3) were applied to acetylene selective hydrogenation, exhibiting much improved ethylene selectivity and high stability. This work offers a promising way to develop stable Pd SACs easily.
Keywordselective hydrogenation of acetylene Pd single-atom catalysts (SACs) weak pi-bonding ethylene adsorption strong metal-support interaction (SMSI)
DOI10.1007/s12274-022-4376-5
WOS KeywordETHENE-RICH STREAMS ; PD/CEO2 CATALYSTS ; INTERMETALLIC COMPOUNDS ; PALLADIUM CATALYSTS ; CARBON-MONOXIDE ; CO OXIDATION ; SEMIHYDROGENATION ; TEMPERATURE ; ETHYNE ; PERFORMANCE
Indexed BySCI
Language英语
Funding ProjectNational Natural Science Foundation of China[21972135] ; National Natural Science Foundation of China[21961142006] ; National Natural Science Foundation of China[51701201] ; CAS Project for Young Scientists in Basic Research[YSBR-022] ; National Key Research and Development Program of China[2021YFA1500503]
WOS Research AreaChemistry ; Science & Technology - Other Topics ; Materials Science ; Physics
Funding OrganizationNational Natural Science Foundation of China ; CAS Project for Young Scientists in Basic Research ; National Key Research and Development Program of China
WOS SubjectChemistry, Physical ; Nanoscience & Nanotechnology ; Materials Science, Multidisciplinary ; Physics, Applied
WOS IDWOS:000797782400009
PublisherTSINGHUA UNIV PRESS
Citation statistics
Cited Times:30[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.giec.ac.cn/handle/344007/36516
Collection中国科学院广州能源研究所
Corresponding AuthorJiang, Qike; Qiao, Botao
Affiliation1.Chinese Acad Sci, Dalian Inst Chem Phys, CAS Key Lab Sci & Technol Appl Catalysis, Dalian 116023, Peoples R China
2.Univ Chinese Acad Sci, Beijing 100049, Peoples R China
3.Chinese Acad Sci, Guangzhou Inst Energy Convers, Guangzhou 510640, Peoples R China
4.Chinese Acad Sci, Dalian Inst Chem Phys, Dalian Natl Lab Clean Energy, Dalian 116023, Peoples R China
Recommended Citation
GB/T 7714
Guo, Yalin,Li, Yangyang,Du, Xiaorui,et al. Pd single-atom catalysts derived from strong metal-support interaction for selective hydrogenation of acetylene[J]. NANO RESEARCH,2022:7.
APA Guo, Yalin,Li, Yangyang,Du, Xiaorui,Li, Lin,Jiang, Qike,&Qiao, Botao.(2022).Pd single-atom catalysts derived from strong metal-support interaction for selective hydrogenation of acetylene.NANO RESEARCH,7.
MLA Guo, Yalin,et al."Pd single-atom catalysts derived from strong metal-support interaction for selective hydrogenation of acetylene".NANO RESEARCH (2022):7.
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