Knowledge Management System Of Guangzhou Institute of Energy Conversion, CAS
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 Publication | NANO RESEARCH |
ISSN | 1998-0124 |
Pages | 7 |
Corresponding Author | Jiang, Qike(qike@dicp.ac.cn) ; Qiao, Botao(bqiao@dicp.ac.cn) |
Abstract | Selective 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. |
Keyword | selective hydrogenation of acetylene Pd single-atom catalysts (SACs) weak pi-bonding ethylene adsorption strong metal-support interaction (SMSI) |
DOI | 10.1007/s12274-022-4376-5 |
WOS Keyword | ETHENE-RICH STREAMS ; PD/CEO2 CATALYSTS ; INTERMETALLIC COMPOUNDS ; PALLADIUM CATALYSTS ; CARBON-MONOXIDE ; CO OXIDATION ; SEMIHYDROGENATION ; TEMPERATURE ; ETHYNE ; PERFORMANCE |
Indexed By | SCI |
Language | 英语 |
Funding Project | National 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 Area | Chemistry ; Science & Technology - Other Topics ; Materials Science ; Physics |
Funding Organization | National Natural Science Foundation of China ; CAS Project for Young Scientists in Basic Research ; National Key Research and Development Program of China |
WOS Subject | Chemistry, Physical ; Nanoscience & Nanotechnology ; Materials Science, Multidisciplinary ; Physics, Applied |
WOS ID | WOS:000797782400009 |
Publisher | TSINGHUA UNIV PRESS |
Citation statistics | |
Document Type | 期刊论文 |
Identifier | http://ir.giec.ac.cn/handle/344007/36516 |
Collection | 中国科学院广州能源研究所 |
Corresponding Author | Jiang, Qike; Qiao, Botao |
Affiliation | 1.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. |
Files in This Item: | There are no files associated with this item. |
Items in the repository are protected by copyright, with all rights reserved, unless otherwise indicated.
Edit Comment