Patterning the consecutive Pd3 to Pd1 on Pd2Ga surface via temperature-promoted reactive metal-support interaction
文献类型:期刊论文
作者 | Niu, Yiming2,4; Wang, Yongzhao2,4; Chen, Junnan2,4; Li, Shiyan1; Huang, Xing3,5; Willinger, Marc-Georg3,6; Zhang, Wei7,8; Liu, Yuefeng1; Zhang, Bingsen1,2,4 |
刊名 | SCIENCE ADVANCES |
出版日期 | 2022-12-07 |
卷号 | 8期号:49页码:10 |
ISSN号 | 2375-2548 |
DOI | 10.1126/sciadv.abq5751 |
通讯作者 | Zhang, Wei(weizhang@jlu.edu.cn) ; Liu, Yuefeng(yuefeng.liu@dicp.ac.cn) ; Zhang, Bingsen(bszhang@imr.ac.cn) |
英文摘要 | Atom-by-atom control of a catalyst surface is a central yet challenging topic in heterogeneous catalysis, which enables precisely confined adsorption and oriented approach of reactant molecules. Here, exposed surfaces with either consecutive Pd trimers (Pd3) or isolated Pd atoms (Pd1) are architected for Pd2Ga intermetallic nano -particles (NPs) using reactive metal-support interaction (RMSI). At elevated temperatures under hydrogen, in situ atomic-scale transmission electron microscopy directly visualizes the refacetting of Pd2Ga NPs from ener-getically favorable (013)/(020) facets to (011)/(002). Infrared spectroscopy and acetylene hydrogenation reaction complementarily confirm the evolution from consecutive Pd3 to Pd1 sites of Pd2Ga catalysts with the concurrent fingerprinting CO adsorption and featured reactivities. Through theoretical calculations and modeling, we reveal that the restructured Pd2Ga surface results from the preferential arrangement of additionally reduced Ga atoms on the surface. Our work provides previously unidentified mechanistic insight into temperature -pro-moted RMSI and possible solutions to control and rearrange the surface atoms of supported intermetallic catalyst. |
资助项目 | National Natural Science Foundation of China[22072164] ; National Natural Science Foundation of China[22002173] ; National Natural Science Foundation of China[52161145403] ; National Natural Science Foundation of China[51932005] ; National Natural Science Foundation of China[21761132025] ; National Natural Science Foundation of China[21972140] ; Postdoctoral Science Foundation of China[2020M680999] ; LiaoNing Revitalization Talents Program[XLYC1807175] ; LiaoNing Revitalization Talents Program[XLYC1907053] ; Research Fund of SYNL |
WOS研究方向 | Science & Technology - Other Topics |
语种 | 英语 |
出版者 | AMER ASSOC ADVANCEMENT SCIENCE |
WOS记录号 | WOS:000913179000011 |
资助机构 | National Natural Science Foundation of China ; Postdoctoral Science Foundation of China ; LiaoNing Revitalization Talents Program ; Research Fund of SYNL |
源URL | [http://ir.imr.ac.cn/handle/321006/175115] |
专题 | 金属研究所_中国科学院金属研究所 |
通讯作者 | Zhang, Wei; Liu, Yuefeng; Zhang, Bingsen |
作者单位 | 1.Chinese Acad Sci, Dalian Inst Chem Phys, Dalian Natl Lab Clean Energy, Dalian 116023, Peoples R China 2.Chinese Acad Sci, Inst Met Res, Shenyang Natl Lab Mat Sci, Shenyang 110016, Peoples R China 3.Swiss Fed Inst Technol, Sci Ctr Opt & Electron Microscopy, Otto Stern Weg 3, CH-8093 Zurich, Switzerland 4.Univ Sci & Technol China, Dept Mat Sci & Engn, Shenyang 110016, Peoples R China 5.Fuzhou Univ, Coll Chem, Fuzhou 36108, Peoples R China 6.Tech Univ Munich, Sch Nat Sci NAT, Dept Chem, Lichtenbergstr 4, D-85747 Garching, Germany 7.Jilin Univ, Sch Mat Sci & Engn, Key Lab Automobile Mat MOE, Changchun 130012, Peoples R China 8.Jilin Univ, Electron Microscopy Ctr, Jilin Prov Int Cooperat Key Lab High Efficiency Cl, Changchun 130012, Peoples R China |
推荐引用方式 GB/T 7714 | Niu, Yiming,Wang, Yongzhao,Chen, Junnan,et al. Patterning the consecutive Pd3 to Pd1 on Pd2Ga surface via temperature-promoted reactive metal-support interaction[J]. SCIENCE ADVANCES,2022,8(49):10. |
APA | Niu, Yiming.,Wang, Yongzhao.,Chen, Junnan.,Li, Shiyan.,Huang, Xing.,...&Zhang, Bingsen.(2022).Patterning the consecutive Pd3 to Pd1 on Pd2Ga surface via temperature-promoted reactive metal-support interaction.SCIENCE ADVANCES,8(49),10. |
MLA | Niu, Yiming,et al."Patterning the consecutive Pd3 to Pd1 on Pd2Ga surface via temperature-promoted reactive metal-support interaction".SCIENCE ADVANCES 8.49(2022):10. |
入库方式: OAI收割
来源:金属研究所
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