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A General Strategy for Fabricating Isolated Single Metal Atomic Site Catalysts in Y Zeolite

机译:在Y型沸石中制备孤立的单金属原子部位催化剂的一般策略。

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摘要

Exploring high-performance zeolite-supported metal catalysts is of great significance. Herein, we develop a strategy for fabricating isolated single metal atomic site catalysts in Y zeolite (M-ISAS@Y, M = Pt, Pd, Ru, Rh, Co, Ni, Cu) by in situ separating and confining a metal-ethanediamine complex into beta-cages during the crystallization process followed by thermal treatment. The M-ISAS are stabilized by skeletal oxygens of Y zeolite, and the crystallinity, porosity, and large surface area are well inherited in m-ISASp Y. As a demonstration, acidic Pt-ISAS@Y is used for n-hexane isomerization involving consecutive catalytic dehydrogenation/hydrogenation on Pt-ISAS and isomerization on Bronsted acid sites. The turnover frequency value of Pt-ISAS reaches 727 h(-1), 5 times more than Pt nanoparticles (similar to 3.5 nm), with a total isomer selectivity of more than 98%. This strategy provides a convenient route to fabricate promising zeolite-based M-ISAS catalysts for industrial applications.
机译:探索高性能的沸石负载金属催化剂具有重要意义。本文中,我们开发了一种通过原位分离和封闭金属乙二胺在Y型沸石(M-ISAS @ Y,M = Pt,Pd,Ru,Rh,Co,Ni,Cu)中制备孤立的单金属原子中心催化剂的策略在结晶过程中进行热处理,然后将其复合成β笼。 M-ISAS由Y沸石的骨架氧稳定,在m-ISASp Y中很好地继承了结晶度,孔隙率和大表面积。作为演示,酸性Pt-ISAS @ Y用于正己烷异构化,包括在Pt-ISAS上进行连续的催化脱氢/加氢,并在布朗斯台德酸位上进行异构化。 Pt-ISAS的周转频率值达到727 h(-1),是Pt纳米颗粒(约3.5 nm)的5倍以上,总异构体选择性超过98%。该策略提供了一条方便的途径,可用于制造工业应用中有前景的基于沸石的M-ISAS催化剂。

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  • 来源
    《Journal of the American Chemical Society》 |2019年第23期|9305-9311|共7页
  • 作者单位

    Tsinghua Univ, Dept Chem, Beijing 100084, Peoples R China|Chinese Acad Sci, Shanghai Inst Appl Phys, Shanghai Synchrotron Radiat Facil, Shanghai 201800, Peoples R China;

    Tsinghua Univ, Dept Chem, Beijing 100084, Peoples R China|Chinese Acad Sci, Shanghai Inst Appl Phys, Shanghai Synchrotron Radiat Facil, Shanghai 201800, Peoples R China;

    Shanghai Jiao Tong Univ, Sch Chem & Chem Engn, Shanghai 200240, Peoples R China;

    China Univ Petr, State Key Lab Heavy Oil Proc, Key Lab Catalysis, Qingdao 266580, Shandong, Peoples R China;

    Beijing Computat Sci Res Ctr, Beijing 100193, Peoples R China;

    East China Normal Univ, Sch Chem & Mol Engn, Shanghai 200062, Peoples R China;

    Anhui Normal Univ, Coll Chem & Mat Sci, Wuhu 241000, Anhui, Peoples R China;

    Tsinghua Univ, Dept Chem, Beijing 100084, Peoples R China;

    Tsinghua Univ, Dept Chem, Beijing 100084, Peoples R China;

    Chinese Acad Sci, Inst Phys, Beijing 100190, Peoples R China;

    Chinese Acad Sci, Inst Phys, Beijing 100190, Peoples R China;

    Chinese Acad Sci, Inst High Energy Phys, Beijing Synchrotron Radiat Facil, Beijing 100049, Peoples R China;

    Chinese Acad Sci, Shanghai Inst Appl Phys, Shanghai Synchrotron Radiat Facil, Shanghai 201800, Peoples R China;

    East China Normal Univ, Sch Chem & Mol Engn, Shanghai 200062, Peoples R China;

    Tsinghua Univ, Dept Chem, Beijing 100084, Peoples R China;

    Tsinghua Univ, Dept Chem, Beijing 100084, Peoples R China;

    Tsinghua Univ, Dept Chem, Beijing 100084, Peoples R China;

    China Univ Petr, State Key Lab Heavy Oil Proc, Key Lab Catalysis, Qingdao 266580, Shandong, Peoples R China;

    Beijing Computat Sci Res Ctr, Beijing 100193, Peoples R China;

    Shanghai Jiao Tong Univ, Sch Chem & Chem Engn, Shanghai 200240, Peoples R China;

    Tsinghua Univ, Dept Chem, Beijing 100084, Peoples R China;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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  • 入库时间 2022-08-18 04:18:05

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