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Confinement of Ultrasmall Cu/ZnO_x Nanoparticles in Metal-Organic Frameworks for Selective Methanol Synthesis from Catalytic Hydrogenation of CO_2

机译:超小Cu / ZnO_x纳米粒子在金属有机骨架中的限制,用于CO_2催化加氢选择性合成甲醇

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摘要

The interfaces of Cu/ZnO and Cu/ZrO_2 play vital roles in the hydrogenation of CO_2 to methanol by these composite catalysts. Surface structural reorganization and particle growth during catalysis deleteriously reduce these active interfaces, diminishing both catalytic activities and MeOH selectivities. Here we report the use of preassembled bpy and Zr_6(µ_3O)_4(µy-OH)_4 sites in UiO-bpy metal-organic frameworks (MOFs) to anchor ultrasmall Cu/ZnO_x nanoparticles, thus preventing the agglomeration of Cu NPs and phase separation between Cu and ZnO_x in MOF-cavity-confined Cu/ZnO_x. nanoparticles. The resultant Cu/ZnO_x@MOF catalysts show very high activity with a space-time yield of up to 2.59 g_(MeOH) Kg_(cu)~(-1) h~(-1), 100% selectivity for CO_2 hydrogenation to methanol, and high stability over 100 h. These new types of strong metal-support interactions between metallic nanoparticles and organic chelates/metal-oxo clusters offer new opportunities in fine-tuning catalytic activities and selectivities of metal nanoparticles@MOFs.
机译:这些复合催化剂将Cu / ZnO和Cu / ZrO_2的界面在CO_2加氢成甲醇中起着至关重要的作用。催化过程中的表面结构重组和颗粒生长会有害地减少这些活性界面,从而降低催化活性和MeOH的选择性。在这里,我们报告了在UiO-bpy金属有机框架(MOF)中使用预组装的bpy和Zr_6(µ_3O)_4(µy-OH)_4位点来锚定超小的Cu / ZnO_x纳米颗粒,从而防止了Cu NP的团聚和相分离在MOF腔约束的Cu / ZnO_x中,Cu和ZnO_x之间的关系。纳米粒子。所得的Cu / ZnO_x @ MOF催化剂显示出很高的活性,时空产率高达2.59 g_(MeOH)Kg_(cu)〜(-1)h〜(-1),CO_2加氢制甲醇的选择性为100% ,并且在100小时内具有很高的稳定性。金属纳米颗粒与有机螯合物/金属氧簇之间的新型新型强金属-载体相互作用为微调金属纳米颗粒@MOFs的催化活性和选择性提供了新的机会。

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  • 来源
    《Journal of the American Chemical Society》 |2017年第10期|3834-3840|共7页
  • 作者单位

    Collaborative Innovation Center of Chemistry for Energy Materials, State Key Laboratory of Physical Chemistry of Solid Surfaces, Department of Chemistry, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, PR China;

    Collaborative Innovation Center of Chemistry for Energy Materials, State Key Laboratory of Physical Chemistry of Solid Surfaces, Department of Chemistry, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, PR China;

    Collaborative Innovation Center of Chemistry for Energy Materials, State Key Laboratory of Physical Chemistry of Solid Surfaces, Department of Chemistry, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, PR China;

    Department of Chemistry, University of Chicago, 929 East 57th Street, Chicago, Illnois 60637, United States;

    Collaborative Innovation Center of Chemistry for Energy Materials, State Key Laboratory of Physical Chemistry of Solid Surfaces, Department of Chemistry, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, PR China;

    Collaborative Innovation Center of Chemistry for Energy Materials, State Key Laboratory of Physical Chemistry of Solid Surfaces, Department of Chemistry, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, PR China, Department of Chemistry, University of Chicago, 929 East 57th Street, Chicago, Illnois 60637, United States;

  • 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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