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镍催化氢化反应的原位壳层隔离纳米粒子增强拉曼光谱

In Situ Shell-Isolated Nanoparticle-Enhanced Raman Spectroscopy of Nickel-Catalyzed Hydrogenation Reactions.

作者信息

Wondergem Caterina S, Kromwijk Josepha J G, Slagter Mark, Vrijburg Wilbert L, Hensen Emiel J M, Monai Matteo, Vogt Charlotte, Weckhuysen Bert M

机构信息

Inorganic Chemistry and Catalysis Group Debye Institute for Nanomaterials Science, Utrecht University, Universiteitsweg 99, 3584 CG, Utrecht, The Netherlands.

Laboratory of Inorganic Materials and Catalysis, Eindhoven University of Technology P.O. Box 513, 5600 MB, Eindhoven, The Netherlands.

出版信息

Chemphyschem. 2020 Apr 2;21(7):625-632. doi: 10.1002/cphc.201901162. Epub 2020 Feb 4.

Abstract

Synthesis methods to prepare lower transition metal catalysts and specifically Ni for Shell-Isolated Nanoparticle-Enhanced Raman Spectroscopy (SHINERS) are explored. Impregnation, colloidal deposition, and spark ablation have been investigated as suitable synthesis routes to prepare SHINERS-active Ni/Au@SiO catalyst/Shell-Isolated Nanoparticles (SHINs). Ni precursors are confirmed to be notoriously difficult to reduce and the temperatures required are generally harsh enough to destroy SHINs, rendering SHINERS experiments on Ni infeasible using this approach. For colloidally synthesized Ni nanoparticles deposited on Au@SiO SHINs, stabilizing ligands first need to be removed before application is possible in catalysis. The required procedure results in transformation of the metallic Ni core to a fully oxidized metal nanoparticle, again too challenging to reduce at temperatures still compatible with SHINs. Finally, by use of spark ablation we were able to prepare metallic Ni catalysts directly on Au@SiO SHINs deposited on a Si wafer. These Ni/Au@SiO catalyst/SHINs were subsequently successfully probed with several molecules (i. e. CO and acetylene) of interest for heterogeneous catalysis, and we show that they could be used to study the in situ hydrogenation of acetylene. We observe the interaction of acetylene with the Ni surface. This study further illustrates the true potential of SHINERS by opening the door to studying industrially relevant reactions under in situ or operando reaction conditions.

摘要

探索了制备用于壳层隔离纳米粒子增强拉曼光谱(SHINERS)的低价过渡金属催化剂,特别是镍催化剂的合成方法。浸渍法、胶体沉积法和火花烧蚀法已被研究作为制备具有SHINERS活性的Ni/Au@SiO催化剂/壳层隔离纳米粒子(SHINs)的合适合成路线。已证实镍前驱体极难还原,所需温度通常苛刻到足以破坏SHINs,使得使用这种方法对镍进行SHINERS实验不可行。对于胶体合成的沉积在Au@SiO SHINs上的镍纳米粒子,在催化应用之前首先需要去除稳定配体。所需的程序导致金属镍核转变为完全氧化的金属纳米粒子,在仍与SHINs兼容的温度下再次还原也极具挑战性。最后,通过使用火花烧蚀,我们能够直接在沉积在硅片上的Au@SiO SHINs上制备金属镍催化剂。这些Ni/Au@SiO催化剂/SHINs随后成功地用几种用于多相催化的感兴趣分子(即CO和乙炔)进行了探测,并且我们表明它们可用于研究乙炔的原位加氢反应。我们观察到乙炔与镍表面的相互作用。这项研究通过开启在原位或操作反应条件下研究工业相关反应的大门,进一步说明了SHINERS的真正潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/482a/7187311/568ae80f4adc/CPHC-21-625-g001.jpg

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