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在多相催化中控制形状的纳米结构。

Shape-controlled nanostructures in heterogeneous catalysis.

机构信息

Department of Chemistry, University of California, Riverside, CA 92521 (USA).

出版信息

ChemSusChem. 2013 Oct;6(10):1797-820. doi: 10.1002/cssc.201300398. Epub 2013 Sep 6.

Abstract

Nanotechnologies have provided new methods for the preparation of nanomaterials with well-defined sizes and shapes, and many of those procedures have been recently implemented for applications in heterogeneous catalysis. The control of nanoparticle shape in particular offers the promise of a better definition of catalytic activity and selectivity through the optimization of the structure of the catalytic active site. This extension of new nanoparticle synthetic procedures to catalysis is in its early stages, but has shown some promising leads already. Here, we survey the major issues associated with this nanotechnology-catalysis synergy. First, we discuss new possibilities associated with distinguishing between the effects originating from nanoparticle size versus those originating from nanoparticle shape. Next, we survey the information available to date on the use of well-shaped metal and non-metal nanoparticles as active phases to control the surface atom ensembles that define the catalytic site in different catalytic applications. We follow with a brief review of the use of well-defined porous materials for the control of the shape of the space around that catalytic site. A specific example is provided to illustrate how new selective catalysts based on shape-defined nanoparticles can be designed from first principles by using fundamental mechanistic information on the reaction of interest obtained from surface-science experiments and quantum-mechanics calculations. Finally, we conclude with some thoughts on the state of the field in terms of the advances already made, the future potentials, and the possible limitations to be overcome.

摘要

纳米技术为制备具有明确尺寸和形状的纳米材料提供了新方法,其中许多方法最近已应用于多相催化领域。特别是控制纳米颗粒的形状有望通过优化催化活性位点的结构来更好地定义催化活性和选择性。将新的纳米颗粒合成方法扩展到催化领域还处于早期阶段,但已经显示出了一些有前途的线索。在这里,我们调查了与这种纳米技术-催化协同作用相关的主要问题。首先,我们讨论了区分源自纳米颗粒尺寸的效应与源自纳米颗粒形状的效应的新可能性。接下来,我们调查了迄今为止关于使用形状良好的金属和非金属纳米颗粒作为活性相来控制不同催化应用中定义催化位点的表面原子集合的信息。我们简要回顾了使用定义良好的多孔材料来控制催化位点周围空间形状的情况。提供了一个具体的例子来说明如何通过使用从表面科学实验和量子力学计算获得的关于感兴趣反应的基本机理信息,从第一性原理设计基于形状定义的纳米颗粒的新型选择性催化剂。最后,我们根据已经取得的进展、未来的潜力以及可能需要克服的限制,对该领域的状况进行了一些思考。

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