Inorganic Chemistry and Catalysis, Debye institute for Nanomaterials, Utrecht University, Utrecht, Netherlands.
Schulich Faculty of Chemistry, Technion - Israel Institute of Technology, Haifa, Israel.
Nat Rev Chem. 2022 Feb;6(2):89-111. doi: 10.1038/s41570-021-00340-y. Epub 2022 Jan 6.
Catalysis is at the core of chemistry and has been essential to make all the goods surrounding us, including fuels, coatings, plastics and other functional materials. In the near future, catalysis will also be an essential tool in making the shift from a fossil-fuel-based to a more renewable and circular society. To make this reality, we have to better understand the fundamental concept of the active site in catalysis. Here, we discuss the physical meaning - and deduce the validity and, therefore, usefulness - of some common approaches in heterogeneous catalysis, such as linking catalyst activity to a 'turnover frequency' and explaining catalytic performance in terms of 'structure sensitivity' or 'structure insensitivity'. Catalytic concepts from the fields of enzymatic and homogeneous catalysis are compared, ultimately realizing that the struggle that one encounters in defining the active site in most solid catalysts is likely the one we must overcome to reach our end goal: tailoring the precise functioning of the active sites with respect to many different parameters to satisfy our ever-growing needs. This article ends with an outlook of what may become feasible within the not-too-distant future with modern experimental and theoretical tools at hand.
催化是化学的核心,对于制造我们周围所有的物品,包括燃料、涂料、塑料和其他功能材料,都是必不可少的。在不久的将来,催化也将成为从基于化石燃料的社会向更可再生和循环的社会转变的重要工具。为了实现这一目标,我们必须更好地理解催化中活性位的基本概念。在这里,我们讨论了一些常见的非均相催化方法的物理意义——并推断出它们的有效性和因此的有用性,例如将催化剂活性与“周转率”联系起来,并根据“结构敏感性”或“结构不敏感性”来解释催化性能。比较了酶催化和均相催化领域的催化概念,最终认识到,在定义大多数固体催化剂中的活性位时遇到的困难,很可能是我们必须克服的困难,以达到我们的最终目标:根据许多不同的参数来精确调整活性位的功能,以满足我们不断增长的需求。本文以现代实验和理论工具为背景,展望了在不久的将来可能实现的目标。