Dimitratos Nikolaos, Vilé Gianvito, Albonetti Stefania, Cavani Fabrizio, Fiorio Jhonatan, López Núria, Rossi Liane M, Wojcieszak Robert
Dipartimento di Chimica Industriale "Toso Montanari", Alma Mater Studiorum Università di Bologna, Bologna, Italy.
Center for Chemical Catalysis-C3, Alma Mater Studiorum Università di Bologna, Bologna, Italy.
Nat Rev Chem. 2024 Mar;8(3):195-210. doi: 10.1038/s41570-024-00578-2. Epub 2024 Feb 23.
Catalytic reactions involving molecular hydrogen are at the heart of many transformations in the chemical industry. Classically, hydrogenations are carried out on Pd, Pt, Ru or Ni catalysts. However, the use of supported Au catalysts has garnered attention in recent years owing to their exceptional selectivity in hydrogenation reactions. This is despite the limited understanding of the physicochemical aspects of hydrogen activation and reaction on Au surfaces. A rational design of new improved catalysts relies on making better use of the hydrogenating properties of Au. This Review analyses the strategies utilized to improve hydrogen-Au interactions, from addressing the importance of the Au particle size to exploring alternative mechanisms for H dissociation on Au cations and Au-ligand interfaces. These insights hold the potential to drive future applications of Au catalysis.
涉及分子氢的催化反应是化学工业中许多转化过程的核心。传统上,氢化反应是在钯、铂、钌或镍催化剂上进行的。然而,近年来负载型金催化剂的使用因其在氢化反应中具有特殊的选择性而备受关注。尽管人们对金表面氢活化和反应的物理化学方面了解有限。合理设计新型改进催化剂依赖于更好地利用金的氢化特性。本综述分析了用于改善氢与金相互作用的策略,从探讨金颗粒尺寸的重要性到探索金阳离子和金 - 配体界面上氢解离的替代机制。这些见解有可能推动金催化的未来应用。