Wang Qilun, Cheng Yaqi, Yang Hong Bin, Su Chenliang, Liu Bin
Department of Materials Science and Engineering, City University of Hong Kong, Hong Kong SAR, China.
International Collaboration Laboratory of 2D Materials for Optoelectronics Science and Technology of Ministry of Education, Institute of Microscale Optoelectronics, Shenzhen University, Shenzhen, China.
Nat Nanotechnol. 2024 Oct;19(10):1442-1451. doi: 10.1038/s41565-024-01716-z. Epub 2024 Aug 5.
Single-atom catalysts (SACs) have attracted considerable research interest owing to their combined merits of homogeneous and heterogeneous catalysts. However, the uniform and isolated active sites of SACs fall short in catalysing complex chemical processes that simultaneously involve multiple intermediates. In this Review, we highlight an emerging class of catalysts with adjacent binary active centres, which is called integrative catalytic pairs (ICPs), showing not only atomic-scale site-to-site electronic interactions but also synergistic catalytic effects. Compared with SACs or their derivative dual-atom catalysts (DACs), multi-interactive intermediates on ICPs can overcome kinetic barriers, adjust reaction pathways and break the universal linear scaling relations as the smallest active units. Starting from this active-site design principle, each single active atom can be considered as a brick to further build integrative catalytic clusters (ICCs) with desirable configurations, towards trimer or even larger multi-atom units depending on the requirement of a given reaction.
单原子催化剂(SACs)因其兼具均相催化剂和多相催化剂的优点而引起了广泛的研究兴趣。然而,SACs均匀且孤立的活性位点在催化同时涉及多种中间体的复杂化学过程时存在不足。在本综述中,我们重点介绍了一类新兴的具有相邻二元活性中心的催化剂,即整合催化对(ICP),它不仅显示出原子尺度的位点间电子相互作用,还具有协同催化效应。与SACs或其衍生的双原子催化剂(DACs)相比,ICP上的多相互作用中间体可以作为最小的活性单元克服动力学障碍、调整反应途径并打破普遍的线性标度关系。基于这种活性位点设计原则,每个单个活性原子都可被视为一块“砖”,以进一步构建具有理想构型的整合催化簇(ICC),根据特定反应的需求形成三聚体甚至更大的多原子单元。