Han Lili, Cheng Hao, Liu Wei, Li Haoqiang, Ou Pengfei, Lin Ruoqian, Wang Hsiao-Tsu, Pao Chih-Wen, Head Ashley R, Wang Chia-Hsin, Tong Xiao, Sun Cheng-Jun, Pong Way-Faung, Luo Jun, Zheng Jin-Cheng, Xin Huolin L
Department of Physics and Astronomy, University of California, Irvine, CA, USA.
School of Materials Science and Engineering, Tianjin Key Lab of Photoelectric Materials & Devices, Tianjin University of Technology, Tianjin, China.
Nat Mater. 2022 Jun;21(6):681-688. doi: 10.1038/s41563-022-01252-y. Epub 2022 May 23.
Atomically dispersed single-atom catalysts have the potential to bridge heterogeneous and homogeneous catalysis. Dozens of single-atom catalysts have been developed, and they exhibit notable catalytic activity and selectivity that are not achievable on metal surfaces. Although promising, there is limited knowledge about the boundaries for the monometallic single-atom phase space, not to mention multimetallic phase spaces. Here, single-atom catalysts based on 37 monometallic elements are synthesized using a dissolution-and-carbonization method, characterized and analysed to build the largest reported library of single-atom catalysts. In conjunction with in situ studies, we uncover unified principles on the oxidation state, coordination number, bond length, coordination element and metal loading of single atoms to guide the design of single-atom catalysts with atomically dispersed atoms anchored on N-doped carbon. We utilize the library to open up complex multimetallic phase spaces for single-atom catalysts and demonstrate that there is no fundamental limit on using single-atom anchor sites as structural units to assemble concentration-complex single-atom catalyst materials with up to 12 different elements. Our work offers a single-atom library spanning from monometallic to concentration-complex multimetallic materials for the rational design of single-atom catalysts.
原子分散的单原子催化剂有潜力弥合多相催化和均相催化之间的差距。目前已经开发出了几十种单原子催化剂,它们展现出了在金属表面无法实现的显著催化活性和选择性。尽管前景广阔,但对于单金属单原子相空间的边界,我们所知有限,更不用说多金属相空间了。在此,我们采用溶解-碳化法合成了基于37种单金属元素的单原子催化剂,并对其进行表征和分析,构建了目前报道的最大的单原子催化剂库。结合原位研究,我们揭示了关于单原子的氧化态、配位数、键长、配位元素和金属负载量的统一原则,以指导将原子分散的原子锚定在氮掺杂碳上的单原子催化剂的设计。我们利用这个库为单原子催化剂开辟了复杂的多金属相空间,并证明将单原子锚定位点用作结构单元来组装包含多达12种不同元素的浓度复杂的单原子催化剂材料没有根本限制。我们的工作提供了一个从单金属到浓度复杂的多金属材料的单原子库,用于合理设计单原子催化剂。
Acc Chem Res. 2019-1-22
J Colloid Interface Sci. 2022-10-15
Proc Natl Acad Sci U S A. 2024-3-5
Nat Commun. 2020-8-13
Angew Chem Int Ed Engl. 2025-6-17
Nat Commun. 2025-1-28
Sci Adv. 2025-1-17
Nat Commun. 2025-1-10