Duan Manyi, Yu Jian, Meng Jun, Zhu Beien, Wang Yong, Gao Yi
College of Physics and Electronic Engineering, Sichuan Normal University, Chengdu, 610101, China.
Division of Interfacial Water and Key Laboratory of Interfacial Physics and Technology, Shanghai Institute of Applied Physics, Chinese Academy of Sciences, Shanghai, 201800, China.
Angew Chem Int Ed Engl. 2018 May 28;57(22):6464-6469. doi: 10.1002/anie.201800925. Epub 2018 May 3.
Metal nanoparticles (NPs) dispersed on a high-surface-area support are normally used as heterogeneous catalysts. Recent in situ experiments have shown that structure reconstruction of the NP occurs in real catalysis. However, the role played by supports in these processes is still unclear. Supports can be very important in real catalysis because of the new active sites at the perimeter interface between nanoparticles and supports. Herein, using a developed multiscale model coupled with in situ spherical aberration-corrected (Cs-corrected) TEM experiments, we show that the interaction between the support and the gas environment greatly changes the contact surface area between the metal and support, which further leads to the critical change in the perimeter interface. The dynamic changes of the interface in reactive environments can thus be predicted and be included in the rational design of supported metal nanocatalysts. In particular, our multiscale model shows quantitative consistency with experimental observations. This work offers possibilities for obtaining atomic-scale structures and insights beyond the experimental limits.
分散在高比表面积载体上的金属纳米颗粒(NPs)通常用作多相催化剂。最近的原位实验表明,在实际催化过程中会发生纳米颗粒的结构重构。然而,载体在这些过程中所起的作用仍不清楚。由于纳米颗粒与载体之间的周边界面处会产生新的活性位点,因此载体在实际催化中可能非常重要。在此,我们使用一个开发的多尺度模型,并结合原位球差校正(Cs校正)TEM实验,表明载体与气体环境之间的相互作用极大地改变了金属与载体之间的接触表面积,进而导致周边界面发生关键变化。因此,可以预测反应环境中界面的动态变化,并将其纳入负载型金属纳米催化剂的合理设计中。特别是,我们的多尺度模型与实验观察结果显示出定量一致性。这项工作为获得超越实验极限的原子尺度结构和见解提供了可能性。