| Literature DB >> 31356053 |
Yonggang Yao1, Zhennan Huang2, Pengfei Xie3, Tangyuan Li1, Steven D Lacey1, Miaolun Jiao1, Hua Xie1, Kun Kelvin Fu1, Rohit Jiji Jacob4, Dylan Jacob Kline4, Yong Yang4, Michael R Zachariah4, Chao Wang3, Reza Shahbazian-Yassar2, Liangbing Hu1.
Abstract
Supported metallic nanoclusters (NCs, < 2 nm) are of great interests in various catalytic reactions with enhanced activities and selectivities, yet it is still challenging to efficiently and controllably synthesize ultrasmall NCs with a high-dispersal density. Here we report the in situ synthesis of surfactant-free, ultrasmall, and uniform NCs via a rapid thermal shock on defective substrates. This is achieved by using high-temperature synthesis with extremely fast kinetics while limiting the synthesis time down to milliseconds (e.g., ∼1800 K for 55 ms) to avoid aggregation. Through defect engineering and optimized loading, the particle size can be robustly tuned from >50 nm nanoparticles to <1 nm uniform NCs with a high-dispersal density. We demonstrate that the ultrasmall NCs exhibit drastically improved activities for catalytic CO oxidation as compared to their nanoparticulated counterparts. In addition, the reported method shows generality in synthesizing most metallic NCs (e.g., Pt, Ru, Ir, Ni) in an extremely facile and efficient manner. The ultrafast and controllable synthesis of uniform, high-density, and size-controllable NCs paves the way for the utilization and nanomanufacturing of NCs for a range of catalytic reactions.Keywords: CO oxidation; defects; high-density dispersion; nanoclusters; thermal shock
Year: 2019 PMID: 31356053 DOI: 10.1021/acsami.9b07198
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229