Source abstract
Abstract
Abstract Supported metal nanoparticles play key roles in nanoelectronics, sensors, energy storage/conversion, and catalysts for the sustainable production of fuels and chemicals. Direct observation of the dynamic processes of nanocatalysts at high temperatures and the confinement of supports is of great significance to investigate nanoparticle structure and functions for practical utilization. Here, in situ high‐resolution transmission electron microscopy photos and videos are combined with dynamics simulations to reveal the real‐time dynamic behavior of Pt nanocatalysts at operation temperatures. Amorphous Pt surface on moving and deforming particles is the working structure during the high operation temperature rather than a static crystal surface and immobilization on supports as proposed before. The free rearrangement of the shape of Pt nanoparticles allows them to pass through narrow windows, which is generally considered to immobilize the particles. The Pt particles, no matter what their sizes, prefer to stay inside nanopores even when they are fast moving near an opening at temperatures up to 900 °C. The porous confinement also blocks the sintering of the particles under the confinement size of pores. These contribute to the continuous high activity and stability of Pt nanocatalysts inside nanoporous supports during a long‐term evaluation of catalytic reforming reaction.
Source: crossref · Quality: baseline
Affiliations
Laboratory for Catalysis Engineering School of Chemical and Biomolecular Engineering The University of Sydney NSW 2006 Australia
Department CAS Key Laboratory for Nanosystem and Hierarchy Fabrication CAS Center for Excellence in Nanoscience National Center for Nanoscience and Technology Chinese Academy of Sciences Beijing 100190 China
The University of Sydney Nano Institute NSW 2006 Australia
University of Chinese Academy of Sciences Beijing 100049 China
School of Physics The University of Sydney NSW 2006 Australia
School of Aerospace Mechanical and Mechatronic Engineering The University of Sydney NSW 2006 Australia
Funding
Australian Research Council · National Natural Science Foundation of China