Abstract
The treatment of emissions from natural gas engines is an important area of research since methane is a potent greenhouse gas. The benchmark catalysts, based on Pd, still face challenges such as water poisoning and long-term stability. Here we report an approach for catalyst synthesis that relies on the trapping of metal single atoms on the support surface, in thermally stable form, to modify the nature of further deposited metal/metal oxide. By anchoring Pt ions on a catalyst support we can tailor the morphology of the deposited phase. In particular, two-dimensional (2D) rafts of PdOx are formed, resulting in higher reaction rates and improved water tolerance during methane oxidation. The results show that modifying the support by trapping single atoms could provide an important addition to the toolkit of catalyst designers for controlling the nucleation and growth of metal and metal oxide clusters in heterogeneous catalysts. [Figure not available: see fulltext.].
Original language | English |
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Pages (from-to) | 830-839 |
Number of pages | 10 |
Journal | Nature Catalysis |
Volume | 4 |
Issue number | 10 |
DOIs | |
State | Published - Oct 2021 |
Externally published | Yes |
Funding
The catalyst synthesis and characterization via transmission electron microscopy (TEM) and DRIFTS was partly supported by DOE/BES Catalysis Science program, grant no. DE-FG02-05ER15712. Reactivity measurements were supported by the US Department of Energy (DOE) Office of Energy Efficiency and Renewable Energy under the Advanced Manufacturing Office, award number DE-LC 000L059 and from the Vehicle Technologies Office. H.X. acknowledges support from the National High-Level Young Talents programme and National Natural Science Foundation of China (grant nos. 22072118 and 2212100020). The computational work on catalysis was supported by the National Natural Science Foundation of China (grant nos. 21673040 and 21973013) and Air Force Office of Scientific Research (grant no. FA9550-18-1-0413). S.S.C. acknowledges support from the Center for Integrated Nanotechnologies (CINT), a user facility operated for the US DOE Office of Science where some of the characterization was performed. J.H. thanks National Natural Science Foundation of China (grant nos. 51772262, U20A20336 and 21935009), Natural Science Foundation of Hebei Province (grant no. B2020203037) and the Hunan Innovation Team (grant no. 2018RS3091) for financial support of this research. The characterization via XAS was supported by the National Science Foundation under Cooperative Agreement no. EEC-1647722 (CISTAR). Use of the Advanced Photon Source was supported by the US DOE Office of Basic Energy Sciences under contract no. DE-AC02-06CH11357. MRCAT operations, beamline 10-BM and 10-ID, are supported by the DOE and the MRCAT member institutions. We thank A. Genc, H. Pham and F. Shi for assistance with the TEM measurements that were performed, in part, at Thermo Fisher and at the University of Illinois at Chicago, Research Resources Center, Electron Microscopy Core. K.L. and S.S.C. acknowledge support from Sandia National Laboratories, a multi-mission laboratory managed and operated by National Technology and Engineering Solutions of Sandia, LLC, a wholly owned subsidiary of Honeywell International, Inc., for the US DOE’s National Nuclear Security Administration under contract no. DE-NA0003525. This paper describes objective technical results and analysis. Any subjective views or opinions that might be expressed in the document do not necessarily represent the views of the US DOE or the United States Government.