Highly Efficient CO Oxidation on Atomically Thin Pt Plates Supported on Irreducible Si 7 × 7

Abstract
Electronic interaction between metal nanoparticles and irreducible supports is an important aspect of heterogeneous catalysis due to its capability of controlling the associated catalytic performance. We elucidate the relationship between metal–support electronic interactions and catalytic activity on size-selected singe layered platinum plates Ptn (n = 10, 20, 30, and 45) supported on a Si (111)-7 × 7 reconstructed surface (Si-RS). Our first-principles density functional theory study shows that CO oxidation catalysis over Pt supported on the nonreducible Si-RS is affected by variations in charge transfer, cluster size, and electronic interactions between clusters and support. CO adsorbs on Ptn adsorption sites in two distinct ranges of adsorption energies, which explains the experimentally observed two different desorption temperatures of CO. Pt30/Si-RS is more active than other Ptn/Si-RS under the same conditions, showing markedly enhanced catalytic activity in terms of high turnover frequency of CO2 production. This superior activity originates from the optimum CO and O2 adsorption on Pt30 arising from the position of the d-band center being midway between their π orbitals. Experimental observations convey that the TOFs of CO2 production on Pt30(45)/Si-RS are very high, and these are tolerant to CO poisoning between 450 and 550 K. DFT computations of TOF on Pt30(45)/Si-RS for CO2 validate the experimentally observed trends at 350, 450, and 550 K and exhibit that the CO oxidation activity exceeds that of the conventional catalysts between 450 and 550 K. Our results depict the importance of size control and electronic structure tailoring while designing Pt-based catalysts and will motivate the effective utilization of rare elements on irreducible substrates.

Citation
Ahmad, R., Yasumatsu, H., & Singh, A. K. (2023). Highly Efficient CO Oxidation on Atomically Thin Pt Plates Supported on Irreducible Si 7 × 7. The Journal of Physical Chemistry C. https://doi.org/10.1021/acs.jpcc.2c08106

Acknowledgements
This work was financially supported by DST Nanomission. The authors thank Materials Research Center, Indian Institute of Science, Bangalore, for providing the required computational facilities. R.A. acknowledges support from DST through the INSPIRE Fellowship. H.Y. is grateful to the Special Cluster Research Project of Genesis Research Institute, Inc., JSPS Grant-in-Aid for Scientific Research (KAKENHI) (C) Grant Number 15K04594 and JSPS Invitational Fellowships for Research in Japan (ID No. S15038, Dr. Claude Henry, CINaM-CNRS). A.K.S is also grateful to JSPS Invitational Fellowships for Research in Japan (ID No. S20076 hosted by Prof. Hisato Yasumatsu).

Publisher
American Chemical Society (ACS)

Journal
The Journal of Physical Chemistry C

DOI
10.1021/acs.jpcc.2c08106

Additional Links
https://pubs.acs.org/doi/10.1021/acs.jpcc.2c08106

Permanent link to this record