The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.
The dynamics of overlayer formation on catalyst nanoparticles and strong metal-support interaction
Open accessAbstract
Heterogeneous catalysts play a pivotal role in the chemical industry. The strong metal-support interaction (SMSI), which affects the catalytic activity, is a phenomenon researched for decades. However, detailed mechanistic understanding on real catalytic systems is lacking. Here, this surface phenomenon was studied on an actual platinum-titania catalyst by state-of-the-art in situ electron microscopy, in situ X-ray photoemission spectroscopy and in situ X-ray diffraction, aided by density functional theory calculations, providing a novel real time view on how the phenomenon occurs. The migration of reduced titanium oxide, limited in thickness, and the formation of an alloy are competing mechanisms during high temperature reduction. Subsequent exposure to oxygen segregates the titanium from the alloy, and a thicker titania overlayer forms. This role of oxygen in the formation process and stabilization of the overlayer was not recognized before. It provides new application potential in catalysis and materials science.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
The surface science of titanium dioxide
Diebold, U. (2003) · Surface Science Reports · doi:10.1016/s0167-5729(02)00100-0 · Cited by 7,944
Strong metal-support interactions. Group 8 noble metals supported on titanium dioxide
Tauster, S. J., Fung, S. C., & Garten, R. L. (1978) · Journal of the American Chemical Society · doi:10.1021/ja00469a029 · Cited by 3,188
Atom-Resolved Imaging of Dynamic Shape Changes in Supported Copper Nanocrystals
Hansen, P. L., Wagner, J. B., Helveg, S., Rostrup-Nielsen, J. R., Clausen, B. S., & Topsøe, H. (2002) · Science · doi:10.1126/science.1069325 · Cited by 1,261
Li, Z., Qi, Z., Wang, S., Ma, T., Zhou, L., Wu, Z., Luan, X., Lin, F.-Y., Chen, M., Miller, J. T., et al. (2019) · Nano Letters · doi:10.1021/acs.nanolett.9b01381 · Cited by 210
Research works printed but not linked: 48
- Grubb, W. T. & McKee, D. W. Boron carbide, a new substrate for fuel cell electrocatalysts. Nature 210, 192–194 (1966). · DOI
- Lox, E. S. J. in Handbook of Heterogeneous Catalysis, 2274–2345 https://doi.org/10.1002/9783527610044.hetcat0120 (Wiley-VCH Verlag GmbH & Co. KGaA, 2008), · doi:10.1002/9783527610044.hetcat0120
- Tauster, S. J. & Fung, S. C. Strong metal-support interactions: occurrence among the binary oxides of groups IIA-VB. J. Catal. 55, 29–35 (1978). · DOI · Paper page
- Tauster, S. J., Fung, S. C., Baker, R. T. K. & Horsley, J. A. Strong-interactions in supported-metal catalysts. Science 211, 1121–1125 (1981). · DOI · Paper page
- Zhang, J. et al. Wet-chemistry strong metal–support interactions in titania-supported Au catalysts. J. Am. Chem. Soc. 141, 2975–2983 (2019). · DOI · Paper page
- Zhu, M. et al. Strong metal-support interactions between copper and iron oxide during the high-temperature water-gas shift reaction. Angew. Chem. Int. Ed. 58, 9083–9087 (2019). · DOI
- Hernández Mejía, C., van Deelen, T. W. & de Jong, K. P. Activity enhancement of cobalt catalysts by tuning metal-support interactions. Nat. Commun. 9, 4459 (2018). · DOI · Paper page
- Corma, A., Serna, P., Concepción, P. & Calvino, J. J. Transforming nonselective into chemoselective metal catalysts for the hydrogenation of substituted nitroaromatics. J. Am. Chem. Soc. 130, 8748–8753 (2008). · DOI · Paper page
- Macino, M. et al. Tuning of catalytic sites in Pt/TiO2 catalysts for the chemoselective hydrogenation of 3-nitrostyrene. Nat. Catal. 2, 873–881 (2019). · DOI · Paper page
- Matsubu, J. C. et al. Adsorbate-mediated strong metal–support interactions in oxide-supported Rh catalysts. Nat. Chem. 9, 120–127 (2016). · DOI · Paper page
- Spencer, M. S. Models of strong metal-support interaction (SMSI) in Pt on TiO2 catalysts. J. Catal. 93, 216–223 (1985). · DOI
- Bernal, S. et al. Some recent results on metal/support interaction effects in NM/CeO2 (NM: noble metal) catalysts. Catal. Today 50, 175–206 (1999). · DOI · Paper page
- Dulub, O., Hebenstreit, W. & Diebold, U. Imaging cluster surfaces with atomic resolution: the strong metal-support interaction state of Pt supported on TiO2. Phys. Rev. Lett. 84, 3646–3649 (2000). · DOI · Paper page
- Braunschweig, E. J., Logan, A. D., Datye, A. K. & Smith, D. J. Reversibility of strong metal-support interactions on Rh/TiO2. J. Catal. 118, 227–237 (1989). · DOI
- Zhang, S. et al. Dynamical observation and detailed description of catalysts under strong metal–support interaction. Nano Lett. 16, 4528–4534 (2016). · DOI · Paper page
- Deng, L. et al. Strong metal-support interaction between Pt and SiO2 following high-temperature reduction: a catalytic interface for propane dehydrogenation. Chem. Commun. 53, 6937–6940 (2017). · DOI
- Behrens, M. et al. The active site of methanol synthesis over Cu/ZnO/Al2O3 industrial catalysts. Science 336, 893–897 (2012). · DOI · Paper page
- Willinger, M. G. et al. A case of strong metal-support interactions: combining advanced microscopy and model systems to elucidate the atomic structure of interfaces. Angew. Chem. Int. Ed. 53, 5998–6001 (2014). · DOI · Paper page
- Bernal, S. et al. High-resolution electron microscopy investigation of metal-support interactions in Rh/TiO2. J. Chem. Soc. Faraday Trans. 92, 2799–2809 (1996). · DOI
- Hansen, T. W. Atomic-resolution in situ transmission electron microscopy of a promoter of a heterogeneous catalyst. Science 294, 1508–1510 (2001). · DOI · Paper page
- Grass, M. E. et al. A reactive oxide overlayer on rhodium nanoparticles during CO oxidation and its size dependence studied by in situ ambient-pressure X-ray photoelectron spectroscopy. Angew. Chem. Int. Ed. 47, 8893–8896 (2008). · DOI · Paper page
- Starr, D. E., Liu, Z., Hävecker, M., Knop-Gericke, A. & Bluhm, H. Investigation of solid/vapor interfaces using ambient pressure X-ray photoelectron spectroscopy. Chem. Soc. Rev. 42, 5833 (2013). · DOI · Paper page
- Roy, K., Artiglia, L. & van Bokhoven, J. A. Ambient pressure photoelectron spectroscopy: opportunities in catalysis from solids to liquids and introducing time resolution. ChemCatChem 10, 666–682 (2018). · DOI
- Haller, G. L. & Resasco, D. E. Metal support interaction - Group-VIII metals and reducible oxides. Adv. Catal. 36, 173–235 (1989). · DOI · Paper page
- Zhu, Z. et al. Formation of nanometer-sized surface platinum oxide clusters on a stepped Pt(557) single crystal surface induced by oxygen: a high-pressure STM and ambient-pressure XPS study. Nano Lett. 12, 1491–1497 (2012). · DOI
- Baetzold, R. C., Apai, G., Shustorovich, E. & Jaeger, R. Surface core-level shifts for Pt single-crystal surfaces. Phys. Rev. B 26, 4022–4027 (1982). · DOI
- Pereira-Hernández, X. I. et al. Tuning Pt-CeO2 interactions by high-temperature vapor-phase synthesis for improved reducibility of lattice oxygen. Nat. Commun. 10, 1358 (2019). · DOI · Paper page
- Diebold, U. & Madey, T. E. TiO2 by XPS. Surf. Sci. Spectra 4, 227–231 (1996). · DOI
- Henderson, G. S., de Groot, F. M. F. & Moulton, B. J. A. X-ray absorption near-edge structure (XANES) spectroscopy. Rev. Mineral. Geochem. 78, 75–138 (2014). · doi:10.2138/rmg.2014.78.3
- Fadley, C. S., Baird, R. J., Siekhaus, W., Novakov, T. & Bergström, S. Å. L. Surface analysis and angular distributions in x-ray photoelectron spectroscopy. J. Electron Spectros. Relat. Phenom. 4, 93–137 (1974). · doi:10.1016/0368-2048(74)90001-2
- Cesar, L. G. et al. Identification of a Pt3Co surface intermetallic alloy in Pt–Co propane dehydrogenation catalysts. ACS Catal. 5231–5244 https://doi.org/10.1021/acscatal.9b00549 (2019). · DOI · Paper page
- Pietrokowsky, P. Novel ordered phase, Pt8Ti. Nature 206, 291–291 (1965). · doi:10.1038/206291a0
- LiBretto, N. J., Yang, C., Ren, Y., Zhang, G. & Miller, J. T. Identification of Surface Structures in Pt3Cr Intermetallic Nanocatalysts. Chem. Mater. 31, 1597–1609 (2019). · DOI
- Orlando, F. et al. The environmental photochemistry of oxide surfaces and the nature of frozen salt solutions: a new in situ XPS approach. Top. Catal. 59, 591–604 (2016). · DOI
- Artiglia, L. et al. Introducing time resolution to detect Ce3+ catalytically active sites at the Pt/CeO2 interface through ambient pressure X-ray photoelectron spectroscopy. J. Phys. Chem. Lett. 8, 102–108 (2017). · DOI
- Artiglia, L. et al. In Situ X-ray photoelectron spectroscopy detects multiple active sites involved in the selective anaerobic oxidation of methane in copper-exchanged zeolites. ACS Catal. 6728–6737 (2019). · DOI
- Doniach, S. & Sunjic, M. Many-electron singularity in X-ray photoemission and X-ray line spectra from metals. J. Phys. C. Solid State Phys. 3, 285–291 (1970). · DOI · Paper page
- Tanuma, S., Powell, C. J. & Penn, D. R. Use of sum rules on the energy-loss function for the evaluation of experimental optical data. J. Electron Spectros. Relat. Phenom. 62, 95–109 (1993). · doi:10.1016/0368-2048(93)80008-a
- Tanuma, S., Powell, C. J. & Penn, D. R. Calculations of electorn inelastic mean free paths. II. Data for 27 elements over the 50–2000 eV range. Surf. Interface Anal. 17, 911–926 (1991). · DOI · Paper page
- Yeh, J. J. & Lindau, I. Atomic subshell photoionization cross sections and asymmetry parameters: 1 ≤ Z ≤ 103. Data Nucl. Data Tables 32, 1–155 (1985). · DOI · Paper page
- Coelho, A. A. TOPAS and TOPAS-Academic: an optimization program integrating computer algebra and crystallographic objects written in C++. J. Appl. Crystallogr. 51, 210–218 (2018). · DOI · Paper page
- Vandevondele, J. et al. Quickstep: fast and accurate density functional calculations using a mixed Gaussian and plane waves approach. Comput. Phys. Commun. 167, 103–128 (2005). · DOI · Paper page
- Perdew, J. P., Burke, K. & Ernzerhof, M. Generalized gradient approximation made simple. Phys. Rev. Lett. 77, 3865–3868 (1996). · DOI · Paper page
- Goedecker, S., Teter, M. & Hutter, J. Separable dual-space Gaussian pseudopotentials. Phys. Rev. B 54, 1703–1710 (1996). · DOI · Paper page
- Lippert, G., Hutter, J. & Parrinello, M. A hybrid Gaussian and plane wave density functional scheme. Mol. Phys. 92, 477–488 (1997). · DOI · Paper page
- Reuter, K. & Scheffler, M. First-principles atomistic thermodynamics for oxidation catalysis: surface phase diagrams and catalytically interesting regions. Phys. Rev. Lett. 90, 046103 (2003). · DOI · Paper page
- Larsen et al. The atomic simulation environment — a Python library for working with atoms. J. Phys.: Condens. Matter 29, 273002–273032. · DOI · Paper page
- Barcaro, G. et al. Building principles and structural motifs in TiOx ultrathin films on a (111) substrate. J. Phys. Chem. C. 116, 13302–13306 (2012). · doi:10.1021/jp303730j
Cited by
Liu, L., & Corma, A. (2023) · Chemical Reviews · doi:10.1021/acs.chemrev.2c00733 · Cited by 689
Li, Y., Zhang, Y., Qian, K., & Huang, W. (2022) · ACS Catalysis · doi:10.1021/acscatal.1c04854 · Cited by 538
Subhan, A., Mourad, A.-H. I., & Al-Douri, Y. (2022) · Nanomaterials · doi:10.3390/nano12132144 · Cited by 95
“In the viewpoint of application, metal NPs have been extensively used in various industrial applications, such as in nanofilters for wastewater treatment in the petroleum industry [3], heterogeneous catalysts in the chemical industry [4], photodetectors in the automotive and space industries [5,6], quantum dots in the…”
Background
Metadata
- Authors
- Beck, A., Huang, X., Artiglia, L., Zabilskiy, M., Wang, X., Rzepka, P., Palagin, D., Willinger, M.-G., & van Bokhoven, J. A.
- Venue
- Nature Communications
- Published
- 2020-06-26
- Volume
- 11
- Issue
- 1
- Pages
- 3220-3220
- ISSN
- 2041-1723 (ISSN-L)
- OpenAlex
- W3037837763
- Cited by
- 317
- References
- 4
- FWCI
- 13.89
- Type
- journal article
- Language
- en
- Open access
- gold
- Licence
- creativecommons.org/licenses/by/4.0 (tdm)
- creativecommons.org/licenses/by/4.0 (vor)
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: The dynamics of overlayer formation on catalyst nanoparticles and strong metal-support interaction. https://app.cochat.ai/papers/10.1038/s41467-020-17070-2
- The paper
- Beck, A., Huang, X., Artiglia, L., Zabilskiy, M., Wang, X., Rzepka, P., Palagin, D., Willinger, M.-G., & van Bokhoven, J. A. (2020). The dynamics of overlayer formation on catalyst nanoparticles and strong metal-support interaction. Nature Communications. https://doi.org/10.1038/s41467-020-17070-2
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.