Pt/MnO Interface Induced Defects for High Reverse Water Gas Shift Activity

The implementation of supported metal catalysts heavily relies on the synergistic interactions between metal nanoparticles and the material they are dispersed on. It is clear that interfacial perimeter sites have outstanding skills for turning catalytic reactions over, however, high activity and sel...

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Szenti Imre
Efremova Anastasiia
Kiss János
Sápi András
Óvári László
Halasi Gyula
Haselmann Ulrich
Zhang Zhaoli
Morales-Vidal Jordi
Baán Kornélia
Kukovecz Ákos
López Núria
Kónya Zoltán
Dokumentumtípus: Cikk
Megjelent: 2024
Sorozat:ANGEWANDTE CHEMIE-INTERNATIONAL EDITION 63 No. 8
Tárgyszavak:
doi:10.1002/anie.202317343

mtmt:34471429
Online Access:http://publicatio.bibl.u-szeged.hu/32711
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490 0 |a ANGEWANDTE CHEMIE-INTERNATIONAL EDITION  |v 63 No. 8 
520 3 |a The implementation of supported metal catalysts heavily relies on the synergistic interactions between metal nanoparticles and the material they are dispersed on. It is clear that interfacial perimeter sites have outstanding skills for turning catalytic reactions over, however, high activity and selectivity of the designed interface‐induced metal distortion can also obtain catalysts for the most crucial industrial processes as evidenced in this paper. Herein, the beneficial synergy established between designed Pt nanoparticles and MnO in the course of the reverse water gas shift (RWGS) reaction resulted in a Pt/MnO catalyst having ~10 times higher activity compared to the reference Pt/SBA‐15 catalyst with >99% CO selectivity. Under activation, a crystal assembly through the metallic Pt (110) and MnO evolved, where the plane distance differences caused a mismatched row structure in softer Pt nanoparticles, which was identified by microscopic and surface‐sensitive spectroscopic characterizations combined with density functional theory simulations. The generated edge dislocations caused the Pt lattice expansion which led to the weakening of the Pt‐CO bond. Even though MnO also exhibited an adverse effect on Pt by lowering the number of exposed metal sites, rapid desorption of the linearly adsorbed CO species governed the performance of the Pt/MnO in the RWGS. 
650 4 |a Kémiai tudományok 
650 4 |a Nanotechnológia 
700 0 1 |a Efremova Anastasiia  |e aut 
700 0 1 |a Kiss János  |e aut 
700 0 1 |a Sápi András  |e aut 
700 0 1 |a Óvári László  |e aut 
700 0 1 |a Halasi Gyula  |e aut 
700 0 1 |a Haselmann Ulrich  |e aut 
700 0 1 |a Zhang Zhaoli  |e aut 
700 0 2 |a Morales-Vidal Jordi  |e aut 
700 0 2 |a Baán Kornélia  |e aut 
700 0 2 |a Kukovecz Ákos  |e aut 
700 0 2 |a López Núria  |e aut 
700 0 2 |a Kónya Zoltán  |e aut 
856 4 0 |u http://publicatio.bibl.u-szeged.hu/32711/1/AngewChemIntEd-2023-Szenti-PtMnOInterfaceInducedDefectsforHighReverseWaterGasShiftActivity.pdf  |z Dokumentum-elérés