Subnanometric Pt clusters dispersed over Cs-doped TiO2 for CO2 upgrading via low-temperature RWGS: operando mechanistic insights to guide an optimal catalyst design

Literature Information

Publication Date 2023-12-11
DOI 10.1039/D3TA05482A
Impact Factor 12.732
Authors

Guillermo Torres-Sempere, Rubén Blay-Roger, Ligia A. Luque-Álvarez, Luis F. Bobadilla, Laura Pastor-Pérez, Miguel A. Centeno, Willinton Y. Hernández, Ibraheem Yousef, José A. Odriozola, Tomas R. Reina


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Abstract

The RWGS reaction is gathering momentum as an effective route for CO2 valorisation and given its endothermic nature the challenge lies in the design of active low-temperature catalysts. Herein we have designed two catalysts based on subnanometric Pt clusters providing effective CO2 conversion and, more importantly, high CO selectivity in the low-temperature range. The impact of Cs as a dopant in the catalyst's formulation is crucial leading to full selectivity at 300 °C. The reaction mechanisms for the studied systems namely Pt/TiO2 and PtCs/TiO2 are significantly different due to the presence of the alkali promoter. The presence of Cs neutralises the hydroxide groups of the TiO2 surface, changing the reaction pathway. The Pt/TiO2 catalyst follows a redox mechanism where CO2 dissociates to CO in the oxygen vacancies, and then these vacancies are recovered by the migration of H2 by spill over phenomena. On the other hand, the Cs doped catalyst has two possible mechanism pathways: the (ii) formyl/acyl pathway, where –CHO species are formed and, depending on the reaction conditions, evolve to CO gas or oxygenated compounds, and (ii) frustrated Lewis pair (FLP) assisted CO2 reduction route, in which the FLP induces the heterolytic dissociation of H2 and the subsequent hydrogenation of CO2 to CO. The latter route enabled by Cs-doping combined with the subnanometric Pt domains seems to be responsible for the excellent catalytic behaviour leading to fully selective low-temperature RWGS systems and thus unlocking new possibilities for less energy demanding CO2 valorisation units based on RWGS.

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DOI: 10.1039/AN99621BX011

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