1. Enhanced Proximity of Rh 1,2 -Rh n Ensembles Encaged in UiO-67 Boosting Catalytic Conversion of Syngas to Oxygenates.
- Author
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Yu J, Liu T, Gu Q, Wang J, Han Y, Li G, Guo Q, Gu Y, Wu X, Gong X, Yang B, and Mao D
- Abstract
Maintaining high conversion under the premise of high oxygenates selectivity in syngas conversion is important but a formidable challenge in Rh catalysis. Monometallic Rh catalysts provide poor oxygenate conversion efficiency, and efforts have been focused on constructing adjacent polymetallic sites; however, the one-pass yields of C
2+ oxygenates over the reported Rh-based catalysts were mostly <20 %. In this study, we constructed a monometallic Rh catalyst encapsulated in UiO-67 (Rh/UiO-67) with enhanced proximity to dual-site Rh1,2 -Rhn ensembles. Unexpectedly, this catalyst exhibited high efficacy for oxygenate synthesis from syngas, giving a high oxygenate selectivity of 72.0 % with a remarkable CO conversion of 50.4 %, and the one-pass yield of C2+ oxygenates exceeded 25 %. The state-of-the-art characterizations further revealed the spontaneous formation of an ensemble of Rh single atoms/dimers (Rh1,2 ) in the proximity of ultrasmall Rh clusters (Rhn ) confined within the nanocavity of UiO-67, providing adjacent Rh+ -Rh0 dual sites dynamically during the reaction that promote the relay of the undissociated CHO species to the CHx species. Thus, our results open a new route for designing highly efficient Rh catalysts for the conversion of syngas to oxygenates by precisely tuning the ensemble and proximity of the dual active sites in a confined space., (© 2024 Wiley-VCH GmbH.)- Published
- 2024
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