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Flame Spray Pyrolysis as a Synthesis Platform to Assess Metal Promotion in In2O3-Catalyzed CO2 Hydrogenation

Área de investigación Química Homogénea
TítuloFlame Spray Pyrolysis as a Synthesis Platform to Assess Metal Promotion in In2O3-Catalyzed CO2 Hydrogenation
Tipo de publicaciónArtículo de revista
Año de publicación2022
AutoresAraujo, TPinheiro, Morales-Vidal, J, Zou, T, Garcia-Muelas, R, Willi, PO, Engel, KM, Safonova, OV, Akl, DFaust, Krumeich, F, Grass, RN, Mondelli, C, Lopez, N, Perez-Ramirez, J
RevistaADVANCED ENERGY MATERIALS
Type of ArticleArticle; Early Access
Palabras clavesCO2, green methanol, hydrogenation, indium oxide, metal speciation, promotion
Abstract

A plethora of metal promoters have been applied to enhance the performance of In2O3 in CO2 hydrogenation to methanol, a prospective energy carrier. However, the lack of systematic catalyst preparation and evaluation precludes a direct comparison of their speciation and promotional effects, and consequently, the design of an optimal system. Herein, flame spray pyrolysis (FSP) is employed as a standardized synthesis method to introduce nine metal promoters (0.5 wt.%) into In2O3. Methanol productivity generally increased on M-In2O3 with selectivity following Pd approximate to Pt > Rh approximate to Ru approximate to Ir > Ni approximate to Co > Ag approximate to In2O3 > Au. In-depth characterization, kinetic analyses, and theoretical calculations reveal a range of metal-dependent speciation which dictate catalyst architecture and degree of promotion. Atomically-dispersed promoters (Pd, Pt, Rh, Ru, and Ir) grant the highest improvement in performance, particularly Pd and Pt, which markedly promote hydrogen activation while hindering undesired CO formation. In contrast, metals in clustered (Ni and Co) and nanoparticle (Ag and Au) forms display moderate and no promotion, respectively. This study provides an atomic-level understanding of In2O3 promotion based on a unified protocol, and highlights the potential of FSP to engineer complex catalytic systems toward more efficient energy transformations.

DOI10.1002/aenm.202103707