CO2 hydrogenation selectivity shift over In-Co binary oxides catalysts: Catalytic mechanism and structure-property relationship

نویسندگان

چکیده

The hydrogenation of CO2 into methanol has attracted much attention and In2O3 is a promising catalyst. Introducing metal elements (M/In2O3) one the main strategies to improve its performance. However, mechanism active sites remain unclear need be further elucidated. Here, noble-metal-free Inx-Coy oxides catalysts were prepared. Much-improved performance obvious product selectivity shift observed. optimized catalyst (In1-Co4) (9.7 mmol gcat−1 h−1) showed five times yields than pure (2.2 (P = 4.0 MPa, T 300 °C, GHSV 24000 cm3STP h−1, H2:CO2 3). And cobalt-catalyzed methanation activity was suppressed, although cobalt most element. To unravel this shift, detailed evaluation, together with several in-situ ex-situ characterizations, employed on In-Co for comparative study. results indicated both followed formate pathway, reconstructed generated surface In2O3-enriched core-shell-like structure under reductive atmosphere. enriched at significantly enhanced adsorption capacity well stabilized intermediates hydrogenation. carbon-containing adsorbed stronger led feasible C/H ratio, thus allowing *CH3O desorb produce CH3OH instead being over-hydrogenated CH4.

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ژورنال

عنوان ژورنال: Chinese Journal of Catalysis

سال: 2022

ISSN: ['0253-9837', '1872-2067']

DOI: https://doi.org/10.1016/s1872-2067(21)63870-6