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CO2 Activation over Nanoshaped CeO2 Decorated with Nickel for Low-Temperature Methane Dry Reforming
Author(s) -
Kristijan Lorber,
Janez Zavašnik,
Iztok Arčon,
Matej Huš,
Janvit Teržan,
Blaž Likozar,
Petar Djinović
Publication year - 2022
Publication title -
acs applied materials and interfaces
Language(s) - English
Resource type - Journals
eISSN - 1944-8252
pISSN - 1944-8244
DOI - 10.1021/acsami.2c05221
Subject(s) - materials science , carbon dioxide reforming , methane , formate , syngas , dissociation (chemistry) , hydrogen , chemical engineering , xanes , nanorod , extended x ray absorption fine structure , inert gas , inorganic chemistry , catalysis , nanotechnology , chemistry , absorption spectroscopy , organic chemistry , physics , composite material , quantum mechanics , spectroscopy , engineering
Dry reforming of methane (DRM) is a promising way to convert methane and carbon dioxide into H 2 and CO (syngas). CeO 2 nanorods, nanocubes, and nanospheres were decorated with 1-4 wt % Ni. The materials were structurally characterized using TEM and in situ XANES/EXAFS. The CO 2 activation was analyzed by DFT and temperature-programmed techniques combined with MS-DRIFTS. Synthesized CeO 2 morphologies expose {111} and {100} terminating facets, varying the strength of the CO 2 interaction and redox properties, which influence the CO 2 activation. Temperature-programmed CO 2 DRIFTS analysis revealed that under hydrogen-lean conditions mono- and bidentate carbonates are hydrogenated to formate intermediates, which decompose to H 2 O and CO. In excess hydrogen, methane is the preferred reaction product. The CeO 2 cubes favor the formation of a polydentate carbonate species, which is an inert spectator during DRM at 500 °C. Polydentate covers a considerable fraction of ceria's surface, resulting in less-abundant surface sites for CO 2 dissociation.

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