Tuning Ni-catalyzed CO2 hydrogenation selectivity via Ni-ceria support interactions and Ni-Fe bimetallic formation
Abstract
CO2 hydrogenation over Fe-modified Ni/CeO2 catalysts was investigated in a batch reactor using time-resolved in situ FTIR spectroscopy. Low loading of Ni/CeO2 was associated with high selectivity to CO over CH4, while higher Ni loading improved CO2 hydrogenation activity with a reduced CO selectivity. X-ray absorption near-edge structure (XANES) analysis revealed Ni to be metallic for all catalysts including the CO-selective low loading 0.5% Ni catalyst, suggesting that the selectivity trend is due to structural rather than oxidation state effects. The loading amount of 1.5% Ni was selected for co-impregnation with Fe, based on the significant shift in product selectivity towards CH4 for that loading amount, in order to shift the selectivity towards CO while maintaining high activity. Temperature programmed reduction (TPR) results indicated bimetallic interactions between Ni and Fe, and XANES analysis showed that about 70% of Fe in the bimetallic catalysts was oxidized. The Ni-Fe catalysts demonstrated improved selectivity towards CO without significantly compromising activity, coupling the high activity of Ni catalysts and the high CO selectivity of Fe. The general trends in Ni loading and bimetallic modification should guide efforts to develop non-precious metal catalysts for the selective production of CO by CO2 hydrogenation.
- Authors:
-
- Columbia Univ., New York, NY (United States). Department of Chemical Engineering
- Brookhaven National Lab. (BNL), Upton, NY (United States). Chemistry Department
- Columbia Univ., New York, NY (United States). Department of Chemical Engineering; Brookhaven National Lab. (BNL), Upton, NY (United States). Chemistry Department
- Publication Date:
- Research Org.:
- Brookhaven National Lab. (BNL), Upton, NY (United States)
- Sponsoring Org.:
- USDOE Office of Science (SC), Basic Energy Sciences (BES)
- OSTI Identifier:
- 1430879
- Alternate Identifier(s):
- OSTI ID: 1549473
- Report Number(s):
- BNL-203438-2018-JAAM
Journal ID: ISSN 0926-3373
- Grant/Contract Number:
- SC0012704
- Resource Type:
- Accepted Manuscript
- Journal Name:
- Applied Catalysis B: Environmental
- Additional Journal Information:
- Journal Volume: 224; Journal Issue: C; Journal ID: ISSN 0926-3373
- Publisher:
- Elsevier
- Country of Publication:
- United States
- Language:
- English
- Subject:
- 37 INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY; CO2 reduction; Ni loading; Ni-Fe bimetallic catalysts; Metal oxide; XANES
Citation Formats
Winter, Lea R., Gomez, Elaine, Yan, Binhang, Yao, Siyu, and Chen, Jingguang G. Tuning Ni-catalyzed CO2 hydrogenation selectivity via Ni-ceria support interactions and Ni-Fe bimetallic formation. United States: N. p., 2017.
Web. doi:10.1016/j.apcatb.2017.10.036.
Winter, Lea R., Gomez, Elaine, Yan, Binhang, Yao, Siyu, & Chen, Jingguang G. Tuning Ni-catalyzed CO2 hydrogenation selectivity via Ni-ceria support interactions and Ni-Fe bimetallic formation. United States. https://doi.org/10.1016/j.apcatb.2017.10.036
Winter, Lea R., Gomez, Elaine, Yan, Binhang, Yao, Siyu, and Chen, Jingguang G. Mon .
"Tuning Ni-catalyzed CO2 hydrogenation selectivity via Ni-ceria support interactions and Ni-Fe bimetallic formation". United States. https://doi.org/10.1016/j.apcatb.2017.10.036. https://www.osti.gov/servlets/purl/1430879.
@article{osti_1430879,
title = {Tuning Ni-catalyzed CO2 hydrogenation selectivity via Ni-ceria support interactions and Ni-Fe bimetallic formation},
author = {Winter, Lea R. and Gomez, Elaine and Yan, Binhang and Yao, Siyu and Chen, Jingguang G.},
abstractNote = {CO2 hydrogenation over Fe-modified Ni/CeO2 catalysts was investigated in a batch reactor using time-resolved in situ FTIR spectroscopy. Low loading of Ni/CeO2 was associated with high selectivity to CO over CH4, while higher Ni loading improved CO2 hydrogenation activity with a reduced CO selectivity. X-ray absorption near-edge structure (XANES) analysis revealed Ni to be metallic for all catalysts including the CO-selective low loading 0.5% Ni catalyst, suggesting that the selectivity trend is due to structural rather than oxidation state effects. The loading amount of 1.5% Ni was selected for co-impregnation with Fe, based on the significant shift in product selectivity towards CH4 for that loading amount, in order to shift the selectivity towards CO while maintaining high activity. Temperature programmed reduction (TPR) results indicated bimetallic interactions between Ni and Fe, and XANES analysis showed that about 70% of Fe in the bimetallic catalysts was oxidized. The Ni-Fe catalysts demonstrated improved selectivity towards CO without significantly compromising activity, coupling the high activity of Ni catalysts and the high CO selectivity of Fe. The general trends in Ni loading and bimetallic modification should guide efforts to develop non-precious metal catalysts for the selective production of CO by CO2 hydrogenation.},
doi = {10.1016/j.apcatb.2017.10.036},
journal = {Applied Catalysis B: Environmental},
number = C,
volume = 224,
place = {United States},
year = {Mon Oct 16 00:00:00 EDT 2017},
month = {Mon Oct 16 00:00:00 EDT 2017}
}
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