Journal
ENERGY & ENVIRONMENTAL SCIENCE
Volume 14, Issue 9, Pages 4847-4857Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d1ee01592c
Keywords
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Funding
- Generalitat de Catalunya [2017 SGR 327, 2017 SGR 1246]
- Spanish MINECO [PID2020-116093RB-C43]
- Severo Ochoa program from Spanish MINECO [SEV-2017-0706]
- CERCA Programme/Generalitat de Catalunya
- Humboldt Research Fellowship by the Alexander von Humboldt Foundation [3.5-CHN-1206832-HFST-P]
- FWO project [12ZV320N]
- China Scholarship Council [201706180028, 201804910551]
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A quasi-double star catalyst composed of nearby Ni and Fe active sites was developed to achieve high selectivity and low overpotential during the CO2 reduction reaction. The optimized Ni/Fe-N-C catalyst exhibited exclusive selectivity with a maximum FE(CO) of 98% at a low overpotential of 390 mV vs. RHE, outperforming single metal counterparts and other state-of-the-art M-N-C catalysts. The DFT results suggest that the neighboring Ni and Fe active sites synergistically decrease reaction barriers and prevent undesired hydrogen evolution reaction, potentially surpassing the activity benchmark of single metal counterparts.
Although the Faraday efficiencies (FEs) obtained on most of the Ni based single-atom catalysts (Ni-N-C) are satisfactory (generally >90%) for the electrochemical transfer CO2 to CO, their practical application is still limited by their high overpotentials (>600 mV vs. RHE), which implies a higher energy consumption to drive the CO2 RR. In this work, we have prepared a quasi-double star catalyst composed of nearby Ni and Fe active sites via a simple pyrolysis of Ni and Fe co-doped Zn-based MOFs in order to achieve a high selectivity at a low overpotential during the CO2 RR. Specifically, the optimized Ni/Fe-N-C catalyst shows an exclusive selectivity (a maximum FE(CO) of 98%) at a low overpotential of 390 mV vs. RHE, which is superior to both the single metal counterparts (Ni-N-C and Fe-N-C catalysts) and other state-of-the-art M-N-C catalysts. The DFT results further reveal that regulating the catalytic CO2 RR performance via nearby Ni and Fe active sites can potentially break the activity benchmark of the single metal counterparts because the neighboring Ni and Fe active sites not only function in synergy to decrease the reaction barrier for the formation of COOH* and desorption of CO* in comparison to their single metal counterparts, but also prevent the undesired hydrogen evolution reaction (HER). This work presents a quasi-double-star catalyst composed of two metal sites for high-efficiency CO2 reduction, which paves the way for the rational design of bimetallic catalysts with separated active sites for other reactions.
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