Abstract
Clusters of nitrogen- and carbon-coordinated transition metals dispersed in a carbon matrix (e. g., Fe−N−C) have emerged as an inexpensive class of electrocatalysts for the oxygen reduction reaction (ORR). Here, it was shown that optimizing the interaction between the nitrogen-coordinated transition metal clusters embedded in a more stable and corrosion-resistant carbide matrix yielded an ORR electrocatalyst with enhanced activity and stability compared to Fe−N−C catalysts. Utilizing first-principles calculations, an electrostatics-based descriptor of catalytic activity was identified, and nitrogen-coordinated iron (FeN4) clusters embedded in a TiC matrix were predicted to be an efficient platinum-group metal (PGM)-free ORR electrocatalyst. Guided by theory, selected catalyst formulations were synthesized, and it was demonstrated that the experimentally observed trends in activity fell exactly in line with the descriptor-derived theoretical predictions. The Fe−N−TiC catalyst exhibited enhanced activity (20 %) and durability (3.5-fold improvement) compared to a traditional Fe−N−C catalyst. It was posited that the electrostatics-based descriptor provides a powerful platform for the design of active and stable PGM-free electrocatalysts and heterogenous single-atom catalysts for other electrochemical reactions.
Original language | English |
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Pages (from-to) | 4680-4689 |
Number of pages | 10 |
Journal | ChemSusChem |
Volume | 14 |
Issue number | 21 |
DOIs | |
State | Published - Nov 4 2021 |
Funding
This work was partially supported through National Science Foundation grant numbers 1729787 and 1806147. A portion of the STEM experiments was conducted at the Center for Nanophase Materials Sciences at Oak Ridge National Laboratory, which is a Department of Energy (DOE) Office of Science User Facility, through a user project (J.A.H., A.Y.B., J.C.I.). This work used the computational resources of the Extreme Science and Engineering Discovery Environment (XSEDE), which is supported by National Science Foundation grants ACI-1053575 and ACI-1548562. V.R. acknowledges with gratitude the Roma B. and Raymond H. Wittcoff Distinguished University Professorship. This work was partially supported through National Science Foundation grant numbers 1729787 and 1806147. A portion of the STEM experiments was conducted at the Center for Nanophase Materials Sciences at Oak Ridge National Laboratory, which is a Department of Energy (DOE) Office of Science User Facility, through a user project (J.A.H., A.Y.B., J.C.I.). This work used the computational resources of the Extreme Science and Engineering Discovery Environment (XSEDE), which is supported by National Science Foundation grants ACI‐1053575 and ACI‐1548562. V.R. acknowledges with gratitude the Roma B. and Raymond H. Wittcoff Distinguished University Professorship.
Funders | Funder number |
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Roma B. and Raymond H. Wittcoff Distinguished University | |
National Science Foundation | ACI‐1053575, ACI‐1548562, 1806147, 1729787 |
U.S. Department of Energy | |
Office of Science | ACI-1548562, ACI-1053575 |
Keywords
- Bader charge
- electrochemistry
- oxidative degradation
- oxygen reduction reaction
- proton exchange membrane fuel cells