This study is led by Associate Researcher Ding Tao and Professor Yao Tao, University of Science and Technology of China. The experiments were performed by Density functional theory calculation and synchrotron radiation characterization techniques.
The authors systematically design and investigate the site-distance effect of Fe-Rh atom catalysts (Fe-Rh x @NC) supported by N-doped graphene for ORR by an integrated theoretical and experimental approach. By using electrostatic potential (ESP) and bader charge analysis, theoretical calculations predict that the site-distance effect changes the catalytic electronic structure of different Fe-Rh atomic site distances (d Fe-Rh ), optimizing the adsorption strength of the catalyst.
Consequently, motivated by this theoretical calculations, the authors designed the Fe-Rh x @NC catalysts through a spatial confinement strategy, and synthesized the Fe-Rh x @NC catalysts with different d Fe-Rh . High-angle toroidal dark field scanning TEM (HAADF-STEM) images further demonstrate the successful synthesis of catalysts at different Fe-Rh atomic distances. X-ray photoelectron spectroscopy (XPS) and X-ray absorption spectroscopy (XAS) demonstrated the effect of site-distance on the strength of interaction between Fe and Rh.
The Fe-Rh 2 @NC has the optimal atomic distance to provide the most positive onset potential (E onset ) and a half-wave potential (E 1/2 ) of 1.01 and 0.91 V vs. RHE as compared to Fe-Rh 1 @NC (0.96 and 0.88 V) and Fe@NC (0.96 and 0.87 V), even higher than commercial Pt/C (0.98 and 0.86 V).
Density functional theory (DFT) calculations reveal that Fe-Rh 2 @NC can interact with O 2 moderately, with suitable adsorption energy, conducive to promote the kinetic process of ORR. Compared with Fe@NC, the Fe-Rh 2 @NC catalyst has a higher projected the state density near the Fermi level, indicating that Fe-Rh 2 @NC bimetallic catalyst has stronger electron transfer ability and higher catalytic performance.
See the article:
Regulating atomic Fe-Rh site distance for efficient oxygen reduction reaction
https://doi.org/10.1007/s11426-023-1889-6
Science China Chemistry