Atomic Imaging of Fe, N-doped Carbon Electrocatalysts' Active Sites and Their Stability
Résumé
Fe, N-doped carbon electrocatalysts (i.e. Fe-N-C) are of interest for the oxygen reduction reaction because they can solve the geological and economic constraints associated with the use of Pt-based electrocatalysts. However, the nature and the stability of their active sites is yet to be fully understood. The presence of nitrogen and atomically dispersed Fe is believed to result in the presence of various moieties, i.e. Fe-N x , N-pyridinic, N-pyrrolic, etc. Such assumptions are based on the fitting of the N1s peak observed by X-ray photoelectron spec-troscopy (XPS) 1,2 and, for the Fe-N x moieties, extended X-ray absorption fine structure (EXAFS) 3. Imaging a non-model Fe-N-C electrocatalyst at an atomic scale could provide additional insights onto the exact structure of those moieties, and, in combination with electrochemical ageing, ease the assessment of their stability. Here, we discuss the multiplicity of actives sites in an Fe-N-C electrocatalyst synthesized by the sacrificial support method. We use a combination of XPS, EXAFS, scanning transmission electron micrographs (STEM) and electron energy loss elemental mapping (EELS-see Figure 1) to unveil the presence, additional to Fe-N x , of other active sites, e.g. Fe-N x C y or nitrogen moieties. Then, we investigate the stability of said moieties (with a focus onto Fe-N x) using a combination of step-cycles (10,000 cycles; 0.6-1.0 V vs. RHE, 3s-3s, in Ar-saturated 0.1 M H 2 SO 4 , T = 80°C) and STEM (see Figure 1), showing that, in these experimental conditions and for this specific family of Fe-N-C electrocatalysts, the atomically dispersed Fe forms clusters-but not nano-particles-during the ageing process.
Domaines
Matériaux
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