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Synergistic Effects of Co and Fe on the Oxygen Evolution Reaction Activity of LaCo x Fe 1− x O 3
Author(s) -
Füngerlings Achim,
Koul Adarsh,
Dreyer Maik,
Rabe Anna,
Morales Dulce M.,
Schuhmann Wolfgang,
Behrens Malte,
Pentcheva Rossitza
Publication year - 2021
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.202102829
Subject(s) - overpotential , oxygen evolution , density functional theory , linear sweep voltammetry , deprotonation , chemistry , oxygen , protonation , materials science , crystallography , electrochemistry , analytical chemistry (journal) , ion , cyclic voltammetry , computational chemistry , electrode , organic chemistry , chromatography
In a combined experimental and theoretical study we assess the role of Co incorporation on the OER activity of LaCo x Fe 1− x O 3 . Phase pure perovskites were synthesized up to x = 0 . 300 in 0.025/0.050 steps. HAADF STEM and EDX analysis points towards FeO 2 ‐terminated (001)‐facets in LaFeO 3 , in accordance with the stability diagram obtained from density functional theory calculations with a Hubbard U term (DFT+ U ). Linear sweep voltammetry conducted in a rotating disk electrode setup shows a reduction of the OER overpotential and a nonmonotonic trend with x , with double layer capacitance measurements indicating an intrinsic nature of activity. This is supported by DFT+ U results that show reduced overpotentials for both Fe and Co reaction sites with the latter reaching values of 0.32–0.40 V, ∼0.3 V lower than for Fe. This correlates with a stronger reduction of the binding energy difference of the *O and *OH intermediates towards an optimum value of 1.6 eV for x = 0 . 250 , the OH deprotonation being the potential limiting step in most cases. Significant variations of the magnetic moments of both surface and subsurface Co and Fe during OER demonstrate that the beneficial effect is a result of a concerted action involving many surrounding ions, which extends the concept of the active site.