Details

Autor(en) / Beteiligte

• Burke, Michaela S
• Kast, Matthew G
• Trotochaud, Lena
• Smith, Adam M
• Boettcher, Shannon W

Titel

Cobalt–Iron (Oxy)hydroxide Oxygen Evolution Electrocatalysts: The Role of Structure and Composition on Activity, Stability, and Mechanism

Ist Teil von

• Journal of the American Chemical Society, 2015-03, Vol.137 (10), p.3638-3648

Ort / Verlag

United States: American Chemical Society

Erscheinungsjahr

2015

Quelle

Alma/SFX Local Collection

Beschreibungen/Notizen

• Cobalt oxides and (oxy)­hydroxides have been widely studied as electrocatalysts for the oxygen evolution reaction (OER). For related Ni-based materials, the addition of Fe dramatically enhances OER activity. The role of Fe in Co-based materials is not well-documented. We show that the intrinsic OER activity of Co1–x Fe x (OOH) is ∼100-fold higher for x ≈ 0.6–0.7 than for x = 0 on a per-metal turnover frequency basis. Fe-free CoOOH absorbs Fe from electrolyte impurities if the electrolyte is not rigorously purified. Fe incorporation and increased activity correlate with an anodic shift in the nominally Co2+/3+ redox wave, indicating strong electronic interactions between the two elements and likely substitutional doping of Fe for Co. In situ electrical measurements show that Co1–x Fe x (OOH) is conductive under OER conditions (∼0.7–4 mS cm–1 at ∼300 mV overpotential), but that FeOOH is an insulator with measurable conductivity (2.2 × 10–2 mS cm–1) only at high overpotentials >400 mV. The apparent OER activity of FeOOH is thus limited by low conductivity. Microbalance measurements show that films with x ≥ 0.54 (i.e., Fe-rich) dissolve in 1 M KOH electrolyte under OER conditions. For x < 0.54, the films appear chemically stable, but the OER activity decreases by 16–62% over 2 h, likely due to conversion into denser, oxide-like phases. We thus hypothesize that Fe is the most-active site in the catalyst, while CoOOH primarily provides a conductive, high-surface area, chemically stabilizing host. These results are important as Fe-containing Co- and Ni-(oxy)­hydroxides are the fastest OER catalysts known.