期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 137, 期 10, 页码 3638-3648出版社
AMER CHEMICAL SOC
DOI: 10.1021/jacs.5b00281
关键词
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资金
- National Science Foundation [CHE-1301461, 0923577, 0421086]
- Center for Sustainable Materials Chemistry through the National Science Foundation [CHE-1102637]
- W. M. Keck Foundation
- M. J. Murdock Charitable Trust
- ONAMI
- Air Force Research Laboratory [FA8650-05-1-5041]
- University of Oregon
- Division Of Chemistry
- Direct For Mathematical & Physical Scien [1102637] Funding Source: National Science Foundation
- Division Of Chemistry
- Direct For Mathematical & Physical Scien [1301461] Funding Source: National Science Foundation
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-xFex(OOH) is similar to 100-fold higher for x approximate to 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-xFex(OOH) is conductive under OER conditions (similar to 0.7-4 mS cm(-1) at similar to 300 mV overpotential), but that FeOOH is an insulator with measurable conductivity (2.2 x 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.
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