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. Author manuscript; available in PMC: 2013 Oct 29.
Published in final edited form as: J Phys Chem C Nanomater Interfaces. 2011 Jul 12;115(32):10.1021/jp2042526. doi: 10.1021/jp2042526

Figure 3. Activity recovery by re-heat-treatment in argon of acid-washed catalysts.

Figure 3

(A) Normalized activity based on that of the original catalyst (O-catalyst) vs. re-heat-treatment temperature in argon, as measured in RDE (open circles) and PEMFC (filled squares).

The acid-washing was performed in a pH 1 H2SO4-solution for 24 h, then the powder was filtered, rinsed with deionized water and dried. Several aliquots of the acid-washed catalyst (AW-catalyst) were re-heat-treated in argon at various temperatures for 1 h. The initial activities of the O-catalyst were 2.8 and 15.1 A g-1 in RDE and PEMFC, respectively. Aliquots of a test precursor initially free of active sites (see section 2.1.4) were heat-treated in argon at various temperatures for 1 h (asterisks) in order to determine the minimum temperature required for catalytic-site formation.

(B) Normalized activity as measured in RDE (open circles) or PEMFC (filled squares) at various steps of five successive acid-washing/re-heat-treatment cycles. Acid-washed and re-heat-treated catalysts are labeled AWX and RHTX, respectively, X denoting the cycle number. Each acid-washing lasted 24 h in a pH 1 H2SO4-solution, then the powder was filtered, rinsed and dried. Each AW-catalyst was re-heat-treated for 1 h at 950°C in argon.

(C) Bulk Fe content at each step of the five acid-washing/re-heat-treatment cycles described in (B), as measured by neutron activation analysis.