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The low mass activity of the PtCo/C-900 catalyst was explained by small electrochemically active surface area (EAS).
Au0.45Pd0.55-5 nm exhibited the superior specific activity of 1.11 mandmassnd mactivityvity of >0.4 A/mgmetal toward ethanol oxidation, approximately 5 times more active than commercial Pd/C.
In addition to the intrinsic activity, the mass activity of the catalyst will be more crucial to the practical application.
Mass activity of Pd nanocubes increased with decreasing the particle size.
The mass activity of 20 wt% Au/C catalysts was higher due to smaller particle size.
It is noteworthy that the mass activity of NC@CoPx/PyCNTs was 9.8 times higher than commercial 20% Pt/C.
Among these catalysts, the Pt45Ru45Fe10/C catalyst exhibited the highest mass activity of 2.6 A/g catal.
The mass activity of C-TNTs-Pt-1 at 0.85 V was about 0.44 A mgPt−1.
The specific activity and mass activity of Pt/ITO were about 2.5 times that of Pt/Vulcan.
Furthermore, in the GDE configuration this catalyst reached a mass activity of –1.4 mA mg−1, after IR correction.
The mass activity of as-prepared PtAg2/C-D catalyst reaches 3.35 times as high as that of Pt/C.
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