Abstract

The high-efficient C-C bond cleavage is the key for ethanol electrooxidation. In this work, PtCu/Cu 2−x Se nanowires (NWs) with abundant surface defects were constructed and exhibited remarkable activity of 5.03 A mg −1 Pt as well as 5.29 A mg −1 Pt for ethanol oxidation and methanol oxidation, respectively, which are 5.0 and 5.3 fold of commercial Pt/C. ex situ, in situ experiments and calculation results reveal that the formation of PtCu alloys lowered the d -band level to promote the adsorption of hydroxyl species. The abundant defects created high density of low-coordinated atoms to boost the reaction kinetics. Thus, PtCu/Cu 2−x Se NWs displayed enhanced C-C bond cleavage ability and high selectivity for C1 products (CO 2 ). The assembled direct ethanol fuel cells (DEFCs) with PtCu/Cu 2−x Se NWs as anode provided an open-circuit voltage (OCV) of 0.773 V and a peak power density of 7.8 mW cm −2 . This work not only give us a potential catalyst for C-C bond cleavage, but also provides an effective strategy to enhance the electrocatalytic activity of ethanol/methanol oxidation. • To boost the C-C bond cleavage for ethanol oxidation, a one-stone, two birds strategy was demonstrated. • PtCu/Cu 2-x Se NWs displayed 5.0 and 5.3-fold mass activity than commercial Pt/C for ethanol and methanol oxidation reaction. • PtCu/Cu 2-x Se NWs displayed higher efficiency to break C-C bond to produce more C1 intermediates than commercial Pt/C.

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