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Chen et al. Energy Mater 2022;2:200033  https://dx.doi.org/10.20517/energymater.2022.36  Page 9 of 11

               Table 1. Comparison of electrochemical catalysis
                                      ECSA (m /g)              MA (mA/mg )           Half-wave potential (V)
                                             2
                Samples                                                 Pt
                               Initial  After ADT  Loss  Initial  After ADT  Loss  Initial  After ADT  Loss
                PtCu aerogels/C  43.6  34.0       22.1%  369.4  213.7      42.3%  0.926  0.906      0.020
                Pt/C           54.3   47.1        13.4%  140.0  105.0      25.0%  0.885  0.873      0.012

















                Figure 7. Structural characterization of PtCu aerogels/C obtained after ADT. (A, B) HRTEM images and (C) HAADF-STEM and EDX
                mapping images.


               We considered that the enhanced ORR activity of the PtCu aerogels may originate from two aspects. For the
               topological structure of the PtCu aerogels, the high specific area provided more active sites and the larger
               porosity helped improve the mass transfer. For the crystal structure of the PtCu alloy, alloying with Cu
               lowers the d-band center of Pt and consequently weakens the oxygen adsorption energy of Pt, helping
                                 [1]
               increase the activity . Furthermore, the PtCu exposed mainly (111) facets, which is the best facet for
               catalyzing ORR . As a result, the PtCu aerogels exhibited excellent electrochemical catalysis towards the
                            [36]
               ORR.

               CONCLUSIONS
               In conclusion, PtCu aerogels were successfully synthesized by a facile NaBH  reduction reaction and showed
                                                                               4
               a porous structure with high specific surface areas. The synthesis period was effectively reduced from tens of
               hours to tens of minutes. By controlling the addition of citrate, we discussed that the gelation of PtCu
               followed the rapid nucleation mechanism. Moreover, the as-prepared PtCu aerogels exposed mainly the
               most active facets for the ORR and consequently exhibited a remarkable ORR performance compared to
               Pt/C. This facile route and good catalytic activity may help develop efficient catalysts for fuel cell
               applications.


               DECLARATIONS
               Authors’ contributions
               Experiments, data analysis and manuscript writing: Chen Z
               Assistance in experiments and data analysis: Liao Y
               Supervision of the research: Chen S


               Availability of data and materials
               Not applicable.
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