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Li et al. Energy Mater 2023;3:300021  https://dx.doi.org/10.20517/energymater.2023.09  Page 11 of 16













































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                Figure 5. (A) LSV curves, (B) Corresponding overpotentials at 10 mA cm  (η ), and (C) Tafel plots of Se@NiFe, FePc/Se@NiFe,
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                FePc/Se@Ni, FePc/Se@Fe and RuO  in O -saturated 1.0 M KOH. (D) LSV recorded before and after ADT for 5,000 cycles and (E) OER
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                I-T tests of FePc/Se@NiFe and RuO  at overpotential. (F) Polarization curves of FePc/Se@NiFe for dual-functional catalytic activity. (G)
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                Dual-functional electrocatalytic activity of the FePc/Se@NiFe, Pt/C + RuO , and the previously reported electrocatalysts based on
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                transition metal selenides.
               (212.7 mV dec ) and the state-of-the-art RuO  catalyst (187.2 mV dec ). Then, the FePc/Se@NiFe also
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               exhibits excellent durability in terms of OER. As depicted in Figure 5D, the FePc/Se@NiFe display almost a
               negligible decay of OER activity after 5,000 CV cycles through an ADT. However, the overpotential of RuO
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               increased significantly under the same testing conditions. After the ADT test, there is no noticeable change
               in  the  structure  and  morphology  of  FePc/Se@NiFe,  as  evident  from  the  XRD  and  SEM  in
               Supplementary Figure 5C and D. Furthermore, I-T examinations also are implemented to detect the
               durability of FePc/Se@NiFe at a given potential of 1.55 V (vs. RHE). As displayed in Figure 5E, FePc/
               Se@NiFe can retain its 80.8% catalytic activity after 24 h stability tests. In contrast, the current response of
               RuO  manifests significant fluctuations with a low retention rate of initial current densities (70.8%),
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               suggesting further the excellent durability of FePc/Se@NiFe. In general, the dual-functional electrocatalytic
               activity and reversibility are estimated from the potential difference ΔE (E = E  - E ), where a smaller
                                                                                    j=10
                                                                                         1/2
               value of E implies better dual-functional activity. Remarkably, the FePc/Se@NiFe electrocatalyst reached an
               impressive ΔE value of 0.622 V, which is better than FePc (0.91 V), NiFe-LDH (0.96 V), Pt/C + RuO
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               (0.685 V) [Supplementary Figure 7D] and most previously reported high-performance dual-functional
               catalysts based on transition metal selenides [Figure 5F and G]. The smallest potential gap indicates the
               tremendous potential of FePc/Se@NiFe for practical application in rechargeable ZABs. Exceptional
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