| Abstrakt: |
The electrocatalytic oxygen evolution reaction (OER) and oxygen reduction reaction (ORR) are the core reactions in reversible zinc-air batteries but are kinetically challenging because of their complex multielectron transfer process. In this case, the exploration and rational design of non-precious bifunctional oxygen electrocatalysts with dense active sites and optimized electronic structures can facilitate favorable 4e-transfer. In this study, we report a highly reversible bifunctional electrocatalyst for flexible Zn-air batteries featuring pyridinic-N exclusively enriched carbon-nanotube-encased nickel-iron (NiFe) interfacial alloy nanoparticles derived from an LDH template on knitted carbon fiber cloth. The NiFe nanoparticles were catalytically released from NiFe-MOFs to form CNT tentacles when pyrolyzed in an inert atmosphere. XPS and XAS studies revealed the dominant presence of pyridinic-N, which reduces electron localization around NiFe centers and improves the interaction with oxygenated species. As a result, NiFe-N-CNT-KCC catalysts exhibited a low operating overpotential (h10) of 173 mV for the OER and a half-wave potential (E1/2) of 0.87 V for the ORR, which are superior to benchmark electrocatalysts. As an air cathode for zinc-air batteries, the NiFe-N-CNT-KCC-based battery showed an excellent electrochemical performance, with an open circuit voltage (OCV) of 1.55 V, high power density of 153 mW cm-2, excellent specific capacity of 793.2 mA h g-1, and long-term stability. Impressively, a solidstate flexible zinc-air battery with the NiFe-N-CNT-KCC cathode showed an admirable rate performance and exceptional mechanical stability under arbitrary bending and twisting conditions, showing great potential for practical implementation in next-generation high-power and high-energydensity batteries wearable applications. [ABSTRACT FROM AUTHOR] |
