Abstract
This study reports the successful synthesis of a novel electrocatalyst for oxygen reduction reactions (ORR), comprising S,N dual-doped carbon nanofibers with atomically dispersed Co/Ni species (denoted as Co,Ni-SAs/S,N-CNFs), leveraging electrostatic spinning to achieve a unique spatial architecture that maximizes both active site density and mass transport efficiency. Density functional theory (DFT) analysis identified the initial proton-electron transfer to adsorbed O2 as the rate-limiting step, with CoN3S1-NiN3S1 emerging as the pivotal active site structure catalyzing this critical reaction. The fabricated Co,Ni-SAs/S,N-CNFs electrocatalyst exhibited remarkable ORR performance, characterized by a high half-wave potential of 0.84 V and a low Tafel slope of 57.9 mV dec-1. To gain a comprehensive understanding of its catalytic behavior, a tailored temperature-controlled scanning electrochemical microscopy (SECM) was employed, enabling the mapping of reactivity distribution under simulated operating conditions while preserving structural integrity. Liquid zinc-air batteries (ZABs) with this electrocatalyst excelled, reaching 175 mW/cm2 power density and enduring 1240 cycles. The electrospun membrane catalyst enabled both button and flexible ZABs, adaptable to diverse environments. This study advances non-precious metal electrocatalyst design and offers insights for ZAB applications, fostering green energy prospects.
Published Version
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