4.8 Article

Conductive N, S doped Copolymers as Stable Metal-Free Electrocatalysts for Water Splitting

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ACS APPLIED MATERIALS & INTERFACES
卷 15, 期 40, 页码 46829-46839

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AMER CHEMICAL SOC
DOI: 10.1021/acsami.3c08234

关键词

water splitting; copolymers; conducting polymers; metal-free catalyst; hydrogenevolution reaction; oxygen evolution reaction; protonaffinity

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A novel metal-free catalyst with remarkable activity in the oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) was synthesized. The catalyst exhibited low overpotential when deposited on a conductive nickel foam substrate. Additionally, it displayed lower operating potentials and good stability in an alkaline anion-exchange membrane electrolyzer.
Noble metals (Pt) and metal oxides (IrC and RuO2) are heavily utilized as benchmark electrocatalysts for alkaline water splitting; however, these materials possess several drawbacks including high cost, poor selectivity and stability, and high environmental impact. To address these issues, we synthesized a novel metal-free conducting polypyrrole-polythiophene (Ppy-Ptp) copolymer and a separate Ppy electrode material for water-splitting applications. The Ppy-Ptp and Ppy electrocatalysts exhibited remarkable activity in the oxygen evolution reaction (OER) and hydrogen evolution reaction (HER), respectively. The optimal Ppy-Ptp (1:3) formulation, when deposited on a conductive nickel foam (NF) substrate, exhibited an exceptional OER performance with a low overpotential of approximately 250 mV at 20 mAcm(-2), thereby outperforming the benchmark IrC/NF electrocatalyst (290 mV, 20 mAcm(-2)). Additionally, a similarly prepared Ppy/NF electrocatalyst exhibited an extraordinary HER performance with an overpotential of approximately 72 mV at 10 mA cm(-2). Furthermore, an alkaline anion-exchange membrane (AEM) electrolyzer incorporating Ppy-Ptp (1:3) and Ppy as the anode and cathode materials, respectively, displayed operating potentials of 1.55, 1.70, and 1.78 V at 10, 50, and 100 mA cm(-2), which are lower than those observed in previously reported electrolyzers. This electrolyzer also exhibited considerable operational endurance over 50 h at 50 mA cm(-2), over which a negligible decay of 0.02 V was observed. The novel polymer-based metal-free catalysts presented herein therefore exhibit considerable potential as alternative electrocatalytic materials for sustainable industrial-scale H-2 synthesis.

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