海水
硫化钴
过电位
钴
硫化物
催化作用
分解水
析氧
化学
离解(化学)
法拉第效率
无机化学
镍
电解水
氧化物
电解
材料科学
电解质
地质学
海洋学
电化学
物理化学
电极
有机化学
光催化
生物化学
作者
Ahmed Badreldin,Jehad Abed,Noor Hafizah Hassan,Abdellatif El-Ghenymy,Wafa Suwaileh,Wubulikasimu Yiming,Zafar Khan Ghouri,Karim Hassan Youssef,Dharmesh Kumar,Khaled Elsaid,Edward H. Sargent,Ahmed Abdel‐Wahab
标识
DOI:10.1016/j.apcatb.2023.122599
摘要
Sluggish kinetics of the anodic oxygen evolution reaction (OER) and minor upstream upsets in feed water quality remain bottlenecks for efficient water electrolysis, which is exacerbated under near-neutral pH environments due to H2O dissociation. In this work, we report the introduction of a NiSx interlayer in a Co-(NiFe) oxide/nitride catalyst on nickel foam substrate. Postmortem OER characterization in neutral pH synthetic seawater (SSW) shows that stable cationic [Co-(NiFe)]δ+ and anionic [O-N]δ– surface species coupled with the NiSx interlayer accelerate H2O dissociation, thereby enhancing activity and kinetics. The electrocatalysts exhibit stable performance at 100 mA cm−2 for 50 h in alkaline and neutral pH SSW with 350 and 425 mV of overpotential, respectively. The faradaic efficiency of the NiSx interlayer catalysts is enhanced by 10.3% and 8.5% achieving 94.5% and 87.4% under alkaline and neutral pH SSW, respectively, during chronoamperometry tests at a high applied voltage of 1.75 V (vs. RHE).
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