X射线光电子能谱
电化学
电催化剂
催化作用
电解
析氧
化学工程
价(化学)
材料科学
密度泛函理论
化学
电极
物理化学
计算化学
工程类
电解质
生物化学
有机化学
作者
Jiaxin Liu,Yue Shi,Yanli Gu,Zheng Lv,Liang Zhao,Yu Yang,Tianrong Zhan,Jianping Lai,Lei Wang
出处
期刊:Nano Research
[Springer Nature]
日期:2023-11-21
卷期号:17 (5): 3675-3683
被引量:10
标识
DOI:10.1007/s12274-023-6264-z
摘要
FeOOH have received considerable attention due to their natural abundance and cost-effectiveness. Despite the significant progress achieved, the one-step synthesis of integrated FeOOH is still a major challenge. Meanwhile, the current research on FeOOH catalyst still suffers from the unclear mechanism of controlling morphology. Here, density functional theory (DFT) calculations and X-ray photoelectron spectroscopy (XPS) demonstrated the strong electron-capturing and hydrogen absorption ability of Co in FeOOH, which further promotes the formation and stabilization of FeOOH. We used a one-step electrodeposition method to synthesize Co introduced FeOOH integrated electrocatalyst and propose to introduce ions with different valence states to regulate the morphology of FeOOH by precise modulation of electric double layer (EDL) composition and thickness. The prepared Co-FeOOH-K+ has a larger electrochemically active surface area (ECSA) (325 cm2) and turnover frequency (TOF) value (0.75 s−1). In the electrochemical experiments of an alkaline anion exchange membrane electrolyzer, Co-FeOOH-K+ shows better oxygen evolution performance than commercial RuO2 under industrial production conditions and has good industrial application prospects.
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