纳米片
双锰矿
催化作用
海水
普鲁士蓝
材料科学
化学工程
纳米技术
化学
无机化学
环境科学
环境化学
电化学
海洋学
电极
有机化学
地质学
物理化学
工程类
氧化锰
作者
Yuting Yang,Jixin Li,Wei Qiao,Han Yang,Yuqi Huang,Fengli Li,Yu Yu,Jingyun Fang,Ping Li
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2025-04-15
卷期号:15 (9): 6954-6968
被引量:29
标识
DOI:10.1021/acscatal.5c00581
摘要
Seawater electrolysis is appealing for mass production of high-purity H2, yet it remains challenging in engineering an efficient and robust oxygen evolution reaction (OER) anode to avoid undesired chloride oxidation reactions and resist chloride corrosion. Herein, we report a multilayered electrode with a Fe-phytate (Fe-PA) complex armor capped on the defect-rich Ni-doped δ-MnO2 ultrathin nanosheet array aligned on 3D macroporous Ni foam for boosted and sustained seawater oxidation at an industrial-level current density. From comprehensive experimental and theoretical investigations, the integration of the defect-rich Ni-MnO2 ultrathin nanosheet array configuration with a surface Fe-PA modification can provide abundant catalytic sites featuring an optimized electronic structure to promote the rate-determining step of *OH deprotonation to inherently boost the OER, and meanwhile impart superhydrophilicity and quasi-superaerophobicity to accelerate electrolyte infiltration and bubble detachment for facilitated mass transport. Impressively, the multilayered architecture comprising an inherently anticorrosive δ-MnO2 core and Fe-PA complex armor could cooperatively contribute to promoting corrosion resistance via effective chloride repelling. This work opens up a promising avenue for constructing MnO2-based materials toward promoted and long-lasting seawater oxidation via geometric and electronic modulation, which represents a significant step in advancing seawater electrolysis technology.
科研通智能强力驱动
Strongly Powered by AbleSci AI