Defect-rich Birnessite Ultrathin Nanosheet Array Armed with Fe-Phytate Complex Enables Boosted and Long-Lasting Seawater Oxidation at Industrial-Level Current Density

IF 13.1 1区 化学 Q1 CHEMISTRY, PHYSICAL ACS Catalysis Pub Date : 2025-04-15 DOI:10.1021/acscatal.5c00581
Yuting Yang, Jixin Li, Wei Qiao, Han Yang, Yuqi Huang, Fengli Li, Yu Yu, Jingyun Fang, Ping Li
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Abstract

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.

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富含缺陷的桦褐铁矿超薄纳米片阵列与铁-hytate复合物可在工业级电流密度下实现高效持久的海水氧化作用
海水电解对大规模生产高纯度H2具有吸引力,但在设计高效且坚固的析氧反应(OER)阳极以避免不期望的氯化物氧化反应和抗氯化物腐蚀方面仍然具有挑战性。在此,我们报道了一种多层电极,其上覆盖有铁-植酸盐(Fe-PA)复合护甲,覆盖在富含缺陷的Ni掺杂δ-MnO2超薄纳米片阵列上,这些纳米片阵列排列在3D大孔Ni泡沫上,用于在工业级电流密度下促进和持续的海水氧化。综合实验和理论研究发现,将缺陷丰富的Ni-MnO2超薄纳米片阵列构型与Fe-PA表面改性相结合,可以提供丰富的具有优化电子结构的催化位点,促进*OH去质子化的速率决定步骤,从而内在地提高OER。同时赋予超亲水性和准超疏水性以加速电解质的渗透和气泡脱离,促进质量的传递。令人印象深刻的是,由固有防腐δ-MnO2核心和Fe-PA复合装甲组成的多层结构可以通过有效的氯化物排斥来共同促进耐腐蚀性。这项工作为构建基于二氧化锰的材料,通过几何和电子调制促进和持久的海水氧化开辟了一条有前途的途径,这是推进海水电解技术的重要一步。
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来源期刊
ACS Catalysis
ACS Catalysis CHEMISTRY, PHYSICAL-
CiteScore
20.80
自引率
6.20%
发文量
1253
审稿时长
1.5 months
期刊介绍: ACS Catalysis is an esteemed journal that publishes original research in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. It offers broad coverage across diverse areas such as life sciences, organometallics and synthesis, photochemistry and electrochemistry, drug discovery and synthesis, materials science, environmental protection, polymer discovery and synthesis, and energy and fuels. The scope of the journal is to showcase innovative work in various aspects of catalysis. This includes new reactions and novel synthetic approaches utilizing known catalysts, the discovery or modification of new catalysts, elucidation of catalytic mechanisms through cutting-edge investigations, practical enhancements of existing processes, as well as conceptual advances in the field. Contributions to ACS Catalysis can encompass both experimental and theoretical research focused on catalytic molecules, macromolecules, and materials that exhibit catalytic turnover.
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