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将废弃磷酸铁锂阴极升级为用于稳定直接海水分解的异质结构电催化剂。

Upcycling of Spent LiFePO Cathodes to Heterostructured Electrocatalysts for Stable Direct Seawater Splitting.

作者信息

Li Zhen, Li Mengting, Chen Yiqun, Ye Xucun, Liu Mengjie, Lee Lawrence Yoon Suk

机构信息

Department of Applied Biology and Chemical Technology and Research Institute for Smart Energy, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong SAR, China.

出版信息

Angew Chem Int Ed Engl. 2024 Oct 24;63(44):e202410396. doi: 10.1002/anie.202410396. Epub 2024 Sep 24.

Abstract

The pursuit of carbon-neutral energy has intensified the interest in green hydrogen production from direct seawater electrolysis, given the scarcity of freshwater resources. While Ni-based catalysts are known for their robust activity in alkaline water oxidation, their catalytic sites are prone to rapid degradation in the chlorine-rich environments of seawater, leading to limited operation time. Herein, we report a Ni(OH) catalyst interfaced with laser-ablated LiFePO (Ni(OH)/L-LFP), derived from spent Li-ion batteries (LIBs), as an effective and stable electrocatalyst for direct seawater oxidation. Our comprehensive analyses reveal that the PO species, formed around L-LFP, effectively repels Cl ions during seawater oxidation, mitigating corrosion. Simultaneously, the interface between in situ generated NiOOH and Fe(PO) enhances OH adsorption and electron transfer during the oxygen evolution reaction. This synergistic effect leads to a low overpotential of 237 mV to attain a current density of 10 mA cm and remarkable durability, with only a 3.3 % activity loss after 600 h at 100 mA cm in alkaline seawater. Our findings present a viable strategy for repurposing spent LIBs into high-performance catalysts for sustainable seawater electrolysis, contributing to the advancement of green hydrogen production technologies.

摘要

鉴于淡水资源的稀缺,对碳中和能源的追求加剧了人们对直接海水电解生产绿色氢气的兴趣。虽然镍基催化剂在碱性水氧化中具有强大的活性,但它们的催化位点在海水富含氯的环境中容易迅速降解,导致运行时间有限。在此,我们报告了一种由废旧锂离子电池(LIBs)衍生的、与激光烧蚀的LiFePO(Ni(OH)/L-LFP)界面结合的Ni(OH)催化剂,作为一种用于直接海水氧化的有效且稳定的电催化剂。我们的综合分析表明,在L-LFP周围形成的PO物种在海水氧化过程中有效地排斥Cl离子,减轻腐蚀。同时,原位生成的NiOOH与Fe(PO)之间的界面在析氧反应过程中增强了OH吸附和电子转移。这种协同效应导致在达到10 mA cm的电流密度时过电位低至237 mV,并且具有出色的耐久性,在碱性海水中于100 mA cm下600小时后活性仅损失3.3%。我们的研究结果提出了一种可行的策略,即将废旧LIBs重新用作可持续海水电解的高性能催化剂,为绿色氢气生产技术的进步做出贡献。

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