Chen Mengxin, Zhang Yuanyuan, Chen Ji, Wang Ran, Zhang Bin, Song Bo, Xu Ping
MIIT Key Laboratory of Critical Materials Technology for New Energy Conversion and Storage, School of Chemistry and Chemical Engineering, Harbin Institute of Technology, Harbin, 150001, P. R. China.
Key Laboratory for Photonic and Electronic Bandgap Materials, Harbin Normal University, Harbin, 150025, P. R. China.
Small. 2024 Jun;20(23):e2309371. doi: 10.1002/smll.202309371. Epub 2024 Jan 2.
Construction of heterojunctions is an effective strategy to enhanced electrocatalytic oxygen evolution reaction (OER), but the structural evolution of the active phases and synergistic mechanism still lack in-depth understanding. Here, an FeOOH/NiS heterostructure supported on nickel foam (NF) through a two-step hydrothermal-chemical etching method is reported. In situ Raman spectroscopy study of the surface reconstruction behaviors of FeOOH/NiS/NF indicates that NiS can be rapidly converted to NiOOH, accompanied by the phase transition from α-FeOOH to β-FeOOH during the OER process. Importantly, a deep analysis of Ni─O bond reveals that the phase transition of FeOOH can regulate the lattice disorder of NiOOH for improved catalytic activity. Density functional theory (DFT) calculations further confirm that NiOOH/FeOOH heterostructure possess strengthened adsorption for O-containing intermediates, as well as lower energy barrier toward the OER. As a result, FeOOH/NiS/NF exhibits promising OER activity and stability in alkaline conditions, requiring an overpotential of 268 mV @ 100 mA cm and long-term stability over 200 h at a current density of 200 mA cm. This work provides a new perspective for understanding the synergistic mechanism of heterogeneous electrocatalysts during the OER process.
构建异质结是增强电催化析氧反应(OER)的有效策略,但活性相的结构演变和协同机制仍缺乏深入了解。在此,报道了一种通过两步水热-化学蚀刻法负载在泡沫镍(NF)上的FeOOH/NiS异质结构。对FeOOH/NiS/NF表面重构行为的原位拉曼光谱研究表明,在OER过程中,NiS可迅速转化为NiOOH,同时伴随着α-FeOOH向β-FeOOH的相变。重要的是,对Ni─O键的深入分析表明,FeOOH的相变可调节NiOOH的晶格无序度,从而提高催化活性。密度泛函理论(DFT)计算进一步证实,NiOOH/FeOOH异质结构对含O中间体具有增强的吸附作用,并且对OER具有较低的能垒。因此,FeOOH/NiS/NF在碱性条件下表现出有前景的OER活性和稳定性,在100 mA cm时过电位为268 mV,在200 mA cm的电流密度下具有超过200 h的长期稳定性。这项工作为理解OER过程中异质电催化剂的协同机制提供了新的视角。