Ma Fahao, Wu Qian, Liu Mu, Zheng Liren, Tong Fengxia, Wang Zeyan, Wang Peng, Liu Yuanyuan, Cheng Hefeng, Dai Ying, Zheng Zhaoke, Fan Yuchen, Huang Baibiao
State Key Laboratory of Crystal Materials, Shandong University, Jinan 250100, P. R. China.
School of Physics, Shandong University, Jinan 250100, P. R. China.
ACS Appl Mater Interfaces. 2021 Feb 3;13(4):5142-5152. doi: 10.1021/acsami.0c20886. Epub 2021 Jan 22.
Surface engineering is of importance to reduce the reaction barrier of oxygen evolution reaction (OER). Herein, the NiFe Prussian blue analogue (NiFe-PBA)-F catalyst with a multilevel structure was obtained from NiFe-PBAs via a fluorination strategy, which presents an ultralow OER overpotential of 190 mV at 10 mA cm in alkaline solution, with a small Tafel slope of 57 mV dec and excellent stability. Interestingly, surface fluorination engineering could achieve a controllable removal of ligands of the cyan group, contributing to keep the framework structure of NiFe-PBAs. Particularly, NiFe-PBAs-F undergoes a dramatic reconstruction with the dynamic migration of F ions, which creates more active sites of F-doped NiFeOOH and affords more favorable adsorption of oxygen intermediates. Density functional theory calculations suggest that F doping increases the state density of Ni 3d orbital around the Fermi level, thus improving the conductivity of NiFeOOH. Furthermore, based on our experimental results, the lattice oxygen oxidation mechanism for NiFe-PBAs-F was proposed. Our work not only provides a new pathway to realize the controllable pyrolysis of NiFe-PBAs but also gives more insights into the reconstruction and the mechanism for the OER process.
表面工程对于降低析氧反应(OER)的反应势垒具有重要意义。在此,通过氟化策略从镍铁普鲁士蓝类似物(NiFe-PBA)制备了具有多级结构的NiFe普鲁士蓝类似物-F(NiFe-PBA-F)催化剂,该催化剂在碱性溶液中10 mA cm时呈现出190 mV的超低OER过电位,塔菲尔斜率小至57 mV dec,且具有出色的稳定性。有趣的是,表面氟化工程可实现对氰基配体的可控去除,有助于保持NiFe-PBA的骨架结构。特别地,NiFe-PBA-F随着F离子的动态迁移经历了显著的重构,形成了更多F掺杂的NiFeOOH活性位点,并为氧中间体提供了更有利的吸附。密度泛函理论计算表明,F掺杂增加了费米能级附近Ni 3d轨道的态密度,从而提高了NiFeOOH的导电性。此外,基于我们的实验结果,提出了NiFe-PBA-F的晶格氧氧化机制。我们的工作不仅为实现NiFe-PBA的可控热解提供了一条新途径,也为OER过程的重构和机制提供了更多见解。