He Bowen, Kuang Panyong, Li Xiaohe, Chen Hu, Yu Jiaguo, Fan Ke
State Key Laboratory of Advanced Technology for, Materials Synthesis and Processing, Wuhan University of Technology, Wuhan, 430070, P. R. China.
International School of Material Science and Engineering, Wuhan University of Technology, Wuhan, 430070, P. R. China.
Chemistry. 2020 Mar 26;26(18):4052-4062. doi: 10.1002/chem.201902659. Epub 2019 Sep 10.
Using bimetallic Prussian blue analogue (PBA) as a precursor is effective for preparing electrocatalysts for the oxygen evolution reaction (OER); however, the role of these PBA-derived catalysts in the OER is still ambiguous. Herein, by simply controlling synthesis temperature, a bimetallic PBA-derived O,N-codoped Ni-Fe carbide, can be well tuned to optimize structure and OER performance. Importantly, by a series of ex situ and in situ investigations, real active species of NiFeO H are in situ formed on the surface during the OER, which reveals a "pre-catalyst" role of O,N-codoped Ni-Fe carbides. Furthermore, it has been successfully applied to highly efficient Zn-air batteries and outplays its RuO counterpart. When applied to photoelectrocatalytic water oxidation as the co-catalyst, it improves the performance of the BiVO photoanode by enhancing hole collecting and transporting ability. We believe this research not only provides a highly efficient and low-cost electrocatalyst for the OER, but also unveils the "pre-catalyst" role of PBA-derived materials in energy-storage and conversion devices.
使用双金属普鲁士蓝类似物(PBA)作为前驱体对于制备用于析氧反应(OER)的电催化剂是有效的;然而,这些源自PBA的催化剂在OER中的作用仍然不明确。在此,通过简单地控制合成温度,可以很好地调节一种源自双金属PBA的O、N共掺杂的Ni-Fe碳化物,以优化其结构和OER性能。重要的是,通过一系列非原位和原位研究,在OER过程中,表面原位形成了真正的活性物种NiFeO H,这揭示了O、N共掺杂的Ni-Fe碳化物的“预催化剂”作用。此外,它已成功应用于高效锌空气电池,并优于其RuO对应物。当作为共催化剂应用于光电催化水氧化时,它通过增强空穴收集和传输能力提高了BiVO光阳极的性能。我们相信这项研究不仅为OER提供了一种高效且低成本的电催化剂,还揭示了源自PBA的材料在能量存储和转换装置中的“预催化剂”作用。