Zhu Kaijian, Luo Wenjun, Zhu Guoxiang, Wang Jun, Zhu Yongfa, Zou Zhigang, Huang Wei
Key Laboratory of Flexible Electronics (KLOFE), Institute of Advanced Materials (IAM), Jiangsu National Synergetic Innovation Center for Advanced, Materials (SICAM), Nanjing Tech University (NanjingTech), 30 South Puzhu Road, Nanjing, 211816, P.R. China.
Department of Chemistry, Tsinghua University, Beijing, 100084, P.R. China.
Chem Asian J. 2017 Oct 18;12(20):2720-2726. doi: 10.1002/asia.201700964. Epub 2017 Sep 21.
Iron-based (oxy)hydroxides are especially attractive electrocatalysts for the oxygen evolution reaction (OER) owing to their earth abundance, low cost, and nontoxicity. However, poor OER kinetics on the surface restricts the performance of the FeOOH electrocatalyst. Herein, a highly efficient and stable Ni(OH) /β-like FeOOH electrocatalyst is obtained by facile electroactivation treatment. The activated Ni(OH) /β-like FeOOH sample indicates an overpotential of 300 mV at 10 mA cm for the OER, and no clear current decay after 50 h of testing; this is comparable to the most efficient nickel- and cobalt-based electrocatalysts on planar substrates. Furthermore, studies suggest that β-like FeOOH plays a key role in remarkably enhancing the performance during the electroactivation process owing to its metastable tunnel structure with a lower barrier for interface diffusion of Ni ions between the bilayer electrocatalyst. This study develops a new strategy to explore efficient and low-cost electrocatalysts and deepens understanding of bilayer electrocatalysts for the OER.
铁基(羟基)氧化物因其在地壳中储量丰富、成本低且无毒,是析氧反应(OER)极具吸引力的电催化剂。然而,其表面较差的析氧反应动力学限制了FeOOH电催化剂的性能。在此,通过简便的电活化处理获得了一种高效且稳定的Ni(OH) /β型FeOOH电催化剂。活化后的Ni(OH) /β型FeOOH样品在10 mA cm的析氧反应中过电位为300 mV,测试50 h后没有明显的电流衰减;这与平面基底上最有效的镍基和钴基电催化剂相当。此外,研究表明,β型FeOOH因其亚稳态隧道结构在双层电催化剂中对Ni离子的界面扩散具有较低势垒,在电活化过程中对显著提高性能起着关键作用。本研究开发了一种探索高效低成本电催化剂的新策略,并加深了对用于析氧反应的双层电催化剂的理解。