Bai Xue, Wang Qin, Xu Guangran, Ning Yunkun, Huang Keke, He Feng, Wu Zhi-Jian, Zhang Jun
College of Chemistry and Chemical Engineering, Inner Mongolia University, Hohhot, 010021, P. R. China.
Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, 518055, P. R. China.
Chemistry. 2017 Nov 27;23(66):16862-16870. doi: 10.1002/chem.201703712. Epub 2017 Nov 6.
Electrocatalytic splitting of water is becoming increasingly crucial for renewable energy and device technologies. As one of the most important half-reactions for water splitting reactions, the oxygen evolution reaction (OER) is a kinetically sluggish process that will greatly affect the energy conversion efficiency. Therefore, exploring a highly efficient and durable catalyst to boost the OER is of great urgency. In this work, we develop a facile strategy for the synthesis of well-defined phosphorus and fluorine co-doped Ni Co N hybrid nanorods (HNs) by using ionic liquids (ILs; 1-butyl-3-methylimidazolium hexafluorophosphate). In comparison to the IrO catalyst, the as-obtained PF/Ni Co N HNs manifests a low overpotential of 280 mV at 10 mA cm , Tafel slope of 66.1 mV dec , and excellent durability in 1.0 m KOH solution. Furthermore, the iR-corrected electrochemical results indicate it could achieve a current density of 100 mA cm at an overpotential of 350 mV. The combination of cobalt and nickel elements, 1D mesoporous nanostructure, heteroatom incorporation, and ionic liquid-assisted nitridation, which result in faster charge transfer capability and more active surface sites, can facilitate the release of oxygen bubbles from the catalyst surface. Our findings confirm that surface heteroatom doping in bimetallic nitrides could serve as a new class of OER catalyst with excellent catalytic activity.
水的电催化分解对于可再生能源和器件技术而言正变得愈发关键。作为水分解反应中最重要的半反应之一,析氧反应(OER)是一个动力学缓慢的过程,这将极大地影响能量转换效率。因此,探索一种高效且耐用的催化剂来促进OER迫在眉睫。在这项工作中,我们开发了一种简便的策略,通过使用离子液体(ILs;1-丁基-3-甲基咪唑六氟磷酸盐)来合成结构明确的磷和氟共掺杂的Ni Co N混合纳米棒(HNs)。与IrO催化剂相比,所制备的PF/Ni Co N HNs在10 mA cm时表现出280 mV的低过电位,塔菲尔斜率为66.1 mV dec,并且在1.0 m KOH溶液中具有出色的耐久性。此外,经iR校正的电化学结果表明,它在350 mV的过电位下可实现100 mA cm的电流密度。钴和镍元素的组合、一维介孔纳米结构、杂原子掺入以及离子液体辅助氮化,导致更快的电荷转移能力和更多的活性表面位点,能够促进氧气泡从催化剂表面释放。我们的研究结果证实,双金属氮化物中的表面杂原子掺杂可作为一类具有优异催化活性的新型OER催化剂。