Yun He , Zheng Wang , Zhikai Hu , Yanling Hu , Xinxin Fan , Shuling Liu , Chao Wang
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引用次数: 0
Abstract
Active and stable electrocatalysts for oxygen evolution reaction (OER) is crutial in the widespread application of hydrogen production from water electrolyzers. Here, deep eutectic solvents formed from metal chlorides and l-serine are utilized as the electrolyte to deposit metal films (Ni, Fe, and Ni-Fe alloys) under potentiostatic conditions onto nickel foam (NF) substrate. The deposited films are characterized, and the Ni-Fe alloy films constituting of nanometer-sized crystalline regions. Electron interaction between Ni and Fe is observed. In 1 M KOH, Ni-Fe/NF requires only 219 mV overpotential to achieve a current density of 10 mA cm−2, and can stably catalyze OER in alkaline solutions. Compared to the Ni/NF and Fe/NF, the high OER activity of Ni-Fe/NF is not originated from improved number of active sites, but from the enhanced intrinsic activity, evidenced by the improved OER kinetics caused by the electron interaction. The acidity of the Ni site increases due to the introduction of Fe, and lattice oxygen mechanism is involved in the OER process on Ni-Fe/NF. After long-term OER, metal oxides and (oxy)hydroxides are formed at the surface.
活性稳定的析氧反应电催化剂是水电解槽制氢技术广泛应用的关键。在这里,由金属氯化物和l-丝氨酸形成的深共晶溶剂被用作电解液,在恒电位条件下将金属薄膜(Ni, Fe和Ni-Fe合金)沉积在泡沫镍(NF)衬底上。对沉积膜进行了表征,发现镍铁合金薄膜由纳米级结晶区组成。观察到Ni和Fe之间的电子相互作用。在1 M KOH条件下,Ni-Fe/NF只需要219 mV过电位就可以达到10 mA cm−2的电流密度,并且可以在碱性溶液中稳定催化OER。与Ni/NF和Fe/NF相比,Ni-Fe/NF的高OER活性不是源于活性位点数量的增加,而是源于内在活性的增强,这可以通过电子相互作用引起的OER动力学的改善来证明。Fe的加入使Ni位点的酸度增加,晶格氧机制参与了Ni-Fe/NF的OER过程。经过长期OER,金属氧化物和(氧)氢氧化物在表面形成。
期刊介绍:
The Journal of Colloid and Interface Science publishes original research findings on the fundamental principles of colloid and interface science, as well as innovative applications in various fields. The criteria for publication include impact, quality, novelty, and originality.
Emphasis:
The journal emphasizes fundamental scientific innovation within the following categories:
A.Colloidal Materials and Nanomaterials
B.Soft Colloidal and Self-Assembly Systems
C.Adsorption, Catalysis, and Electrochemistry
D.Interfacial Processes, Capillarity, and Wetting
E.Biomaterials and Nanomedicine
F.Energy Conversion and Storage, and Environmental Technologies