Feng Zhonghan, Pu Jiayan, Liu Maosheng, Zhang Wenxiu, Zhang Xinyue, Cui Liang, Liu Jingquan
College of Materials Science and Engineering, Institute for Graphene Applied Technology Innovation, Qingdao University, Qingdao 266071, China.
College of Materials Science and Engineering, Linyi University, Linyi 276000, Shandong, China.
J Colloid Interface Sci. 2022 May;613:806-813. doi: 10.1016/j.jcis.2022.01.081. Epub 2022 Jan 15.
Herein, a hierarchical CoS/CeO nanorod array on cobalt foam (CoS/CeO-CF) was successfully constructed via a facile one-step hydrothermal method. The fabrication of CoS/CeO-CF was confirmed by X-ray diffraction, scanning electron microscope (SEM), high resolution transmission electron microscope (HRTEM). It is observed that CeO nanorod was fully covered with CoS nanosheets, forming a hierarchical core-shell nanostructure. Furthermore, CeO and CoS were doped with each other during the one-step hydrothermal process, forming a heterogeneous CoS/CeO nanostructure. Density functional theory (DFT) calculations suggest that the introduction of CeO in CoS is effective in reducing the free energy barrier of OER process. To achieve current density of 10 mA cm, only small overpotentials of 74.9 mV and 213 mV are required for HER and OER in 1.0 M KOH solution, respectively. In particular, the CoS/CeO-CF based electrolysis cell for overall water splitting only needs an output voltage of 1.64 V in the alkaline medium, lower than that of Pt/C-RuO-based electrolysis cells (1.70 V). Such hierarchical heterogeneous catalyst also shows ultra-stable catalytic activity. Therefore, with the favorable heterointerfaces and hierarchical structures, CoS/CeO-CF could be a promising bifunctional electrocatalyst for overall water splitting and this study may also provide a facile method for the preparation of hierarchical heterogeneous nanostructured materials.
在此,通过简便的一步水热法成功构建了泡沫钴上的分级CoS/CeO纳米棒阵列(CoS/CeO-CF)。通过X射线衍射、扫描电子显微镜(SEM)、高分辨率透射电子显微镜(HRTEM)对CoS/CeO-CF的制备进行了确认。观察到CeO纳米棒被CoS纳米片完全覆盖,形成了分级核壳纳米结构。此外,在一步水热过程中CeO和CoS相互掺杂,形成了异质CoS/CeO纳米结构。密度泛函理论(DFT)计算表明,在CoS中引入CeO有效地降低了析氧反应(OER)过程的自由能垒。在1.0 M KOH溶液中,要达到10 mA cm的电流密度,析氢反应(HER)和析氧反应分别仅需要74.9 mV和213 mV的小过电位。特别是,用于全水分解的基于CoS/CeO-CF的电解池在碱性介质中仅需要1.64 V的输出电压,低于基于Pt/C-RuO的电解池(1.70 V)。这种分级异质催化剂还表现出超稳定的催化活性。因此,凭借良好的异质界面和分级结构,CoS/CeO-CF可能是一种有前景的用于全水分解的双功能电催化剂,并且本研究也可能为制备分级异质纳米结构材料提供一种简便方法。