Liu Xiaoming, Zhuo Mulin, Zhang Wendi, Gao Man, Liu Xuan-He, Sun Bing, Wu Jing
School of Science, China University of Geosciences (Beijing), Beijing 100083, People's Republic of China.
School of Science, China University of Geosciences (Beijing), Beijing 100083, People's Republic of China.
Ultrason Sonochem. 2020 Oct;67:105179. doi: 10.1016/j.ultsonch.2020.105179. Epub 2020 May 19.
The inherent periodically arranged M-N, M-S and M-O units (M are usually Fe, Co, Ni, etc.) in metal-organic frameworks (MOFs) can be promising active centers in electrocatalysis. In previous studies, MOFs were usually constructed by energy-consuming hydro- or solvo-thermal reactions. Ultrasonic synthesis is a rapid and environment-friendly technique when envisaging MOFs' industrial applications. In addition, different synthetic pathways for MOFs may lead to difference in their microstructure, resulting in different electrocatalytic performance. Nevertheless, only a handful of MOFs were successfully prepared by ultrasonic synthesis and few were applied in electrochemical catalysis. Herein, we constructed Ni/Co-catecholates (Ni/Co-CATs) synthesized by one-step ultrasonic method (250 W, 40 KHz, 25 W/L, Ultrasonic clearing machine) and compared their performance in oxygen reduction reaction (ORR) with that of Ni/Co-CATs synthesized by hydrothermal method. Ni-CAT and Co-CAT prepared by ultrasonic showed the half-wave potential of -0.196 V and -0.116 V (vs. Ag/AgCl), respectively. The potentials were more positive than those prepared by hydro-thermal method. And they showed excellent electrochemical stability in neutral solution. The latter was only 32 mV lower than that of commercial Pt/C. The improved performance in ORR was attributed to higher specific surface area and mesopore volume as well as more structural defects generated in the ultrasonic synthesis process, which could facilitate their exposure of electrocatalytic active sites and their mass transport. This work gives some perspective into cost-effective synthetic strategies of efficient MOFs-based electrocatalysts.
金属有机框架材料(MOFs)中固有的周期性排列的M-N、M-S和M-O单元(M通常为铁、钴、镍等)有望成为电催化中的活性中心。在以往的研究中,MOFs通常通过耗能的水热或溶剂热反应构建。考虑到MOFs的工业应用,超声合成是一种快速且环境友好的技术。此外,MOFs的不同合成途径可能导致其微观结构存在差异,从而产生不同的电催化性能。然而,通过超声合成成功制备的MOFs数量很少,应用于电化学催化的更是寥寥无几。在此,我们构建了通过一步超声法(250 W,40 KHz,25 W/L,超声清洗机)合成的镍/钴儿茶酚盐(Ni/Co-CATs),并将其在氧还原反应(ORR)中的性能与水热法合成的Ni/Co-CATs进行了比较。超声法制备的Ni-CAT和Co-CAT的半波电位分别为-0.196 V和-0.116 V(相对于Ag/AgCl)。这些电位比水热法制备的更正向。并且它们在中性溶液中表现出优异的电化学稳定性。后者仅比商业Pt/C低32 mV。ORR性能的提高归因于更高的比表面积和中孔体积,以及超声合成过程中产生的更多结构缺陷,这有利于电催化活性位点的暴露及其传质。这项工作为基于MOFs的高效电催化剂的经济高效合成策略提供了一些思路。