Department of Chemical Technology, Faculty of Chemistry, Adam Mickiewicz University in Poznań, Uniwersytetu Poznańskiego 8, 61-614Poznań, Poland.
Faculty of Chemistry, Jagiellonian University, Gronostajowa 2, 30-387Krakow, Poland.
ACS Appl Mater Interfaces. 2023 Feb 1;15(4):5148-5160. doi: 10.1021/acsami.2c18403. Epub 2023 Jan 19.
The effective use of the active phase is the main goal of the optimization of supported catalysts. However, carbon supports do not interact strongly with metal oxides, thus, oxidative treatment is often used to enhance the number of anchoring sites for deposited particles. In this study, we set out to investigate whether the oxidation pretreatment of mesoporous carbon allows the depositing of a higher loading and a more dispersed cobalt active phase. We used graphitic ordered mesoporous carbon obtained by a hard-template method as active phase support. To obtain different surface concentrations and speciation of oxygen functional groups, we used a low-temperature oxygen plasma. The main methods used to characterize the studied materials were X-ray photoelectron spectroscopy, transmission electron microscopy, and electrocatalytic tests in the oxygen evolution reaction. We have found that the oxidative pretreatment of mesoporous carbon influences the speciation of the deposited cobalt oxide phase. Moreover, the activity of the electrocatalysts in oxygen evolution is positively correlated with the relative content of the COO-type groups and negatively correlated with the C═O-type groups on the carbon support. Furthermore, the high relative content of COO-type groups on the carbon support is correlated with the presence of well-dispersed CoO nanoparticles. The results obtained indicate that to achieve a better dispersed and thus more catalytically active material, it is more important to control the speciation of the oxygen functional groups rather than to maximize their total concentration.
有效利用活性相是优化负载型催化剂的主要目标。然而,碳载体与金属氧化物的相互作用不强,因此,通常采用氧化处理来增强沉积颗粒的锚固位点数。在本研究中,我们旨在研究介孔碳的氧化预处理是否允许沉积更高负载量和更分散的钴活性相。我们使用硬模板法制备的石墨有序介孔碳作为活性相载体。为了获得不同的表面氧官能团浓度和形态,我们使用了低温氧等离子体。用于表征所研究材料的主要方法是 X 射线光电子能谱、透射电子显微镜和析氧反应中的电催化测试。我们发现,介孔碳的氧化预处理会影响沉积的氧化钴相的形态。此外,电催化剂在析氧反应中的活性与 COO 型基团的相对含量呈正相关,与碳载体上的 C═O 型基团呈负相关。此外,碳载体上 COO 型基团的高相对含量与分散良好的 CoO 纳米颗粒的存在有关。研究结果表明,为了获得分散性更好、因此催化活性更高的材料,控制氧官能团的形态比最大化其总浓度更为重要。