Khdary Nezar H, El-Gohary Asmaa R M, Galal Ahmed, Alhassan Ahmed M, Alzahrain Sami D
King Abdulaziz City for Science and Technology Riyadh 11442 Kingdom of Saudi Arabia
Cairo University, Faculty of Science, Chemistry Department Giza 12613 Egypt.
RSC Adv. 2024 Aug 16;14(35):25830-25843. doi: 10.1039/d4ra03998j. eCollection 2024 Aug 12.
In this study, we prepared a potential catalyst as an electrode modifier for electrolytic water splitting. In the preparation step, the amine was decorated with copper-phosphorus. It was immobilized over the silica surface, and the surface was engineered using -(3-(trimethoxysilyl) propyl)ethylenediamine for the synthesis of the catalysts (AS). The morphological and structural aspects of the catalyst (AFS-Cu-P) were determined using FE-SEM/EDAX, FTIR, elemental analysis, BET, TGA, and XPS. The catalyst's efficacy for the oxygen evolution reaction (OER) was assessed in an alkaline medium with and without hydrazine. The hydrazine oxidation reaction enhanced the sluggish OER and facilitated water splitting. Detailed electrochemical measurements confirmed an increase in the kinetics of the process and a reduction in the activation energy needed to complete the process. The Tafel slopes, charge transfer coefficients, exchange-specific current densities, apparent rate constants, and diffusion coefficients are provided along with their respective values. The results showed that the presence of Cu and CNT is crucial in the conversion process.
在本研究中,我们制备了一种潜在的催化剂作为电解水分解的电极修饰剂。在制备步骤中,胺用铜 - 磷进行了修饰。它被固定在二氧化硅表面,并且使用 -(3 -(三甲氧基甲硅烷基)丙基)乙二胺对表面进行工程设计以合成催化剂(AS)。使用场发射扫描电子显微镜/能谱仪(FE - SEM/EDAX)、傅里叶变换红外光谱仪(FTIR)、元素分析、比表面积分析仪(BET)、热重分析仪(TGA)和X射线光电子能谱仪(XPS)确定了催化剂(AFS - Cu - P)的形态和结构方面。在有和没有肼的碱性介质中评估了催化剂对析氧反应(OER)的功效。肼氧化反应增强了缓慢的析氧反应并促进了水分解。详细的电化学测量证实了该过程动力学的增加以及完成该过程所需活化能的降低。给出了塔菲尔斜率、电荷转移系数、交换特定电流密度、表观速率常数和扩散系数及其各自的值。结果表明,铜和碳纳米管的存在在转化过程中至关重要。