Alamro Fowzia S, Medany Shymaa S, Al-Kadhi Nada S, Ahmed Hoda A, Hefnawy Mahmoud A
Department of Chemistry, College of Science, Princess Nourah bint Abdulrahman University, P.O. Box 84428, Riyadh 11671, Saudi Arabia.
Chemistry Department, Faculty of Science, Cairo University, Giza 12613, Egypt.
Molecules. 2024 Mar 8;29(6):1215. doi: 10.3390/molecules29061215.
The production of green hydrogen using water electrolysis is widely regarded as one of the most promising technologies. On the other hand, the oxygen evolution reaction (OER) is thermodynamically unfavorable and needs significant overpotential to proceed at a sufficient rate. Here, we outline important structural and chemical factors that affect how well a representative nickel ferrite-modified graphene oxide electrocatalyst performs in efficient water splitting applications. The activities of the modified pristine and graphene oxide-supported nickel ferrite were thoroughly characterized in terms of their structural, morphological, and electrochemical properties. This research shows that the NiFeO@GO electrode has an impact on both the urea oxidation reaction (UOR) and water splitting applications. NiFeO@GO was observed to have a current density of 26.6 mA cm in 1.0 M urea and 1.0 M KOH at a scan rate of 20 mV s. The Tafel slope provided for UOR was 39 mV dec, whereas the GC/NiFeO@GO electrode reached a current of 10 mA cm at potentials of +1.5 and -0.21 V (vs. RHE) for the OER and hydrogen evolution reaction (HER), respectively. Furthermore, charge transfer resistances were estimated for OER and HER as 133 and 347 Ω cm, respectively.
利用水电解生产绿色氢能被广泛认为是最具前景的技术之一。另一方面,析氧反应(OER)在热力学上是不利的,需要显著的过电位才能以足够的速率进行。在此,我们概述了影响代表性镍铁氧体修饰氧化石墨烯电催化剂在高效水分解应用中性能的重要结构和化学因素。从结构、形态和电化学性质方面对修饰的原始镍铁氧体和氧化石墨烯负载的镍铁氧体的活性进行了全面表征。这项研究表明,NiFeO@GO电极对尿素氧化反应(UOR)和水分解应用都有影响。在1.0 M尿素和1.0 M KOH中,扫描速率为20 mV s时,观察到NiFeO@GO的电流密度为26.6 mA cm。UOR的塔菲尔斜率为39 mV dec,而GC/NiFeO@GO电极在析氧反应(OER)和析氢反应(HER)的电位分别为+1.5和 -0.21 V(相对于可逆氢电极,RHE)时达到10 mA cm的电流。此外,OER和HER的电荷转移电阻分别估计为133和347 Ω cm。