析氧
石墨烯
塔菲尔方程
过电位
分解水
电催化剂
氧化物
电化学
材料科学
电解水
无机化学
制氢
化学工程
镍
电解
电极
化学
氢
催化作用
纳米技术
冶金
物理化学
有机化学
光催化
工程类
生物化学
电解质
作者
Fowzia S. Alamro,Shymaa S. Medany,Nada S. Al‐Kadhi,Hoda A. Ahmed,Mahmoud A. Hefnawy
出处
期刊:Molecules
[Multidisciplinary Digital Publishing Institute]
日期:2024-03-08
卷期号:29 (6): 1215-1215
被引量:11
标识
DOI:10.3390/molecules29061215
摘要
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 NiFe2O4@GO electrode has an impact on both the urea oxidation reaction (UOR) and water splitting applications. NiFe2O4@GO was observed to have a current density of 26.6 mA cm−2 in 1.0 M urea and 1.0 M KOH at a scan rate of 20 mV s−1. The Tafel slope provided for UOR was 39 mV dec−1, whereas the GC/NiFe2O4@GO electrode reached a current of 10 mA cm−2 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 cm2, respectively.
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