Chemical Engineering Department, Faculty of Engineering, Minia University, El-Minia, Egypt.
Department of Chemistry, College of Science and Humanities, Ad-Dawadmi, Shaqra University, Shaqra, Saudi Arabia.
PLoS One. 2024 Oct 3;19(10):e0308365. doi: 10.1371/journal.pone.0308365. eCollection 2024.
A novel nickel-molybdenum carbide-graphite nanofiber composite is introduced as an electrocatalyst for ethanol electrooxidation. The proposed nanofibers have been prepared by calcinating electrospun nanofibers composed of nickel acetate tetrahydrate, molybdenum chloride, and polyvinyl alcohol. The calcination process was conducted at different temperatures (700, 850, and 1000°C) under a nitrogen gas atmosphere with a heating rate of 2.5 deg/min and a holding time of 5 h. Physicochemical characterizations have indicated that nickel acetate is entirely reduced to nickel metal during the sintering process, and molybdenum has bonded with carbon to produce molybdenum carbide. At the same time, the used polymer has been pyrolyzed to produce a carbon nanofiber matrix embedding formed inorganic nanoparticles. Electrochemical measurements concluded that molybdenum content and calcination temperature should be controlled to maximize the electrocatalytic activity of the proposed catalyst. Typically, the oxidation peak current density was 28.5, 28.8, 51.5, 128.3, 25.6, and 3 mA/cm2 for nanofibers prepared from an electrospun solution containing 0, 5, 10, 15, 25, and 35 wt% molybdenum carbide, respectively. Moreover, it was observed that increasing the calcination temperature distinctly improves the electrocatalytic activity. Kinetic studies have indicated that the reaction order is close to zero with a reaction temperature-dependent value. Moreover, it was detected that the electrooxidation reaction of ethanol over the proposed nanofiber composite follows the Arrhenius equation. The determined activation energy is 33 kJ/mol, which indicates good catalytic activity for the introduced nanofibers. Through the application of a set of visualization-based tools and the general linear model (GLM), the optimal conditions that generate the highest current density were identified. The computations unveiled that the optimal parameter settings are as follows: Mo content at 15 wt.%, methanol concentration of 1.55 M, and reaction temperature of 59°C.
一种新型的镍-钼碳化石墨纳米纤维复合材料被引入作为乙醇电氧化的电催化剂。所提出的纳米纤维是通过煅烧由四水合醋酸镍、氯化钼和聚乙烯醇组成的电纺纳米纤维制备的。煅烧过程在氮气气氛下以 2.5°C/min 的加热速率进行,并在 5 小时的保持时间下进行不同的温度(700、850 和 1000°C)。物理化学特性表明,在烧结过程中,四水合醋酸镍完全还原为镍金属,而钼与碳结合生成碳化钼。同时,所用聚合物已热解生成嵌入形成的无机纳米颗粒的碳纳米纤维基质。电化学测量得出结论,应该控制钼含量和煅烧温度,以最大限度地提高所提出催化剂的电催化活性。通常,氧化峰电流密度分别为 28.5、28.8、51.5、128.3、25.6 和 3 mA/cm2,对于分别由包含 0、5、10、15、25 和 35wt%碳化钼的电纺溶液制备的纳米纤维。此外,观察到增加煅烧温度明显提高了电催化活性。动力学研究表明,反应级数接近零,且与反应温度有关。此外,检测到在提出的纳米纤维复合材料上,乙醇的电氧化反应遵循阿累尼乌斯方程。确定的活化能为 33 kJ/mol,表明引入的纳米纤维具有良好的催化活性。通过应用一组基于可视化的工具和广义线性模型(GLM),确定了产生最高电流密度的最佳条件。计算结果表明,最佳参数设置如下:Mo 含量为 15wt.%,甲醇浓度为 1.55 M,反应温度为 59°C。