Calcined Nickel Oxide Nanostructures at Different Temperatures Onto Graphite for Efficient Electro-Oxidation of Ethylene Glycol in Basic Electrolyte

IF 3.7 2区 化学 Q2 CHEMISTRY, APPLIED
Nasser Zouli, R. M. Abdel Hameed, Ahmed Abutaleb, Ibrahim M. Maafa, Ayman Yousef
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Abstract

Fabricating a highly active and stable nanocatalyst material displays a great concern when constructing a commercially viable ethylene glycol (EG) fuel cell. Herein, nickel oxide nanostructures were grown onto graphite (NO/T) using coprecipitation and calcination protocol at different temperatures. Techniques for XRD, TEM, SEM, and EDX investigations were used to look into the produced crystal planes, shape, and elemental mapping of synthesized nickel oxide nanoparticles. Different NO/T nanocatalyst electroactivities were examined in order to oxidize EG molecules in basic electrolyte. The surface area values of calcined nanostructures at 200°C and 300°C were much higher than those measured at NO/T-400 by 7.62 and 3.71 folds to explain their outstanding performance. Some kinetic information for varied NO/T nanocatalysts was derived including the electron transfer coefficient, rate constant, and surface coverage values. Electron transfer rate constants of 0.1946, 0.3734, 0.0113, and 0.0303 s−1 were calculated at NO/T-200, NO/T-300, NO/T-400, and NO/T-500, respectively. Increased oxidation current densities could be achieved when NO/T nanomaterials were subjected to lowered calcination temperatures. NO/T-200 and NO/T-300 nanocatalysts also displayed decreased Eonset for alcohol oxidation process by 20 and 41 mV in relation to that at NO/T-400. Moreover, chronoamperometric experiments revealed the prevalence of the stable behavior during EG oxidation at these nanostructures, especially for calcined ones at 200°C and 300°C. Much reduced poisoning rates were measured at NO/T-200 (0.171 s−1) and NO/T-300 (0.067 s−1) when contrasted to that at NO/T-500 (0.727 s−1). Increasing the alcohol and supporting electrolyte concentrations was beneficial in improving the charge transfer characteristics of NO/T nanocatalysts as demonstrated by EIS measurements. This study supports the promising activity of NiO nanoparticles onto graphite as anode materials for direct alcohol fuel cells.

Abstract Image

Abstract Image

不同温度下在石墨上煅烧氧化镍纳米结构,实现乙二醇在碱性电解液中的高效电氧化
在构建商业上可行的乙二醇(EG)燃料电池时,制造高活性、高稳定性的纳米催化剂材料是一个非常重要的问题。本文采用共沉淀和煅烧协议,在不同温度下在石墨(NO/T)上生长了氧化镍纳米结构。利用 XRD、TEM、SEM 和 EDX 技术对合成的氧化镍纳米粒子的晶面、形状和元素分布进行了研究。为了在碱性电解液中氧化 EG 分子,研究人员考察了不同 NO/T 纳米催化剂的电活性。在 200°C 和 300°C 煅烧的纳米结构的表面积值比在 NO/T-400 条件下测得的表面积值高出 7.62 倍和 3.71 倍,这就解释了它们的优异性能。研究人员得出了不同 NO/T 纳米催化剂的一些动力学信息,包括电子转移系数、速率常数和表面覆盖值。计算得出 NO/T-200、NO/T-300、NO/T-400 和 NO/T-500 的电子转移速率常数分别为 0.1946、0.3734、0.0113 和 0.0303 s-1。降低 NO/T 纳米材料的煅烧温度可提高氧化电流密度。与 NO/T-400 相比,NO/T-200 和 NO/T-300 纳米催化剂在酒精氧化过程中的 Eonset 值也分别降低了 20 和 41 mV。此外,时变实验表明,这些纳米结构在 EG 氧化过程中表现稳定,尤其是在 200°C 和 300°C 煅烧过的纳米结构。与 NO/T-500 时的中毒速率(0.727 秒-1)相比,NO/T-200 时(0.171 秒-1)和 NO/T-300 时(0.067 秒-1)的中毒速率大大降低。EIS 测量结果表明,提高酒精和支撑电解质的浓度有利于改善 NO/T 纳米催化剂的电荷转移特性。这项研究证明了石墨上的氧化镍纳米颗粒作为直接醇燃料电池的阳极材料具有良好的活性。
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来源期刊
Applied Organometallic Chemistry
Applied Organometallic Chemistry 化学-无机化学与核化学
CiteScore
7.80
自引率
10.30%
发文量
408
审稿时长
2.2 months
期刊介绍: All new compounds should be satisfactorily identified and proof of their structure given according to generally accepted standards. Structural reports, such as papers exclusively dealing with synthesis and characterization, analytical techniques, or X-ray diffraction studies of metal-organic or organometallic compounds will not be considered. The editors reserve the right to refuse without peer review any manuscript that does not comply with the aims and scope of the journal. Applied Organometallic Chemistry publishes Full Papers, Reviews, Mini Reviews and Communications of scientific research in all areas of organometallic and metal-organic chemistry involving main group metals, transition metals, lanthanides and actinides. All contributions should contain an explicit application of novel compounds, for instance in materials science, nano science, catalysis, chemical vapour deposition, metal-mediated organic synthesis, polymers, bio-organometallics, metallo-therapy, metallo-diagnostics and medicine. Reviews of books covering aspects of the fields of focus are also published.
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