Fe3O4-S-rGO表面电沉积Pd纳米粒子用于甲醇电氧化

IF 2.7 4区 化学 Q3 CHEMISTRY, PHYSICAL
Rukan Suna Karatekin, Sedef Kaplan
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引用次数: 0

摘要

在不同Pd沉积时间下合成了一系列Pd/Fe3O4@S-rGO,并通过计时安培法(CA)、循环伏安法(CVs)和电化学阻抗谱法(EIS)研究了它们在碱性介质中对甲醇氧化反应的催化活性。对于S源,使用十二烷基苯磺酸钠(SDBS)获得超细Fe3O4颗粒,并增强石墨烯层性能。通过表征测量,得出Pd成功沉积在具有纳米级立方晶格纳米结构的Fe3O4@S-rGO (S和Fe3O4双掺杂还原氧化石墨烯)上。在Fe3O4的存在下,Pd450/ITO的带隙从3.46 eV减小到1.74 eV。制备的催化剂带隙随钯沉积时间的变化而变化。此外,Pd与Fe3O4的协同作用增强了电极对甲醇氧化的催化活性。Pd450/Fe3O4@S-rGO电催化剂在扫描速率为30 mV s−1时电流密度为22.3 mA cm−2,在0.5 M甲醇和1 M NaOH中具有良好的长期稳定性。该值是相同条件下Pt/C (10 mAcm−2)催化剂的2.2倍。添加Fe3O4后,Pd450/ITO的Tafel斜率从180 mVdec−1降低到118 mVdec−1。图形抽象
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Electrodeposited Pd Nanoparticles onto Fe3O4-S-rGO for Methanol Electro-oxidation

Electrodeposited Pd Nanoparticles onto Fe3O4-S-rGO for Methanol Electro-oxidation

A series of Pd/Fe3O4@S-rGO was synthesized under various deposition times of Pd and their catalytic activity was investigated in alkaline media via chronoamperometry (CA), cyclic voltammetry (CVs), and electrochemical impedance spectroscopy (EIS) for the methanol oxidation reaction. For the S source, sodium dodecylbenzene sulfonate (SDBS) was used to obtain ultrafine Fe3O4 particles and enhance the graphene layer properties. Through the characterization measurements, it is concluded that Pd was deposited successfully onto Fe3O4@S-rGO (S and Fe3O4 dual-doped reduced graphene oxide) with nanoscale cubic lattice nanostructure. In the presence of Fe3O4, the band gap of Pd450/ITO decreased from 3.46 to 1.74 eV. The band gap of fabricated catalyzes changed with the deposition time of Pd. In addition, the synergistic effect between Pd and Fe3O4 enhances the catalytic activity of the electrode toward methanol oxidation when compared bulk Pd electrode. The Pd450/Fe3O4@S-rGO electrocatalyst showed a current density of 22.3 mA cm−2 at a scan rate of 30 mV s−1 with remarkable long-term stability in 0.5 M methanol in 1 M NaOH. This value is 2.2 times higher than the Pt/C (10 mAcm−2) catalyst under the same conditions. With modifying Fe3O4 the Tafel slope of Pd450/ITO decreased from 180 to 118 mVdec−1.

Graphical Abstract

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来源期刊
Electrocatalysis
Electrocatalysis CHEMISTRY, PHYSICAL-ELECTROCHEMISTRY
CiteScore
4.80
自引率
6.50%
发文量
93
审稿时长
>12 weeks
期刊介绍: Electrocatalysis is cross-disciplinary in nature, and attracts the interest of chemists, physicists, biochemists, surface and materials scientists, and engineers. Electrocatalysis provides the unique international forum solely dedicated to the exchange of novel ideas in electrocatalysis for academic, government, and industrial researchers. Quick publication of new results, concepts, and inventions made involving Electrocatalysis stimulates scientific discoveries and breakthroughs, promotes the scientific and engineering concepts that are critical to the development of novel electrochemical technologies. Electrocatalysis publishes original submissions in the form of letters, research papers, review articles, book reviews, and educational papers. Letters are preliminary reports that communicate new and important findings. Regular research papers are complete reports of new results, and their analysis and discussion. Review articles critically and constructively examine development in areas of electrocatalysis that are of broad interest and importance. Educational papers discuss important concepts whose understanding is vital to advances in theoretical and experimental aspects of electrochemical reactions.
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