Department of Physics, Faculty of Science, University of Guilan, P.O. Box 41335-1914, Rasht, Iran; Department of Physics, Payame Noor University (PNU), P.O.Box:19395-3697, Tehran, Iran.
Department of Chemistry, Payame Noor University (PNU), P.O. Box 19395-4697, Tehran, Iran.
J Colloid Interface Sci. 2019 Mar 1;537:186-196. doi: 10.1016/j.jcis.2018.11.019. Epub 2018 Nov 8.
A three-component nano-electrocatalyst, magnetite coated molybdenum disulfide hybridized with reduced graphene oxide (FeO@MoS/RGO), is synthesized by a two-step hydrothermal method. This catalyst is applied as an effective substitution for the platinum catalyst in methanol oxidation and hydrogen evolution reactions. Cyclic voltammetry, chronoamperometry, and linear sweep voltammetry are used to evaluate the performance of the electrocatalyst in acidic and basic media. The results of methanol oxidation reaction on the hybridized nano-electrocatalyst showed good electrocatalytic properties with considerable diffusion currents. This fact is confirmed by the Tafel plots and the calculated kinetic parameters of electron transfer. FeO@MoS/RGO showed an anodic transfer coefficient and exchange current of 0.464 and 4.80 × 10, respectively that are higher than FeO/RGO. The presence of the porous MoS in catalyst has a key effect on supplying electroactive sites for electron transfer. Also, the high actual surface area obtained for the hybridized nano-electrocatalyst (A = 0.0295 cm). The maximum power density of 35.03 mW cm obtained for a single cell containing the prepared hybridized catalyst as the anode which shows a competitive feature of the synthetic catalyst compared to other reports. Furthermore, the synthetic catalyst shows the low-value overpotential of 108 mV and Tafel slope of 48 mV dec during the hydrogen evolution process in acidic media. This is attributed to the synergistic effect between FeO and MoS and also increase the electron transfer rate due to adding conductive RGO to the catalyst. The results show that the synthetic nanocatalyst can have promising applications for hydrogen evolution and methanol oxidation reactions.
采用两步水热法合成了一种由磁铁矿包裹的二硫化钼与还原氧化石墨烯杂化的三组分纳米电催化剂(FeO@MoS/RGO)。该催化剂作为甲醇氧化和析氢反应中铂催化剂的有效替代品得到了应用。在酸性和碱性介质中,通过循环伏安法、计时电流法和线性扫描伏安法评估了电催化剂的性能。在杂化纳米电催化剂上进行的甲醇氧化反应的结果表明,具有相当大的扩散电流,具有良好的电催化性能。这一事实通过塔菲尔图和计算的电子转移动力学参数得到了证实。FeO@MoS/RGO 的阳极转移系数和交换电流分别为 0.464 和 4.80×10,高于 FeO/RGO。催化剂中多孔 MoS 的存在对提供电子转移的电活性位点具有关键作用。此外,杂化纳米电催化剂获得的实际高表面积(A=0.0295cm)。含有制备的杂化催化剂作为阳极的单电池获得了 35.03mWcm 的最大功率密度,这表明与其他报道相比,合成催化剂具有竞争优势。此外,在酸性介质中析氢过程中,合成催化剂的过电位低至 108mV,塔菲尔斜率为 48mVdec。这归因于 FeO 和 MoS 之间的协同效应,以及向催化剂中添加导电 RGO 导致电子转移率提高。结果表明,合成纳米催化剂在析氢和甲醇氧化反应中具有广阔的应用前景。