Fabio A. Gómez-Gómez, Eleazar Castañeda-Morales, Arturo Manzo-Robledo
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引用次数: 0
Abstract
A promising approach for hydrogen evolution reaction (HER) as energy source and nitrates reduction (NO3−-RR) towards control pollution and/or the generation of various nitrogenous added-value products is presented in this study. The investigation is focused on the electrocatalytic activity at acid conditions (0.5 M H2SO4 and 1.0 M HNO3 solutions) of MoS2 nanoflower-like morphology synthesized via hydrothermal route. The electrocatalytic characterization indicates that depending on the acid in turn, the overpotential for HER is altered. In this context, Tafel slopes and capacitance measurements give more insights on the interactions of MoS2 catalyst in each acid. Whereas the charge-transfer resistance (ohms) was found to be RHNO3 > RH2SO4 as observed from galvanostatic-EIS experiments. Herein, DEMS results demonstrated that the reaction products are modulated by the acid nature, where hydrogen was observed as unique product in H2SO4; conversely, at HNO3 electrolyte, the reduction of NO3− species was carried out leading to generation of N2, N2H4 and NH3, among other compounds, delaying HER-kinetic. Specialized techniques such XRD, SEM-EDS, RAMAN and XPS give some clues concerning the surface state of the materials in study.
本研究提出了一种利用析氢反应(HER)作为能源和硝酸盐还原(NO3−-RR)来控制污染和/或产生各种含氮增值产品的有前途的方法。研究了水热法合成的二硫化钼纳米花在酸性条件下(0.5 M H2SO4和1.0 M HNO3溶液)的电催化活性。电催化表征表明,根据酸的不同,HER的过电位会发生改变。在这种情况下,Tafel斜率和电容测量可以更深入地了解MoS2催化剂在每种酸中的相互作用。而恒流电阻抗实验发现,电荷转移电阻(欧姆)为RHNO3 >; RH2SO4。其中,dms结果表明,反应产物受酸性质的调节,其中氢是H2SO4中唯一的产物;相反,在HNO3电解质下,NO3−的还原导致了N2、N2H4和NH3等化合物的生成,延迟了her -动力学。XRD、SEM-EDS、RAMAN和XPS等专业技术为研究材料的表面状态提供了线索。
期刊介绍:
The Journal of Electroanalytical Chemistry is the foremost international journal devoted to the interdisciplinary subject of electrochemistry in all its aspects, theoretical as well as applied.
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