ELECTROLYTIC CATALYSTS BASED ON TUNGSTEN AND CARBON COMPOUNDS FOR THE HYDROGEN EVOLUTION REACTION

S. Kuleshov, I. Novoselova, Olha Medvezhynska
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Abstract

The hydrogen evolution reaction (HER) is one of the most promising methods of obtaining high-purity hydrogen. However, the high cost and limited resources of materials with low cathodic hydrogen evolution overvoltage values, such as platinum group metals, are the main obstacles to the use HER for obtaining hydrogen on an industrial scale. Therefore, it is necessary to develop new alternative materials and methods of their production. One of the promising materials are catalysts based on refractory metals, in particular tungsten carbides. Metal tungsten can also be used for these purposes. In our opinion, high-temperature electrochemical synthesis (HTES) in molten salts can be a promising method of obtaining materials with properties that meet the requirements for effective catalysts, namely: ultra-dispersity, high specific surface area, mesoporosity and defective structure, high chemical and electrochemical stability. Therefore, the purpose of this work is to evaluate the electrocatalytic activity of a group of materials for HER, which are obtained by HTES in melts. Four samples of electrolytic materials were chosen for the study: tungsten, carbon, tungsten mono- and semi-carbides (WC and W2С). All samples were characterized in detail using X-ray diffraction (phase composition), SEM (morphology), Raman spectroscopy (structure of carbon phases), DTG (free carbon content). Based on the analysis of the obtained data, it was established that all samples can be used as catalysts: crystallites have a nanometer size and a large number of structural defects; morpho­logy provides increased surface area; tungsten carbide particles are covered with a layer of free carbon, which prevents oxidation of carbide to WO3, which has a lower catalytic acti­vity; carbon particles are nanosized (20–30 nm) and contain a large number of structural defects; tungsten carbide-based samples contain free carbon, which increases the specific surface area, but does not cause clogging of pores. Polarization measurements were carried out at room temperature at a polarization rate of 5 mV/s in a standard three-electrode cell with an Ag|AgCl reference electrode. 1N H2SO4 was used as a base solution, which was bubbled with high-purity argon. Onset potentials for all samples are -0.05 – -0.25 V (in order WC/C – W2C/WC/C – C – W). The overvoltage and Tafel slope were calculated and WC/C composite was shown to have the lowest values of -0.2 V and -75 mV, respectively. Electrolytic composite of tungsten carbide/carbon have demonstrated the best characteristics, so we plan to continue the development of synthesis method of carbide compounds, which will allow us to reveal even greater potential of carbide catalysts and pave the way for their wide application in catalytic processes.
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基于钨和碳化合物的析氢反应电解催化剂
析氢反应(HER)是制备高纯氢最有前途的方法之一。然而,具有低阴极析氢过电压值的材料(如铂族金属)的高成本和有限资源是利用HER实现工业规模制氢的主要障碍。因此,有必要开发新的替代材料及其生产方法。其中一个有前途的材料是基于难熔金属的催化剂,特别是碳化钨。金属钨也可用于这些目的。我们认为,熔盐高温电化学合成(HTES)是一种很有前途的方法,可以获得满足有效催化剂要求的材料,即:超分散性、高比表面积、介孔和缺陷结构、高化学和电化学稳定性。因此,本工作的目的是评估HTES在熔体中获得的一组材料的HER电催化活性。研究中选择了四种电解材料样品:钨、碳、钨单碳化物和半碳化物(WC和W2С)。采用x射线衍射(相组成)、SEM(形貌)、拉曼光谱(碳相结构)、DTG(游离碳含量)对样品进行了详细表征。通过对所得数据的分析,确定了所有样品都可以作为催化剂:晶体具有纳米尺寸和大量的结构缺陷;形态提供了增加的表面积;碳化钨颗粒上覆盖有一层游离碳,防止碳化钨氧化为WO3,催化活性较低;碳颗粒是纳米级的(20-30 nm),含有大量的结构缺陷;碳化钨基样品含有游离碳,这增加了比表面积,但不会造成孔隙堵塞。在标准三电极电池中,以Ag / AgCl为基准电极,在室温下以5 mV/s的极化速率进行极化测量。以1N H2SO4为底液,用高纯氩气吹泡。所有样品的起始电位为-0.05 ~ -0.25 V(顺序为WC/C - W2C/WC/C - C - W)。计算过电压和Tafel斜率,WC/C复合物的最低值分别为-0.2 V和-75 mV。碳化钨/碳的电解复合材料已经表现出了最好的特性,因此我们计划继续开发碳化钨化合物的合成方法,这将使我们能够揭示碳化钨催化剂的更大潜力,并为其在催化过程中的广泛应用铺平道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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