Intercalation of Potassium Ions in Molybdenum Sulfide as Catalyst for CO2 Reduction

Eszter Mádai, Arjan Mol, Remco Hartkamp, Peyman Taheri
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Abstract

The increasing CO 2 emission during the last decades highly contributed to global warming and as a consequence, we are facing the disruption of nature and more and more extreme weather conditions nowadays [1]. One way of dealing with the emitted excess CO 2 is to create a synthetic carbon cycle, where the emitted CO 2 is captured and turned into fuel using electrocatalysis and green energy. However, in order to achieve this, the exploration of new electrocatalysts is needed for the sake of cost and process efficiency and environmental friendliness. Two dimensional materials have a promising future as catalysts due to their high surface-to-volume ratio. A potential catalyst material for CO 2 reduction is molybdenite (MoS 2 ), a cheap, layered semiconductor which already showed selectivity towards CO 2 reduction in non-aqueous media [2,3]. Its layered structure allows not only to have a high specific surface area but also makes the intercalation of different ions possible. These features enable us to enhance the conductivity of the material via electron donation by the intercalated species [4]. The improved conductivity and the changed band gap can contribute to a higher efficiency of electrochemical processes. Our research investigates the intercalation mechanism of potassium ions into MoS 2 layers and the effects of the intercalated potassium on the CO 2 reduction efficiency. The intercalation process is studied experimentally through electrochemical impedance spectroscopy (EIS) and confirmed by X-ray diffraction (XRD). Furthermore, the Gibbs free energy profile of the intercalation is obtained by Molecular Dynamics (MD) simulations using umbrella sampling. The electronic properties are measured with X-ray photoelectron spectroscopy (XPS) and the products of the CO 2 reduction reaction is measured with gas chromatography (GC). The results suggest that the potassium intercalation improves the conductivity of the MoS 2 and consequently the CO 2 reduction efficiency. [1] McCrystall et al. New climate models reveal faster and larger increases in Arctic precipitation than previously projected. Nat. Commun. 12:6765, 2021. [2] Asadi et al. Robust carbon dioxide reduction on molybdenum disulphide edges. Nature Communications, 5(1), 2014. [3] Asadi et al. Nanostructured transition metal dichalcogenide electrocatalysts for CO 2 reduction in ionic liquid. Science, 353(6298):467–470, 2016. [4] Wang et al. Atomic-scale clarification of structural transition of MoS 2 upon sodium intercalation. ACS Nano, 8(11):11394– 11400, 2014.
硫化钼中钾离子插层催化CO2还原
近几十年来二氧化碳排放量的增加是全球变暖的主要原因,因此,我们正面临着自然的破坏和越来越多的极端天气条件[1]。处理排放过量二氧化碳的一种方法是创造一个合成碳循环,在这个循环中,排放的二氧化碳被捕获,并利用电催化和绿色能源转化为燃料。然而,为了实现这一目标,需要探索新的电催化剂,以提高成本和工艺效率,并对环境友好。由于二维材料具有较高的表面体积比,作为催化剂具有广阔的应用前景。辉钼矿(MoS 2)是一种潜在的CO 2还原催化剂材料,它是一种廉价的层状半导体,已经在非水介质中表现出对CO 2还原的选择性[2,3]。它的层状结构不仅使其具有较高的比表面积,而且使不同离子的插入成为可能。这些特性使我们能够通过插层物质的电子赋能来增强材料的导电性[4]。电导率的提高和带隙的改变有助于提高电化学过程的效率。本研究探讨了钾离子在MoS - 2层中的嵌入机理,以及嵌入的钾离子对CO 2还原效率的影响。通过电化学阻抗谱(EIS)和x射线衍射(XRD)实验研究了插层过程。此外,利用分子动力学(MD)模拟伞式采样得到了插层的吉布斯自由能分布。用x射线光电子能谱(XPS)测定了产物的电子性质,用气相色谱(GC)测定了CO 2还原反应的产物。结果表明,钾的插入提高了MoS 2的电导率,从而提高了CO 2的还原效率。[1]李志强,李志强。新的气候模式显示,北极降水的增长速度比先前预测的更快、更大。民法典。12:67 . 65,2021。[2]张晓明,张晓明。在二硫化钼边缘上强有力的二氧化碳还原。自然通讯,5(1),2014。[3]刘建平,刘建平。离子液体中CO 2还原纳米结构过渡金属二硫化物电催化剂。科学通报,2016,35(6):457 - 457。[4]王等。钠嵌入后二氧化钼结构转变的原子尺度澄清。生物质化学工程学报,2014,35(6):1183 - 1183。
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