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新型液态有机氢载体:吲哚、二氢吲哚和八氢吲哚在Pt(111)上的模型催化研究

Model Catalytic Studies of Novel Liquid Organic Hydrogen Carriers: Indole, Indoline and Octahydroindole on Pt(111).

作者信息

Schwarz Matthias, Bachmann Philipp, Silva Thais Nascimento, Mohr Susanne, Scheuermeyer Marlene, Späth Florian, Bauer Udo, Düll Fabian, Steinhauer Johann, Hohner Chantal, Döpper Tibor, Noei Heshmat, Stierle Andreas, Papp Christian, Steinrück H-P, Wasserscheid Peter, Görling Andreas, Libuda Jörg

机构信息

Lehrstuhl für Physikalische Chemie II, Friedrich-Alexander-Universität Erlangen-Nürnberg, Egerlandstraße 3, 91058, Erlangen, Germany.

Lehrstuhl für Chemische Reaktionstechnik, Friedrich-Alexander-Universität Erlangen-Nürnberg, Egerlandstraße 3, 91058, Erlangen, Germany.

出版信息

Chemistry. 2017 Oct 20;23(59):14806-14818. doi: 10.1002/chem.201702333. Epub 2017 Sep 26.

DOI:10.1002/chem.201702333
PMID:28815946
Abstract

Indole derivatives were recently proposed as potential liquid organic hydrogen carriers (LOHC) for storage of renewable energies. In this work, we have investigated the adsorption, dehydrogenation and degradation mechanisms in the indole/indoline/octahydroindole system on Pt(111). We have combined infrared reflection absorption spectroscopy (IRAS), X-ray photoelectron spectroscopy (XPS) and DFT calculations. Indole multilayers show a crystallization transition at 200 K, in which the molecules adopt a strongly tilted orientation, before the multilayer desorbs at 220 K. For indoline, a less pronounced restructuring transition occurs at 150 K and multilayer desorption is observed at 200 K. Octahydroindole multilayers desorb already at 185 K, without any indication for restructuring. Adsorbed monolayers of all three compounds are stable up to room temperature and undergo deprotonation at the NH bond above 300 K. For indoline, the reaction is followed by partial dehydrogenation at the 5-membered ring, leading to the formation of a flat-lying di-σ-indolide in the temperature range from 330-390 K. Noteworthy, the same surface intermediate is formed from indole. In contrast, the reaction of octahydroindole with Pt(111) leads to the formation of a different intermediate, which originates from partial dehydrogenation of the 6-membered ring. Above 390 K, all three compounds again form the same strongly dehydrogenated and partially decomposed surface species.

摘要

吲哚衍生物最近被提议作为潜在的液态有机氢载体(LOHC)用于可再生能源的储存。在这项工作中,我们研究了吲哚/二氢吲哚/八氢吲哚体系在Pt(111)上的吸附、脱氢和降解机制。我们结合了红外反射吸收光谱(IRAS)、X射线光电子能谱(XPS)和密度泛函理论(DFT)计算。吲哚多层膜在200 K时发生结晶转变,在此转变过程中分子采取强烈倾斜的取向,然后在220 K时多层膜脱附。对于二氢吲哚,在150 K时发生不太明显的结构转变,在200 K时观察到多层膜脱附。八氢吲哚多层膜在185 K时就已脱附,没有任何结构转变的迹象。所有这三种化合物的吸附单层在室温下都是稳定的,并且在300 K以上NH键处发生去质子化。对于二氢吲哚,该反应随后在五元环处发生部分脱氢,导致在330 - 390 K的温度范围内形成平躺的双σ-吲哚化物。值得注意的是,吲哚也形成相同的表面中间体。相比之下,八氢吲哚与Pt(111)的反应导致形成不同的中间体,它源于六元环的部分脱氢。在390 K以上,所有这三种化合物再次形成相同的高度脱氢和部分分解的表面物种。

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