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表面氧化诱导的液态钯镓SCALMS模型催化剂的结构重组

Surface oxidation-induced restructuring of liquid Pd-Ga SCALMS model catalysts.

作者信息

Wittkämper Haiko, Maisel Sven, Moritz Michael, Grabau Mathias, Görling Andreas, Steinrück Hans-Peter, Papp Christian

机构信息

Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Lehrstuhl für Physikalische Chemie II, Egerlandstr. 3, 91058 Erlangen, Germany.

出版信息

Phys Chem Chem Phys. 2021 Aug 4;23(30):16324-16333. doi: 10.1039/d1cp02458b.

Abstract

We have examined model systems for the recently reported Pd-Ga Supported Catalytically Active Liquid Metal Solutions (SCALMS) catalysts using near-ambient pressure X-ray photoelectron spectroscopy (NAP-XPS) under oxidizing conditions. Gallium is known to be highly prone to oxidation and in practical applications, handling of the catalyst material in air or the presence of traces of oxygen in the reactor are unavoidable. Therefore, we expect our results to be of high relevance for the application of Ga-based SCALMS catalysts. Pd-Ga alloy samples of 1.3 and 1.8 at% Pd content were exposed to molecular oxygen at different pressures between 3 × 10-7 and 1 mbar and a temperature of 550 K. We observe the formation of wetting Ga2O3 films upon exposure to molecular oxygen. The absolute thicknesses of the oxide films depend on oxygen pressure, with values ranging from ∼12 Å at 10-7 to 10-5 mbar to ∼50 Å at 1 mbar. The formed metal-oxide interface leads to a redistribution of Pd, which accumulates at the boundary between the wetting oxide film and the metal substrate as a response to the oxide film growth. A maximum Pd 3d intensity is observed at an oxide thickness of 5 Å. For thicker films, the Pd 3d signal and the Ga 3d signal ascribed to the metallic substrate decrease in parallel, which is attributed to the oxide layer growing on top of the liquid metal alloy. From this observation, we conclude that no significant amount of Pd is bound in the newly formed oxide film. Density-functional theory (DFT) calculations support the experimental observations.

摘要

我们使用近常压X射线光电子能谱(NAP-XPS)在氧化条件下研究了最近报道的钯-镓负载催化活性液态金属溶液(SCALMS)催化剂的模型系统。众所周知,镓极易氧化,在实际应用中,催化剂材料在空气中处理或反应器中存在微量氧气是不可避免的。因此,我们预计我们的结果与基于镓的SCALMS催化剂的应用高度相关。钯含量为1.3和1.8原子百分比的钯-镓合金样品在3×10-7至1毫巴的不同压力和550 K的温度下暴露于分子氧中。我们观察到暴露于分子氧后形成了润湿性的Ga2O3薄膜。氧化膜的绝对厚度取决于氧气压力,值范围从10-7至10-5毫巴时的约12 Å到1毫巴时的约50 Å。形成的金属-氧化物界面导致钯的重新分布,作为对氧化膜生长的响应,钯在润湿性氧化膜和金属基底之间的边界处积累。在氧化膜厚度为5 Å时观察到最大的钯3d强度。对于更厚的薄膜,归因于金属基底的钯3d信号和镓3d信号平行下降,这归因于在液态金属合金顶部生长的氧化层。从这一观察结果,我们得出结论,新形成的氧化膜中没有大量的钯被结合。密度泛函理论(DFT)计算支持了实验观察结果。

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