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氧化催化剂上原子层沉积的机理研究——AlO和PO沉积

Mechanistic studies of atomic layer deposition on oxidation catalysts - AlO and PO deposition.

作者信息

Knemeyer Kristian, Piernavieja Hermida Mar, Ingale Piyush, Schmidt Johannes, Kröhnert Jutta, Naumann d'Alnoncourt Raoul, Driess Matthias, Rosowski Frank

机构信息

BasCat-UniCat BASF JointLab, Technische Universität Berlin, Hardenbergstraße 36, 10623 Berlin, Germany.

出版信息

Phys Chem Chem Phys. 2020 Aug 28;22(32):17999-18006. doi: 10.1039/d0cp02572k. Epub 2020 Aug 4.

DOI:10.1039/d0cp02572k
PMID:32749415
Abstract

Atomic layer deposition is a rising technique for catalyst synthesis and modification. Typically, the focus of ALD in catalysis is on supported metal nanoparticles. Here, the authors give mechanistic insights into the ALD of oxides on redox active catalysts by a combination of in situ analytics, such as XPS, DRIFTS and gravimetric measurements. Phosphorus oxide and aluminum oxide were deposited on divanadium pentoxide powder in a fixed bed reactor. In contrast to the generally accepted concepts, the first half cycle does not proceed over surface hydroxyl groups but involves redox chemistry between the precursor and the vanadium atoms, as shown by P-SSNMR and XPS. For PO deposition, a temperature step from 150 °C in the first half cycle to 450 °C in the second half cycle is needed to obtain linear mass gain per cycle as the remaining ligands are combusted and reduced vanadium atoms are reoxidized. Homogeneous deposition was confirmed by STEM-EDX and XRD showing no additional phases, despite performing up to 10 ALD cycles. Even the well-known process of alumina ALD confirms the involvement of reduction-oxidation reactions between the ALD precursor and the substrate VO. However, redox chemistry can be suppressed for alumina ALD at low temperatures of 50 °C. Therefore, this study shows that ALD on oxidation catalysts is complex and thus the developed ALD processes are unusual compared to ALD on typical supports, such as SiO or AlO.

摘要

原子层沉积是一种新兴的催化剂合成与改性技术。通常,催化领域中原子层沉积的重点在于负载型金属纳米颗粒。在此,作者通过结合原位分析技术,如X射线光电子能谱(XPS)、漫反射红外傅里叶变换光谱(DRIFTS)和重量测量,对氧化还原活性催化剂上氧化物的原子层沉积机理进行了深入研究。在固定床反应器中,将磷氧化物和铝氧化物沉积在五氧化二钒粉末上。与普遍接受的概念不同,前半周期并非通过表面羟基进行,而是涉及前驱体与钒原子之间的氧化还原化学过程,这由磷固体核磁共振(P - SSNMR)和XPS所证实。对于PO沉积,需要一个温度步骤,即从前半周期的150°C升至后半周期的450°C,以便在剩余配体燃烧且还原的钒原子重新氧化时,获得每周期线性的质量增加。扫描透射电子显微镜 - 能谱仪(STEM - EDX)和X射线衍射(XRD)证实了均匀沉积,尽管进行了多达10个原子层沉积循环,但未显示出额外的相。即使是众所周知的氧化铝原子层沉积过程也证实了原子层沉积前驱体与底物VO之间存在氧化还原反应。然而,在50°C的低温下,氧化铝原子层沉积的氧化还原化学过程可以被抑制。因此,本研究表明氧化催化剂上的原子层沉积是复杂的,与在典型载体(如SiO或AlO)上的原子层沉积相比,所开发的原子层沉积过程并不寻常。

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