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基于胍盐和脒盐的铈和镱配合物作为原子层沉积前驱体的合理开发:合成、建模与应用

Rational Development of Guanidinate and Amidinate Based Cerium and Ytterbium Complexes as Atomic Layer Deposition Precursors: Synthesis, Modeling, and Application.

作者信息

Kaur Parmish, Mai Lukas, Muriqi Arbresha, Zanders David, Ghiyasi Ramin, Safdar Muhammad, Boysen Nils, Winter Manuela, Nolan Michael, Karppinen Maarit, Devi Anjana

机构信息

Inorganic Materials Chemistry, Ruhr University Bochum, Universitätsstraße 150, 44801, Bochum, Germany.

Tyndall National Institute, University College Cork, Lee Maltings, Cork, T12 R5CP, Ireland.

出版信息

Chemistry. 2021 Mar 12;27(15):4913-4926. doi: 10.1002/chem.202003907. Epub 2021 Jan 20.

Abstract

Owing to the limited availability of suitable precursors for vapor phase deposition of rare-earth containing thin-film materials, new or improved precursors are sought after. In this study, we explored new precursors for atomic layer deposition (ALD) of cerium (Ce) and ytterbium (Yb) containing thin films. A series of homoleptic tris-guanidinate and tris-amidinate complexes of cerium (Ce) and ytterbium (Yb) were synthesized and thoroughly characterized. The C-substituents on the N-C-N backbone (Me, NMe , NEt , where Me=methyl, Et=ethyl) and the N-substituents from symmetrical iso-propyl (iPr) to asymmetrical tertiary-butyl (tBu) and Et were systematically varied to study the influence of the substituents on the physicochemical properties of the resulting compounds. Single crystal structures of [Ce(dpdmg) ] 1 and [Yb(dpdmg) ] 6 (dpdmg=N,N'-diisopropyl-2-dimethylamido-guanidinate) highlight a monomeric nature in the solid-state with a distorted trigonal prismatic geometry. The thermogravimetric analysis shows that the complexes are volatile and emphasize that increasing asymmetry in the complexes lowers their melting points while reducing their thermal stability. Density functional theory (DFT) was used to study the reactivity of amidinates and guanidinates of Ce and Yb complexes towards oxygen (O ) and water (H O). Signified by the DFT calculations, the guanidinates show an increased reactivity toward water compared to the amidinate complexes. Furthermore, the Ce complexes are more reactive compared to the Yb complexes, indicating even a reactivity towards oxygen potentially exploitable for ALD purposes. As a representative precursor, the highly reactive [Ce(dpdmg) ] 1 was used for proof-of-principle ALD depositions of CeO thin films using water as co-reactant. The self-limited ALD growth process could be confirmed at 160 °C with polycrystalline cubic CeO films formed on Si(100) substrates. This study confirms that moving towards nitrogen-coordinated rare-earth complexes bearing the guanidinate and amidinate ligands can indeed be very appealing in terms of new precursors for ALD of rare earth based materials.

摘要

由于用于气相沉积含稀土薄膜材料的合适前驱体供应有限,因此需要寻找新的或改进的前驱体。在本研究中,我们探索了用于原子层沉积(ALD)含铈(Ce)和镱(Yb)薄膜的新前驱体。合成了一系列铈(Ce)和镱(Yb)的均配三胍基和三亚胺基配合物,并进行了全面表征。N-C-N主链上的C取代基(Me、NMe₂、NEt₂,其中Me = 甲基,Et = 乙基)以及从对称异丙基(iPr)到不对称叔丁基(tBu)和Et的N取代基被系统地改变,以研究取代基对所得化合物物理化学性质的影响。[Ce(dpdmg)₃] 1和[Yb(dpdmg)₃] 6(dpdmg = N,N'-二异丙基-2-二甲基氨基胍基)的单晶结构突出了固态下的单体性质,具有扭曲的三角棱柱几何形状。热重分析表明这些配合物具有挥发性,并强调配合物中不对称性的增加会降低其熔点,同时降低其热稳定性。密度泛函理论(DFT)用于研究Ce和Yb配合物的亚胺基和胍基对氧气(O₂)和水(H₂O)的反应活性。DFT计算表明,与亚胺基配合物相比,胍基对水的反应活性增加。此外,Ce配合物比Yb配合物更具反应活性,这表明其对氧气的反应活性甚至可能用于ALD目的。作为代表性前驱体,高反应活性的[Ce(dpdmg)₃] 1被用于以水作为共反应物进行CeO₂薄膜的原理验证ALD沉积。在160°C下可以确认自限性ALD生长过程,在Si(100)衬底上形成了多晶立方CeO₂薄膜。这项研究证实,对于基于稀土材料的ALD新前驱体而言,转向带有胍基和亚胺基配体的氮配位稀土配合物确实可能非常有吸引力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4aba/7986905/8a4b2c518673/CHEM-27-4913-g001.jpg

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