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Article

Two-Dimensional Perovskite Crystals Formed by Atomic Layer Deposition of CaTiO3 on γ-Al2O3

Department of Chemical and Biomolecular Engineering, University of Pennsylvania, Philadelphia, PA 19104, USA
*
Author to whom correspondence should be addressed.
Submission received: 3 August 2021 / Revised: 24 August 2021 / Accepted: 25 August 2021 / Published: 27 August 2021

Abstract

:
CaTiO3 films with an average thickness of 0.5 nm were deposited onto γ-Al2O3 by Atomic Layer Deposition (ALD) and then characterized by a range of techniques, including X-ray Diffraction (XRD) and High-Resolution, Transmission Electron Microscopy (HRTEM). The results demonstrate that the films form two-dimensional crystallites over the entire surface. Lattice fringes from HRTEM indicate that the crystallites range in size from 5 to 20 nm and are oriented in various directions. Films of the same thickness on SiO2 remained amorphous, indicating that the support played a role in forming the crystallites.

1. Introduction

Thin oxide films on high-surface-area substrates could be important for a number of applications, including novel heterogeneous catalysts [1] and new materials for chemical looping [2]. The standard impregnation of metal salts can give monolayer oxides when there are favorable interactions with the support, such as in the case of titania-supported vanadia catalysts [3]; however, when the impregnated amount is in excess of a monolayer, three-dimensional particles are usually formed [4]. Recent interest in adding the second oxide by Atomic Layer Deposition (ALD) results from the fact that uniform, two-dimensional layers which are thicker than one monolayer can be formed by this procedure [5,6,7,8]. In some applications, the crystallinity of the two-dimensional film could be very important.
An interesting example where thin films are important is that of perovskite-supported metals. These have been referred to as “Intelligent Catalysts” because the reversible ingress and egress of the metal catalyst into the perovskite lattice can potentially be used to redisperse the metal after sintering [9,10]. Strong interactions between the perovskite and the metal can also affect other properties of the metal. For example, Ni supported on Ti-based perovskites have been shown to exhibit extreme tolerance against coking [11] while still showing a high activity for the reforming of methane [12]. However, the implementation of these catalysts has been limited by the low surface areas of typical perovskites and by the fact that much of the metal remains in the perovskite lattice, inaccessible for reactions [1]. Both problems can be solved by having the perovskite in the form of a thin film on a second, high-surface-area oxide. Since the perovskite structure of the oxide is critical for establishing the catalytic properties of Intelligent Catalysts [13], the characterization of the structure of the film is critical.
For a supported thin film to retain a high surface area, the thickness cannot be greater than about 1 nm. This is illustrated by considering that a 1 nm film with a density of 5 g/cm3 on a 200 m2/g support would have a mass equal to that of the underlying support. Assuming that the surface area does not decrease even more due to the shrinkage of the pores, the specific surface area would still decrease by a factor of two simply due to the increase in the mass of the sample. However, since the unit cell size of oxides with perovskite or fluorite structures is only about 0.5 nm, the crystallinity of a 1 nm film would depend on the in-plane ordering of the cations. The characterization of this ordering by techniques like X-ray Diffraction (XRD) is challenging since the film thickness is less than the X-ray coherence length.
Consistent with the films being thinner than the X-ray coherence length, studies from our laboratories of CeO2 [14], ZrO2 [15], and CeZrO4 [16] films less than 1 nm in thickness and deposited onto Al2O3 by ALD showed these to be X-ray amorphous, even for oxide loadings as high as nearly 40 wt% and calcination temperatures above 1073 K. However, later investigations of mixed oxides with stoichiometries of LaFeO3 [17,18] and CaTiO3 [12,19] reported intense perovskite XRD peaks for even lower loadings on MgAl2O4 supports, even though other characterization techniques indicated that the films remained intact and did not coalesce into particles. Furthermore, X-ray line broadening of the perovskite features indicated crystallite sizes between 10 and 20 nm [1], which was inconsistent with there being sufficient material to cover the surface of the support. Since diffraction in the direction perpendicular to the plane of a two-dimensional crystallite is possible [20], it was suggested that the films formed flat crystallites with random surface orientations [1]. The direct observation of these crystallites by electron microscopy was difficult however, due to the underlying crystallinity of the MgAl2O4 support.
In the present study, we investigated CaTiO3 films on a γ-Al2O3 support to look for direct evidence of crystallinity in two-dimensional films. In previous research, CaTiO3 film has proven itself a promising support for both noble metal catalysts [19,21] and Ni-based catalysts [12]. γ-Al2O3 was chosen as the support because of its relatively poor crystallinity and low reactivity with CaTiO3. Although CaAl2O4 formation is possible, the spinel structure is easily distinguished from that of a perovskite phase if it should form.

2. Materials and Methods

2.1. Sample Preparation

Fresh γ-Al2O3 (Strem Chemicals, Inc., Newburyport, MA, USA, 180 m2/g) was first calcined in air at 1173 K for 24 h to achieve a stable support with a surface area of 105 m2/g, and the diameter of the calcined Al2O3 particles ranged between 5–30 nm. ALD was performed in a static system that has been described in detail elsewhere [15]. The precursors were Ca(TMHD)2 (TMHD=2,2,6,6-tetramethyl-3,5-heptanedionato, Strem Chemicals, Inc., Newburyport, MA, USA) and TiCl4 (Sigma-Aldrich, St. Louis, MO, USA). For CaO deposition, the sample was exposed to vapors from the Ca precursor for 5 min at 573 K; ligand removal was accomplished by oxidizing the sample in air at 873 K in a muffle oven for 5 min. For TiO2 deposition, the sample was exposed to TiCl4 vapor at 423 K for 3 min; oxidation was accomplished by exposure to humidified air (containing 10% steam) at 423 K. Growth rates were determined by weighing the sample after every ALD cycle, as shown in Figure S3, and were found to be 6.6 × 1013 Ca atom/cm2-cycle (equivalent to 0.018 nm of CaO per cycle, assuming a bulk density for the film) and 9.6 × 1013 Ti atom/cm2-cycle (0.030 nm of TiO2 per cycle). To achieve the correct perovskite stoichiometry, we performed six ALD cycles of CaO, followed by four cycles of TiO2. The elemental composition of the deposited sample was further tested by the inductively coupled plasma−optical emission spectrometry (ICP-OES) method on a Spectro Genesis spectrometer equipped with a Mod Lichte nebulizer. Finally, the CaTiO3/Al2O3 sample was calcined in air at 1073 K for 3 h. The calculated thickness of the CaTiO3 film was 0.52 nm, determined from the mass of deposited CaTiO3 and the BET surface area of the Al2O3, assuming a uniform film with the bulk density of CaTiO3 (3.98 g cm−3) [12].

2.2. Sample Characterization

X-ray Diffraction (XRD) was performed on a Rigaku MiniFlex diffractometer (Rigaku Analytical Devices, Inc., Wilmington, MA, USA) equipped with a Cu K-α source (λ = 0.15406 nm). Scanning transmission electron microscopy (STEM) and high-resolution transmission electron microscopy (HR-TEM) images and Energy Dispersive X-ray Spectra (EDS) were acquired on a JEOL JEM-F200 STEM (JEOL USA Inc., Peabody, MA, USA), operated at 200 kV. For the TEM analysis, the sample was ground with a mortar and pestle and then dispersed in ethanol to form a suspension. A single drop of the suspension was then added to a standard TEM sample grid (Ted Pella, Inc., Redding, CA, USA), which was then allowed to dry. Temperature Programmed Desorption (TPD) measurements were performed in high vacuum using equipment that is described in detail elsewhere [22]. During the TPD experiment, the samples were first exposed to 2-propanol vapor at room temperature, then evacuated for 1 h using a turbo-molecular pump. The sample temperature was then ramped at 10 K min−1 while monitoring the desorbing species using a quadrupole mass spectrometer (SRS-RGA-100, Stanford Research Systems, Sunnyvale, CA, USA).

3. Results

The XRD patterns of the 18 wt% CaTiO3/Al2O3 sample and the bare Al2O3 support are presented in Figure 1. The pattern for bare Al2O3 shows weak, broad peaks, consistent with a low degree of crystallinity, while the CaTiO3-containing sample shows additional features at 23, 33, 48, 59 degrees 2θ that can be assigned to the CaTiO3 perovskite phase, even though the thickness of the film (0.52 nm) was much smaller than the coherence length of XRD. Based on the linewidth of the feature at ~33 degrees, the crystallite size of the perovskite phase is estimated to be ~17 nm. The two small peaks at 25 and 27 degrees can be assigned to the (101) peak of an anatase phase and the (110) peak of a rutile phase. Both peaks are the strongest features of their respective phases and suggest that there was a slight excess of TiO2 in the sample. The ICP-OES results showed that the weight loading of CaTiO3 on Al2O3 was 16.7 wt%, consistent with that acquired by weight tracking. The ratio between Ca and Ti was 0.95:1 and agreed with the XRD results. It is worth noting that if all of the perovskite phase were present as three-dimensional particles, 17 nm in size, the amount of CaTiO3 in the sample would be sufficient to cover only a very small fraction of the Al2O3.
To determine the morphology of the added CaTiO3, Scanning Transmission Electron Microscope (STEM) images with Energy Dispersive X-ray Spectra (EDS) were obtained, as shown in Figure 2a–d. The STEM images of CaTiO3/Al2O3 were indistinguishable from those of Al2O3. The EDS maps of Ca, Ti and Al were more informative and show uniform distributions of Ca and Ti over the entire surface.
Further evidence for the CaTiO3 forming a uniform film comes from Temperature Programmed Desorption (TPD) measurements reported in Figure 3. Al2O3 is a Lewis acid and is a good catalyst for alcohol dehydration. As discussed in more detail elsewhere [23], room-temperature exposure of Al2O3 to 2-propanol, followed by evacuation, leaves approximately one monolayer of the alcohol on the surface. As shown by the TPD in Figure 3a, about half of this adsorbed alcohol leaves the surface as 2-propanol (m/e = 45, 43, and 41) below 400 K, with the rest reacting to propene (m/e = 41) and water, with propene desorbing between 400 and 500 K. The analogous results for the 18 wt% CaTiO3/Al2O3 sample are presented in Figure 3b. Significant amounts of unreacted 2-propanol again desorbed from the sample below 400 K. However, we also observed acetone (m/e = 43) and propene from 575 K to 700 K. For the present purposes, it is noteworthy that desorption features associated with the bare Al2O3 are completely absent. If a significant fraction of the Al2O3 remained uncovered, one would have observed a propene feature in the TPD below 500 K.
While the XRD pattern suggested that the CaTiO3 was present in the form of ~17 nm crystallites, the STEM results in Figure 2 and the TPD results in Figure 3 demonstrated that the CaTiO3 must be present as a uniform film no more than ~0.5 nm in thickness. However, if even a fraction of the 17 nm crystallites were three-dimensional, there would be insufficient material to completely cover the Al2O3 support. This is shown diagrammatically in Figure 4, in which Figure 4a demonstrates the pristine state of the Al2O3 support. If the crystallized CaTiO3 were present as three-dimensional, cubic crystallites with an edge length of 10 nm shown in Figure 4c, then 18 wt% CaTiO3 would be sufficient to occupy only 5% of the 105 m2/g Al2O3. Both the STEM/EDS and 2-propanol TPD results imply that the morphology of the film must be more similar to that shown in Figure 4b.
The crystallinity of the CaTiO3 films was further assessed by High Resolution Transmission Electron Microscopy (HR-TEM), with representative images of the bare and CaTiO3-covered Al2O3 reported in Figure 5. The image of Al2O3 in Figure 5a does not exhibit any well-defined lattice fringes, consistent with the broad peaks found in the XRD pattern of Figure 1. By contrast, the entire surface of the CaTiO3/Al2O3 sample, shown in Figure 5b, is covered with lattice fringes. Distinguishable crystallites in Figure 5b are framed by the dashed red lines. Most of the crystallites seem to be between 5 and 10 nm in size, with some of the fringes extending over significantly larger dimensions.
In the HR-TEM image of the CaTiO3/Al2O3 sample in Figure 6, we focused on regions of the sample that exhibited better crystallization in order to index some of the observed planes. As shown in yellow, fringes could be easily identified with d-spacing corresponding to (002) planes, consistent with these being the most intense feature in the XRD patterns presented in Figure 1. At least one of these crystallites appears to be greater than 20 nm in size (denoted as the red-framed region in Figure 6), consistent with the crystallite-size estimates from XRD. Lattice spacings corresponding to the (202) planes were observed in other images, as shown in Figure S1 (The lattice parameters as well as the d-spacing values for bulk CaTiO3 are presented in Table S1).
The question arises whether the Al2O3 support plays a role in crystallizing the perovskite film. To address this issue, we also deposited a 0.5 nm film (0.37 g/g SiO2) of a mixed oxide with the CaTiO3 stoichiometry (The Ca:Ti ratio of the sample was 0.93:1 based on the ICP-OES results) onto an amorphous silica that had a surface area of 180 m2/g. Growth rates of CaO and TiO2 on SiO2 are presented in Figure S4. The sample was again oxidized at 1073 K for 3 h. As shown in Figure S2, the film was largely amorphous, except for a few minor peaks corresponding to an anatase phase (TiO2). The absence of diffraction peaks showed conclusively that three-dimensional particles were not formed and that the film was also not crystalline on the length scale of the X-ray. This result is similar to what was observed in earlier attempts to prepare LaFeO3 films on silica, which also failed to find evidence of a perovskite phase from diffraction measurements [24].

4. Discussion

It is interesting to ask why the results on SiO2 are so different from those on Al2O3 and MgAl2O4 [21,25]. Clearly, the perovskite films are not epitaxially matched to the crystal structures of Al2O3 (cubic, a = 0.7912 nm) or MgAl2O4 (cubic, a = 0.8081 nm) [12]. However, it appears that both Al2O3 and MgAl2O4 are able to nucleate the formation of larger, two-dimensional crystallites while SiO2 is not. Because the crystallization of a perovskite thin film is a nucleation-controlled process, understanding the manner of nucleation is important. Given the thickness of the thin film in the present research (~0.5 nm), the perovskite film must have crystallized in a “heterogeneous nucleation” manner, during which the “seeding effect” played a major role [26]. The nanoscale seeds at the interface between the overlayer and its support presumably reduce the energy barrier for forming crystallites by promoting nucleation at a specific surface site, thus lowering the temperature required to crystallize the perovskite phase. Seeds that were previously reported to facilitate nucleation are crystallized materials, such as perovskite [27] or an intermetal [28]. In the present study, surface crystallites of Al2O3 likely served as the seeds in the nucleation of CaTiO3. By contrast, the crystallization of a perovskite phase on the surface of SiO2 is more difficult due to a scarcity of nucleation sites. A better understanding of the crystallization process could be achieved with theoretical tools such as the density function theory (DFT).
The diffraction pattern for CaTiO3/Al2O3 exhibits the typical powder-pattern behavior, and a better understanding of the nucleation process may provide an opportunity to prepare materials in which certain crystal planes are preferred.

5. Conclusions

We demonstrated that relatively large, two-dimensional perovskite platelets were formed when CaTiO3 films were deposited onto γ-Al2O3 by ALD. The Al2O3 support facilitated the crystallization of its perovskite overlayer by providing sites for nucleation. The formation of CaTiO3 crystallites on the amorphous SiO2 support, however, is more difficult.

Supplementary Materials

The following are available online at https://0-www-mdpi-com.brum.beds.ac.uk/article/10.3390/nano11092207/s1, Figure S1: (a) High angle annular dark field (HAADF) STEM image of the 18-wt% CaTiO3/Al2O3 sample; (b–d) are EDS maps of Ca, Ti and Al, taken from the region indicated by the dashed red frame; (e) HR-TEM of the sample, image acquired from the orange framed region, Figure S2: XRD patterns of CaTiO3 deposited on SiO2, the black line denotes bare SiO2 and the red line denotes CaTiO3/SiO2, Figure S3: Growth rate of CaO, TiO2 on γ-Al2O3 as a function of ALD cycles. (a) CaO; (b) TiO2, Figure S4: Growth rate of CaO, TiO2 on SiO2 as a function of ALD cycles. (a) CaO; (b) TiO2, Table S1: Lattice perimeters and d-spacing values of standard CaTiO3 crystal system.

Author Contributions

Conceptualization, investigation and writing the original draft, T.C.; S/TEM experiments, O.K.; Sample preparation, C.L., T.C.; supervision, reviewing and editing, J.M.V. and R.J.G. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by the Air Force Office of Scientific Research, under AFOSR Award No. FA9550-19-1-0326. Some of this work was carried out at the Singh Center for Nanotechnology, part of the National Nanotechnology Coordinated Infrastructure Program, which is supported by the National Science Foundation grant NNCI- 2025608.

Data Availability Statement

The data presented in this study are available upon request from the corresponding author.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. XRD patterns of bare Al2O3 (γ-phase, denoted as the black line) and the 18 wt% CaTiO3/Al2O3 sample (denoted as the red line). Features shaded in grey correspond to peaks of the perovskite phase.
Figure 1. XRD patterns of bare Al2O3 (γ-phase, denoted as the black line) and the 18 wt% CaTiO3/Al2O3 sample (denoted as the red line). Features shaded in grey correspond to peaks of the perovskite phase.
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Figure 2. (a) High angle annular dark field (HAADF) STEM image of the 18 wt% CaTiO3/Al2O3 sample; (bd) are EDS maps of Ca, Ti and Al, taken from the region indicated by the red frame.
Figure 2. (a) High angle annular dark field (HAADF) STEM image of the 18 wt% CaTiO3/Al2O3 sample; (bd) are EDS maps of Ca, Ti and Al, taken from the region indicated by the red frame.
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Figure 3. TPD of 2-propanol from (a) bare Al2O3; (b) Al2O3 loaded with 18 wt% CaTiO3. Desorption features correspond to propene (m/e = 41), acetone (m/e = 43), and unreacted 2-propanol (m/e = 41, 43, and 45).
Figure 3. TPD of 2-propanol from (a) bare Al2O3; (b) Al2O3 loaded with 18 wt% CaTiO3. Desorption features correspond to propene (m/e = 41), acetone (m/e = 43), and unreacted 2-propanol (m/e = 41, 43, and 45).
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Figure 4. Morphology of the CaTiO3 film on the surface of the Al2O3 support. (a) Bare support; (b) support coated with a uniform film; (c) support decorated with three-dimensional cubic crystallites.
Figure 4. Morphology of the CaTiO3 film on the surface of the Al2O3 support. (a) Bare support; (b) support coated with a uniform film; (c) support decorated with three-dimensional cubic crystallites.
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Figure 5. HR-TEM image of (a) bare Al2O3; (b) 18 wt% CaTiO3/Al2O3.
Figure 5. HR-TEM image of (a) bare Al2O3; (b) 18 wt% CaTiO3/Al2O3.
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Figure 6. HR-TEM image of the 18 wt% CaTiO3/Al2O3 sample.
Figure 6. HR-TEM image of the 18 wt% CaTiO3/Al2O3 sample.
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Cao, T.; Kwon, O.; Lin, C.; Vohs, J.M.; Gorte, R.J. Two-Dimensional Perovskite Crystals Formed by Atomic Layer Deposition of CaTiO3 on γ-Al2O3. Nanomaterials 2021, 11, 2207. https://0-doi-org.brum.beds.ac.uk/10.3390/nano11092207

AMA Style

Cao T, Kwon O, Lin C, Vohs JM, Gorte RJ. Two-Dimensional Perovskite Crystals Formed by Atomic Layer Deposition of CaTiO3 on γ-Al2O3. Nanomaterials. 2021; 11(9):2207. https://0-doi-org.brum.beds.ac.uk/10.3390/nano11092207

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Cao, Tianyu, Ohhun Kwon, Chao Lin, John M. Vohs, and Raymond J. Gorte. 2021. "Two-Dimensional Perovskite Crystals Formed by Atomic Layer Deposition of CaTiO3 on γ-Al2O3" Nanomaterials 11, no. 9: 2207. https://0-doi-org.brum.beds.ac.uk/10.3390/nano11092207

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