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At least 631 records · Page 35

Irradiation-induced amorphization of UO 2 films prepared by spraying-assisted combustion synthesis

Spraying-assisted combustion synthesis with uranyl nitrate – acetylacetone – 2-methoxyethanol solutions was used to prepare UO 2 films on an aluminum alloy substrate. The tuning of the spraying parameters and annealing temperatures allowed the preparation of UO 2 films with thicknesses varying from 10–300 nm and 5–10 nm UO 2 grain size. High-resolution electron microscopy and X-ray photoelectron spectroscopy showed that increasing the annealing temperature promotes Mg diffusion from the substrate into the films. The incorporation of Mg reduced the overall crystallinity of the films. The irradiation with Ar 2+ ions (1.7 MeV energy and a fluence of 2 × 10 16 ions/cm 2 ) did not degrade the quality of the films. However, the Mg content significantly influenced the irradiation-induced restructuring of the UO 2 films. Irradiated films with low or no Mg content exhibit high crystallinity, and the UO 2 /Al interfacial layer becomes highly porous. Films with higher Mg content are mostly amorphized after irradiation. The origin of irradiation-induced amorphization was related to the formation of Mg y U 1-y O 2±x solid solutions. Chemically complex, pore-free, and amorphous Mg-Al-O film/substrate interfacial layers enable continuous Mg diffusion during irradiation. As a result, the gradual increase in Mg amounts triggers irradiation-induced precipitation of a crystalline MgO-rich phase within the amorphous films.

38 RADIATION CHEMISTRY, RADIOCHEMISTRY, AND NUCLEA↗

A chemical bath deposition route to facet-controlled Ag{sub 3}PO{sub 4} thin films with improved visible light photocatalytic activity

A facile, economic, and reproducible chemical bath deposition (CBD) method is developed for the fabrication of facet-controlled Ag{sub 3}PO{sub 4} thin films with enhanced visible light photocatalytic activity. The fine-control of bath temperature, precursor, complexing agent, substrate, and solution pH is fairly crucial in preparing the facet-selective thin film of Ag{sub 3}PO{sub 4} nanocrystal. The change of precursor from silver nitrate to silver acetate makes possible the tailoring of the crystal shape of Ag{sub 3}PO{sub 4} from cube to rhombic dodecahedron and also the bandgap tuning of the deposited films. The control of [Ag{sup +}]/[phosphate] ratio enables to maximize the loading amount of Ag{sub 3}PO{sub 4} crystals per the unit area of the deposited film. All the fabricated Ag{sub 3}PO{sub 4} thin films show high photocatalytic activity for visible light-induced degradation of organic molecules, which can be optimized by tailoring the crystal shape of the deposited crystals. This CBD method is also useful in preparing the facet-controlled hybrid film of Ag{sub 3}PO{sub 4}–ZnO photocatalyst. The present study clearly demonstrates the usefulness of the present CBD method for fabricating facet-controlled thin films of metal oxosalt and its nanohybrid. - Highlights: • The crystal facet of Ag{sub 3}PO{sub 4} films can be tuned by chemical bath deposition. • The crystal shape of Ag{sub 3}PO{sub 4} is tailorable from cube to rhombic dodecahedron. • Facet-tuned Ag{sub 3}PO{sub 4} film shows enhanced visible light photocatalyst activity.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Aluminum doped nickel oxide thin film with improved electrochromic performance from layered double hydroxides precursor in situ pyrolytic route

Electrochromic materials with unique performance arouse great interest on account of potential application values in smart window, low-power display, automobile anti-glare rearview mirror, and e-papers. In this paper, high-performing Al-doped NiO porous electrochromic film grown on ITO substrate has been prepared via a layered double hydroxides(LDHs) precursor in situ pyrolytic route. The Al{sup 3+} ions distributed homogenously within the NiO matrix can significantly influence the crystallinity of Ni-Al LDH and NiO:Al{sup 3+} films. The electrochromic performance of the films were evaluated by means of UV–vis absorption spectroscopy, cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and chronoamperometry(CA) measurements. In addition, the ratio of Ni{sup 3+}/Ni{sup 2+} also varies with Al content which can lead to different electrochemical performances. Among the as-prepared films, NiO film prepared from Ni-Al (19:1) LDH show the best electrochromic performance with a high transparency of 96%, large optical modulation range (58.4%), fast switching speed (bleaching/coloration times are 1.8/4.2 s, respectively) and excellent durability (30% decrease after 2000 cycles). The improved performance was owed to the synergy of large NiO film specific surface area and porous morphology, as well as Al doping stifled the formation of Ni{sup 3+} making bleached state more pure. This LDHs precursor pyrolytic method is simple, low-cost and environmental benign and is feasible for the preparation of NiO:Al and other Al-doped oxide thin film. - Graphical abstract: The ratio of Ni{sup 3+}/Ni{sup 2+} varies with Al content which can lead to different electrochemical performances. Among the as-prepared films, NiO film prepared from Ni-Al (19:1) LDH show the best electrochromic performance with a high transparency of 96%, large optical modulation range, fast switching speed and excellent durability. Display Omitted.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

The role of polymer films on the oxidation of magnetite nanoparticles

A detailed investigation about the role of polymer films on the oxidation process of magnetite nanoparticles (∼7 nm diameter), under laser irradiation is performed employing micro Raman spectroscopy. To support this investigation, Fe{sub 3}O{sub 4}-np are synthesized by the co-precipitation method and assembled layer-by-layer with sodium sulfonated polystyrene (PSS). Polymer films (Fe{sub 3}O{sub 4}-np/PSS){sub n} with n=2,3,5,7,10 and 25 bilayers are employed as a model system to study the oxidation process under laser irradiation. Raman data are further processed by principal component analysis. Our findings suggest that PSS protects Fe{sub 3}O{sub 4}-np from oxidation when compared to powder samples, even for the sample with the greater number of bilayers. Further, the oxidation of magnetite to maghemite occurs preferably for thinner films up to 7 bilayers, while the onset for the formation of the hematite phase depends on the laser intensity for thicker films. Water takes part on the oxidation processes of magnetite, the oxidation/phase transformation of Fe{sub 3}O{sub 4}-np is intensified in films with more bilayers, since more water is included in those films. Encapsulation of Fe{sub 3}O{sub 4}-np by PSS in layer-by-layer films showed to be very efficient to avoid the oxidation process in nanosized magnetite. - Graphical abstract: Encapsulation of Fe{sub 3}O{sub 4}-np by PSS in layer-by-layer films avoids the oxidation and phase transformation of nanosized magnetite. - Highlights: • (Fe{sub 3}O{sub 4}-np/PSS){sub n} nanofilms, with n=2 up to 25, where layer-by-layer assembled. • The influence of film architecture on the Fe{sub 3}O{sub 4}-np oxidation was investigated through Raman spectroscopy. • Encapsulation of Fe{sub 3}O{sub 4}-np by PSS showed to be very efficient to avoid the Fe{sub 3}O{sub 4}-np oxidation.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Growth and magnetoelectric properties of (00l)-oriented La{sub 0.67}Sr{sub 0.33}MnO{sub 3}/PbZr{sub 0.52}Ti{sub 0.48}O{sub 3} heterostructure films

C-axis oriented La{sub 0.67}Sr{sub 0.33}MnO{sub 3}(LSMO)/PbZr{sub 0.52}Ti{sub 0.48}O{sub 3}(PZT) films are fabricated successfully by sol-gel method on LaAlO{sub 3} (00l) substrates. The structure, composition and morphology of the films are investigated by X-ray diffractometer (XRD, θ-2θ scan, ω-scan and ϕ-scan), X-ray photoelectron spectroscope (XPS), field emission scanning electron microscope (FESEM) and high resolution transmission electron microscope (HRTEM). The electric and magnetic properties of randomly and c-axis oriented LSMO/PZT films are studied comparably using ferroelectric testing apparatus and physical property measurement system (PPMS). It is found that the epitaxial LSMO/PZT composite films show well controlled growth along c-axis, and much better magnetoelectric properties than the randomly oriented ones. The ME voltage coefficient increases from 23 mV cm{sup −1} Oe{sup −1} for the randomly oriented LSMO/PZT composite films to 52 mV cm{sup −1} Oe{sup −1} for c-axis oriented ones prepared using the low cost sol-gel method presented in this study, which shows high potential in promising applications. - Highlights: •Epitaxial LSMO/PZT films were fabricated successfully by sol-gel method on LAO (00l) substrate. •The prepared films exhibit well-defined multiferroic properties for the epitaxial LSMO/PZT films. •Epitaxial LSMO/PZT films show superior magnetoelectric properties to the randomly oriented ones.

36 MATERIALS SCIENCE↗

Characterization of thin films prepared by co-sputtering iron and titanium precursors and thermal oxidation under air atmosphere

Highlights: • Thin films of mixed iron and titanium oxide were prepared by Ti-Fe annealing. • Segregation and phase separation of iron and titanium oxides are observed. • Formation of iron rich (Fe{sub x}O) nanoparticles at the surface region is revealed. • Formation of thin films with high refractive index can be obtained. - Abstract: Nanocomposites of metal oxides are useful materials for operation in many energy conversion systems. In this study, such nanocomposites were prepared by oxidation of mixtures of iron and titanium precursor metallic thin films at 520 °C under air atmosphere. The metallic films with different iron percentages were obtained by radio frequency (RF) magnetron sputtering on glass and silicon substrates. The films were characterized by means of X-ray Diffraction (XRD), Raman spectroscopy, UV–Vis spectroscopy, High Resolution Scanning Transmission Electron Microscopy (HRSTEM), Ellipsometry and X-ray Photo-electron Spectroscopy (XPS). The results show that these films present mainly two nanometric phases, namely Fe{sub 2}O{sub 3} and TiO{sub 2}. A phase separation was observed; the film surface was found to be iron rich oxide or clusters of iron rich oxide (Fe{sub x}O{sub y}, x > y), whereas titanium accumulated deeply in the bulk, forming TiO{sub 2} far below the film surface. A red shift of optical absorption as well as a relatively stable high refractive index (varying between 3.1 and 3.5) over a broad band of optical frequencies was observed for the films containing higher iron initial concentrations.

36 MATERIALS SCIENCE↗

Correlation between thickness dependent nanoscale structural chemistry and superconducting properties of ultrathin epitaxial NbN films

NbN-based superconductors have attracted interest for superconducting circuits, quantum computation and high frequency devices. The superconducting properties of NbN films are predominately reliant on the microstructure, therefore, an atomic-level understanding of the structure-chemistry is required to achieve high quality epitaxial NbN films. Here, in this study, the thickness-dependent superconducting properties of NbN films (5, 10, and 50 nm) within NbN/AlN/Al 2 O 3 heterostructures are investigated. NbN and AlN were epitaxially grown by an industrial scale physical vapor deposition technique. The role of nanoscale chemistry on the ultrathin NbN superconducting film is investigated at the atomic level for the first time via atom probe tomography, providing three-dimensional atomic distribution, chemical homogeneity, effect of impurities, specially, in secondary phase formations and interfacial abruptness. The NbN film with 5 nm of thickness demonstrates a superconducting transition temperature of 11.2 K as compared to 50 nm NbN films with a transition temperature of 15.3 K. These thickness dependent variation of superconducting properties are associated with the chemical inhomogeneity in terms of in-plane N:Nb distribution, secondary phase formations and NbN/AlN interfacial abruptness as a function of the NbN films thicknesses. The analysis depicts the interplay between the surface/interface and the superconducting properties of ultrathin NbN films. These results provide insights on material design and growth that will enable the development of optimized superconducting NbN films for quantum devices.

36 MATERIALS SCIENCE↗

Influence of activation parameters on the thickness of MgO thin film on Ag-3Mg alloy and its secondary electron emission property

Highlights: • MgO films with controlled thicknesses on Ag-3Mg alloys were prepared by activation in low vacuum with oxygen. • Superior secondary electron yield was obtained for the Ag-3Mg alloy with proper thickness of MgO film. • Oxygen pressure during the activation process is crucial for obtaining good secondary electron yield for Ag-3Mg alloys. • The mechanism of secondary electron emission in MgO films is discussed. - Abstract: MgO thin films of different thicknesses were prepared on polished Ag-3wt%Mg alloy by an activation process at 500–650 °C under oxygen pressures of 0.5–10.0 Pa. The influence of the thickness of MgO film on the secondary electron yield of the Ag-3wt%Mg alloy is investigated. The alloy with an MgO film of moderate thickness of 65 ± 1 nm shows the highest secondary electron yield of 10. Oxygen pressure below 10.0 Pa is crucial for the formation of intact MgO film on the top surface. Computational simulation analysis reveals that the maximum yield occurs when the penetration depth of primary electrons is 13–18 nm less than the thickness of MgO film. Electron supply of this extra MgO film is allowed by an electron tunneling mechanism under certain bias voltage. The replenishment of new electrons to the electron deficient surface is crucial for obtaining optimized secondary electron yields for Ag-Mg alloy cathodes.

36 MATERIALS SCIENCE↗

Influence of Fluorine incorporation on the photocatalytic activity of Tin Oxide thin films

Highlights: • Fluorine doped SnO{sub 2} thin films prepared by a facile homemade jet nebulizer spray pyrolysis technique. • XRD, XPS, PL, FESEM, AFM studies support the discussions. • The photocatalytic activities of the prepared tin oxide (TO) and FTO thin films for the degradation of MB aqueous solution were tested. . - Abstract: This work reports the photocatalytic activity of undoped tin oxide (TO) and F doped tin oxide (FTO) thin films for MB dye degradation under visible light irradiation. A facile homemade jet nebulizer spray pyrolysis technique was employed to prepare these samples. The results indicate that FTO film exhibits superior photocatalytic activity compared to TO film. Dye degradation of nearly 95% is achieved using FTO film at 90 min whereas TO film degrades only 78% of dye molecules in the same time interval. This enhancement for FTO films might be due to the generation of large number of free electrons caused by the fluorine incorporation. The mechanism behind the enhancement of photocatalytic activity of FTO films is discussed elaborately with the aid of optical and PL studies. The structure, composition and morphology of the samples were analyzed using XRD, XPS, FTIR, FESEM and AFM. The incorporation of F into SnO{sub 2} lattice is confirmed through FTIR analysis.

36 MATERIALS SCIENCE↗

A rapid and convenient method for the preparation of thermochromic VO{sub 2} thin films

Highlights: • A simple and efficient route has been developed for the preparation of VO{sub 2} thin films. • VO{sub 2} films annealed at high enough crystallization temperature were obtained and analyzed. • Excellent optical modulation both in the visible and near-infrared region has been achieved in the prepared VO{sub 2} film. - Abstract: The annealing temperature for the preparation of VO{sub 2} films with sputtering method have always been applied in the range of 300–500 °C. Herein, a simple and efficient route has been developed for the preparation of VO{sub 2} thin films through the thermal oxidation of sputtered vanadium film at 585 °C. Structural, morphological, elemental analysis and thermochromic properties of synthesized VO{sub 2} films are reported. Different from the traditional sputtered VO{sub 2} films, large change of transmittance has been found in the visible region during phase transition. The present work shows the feasibility to fabricate reliably reproduced high quality VO{sub 2} films with reversible phase transition and excellent optical modulation both in the visible and near-infrared region.

36 MATERIALS SCIENCE↗

One-pot electrochemical preparation of BiOCl/BiPO{sub 4} double-layer heterojunction film with efficient photocatalytic performance

Highlights: • A novel BiOCl/BiPO{sub 4} heterojunction film has been synthesized by one-pot electrochemical method. • The as-prepared BiOCl/BiPO{sub 4} heterojunction film exhibited high photocatalytic activity and stability. • The plausible formation process of BiOCl/BiPO{sub 4} heterojunction film has been proposed and demonstrated. • The photocatalytic mechanism of phenol degradation presented by BiOCl/BiPO{sub 4} heterojunction film was investigated and analyzed. - Abstract: A BiOCl/BiPO{sub 4} double-layer heterojunction film on metal Bi plate with reduced recombination of photo-induced carriers has been successfully prepared by one-step electrochemical anodization process. The morphology characterizations displayed that the double-layer film consisted of BiPO{sub 4} rods array at the bottom and BiOCl nanosheets on the top. Meanwhile, the control experiments indicated that the BiPO{sub 4} rods array was transformed by BiOCl rather than Bi{sup 3+} reacting with PO{sub 4}{sup 3−} directly. In addition, the resulting BiOCl/BiPO{sub 4} heterojunction film exhibited excellent photocatalytic activity and stability on the degradation of phenol comparing with pure BiOCl film. Transient photocurrent measurements and PL spectra proved that the enhanced photocatalytic performance of BiOCl/BiPO{sub 4} heterojunction film was attributed to the effective separation of photo-generated electron-hole pairs excited on BiOCl. Moreover, ·O{sub 2}{sup −} and ·OH played a crucial role in the photodegradation process of phenol. Based on these analytical results, a plausible photocatalytic mechanism has been proposed.

36 MATERIALS SCIENCE↗

Wafer-scale two-dimensional Au-TiO{sub 2} bilayer films for photocatalytic degradation of Palmitic acid under UV and visible light illumination

Highlights: • Successful wafer-scale atomic layer deposition of 2D Au-TiO{sub 2} bilayer photocatalyst films. • The efficient degradation of fatty acid by tailoring 2D TiO{sub 2} films under UV and visible light illumination. • Improved visible light photocatalytic activity and photocurrent density of 2D Au-TiO{sub 2} bilayer films. • Comparable photocatalytic performance of ultra-thin 2D TiO{sub 2} and thick TiO{sub 2} films under UV light illumination. - Abstract: Bilayer Au-TiO{sub 2} configuration with two-dimensional (2D) TiO{sub 2} films enabled sensible improvement in photocatalytic degradation of Palmitic Acid (PA) and also the enhancement of current density under visible light illumination. The improved visible light photocatalytic and photocurrent properties were attained when 35 nm thick 2D TiO{sub 2} film was developed by atomic layer deposition (ALD) on Si/SiO{sub 2}-Au substrate. The Au-TiO{sub 2} bilayer demonstrated the improved photocatalytic and photovoltaic performances compared with those TiO{sub 2} films developed on Si/SiO{sub 2} bare substrate. These improvements can be attributed to the plasmonic effects of Au film acting as antenna for visible light and also serving as hole acceptor during photocatalysis process. The proposed mechanisms for enhanced visible light performance of bilayer films are hot electron injection and the formation of hot spots at Au-TiO{sub 2} interface which contributed to the electron injection to conduction band of TiO{sub 2} or facilitated the separation of generated electron-hole pairs at Au-TiO{sub 2} Schottky junction.

36 MATERIALS SCIENCE↗

Anomalous Raman and photoluminescence blue shift in mono- and a few layered pulsed laser deposited MoS2 thin films

Highlights: • Mono- and a few layered MoS{sub 2} films deposited using pulsed laser deposition technique by varying the deposition time. • The films experienced an epitaxial compression due to its adhesion with the substrate. • Lattice strain of the films led to a significant Raman frequency shift. • An anomalous PL peak was observed which is attributed to quantum confinement. - Abstract: We report on the Raman blue shift of layered MoS{sub 2} films as well as an anomalous blue shift of the photoluminescence spectra of nanocrystallite MoS{sub 2} films grown by pulsed laser deposition. Monolayer, bilayer and trilayer MoS{sub 2} films were fabricated by ablating MoS{sub 2} target for a deposition time of around 14, 24 and 30 s at a laser fluence of 2.2 Jcm{sup −2}. The two Raman active modes showed lattice strain-induced blue shift of 1–3 cm{sup −1}. The layered films showed an out-of-plane compressive strain as well as an in-plane tensile strain confirmed by Riet-Veld refinement of the X-ray diffraction pattern. TEM image of the MoS{sub 2} film for 14 s demonstrated the presence of nanocrystallites of an average size of 13 nm along with the layered film of MoS{sub 2}. An anomalous photoluminescence peak was observed corresponding to the MoS{sub 2} nanocrystallites at 2.18 eV, attributed to quantum confinement effect.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Solution-based spin-coated tin sulfide thin films for photovoltaic and supercapacitor applications

Highlights: • Tin sulfide (SnS{sub x}) thin films were prepared by solution-based spin coating. • The SnS{sub x} films annealed at 500 °C exhibited a pure SnS phase. • The films exhibited direct band gap of 1.4 eV which is near to solar maximum. • The films with the pure SnS phase exhibited a specific capacitance of 42 F g{sup ―1}. - Abstract: In this study, tin sulfide (SnS{sub x}) thin films were prepared using a solution-based spin-coating method. The annealing temperature was observed to play a dominant role in determining the phase, crystallinity, and morphology of the SnS{sub x} thin films. The results obtained from X-ray diffraction, as well as optical and electrical measurements, revealed that the films annealed at 500 °C exhibit a pure SnS phase, with a carrier concentration and direct band gap of ∼10{sup 12} and 1.4 eV, respectively. To explore the applications of SnS in supercapacitors, electrochemical measurements were performed in a 0.2 M NaOH solution. The results indicated that films with a pure SnS phase have a high specific capacitance of 42 F g{sup ―1} at a current density of 2 A g{sup ―1}. The synthesized SnS thin films demonstrate potential for applications in electrochemical capacitors and solar cells.

14 SOLAR ENERGY↗

High-temperature chemical expansion of Pr0.1Ce0.9O2-δ thin films determined by Differential Laser Doppler Vibrometry

The chemical expansion of thin-film praseodymium-cerium oxide solid solutions (Pr 0.1 Ce 0.9 O 2-δ , PCO10) is investigated at temperatures ranging from 500 °C to 800 °C and oxygen activities down to about 10 -22 . Differential Laser Doppler Vibrometry (D-LDV) in combination with periodic electrochemical pumping of oxygen is used to detect very small displacements of the sample surface. With decreasing pumping frequency, the film approaches chemical equilibrium, which is nearly reached at 700 °C below 0.01 Hz. D-LDV enables direct measurement of film thickness changes as well as the bending of the underlying substrates due electrochemically induced lateral mechanical stress. The substrate bending is found to be more than an order of magnitude larger than the film thickness change, increasing the detection limit by the same factor. The thickness change of the thin film is calculated from the measured displacement of the sample surface and compared with directly measured values. Thin-film literature data available for low oxygen activities up to 650 °C agree with our measurements. In addition, the thickness change of the film is determined from the displacement at different sample positions, which validates previous measurements. Finally, thin film chemical expansion is found to be larger by a factor of about 2 than the corresponding bulk value in agreement with predictions from a mechanical model that the out-of-plane expansion of a constrained film is increased.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Epitaxial growth of oriented CoO films by radio-frequency sputtering deposition

Rock-salt CoO is a p-type semiconductor and its Neel temperature is close to room temperature. CoO-based compounds are known as promising systems for renewable energy harvest with high efficiency. CoO with catalytic and exchange bias properties can be widely used for industrial applications. In this paper, we report high-quality stable CoO(111) and (100) films epitaxially grown on c-cut (0001) and r-cut ($10\bar1$2) alpha-Al 2 O 3 substrates, respectively, using radio-frequency sputtering deposition. X-ray diffraction (XRD) measurements revealed that the CoO films had a rock-salt structure (Fm3m) with lattice constants of 4.2477 Å and 4.2617 Å for film grown on (0001) and ($10\bar1$2) α-Al 2 O 3 substrates, respectively. CoO films with the best crystal quality were grown at a substrate temperature of similar to ~700°C. XRD measurements of CoO(111) films indicated a lack of structural residual strain, whereas CoO(100) films had substantial amounts of structural strain. X-ray reflectivity (XRR) and transmission electron microscopy measurements showed neither oxygen vacancy nor defects in both CoO(111) and (100) films. Further, XRR revealed that the mean electron density of the CoO films was nearly identical to a pure CoO and that the films were considerably stable under the atmosphere.

36 MATERIALS SCIENCE↗

Impact of Relative Humidity during Spin-Deposition of Metal Oxide Thin Films from Aqueous Solution Precursors

Relative humidity during the spin-processing of thin film solution precursors is often not controlled or measured, and its effect on film thickness is generally unappreciated. Herein, we report that the relative humidity during spin-processing has a marked impact on the film thickness of amorphous metal oxide (aluminum oxide and lanthanum zirconium oxide) and hafnium oxide-sulfate (HafSOx) thin films deposited from aqueous precursors. In the humidity range studied [20–95% relative humidity (RH)], film thicknesses varied by a factor of nearly 3, and this effect is independent of the metal precursor identity. Our data suggest that film thickness depends linearly on evaporation rate (100 – RH) for all systems studied, suggesting this effect is predominantly due to the unique characteristics of water as a solvent. In situ X-ray reflectivity studies of HafSOx films deposited under different humidities reveal that, while the thickness varies significantly with humidity, the density of the as-deposited films is similar, suggesting that humidity primarily affects the relative amount of material deposited. Because reproducible film thickness is critical for many applications, our data highlight the importance of controlling humidity during spin-processing.

36 MATERIALS SCIENCE↗

Controlling Preferred Grain Orientation in Vapor-Deposited Metal-Halide Perovskite Thin Films

Metal-halide perovskites are promising semiconductor materials for light-absorber layers in solar cells due to their optimized band gap, defect tolerance, and relative ease of synthesis. In this work, we demonstrate the viability of vapor transport deposition (VTD), a solvent-free processing method, to realize polycrystalline films of both lead iodide (PbI 2 ) and methylammonium lead iodide (MAPbI 3 ) perovskites showing preferential crystallographic orientation. Notable is the difference in perovskite film texturing observed for sequentially and co-deposited VTD films of MAPbI 3 , as well as the lack of strong preferential orientation in solution-processed MAPbI 3 films. While sequential deposition of the perovskite precursors PbI 2 and methylammonium iodide (MAI) leads to a MAPbI 3 film with a limited preferential grain orientation, co-deposited MAPbI 3 films mirror the orientation of excess PbI 2 present in the film. The latter is confirmed by the similar dependence of preferential orientation for PbI 2 and co-deposited MAPbI 3 on underlayer roughness, as well as the emergence of preferential orientation in MAPbI 3 only when excess PbI 2 is present. Both MAPbI 3 and PbI 2 films show a strong preferred lattice orientation on smooth substrates, while on rougher substrates, this orientation is disrupted. Furthermore, these results are interpreted as excess PbI 2 frustrating the diffusion of MAI in the film, which would otherwise disrupt the preferred orientation, pointing to a notable difference in lattice orientation arising from processing technique and conditions.

Deposition↗