Intermediate Crystalline Phase Research Articles

Modulation of Phase Behavior and Microscopic Dynamics in Cationic Vesicles by 1-Decyl-3-methylimidazolium Bromide.

Synthetic cationic lipids have garnered significant attention as promising candidates for gene/DNA transfection in therapeutic applications. The phase behavior of the vesicles formed by these lipids is intriguing, revealing intricate connections to the structure and dynamics of the membrane. These phenomena emerge from the complex interplay between hydrophobic and electrostatic interactions of the lipids. In this study, we explore the impact of an ionic liquid-based surfactant, 1-decyl-3-methylimidazolium bromide (DMIM[Br]), on the structural, dynamical, and phase behavior of cationic dihexadecyldimethylammonium bromide (DHDAB) vesicles. Our investigations indicate that the addition of DMIM[Br] increases the vesicle size while thinning the membrane. Further, DMIM[Br] also induces substantial changes in the membrane phase behavior. At 10 and 25 mol %, DMIM[Br] eliminates the pre-transition from coagel to intermediate crystalline (IC) phase and decreases the onset temperature of the main phase transition to the fluid phase. In the cooling cycle, the addition of DMIM[Br] further induces the formation of an intermediate gel phase. This behavior is reminiscent of the non-synchronous ordering observed in the DODAB membrane, a longer-chain counterpart of DHDAB. Interestingly, at 40 mol % of DMIM[Br], the formation of the intermediate gel phase is largely suppressed. Neutron scattering data provide evidence that the addition of DMIM[Br] enhances lipid mobility in coagel and fluid phases, suggesting that DMIM[Br] acts as a plasticizer, enhancing membrane fluidity across all of the phases. Our findings infer that DMIM[Br] modulates the membrane's phase behavior and fluidity, two essential ingredients for the efficient transport of cargo, by controlling the balance of electrostatic and hydrophobic interactions.

Amorphous Solid Forms of Ranolazine and Tryptophan and Their Relaxation to Metastable Polymorphs.

Different methods were explored for the amorphization of ranolazine, a sparingly soluble anti-anginal drug, such as mechanochemistry, quench-cooling, and solvent evaporation from solutions. Amorphous phases, with Tg values lower than room temperature, were obtained by cryo-milling and quench-cooling. New forms of ranolazine, named II and III, were identified from the relaxation of the ranolazine amorphous phase produced by cryo-milling, which takes place within several hours after grinding. At room temperature, these metastable polymorphs relax to the lower energy polymorph I, whose crystal structure was solved in this work for the first time. A binary co-amorphous mixture of ranolazine and tryptophan was produced, with three important advantages: higher glass transition temperature, increased kinetic stability preventing relaxation of the amorphous to crystalline phases for at least two months, and improved aqueous solubility. Concomitantly, the thermal behavior of amorphous tryptophan obtained by cryo-milling was studied by DSC. Depending on experimental conditions, it was possible to observe relaxation directly to the lower energy form or by an intermediate metastable crystalline phase and the serendipitous production of the neutral form of this amino acid in the pure solid phase.

Transition Mechanism from the Metastable Two-Dimensional Gel to the Stable Three-Dimensional Crystal of Imidazolium-Based Ionic Liquids.

One important quest for making high quality materials with amphiphiles is to understand how a disordered self-assembly changes to a stable crystalline state. Herein, we addressed the basic question by investigating the phase transition mechanism of imidazolium-based ionic liquid (IL) [C16mim]Br, using time-resolved small- and wide-angle X-ray scattering (SAXS-WAXS), differential scanning calorimetry, and Fourier transform infrared spectroscopy techniques. Totally, a hexagonal phase, two lamellar-gel phases, and three lamellar-crystalline phases were observed, showing the special polymorphism of the system. It was demonstrated that at low concentrations the two-dimensional gel phase (Lβ1) transforms into the most stable lamellar-crystal phase (Lc3) through two intermediate crystalline phases Lc1 and Lc2. At high concentrations, the Lβ1 phase changes to a condensed lamellar gel phase (Lβ2) before changing to Lc2 and eventually to Lc3. Comparative studies using [C16mim]Cl and [C16mim]NO3 unveiled that the interactions between the counterions and the headgroups of the IL, as well as the dehydration process, govern the nucleation process of Lc3 and thus the formation of the crystal. The in-depth investigation on the transition mechanism and the phase polymorphism in the present work advances our understanding of the crystallization of amphiphilic ionic liquids in dispersions and would promote future applications.

Unraveling Deposition Atmosphere Impact on Reproducibility of Perovskite Light-Emitting Diodes.

Manipulating the crystallization dynamics of perovskite emitters is an effective strategy for preparing high-performance perovskite light-emitting diodes (PeLEDs). In general, amorphous-like thermodynamically stable intermediates are desirable for a retarded and controllable crystallization process of perovskite emitters. Despite a variety of well-demonstrated strategies for crystallization control, it has been generally realized that perovskite thin-film emitters show problematic reproducibility. Here, we unraveled that the coordinating solvent vapor residues could raise deleterious influences on the formation of amorphous intermediate phases, which thus leads to varying crystal qualities from batch to batch. We demonstrated that undesirable crystalline intermediate phases tend to form with a strong coordination solvent vapor atmosphere, which alters the crystallization process and thus brings about additional ionic defects. By applying an inert gas flush strategy, this detrimental effect could be effectively mitigated, enabling PeLEDs with high reproducibility. This work provides new insight into the fabrication of efficient and reproducible perovskite optoelectronics.

TEM Investigation of Asymmetric Deposition-Driven Crystalline-to-Amorphous Transition in Silicon Nanowires.

Controlling the shape and internal strain of nanowires (NWs) is critical for their safe and reliable use and for the exploration of novel functionalities of nanodevices. In this work, transmission electron microscopy was employed to examine bent Si NWs prepared by asymmetric electron-beam evaporation. The asymmetric deposition of Cr caused the formation of nanosized amorphous-Si domains; the non-crystallinity of the Si NWs was controlled by the bending radius. No other intermediate crystalline phase was present during the crystalline-to-amorphous transition, indicating a direct phase transition from the original crystalline phase to the amorphous phase. Moreover, amorphous microstructures caused by compressive stress, such as amorphous Cr domains and boxes, were also observed in the asymmetric Cr layer used to induce bending, and the local non-crystallinity of Cr was lower than that of Si under the same bending radius.

Metal-induced crystallization of amorphous semiconductor films: Nucleation phenomena in Ag-Ge films

The initial stages of interfacial interactions between Ag nanoparticles and amorphous Ge (a-Ge) films, in particular the mechanism and kinetics of metal-induced crystallization (MIC) of a-Ge films are investigated herein. Unsupported Ag-Ge films formed by PVD were used as a model. In situ high-resolution (S)TEM and low-loss monochromated STEM-EELS techniques were used for real-time observation of the nucleation and growth of crystalline Ge and intermediate phases, as well as mapping of chemical elements at the reaction zone. We show that crystallization is activated at the metal–semiconductor interface around ≈200 °C, followed by lateral crystallization of a-Ge film at temperatures above ≈400 °C. It was revealed that the MIC process occurs through intermediate phases. Metastable Ag0.8Ge0.2 hcp phase was identified at the reaction front at elevated temperatures, thus revealing the non-equilibrium melting of a eutectic alloy as the most probable mechanism of Ag-induced crystallization of a-Ge film. We show that the MIC process is activated only if the size of Ag nanoparticles exceeds a critical value, which is ≈8 nm in our case and equal to the thickness of the a-Ge film.

Impact of urea-based deep eutectic solvents on Mg-MOF-74 morphology and sorption properties

Deep eutectic solvents (DES) based on different urea derivatives have been demonstrated to be efficient green alternatives for the ionothermal synthesis of the prototypical Mg-MOF-74 with a strong impact on the morphology and sorption properties of the material. While the synthesis of the material is rather straightforward in the reline (choline chloride:urea 1:2) DES, higher temperatures and longer reaction times are necessary in the e-urea (2-imidazolidinone, ethylene-urea) based analogous system. Interestingly, in the latter, a variety of intermediate crystalline phases could be observed and characterized by single-crystal X-ray diffraction. In these compounds, coordination of the DES components – the chloride anion and e-urea derivative – to the Mg(II) cation was found to compete with the carboxylate linker. It was rationalized that the difference in the synthesis conditions and in the isolation of intermediate systems originate from the varying decomposition kinetics of the DES and hence from the basicity of the solvent. Although the same material is obtained as ascertained by powder X-ray diffraction and elemental analysis, the final morphology characterized by SEM and TEM is dependent on the nature of the solvent. Whereas the classical rod-like shape is observed in reline, an unusual morphology showing slices perpendicular to the main growth axis is present in the e-urea based DES. For the material featuring this unusual morphology, a higher specific surface area and CO2 uptake were found, which were associated with a higher degree of microporosity.

Microscopic diffusion in cationic vesicles across different phases

Understanding the phase behavior and microscopic diffusion mechanism of cationic vesicles is crucial for controlled-release kinetics in gene/DNA transfection. Here, we report our findings on the structure, phase behavior, and microscopic dynamics of a vesicle based on a cationic double-chained surfactant, dihexadecyldimethylammonium bromide (DHDAB), which is a promising candidate for a nonviral gene/DNA carrier. Small-angle neutron-scattering measurements reveal that DHDAB aggregates are in the form of unilamellar vesicles. Calorimetric studies show a strong thermal hysteresis in the heating and cooling cycles following different pathways. Two first-order transitions are observed at 303 and 318 K in the heating cycle. Fourier transform infrared spectroscopy reveals that the first transition (at 303 K) is associated with a polymorphic (solid-solid) transition from coagel to an intermediate crystalline (IC) phase, and subsequently the second transition (at 318 K) is an order-disorder transition from IC to the fluid phase. Interestingly, it is found that in the cooling cycle, the fluid phase directly transforms back into the coagel phase without passing through the IC phase. This is also confirmed by an elastic fixed window scan (EFWS) using incoherent neutron scattering. The phase behavior of DHDAB is in strong contrast to that of its longer-chain counterpart, dioctadecyldimethylammonium bromide (DODAB), where the intermediate gel phase was observed during the cooling cycle. Moreover, no polymorphic transition was observed in the heating cycle of DODAB, in which the coagel phase directly converts to the fluid phase. These sharply contrasting phase behaviors for DHDAB and DODAB suggest the strong dependence of membrane phase behavior to the alkyl chain length. EFWS measurements reveal that the phase transitions observed in the DHDAB membrane are associated with strong changes in the DHDAB dynamics. The changes in conformational entropy of DHDAB molecules estimated from EFWS confirm that the coagel-fluid and IC-fluid phase transitions are accompanied by strong changes in the conformations of the alkyl chains. The microscopic dynamics of DHDAB molecules in each of these phases is investigated by employing quasielastic neutron-scattering (QENS). In the ordered phases (coagel and IC), only localized internal dynamics of the DHDAB is observed in the QENS spectra. However, in the fluid phase, the presence of a long-range lateral diffusion is detected in addition to the localized internal dynamics of the alkyl chain. The lateral motion is found to follow Fickian diffusion. The internal dynamics of DHDAB depends on the phase state of the bilayer. In the ordered phase, the internal dynamics is described by a fractional uniaxial rotational diffusion model. However, in the fluid phase, where alkyl tails are disordered with significant gauche defects, the internal dynamics is described using localized translation within confined spheres. This study highlights the rich phase behavior of the DHDAB membrane and the surfactant dynamics across these phases.

Nanolattice-Forming Hybrid Collagens in Protective Shark Egg Cases.

Nanoscopic structural control with long-range ordering remains a profound challenge in nanomaterial fabrication. The nanoarchitectured egg cases of elasmobranchs rely on a hierarchically ordered latticework for their protective function─serving as an exemplary system for nanoscale self-assembly. Although the proteinaceous precursors are known to undergo intermediate liquid crystalline phase transitions before being structurally arrested in the final nanolattice architecture, their sequences have so far remained unknown. By leveraging RNA-seq and proteomic techniques, we identified a cohort of nanolattice-forming proteins comprising a collagenous midblock flanked by domains typically associated with innate immunity and network-forming collagens. Structurally homologous proteins were found in the genomes of other egg-case-producing cartilaginous fishes, suggesting a conserved molecular self-assembly strategy. The identity and stabilizing role of cross-links were subsequently elucidated using mass spectrometry and in situ small-angle X-ray scattering. Our findings provide a new design approach for protein-based liquid crystalline elastomers and the self-assembly of nanolattices.

Synthesis of Phase-Pure Thermochromic VO2 (M1).

A highly reproducible, simple, and inexpensive synthesis method for obtaining phase-pure thermochromic monoclinic VO2 (M1) is presented. Vanadium(III) oxide and ammonium metavanadate were used as starting materials and no additional reducing agents are required. Heating a mixture of these two components under an argon atmosphere at 750 °C for 2-4 h provides the direct formation of VO2 (M1) without detectable impurity phases. The formation reaction of VO2 (M1) was studied using in situ powder X-ray diffraction (PXRD), where a pressed pellet of the precursor material was heated during the continuous collection of PXRD data on a two-dimensional detector. The formation takes place via at least two crystalline intermediate phases where the first forms at 170-185 °C (likely an ammonium and oxygen deficient (NH4)1-δVO3-δ phase), and the second at 230 °C (likely a more disordered phase due to the increased background intensity). We assume that the solid-state reaction between the unknown but likely disordered vanadate phase and vanadium(III) oxide starts at 395 °C in concert with the appearance of several other unknown crystalline phases. At 610-750 °C, phase-pure rutile VO2 (P42/mnm) is obtained, which upon cooling converts to monoclinic VO2 (M1). The product composition, microstructure, and homogeneity are characterized by Raman spectroscopy, scanning electron microscopy, transmission electron microscopy, and energy-dispersive X-ray spectroscopy. The synthesized VO2 (M1) has a sharp reversible insulator-to-metal transition at 71.3 °C during heating and 59.5 °C during cooling, as characterized using differential scanning calorimetry, and resistivity and magnetic property measurements.

The coprecipitation formation study of iron oxide nanoparticles with the assist of a gas/liquid mixed phase fluidic reactor

Coprecipitation is the most commonly used method to synthesize iron oxide nanoparticles (IONPs) due to its low cost and environmentally friendly synthesis process. Recently, several studies have proposed that the coprecipitation formation of IONPs is through the aggregation of initially formed primary particles. However, there are still lack of systematic researches about the room temperature coprecipitation formation process of IONPs under quick mixing mode. Here, a gas/liquid mixed phase fluidic reactor was specially designed, and the influences of reaction time, reaction pH and valence of iron ions on the coprecipitation formation of IONPs in quick mixing mode were studied. The NH3 gas was used as the alkaline reactant. At pH above 10.0, the iron ions promptly hydrolyzed and precipitated to form primary nanoparticles, and then the primary nanoparticles accreted to form Fe3O4 nanoparticles in 2 min 30 s. As the reaction pH increased from 2.5 to 9.5, extremely small particles gradually aggregated to form Fe3O4 nanoparticles. Large Fe3O4 nanoparticles with a mean diameter of ~ 8.1 nm were completely formed at pH 9.5. And a small amount of poorly crystalline intermediate phases including akageneite, ferrihydrite and goethite were observed during this process. When Fe2+ ions were absent during the reaction process, the final products had poor crystallinity and weak magnetic properties. While if only Fe2+ ions were used in the precursor, the sheet-like green rusts generated firstly, and Fe3O4 nanoparticles would gradually form on the surface of green rusts with the partial oxidation of Fe2+ ions. The results of regulating the reaction conditions especially reaction pH indicate that this reaction design can effectively reduce the formation of intermediate crystal phases.

Supramolecular meso-Trick: Ambidextrous Mirror Symmetry Breaking in a Liquid Crystalline Network with Tetragonal Symmetry.

Bicontinuous and multicontinuous network phases are among nature's most complex structures in soft matter systems. Here, a chiral bicontinuous tetragonal phase is reported as a new stable liquid crystalline intermediate phase at the transition between two cubic phases, the achiral double gyroid and the chiral triple network cubic phase with an I23 space group, both formed by dynamic networks of helices. The mirror symmetry of the double gyroid, representing a meso-structure of two enantiomorphic networks, is broken at the transition to this tetragonal phase by retaining uniform helicity only along one network while losing it along the other one. This leads to a conglomerate of enantiomorphic tetragonal space groups, P41212 and P43212. Phase structures and chirality were analyzed by small-angle X-ray scattering (SAXS), grazing-incidence small-angle X-ray scattering (GISAXS), resonant soft X-ray scattering (RSoXS) at the carbon K-edge, and model-dependent SAXS/RSoXS simulation. Our findings not only lead to a new bicontinuous network-type three-dimensional mesophase but also reveal a mechanism of mirror symmetry breaking in soft matter by partial meso-structure racemization at the transition from enantiophilic to enantiophobic interhelical self-assembly.

Room Temperature Synthesis of [Pd(cyclam)]5{H3Nb6O19}2 ⋅ 26H2O: a Suitable Precursor for the in‐situ Generation of a Highly Active Catalyst for Light‐Driven Hydrogen Evolution

AbstractThe first Pd2+ containing polyoxoniobate [Pd(cyclam)]5{H3Nb6O19}2 ⋅ 26H2O (I) was prepared at room temperature. In the structure, two hexaniobate clusters are surrounded by a bi‐capped cube formed by Pd2+ centered complexes. This motif is arranged in a layer‐like fashion with crystal water molecules located between cations and anions. Temperature resolved in‐situ X‐ray diffraction experiments demonstrate that successive removal of the crystal water molecules leads to formation of several crystalline intermediate phases. Water sorption investigations show that thermally removed H2O can be successfully reintegrated proceeding via two distinct steps. The catalytic performance for the light‐driven hydrogen evolution reaction (HER) was investigated in a sacrificial system and fluorescein Na+ salt as sensitizer yielding a high value of 90 μmol/h H2. Surprisingly, a composite Pd@Na7[HNb6O19] ⋅ 15H2O is in‐situ formed during the catalytic reaction by cation exchange with simultaneous reduction of Pd2+ nanoparticles decorating the hexaniobate support. The recovered catalyst was even more active producing 157 μmol/h H2 with an apparent quantum efficiency of 1.85 %. Photocatalytic experiments performed with ex‐situ generated Pd nanoparticles deposited on Na7[HNb6O19] ⋅ 15H2O show much lower activities indicating a synergistic effect of the in‐situ generated Pd@Na7[HNb6O19] ⋅ 15H2O catalyst.

Unraveling the CO and CO2 reactivity on Li2MnO3: Sorption and catalytic analyses

Lithium manganate (Li2MnO3) was synthesized, characterized and then tested as possible carbon oxides captor material. Thus, Li2MnO3 was dynamic and isothermally tested under different CO2 or CO atmospheres. This ceramic exhibited excellent CO oxidation and subsequent chemisorption properties under reductive atmospheres, while CO2 or CO in oxygen presence were not trapped. Li2MnO3 is the first lithium-containing ceramic reported for a selective CO sorption, in reductive atmospheres, which would be of great interest in different physicochemical processes. In fact, the CO-Li2MnO3 system evolution showed that o-LiMnO2 is produced as an intermediate crystalline phase. Based on that, o-LiMnO2 was analyzed to complement the CO chemisorption analysis. The whole atypical and unique reaction path was evidenced and supported by different structural and chemical analysis performed on the isothermal products, where lithium diffusion and reactivity with CO is performed through partial Mn reduction, allowing oxygen release for CO oxidation to form CO2 which can be captured. Moreover, isothermal data was kinetically analyzed and fitted to the Jander-Zhang mathematical model. Finally, cyclic CO oxidation-carbonation and decarbonation on Li2MnO3 showed interesting efficiencies, which however would be enhanced. Hence, Li2MnO3 presents interesting properties as CO oxidant and captor material, in non-oxidative conditions.

Time-resolved in-situ x-ray diffraction study of CaO and CaO:Ca3Al2O6 composite catalysts for biodiesel production

Alternative and sustainable waste sources are receiving increasing attention as they can be used to produce biofuels with a low carbon footprint. Waste fish oil is one such example and can be considered an abundant and sustainable waste source to produce biodiesel. Ultimately this could lead to fishing communities having their own ‘off-grid’ source of fuel for boats and vehicles. At the industrial level, biodiesel is currently produced by homogeneous catalysis because of the high catalyst activity and selectivity. In contrast, heterogeneous catalysis offers several advantages such as improved reusability, reduced waste and lower processing costs. Here we investigate the phase evolution of two heterogeneous catalysts, CaO and a Ca3Al2O6:CaO (‘C3A:CaO’) composite, under in-situ conditions for biodiesel production from fish oil. A new reactor was designed to monitor the evolution of the crystalline catalyst during the reaction using synchrotron powder x-ray diffraction. The amount of calcium diglyceroxide (CaDG) began to increase rapidly after approximately 30 min, for both catalysts. This rapid increase in CaDG could be linked to ex-situ nuclear magnetic resonance studies which showed that the conversion of fish oil to biodiesel rapidly increased after 30 min. The key to the difference in activity of the two catalysts appears to be that the Ca3Al2O6:CaO composite maintains a high rate of CaDG formation for longer than CaO, although the initial formation rates and reaction kinetics are similar. The Ca for the CaDG mainly comes from the CaO phase. In addition, towards the end of the second test utilising the CaO catalyst (after 120 min), there is a rapid decrease in CaDG and a rapid increase in Ca(OH)2. This was not observed for the Ca3Al2O6:CaO catalyst and this is due to Ca3Al2O6 stabilising the CaO in the composite material. No additional calcium containing intermediate crystalline phases were observed during our in-situ experiment. Overall this specialised in-situ set-up has been shown to be suitable to monitor the phase evolution of heterogeneous crystalline catalysts during the triglycerides transesterification reaction, offering the opportunity to correlate the crystalline phases to activity, deactivation and stability.

Evolution of the Local Structure in the Sol-Gel Synthesis of Fe3C Nanostructures.

The sol–gel synthesis of iron carbide (Fe3C) nanoparticles proceeds through multiple intermediate crystalline phases, including iron oxide (FeOx) and iron nitride (Fe3N). The control of particle size is challenging, and most methods produce polydisperse Fe3C nanoparticles of 20–100 nm in diameter. Given the wide range of applications of Fe3C nanoparticles, it is essential that we understand the evolution of the system during the synthesis. Here, we report an in situ synchrotron total scattering study of the formation of Fe3C from gelatin and iron nitrate sol–gel precursors. A pair distribution function analysis reveals a dramatic increase in local ordering between 300 and 350 °C, indicating rapid nucleation and growth of iron oxide nanoparticles. The oxide intermediate remains stable until the emergence of Fe3N at 600 °C. Structural refinement of the high-temperature data revealed local distortion of the NFe6 octahedra, resulting in a change in the twist angle suggestive of a carbonitride intermediate. This work demonstrates the importance of intermediate phases in controlling the particle size of a sol–gel product. It is also, to the best of our knowledge, the first example of in situ total scattering analysis of a sol–gel system.

Structural evolution in thermoelectric zinc antimonide thin films studied by in situ X-ray scattering techniques.

Zinc antimonides have been widely studied owing to their outstanding thermoelectric properties. Unlike in the bulk state, where various structurally unknown phases have been identified through their specific physical properties, a number of intermediate phases in the thin-film state remain largely unexplored. Here, in situ X-ray diffraction and X-ray total scattering are combined with in situ measurement of electrical resistivity to monitor the crystallization process of as-deposited amorphous Zn-Sb films during post-deposition annealing. The as-deposited Zn-Sb films undergo a structural evolution from an amorphous phase to an intermediate crystalline phase and finally the ZnSb phase during heat treatment up to 573 K. An intermediate phase (phase B) is identified to be a modified β-Zn8Sb7 phase by refinement of the X-ray diffraction data. Within a certain range of Sb content (∼42-55 at%) in the films, phase B is accompanied by an emerging Sb impurity phase. Lower Sb content leads to smaller amounts of Sb impurity and the formation of phase B at lower temperatures, and phase B is stable at room temperature if the annealing temperature is controlled. Pair distribution function analysis of the amorphous phase shows local ordered units of distorted ZnSb4 tetrahedra, and annealing leads to long-range ordering of these units to form the intermediate phase. A higher formation energy is required when the intermediate phase evolves into the ZnSb phase with a significantly more regular arrangement of ZnSb4 tetrahedra.

20.8% Slot‐Die Coated MAPbI3 Perovskite Solar Cells by Optimal DMSO‐Content and Age of 2‐ME Based Precursor Inks

AbstractSolar cells incorporating metal‐halide perovskite (MHP) semiconductors are continuing to break efficiency records for solution‐processed solar cell devices. Scaling MHP‐based devices to larger area prototypes requires the development and optimization of scalable process technology and ink formulations that enable reproducible coating results. It is demonstrated that the power conversion efficiency (PCE) of small‐area methylammonium lead iodide (MAPbI3) devices, slot‐die coated from a 2‐methoxy‐ethanol (2‐ME) based ink with dimethyl‐sulfoxide (DMSO) used as an additive depends on the amount of DMSO and age of the ink formulation. When adding 12 mol% of DMSO, small‐area devices of high performance (20.8%) are achieved. The effect of DMSO content and age on the thin film morphology and device performance through in situ X‐ray diffraction and small‐angle X‐ray scattering experiments is rationalized. Adding a limited amount of DMSO prevents the formation of a crystalline intermediate phase related to MAPbI3 and 2‐ME (MAPbI3‐2‐ME) and induces the formation of the MAPbI3 perovskite phase. Higher DMSO content leads to the precipitation of the (DMSO)2MA2Pb3I8 intermediate phase that negatively affects the thin‐film morphology. These results demonstrate that rational insights into the ink composition and process control are critical to enable reproducible large‐scale manufacturing of MHP‐based devices for commercial applications.

Thermal transition behaviors of vanadium pentoxide film during post-deposition annealing

Vanadium pentoxide (V2O5) films were deposited on sapphire substrates by radio frequency (R.F.) magnetron sputtering at 450 °C and annealed in various ambient atmospheres. The influence of ambient atmospheres on the structure, optical properties, and morphology of the thin films after annealing were characterized, and the transition behaviors in the annealing process were investigated by DSC, temperature-dependent Raman and FTIR. The results demonstrated that V2O5 films underwent four different transition behaviors during post-deposition annealing due to the different oxygen proportion of ambient. Different products (VO2(B), VO2(R)) in the transition process were the main reason for the evolution of optical properties. No transition behaviors occurred because of the oxygen-rich ambient when annealed in air, and no significant change in infrared transmittance was observed. When annealed in 0.1% O2/Ar, the film was converted to VO2(B) with the decrease of infrared transmittance. In the case of 0.01% O2/Ar, metastable VO2(B) and VO2(R) were observed as intermediate crystalline phases before V2O5 finally transformed to VO2(M), and the changes in the three stages of two drops and one rise were shown in infrared transmittance. While annealed in pure argon ambient, V2O5 was turned into VO2 (R) and VO2 (M) without VO2 (B) phase production, accompanied by a single change of infrared transmittance reduction and recovery. This provides a more detailed vanadium oxide thermal transition process and shows data reference for the preparation technology and application of vanadium oxide materials.

Solution-Phase Halide Exchange and Targeted Annealing Kinetics in Lead Chloride Derived Hybrid Perovskites.

Hybrid perovskites are a promising class of materials for a range of optoelectronic applications. Many material properties are dictated by the details of the synthetic process, yet a mechanistic understanding is lacking for the majority of these materials. We have studied the formation of methylammonium lead iodide films derived from a lead chloride precursor to understand both the casting solution chemistry and its influence on the final, largely chlorine-free, film. Using solution-phase extended X-ray absorption spectroscopy, we observe a halide exchange with the primary solution plumbate species identified as PbI2.5Cl0.33. The mixed halide plumbate solution species leads to formation of the crystalline intermediate phase of (CH3NH3)2PbI3Cl. Using in situ synchrotron X-ray diffraction, we show that compositional control of the casting solution can control the annealing kinetics of film formation. Our study demonstrates the importance of solution-phase chemistry and its impact on lead halide perovskite synthesis.