Vapor Phase Deposition Method Research Articles

Room-temperature nanostructured PbSe/CdSe mid-infrared photodetector: Annealing effects

Room-temperature (RT) photoconductor using mid-wave infrared (MWIR) nanostructured lead selenide (PbSe)/cadmium selenide (CdSe) is presented on a commercially available silicon dioxide on silicon (100) (SiO2/Si) wafer. This device is fabricated through vapor phase deposition (VPD) and subsequently annealed in oxygen to create interconnected nanostructures, which establish efficient pathways for photogenerated carriers and passivate defects within the material. RT specific detectivity (D*) of 8.57 × 108 Jones and a peak D* of 2.49 × 109 Jones are achieved with interband cut-off wavelength of 4 μm. Additionally, the utilization of nanostructured thin film deposition on cost-effective SiO2/Si(100) substrates via the affordable VPD method significantly reduces production costs and facilitates the potential of monolithic integration with Si-based readout integrated circuitry enabling low-cost large-scale production.

Low-Temperature Vapor-Phase Growth of 2D Metal Chalcogenides.

2D metal chalcogenides (MCs) have garnered significant attention from both scientific and industrial communities due to their potential in developing next-generation functional devices. Vapor-phase deposition methods have proven highly effective in fabricating high-quality 2D MCs. Nevertheless, the conventionally high thermal budgets required for synthesizing 2D MCs pose limitations, particularly in the integration of multiple components and in specialized applications (such as flexible electronics). To overcome these challenges, it is desirable to reduce the thermal energy requirements, thus facilitating the growth of various 2D MCs at lower temperatures. Numerous endeavors have been undertaken to develop low-temperature vapor-phase growth techniques for 2D MCs, and this review aims to provide an overview of the latest advances in low-temperature vapor-phase growth of 2D MCs. Initially, the review highlights the latest progress in achieving high-quality 2D MCs through various low-temperature vapor-phase techniques, including chemical vapor deposition (CVD), metal-organic CVD, plasma-enhanced CVD, atomic layer deposition (ALD), etc. The strengths and current limitations of these methods are also evaluated. Subsequently, the review consolidates the diverse applications of 2D MCs grown at low temperatures, covering fields such as electronics, optoelectronics, flexible devices, and catalysis. Finally, current challenges and future research directions are briefly discussed, considering the most recent progress in the field.

Lead‐Free CsCu2I3 Halides with 1D Crystal Structure for UV Photodetection

AbstractCopper halide semiconductors are attracting extensive attention due to their nontoxic composition and excellent optoelectronic properties. Most so far are prepared via solution methods; however, grain boundaries and defects existing in those products hinder their further practical applications in solid‐state devices. In this work, CsCu2I3 halides with 1D crystal structure are initially prepared by a vapor phase deposition method. The large Stokes shift coupling with a long photoluminescence decay time (112 ns) suggests the existence of a self‐trapped exciton process in these CsCu2I3 nanowires, responsible for the yellow light emission emerging at 570 nm. UV photodetectors based on individual CsCu2I3 nanowires that are constructed via an etching‐free dry transfer route reveal a responsivity of 122 mA W−1 and rise/decay times of 203/223 ms (310 nm, 5 V bias), comparable to or better than those congeneric UV sensors made of other lead‐free halides. These CsCu2I3 nanowire‐based photodetectors also reveal good stability in the atmosphere (RH = 60–70%, 17 °C), benefitting from their fourfold coordination environment of Cu(I) atoms in the 1D crystal structure. These results imply the technical potential of manufacturing low‐dimensional lead‐free halide semiconductors for next‐generation green optoelectronics.

Van der waals epitaxial growth of mixed-dimensional 1D/2D heterostructures with tellurium nanowires and transition metal dichalcogenide nanosheets for nonlinear optical applications

One-dimensional (1D) tellurium (Te) nanowires (NWs) have triggered intense attention due to their remarkable properties in electronics, optoelectronics and nonlinear optics. However, the saturable absorption properties of Te NWs and the ability to be bleached by strong pulsed energy need to be further improved. Van der Waals (vdW) heterostructures based on two-dimensional (2D) transition metal dichalcogenides (TMDCs) exhibit prominent nonlinear optical properties. Direct epitaxial growth of large-area 1D/2D Te-TMDC vdW heterostructures is still rarely investigated. Herein, we demonstrate the controllable epitaxial growth of large-scale 1D/2D vertical Te-TMDC heterostructures via two-step vapor phase deposition method. Our experimental results have confirmed that the saturable absorption properties of as-prepared Te-TMDC heterostructures can be obviously enhanced. The first principle calculations and surface potential measurements demonstrate that effective interlayer charge transfer between Te NWs and TMDC nanosheets is beneficial for promoting the saturable absorption properties. Systematic investigation of vdW Te-TMDC heterostructures with nonlinear optical properties is vital for the next generation of nanophotonics and integrated photonics, which paves the way for the development of saturable absorbers and light modulators based on Te-TMDC vdW heterostructures.

Direct Z-Scheme SnSe2/SnSe Heterostructure Passivated by Al2O3 for Highly Stable and Sensitive Photoelectrochemical Photodetectors.

To mimic the natural photosynthesis system, a Z-scheme heterostructure is proposed as a viable and effective strategy for efficient solar energy utilization such as photocatalysis and photoelectrochemical (PEC) water splitting due to the high carrier separation efficiency, fast charge transport, strong redox, and wide light absorption. However, it remains a huge challenge to form a direct Z-scheme heterostructure due to the internal electric-field restriction and vital band-alignment at the interface. Herein, the van der Waals heterostructure based on the allotrope SnSe2 and SnSe is designed and synthesized by a two-step vapor phase deposition method to overcome the limitation in the formation of the Z-scheme heterostructure for the first time. The Z-scheme heterostructure of SnSe2/SnSe is confirmed by X-ray photoelectron spectroscopy, ultraviolet photoelectron spectroscopy, PEC measurement, density functional theory calculations, and water splitting. Strikingly, the PEC photodetectors based on the Z-scheme heterostructure show a synergistic effect of superior stability from SnSe and fast photoresponse from SnSe2. As such, the SnSe2/SnSe Z-scheme heterostructure shows a good photodetection performance in the ultraviolet to visible wavelength range. Furthermore, the photodetector shows a faster response/recovery time of 13/14 ms, a higher photosensitivity of 529.13 μA/W, and a higher detectivity of 4.94 × 109 Jones at 475 nm compared with those of single components. Furthermore, the photodetection stability of the SnSe2/SnSe is also greatly improved by a-thin-Al2O3-layer passivation. The results imply the promising rational design of a direct Z-scheme heterostructure with efficient charge transfer for high performance of optoelectronic devices.

Bi2 Te3 /Bi2 Se3 /Bi2 S3 Cascade Heterostructure for Fast-Response and High-Photoresponsivity Photodetector and High-Efficiency Water Splitting with a Small Bias Voltage.

Large-scale multi-heterostructure and optimal band alignment are significantly challenging but vital for photoelectrochemical (PEC)-type photodetector and water splitting. Herein, the centimeter-scale bismuth chalcogenides-based cascade heterostructure is successfully synthesized by a sequential vapor phase deposition method. The multi-staggered band alignment of Bi2 Te3 /Bi2 Se3 /Bi2 S3 is optimized and verified by X-ray photoelectron spectroscopy. The PEC photodetectors based on these cascade heterostructures demonstrate the highest photoresponsivity (103mAW-1 at -0.1V and 3.5mAW-1 at 0V under 475nm light excitation) among the previous reports based on two-dimensional materials and related heterostructures. Furthermore, the photodetectors display a fast response (≈8ms), a high detectivity (8.96×109 Jones), a high external quantum efficiency (26.17%), and a high incident photon-to-current efficiency (27.04%) at 475nm. Due to the rapid charge transport and efficient light absorption, the Bi2 Te3 /Bi2 Se3 /Bi2 S3 cascade heterostructure demonstrates a highly efficient hydrogen production rate (≈0.416mmolcm-2 h-1 and ≈14.320µmolcm-2 h-1 with or without sacrificial agent, respectively), which is far superior to those of pure bismuth chalcogenides and its type-II heterostructures. The large-scale cascade heterostructure offers an innovative method to improve the performance of optoelectronic devices in the future.

Lead Selenide Thin Films and Uncooled Midinfrared Detectors by Vapor Phase Deposition.

The broad application of lead selenide (PbSe)-based uncooled midinfrared (MIR) detectors has been hindered by the nonuniformity of wafer-level films prepared by the conventional chemical bath deposition (CBD) method. Herein, using a vapor phase deposition (VPD) approach, we demonstrate the deposition of 3 in. wafer-scale uniform PbSe thin films with thicknesses of up to 1.5 μm. To trigger the MIR response, the as-grown films were sensitized at an elevated temperature in an oxygen-iodine atmosphere. We discovered that the key to spark off the MIR response of the PbSe detector originated from the self-assembled rodlike microstructures in the thin films, which can be controlled by the I2/PbSe flux ratio in the VPD process. At room temperature, the thin film detector exhibits an excellent optoelectronic performance, with detectivity up to 2.4 × 109 cm Hz1/2 W-1 achieved under optimized conditions. Our results show that the VPD method opens up a new avenue to the industrialization of uncooled lead-salt MIR detectors.

A Sub-20nm Organic/Inorganic Hybrid Dielectric for Ultralow-Power Organic Thin-Film Transistor (OTFT) With Enhanced Operational Stability.

Organic/inorganic hybrid materials are utilized extensively as gate dielectric layers in organic thin-film transistors (OTFTs). However, inherently low dielectric constant of organic materials and lack of a reliable deposition process for organic layers hamper the broad application of hybrid dielectric materials. Here, a universal strategy to synthesize high-k hybrid dielectric materials by incorporating a high-k polymer layer on top of various inorganic layers generated by different fabrication methods, including AlOx and HfOx , is presented. Those hybrid dielectrics commonly exhibit high capacitance (>300 nF·cm-2 ) as well as excellent insulating properties. A vapor-phase deposition method is employed for precise control of the polymer film thickness. The ultralow-voltage (<3V) OTFTs are demonstrated based on the hybrid dielectric layer with 100% yield and uniform electrical characteristics. Moreover, the exceptionally high stability of OTFTs for long-term operation (current change less than 5% even under 30 h of voltage stress at 2.0 MV·cm-1 ) is achieved. The hybrid dielectric is fully compatible with various substrates, which allows for the demonstration of intrinsically flexible OTFTs on the plastic substrate. It is believed that this approach for fabricating hybrid dielectrics by introducing the high-k organic material can be a promising strategy for future low-power, flexible electronics.

Template and Temperature-Controlled Polymorph Formation in Squaraine Thin Films.

Controlling the polymorph formation in organic semiconductor thin films by the choice of processing parameters is a key factor for targeted device performance. Small molecular semiconductors such as the prototypical anilino squaraine compound with branched butyl chains as terminal functionalization (SQIB) allow both solution and vapor phase deposition methods. SQIB has been considered for various photovoltaic applications mainly as amorphous isotropic thin films due to its broad absorption within the visible to deep-red spectral range. The two known crystalline polymorphs adopting a monoclinic and orthorhombic crystal phase show characteristic Frenkel excitonic spectral signatures of overall H-type and J-type aggregates, respectively, with additional pronounced Davydov splitting. This gives a recognizable polarized optical response of crystalline thin films suitable for identification of the polymorphs. Both phases emerge with a strongly preferred out-of-plane and rather random in-plane orientation in spin-casted thin films depending on subsequent thermal annealing. By contrast, upon vapor deposition on dielectric and conductive substrates, such as silicon dioxide, potassium chloride, graphene, and gold, the polymorph expression depends basically on the choice of growth substrate. The same pronounced out-of-plane orientation is adopted in all crystalline cases, but with a surface templated in-plane alignment in case of crystalline substrates. Strikingly, the amorphous isotropic thin films obtained by vapor deposition cannot be crystallized by thermal postannealing, which is a key feature for the spin-casted thin films, here monitored by polarized in situ microscopy. Combining X-ray diffraction, atomic force microscopy, ellipsometry, and polarized spectro-microscopy, we identify the processing-dependent evolution of the crystal phases, correlating morphology and molecular orientations within the textured SQIB films.

A Sub-Micron-Thick stretchable adhesive layer for the lamination of arbitrary elastomeric substrates with enhanced adhesion stability

Binding two separate elastomeric substrates is of great importance for the fabrication of next generation stretchable devices including epidermal electronics and soft robotics. However, it is still extremely challenging to find an adhesive to bind arbitrary elastomers with excellent adhesion strength and reliability without compromising the stretchability of the laminated elastomeric substrates. In this study, a sub-micron-thick (∼500 nm) stretchable adhesive was synthesized by using a vapor-phase deposition method. The stretchable adhesive consists of a copolymer film containing curable epoxy and hydroxyl functionalities with sufficiently low glass transition temperature (Tg) in order to render the adhesive elastomeric. Moreover, depositing the adhesive layer in vapor phase induced an interpenetrating polymer network (IPN) at the interface between the elastomeric substrate and stretchable adhesive layer, which enabled strong binding between arbitrary elastomeric substrates such as polydimethylsiloxane (PDMS), Silbione™, 3 M VHB™, and Ecoflex™, with substantially enhanced adhesion stability and high transparency. The adhesion strength was fully retained even after more than 105 times of repeated stretch-release cycles of 50% strain. The IPN-induced stretchable but ultrathin adhesive layer developed in this study will serve as a platform bonding technology for the wide range of soft matter engineering applications.

Coupling powder bed additive manufacturing and vapor phase deposition methods for elaboration of coated 3D Ti-6Al-4V architectures with enhanced surface properties

We propose an innovative process coupling powder bed additive manufacturing by Electron Beam Melting (EBM) with Chemical Vapor Deposition (CVD) and Atomic Layer Deposition (ALD) to develop 3D Ti-6Al-4V structures covered with AlN coating. Despite of the high reactivity of Ti-6Al-4V with nitrogen, thick (~10 μm) and conformal AlN films are deposited by CVD on Ti-6Al-4V substrates with high surface roughness. An AlN under-layer deposited by ALD is necessary to mitigate the reaction between Ti-6Al-4V and the nitrogen precursor NH3(g) and to limit the formation of brittle titanium nitride phases. We have thus achieved an adherent coating without any modification of the Ti-6Al-4V microstructure at the core of the substrate. We show that a 7 μm thick AlN coating is efficient in protecting Ti-6Al-4V against cyclic oxidation at 650 °C for at least 650 h. This study opens new opportunities for the design of coated 3D Ti-6Al-4V structures for use in high temperature oxidizing environments.

Bridging the Synthesis Gap: Ionic Liquids Enable Solvent-Mediated Reaction in Vapor-Phase Deposition.

Molecular layer deposition (MLD) is an attractive, vapor-phase deposition method for applications requiring ultrathin organic materials, such as photolithography, lithium batteries, and microelectronics. By using sequential self-limiting surface reactions, MLD offers excellent control over thickness and conformality, but there are also challenges such as a limited range of possible film compositions and long deposition times. In this study, we introduce a modified technique, termed ionic liquid assisted MLD (IL-MLD), that can overcome these barriers. By performing the surface reactions inside of an ultrathin layer of a compatible ionic liquid (IL), solvent effects are replicated inside a vacuum system, broadening the possible reactions to a much wider suite of chemistries. Using this strategy, the MLD of polyetherketoneketone, an industrially and research-relevant, high-performance thermoplastic, is reported. With this proof-of-concept, we demonstrate that IL-MLD can enable the synthesis of polymers via solvent- or catalyst-mediated reactions and establish an approach that may allow solution chemistries to be accessed in other vapor deposition techniques as well.

Comparative Study on the Adsorption Capacities of the Three Black Phosphorus-Based Materials for Methylene Blue in Water

Dye effluent has attracted considerable attention from worldwide researchers due to its harm and toxicity in recent years; as a result, the treatment for dye has become one of the focuses in the environmental field. Adsorption has been widely applied in water treatment owing to its various advantages. However, the adsorption behaviors of the new materials, such as the 2D black phosphorus (BP), for pollution were urgently revealed and improved. In this work, BP, black phosphorene (BPR), and sulfonated BPR (BPRS) were prepared by the vapor phase deposition method, liquid-phase exfoliating method, and modification with sulfonation, respectively. The three BP-based materials were characterized and used as adsorbents for the removal of methylene blue (MB) in water. The results showed that the specific surface areas (SSAs) of BP, BPR, and BPRS were only 6.78, 6.92, and 7.72 m2·g−1, respectively. However, the maximum adsorption capacities of BP, BPR, and BPRS for MB could reach up to 84.03, 91.74, and 140.85 mg·g−1, which were higher than other reported materials with large SSAs such as graphene (GP), nanosheet/magnetite, and reduced graphene oxide (rGO). In the process of BP adsorbing MB, wrinkles were generated, and the wrinkles would further induce adsorption. BPR had fewer layers (3–5), more wrinkles, and stronger adsorption capacity (91.74 mg·g−1). The interactions between the BP-based materials and MB might cause the BP-based materials to deform, i.e., to form wrinkles, thereby creating new adsorption sites between layers, and then further inducing adsorption. Although the wrinkles had a certain promotion effect, the adsorption capacity was limited, so the sulfonic acid functional group was introduced to modify BPR to increase its adsorption sites and promote the adsorption effect. These findings could provide a new viewpoint and insight on the adsorption behavior and potential application of the BP-based materials.

Uniform Polypyrrole Layer-Coated Sulfur/Graphene Aerogel via the Vapor-Phase Deposition Technique as the Cathode Material for Li-S Batteries.

The practical application of Li-S batteries is hampered because of their poor cycling stability caused by electrolyte-dissolved lithium polysulfides. Dual functionalities such as strong chemical adsorption stability and high conductivity are highly desired for an ideal host material for the sulfur-based cathode. Herein, a uniform polypyrrole layer-coated sulfur/graphene aerogel composite is designed and synthesized using a novel vapor-phase deposition method. The polypyrrole layer simultaneously acts as a host and an adsorbent for efficient suppression of polysulfide dissolution through strong chemical interaction. The density functional theory calculations reveal that the polypyrrole could trap lithium polysulfides through stronger bonding energy. In addition, the deflation of sulfur/graphene hydrogel during the vapor-phase deposition process enhances the contact of sulfur with matrices, resulting in high sulfur utilization and good rate capability. As a result, the synthesized polypyrrole-coated sulfur/graphene aerogel composite delivers specific discharge capacities of 1167 and 409.1 mA h g-1 at 0.2 and 5 C, respectively. Moreover, the composite can maintain a capacity of 698 mA h g-1 at 0.5 C after 500 cycles, showing an ultraslow decay rate of 0.03% per cycle.

A Micropatterning Strategy to Study Nuclear Mechanotransduction in Cells.

Micropatterning techniques have been widely used in biology, particularly in studies involving cell adhesion and proliferation on different substrates. Cell micropatterning approaches are also increasingly employed as in vitro tools to investigate intracellular mechanotransduction processes. In this report, we examined how modulating cellular shapes on two-dimensional rectangular fibronectin micropatterns of different widths influences nuclear mechanotransduction mediated by emerin, a nuclear envelope protein implicated in Emery–Dreifuss muscular dystrophy (EDMD). Fibronectin microcontact printing was tested onto glass coverslips functionalized with three different silane reagents (hexamethyldisilazane (HMDS), (3-Aminopropyl)triethoxysilane (APTES) and (3-Glycidyloxypropyl)trimethoxysilane (GPTMS)) using a vapor-phase deposition method. We observed that HMDS provides the most reliable printing surface for cell micropatterning, notably because it forms a hydrophobic organosilane monolayer that favors the retainment of surface antifouling agents on the coverslips. We showed that, under specific mechanical cues, emerin-null human skin fibroblasts display a significantly more deformed nucleus than skin fibroblasts expressing wild type emerin, indicating that emerin plays a crucial role in nuclear adaptability to mechanical stresses. We further showed that proper nuclear responses to forces involve a significant relocation of emerin from the inner nuclear envelope towards the outer nuclear envelope and the endoplasmic reticulum membrane network. Cell micropatterning by fibronectin microcontact printing directly on HMDS-treated glass represents a simple approach to apply steady-state biophysical cues to cells and study their specific mechanobiology responses in vitro.

Room-Temperature Cubic Phase Crystallization and High Stability of Vacuum-Deposited Methylammonium Lead Triiodide Thin Films for High-Efficiency Solar Cells.

Methylammonium lead triiodide (MAPI) has emerged as a high-performance photovoltaic material. Common understanding is that at room temperature, it adopts a tetragonal phase and it only converts to the perfect cubic phase around 50-60 °C. Most MAPI films are prepared using a solution-based coating process, yet they can also be obtained by vapor-phase deposition methods. Vapor-phase-processed MAPI films have significantly different characteristics than their solvent-processed analogous, such as relatively small crystal-grain sizes and short excited-state lifetimes. However, solar cells based on vapor-phase-processed MAPI films exhibit high power-conversion efficiencies. Surprisingly, after detailed characterization it is found that the vapor-phase-processed MAPI films adopt a cubic crystal structure at room temperature that is stable for weeks, even in ambient atmosphere. Furthermore, it is demonstrated that by tuning the deposition rates of both precursors during codeposition it is possible to vary the perovskite phase from cubic to tetragonal at room temperature. These findings challenge the common belief that MAPI is only stable in the tetragonal phase at room temperature.

Impregnation Protocols on Alumina Beads for Controlling the Preparation of Supported Metal Catalysts

Whereas the synthesis principles of supported metal catalysts are well documented in the open literature, impregnation protocols on shaped bodies represent sensitive industrial know-how and are, therefore, rarely found. We investigated various synthesis parameters for both wetness (WI) and dry (DI) impregnations to prepare Pd/γ–Al2O3 alumina beads. Two kinds of catalysts were achieved: homogeneously dispersed catalysts with no metal gradient across the beads and eggshell catalysts. A combination of optical images, Castaing microprobe analysis, elemental analysis, and TEM made it possible to discriminate between catalysts according to their metal loading, location across the bead diameter, and metal dispersion. Regardless of the macropore structure of the alumina beads, we found that volatile solvents (acetone) were preferred for preparing homogeneous catalysts by WI, whereas the use of a viscous aqueous solution (water/glycerol) in DI resulted in an eggshell-type catalyst. The atomic layer deposition (ALD) method was also investigated as a physical vapor phase deposition method for preparing eggshell catalysts. Representative-shaped catalysts were tested for CO oxidation as a model reaction in order to highlight the differences between catalysts with a homogeneous metal distribution (no metal gradient) and eggshell-type.

Photoluminescence properties of ultrathin CsPbCl3 nanowires on mica substrate

Fabricating high-quality cesium lead chloride (CsPbCl3) perovskite nanowires (NWs) with dimension below 10 nm is not only of interests in fundamental physics, but also holds the great promise for optoelectronic applications. Herein, ultrathin CsPbCl3 NWs with height of ~7 nm, have been achieved via vapor phase deposition method. Power and temperature-dependent photoluminescence (PL) spectroscopy is performed to explore the emission properties of the CsPbCl3 NWs. Strong free exciton recombination is observed at ~3.02 eV as the temperature (T) is 78−294 K with binding energy of ~ 37.5 meV. With the decreasing of T, the PL peaks exhibit a first blueshift by 2 meV for T ~ 294−190 K and then a redshift by 4 meV for T ~ 190−78 K. The exciton–optical phonon interaction plays a major role in the linewidth broadening of the PL spectra with average optical phonon energy of ~48.0 meV and the interaction coefficient of 203.9 meV. These findings advance the fabrication of low dimensional CsPbCl3 perovskite and provide insights into the photophysics of the CsPbCl3 perovskite.

Thermodynamic study of volatile iridium (I) complexes with 1,5-cyclooctadiene and acetylacetonato derivatives: Effect of (O,O) and (O,N) coordination sites

Three hetero-ligand volatile iridium (I) complexes with β-diketonate derivatives [Ir(cod)(L)] (cod = 1,5-cyclooctadiene, L = CH3C(O)CHC(X)CH3, X = O (acac) 1, N–H (i-acac) 2, N–CH3 (Mei-acac) 3) have been synthesized, purified and characterized in order to investigate the influence of (O,O) and (O,N) coordination sites in chelate ligand on the thermochemical properties of this type compounds. β-Ketoiminate complexes (L = i-acac, Mei-acac) were prepared for the first time. Thermal behavior of iridium complexes in condensed phase has been studied by differential scanning calorimetry and thermodynamic parameters of melting processes (Δmelt.Hm.p., Δmelt.S°m.p.) have been determined for the first time. The temperature dependencies of saturated vapor pressures over the solid complexes have been measured by flow (transpiration) method (temperature intervals (363–423) K, (383–431) K and (383–420) K for compounds 1, 2 and 3, respectively). Using these data, the thermodynamic parameters of sublimation processes (ΔsubHT, ΔsubS°T) have been calculated. It has been found that although the ligand modification has a minor effect on the vaporization characteristics of this type complexes, the volatility unexpectedly decreases in the following sequence: L = acac > i-acac > Mei-acac. However, the vapor pressure values in the above-mentioned temperature interval are sufficient to all complexes studied be used as effective volatile precursors to obtain iridium-containing coatings by chemical vapor-phase deposition methods.

Record‐Low‐Threshold Lasers Based on Atomically Smooth Triangular Nanoplatelet Perovskite

AbstractSingle‐crystalline perovskites are ideal candidates for lasing and other optoelectronic applications. Although significant efforts have been made to grow both bulk single‐crystalline perovskites in liquid solution, their dimensions are still too large to make nanoscale whispering‐gallery‐mode (WGM) resonator based lasers that possess high quality (Q) factor and small volume. Besides, most reported perovskite resonators do not possess atomically smooth surfaces and facets, which limits the Q and thereby increases the lasing threshold. Here, atomically smooth triangular PbI2 templates are fabricated on a mica substrate by the vapor phase deposition method and are converted to atomically smooth perovskites which have regular and unwrinkled facets with average surface roughness less than 2 nm. By using a CH3NH3PbI3 nanoplatelet with a side length of 27 µm and thickness of 80 nm, room temperature WGM lasing with a Q up to 2600 is demonstrated, the highest reported for hybrid organic–inorganic perovskite nanoplatelets. In addition, the volume of the WGM mode is reduced significantly in comparison with the prior reports. The realized high‐quality triangular CH3NH3PbI3 perovskite nanoplatelets with high Q factor and small volume are expected to perform as ideal cavities for long pulse durations lasers and would find potential applications in integrated optoelectronic devices.