Origin of Persisting Photoresponse of One-Year Aged Two-Dimensional Lead Halide Perovskites Stored in Air under Dark Conditions.

Two-dimensional halide perovskites are promising for advanced photonic, optoelectronic, and photovoltaic applications. However, their long-term stability is still a critical factor limiting their implementation into further commercial applications. Here, we present an environmental stability analysis of BA(MA)PbI (BA = CHN, MA = CHN) two-dimensional perovskites with the lowest quantum well thicknesses of = 1 and = 2, after 1 year of aging under ambient humidity, oxygen content, and light conditions.

Enabling white color tunability in complex 3D-printed composites by using lead-free self-trapped exciton 2D perovskite/carbon quantum dot inks.

The generation of stable white light emission using lead-free perovskites remains a huge challenge in the development of future display and lighting technologies, due to fast material deterioration and the decrease of the color quality. In this work, we report a combination of diverse types of 2D ASnX (A = bulky cation, X = Br, I) perovskites exhibiting self-trapped exciton (STE) emission and blue luminescent carbon quantum dots (CQDs), with the purpose of generating ASnX/CQD inks with a broadband emission in the visible region and a tunable white light color. By varying the concentration of the 2D perovskite, the white emission of the mixtures is modulated to cool, neutral, and warm tonalities, with a PL quantum yield up to 45%.

A Perovskite Photovoltaic Mini-Module-CsPbBr Photoelectrochemical Cell Tandem Device for Solar-Driven Degradation of Organic Compounds.

Recently, halide perovskites have been widely explored for high-efficiency photocatalysis or photoelectrochemical (PEC) cells. Here, in order to make an efficient photoanode electrode for the degradation of pollutants, concretely 2-mercaptobenzothiazole (MBT), nanoscale cesium lead bromide (CsPbBr) perovskite was directly formed on the surface of mesoporous titanium dioxide (meso-TiO) film using a two-step spin-coating process. This photoelectrode recorded a photocurrent of up to 3.

Impact of core-shell perovskite nanocrystals for LED applications: successes, challenges, and prospects.

Perovskite nanocrystals (PeNCs) synthesized by colloidal solution methods are an outstanding case of study due to their remarkable optical features, different from their bulk counterpart, such as a tuneable band gap and narrower photoluminescence emission, altered by the size and shape. However, the stability of these systems needs to be improved to consolidate their application in optoelectronic devices. Improved PeNC quality is associated with a less defective structure, as it affects negatively the photoluminescence quantum yield (PLQY), due to the essential, but at the same time labile interaction between the colloidal capping ligands and the perovskite core.

Increasing the Performance and Stability of Red-Light-Emitting Diodes Using Guanidinium Mixed-Cation Perovskite Nanocrystals.

Halide perovskite nanocrystals (PNCs) exhibit growing attention in optoelectronics due to their fascinating color purity and improved intrinsic properties. However, structural defects emerging in PNCs progressively hinder the radiative recombination and carrier transfer dynamics, limiting the performance of light-emitting devices. In this work, we explored the introduction of guanidinium (GA) during the synthesis of high-quality CsGAPbI PNCs as a promising approach for the fabrication of efficient bright-red light-emitting diodes (R-LEDs).

Polymeric ionic liquid-based formulations for the fabrication of highly stable perovskite nanocrystal composites for photocatalytic applications.

Halide perovskite nanocrystals (PNCs) have emerged as potential visible-light photocatalysts because of their outstanding intrinsic properties, including high absorption coefficient and tolerance to defects, which reduces non-radiative recombination, and high oxidizing/reducing power coming from their tuneable band structure. Nevertheless, their sensitivity to humidity, light, heat and water represents a great challenge that limits their applications in solar driven photocatalytic applications. Herein, we demonstrate the synergistic potential of embedding PNCs into polymeric ionic liquids () to fabricate suitable composites for photodegradation of organic dyes.

Balanced change in crystal unit cell volume and strain leads to stable halide perovskite with high guanidinium content.

Up-to-date studies propose that strain in halide perovskites is one of the key factors that determine a device's efficiency and stability. Here, we show a systematic approach to characterize the phenomenon in the standard methylammonium lead iodine (MAPbI) perovskite system by: (i) the substitution of some MA by guanidinium (Gu); (ii) the incorporation of PbS quantum dot (QD) additives and (iii) addition of both Gu and PbS at the same time. We studied the effect of these incorporations on the film strain and crystal cell unit volume, and on the solar cell device efficiency and stability.

Revealing Giant Exciton Fine-Structure Splitting in Two-Dimensional Perovskites Using van der Waals Passivation.

Organic-inorganic layered perovskites are currently some of the most promising 2D van der Waals materials. Low crystal quality usually broadens the exciton line width, obscuring the fine structure of the exciton in conventional photoluminescence experiments. Here, we propose a mechanical approach to reducing the effect of spectral diffusion by means of hBN capping on layered perovskites, revealing the exciton fine structure.

Boosting Long-Term Stability of Pure Formamidinium Perovskite Solar Cells by Ambient Air Additive Assisted Fabrication.

Due to the high industrial interest for perovskite-based photovoltaic devices, there is an urgent need to fabricate them under ambient atmosphere, not limited to low relative humidity (RH) conditions. The formamidinium lead iodide (FAPI) perovskite α-black phase is not stable at room temperature and is challenging to stabilize in an ambient environment. In this work, we show that pure FAPI perovskite solar cells (PSCs) have a dramatic increase of device long-term stability when prepared under ambient air compared to FAPI PSCs made under nitrogen, both fabricated with -methylpyrrolidone (NMP).

Purcell Enhancement and Wavelength Shift of Emitted Light by CsPbI Perovskite Nanocrystals Coupled to Hyperbolic Metamaterials.

Manipulation of the exciton emission rate in nanocrystals of lead halide perovskites (LHPs) was demonstrated by means of coupling of excitons with a hyperbolic metamaterial (HMM) consisting of alternating thin metal (Ag) and dielectric (LiF) layers. Such a coupling is found to induce an increase of the exciton radiative recombination rate by more than a factor of three due to the Purcell effect when the distance between the quantum emitter and HMM is nominally as small as 10 nm, which coincides well with the results of our theoretical analysis. Besides, an effect of the coupling-induced long wavelength shift of the exciton emission spectrum is detected and modeled.

Photo-Induced Black Phase Stabilization of CsPbI QDs Films.

α-CsPbI quantum dots (QDs) show outstanding photoelectrical properties that had been harnessed in the fabrication of perovskite QDs solar cells. Nevertheless, the stabilization of the CsPbI perovskite cubic phase remains a challenge due to its own thermodynamic and the presence of surface defects. Herein, we report the optimization of the CsPbI QDs solar cells, by monitoring the structure, the morphology and the optoelectronic properties after a precise treatment, consisting of the conventional solvent washing with a time limited ultraviolet (UV) exposure combination, during the layer-by-layer deposition.

Ligand & band gap engineering: tailoring the protocol synthesis for achieving high-quality CsPbI quantum dots.

Hot-injection has become the most widespread method used for the synthesis of perovskite quantum dots (QDs) with enormous interest for application in optoelectronic devices. However, there are some aspects of the chemistry involved in this synthesis that have not been completely investigated. In this work, we synthesized ultra-high stable CsPbI QDs for more than 15 months by controlling two main parameters: synthesis temperature and the concentration of capping ligands.

Unravelling the Photocatalytic Behavior of All-Inorganic Mixed Halide Perovskites: The Role of Surface Chemical States.

Within the most mesmerizing materials in the world of optoelectronics, mixed halide perovskites (MHPs) have been distinguished because of the tunability of their optoelectronic properties, balancing both the light-harvesting efficiency and the charge extraction into highly efficient solar devices. This feature has drawn the attention of analogous hot topics as photocatalysis for carrying out more efficiently the degradation of organic compounds. However, the photo-oxidation ability of perovskite depends not only on its excellent light-harvesting properties but also on the surface chemical environment provided during its synthesis.

Single-Exciton Amplified Spontaneous Emission in Thin Films of CsPbX (X = Br, I) Perovskite Nanocrystals.

CsPbX perovskite nanocrystals (PNCs) have emerged as an excellent material for stimulated emission purposes, with even more prospective applications than conventional colloidal quantum dots. However, a better understanding of the physical mechanisms responsible for amplified spontaneous emission (ASE) is required to achieve more ambitious targets (lasing under continuous wave optical or electrical excitation). Here, we establish the intrinsic mechanisms underlying ASE in PNCs of three different band gaps (CsPbBr, CsPbBrI, and CsPbI).

Optical Amplification in Hollow-Core Negative-Curvature Fibers Doped with Perovskite CsPbBr Nanocrystals.

We report a hollow-core negative-curvature fiber (HC-NCF) optical signal amplifier fabricated by the filling of the air microchannels of the fiber with all-inorganic CsPbBr perovskite nanocrystals (PNCs). The optimum fabrication conditions were found to enhance the optical gain, up to +3 dB in the best device. Experimental results were approximately reproduced by a gain assisted mechanism based on the nonlinear optical properties of the PNCs, indicating that signal regeneration can be achieved under low pump powers, much below the threshold of stimulated emission.

Photocatalytic and Photoelectrochemical Degradation of Organic Compounds with All-Inorganic Metal Halide Perovskite Quantum Dots.

Inspired by the outstanding optoelectronic properties reported for all-inorganic halide perovskite quantum dots (QDs), we have evaluated the potential of these materials toward the photocatalytic and photoelectrochemical degradation of organic compounds, taking the oxidation of 2-mercaptobenzothiazole (MBT) as a proof-of-concept. First, we determined electrochemically the energy levels of dispersions of perovskite QDs with different band gaps induced by the different ratios between halides (Br and I) and metallic cations (Pb and Sn). Then, we selected CsPbBr QDs to demonstrate the photocatalytic and photoelectrochemical oxidation of MBT, confirming that hole injection takes place from CsPbBr QDs to MBT, resulting in the total degradation of MBT as evidenced by electrospray mass spectrometry analyses.

Controlling the Phase Segregation in Mixed Halide Perovskites through Nanocrystal Size.

Mixed halide perovskites are one of the promising candidates in developing solar cells and light-emitting diodes (LEDs), among other applications, because of their tunable optical properties. Nonetheless, photoinduced phase segregation, by formation of segregated Br-rich and I-rich domains, limits the overall applicability. We tracked the phase segregation with increasing crystalline size of CsPbBr I and their photoluminescence under continuous-wave laser irradiation (405 nm, 10 mW cm) and observed the occurrence of the phase segregation from the threshold size of 46 ± 7 nm.

Hidden energy levels? Carrier transport ability of CdS/CdSSe quantum dot solar cells impacted by Cd-Cd level formation.

In quantum dot sensitized solar cells (QDSSC), a cascade energy level structure controlled by assembly of cadmium-chalcogenide quantum dots can remarkably improve the sunlight harvesting and charge carrier lifetime. Despite the advantages of using co-sensitizers, energy conversion efficiencies are still low. An increased understanding of the causes of the low photoconversion efficiency (PCE) will contribute to the development of a straightforward approach to improve solar cell performance by exploiting co-sensitization.