Electronically tunable anion-π interactions in pyrylium complexes: experimental and theoretical studies.

Noncovalent interactions of anions with electron-deficient aromatic rings that have been studied so far involve non-heteroaromatic or nitrogen-based heteroaromatic systems. Here we report the first case of an organic oxygenated aromatic system, in particular the tri-aryl-pyrylium tetrafluoroborate system, for which noncovalent anion-π interactions of the pyrylium cation with the tetrafluoroborate anion have been experimentally detected and demonstrated by means of (19)F NMR spectroscopy in solution. A series of pyrylium tetrafluoroborate salts were synthesized in the presence of BF3·Et2O, by direct reaction of 4-substituted benzaldehydes with 4-substituted acetophenones or via the previously obtained chalcone of the less reactive ketone. Correlations of (19)F NMR chemical shifts of tetrafluoroborate anion for most of the synthesized tri-arylpyrylium tetrafluoroborate complexes with both the pyrylium cation molecular weight and the standard substituent Hammett constants, demonstrate anion-π(+) interaction to act between the polyatomic anion BF4(-) and the pyrylium aromatic system. DFT calculations reveal that an additional (C-H)(+)-anion hydrogen bond involving the H(5) of pyrylium ring exists for these fluorescent dyes that show a tunable cup-to-cap shape cavity. The strong fluorescence emission observed for some representative pyrylium tetrafluoroborates described herein, makes them a promising class of tunable emission wavelength dyes for laser technology applications.

Highly Anisotropic Organometal Halide Perovskite Nanowalls Grown by Glancing-Angle Deposition.

Polarizers are ubiquitous components in current optoelectronic devices as displays or photographic cameras. Yet, control over light polarization is an unsolved challenge, since the main drawback of the existing display technologies is the significant optical losses. In such a context, organometal halide perovskites (OMHP) can play a decisive role given their flexible synthesis with tunable optical properties such as bandgap and photoluminescence, and excellent light emission with a low non-radiative recombination rate. Therefore, along with their outstanding electrical properties have elevated hybrid perovskites as the material of choice in photovoltaics and optoelectronics. Among the different OMHP nanostructures, nanowires and nanorods have lately arisen as key players in the control of light polarization for lighting or detector applications. Herein, the fabrication of highly aligned and anisotropic methylammonium lead iodide perovskite nanowalls by glancing-angle deposition, which is compatible with most substrates, is presented. Their high alignment degree provides the samples with anisotropic optical properties such as light absorption and photoluminescence. Furthermore, their implementation in photovoltaic devices provides them with a polarization-sensitive response. This facile vacuum-based approach embodies a milestone in the development of last-generation polarization-sensitive perovskite-based optoelectronic devices such as lighting appliances or self-powered photodetectors.

Identification of recombination losses and charge collection efficiency in a perovskite solar cell by comparing impedance response to a drift-diffusion model.

Interpreting the impedance response of perovskite solar cells (PSCs) is significantly more challenging than for most other photovoltaics. This is for a variety of reasons, of which the most significant are the mixed ionic-electronic conduction properties of metal halide perovskites and the difficulty in fabricating stable, and reproducible, devices. Experimental studies, conducted on a variety of PSCs, produce a variety of impedance spectra shapes. However, they all possess common features, the most noteworthy of which is that they have at least two features, at high and low frequency, with different characteristic responses to temperature, illumination and electrical bias. The impedance response has commonly been analyzed in terms of sophisticated equivalent circuits that can be hard to relate to the underlying physics and which complicates the extraction of efficiency-determining parameters. In this paper we show that, by a combination of experiment and drift-diffusion (DD) modelling of the ion and charge carrier transport and recombination within the cell, the main features of common impedance spectra are well reproduced by the DD simulation. Based on this comparison, we show that the high frequency response contains all the key information relating to the steady-state performance of a PSC, i.e. it is a signature of the recombination mechanisms and provides a measure of charge collection efficiency. Moreover, steady-state performance is significantly affected by the distribution of mobile ionic charge within the perovskite layer. Comparison between the electrical properties of different devices should therefore be made using high frequency impedance measurements performed in the steady-state voltage regime in which the cell is expected to operate.

Understanding the Interfaces between Triple-Cation Perovskite and Electron or Hole Transporting Material.

The properties of efficient solar cells fabricated with triple-cation perovskite placed between a mesoporous titania layer and a spiro-OMeTAD layer are studied by using devices either prepared under water-free drybox conditions or fabricated under ambient room humidity. The morphological studies indicate that the content of unreacted PbI2 phase in the perovskite structure is much higher near the interface with titania than near the interface with spiro-OMeTAD. The stationary emission spectra and transient bleach peaks of perovskites show additional long-wavelength features close to the titania side. Time-resolved techniques ranging from femtoseconds to seconds reveal further differences in charge dynamics at both interfaces. The population decay is significantly faster at the titania side than at the spiro-OMeTAD side for the cells prepared under ambient conditions. An increased hole injection rate correlates with higher photocurrent seen in the devices prepared under drybox conditions. The charge recombination loss on the millisecond time scale is found to be slower at the interface with titania than at the interface with spiro-OMeTAD. The ideality factor of the cells is found to increase with increasing DMSO content in the precursor solution, indicating a change in recombination mechanism from bulk to surface recombination. We also found that the charge dynamics are not uniform within the whole perovskite layer. This feature has significant implications for understanding the operation and optimizing the performance of solar devices based on mixed cation perovskites.

Understanding the Influence of Interface Morphology on the Performance of Perovskite Solar Cells.

In recent years, organo-halide perovskite solar cells have garnered a surge of interest due to their high performance and low-cost fabrication processing. Owing to the multilayer architecture of perovskite solar cells, interface not only has a pivotal role to play in performance, but also influences long-term stability. Here we have employed diverse morphologies of electron selective layer (ESL) to elucidate charge extraction behavior in perovskite solar cells. The TiO2 mesoporous structure (three-dimensional) having varied thickness, and nanocolumns (1-dimensional) with tunable length were employed. We found that a TiO2 electron selective layer with thickness of about c.a. 100 nm, irrespective of its microstructure, was optimal for efficient charge extraction. Furthermore, by employing impedance spectroscopy at different excitation wavelengths, we studied the nature of recombination and its dependence on the charge generation profile, and results showed that, irrespective of the wavelength region, the fresh devices do not possess any preferential recombination site, and recombination process is governed by the bulk of the perovskite layer. Moreover, depending on the type of ESL, a different recombination mechanism was observed that influences the final behavior of the devices.

Enhancing Moisture and Water Resistance in Perovskite Solar Cells by Encapsulation with Ultrathin Plasma Polymers.

A compromise between high power conversion efficiency and long-term stability of hybrid organic-inorganic metal halide perovskite solar cells is necessary for their outdoor photovoltaic application and commercialization. Herein, a method to improve the stability of perovskite solar cells under water and moisture exposure consisting of the encapsulation of the cell with an ultrathin plasma polymer is reported. The deposition of the polymer is carried out at room temperature by the remote plasma vacuum deposition of adamantane powder. This encapsulation method does not affect the photovoltaic performance of the tested devices and is virtually compatible with any device configuration independent of the chemical composition. After 30 days under ambient conditions with a relative humidity (RH) in the range of 35-60%, the absorbance of encapsulated perovskite films remains practically unaltered. The deterioration in the photovoltaic performance of the corresponding encapsulated devices also becomes significantly delayed with respect to devices without encapsulation when vented continuously with very humid air (RH > 85%). More impressively, when encapsulated solar devices were immersed in liquid water, the photovoltaic performance was not affected at least within the first 60 s. In fact, it has been possible to measure the power conversion efficiency of encapsulated devices under operation in water. The proposed method opens up a new promising strategy to develop stable photovoltaic and photocatalytic perovskite devices.