Semiconductors group

Abstract:

Two-dimensional (2D) halide perovskites are a versatile material class, exhibiting a layered crystal structure, consisting of inorganic metal–halide sheets separated by organic spacer cations. Unlike their 3D counterparts, 2D perovskites have less strict geometric requirements, allowing for a wider range of molecules to be incorporated. This potentially offers a way to engineer the properties of a 2D perovskite through adequate selection of the organic spacer cations. Our study systematically analyzes the effect of spacer cation length on the electronic and optical properties of Ruddlesden–Popper lead-iodide-based 2D perovskites, using alkylammonium cations of varying chain lengths. Intriguingly, no linear correlation between interlayer distance and the optical gap or valence band position is observed in our measurements. Rather it matters whether the spacer cation contains an odd or even number of carbon atoms in the chain. Notably, these odd-even effects manifest in variations of ionization energy, optical gap as well as charge carrier mobility. Density functional theory calculations reproduce the changes in optical properties, allowing us to identify the underlying mechanism: while even-numbered carbon chains pack efficiently within the organic spacer layer, the shorter odd-numbered chains increase distortions. These distortions lead to variations in the Pb–I–Pb bond angle within the inorganic sheets, resulting in the observed odd-even effect in the (opto-)electronic properties. This understanding will be helpful to make more informed choices regarding the incorporated spacer molecules which can potentially help to enhance performance when integrating such 2D perovskite interlayers into devices.

Abstract:

Two-dimensional perovskites show intriguing optoelectronic properties due to their anisotropic structure and multiple quantum well structure. Here, we report the first three gold-based Ruddlesden–Popper type two-dimensional double perovskites with a general formula (NOP)4AuIBIIII8 (B = Au, Bi, Sb) employing naphthalene-O-propylammonium (NOP) as an organic cation. They were found to form highly crystalline thin films on various substrates, predominantly oriented in the [001] direction featuring continuous, crack-free film areas on the μm2 scale. The thin films show strong optical absorption in the visible region, with band gap energies between 1.48 and 2.32 eV. Density functional theory calculations support the experimentally obtained band gap energies and predict high charge-carrier mobilities and effective charge separation. A comprehensive study with time-resolved microwave conductivity (TRMC) and optical-pump-THz-probe (OPTP) spectroscopy revealed high charge-carrier mobilities for lead-free two-dimensional perovskites of 4.0 ± 0.2 cm2(V s)−1 and charge-carrier lifetimes in the range of μs. Photoconductivity measurements under 1 sun illumination demonstrated the material’s application as a photodetector, showing a 2-fold increase in conductivity when exposed to light.

Abstract:

Vacuum deposition of metal halide perovskite is a scalable and adaptable method. In this study, we adopt sequential evaporation to form the perovskite layer and reveal how the relative humidity during the annealing step, impacts its crystallinity and the photoluminescence quantum yield (PLQY). By controlling the humidity, we achieved a significant enhancement of 50 times in PLQY from 0.12% to 6%. This improvement corresponds to an increase in implied open-circuit voltage (Voc) of over 100 meV. We investigate the origin of this enhanced PLQY by combining structural, chemical and spectroscopic methods. Our results show that annealing in a controlled humid environment improves the organic and inorganic halides' interdiffusion throughout the bulk, which in turn significantly reduces non-radiative recombination both in the bulk and at the interfaces with the charge transport layers, which enhanced both the attainable open-circuit voltage and the charge carrier diffusion length. We further demonstrate that the enhanced intermixing results in fully vacuum-deposited FA0.85Cs0.15Pb(IxCl1−x)3 p-i-n perovskite solar cells (PSCs) with a maximum power point tracked efficiency of 21.0% under simulated air mass (AM) 1.5G 100 mW cm−2 irradiance. Additionally, controlled humidity annealed PSCs exhibit superior stability when aged under full spectrum simulated solar illumination at 85 °C and in open-circuit conditions.

Abstract:

Perovskite-inspired materials (PIMs) are gaining increasing attention among emerging photovoltaic absorbers due to their inherent air stability and low-toxicity potential. However, operational stability, the Achilles' heel of all emerging photovoltaics, has been largely overlooked in PIMs research so far, making it difficult to forecast their practical use in real-world applications. In this work, we analyse the operational stability of a promising new PIM composition, CsMAFA-Sb:Bi, generated through the antimony : bismuth co-alloying of a triple cation vacancy-ordered antimony-based PIM. Through an in-depth theoretical and experimental investigation, we demonstrate that the co-alloying induces local structural changes that lead to enhanced microstructure, reduced trap-assisted recombination, and increased solar cell power conversion efficiency (PCE), with the highest value being 3.05%. Accelerated aging tests according to ISOS L-1 and L-2 protocols highlight the crucial role of co-alloying in enhancing stability. Specifically, maximum power point tracking at 85 °C shows a projected T80 lifetime of 275 hours for CsMAFA-Sb:Bi devices, which has never been achieved not only for any other PIM-based device but also for high-efficiency technologies, such as lead halide perovskite solar cells with similar device constituents. This work encourages future studies on PIM-based photovoltaics for their potential operational stability, with the goal of reducing the performance gap with established technologies.

Abstract:

This dataset accompanies the publication "Re-defining non-tracking solar cell efficiency limits with directional spectral filters" published in ACS Photonics (10.1021/acsphotonics.4c02181). The data can be used to reproduce figures 2-4 in the main text and all plots with data in the supporting information (noting figure 1 in the main text is only schematics). All data was generated via home-built modelling codes. All files are in .CSV and easily readable. The abstract for the associated paper is as follows: Optical filters that respond to the wavelength and direction of incident light can be used to increase the efficiency of tracking solar cells. However, as tracking solar cells are more expensive to install and maintain, it is likely that non-tracking solar cells will remain the main product of the (terrestrial) solar cell industry.  Here we demonstrate that wavelength and directionally selective filters can also be used to increase the efficiency limit of non-tracking solar cells at the equator beyond what is currently understood by up to ~ 0.5 % (relative ~ 1.8 %). We also reveal that such filters can be used to regulate the energy output of solar cells throughout a day or year, and can reduce the thickness of the absorber layer by up to 40 %. We anticipate that similar gains would be seen at other latitudes. As this filter has complex wavelength-direction functionality, we present a proof-of-concept design based on Luneburg lenses, demonstrating these filters can be realized. Our results will enable solar cells with higher efficiency and more stable output while using less material.LNETv