Vacuum-based deposition of optoelectronic thin films has a long-standing history. However, in the field of perovskite-based photovoltaics, these techniques are still not as advanced as their solution-based counterparts. Although high-efficiency vacuum-based perovskite solar cells reaching power conversion efficiencies (PCEs) above 20% are reported, the number of studies on the underlying physical and chemical mechanism of the co-evaporation of lead iodide and methylammonium iodide is low. In this study, the impact of one of the most crucial process parameters in vacuum processes-the substrate material-is studied. It is shown that not only the morphology of the co-evaporated perovskite thin films is significantly influenced by the surface polarity of the substrate material, but also the incorporation of the organic compound into the perovskite framework. Based on these studies, a selection guide for suitable substrate materials for efficient co-evaporated perovskite thin films is derived. This selection guide points out that the organic vacuum-processable hole transport material 2,2″,7,7″-tet ra(N,N-di-p-tolyl)amino-9,9-spirobifluorene is an ideal candidate for the fabrication of efficient all-evaporated perovskite solar cells, demonstrating PCEs above 19%. Furthermore, building on the insights into the formation of the perovskite thin films on different substrate materials, a basic crystallization model for co-evaporated perovskite thin films is suggested.
We investigate the T-matrix approach for the simulation of light scattering by an oblate particle near a planar interface. Its validity has been in question if the interface intersects the particle's circumscribing sphere, where the spherical wave expansion of the scattered field can diverge. However, the plane wave expansion of the scattered field converges everywhere below the particle, and in particular at the planar interface. We demonstrate that the particle-interface scattering interaction is correctly accounted for through a plane wave expansion in combination with Fresnel reflection at the planar interface. We present an in-depth analysis of the involved convergence mechanisms, which are governed by the transformation properties between spherical and plane waves. The method is illustrated with the cases of spherical and oblate spheroidal nanoparticles near a perfectly conducting interface, and its accuracy is demonstrated for different scatterer arrangements and materials.
In this work, we have improved the absorption properties of thin film solar cells by introducing light trapping reflectors deposited onto self-assembled nanostructures. The latter consist of a disordered array of nanopillars and are fabricated by polymer blend lithography. Their broadband light scattering properties are exploited to enhance the photocurrent density of thin film devices, here based on hydrogenated amorphous silicon active layers. We demonstrate that these light scattering nanopillars yield a short-circuit current density increase of +33%rel with respect to equivalent solar cells processed on a planar reflector. Moreover, we experimentally show that they outperform randomly textured substrates that are commonly used for achieving efficient light trapping. Complementary optical simulations are conducted on an accurate 3D model to analyze the superior light harvesting properties of the nanopillar array and to derive general design rules. Our approach allows one to easily tune the morphology of the self-assembled nanostructures, is up-scalable and operated at room temperature, and is applicable to other photovoltaic technologies.
The spontaneous phase separation of two or more polymers is a thermodynamic process that can take place in both biological and synthetic materials and which results in the structuring of the matter from the micro-to the nanoscale. For photonic applications, it allows forming quasi-periodic or disordered assemblies of light scatterers at high throughput and low cost. The wet process methods currently used to fabricate phase-separated nanostructures (PSNs) limit the design possibilities, which in turn hinders the deployment of PSNs in commercialized products. To tackle this shortcoming, we introduce a versatile and industrially scalable deposition method based on the inkjet printing of a polymer blend, leading to PSNs with a feature size that is tuned from a few micrometers down to sub-100 nm. Consequently, PSNs can be rapidly processed into the desired macroscopic design. We demonstrate that these printed PSNs can improve light management in manifold photonic applications, exemplified here by exploiting them as a light extraction layer and a metasurface for light-emitting devices and point-of-care biosensors, respectively.
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