Monolithic all-perovskite tandem photovoltaics promise to combine low-cost and high-efficiency solar energy harvesting with the advantages of all-thin-film technologies. To date, laboratory-scale all-perovskite tandem solar cells have only been fabricated using non-scalable fabrication techniques. In response, this work reports on laser-scribed all-perovskite tandem modules processed exclusively with scalable fabrication methods (blade coating and vacuum deposition), demonstrating power conversion efficiencies up to 19.1% (aperture area, 12.25 cm2; geometric fill factor, 94.7%) and stable power output. Compared to the performance of our spin-coated reference tandem solar cells (efficiency, 23.5%; area, 0.1 cm2), our prototypes demonstrate substantial advances in the technological readiness of all-perovskite tandem photovoltaics. By means of electroluminescence imaging and laser-beam-induced current mapping, we demonstrate the homogeneous current collection in both subcells over the entire module area, which explains low losses (<5%rel) in open-circuit voltage and fill factor for our scalable modules.

Engineering of the interface between perovskite absorber thin films and charge transport layers has fueled the development of perovskite solar cells (PSCs) over the past decade. For p‐i‐n PSCs, the development and adoption of hole transport layers utilizing self‐assembled monolayers (SAM‐HTLs) based on carbazole functional groups with phosphonic acid anchoring groups has enabled almost lossless contacts, minimizing interfacial recombination to advance power conversion efficiency in single‐junction and tandem solar cells. However, so far these materials have been deposited exclusively via solution‐based methods. Here, for the first time, vacuum‐based evaporation of the most common carbazole‐based SAM‐HTLs (2PACz, MeO‐2PACz, and Me‐4PACz) is reported. X‐ray photoelectron spectroscopy and infrared spectroscopy demonstrate no observable chemical differences in the evaporated SAMs compared to solution‐processed counterparts. Consequently, the near lossless interfacial properties are either preserved or even slightly improved as demonstrated via photoluminescence measurements and an enhancement in open‐circuit voltage. Strikingly, applying evaporated SAM‐HTLs to complete PSCs demonstrates comparable performance to their solution‐processed counterparts. Furthermore, vacuum deposition is found to improve perovskite wetting and fabrication yield on previously non‐ideal materials (namely Me‐4PACz) and to display conformal and high‐quality coating of micrometer‐sized textured surfaces, improving the versatility of these materials without sacrificing their beneficial properties.

Given the outstanding progress in research over the past decade, perovskite photovoltaics (PV) is about to step up from laboratory prototypes to commercial products.For this to happen, realizing scalable processes to allow the technology to transition from solar cells to modules is pivotal. This work presents all-evaporated perovskite PV modules with all thin films coated by established vacuum deposition processes. A common 532-nm nanosecond laser source is employed to realize all three interconnection lines of the solar modules. The resulting module interconnections exhibit low series resistance and a small total lateral extension down to 160 μm. In comparison with interconnection fabrication approaches utilizing multiple scribing tools, the process complexity is reduced while the obtained geometrical fill factor of 96% is comparable with established inorganic thin-film PV technologies. The all-evaporated perovskite minimodules demonstrate power conversion efficiencies of 18.0% and 16.6% on aperture areas of 4 and 51 cm 2 , respectively. Most importantly, the allevaporated minimodules exhibit only minimal upscaling losses as low as 3.1% rel per decade of upscaled area, at the same time being the most efficient perovskite PV minimodules based on an all-evaporated layer stack sequence.

Narrow-band gap (NBG) Sn−Pb perovskites with band gaps of ∼1.2 eV, which correspond to a broad photon absorption range up to ∼1033 nm, are highly promising candidates for bottom solar cells in all-perovskite tandem photovoltaics. To exploit their potential, avoiding optical losses in the top layer stacks of the tandem configuration is essential. This study addresses this challenge in two ways (1) removing the hole-transport layer (HTL) and (2) implementing highly transparent hydrogen-doped indium oxide In 2 O 3 :H (IO:H) electrodes instead of the commonly used indium tin oxide (ITO). Removing HTL reduces parasitic absorption loss in shorter wavelengths without compromising the photovoltaic performance. IO:H, with an ultra-low near-infrared optical loss and a high charge carrier mobility, results in a remarkable increase in the photocurrent of the semitransparent top and (HTL-free) NBG bottom perovskite solar cells when substituted for ITO. As a result, an IO:H-based four-terminal all-perovskite tandem solar cell (4T all-PTSCs) with a power conversion efficiency (PCE) as high as 24.8% is demonstrated, outperforming ITObased 4T all-PTSCs with PCE up to 23.3%.

Advanced optical concepts, making use of tailored microstructured front cover glasses, promise to reduce the losses encountered with encapsulated solar modules. However, implementing optical concepts into the conventional architecture of encapsulated solar modules and simultaneously maintaining high durability represent a severe technological challenge. The liquid glass technique offers a route to meet this challenge by enabling the implementation of these optical concepts directly into the durable front cover glass of solar modules. In this work, we demonstrate for the first time two showcases of texturing fused silica front cover glass, using the facile liquid glass technique: (I) multifunctional microcone textures that reduce front-side reflection losses by ∼80% compared to a planar reference, which correlates to an increase in short-circuit current density of encapsulated planar monocrystalline silicon heterojunction solar cells by 2.9 mA cm −2 , and exhibit strong hydrophilic behavior facilitating selfcleaning and (II) embedded freeform surface cloaks that redirect incident light away from the metallic contact grids of the solar cell and demonstrate a cloaking efficiency of ∼88%.

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Transparent photovoltaics provide diverse levels of average visible transmittance (AVT) along concurrent light harvesting, making glass façades and windows accessible for photovoltaics. However, improvements in power conversion efficiency (PCE) and...

The steadily growing market share of building‐integrated photovoltaics (BIPVs) places the aesthetics of solar modules in the focus of research and development. In this work, a colorization method based on inkjet‐printed reflective pigments is adapted for the emerging perovskite photovoltaics. Herein, not only excellent control of color impression, brightness, and pattern is demonstrated, but also angle invariant color perception, which makes the presented approach stand out among the many published colorization strategies for perovskite solar cells (PSCs). Compared to uncolored reference solar cells, bright magenta and yellow PSCs display a remarkable relative power conversion efficiency (PCE) of up to 65% and more than 11% absolute PCE. Moreover, PSCs with more BIPV‐relevant coloring patterns such as a mimic of a marble or corten steel surfaces are demonstrated. The colorization method presented is inexpensive and ready for scalable solar module production. To demonstrate the scalability of the proposed concept, a small‐area perovskite solar module (4 cm2 aperture area) in white marble optics exhibiting a PCE of almost 14% as a potential application is presented.