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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 (rel) in open-circuit voltage and fill factor for our scalable modules.

Soiling can significantly reduce the performance of photovoltaic (PV) modules. One source of soiling is volcano eruptions that eject dust contaminants, which can detrimentally affect PV systems. A microtextured fluoropolymer cover film for a PV module was evaluated as a passive antisoiling solution. In this case, the wind was investigated as a natural force to determine whether it can realize the desired self-cleaning functionality instead of the more commonly employed water droplets. Removal of dust particles of different size categories was investigated inside a wind tunnel. The results demonstrate dust removal of up to ∼90% from wind speeds of 8 m/s. Removal of small dust particles requires higher wind speeds compared with larger dust particles. Smaller dust particles were observed to be trapped within the microtexture cavities. Based on a multicrystalline PV minimodule, a performance recovery between 9.7%–24.0% in terms of short-circuit current density (J_SC), relative to the soiled device, was projected. Utilization of wind for dust removal shows potential but would require further optimization of the microtexture design to enhance the self-cleaning function.

Nanostructured tin oxide (SnO2) is a very promising electron transport layer (ETL) for perovskite solar cells (PSCs) that allows low-temperature processing in the planar n–i–p architecture. However, minimizing current–voltage (J–V) hysteresis and optimizing charge extraction for PSCs in this architecture remains a challenge. In response to this, we study and optimize different types of single- and bilayer SnO2 ETLs. Detailed characterization of the optoelectronic properties reveals that a bilayer ETL composed of lithium (Li)-doped compact SnO2 (c(Li)-SnO2) at the bottom and potassium-capped SnO2 nanoparticle layers (NP-SnO2) at the top enhances the electron extraction and charge transport properties of PSCs and reduces the degree of ion migration. This results in an improved PCE and a strongly reduced J–V hysteresis for PSCs with a bilayer c(Li)-NP-SnO2 ETL as compared to reference PSCs with a single-layer or undoped bilayer ETL. The champion PSC with c(Li)-NP-SnO2 ETL shows a high stabilized PCE of up to 18.5% compared to 15.7%, 12.5% and 16.3% for PSCs with c-SnO2, c(Li)-SnO2 and c-NP-SnO2 as ETL, respectively.

Following the 2nd release of the “Emerging PV reports,” the best achievements in the performance of emerging photovoltaic devices in diverse emerging photovoltaic research subjects are summarized, as reported in peer‐reviewed articles in academic journals since August 2021. Updated graphs, tables, and analyses are provided with several performance parameters, e.g., power conversion efficiency, open‐circuit voltage, short‐circuit current density, fill factor, light utilization efficiency, and stability test energy yield. These parameters are presented as a function of the photovoltaic bandgap energy and the average visible transmittance for each technology and application, and are put into perspective using, e.g., the detailed balance efficiency limit. The 3rd installment of the “Emerging PV reports” extends the scope toward triple junction solar cells.

Methylammonium (MA)-free perovskite solar cells have the potential for better thermal stability than their MA-containing counterparts. However, the efficiency of MA-free perovskite solar cells lags behind due to inferior bulk quality. In this work, 4-methylphenethylammonium chloride (4M-PEACl) is added into a MA-free perovskite precursor, which results in greatly enhanced bulk quality. The perovskite crystal grains are significantly enlarged, and defects are suppressed by a factor of four upon the incorporation of an optimal concentration of 4M-PEACl. Quasi-2D perovskites are formed and passivate defects at the grain boundaries of the perovskite crystals. Furthermore, the perovskite surface chemistry is modified, resulting in surface energies more favorable for hole extraction. This facile approach leads to a steady state efficiency of 23.7% (24.2% in reverse scan, 23.0% in forward scan) for MA-free perovskite solar cells. The devices also show excellent light stability, retaining more than 93% of the initial efficiency after 1000 h of constant illumination in a nitrogen environment. In addition, a four-terminal mechanically stacked perovskite-silicon tandem solar cell with champion efficiency of 30.3% is obtained using this MA-free composition. The encapsulated tandem devices show excellent operational stability, retaining more than 98% of the initial performance after 42 day/night cycles in an ambient atmosphere.

3D-printed conductive structures are highly attractive due to their great potential for customizable electronic devices. While the traditional 3D printing of metal requires high temperatures to sinter metal powders or polymer/metal composites, low or room temperature processes will be advantageous to enable multi-material deposition and integration of optoelectronic applications. Herein, digital light processing technology and inkjet printing are combined as an effective strategy to fabricate customized 3D conductive structures. In this approach, a 3D-printed nanoporous (NPo) polymeric material is used as a substrate onto which a nanoparticle-based Ag ink is printed. SEM and X-ray nano computed tomography (nanoCT) measurements show that the porous morphology of the pristine NPo is retained after deposition and annealing of the Ag ink. By optimizing the deposition conditions, conductive structures with sheet resistance

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 all-evaporated minimodules exhibit only minimal upscaling losses as low as 3.1%$_{rei}$ per decade of upscaled area, at the same time being the most efficient perovskite PV minimodules based on an all-evaporated layer stack sequence.

Lanthanide-based upconversion (UC) allows harvesting sub-bandgap near-infrared photons in photovoltaics. In this work, we investigate UC in perovskite solar cells by implementing UC single crystal BaF2:Yb3+, Er3+ at the rear of the solar cell. Upon illumination with high-intensity sub-bandgap photons at 980 nm, the BaF2:Yb3+, Er3+ crystal emits upconverted photons in the spectral range between 520 and 700 nm. When tested under terrestrial sunlight representing one sun above the perovskite's bandgap and sub-bandgap illumination at 980 nm, upconverted photons contribute a 0.38 mA/cm2 enhancement in the short-circuit current density at lower intensity. The current enhancement scales non-linearly with the incident intensity of sub-bandgap illumination, and at higher intensity, 2.09 mA/cm2 enhancement in current was observed. Hence, our study shows that using a fluoride single crystal like BaF2:Yb3+, Er3+ for UC is a suitable method to extend the response of perovskite solar cells to near-infrared illumination at 980 nm with a subsequent enhancement in current for very high incident intensity.

Among perovskite semiconductors, quasi-two-dimensional (2D) materials are attractive for the pursuit of electrically driven lasing given their excellent performance in light-emitting diodes (LEDs) and their recent success in continuous-wave optically pumped lasing. We investigate the spontaneous photoluminescence emission and amplified spontaneous emission (ASE) of a series of quasi-2D emitters, and their directly analogous 3D materials formed by removing the 2D organic spacer by annealing. Although the PL photoluminescence (PL) (at low optical excitation power) from quasi-2D films with high 2D spacer fractions can be much brighter than that from their 3D counterparts, the ASE thresholds of these quasi-2D materials tend to be higher. This counter-intuitive behavior is investigated through time-resolved photophysical studies, which reveal the emission in the high-spacer-content quasi-2D perovskite can be exclusively excitonic, and the exciton–exciton annihilation of quasi-2D perovskite starts to take over the exciton dynamics at a low exciton density (

Despite promising power conversion efficiencies, a key barrier for the future commercialization of perovskite-based solar cells (PSCs) is their lack of stability when exposed to sunlight for extend...

Monolithic two-terminal (2T) perovskite/CuInSe$_2$ (CIS) tandem solar cells (TSCs) combine the promise of an efficient tandem photovoltaic (PV) technology with the simplicity of an all-thin-film device architecture that is compatible with flexible and lightweight PV. In this work, we present the first-ever 2T perovskite/CIS TSC with a power conversion efficiency (PCE) approaching 25% (23.5% certified, area 0.5 cm$^2$). The relatively planar surface profile and narrow band gap (∼1.03 eV) of our CIS bottom cell allow us to exploit the optoelectronic properties and photostability of a low-Br-containing perovskite top cell as revealed by advanced characterization techniques. Current matching was attained by proper tuning of the thickness and bandgap of the perovskite, along with the optimization of an antireflective coating for improved light in-coupling. Our study sets the baseline for fabricating efficient perovskite/CIS TSCs, paving the way for future developments that might push the efficiencies to over 30%.

Hybrid organic–inorganic perovskites are highly promising candidates for the upcoming generation of single- and multijunction solar cells. Despite their extraordinarily good semiconducting properti...

Summary The fast progress of perovskite-based tandem photovoltaic technology raises the need to identify optimal double-junction tandem architectures with regard to energy yield (EY) under realistic irradiation conditions. Recently, the three-terminal (3T) perovskite-silicon tandem architecture was prototyped for the first time. This technology bears great promise as it combines the advantages of two-terminal (2T) and four-terminal (4T) architectures. This numerical study provides a systematic EY-modeling analysis for perovskite-silicon tandem architectures. According to our study, the 3T architecture delivers the highest EY (from 3% to 9% relative) in every climatic condition, due to ∼6% larger photogenerated current density in the absorber layers compared with 4T architecture and a higher robustness to spectral variations compared with 2T architecture. Finally, we show that the standard deviation of the average utilizable photon energy can be used to predict the gain in EY of 3T architecture compared with 2T architecture.

Perovskite solar cells (PSCs) are among the most promising emerging photovoltaic technologies, demonstrating power conversion efficiencies (PCEs) close to 24%. The major challenge hampering commercialization of this technology is the low stability toward inevitable stress factors of PV modules such as temperature variations. Temperature variations are reported to induce a decline in photocurrent of up to 80%, depending on the device architecture, the charge transport layers, and the perovskite absorber material. The effect is particularly pronounced in methylammonium lead iodide-based PSCs, with TiO2 as the electron transport layer (ETL) and spiro-MeOTAD as the hole transport layer (HTL). This article reports on three different strategies to overcome the temperature-variation-induced degradation by altering the interfaces. The charge selective transport layers, the perovskite absorber layer composition, and the perovskite deposition technique are varied. We find that the interface between the ETL and the perovskite layer is the key to temperature-variation-induced degradation. We demonstrate stable PSCs with regard to temperature variations with PCEs as high as 19.5%. Finally, the relevance of the temperature-variation-induced degradation for outdoor applications is shown by stressing PSCs with real outdoor temperature profiles (between 21 and 75 °C).

In this work we employ the transfer matrix method for the analysis of optical materials properties to simulate and optimize monolithic tandem solar cell devices based on CuIn1−x Ga x Se2, CI(G)S, and perovskite (PVK) absorbers. By finding models that fit well the experimental data of the CI(G)S solar cell, the semitransparent perovskite solar cell (PSC) and the PVK/CI(G)S monolithic tandem solar cell, we were able to perform a detailed optical loss analysis that allowed us to determine sources of parasitic absorption. We found better substitute materials for the transport layers to increase the power conversion efficiency and, in case of semitransparent PSCs, sub-bandgap transmittance. Our results set guidelines for the monolithic PVK/CI(G)S tandem solar cells development, predicting an achievable efficiency of 30%.

Hybrid perovskite photovoltaics combine high performance with the ease of solution processing. However, to date, a poor understanding of morphology formation in coated perovskite precursor thin films casts doubt on the feasibility of scaling-up laboratory-scale solution processes. Oblique slot jet drying is a widely used scalable method to induce fast crystallization in perovskite thin films, but deep knowledge and explicit guidance on how to control this dynamic method are missing. In response, we present a quantitative model of the drying dynamics under oblique slot jets. Using this model, we identify a simple criterion for successful scaling of perovskite solution printing and predict coating windows in terms of air velocity and web speed for reproducible fabrication of perovskite solar cells of ∼15% in power conversion efficiency─in direct correlation with the morphology of fabricated thin films. These findings are a corner stone toward scaling perovskite fabrication from simple principles instead of trial and error optimization.

Recent advances in solution processing of micrometer-thick perovskite solar cells over textured silicon bottom solar cells allowed a new promising approach for the fabrication of 2T perovskite/silicon tandem photovoltaics, combining optimal light management in the textured bottom cell with the ease of solution processing. Detailed simulations are needed to assess the performances of this morphology configuration (thick perovskite configuration). In this work, in-depth optical and energy yield (EY) simulations are performed to compare the thick perovskite configuration with other relevant morphology configurations for 2T perovskite/silicon tandem photovoltaics. Under standard test conditions, the total photogenerated current of the thick perovskite configuration is 1.3 mA cm−2 lower (−3.4% relative) than the one of the conformal perovskite on textured silicon configuration for non-encapsulated cells and only 0.8 mA cm−2 (−2.1% relative) for encapsulated cells. Under realistic outdoor conditions, EY modelling for a wide range of locations shows that, while conformal perovskite on textured silicon configuration remains the optimal configuration, thick perovskite configuration exhibits a mere ∼2.5% lower annual EY. Finally, intermediate scenarios are investigated with the angle of the perovskite front-side texture differing from the silicon texture and critical angles for efficient light management in these configurations are identified.

Perovskite based photovoltaic (PV) cells are unique in combining low open-circuit voltage losses with a broad bandgap tunability. This makes them an ideal PV cell to recycle photons back into electrical power in a variety of illumination systems or light emitting devices. Here, advantage of these features is taken and wide bandgap (WBG) perovskite PV cells are incorporated in devices suitable for display illumination and demonstrate a high yield in stray light recycling back into electricity with up to a 37.5% power conversion efficiency. The specific device considered is a modified half-cylinder photonic plate designed to emit diffused broadband polarized light using a nonabsorbing reflective polarizer based on a random dielectric layer distribution. It is experimentally demonstrated that light recycling using appropriately tuned WBG perovskite PV cells becomes very efficient when implemented in systems where the light is emitted from narrowband sources, even if the emission spans a broad wavelength range.

Fair and meaningful device per- formance comparison among luminescent solar concentrator- photovoltaic (LSC-PV) reports cannot be realized without a gen- eral consensus on reporting stan- dards in LSC-PV research. There- fore, it is imperative to adopt standardized characterization protocols for these emerging types of PV devices that are consistent with other PV devices. This commentary highlights several common limitations in LSC literature and summarizes the best practices moving for- ward to harmonize with standard PV reporting, considering the greater nuances present with LSC-PV. Based on these prac- tices, a checklist of actionable items is provided to help stan- dardize the characterization/re- porting protocols and offer a set of baseline expectations for au- thors, reviewers, and editors. The general consensus combined with the checklist will ultimately guide LSC-PV research towards reliable and meaningful ad- vances.

Vacuum-assisted growth (VAG) control is one of the most promising methods for controlling nucleation and crystallization of printed and coated large area lead halide perovskite-based layers for optoelectronics. To coat or print homogeneous high-quality perovskite thin-films at high fabrication yield, real-time process monitoring of the VAG is pivotal. In response, a 2.1-megapixel multichannel photoluminescence (PL) and reflection imaging system is developed and employed for the simultaneous spatial in situ analysis of drying, nucleation, and crystal growth during VAG and subsequent thermal annealing of inkjet-printed and blade-coated perovskite thin-films. It is shown that the VAG process, for example, evacuation rate and time, affects the film formation and provide detailed insight into traced PL and reflection transients extracted from sub-second videos of each channel. Based on correlative analysis between the transients and, for example, perovskite ink composition, wet-film thickness, or evacuation time, key regions which influence crystal quality, film morphology, and are base for prediction of solar cell performance are identified.

Many economic and environmental studies on novel perovskite solar cells (PSCs), published ex post the development stage to investigate the market competitiveness, have focused on laboratory-scale PSC architectures that are not amenable for upscaling. In this paper, we evaluate the market potential and environmental sustainability of a scalable carbon-electrode-based PSC by benchmarking it to the market dominating c-Si photovoltaics and CIGS thin film photovoltaics. The analysis covers the PSCs full lifecycle, at the module and system levels (residential and utility scale), and is based on realistic annual energy output data derived from energy yield calculations. We find that this PSC can produce electricity at low cost (3–6 €cents/kWh), with lowest energy payback (0.6–0.8years) and greenhouse gas emissions (15–25g CO2eq./kWh) compared with grid-connected PV market alternatives, assuming 25 years of lifetime, expected PV system cost reductions, and PSC module recycling and refurbishment.

Interfacial engineering is the key to high-performance perovskite solar cells (PSCs). While a wide range of fullerene interlayers are investigated for Pb-based counterparts with a bandgap of >1.5 eV, the role of fullerene interlayers is barely investigated in Sn-Pb mixed narrow-bandgap (NBG) PSCs. In this work, two novel solution-processed fullerene derivatives are investigated, namely indene-C60-propionic acid butyl ester and indene-C60-propionic acid hexyl ester (IPH), as the interlayers in NBG PSCs. It is found that the devices with IPH-interlayer show the highest performance with a remarkable short-circuit current density of 30.7 mA cm−2 and a low deficit in open-circuit voltage. The reduction in voltage deficit down to 0.43 V is attributed to reduced non-radiative recombination that the authors attribute to two aspects: 1) a higher conduction band offset of ≈0.2 eV (>0 eV) that hampers charge-carrier-back-transfer recombination; 2) a decrease in trap density at the perovskite/interlayer/C60 interfaces that results in reduced trap-assisted recombination. In addition, incorporating the IPH interlayer enhances charge extraction within the devices that results in considerable enhancement in short-circuit current density. Using a NBG device with an IPH interlayer, a respectable power conversion efficiency of 24.8% is demonstrated in a four-terminal all-perovskite tandem solar cell.

et al., Large datasets are now ubiquitous as technology enables higher-throughput experiments, but rarely can a research field truly benefit from the research data generated due to inconsistent formatting, undocumented storage or improper dissemination. Here we extract all the meaningful device data from peer-reviewed papers on metal-halide perovskite solar cells published so far and make them available in a database. We collect data from over 42,400 photovoltaic devices with up to 100 parameters per device. We then develop open-source and accessible procedures to analyse the data, providing examples of insights that can be gleaned from the analysis of a large dataset. The database, graphics and analysis tools are made available to the community and will continue to evolve as an open-source initiative. This approach of extensively capturing the progress of an entire field, including sorting, interactive exploration and graphical representation of the data, will be applicable to many fields in materials science, engineering and biosciences., Open access funding provided by Helmholtz-Zentrum Berlin für Materialien und Energie GmbH., The core funding of the project has been received from the European Union’s Horizon 2020 research and innovation programme under grant agreement no. 787289. We acknowledge the following sources for individual funding. Cambridge India Ramanujan Scholarship, China Scholarship Council, Deutscher Akademischer Austauschdienst (DAAD), EPSRC (grant no. EP/S009213/1), European Union’s Horizon 2020 research and innovation programme (grant no. 764787, EU Project ‘MAESTRO’), (grant no. 756962, ERC Project ‘HYPERION’), (grant no. 764047, EU Project ‘ESPResSo’ and grant no. 850937), GCRF/EPSRC SUNRISE (EP/P032591/1), German Federal Ministry for Education and Research (BMBF), HyPerFORME, NanoMatFutur (grant no. 03XP0091). PEROSEED (ZT-0024), Helmholtz Energy Materials Foundry, The Helmholtz Innovation Laboratory HySPRINT. BMBF (grant nos. 03SF0540, 03SF0557A), HyPerCells graduate school, Helmholtz Association, Helmholtz International Research School (HI-SCORE), the Erasmus programme (CDT-PV, grant no. EP/L01551X/1), the European Union’s Horizon 2020 research and innovation programme (Marie Skłodowska-Curie grant agreement nos. 841386, 795079 and 840751), Royal Society University Research Fellowship (grant no. UF150033). SNaPSHoTs (BMBF), SPARC II, German Research Foundation (DFG, grant no. SPP2196), The National Natural Science Foundation of China (grant no. 51872014), the Recruitment Programme of Global Experts, Fundamental Research Funds for the Central Universities and the ‘111’ project (grant no. B17002), the US Department of Energy’s Office of Energy Efficiency and Renewable Energy under Solar Energy Technologies Office (SETO) agreement no. DE-EE0008551, the Colombia Scientific Programme in the framework of the call Ecosistema Cientifíco (Contract no. FP44842-218-2018), the committee for the development of research (CODI) of the Universidad de Antioquia (grant no. 2017-16000), Spanish MINECO (Severo Ochoa programme, grant no. SEV‐2015‐0522), the Swedish research council (VR, grant no. 2019-05591) and the Swedish Energy Agency (grant no. 2020-005194).

To scale up production of perovskite photovoltaics, state-of-the-art laboratory recipes and processes must be transferred to large-area coating and drying systems. The development of in situ monitoring methods that provide real-time feedback for process control is pivotal to overcome this challenge. Herein, correlative in situ multichannel imaging (IMI) obtaining reflectance, photoluminescence intensity, and central photoluminescence emission wavelength images on areas larger than 100 cm2 with subsecond temporal resolution using a simple, cost-effective setup is demonstrated. Installed on top of a drying channel with controllable laminar air flow and substrate temperature, IMI is shown to consistently monitor solution film drying, perovskite nucleation, and perovskite crystallization. If the processing parameters differ, IMI reveals characteristic changes in large-area perovskite formation dynamics already before the final annealing step. Moreover, when IMI is used to study >130 blade-coated devices processed at the same parameters, about 90% of low-performing devices contain coating inhomogeneities detected by IMI. The results demonstrate that IMI should be of value for real-time 2D monitoring and feedback control in industrial-scale, high-throughput fabrication such as roll-to-roll printing.

All-perovskite two-terminal tandem photovoltaics offer high power conversion efficiencies (PCEs) that can surpass the limits of single-junction photovoltaics. In this study, energy yield (EY) simulations are performed to assess the performance of bifacial all-perovskite tandem solar cells. Under standard test conditions, in the absence of albedo, bifacial tandems demonstrate a 4.9% relative lower PCE compared to equivalent monofacial tandems due to transparency losses at the semitransparent rear side. However, under realistic irradiation conditions, albedo irradiation leads to an enhancement in EY for bifacial cells. This enhancement enables bifacial cells to produce more energy than monofacial cells, even over relatively low average reflectance (R$_A$) ground such as dark sandstone (R$_A$ = 9%). The EY gain for bifacial cells rises to a maximum of 40–50% for ground modeled as a perfect reflector (R$_A$ = 100%), accompanied by a shift in optimum top subcell bandgap to 1.56 eV. This shift is of particular interest as low-bandgap perovskite semiconductors (with lower bromide concentrations) offer enhanced stability under realistic operation conditions. Finally, this work presents a route to increase the PCE of simulated monofacial and bifacial cells, to 31.9% and 30.8%, respectively, by optimizing the optical and electrical performance of the cells.

The recent development of solution-processed perovskite thin films over micrometer-sized textured silicon bottom solar cells enables tandem solar cells with power conversion efficiencies > 30%. Next to improved light harvesting, textured silicon wafers are the industrial standard. To achieve high performance, the open-circuit voltage losses that occur when fabricating perovskite solar cells over such textures need to be mitigated. This study provides a practical guideline to discriminate and address the voltage losses at the interfaces as well as in the bulk of solution-processed double cation perovskite thin films using photoluminescence quantum yield measurements. Furthermore, the origin of these losses is investigated via morphological, microstructural, and compositional analysis and present possible mitigation strategies. The guideline will be beneficial for scientists working on randomly textured surfaces and provides a deeper understanding on this timely research topic.

Perovskite/silicon tandem photovoltaics have attracted enormous attention in science and technology over recent years. In order to improve the performance and stability of the technology, new materials and processes need to be investigated. However, the established sequential layer deposition methods severely limit the choice of materials and accessible device architectures. In response, a novel lamination process that increases the degree of freedom in processing the top perovskite solar cell (PSC) is proposed. The very first prototypes of laminated monolithic perovskite/silicon tandem solar cells with stable power output efficiencies of up to 20.0% are presented. Moreover, laminated single-junction PSCs are on par with standard sequential layer deposition processed devices in the same architecture. The numerous advantages of the lamination process are highlighted, in particular the opportunities to engineer the perovskite morphology, which leads to a reduction of non-radiative recombination losses and and an enhancement in open-circuit voltage (Voc). Laminated PSCs exhibit improved stability by retaining their initial efficiency after 1-year aging and show good thermal stability under prolonged illumination at 80 °C. This lamination approach enables the research of new architectures for perovskite-based photovoltaics and paves a new route for processing monolithic tandem solar cells even with a scalable lamination process.

We present an innovative optoelectronic design combining wide bandgap perovskite photovoltaic cells and broadband light polarizing structures to recycle the stray light back into electricity in devices requiring polarized light selectivity, such as in LCDs.

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

Achieving efficient devices while maintaining a high fabrication yield is a key challenge in the fabrication of solution-processed, perovskite-based light-emitting diodes (PeLEDs). In this respect, pinholes in the solution-processed perovskite layers are a major obstacle. These are usually mitigated using organic electron-conducting planarization layers. However, these organic interlayers are unstable under applied bias in air and suffer from limited charge carrier mobility. In this work, we present a high brightness p-i-n PeLED based on a novel blade-coated silver microflake (SMF) rear electrode, which allows for a low-cost nanocrystalline ZnO inorganic electron-transporting layer to be used. This novel SMF contact is crucial for achieving high performance as it prevents the electrical shorting suffered when standard thermally evaporated silver rear contacts are used. The fabricated PeLEDs exhibit an excellent maximum luminance of 98,000 cd/m2, a maximum current efficiency of 22.3 cd/A, and a high external quantum efficiency of 4.6% under 5.9 V forward bias. The SMF rear contact can be printed and scaled at low cost to large areas and applied to flexible devices.