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Due to their outstanding optoelectronic properties, lead-based halide perovskite materials have been applied as efficient photoactive materials in solution-processed solar cells. Current record efficiencies offer the promise to surpass those of silicon solar cells. However, uncertainty about the potential toxicity of lead-based halide perovskite materials and their facile dissolution in water requires a search for new alternative perovskite-like materials. Thanks to the foresight of scientists and their experience in lead-based halide perovskite preparation, remarkable results have been obtained in a short period of time using lead-free perovskite compositions. However, the lower solar-to-energy conversion efficiency and long-term stability issues are serious drawbacks that hinder the potential progression of these materials. Here, we review and analyse strategies in the literature and the most promising solutions to identify the factors that limit the power conversion efficiency and long-term stability of lead-free tin-based perovskite solar cells. In the light of the current state-of-the-art, we offer perspectives for further developing these promising materials. Lead-based halide perovskite solar cells offer attractive power conversion efficiencies, but the release of lead into the environment is a major concern. Here, lead-free, tin-based perovskites are reviewed as an alternative, with a focus on how to extend their long-term stability.

The upscaling of perovskite solar cells is one of the challenges that must be addressed to pave the way toward the commercial development of this technology. As for other thin-film photovoltaic technologies, upscaling requires the fabrication of modules composed of series-connected cells. In this work we demonstrate for the first time the interconnection of inverted modules with NiOx using a UV ns laser, obtaining a 10.2 cm2 minimodule with a 15.9% efficiency on the active area, the highest for a NiOx based perovskite module. We use optical microscopy, energy-dispersive X-ray spectroscopy, and transfer length measurement to optimize the interconnection. The results are implemented in a complete electrical simulation of the cell-to-module losses to evaluate the experimental results and to provide an outlook on further development of single junction and multijunction perovskite modules.

The reverse bias stability is a key concern for the commercialization and reliability of halide perovskite photovoltaics. Here, the robustness of perovskite‐silicon tandem solar cells to reverse bias electrical degradation down to −40 V is investigated. The two‐terminal tandem configuration, with the perovskite coupled to silicon, can improve the solar cell resistance to severe negative voltages when the tandem device is properly designed. While perovskite cells typically exhibit early reverse bias breakdown voltages, the serial connection with silicon cells with large shunt resistances and high voltage breakdown limits their negative polarization and prevent the passage of large current densities when reverse biased. The importance of careful optical design is illustrated, with bottom‐limited conditions required to prevent the perovskite top cell from exploring its own breakdown. This aspect is of great importance in the case of partial shading events when the solar spectrum is richer in the IR components than the standard AM1.5G. Notably, 100% of efficiency retained after polarization at −40 V in different stressing conditions is observed. The results presented suggest that standard industrial bypass diode schemes may be compatible with silicon/perovskite tandem photovoltaics and provide new guidelines for the standardization of the stressing protocols. The electrical stability of silicon/perovskite tandem solar cells at −40V is investigated. The voltage breakdown and the shunt resistance of the silicon bottom cell should be maximised to protect the perovskite top cell. In the case of partial shadowing, the cell is stable for hours at −40V in bottom‐limited conditions while it shows a fast degradation in top‐limited conditions.

The enhancement of photoelectrochemical conversion efficiency of p-type dye-sensitized solar cells (p-DSSCs) is necessary to build up effective tandem devices in which both anode and cathode are photoactive. The efficiency of a p-type device (2.5%) is roughly one order of magnitude lower than the n-type counterparts (13.1%), thus limiting the overall efficiency of the tandem cell, especially in terms of powered current density. This is mainly due to the recombination reaction that occurs especially at the photocathode (or Indium-doped Tin Oxide (ITO))/electrolyte interface. To minimize this phenomenon, a widely employed strategy is to deposit a compact film of NiO (acting as a blocking electrode) beneath the porous electrode. Here, we propose electrodeposition as a cheap, easy scalable and environmental-friendly approach to deposit nanometric films directly on ITO glass. The results are compared to a blocking layer made by means of sol-gel technique. Cells embodying a blocking layer substantially outperformed the reference device. Among them, BL_1.10V shows the best photoconversion efficiency (0.166%) and one of the highest values of fill factor (approaching 46%) ever reported. This is mainly due to an optimized surface roughness of the blocking layer assuring a good deposition of the porous layer. The effectiveness of the implementation of the blocking layer is further proved by means of Electrochemical Impedance Spectroscopy.

This work explores two different deposition methods to grow buffer layers of Zn x Cd 1− x S for application in kesterite (Cu 2 ZnSnS 4 (CZTS)) solar cells. The introduction of the mixed sulfide of Cd and Zn in CZTS based solar cells represents an important progress due to the improved device performance and minor toxicity with respect to sole CdS. The explored techniques are the chemical bath deposition (CBD) and the precursor ink. For the CBD we focused on the inclusion of zinc into the buffer, i.e. the target solid solution, taking into account the difference in the solubilities of ZnS and CdS. In aqueous solutions the co-deposition process is controlled by various solubility equilibria with CdS precipitation representing the most favorable process. Under these circumstances the ink method here proposed is a promising approach since it is based on the thermal degradation of stable chemical precursors deposited on a dry film. In doing so, the problematic co-deposition of a mixed sulfide derived from sulfides with considerably different solubilities is circumvented. The most important advantages of this approach are the easiness and scalability of the whole process and the reduction of the amounts of toxic reagents/products.

Improving the long-term stability of perovskite solar cells is critical to the deployment of this technology. Despite the great emphasis laid on stability-related investigations, publications lack consistency in experimental procedures and parameters reported. It is therefore challenging to reproduce and compare results and thereby develop a deep understanding of degradation mechanisms. Here, we report a consensus between researchers in the field on procedures for testing perovskite solar cell stability, which are based on the International Summit on Organic Photovoltaic Stability (ISOS) protocols. We propose additional procedures to account for properties specific to PSCs such as ion redistribution under electric fields, reversible degradation and to distinguish ambient-induced degradation from other stress factors. These protocols are not intended as a replacement of the existing qualification standards, but rather they aim to unify the stability assessment and to understand failure modes. Finally, we identify key procedural information which we suggest reporting in publications to improve reproducibility and enable large data set analysis. Reliability of stability data for perovskite solar cells is undermined by a lack of consistency in the test conditions and reporting. This Consensus Statement outlines practices for testing and reporting stability tailoring ISOS protocols for perovskite devices.

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. Making large datasets findable, accessible, interoperable and reusable could accelerate technology development. Now, Jacobsson et al. present an approach to build an open-access database and analysis tool for perovskite solar cells.

Interface engineering of organic-inorganic halide perovskite solar cells (PSCs) plays a pivotal role in achieving high power conversion efficiency (PCE). Graphene and related two-dimensional materials (GRMs) are promising candidates to tune on demand the interface properties of PSCs. In this work, we fully exploit the potential of GRMs by controlling the optoelectronic properties of hybrids between molybdenum disulfide (MoS2) and reduced graphene oxide (RGO) as hole transport layer (HTL) and active buffer layer (ABL) in mesoscopic methylammonium lead iodide (CH3NH3PbI3) perovskite (MAPbI3)-based PSC. We show that zero-dimensional MoS2 quantum dots (MoS2 QDs), derived by liquid phase exfoliated MoS2 flakes, provide both hole-extraction and electron-blocking properties. In fact, on the one hand, intrinsic n-type doping-induced intra-band gap states effectively extract the holes through an electron injection mechanism. On the other hand, quantum confinement effects increase the optical band gap of MoS2 (from 1.4 eV for the flakes to > 3.2 for QDs), raising the minimum energy of its conduction band (from -4.3 eV for the flakes to -2.2 eV for QDs) above the one of conduction band of MAPbI3 (between -3.7 and -4 eV) and hindering electron collection. The van der Waals hybridization of MoS2 QDs with functionalized reduced graphene oxide (f-RGO), obtained by chemical silanization-induced linkage between RGO and (3-mercaptopropyl)trimethoxysilane, is effective to homogenize the deposition of HTLs or ABLs onto the perovskite film, since the two-dimensional (2D) nature of RGO effectively plug the pinholes of the MoS2 QDs films. Our graphene interface engineering (GIE) strategy based on van der Waals MoS2 QD/graphene hybrids enable MAPbI3-based PSCs to achieve PCE up to 20.12% (average PCE of 18.8%).

Efficient semi-transparent solar cells can trigger the adoption of building integrated photovoltaics. Halide perovskites are particularly suitable in this respect owing to their tunable bandgap. Main drawbacks in the development of transparent perovskite solar cells are the high Voc deficit and the difficulties in depositing thin films over large area substrates, given the low solubility of bromide and chloride precursors. In this work, we develop a 2D and passivation strategies for the high band-gap Br perovskite able to reduce charge recombination and consequently improving the open-circuit voltage. We demonstrate 1cm 2 perovskite solar cells with Voc up to 1.73 V (1.83 eV QFLS) and a PCE of 8.2%. The AVT exceeds 70% by means of a bifacial light management and a record light utilization efficiency of 5.72 is achieved, setting a new standard for transparent photovoltaics. Moreover, we show the high ceiling of our technology towards IoT application due to a bifaciality factor of 87% along with 17% PCE under indoor lighting. Finally, the up-scaling has been demonstrated fabricating 20cm 2 -active area modules with PCE of 7.3% and Voc per cell up to 1.65V.

Cloud-native services face unique cybersecurity challenges due to their distributed infrastructure. They are susceptible to various threats like malware, DDoS attacks, and Man-in-the-Middle (MITM) attacks. Additionally, these services often process sensitive data that must be protected from unauthorized access. On top of that, the dynamic and scalable nature of cloud-native services makes it difficult to maintain consistent security, as deploying new instances and infrastructure introduces new vulnerabilities. To address these challenges, efficient security solutions are needed to mitigate potential threats while aligning with the characteristics of cloud-native services. Despite the abundance of works focusing on security aspects in the cloud, there has been a notable lack of research that is focused on the security of cloud-native services. To address this gap, this work is the first survey that is dedicated to exploring security in cloud-native services. This work aims to provide a comprehensive investigation of the aspects, features, and solutions that are associated with security in cloud-native services. It serves as a uniquely structured mapping study that maps the key aspects to the corresponding features, and these features to numerous contemporary solutions. Furthermore, it includes the identification of various candidate open-source technologies that are capable of supporting the realization of each explored solution. Finally, it showcases how these solutions can work together in order to establish each corresponding feature. The insights and findings of this work can be used by cybersecurity professionals, such as developers and researchers, to enhance the security of cloud-native services.