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The LCOE is a strong techno-economic analysis based on performance, stability, and manufacturing costs to evaluate the potential of perovskites in the solar market. Here, we reported an estimation of perovskites’ LCOE between 4–6 cents (USD) per kWh.

Improving the perovskite/electron-transporting layer (ETL) interface is a crucial task to boost the performance of perovskite solar cells (PSCs).

We applied an organic sensor for the detection and quantification of PbI2 released by perovskite solar cells. The molecule shows a fluorescence intensity enhancement in the presence of Pb2+ cations and is highly selective of the desired analyte.

The entire world has been suffering from the coronavirus disease 2019 (COVID‐19) pandemic since March 11, 2020. More than a year later, the COVID‐19 vaccination brought hope to control this viral pandemic. Here, we review the unknowns of the COVID‐19 vaccination, such as its longevity, asymptomatic spread, long‐term side effects, and its efficacy on immunocompromised patients. In addition, we discuss challenges associated with the COVID‐19 vaccination, such as the global access and distribution of vaccine doses, adherence to hygiene guidelines after vaccination, the emergence of novel severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) variants, and vaccine resistance. Despite all these challenges and the fact that the end of the COVID‐19 pandemic is still unclear, vaccines have brought great hope for the world, with several reports indicating a significant decline in the risk of COVID19‐related infection and hospitalizations., peer-reviewed

Perovskite solar cells (PSCs) longevity is nowadays the bottleneck for their full commercial exploitation. Although lot of research is ongoing, the initial decay of the output power - an effect known as "burn-in" degradation happening in the first 100 h - is still unavoidable, significantly reducing the overall performance (typically of20%). In this paper, the origin of the "burn-in" degradation in n-i-p type PSCs is demonstrated that is directly related to Li

Tuning halide composition in perovskites is a powerful approach demonstrated to enhance the performance of perovskite photovoltaic devices where such compositional modifications drive improvements in open-circuit voltage (Voc) and a reduction in nonradiative voltage losses. Similarly, photodetectors (PDs) operate as light to current conversion devices hence it is relevant to investigate whether performance enhancements can be achieved by similar strategies. Herein, perovskite PDs are fabricated with an inverted photodiode configuration based on a MAPb(I1-xBrx)3 perovskite (MA = methylammonium) active layer over the x = 0–0.25 composition range. Interestingly, it has been found that increasing the Br content up to 0.15 (15%) leads to a significant reduction in dark current (Jd), with values as low as 1.3 × 10−9 A cm−2 being achieved alongside a specific detectivity of 8.7 × 1012 Jones. Significantly, it has been observed an exponential relationship between the Jd of devices and their Voc over the 0–15% Br range. The superior performances of the 15% Br-containing devices are attributed to the reduction of trap states, a better charge extraction of photogenerated carriers, and an improvement in photoactive layer morphology and crystallinity.

Paweł Łukasz Zajdel, David G. Madden, Robin Babu, Marco Tortora, Diego Mirani, Nikolay Nikolaevich Tsyrin, Luis Bartolomé, Eder Amayuelas, David Fairen-Jimenez, Alexander Rowland Lowe, Mirosław Adam Chorążewski, Juscelino B. Leao, Craig M. Brown, Markus Bleuel, Victor Stoudenets, Carlo Massimo Casciola, María Echeverría, Francisco Bonilla, Giulia Grancini, Simone Meloni, Yaroslav Grosu, Controlling the pressure at which liquids intrude (wet) and extrude (dry) a nanopore is of paramount importance for a broad range of applications, such as energy conversion, catalysis, chromatography, separation, ionic channels, and many more. To tune these characteristics, one typically acts on the chemical nature of the system or pore size. In this work, we propose an alternative route for controlling both intrusion and extrusion pressures via proper arrangement of the grains of the nanoporous material. To prove the concept, dynamic intrusion–extrusion cycles for powdered and monolithic ZIF-8 metal–organic framework were conducted by means of water porosimetry and in operando neutron scattering. We report a drastic increase in intrusion–extrusion dynamic hysteresis when going from a fine powder to a dense monolith configuration, transforming an intermediate performance of the ZIF-8 + water system (poor molecular spring) into a desirable shock-absorber with more than 1 order of magnitude enhancement of dissipated energy per cycle. The obtained results are supported by MD simulations and pave the way for an alternative methodology of tuning intrusion–extrusion pressure using a macroscopic arrangement of nanoporous material.

The role of halide substitution in a lead-free 2D hybrid perovskite is investigated on the BZA(2)SnX(4) (BZA = benzylammonium; X = Cl, Br and I) system, by reporting the synthesis and the structural analysis by means of single-crystal X-ray diffraction data of the two novel compositions BZA(2)SnBr(4) and BZA(2)SnCl(4). In addition, the mixed composition BZA(2)Sn(BrxI1-x)(4) (0

Engineering two-/three-dimensional (2D/3D) perovskite solar cells is nowadays a popular strategy for efficient and stable devices. However, the exact function of the 2D/3D interface in controlling the long-term device behavior is still obscure. Here, we reveal a dynamical structural mutation of the 2D/3D interface: the small cations in the 3D cage move towards the 2D layer, which acts as an ion scavenger. If structurally stable, the 2D layer physically blocks the ion movement at the interface boosting the device stability. Otherwise, the 2D layer embeds them, dynamically self-transforming into a quasi-2D structure. The judicious choice of the 2D constituent is decisive in controlling the 2D/3D kinetics and improving the device lifetime, opening a new avenue for perovskite interface design.

Pump-probe microscopy was limited to single-point detection because cameras are too slow for shot-to-shot demodulation. We use off-axis holography to create an all-optical lock-in camera, obtaining pump-probe images spanning 100×100 μm2. We use it to study exciton diffusion in perovskites around 100 diffraction-limited spots.

CA extern Lead-free perovskites are attracting increasing interest as nontoxic materials for advanced optoelectronic applications. Here, we report on a family of silver/bismuth bromide double perovskites with lower dimensionality obtained by incorporating phenethylammonium (PEA) as an organic spacer, leading to the realization of two-dimensional double perovskites in the form of (PEA)(4)AgBiBr8 (n = 1) and the first reported (PEA)(2)CsAgBiBr7 (n = 2). In contrast to the situation prevailing in lead halide perovskites, we find a rather weak influence of electronic and dielectric confinement on the photophysics of the lead-free double perovskites, with both the 3D Cs2AgBiBr6 and the 2D n = 1 and n = 2 materials being dominated by strong excitonic effects. The large measured Stokes shift is explained by the inherent soft character of the double-perovskite lattices, rather than by the often-invoked band to band indirect recombination. We discuss the implications of these results for the use of double perovskites in light-emitting applications.

Layered lead halide perovskites (2D LHPs) are attracting considerable attention as a promising material for a new generation of solar cell devices. LHPs have been presented as a more stable alternative to the more widespread 3D bulk perovskite materials; however, a critical analysis of their photostability is still lacking. In this work, we perform a comparative study between BA

Layered lead halide A'2An-1PbnI3n+1 perovskites (2D LHPs) are attracting considerable attention as a more stable alternative with respect to APbI3 parent phases - a promising material for a new generation of solar cells. However, a critical analysis on the photostability of 2D perovskites homologous row is still lacking. In this work, we perform a comparative study of BA2MAn-1PbnI3n+1 (BA - butylammonium, MA - methylammonium) 2D LHPs with different layer number n = 1-3, considered as study-case systems, and MAPbI3, as a reference. We discuss a stability testing protocol with general validity, comparing photometrical determination of iodine-containing products in nonpolar solvents, X-ray diffraction, and photoluminescence spectroscopy. The resulting photostability trends in inert atmosphere demonstrate a nonmonotonic dependence of degradation rate on the perovskite layer thickness n with a "stability island" at n > 3 which is caused by a combination of antibate factors of electronic structure and chemical composition in the family of 2D perovskites. We also identify a critical oxygen concentration in the surrounding environment that affects the mechanism and strongly enhances the rate of layered perovskites photodegradation.

Scientific collaboration has been a critical aspect of the development of all fields of science, particularly clinical medicine. It is well understood that myriads of benefits can be yielded by interdisciplinary and international collaboration. For instance, our rapidly growing knowledge on COVID-19 and vaccine development could not be attained without expanded collaborative activities. However, achieving fruitful results requires mastering specific tactics in collaborative efforts. These activities can enhance our knowledge, which ultimately benefits society. In addition to tackling the issue of the invisible border between different countries, institutes, and disciplines, the border between the scientific community and society needs to be addressed as well. International and transdisciplinary approaches can potentially be the best solution for bridging science and society. The Universal Scientific Education and Research Network (USERN) is a non-governmental, non-profit organization and network to promote professional, scientific research and education worldwide. The fifth annual congress of USERN was held in Tehran, Iran, in a hybrid manner on November 7-10, 2020, with key aims of bridging science to society and facilitating borderless science. Among speakers of the congress, a group of top scientists unanimously agreed on The USERN 2020 consensus, which is drafted with the goal of connecting society with scientific scholars and facilitating international and interdisciplinary scientific activities in all fields, including clinical medicine.

With the world population swelling and rapid technological innovations imposing global network and connections, the growing energy demand has reached unprecedented levels: “The energy industry is facing decades of transformation,” reported the World Energy Council at the end of 2018 [1]. Increasing use of renewable energy sources and photovoltaics is thus utmost for Europe to meet the goals imposed by the Paris Agreement. From a research point of view, this pushes an enormous effort into discovery of new materials, new physical phenomena and development of new technologies to sustain such paradigm shift to a low-carbon society.

Pandemics are enormous threats to the world that impact all aspects of our lives, especially the global economy. The COVID-19 pandemic has emerged since December 2019 and has affected the global economy in many ways. As the world becomes more interconnected, the economic impacts of the pandemic become more serious. In addition to increased health expenditures and reduced labor force, the pandemic has hit the supply and demand chain massively and caused trouble for manufacturers who have to fire some of their employees or delay their economic activities to prevent more loss. With the closure of manufacturers and companies and reduced travel rates, usage of oil after the beginning of the pandemic has decreased significantly that was unprecedented in the last 30 years. The mining industry is a critical sector in several developing countries, and the COVID-19 pandemic has hit this industry too. Also, world stock markets declined as investors started to become concerned about the economic impacts of the COVID-19 pandemic. The tourism industry and airlines have also experienced an enormous loss too. The GDP has reduced, and this pandemic will cost the world more than 2 trillion at the end of 2020.

Pandemics are enormous threats to the world that impact all aspects of our lives, especially the global economy. The COVID-19 pandemic has emerged since December 2019 and has affected the global economy in many ways. As the world becomes more interconnected, the economic impacts of the pandemic become more serious. In addition to increased health expenditures and reduced labor force, the pandemic has hit the supply and demand chain massively and caused trouble for manufacturers who have to fire some of their employees or delay their economic activities to prevent more loss. With the closure of manufacturers and companies and reduced travel rates, usage of oil after the beginning of the pandemic has decreased significantly that was unprecedented in the last 30 years. The mining industry is a critical sector in several developing countries, and the COVID-19 pandemic has hit this industry too. Also, world stock markets declined as investors started to become concerned about the economic impacts of the COVID-19 pandemic. The tourism industry and airlines have also experienced an enormous loss too. The GDP has reduced, and this pandemic will cost the world more than 2 trillion at the end of 2020.

Invited for this month's cover are collaborators from University of Pavia, Ecole Polytechnique Federale de Lausanne, University of Messina and Istituto Italiano di Tecnologia. The cover picture shows the crystal structure of a Ruddlesden-Popper quasi-2D perovskite with chemical formula (PEA)2 MA39 Pb40 I121 (with PEA: phenylethylammonium and MA: methylammonium). The subscript 40 indicates the number of PbI6 octahedra separated by a double layer of PEA cations. Such quasi-2D perovskites exhibit efficient photovoltaic performances and higher stability with respect to the pure 3D counterpart (MAPbI3 ). This article is part of the Special Collection on "Perovskite Materials and Devices". Read the full text of the article at 10.1002/cplu.202000777.

Funder: Engineering and Physical Sciences Research Council; Id: http://dx.doi.org/10.13039/501100000266, Funder: Cambridge Trust Scholarship, Funder: Robert Gardiner Scholarship, Funder: Royal Society; Id: http://dx.doi.org/10.13039/501100000288, Halide perovskite materials offer an ideal playground for easily tuning their color and, accordingly, the spectral range of their emitted light. In contrast to common procedures, this work demonstrates that halide substitution in Ruddlesden–Popper perovskites not only progressively modulates the bandgap, but it can also be a powerful tool to control the nanoscale phase segregation—by adjusting the halide ratio and therefore the spatial distribution of recombination centers. As a result, thin films of chloride‐rich perovskite are engineered—which appear transparent to the human eye—with controlled tunable emission in the green. This is due to a rational halide substitution with iodide or bromide leading to a spatial distribution of phases where the minor component is responsible for the tunable emission, as identified by combined hyperspectral photoluminescence imaging and elemental mapping. This work paves the way for the next generation of highly tunable transparent emissive materials, which can be used as light‐emitting pixels in advanced and low‐cost optoelectronics.

We report the synthesis and characterization of nanocrystals of a novel fully inorganic lead-free zero-dimensional perovskite, Cs4SnBr6. Samples are made of crystals with an average size of ∼20 nm with green emission centered around 530 nm. Interestingly, both colloidal suspensions and thin films show an enhanced air stability with respect to that of any other previous tin-based nanocrystalline system, with emission persisting for tens of hours under laboratory air.

2D hybrid perovskites (2DP) are versatile materials, whose electronic and optical properties can be tuned through the nature of the organic cations (even when those are seemingly electronically inert). Here, it is demonstrated that fluorination of the organic ligands yields glassy 2DP materials featuring long‐lived correlated electron–hole pairs. Such states have a marked charge‐transfer character, as revealed by the persistent Stark effect in the form of a second derivative in electroabsorption. Modeling shows that electrostatic effects associated with fluorination, combined with the steric hindrance due to the bulky side groups, drive the formation of spatially dislocated charge pairs with reduced recombination rates. This work enriches and broadens the current knowledge of the photophysics of 2DP, which will hopefully guide synthesis efforts toward novel materials with improved functionalities., An anomalous, persistent, Stark effect from electroabsorption and nanosecond transient absorption measurement related to the presence of long‐lived screened electron–hole pairs in 2D perovskite is presented. A peculiarity in these materials, contrasting with large exciton binding energies, is presented, revealing a complex photophysical response and highlighting the role of cation's chemistry on the material's optical response.

This short review aims at summarizing the current challenges related to poor Perovskite Solar Cells (PSCs) stability which nowadays puts severe constrains on near future device commercialization. As a game changer in the field of photovoltaics (PVs), PSCs are highly efficient and cheap to fabricate. However, they suffer from poor long-term stability upon exposure to heat, moisture, oxygen and light, and combinations thereof. Poor device stability originates from intrinsic instability issues of the perovskite active layer itself, as well as extrinsic factors due to partial degradation of the layers composing the device stack. Here we briefly review the chemical and physical processes responsible for intrinsic material instability, and we highlight possible solutions to overcome it; we then consider the whole device, discussing properties and interactions of the stacked layers. Finally, particular emphasis is placed on the need of shared standards for stability tests, which should include detailed report on experimental conditions over a statistically significant number of samples, allowing for a direct comparison of results across different groups and fostering a rapid advance of our understanding of degradation mechanisms and of the solutions to overcome them.

International audience; Low-dimensional hybrid perovskites have triggered significant research interest due to their intrinsically tunable optoelectronic properties and technologically relevant material stability. In particular, the role of the organic spacer on the inherent structural and optical features in two-dimensional (2D) perovskites is paramount for material optimization. To obtain a deeper understanding of the relationship between spacers and the corresponding 2D perovskite film properties, we explore the influence of the partial substitution of hydrogen atoms by fluorine in an alkylammonium organic cation, resulting in (Lc)2PbI4 and (Lf)2PbI4 2D perovskites, respectively. Consequently, optical analysis reveals a clear 0.2 eV blue-shift in the excitonic position at room temperature. This result can be mainly attributed to a band gap opening, with negligible effects on the exciton binding energy. According to Density Functional Theory (DFT) calculations, the band gap increases due to a larger distortion of the structure that decreases the atomic overlap of the wavefunctions and correspondingly bandwidth of the valence and conduction bands. In addition, fluorination impacts the structural rigidity of the 2D perovskite, resulting in a stable structure at room temperature and the absence of phase transitions at a low temperature, in contrast to the widely reported polymorphism in some non-fluorinated materials that exhibit such a phase transition. This indicates that a small perturbation in the material structure can strongly influence the overall structural stability and related phase transition of 2D perovskites, making them more robust to any phase change. This work provides key information on how the fluorine content in organic spacer influence the structural distortion of 2D perovskites and their optical properties which possess remarkable importance for future optoelectronic applications, for instance in the field of light-emitting devices or sensors.

Surface passivation of the perovskite photo absorber is a key factor to improve the photovoltaic performance. So far robust passivation strategies have not yet been revealed. Here, we demonstrate a successful passivation strategy which controls the Fermi-level of the perovskite surface by improving the surface states. Such Fermi-level control caused band-bending between the surface and bulk of the perovskite, which enhanced the hole-extraction from the absorber bulk to the HTM side. As an added benefit, the inorganic passivation layer improved the device light stability. By depositing a thick protection layer on the complete device, a remarkable waterproofing effect was obtained. As a result, an enhancement ofVOCand the conversion efficiency from 20.5% to 22.1% was achieved. We revealed these passivation mechanisms and used perhydropoly(silazane) (PHPS) derived silica to control the perovskite surface states.