Search

Chemically processed methylammonium tin-triiodide (CH3NH3SnI3) films include Sn in different oxidation states, leading to poor stability and low power conversion efficiency of the resulting solar cells (PSCs). The development of absorbers with Sn [2+] only has been identified as one of the critical steps to develop all Sn-based devices. Here, we report on coevaporation of CH3NH3I and SnI2 to obtain absorbers with Sn being only in the preferred oxidation state [+2] as confirmed by X-ray photoelectron spectroscopy. The Sn [4+]-free absorbers exhibit smooth highly crystalline surfaces and photoluminescence measurements corroborating their excellent optoelectronic properties. The films show very good stability under heat and light. Photoluminescence quantum yields up to 4 × 10^-3 translate in a quasi Fermi-level splittings exceeding 850 meV under one sun equivalent conditions showing high promise in developing lead-free, high efficiency, and stable PSCs.

In this review we highlight the benefits of perovskites beyond photovoltaic technology, focusing on their use as lasers, light-emitting diodes or sensors, including technologies such as gamma-ray detection or aerospace applications.

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.

Organic-inorganic hybrid halide perovskite materials have attracted considerable research interest, especially for photovoltaics. In addition, their scope has been extended towards light-emitting devices, photodetectors, or detectors. However, the toxicity of lead (Pb) element in perovskite compositions limits their applications. Therefore, a tremendous research effort on replacing is underway. More specifically, tin-based perovskites have shown the highest potential for this purpose. However, many challenges remain before these materials reach the goals of stability, safety, and eventually commercial application. This perspective considers many aspects and the critical development possibilities of tin-based perovskites, including drawbacks and challenges based on their physical properties. Additionally, it provides insights for future device applications that go beyond solar cells. Finally, the existing challenges and opportunities in tin-based perovskites are discussed.

Daily temperature variations induce phase transitions and lattice strains in halide perovskites, challenging their stability in solar cells. We stabilized the perovskite black phase and improved solar cell performance using the ordered dipolar structure of β-poly(1,1-difluoroethylene) to control perovskite film crystallization and energy alignment. We demonstrated p-i-n perovskite solar cells with a record power conversion efficiency of 24.6% over 18 square millimeters and 23.1% over 1 square centimeter, which retained 96 and 88% of the efficiency after 1000 hours of 1-sun maximum power point tracking at 25° and 75°C, respectively. Devices under rapid thermal cycling between −60° and +80°C showed no sign of fatigue, demonstrating the impact of the ordered dipolar structure on the operational stability of perovskite solar cells.

The emergence of perovskite photovoltaic technology is transforming the landscape of solar energy. Its rapid development has been driven by the advances in our understanding of the thin-film microstructures of metal halide perovskites and their intriguing correlations with optoelectronic properties, device efficiency and long-term stability. Here we discuss the morphological characteristics of three key microstructure types encountered in perovskites, which include grain boundaries, intragrain defects and surfaces. To reveal detailed structural information of these microstructure types via tailored characterizations is crucial to probe their detrimental, neutral or beneficial effects on optoelectronic properties. We further elaborate the impacts of these microstructures on the degradation modes of perovskites. Representative examples are also presented, which have translated fundamental understandings to achieve state-of-the-art perovskite solar cells. Finally, we call for more attention in probing hidden microstructures and developing high-spatiotemporal-resolution characterizations, as well as harnessing the potential merits of microstructural imperfections, towards an elevated understanding of microstructure–property–performance relationships for the next solar cell advances.

For the past 30 years, Lean has become popular throughout organisations across the globe. Based on the Toyota Production System (TPS), Lean is a proven systematic methodology to reduce waste in processes, optimise efficiency and ensure quality in the end products. Although Lean has been proven to be a successful methodology, it also has a high failure rate. Research has identified a range of critical success factors (CSF) that are crucial towards the successful implementation of Lean. This research endeavour takes a qualitative approach, using Grounded Theory (GT) to investigate Lean implementation in Maltese organisations and to determine whether established CSFs are applicable to the Maltese context. Participants from the manufacturing, catering, and logistics industries are interviewed, with the data coded and analysed using MAXQDA2020. The findings suggest the importance of leadership as a catalyst in driving change within an organisation to foster a culture of continuous improvement.

The library of two-dimensional (2D) materials has been enriched over recent years with novel crystal architectures endowed with diverse exciting functionalities. Bulk perovskites, including metal-halide and oxide systems, provide access to a myriad of properties through molecular engineering. Their tunable electronic structure offers remarkable features from long carrier-diffusion lengths and high absorption coefficients in metal-halide perovskites to high-temperature superconductivity, magnetoresistance and ferroelectricity in oxide perovskites. Emboldened by the 2D materials research, perovskites down to the monolayer limit have recently emerged. Like other 2D species, perovskites with reduced dimensionality are expected to exhibit new physics and to herald next-generation multifunctional devices. In this Review, we critically assess the preliminary studies on the synthetic routes and inherent properties of monolayer perovskite materials. We also discuss how to exploit them for widespread applications and provide an outlook on the challenges and opportunities that lie ahead for this enticing class of 2D materials. Metal-halide and oxide perovskites are a rich playground for fundamental studies and applications. This Review focuses on the opportunities opened by reducing the dimensionality of these materials to two-dimensional monolayers.

Perovskite solar cells (PSCs) have shown rapid progress in a decade of extensive research and development, aiming now towards commercialization. However, the development of more facile, reliable, and reproducible manufacturing techniques will be essential for industrial production. Many lamination methods have been initially designed for organic photovoltaics (OPVs), which are conceptually similar to PSCs. Lamination could provide a low-cost and adaptable technique for the roll-to-roll production of solar cells. This review presents an overview of lamination methods for the fabrication of PSCs and OPVs. The lamination of different electrodes consisting of various materials such as metal back contacts, photoactive layers, hole transport layers (HTLs), and electron transport layers (ETLs) is discussed. The efficiency and stability of the laminated devices are also presented. Finally, the challenges and opportunities of laminated solar cells are discussed.

Long-term operational stability remains a major challenge in the commercialization of perovskite solar cells (PSCs). While the major thrust of recent research effort has been on understanding the degradation mechanism, many new approaches are being explored to improve the performance stability of PSCs. In this issue are four Letters that discuss new strategies to achieve stabilization of PSCs. Editorial Advisory Board members highlight these new advances herein.

Lead halide based perovskite semiconductors self-assemble with distinct organic cations in natural multi-quantum-well structures. The emerging electronic properties of these two-dimensional (2D) materials can be controlled by the combination of the halide content and choice of chromophore in the organic layer. Understanding the photophysics of the perovskite semiconductor materials is critical for the optimization of stable and efficient optoelectronic devices. We use femtosecond transient absorption spectroscopy (fs-TAS) to study the mechanism of energy transfer between the organic and inorganic layers in a series of three lead-based mixed-halide perovskites such as benzylammonium (BA), 1-naphthylmethylammonium (NMA), and 1-pyrenemethylammonium (PMA) cations in 2D-lead-based perovskite thin films under similar experimental conditions. After optical excitation of the 2D-confined exciton in the lead halide layer, ultrafast energy transfer is observed to organic singlet and triplet states of the incorporated chromophores. This is explained by an effective Dexter energy transfer, which operates via a correlated electron exchange between the donating 2D-confined exciton and the accepting chromophore under spin conservation.

In the last decade, the power conversion efficiency (PCE) of solution-processed perovskite solar cells (PSCs) in the lab-scale has reached an incredible level of 25.5%. Generally, PSCs are composed of a stack consisting of a perovskite thin-film sandwiched between an electron transporting layer (ETL) and a hole transporting layer (HTL). Although the quality of the ETL and HTL interfaces with the perovskite thin-film is important, the quality of the perovskite thin-film is also critical to achieving high-performance PSCs. Low-temperature deposition of organic–inorganic perovskite thin-films by simple solution processes is one of the significant advantages of PSCs compared to other well-developed semiconductors for manufacturing solar cells. However, growing highly uniform and crystalline solution-processed perovskite thin-films is very challenging due to multiple phenomena during film formation, including solvent evaporation, wetting effects, inhomogeneous film stress and uncontrolled nucleation and growth. Therefore, understanding the different stages of perovskite crystallization is critical for achieving high-quality films and realizing higher PCEs. On the other hand, switching to large-scale solar modules leads to a substantial loss in performance, decreasing the chance of commercialization of this technology. Therefore, developing large-scale deposition techniques for reliable perovskite crystallization is very vital for scaling up PSCs. So far, several solution-processed methods such as anti-solvent and two-step processes have been developed for lab-scale perovskite thin-films deposition. However, these methods are not applicable for large-scale perovskite deposition. This review explores various scalable solution-processed perovskite deposition techniques. Moreover, different solvent quenching techniques as the most critical step of large-scale perovskite crystallization are discussed to provide a comprehensive view for achieving high-quality perovskite thin-films with large areas. Finally, the existing challenges and opportunities to push forward the commercialization of PSCs are discussed.

Funder: Helmholtz Young Investigator Group Frontrunner, Over the past few years, lead‐halide perovskites (LHPs), both in the form of bulk thin films and colloidal nanocrystals (NCs), have revolutionized the field of optoelectronics, emerging at the forefront of next‐generation optoelectronics. The power conversion efficiency (PCE) of halide perovskite solar cells has increased from 3.8% to over 25.7% over a short period of time and is very close to the theoretical limit (33.7%). At the same time, the external quantum efficiency (EQE) of perovskite LEDs has surpassed 23% and 20% for green and red emitters, respectively. Despite great progress in device efficiencies, the photoactive phase instability of perovskites is one of the major concerns for the long‐term stability of the devices and is limiting their transition to commercialization. In this regard, researchers have found that the phase stability of LHPs and the reproducibility of the device performance can be improved by A‐site cation alloying with two or more species, these are named mixed cation (double, triple, or quadruple) perovskites. This review provides a state‐of‐the‐art overview of different types of mixed A‐site cation bulk perovskite thin films and colloidal NCs reported in the literature, along with a discussion of their synthesis, properties, and progress in solar cells and LEDs.

Negative capacitance at the low-frequency domain and inverted hysteresis are familiar features in perovskite solar cells, where the origin is still under discussion. Here we use Impedance Spectroscopy to analyse these responses in methylammonium lead bromide cells treated with lithium cation at the electron selective layer/perovskite interface and in iodide devices exposed to different relative humidity conditions. Employing the Surface Polarization Model, we obtain a time constant associated to the kinetics of the interaction of ions/vacancies with the surface, {\tau}kin, in the range of 10^0 - 10^2 s for all the cases exhibiting both features. These interactions lead to a decrease in the overall recombination resistance, modifying the low-frequency perovskite response and yielding to a flattening of the cyclic voltammetry. As consequence of these results we find that that negative capacitance and inverted hysteresis lead to a decrease in the fill factor and photovoltage values., Comment: 17 pages, 4 figures

Long life of perovskite devices in working conditions remains the bottleneck for technology application. Stable charge carriers’ transport together with nonreactive contact materials contributes to the increase of the device operation time. Still, an appropriate model for transport carrier mechanisms is needed because of the complex ionic–electronic interplay. Herein, methylammonium lead bromide perovskite single crystals are used to analyze the current flowing across the perovskite sample after biasing. Two methods are performed: 1) direct measurement using an amperemeter and 2) indirect method by means of an induced potential in a reference capacitor. Because of the continuity of the current, the latest method measures direct current through the sample by monitoring displacements currents. Intriguing features are observed: the displacement currents result in stable and highly reproducible responses for long-term biasing (≈2000 s), while the direct measurements produce larger and exponentially increasing current dependence on time. These findings highlight the nontrivial effect of contacting and measuring procedures in exploring thick perovskite electrical response. Funding for open access charge: CRUE-Universitat Jaume I

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).