A Newly Crosslinked-double Network PEDOT:PSS@PEGDMA toward Highly-Efficient and Stable Tin-Lead Perovskite Solar Cells.

Until now, poly(3,4-ethylenedioxythiophene):poly(styrensulfonate) (PEDOT:PSS) is widely used in Sn-Pb perovskite solar cells (PSCs) due to its many advantages, including high optical transparency, suitable conductivity, superior wettability, and so on. However, the acidic and hydroscopic properties of the PSS component, as well as the incongruous energy level of the hole transport layer (HTL), may lead to unsatisfying interface properties and decreased device performance. Herein, by adding polyethylene glycol dimethacrylate (PEGDMA) into PEDOT:PSS, a newly crosslinked-double-network obtain of PEDOT:PSS@PEGDMA film, which could not only optimize nucleation and crystallinity of Sn-Pb perovskite films, but also suppress defect density and optimize energy level alignment at the HTL/perovskite interface. As a result, the achieves highly efficient and stable mixed Sn-Pb PSCs with an encouraging power conversion efficiency of 20.9%. Additionally, the device can maintain good stability under N2 atmosphere.

The effect of illumination on the formation of metal halide perovskite films.

Optimizing the morphology of metal halide perovskite films is an important way to improve the performance of solar cells when these materials are used as light harvesters, because film homogeneity is correlated with photovoltaic performance. Many device architectures and processing techniques have been explored with the aim of achieving high-performance devices, including single-step deposition, sequential deposition and anti-solvent methods. Earlier studies have looked at the influence of reaction conditions on film quality, such as the concentration of the reactants and the reaction temperature. However, the precise mechanism of the reaction and the main factors that govern it are poorly understood. The consequent lack of control is the main reason for the large variability observed in perovskite morphology and the related solar-cell performance. Here we show that light has a strong influence on the rate of perovskite formation and on film morphology in both of the main deposition methods currently used: sequential deposition and the anti-solvent method. We study the reaction of a metal halide (lead iodide) with an organic compound (methylammonium iodide) using confocal laser scanning fluorescence microscopy and scanning electron microscopy. The lead iodide crystallizes before the intercalation of methylammonium iodide commences, producing the methylammonium lead iodide perovskite. We find that the formation of perovskite via such a sequential deposition is much accelerated by light. The influence of light on morphology is reflected in a doubling of solar-cell efficiency. Conversely, using the anti-solvent method to form methyl ammonium lead iodide perovskite in a single step from the same starting materials, we find that the best photovoltaic performance is obtained when films are produced in the dark. The discovery of light-activated crystallization not only identifies a previously unknown source of variability in opto-electronic properties, but also opens up new ways of tuning morphology and structuring perovskites for various applications.

Interfaces and Interfacial Layers in Inorganic Perovskite Solar Cells.

Owing to their superior thermal stability, metal halide inorganic perovskite materials continue to attract interest for photovoltaics applications. The highest reported power conversion efficiency (PCE) for solar cells based on inorganic perovskites is over 20 %. As this PCE corresponds to 73 % of the theoretical limit, there remains more room for further improving the device PCEs than for improving organic-inorganic hybrid perovskite solar cells (PSCs). The main loss is in the photovoltage, which is limited by interfaces in terms of non-radiative recombination caused by traps and energy-level mismatch. Furthermore, inefficient charge extraction at interfacial contacts reduces the photocurrent and fill factor. This Minireview summarizes the recent developments in the fundamental understanding of how the interfaces and interfacial layers influence the performance of solar cells based on inorganic perovskite absorbers. An outlook for the development of highly efficient and stable inorganic PSCs from the interface point of view is also given.

Crystal-Size-Induced Band Gap Tuning in Perovskite Films.

A comprehensive picture explaining the effect of the crystal size in metal halide perovskite films on their opto-electronic characteristics is currently lacking. We report that perovskite nanocrystallites exhibit a wider band gap due to concurrent quantum confinement and size dependent structural effects, with the latter being remarkably distinct and attributed to the perturbation from the surface of the nanocrystallites affecting the structure of their core. This phenomenon might assist in the photo-induced charge separation within the perovskite in devices employing mesoporous layers as they restrict the size of nanocrystallites present in them. We demonstrate that the crystal size effect is widely applicable as it is ubiquitous in different compositions and deposition methods employed in the fabrication of state-of-the-art perovskite solar cells. This effect is a convenient and effective way to tune the band gap of perovskites.

Design rules for minimizing voltage losses in high-efficiency organic solar cells.

The open-circuit voltage of organic solar cells is usually lower than the values achieved in inorganic or perovskite photovoltaic devices with comparable bandgaps. Energy losses during charge separation at the donor-acceptor interface and non-radiative recombination are among the main causes of such voltage losses. Here we combine spectroscopic and quantum-chemistry approaches to identify key rules for minimizing voltage losses: (1) a low energy offset between donor and acceptor molecular states and (2) high photoluminescence yield of the low-gap material in the blend. Following these rules, we present a range of existing and new donor-acceptor systems that combine efficient photocurrent generation with electroluminescence yield up to 0.03%, leading to non-radiative voltage losses as small as 0.21 V. This study provides a rationale to explain and further improve the performance of recently demonstrated high-open-circuit-voltage organic solar cells.

Planar Perovskite Solar Cells with High Open-Circuit Voltage Containing a Supramolecular Iron Complex as Hole Transport Material Dopant.

In perovskite solar cells (PSCs), the most commonly used hole transport material (HTM) is spiro-OMeTAD, which is typically doped by metalorganic complexes, for example, based on Co, to improve charge transport properties and thereby enhance the photovoltaic performance of the device. In this study, we report a new hemicage-structured iron complex, 1,3,5-tris(5'-methyl-2,2'-bipyridin-5-yl)ethylbenzene Fe(III)-tris(bis(trifluoromethylsulfonyl)imide), as a p-type dopant for spiro-OMeTAD. The formal redox potential of this compound was measured as 1.29 V vs. the standard hydrogen electrode, which is slightly (20 mV) more positive than that of the commercial cobalt dopant FK209. Photoelectron spectroscopy measurements confirm that the iron complex acts as an efficient p-dopant, as evidenced in an increase of the spiro-OMeTAD work function. When fabricating planar PSCs with the HTM spiro-OMeTAD doped by 5 mol % of the iron complex, a power conversion efficiency of 19.5 % (AM 1.5G, 100 mW cm-2 ) is achieved, compared to 19.3 % for reference devices with FK209. Open circuit voltages exceeding 1.2 V at 1 sun and reaching 1.27 V at 3 suns indicate that recombination at the perovskite/HTM interface is low when employing this iron complex. This work contributes to recent endeavors to reduce recombination losses in perovskite solar cells.

Unreacted PbI2 as a Double-Edged Sword for Enhancing the Performance of Perovskite Solar Cells.

Lead halide perovskites have over the past few years attracted considerable interest as photo absorbers in PV applications with record efficiencies now reaching 22%. It has recently been found that not only the composition but also the precise stoichiometry is important for the device performance. Recent reports have, for example, demonstrated small amount of PbI2 in the perovskite films to be beneficial for the overall performance of both the standard perovskite, CH3NH3PbI3, as well as for the mixed perovskites (CH3NH3)x(CH(NH2)2)(1-x)PbBryI(3-y). In this work a broad range of characterization techniques including X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), photo electron spectroscopy (PES), transient absorption spectroscopy (TAS), UV-vis, electroluminescence (EL), photoluminescence (PL), and confocal PL mapping have been used to further understand the importance of remnant PbI2 in perovskite solar cells. Our best devices were over 18% efficient, and had in line with previous results a small amount of excess PbI2. For the PbI2-deficient samples, the photocurrent dropped, which could be attributed to accumulation of organic species at the grain boundaries, low charge carrier mobility, and decreased electron injection into the TiO2. The PbI2-deficient compositions did, however, also have advantages. The record Voc was as high as 1.20 V and was found in PbI2-deficient samples. This was correlated with high crystal quality, longer charge carrier lifetimes, and high PL yields and was rationalized as a consequence of the dynamics of the perovskite formation. We further found the ion migration to be obstructed in the PbI2-deficient samples, which decreased the JV hysteresis and increased the photostability. PbI2-deficient synthesis conditions can thus be used to deposit perovskites with excellent crystal quality but with the downside of grain boundaries enriched in organic species, which act as a barrier toward current transport. Exploring ways to tune the synthesis conditions to give the high crystal quality obtained under PbI2-poor condition while maintaining the favorable grain boundary characteristics obtained under PbI2-rich conditions would thus be a strategy toward more efficiency devices.

Temperature dependence of charge carrier generation in organic photovoltaics.

The charge generation mechanism in organic photovoltaics is a fundamental yet heavily debated issue. All the generated charges recombine at the open-circuit voltage (V_{OC}), so that investigation of recombined charges at V_{OC} provides a unique approach to understanding charge generation. At low temperatures, we observe a decrease of V_{OC}, which is attributed to reduced charge separation. Comparison between benchmark polymer:fullerene and polymer:polymer blends highlights the critical role of charge delocalization in charge separation and emphasizes the importance of entropy in charge generation.

[Psychodynamically oriented inpatient psychotherapy of depressive disorders - First findings from a naturalistic, multicenter study]. / Stationäre tiefenpsychologisch orientierte Psychotherapie bei depressiven Störungen (STOP-D) - Erste Befunde einer naturalistischen, multizentrischen Wirksamkeitsstudie.

OBJECTIVES: While the general effectiveness of psychodynamic psychotherapy in both outpatient and inpatient treatment has been proven, few studies document the effectiveness of clinical inpatient treatment of depression through psychodynamic psychotherapy. METHODS: This paper presents first results of a naturalistic multicenter intervention study. Included were female inpatients suffering from depressive symptoms who had been admitted to 15 psychodynamically oriented psychosomatic hospital units (N = 487). The mean duration of treatment was 61.8 days. Data were acquired at admission (T1) and discharge (T2). RESULTS: Our findings support previous evidence and show that psychodynamically oriented inpatient psychotherapy of depressive disorders is efficient. High pre-post effect sizes were documented in all psychometric instruments used (BDI, HAM-D, SCL-90-R, BSS, GAF). Initial subgroup comparisons reveal that the benefits for patients with comorbid personality disorder are significantly lower than for depressed patients without comorbid personality disorder. CONCLUSION: Psychodynamic inpatient psychotherapy, as practiced under naturalistic conditions, is an effective treatment of depression. Predictors of therapeutic effects within different therapeutic settings, however, remain unclear. The sustainability of the therapeutic effects found and their impact on psychodynamic relevant constructs have still to be proven.

Decreasing exciton dissociation rates for reduced voltage losses in organic solar cells.

Enhancing the device electroluminescence quantum efficiency (EQEEL) is a critical factor in mitigating non-radiative voltage losses (VNR) and further improving the performance of organic solar cells (OSCs). While the common understanding attributes EQEEL in OSCs to the dynamics of charge transfer (CT) states, persistent efforts to manipulate these decay dynamics have yielded limited results, with the EQEEL of high-efficiency OSCs typically remaining below 10-2%. This value is considerably lower than that observed in high efficiency inorganic photovoltaic devices. Here, we report that EQEEL is also influenced by the dissociation rate constant of singlet states (kDS). Importantly, in contrast to the traditional belief that advocates maximizing kDS for superior photovoltaic quantum efficiency (EQEPV), a controlled reduction in kDS is shown to enhance EQEEL without compromising EQEPV. Consequently, a promising experimental approach to address the VNR challenge is proposed, resulting in a significant improvement in the performance of OSCs.

Interface Modification for Efficient and Stable Inverted Inorganic Perovskite Solar Cells.

Due to their excellent thermal stability and ideal bandgap, metal halide inorganic perovskite based solar cells (PSCs) with inverted structure are considered as an excellent choice for perovskite/silicon tandem solar cells. However, the power conversion efficiency (PCE) of inverted inorganic perovskite solar cells (PSCs) still lags far behind that of conventional n-i-p PSCs due to interfacial energy level mismatch and high nonradiative charge recombination. Herein, the performance of inverted PSCs is significantly improved by interfacial engineering of CsPbI3- x Brx films with 2-mercapto-1-methylimidazole (MMI). It is found that the mercapto group can preferably react with the undercoordinated Pb2+ from perovskite by forming Pb-S bonds, which appreciably reduces the surface trap density. Moreover, MMI modification results in a better energy level alignment with the electron-transporting material, promoting carrier transfer and reducing voltage deficit. The above combination results in an open-circuit voltage enhancement by 120 mV, yielding a champion PCE of 20.6% for 0.09 cm2 area and 17.3% for 1 cm2 area. Furthermore, the ambient, operational and heat stabilities of inorganic PSCs with MMI modification are also greatly improved. The work demonstrates a simple but effective approach for fabricating highly efficient and stable inverted inorganic PSCs.

Combined Vacuum Evaporation and Solution Process for High-Efficiency Large-Area Perovskite Solar Cells with Exceptional Reproducibility.

Organic-inorganic hybrid perovskites exhibit outstanding performances in perovskite solar cells (PSCs). However, the complex solution chemistry of perovskites precursors renders it difficult to prepare large-area devices in a reproducible way, which is a prerequisite for the technology to make an impact beyond lab scale. Vacuum processing, instead, is an established technology for large-scale coating of thin films. However, with respect to the hybrid perovskites it is highly challenging due to the high vapor pressure of the organic ammonium halide. In this work, vacuum evaporation of lead iodide and solution processing of organic ammonium halide is combined to produce large-area homogeneous perovskite films with large grains in a highly reproducible way. The resulting PSCs achieve a power conversion efficiency (PCE) of 24.3% (certified 23.9%) on small area (0.10 cm2 ), 24.0% (certified 23.7%) on large area (1 cm2 ) and 20.0% for minimodule (16 cm2 ), and maintain 90% of its initial efficiency after 1000 h 1-sun operation. The vacuum evaporation prevents advert environmental effects on lead halide formation and guarantees a reproducible fabrication of high-quality large-area perovskite films, which opens a promising way for large-scale fabrication of perovskite optoelectronics.

[The influence of the attachment dimensions "anxiety" and "avoidance" on psychosomatic complaints]. / Zum Einfluss der Bindungsdimensionen "Angst" und "Vermeidung" auf den psychosomatischen Beschwerdedruck.

OBJECTIVES: In contemporary literature, insecure attachment styles have been identified as nonspecific vulnerability factors for psychosomatic disorders. Further, they are also associated with aggravation of the assessment of complaints (Maunder and Hunter 2001; Strauß and Schwark 2007). The present study investigates the extent to which attachment-related anxiety and avoidance are related with the intensity of psychosomatic complaints. METHODS: Prior to an initial diagnostic interview, 166 patients from a psychosomatic outpatient department were tested with the questionnaires ECR-RD and SCL-90-R. A model of two latent attachment dimensions, fear (BANG) and avoidance (BVER) in close relationships, underlying the scales of the ECR-RD, was used (Ehrenthal et al. 2009). The GSI was chosen as a good validated, global value from SCL-90-R (Franke 2002) for measuring the psychosomatic pressure caused by complaints. RESULT: As expected, our results demonstrate strong positive correlations between BANG and GSI, whereas BVER and GSI showed a moderate, positive connection. Thus, both attachment dimensions were able to predict a significant ratio of GSI in a multiple regression analysis. CONCLUSION: This study confirmed a systematic relationship between insecure attachment representations and psychosomatic complaints, although some limitations must be noted due to the heterogeneous answer patterns of the BVER-scale. However, in our view, the ECR-RD measure should be used in other clinical studies, the goal being to become a diagnostic standard screening tool for assessing the influence of patients' attachment style on their presentation of psychosomatic complaints.

Simultaneous Lattice Engineering and Defect Control via Cadmium Incorporation for High-Performance Inorganic Perovskite Solar Cells.

Doping of all-inorganic lead halide perovskites to enhance their photovoltaic performance and stability has been reported to be effective. Up to now most studies have focused on the doping of elements in to the perovskite lattice. However, most of them cannot be doped into the perovskite lattice and the roles of these dopants are still controversial. Herein,the authors introduce CdI2 as an additive into CsPbI3-x Brx and use it as active layer to fabricate high-performance inorganic perovskite solar cells (PSCs). Cd with a smaller radius than Pb can partially substitute Pb in the perovskite lattice by up to 2 mol%. Meanwhile, the remaining Cd stays on the surface and grain boundaries (GB) of the perovskite film in the form of Cs2 CdI4-x Br-x , which is found to reduce non-radiative recombination. These effects result in prolonged charge carrier lifetime, suppressed defect formation, decreased GBs, and an upward shift of energybands in the Cd-containing film. A champion efficiency of 20.8% is achieved for Cd-incorporated PSCs, together with improved device ambient stability. This work highlights the importance of simultaneous lattice engineering, defectcontrol and atomic-level characterization in achieving high-performance inorganic PSCs with well-defined structure-property relationships.

Double Layer Composite Electrode Strategy for Efficient Perovskite Solar Cells with Excellent Reverse-Bias Stability.

Perovskite solar cells (PSCs) have become the representatives of next generation of photovoltaics; nevertheless, their stability is insufficient for large scale deployment, particularly the reverse bias stability. Here, we propose a transparent conducting oxide (TCO) and low-cost metal composite electrode to improve the stability of PSCs without sacrificing the efficiency. The TCO can block ion migrations and chemical reactions between the metal and perovskite, while the metal greatly enhances the conductivity of the composite electrode. As a result, composite electrode-PSCs achieved a power conversion efficiency (PCE) of 23.7% (certified 23.2%) and exhibited excellent stability, maintaining 95% of the initial PCE when applying a reverse bias of 4.0 V for 60 s and over 92% of the initial PCE after 1000 h continuous light soaking. This composite electrode strategy can be extended to different combinations of TCOs and metals. It opens a new avenue for improving the stability of PSCs.

A Transparent Electrode Based on Solution-Processed ZnO for Organic Optoelectronic Devices.

Achieving high-efficiency indium tin oxide (ITO)-free organic optoelectronic devices requires the development of high-conductivity and high-transparency materials for being used as the front electrode. Herein, sol-gel-grown zinc oxide (ZnO) films with high conductivity (460 S cm-1) and low optical absorption losses in both visible and near-infrared (NIR) spectral regions are realized utilizing the persistent photoinduced doping effect. The origin of the increased conductivity after photo-doping is ascribed to selective trapping of photogenerated holes by oxygen vacancies at the surface of the ZnO film. Then, the conductivity of the sol-gel-grown ZnO is further increased by stacking the ZnO using a newly developed sequential deposition strategy. Finally, the stacked ZnO is used as the cathode to construct ITO-free organic solar cells, photodetectors, and light emitting diodes: The devices based on ZnO outperform those based on ITO, owing to the reduced surface recombination losses at the cathode/active layer interface, and the reduced parasitic absorption losses in the electrodes of the ZnO based devices.

Multifunctional succinate additive for flexible perovskite solar cells with more than 23% power-conversion efficiency.

Flexible perovskite solar cells (FPSCs) have emerged as power sources in versatile applications owing to their high-efficiency characteristics, excellent flexibility, and relatively low cost. Nevertheless, undesired strain in perovskite films greatly impacts the power-conversion efficiency (PCE) and stability of PSCs, particularly in FPSCs. Herein, a novel multifunctional organic salt, methylammonium succinate, which can alleviate strain and reinforce grain boundaries, was incorporated into the perovskite film, leading to relaxed microstrain and a lower defect concentration. As a result, a PCE of 25.4% for rigid PSCs and a record PCE of 23.6% (certified 22.5%) for FPSCs have been achieved. In addition, the corresponding FPSCs exhibited excellent bending durability, maintaining ∼85% of their initial efficiency after bending at a 6 mm radius for 10 000 cycles.

Sequential vacuum-evaporated perovskite solar cells with more than 24% efficiency.

Vacuum evaporation is promising for the high-throughput fabrication of perovskite solar cells (PSCs) because of its solvent-free characteristic, precise control of film thickness, and compatibility with large-scale production. Nevertheless, the power conversion efficiency (PCE) of PSCs fabricated by vacuum evaporation lags behind that of solution-processed PSCs. Here, we report a Cl-containing alloy-mediated sequential vacuum evaporation approach to fabricate perovskite films. The presence of Cl in the alloy facilitates organic ammonium halide diffusion and the subsequent perovskite conversion reaction, leading to homogeneous pinhole-free perovskite films with few defects. The resulting PSCs yield a PCE of 24.42%, 23.44% (certified 22.6%), and 19.87% for 0.1, 1.0, and 14.4 square centimeters (mini-module, aperture area), respectively. The unencapsulated PSCs show good stability with negligible decline in performance after storage in dry air for more than 4000 hours. Our method provides a reproducible approach for scalable fabrication of large-area, high-efficiency PSCs and other perovskite-based optoelectronics.

Conformal quantum dot-SnO2 layers as electron transporters for efficient perovskite solar cells.

Improvements to perovskite solar cells (PSCs) have focused on increasing their power conversion efficiency (PCE) and operational stability and maintaining high performance upon scale-up to module sizes. We report that replacing the commonly used mesoporous-titanium dioxide electron transport layer (ETL) with a thin layer of polyacrylic acid-stabilized tin(IV) oxide quantum dots (paa-QD-SnO2) on the compact-titanium dioxide enhanced light capture and largely suppressed nonradiative recombination at the ETL-perovskite interface. The use of paa-QD-SnO2 as electron-selective contact enabled PSCs (0.08 square centimeters) with a PCE of 25.7% (certified 25.4%) and high operational stability and facilitated the scale-up of the PSCs to larger areas. PCEs of 23.3, 21.7, and 20.6% were achieved for PSCs with active areas of 1, 20, and 64 square centimeters, respectively.

[The so-called body-mind problem]. / Das so genannte Leib-Seele-Problem.

THE PROBLEM: Even psychosomatic researchers seem to want to avoid the so-called body-mind problem, which is actually a mind-brain problem. In line with Beckermann (2008), the first the four possible positions on the mind-brain problem are presented. The debate over the past 100 years has revolved around the question of whether mental events are ontologically independent of brain physiology or whether they are in fact entirely determined by it. Such a physicalism approach based on properties (i.e., mental characteristics or phenomena are physical or can be completely reduced to physical characteristics), however, is diametrically opposed to some of our strongest intuitions, e.g., that computers will never be able to develop qualities of human experience (qualia) and thus become subjects in the first person singular. Yet we are equally unable to prove the fundamental impossibility of such a development. THESIS: In this stalemate situation, a differentiation was undertaken by Gottlob Frege (1892) which could be of help: Expressed in today's language, a distinction is made between the sense of an expression, its contextual presentation (e.g., where there is a difference between "the evening star" and "the morning star"), on the one hand, and its so-called reference (the object to which it refers, here the planet Venus in both cases) on the other. The school of Gestalt psychology that developed in Berlin at the start of the last century similarly posited a "psychophysical level of the CNS," a continuum in a pattern of electrical field forces which manifests itself first in cerebral physiological-neuronal processes as well as in other perspectives such as consciousness and experience. A subsequent speculative concept then extends this model to assume also an (as yet) unknown Alpha configuration as being a common reference of two sense contents: (1) the results of the neurophysiological third-person perspective and (2) of the emotional-cognitive first-person perspectives. Only through the latter will Alpha be able to become self-conscious and an instance acting in his world. RESULTS: Only through the latter will Alpha be able to become self-conscious and an instance acting in his world. The postulate of an Alpha configuration thus retains the possibility of a biology not (yet) accessible to our knowledge, such that our fundamental conviction regarding the holism of soma and psyche can be maintained for us as medical practitioners and scientific physicians. Our patients need both, our medical-scientific competence (3rd-person perspective) as well as our empathic sensibility in exploring their phenomenal experience (1st-person perspective). They need us as medical artists.