Search Results (16)

Organic–inorganic hybrid flexible perovskite solar cells (F-PSCs) have garnered considerable interest owing to their exceptional power conversion efficiency (PCE) and stable operational characteristics. However, F-PSCs continue to exhibit significantly lower PCE than their rigid counterparts. Herein, we employed 3-chloro-4-methoxybenzylamine hydrochloride (CMBACl) treatment to grow in situ two-dimensional (2D) perovskite layers on three-dimensional (3D) perovskite films. Through comprehensive physicochemical characterization, including X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and photoluminescence (PL) mapping, we demonstrated that CMBACl treatment enabled the in situ growth of two-dimensional (2D) perovskite layers on three-dimensional (3D) perovskite films via chemical interactions between CMBA⁺ cations and undercoordinated Pb²⁺ sites. The organic cation (CMBA⁺) bound to uncoordinated Pb²⁺ ions and residual PbI₂, while the chlorine anion (Cl⁻) filled iodine vacancies in the perovskite lattice, thereby forming a high-quality 2D/3D heterojunction structure. The CMBACl treatment effectively passivated surface defects in the perovskite films, prolonged charge carrier lifetimes, and enhanced the operational stability of the photovoltaic devices. Additionally, the hybrid 2D/3D architecture also improved energy band matching, thereby boosting charge transfer performance. The optimized flexible devices demonstrated a PCE of 23.15%, while retaining over 82% of their initial efficiency after enduring 5000 bending cycles under a 5 mm curvature radius (R = 5 mm). The unpackaged devices retained 94% of their initial efficiency after 1000 h under ambient conditions with a relative humidity (RH) of 45 ± 5%. This strategy offers practical guidelines for selecting interface passivation materials to enhance the efficiency and stability of F-PSCs. Full article

A facile interconnected nanofibre electrode material derived from polybenzimidazol (PBI) was fabricated for a supercapacitor using a centrifugal spinning technique. The PBI solution in a mixture of dimethyl acetamide (DMA) and N, N-dimethylformamide (DMF) was electrospun to an interconnection of fine nanofibres. The as-prepared material was characterised by using various techniques, which include scanning electron microscopy (SEM), X-ray diffractometry (XRD), Raman, X-ray photoelectron spectroscopy (XPS), and Brunauer–Emmett–Teller (BET) among others. The specific surface area of the interconnected NCF material was noticed to be around 49 m² g⁻¹. Electrochemical properties of the material prepared as a single-electrode are methodically studied by adopting cyclic voltammetry, electrochemical impedance spectroscopy, and constant-current charge–discharge techniques. A maximum specific capacitance of 78.4 F g⁻¹ was observed for the electrode at a specific current of 0.5 A g⁻¹ in a 2.5 M KNO₃ solution. The electrode could also retain 96.7% of its initial capacitance after a 5000 charge–discharge cycles at 5 A g⁻¹. The observed capacitance and good cycling stability of the electrode are supported by its specific surface area, pore volume, and conductivity. The results obtained for this material indicate its potential as suitable candidate electrode for supercapacitor application. Full article

In the field of perovskite optoelectronics, developing hole-transporting materials (HTMs) on the spiro[fluorene-9,9′-xanthene] (SFX) platform is one of the current research focuses. The SFX inherits the merits of spirobifluorene in terms of the configuration and property, but it is more easily derivatized and regulated by virtue of its binary structure. In this work, we design and synthesize four isomeric SFX-based HTMs, namely m-SFX-mF, p-SFX-mF, m-SFX-oF, and p-SFX-oF, through varying the positions of fluorination on the peripheral aniline units and their substitutions on the SFX core, and the optoelectronic performance of the resulting HTMs is evaluated in both perovskite solar cells (PSCs) and light-emitting diodes (PeLEDs) by the vacuum thermal evaporating hole-transporting layers (HTLs). The HTM p-SFX-oF exhibits an improved power conversion efficiency of 15.21% in an inverted PSC using CH₃NH₃PbI₃ as an absorber, benefiting from the deep HOMO level and good HTL/perovskite interface contact. Meanwhile, the HTM m-SFX-mF provides a maximum external quantum efficiency of 3.15% in CsPb(Br/Cl)₃-based PeLEDs, which is attributed to its perched HOMO level and shrunken band-gap for facilitating charge carrier injection and then exciton combination. Through elucidating the synergistic position effect of fluorination on aniline units and their substitutions on the SFX core, this work lays the foundation for developing low-cost and efficient HTMs in the future. Full article

High-temperature polymer-electrolyte membrane fuel cells (HT-PEMFCs) are a very important type of fuel cells since they operate at 150–200 °C, making it possible to use hydrogen contaminated with CO. However, the need to improve the stability and other properties of gas-diffusion electrodes still impedes their distribution. Self-supporting anodes based on carbon nanofibers (CNF) are prepared using the electrospinning method from a polyacrylonitrile solution containing zirconium salt, followed by pyrolysis. After the deposition of Pt nanoparticles on the CNF surface, the composite anodes are obtained. A new self-phosphorylating polybenzimidazole of the 6F family is applied to the Pt/CNF surface to improve the triple-phase boundary, gas transport, and proton conductivity of the anode. This polymer coating ensures a continuous interface between the anode and proton-conducting membrane. The polymer is investigated using CO₂ adsorption, TGA, DTA, FTIR, GPC, and gas permeability measurements. The anodes are studied using SEM, HAADF STEM, and CV. The operation of the membrane–electrode assembly in the H₂/air HT-PEMFC shows that the application of the new PBI of the 6F family with good gas permeability as a coating for the CNF anodes results in an enhancement of HT-PEMFC performance, reaching 500 mW/cm² at 1.3 A/cm² (at 180 °C), compared with the previously studied PBI-O-PhT-P polymer. Full article

In this study, a KrF excimer laser with a high-absorption coefficient in metal oxide films and a wavelength of 248 nm was selected for the post-processing of a film and metal oxide thin film transistor (MOTFT). Due to the poor negative bias illumination stress (NBIS) stability of indium gallium zinc oxide thin film transistor (IGZO-TFT) devices, terbium-doped Tb:In₂O₃ material was selected as the target of this study. The XPS test revealed the presence of both Tb³⁺ and Tb⁴⁺ ions in the Tb:In₂O₃ film. It was hypothesized that the peak of the laser thermal effect was reduced and the action time was prolonged by the f-f jump of Tb³⁺ ions and the C-T jump of Tb⁴⁺ ions during the laser treatment. Studies related to the treatment of Tb:In₂O₃ films with different laser energy densities have been carried out. It is shown that as the laser energy density increases, the film density increases, the thickness decreases, the carrier concentration increases, and the optical band gap widens. Terbium has a low electronegativity (1.1 eV) and a high Tb-O dissociation energy (707 kJ/mol), which brings about a large lattice distortion. The Tb:In₂O₃ films did not show significant crystallization even under laser energy density treatment of up to 250 mJ/cm². Compared with pure In₂O₃-TFT, the doping of Tb ions effectively reduces the off-state current (1.16 × 10⁻¹¹ A vs. 1.66 × 10⁻¹² A), improves the switching current ratio (1.63 × 10⁶ vs. 1.34 × 10⁷) and improves the NBIS stability (ΔV_ON = −10.4 V vs. 6.4 V) and positive bias illumination stress (PBIS) stability (ΔV_ON = 8 V vs. 1.6 V). Full article

We investigated the photochemical stability of PbX₂ (X = I and Br) halides by optical and X-ray photoelectron spectroscopy (XPS). The optical absorbance displayed a strong reduction for PbI2 with light soaking and permanent behavior for PbBr₂. The XPS survey spectra showed a sharp drop in the I:Pb ratio for PbI₂ from 1.63 to 1.14 with exposure time from 0 to 1000 h while for PbBr2, it remains practically unchanged (1.59–1.55). The measurements of the XPS Pb 4f and Pb 5d spectra have shown the partial photolysis of PbI₂ with the release of metallic lead whereas PbBr₂ demonstrated remarkable photochemical stability. According to the density functional theory (DFT), calculations of the metal and iodide vacancy formation energies for PbBr₂ are higher than for PbI₂ which confirms the better stability to light soaking. The high photochemical stability of PbBr₂ means that it can be used as excess under MAPbBr₃ perovskite synthesis to improve not only the power conversion efficiency but also stability to light soaking. Full article

This study is devoted to investigating the stability of metal–organic framework (MOF)-hybrid perovskites consisting of CH₃NH₃PbI₃ (MAPbI₃) and UiO-66 without a functional group and UiO-66 with different COOH, NH₂,and F functional groups under external influences including heat, light, and humidity. By conducting crystallinity, optical, and X-ray photoelectron spectra (XPS) measurements after long-term aging, all of the prepared MAPbI3@UiO-66 nanocomposites (with pristine UiO-66 or UiO-66 with additional functional groups) were stable to light soaking and a relative humidity (RH) of 50%. Moreover, the UiO-66 and UiO-66-(F)₄ hybrid perovskite films possessed a higher heat tolerance than the other two UiO-66 with the additional functional groups of NH₂ and COOH. Tthe MAPbI3@UiO-66-(F)₄ delivered the highest stability and improved optical properties after aging. This study provides a deeper understanding of the impact of the structure of hybrid MOFs on the stability of the composite films. Full article

This retrospective cross-sectional study aimed to explore interactions between signs of periodontal inflammation and systemic parameters in athletes. Members of German squads with available data on sports medical and oral examination were included. Groups were divided by gingival inflammation (median of papillary bleeding index, PBI ≥ median) and signs of periodontitis (Periodontal Screening Index, PSI ≥ 3). Age, gender, anthropometry, blood parameters, echocardiography, sports performance on ergometer, and maximal aerobic capacity (VO_2max) were evaluated. Eighty-five athletes (f = 51%, 20.6 ± 3.5 years) were included (PBI < 0.42: 45%; PSI ≥ 3: 38%). Most associations were not statistically significant. Significant group differences were found for body fat percentage and body mass index. All blood parameters were in reference ranges. Minor differences in hematocrit, hemoglobin, basophils, erythrocyte sedimentation rates, urea, and HDL cholesterol were found for PBI, in uric acid for PSI. Echocardiographic parameters (n = 40) did not show any associations. Athletes with PSI ≥ 3 had lower VO_2max values (55.9 ± 6.7 mL/min/kg vs. 59.3 ± 7.0 mL/min/kg; p = 0.03). In exercise tests (n = 30), athletes with PBI < 0.42 achieved higher relative maximal load on the cycling ergometer (5.0 ± 0.5 W/kg vs. 4.4 ± 0.3 W/kg; p = 0.03). Despite the limitations of this study, potential associations between signs of periodontal inflammation and body composition, blood parameters, and performance were identified. Further studies on the systemic impact of oral inflammation in athletes, especially regarding performance, are necessary. Full article

A facile solution process was employed to prepare CsPbI₃ as an anode material for Li-ion batteries. Rietveld refinement of the X-ray data confirms the orthorhombic phase of CsPbI₃ at room temperature. As obtained from bond valence calculations, strained bonds between Pb and I are identified within PbI₆ octahedral units. Morphological study shows that the as-prepared δ-CsPbI₃ forms a nanorod-like structure. The XPS analysis confirm the presence of Cs (3d, 4d), Pb (4d, 4f, 5d) and I (3p, 3d, 4d). The lithiation process involves both intercalation and conversion reactions, as confirmed by cyclic voltammetry (CV) and first-principles calculations. Impedance spectroscopy coupled with the distribution function of relaxation times identifies charge transfer processes due to Li metal foil and anode/electrolyte interfaces. An initial discharge capacity of 151 mAhg⁻¹ is found to continuously increase to reach a maximum of ~275 mAhg⁻¹ at 65 cycles, while it drops to ~240 mAhg⁻¹ at 75 cycles and then slowly decreases to 235 mAhg⁻¹ at 100 cycles. Considering the performance and structural integrity during electrochemical performance, δ-CsPbI₃ is a promising material for future Li-ion battery (LIB) application. Full article

Within the subcutaneous adipose tissue diseases, multiple symmetric lipomatosis (MSL) (syn.: Launois Bensaude Syndrome, Morbus Madelung, benign symmetric lipomatosis) is rare. The pathogenesis of MSL remains unclear. We investigated the largest German cohort of MSL patients to obtain anamnestic data and quality of life with a standard questionnaire. Twenty-nine patients with confirmed MSL were included and filled in a questionnaire designed for this study. The questionnaire assessed common anamnestic factors, such as quality of life (EQ-5D-3L) and subjective treatment goals and success (“Patient-Benefit-Index-Lymphedema”, PBI-L). The gender distribution of the patients involved in the study was m/f: 1/4 (male: n = 6 (21%); female n = 23 (79%)). While the exact pathophysiology of MSL remains unclear, a subset of patients’ positive family history suggests a strong genetic factor, sometimes compatible with autosomal dominant inheritance. Patients with MSL showed lower health states (EQ VAS Score: m = 51, sd = 24, range = 0–90) than the German norm population (m = 77). Around two thirds (68%) of patients reported relevant benefits of therapy (liposuction/lipectomy). In our cohort about one third of the patients reported a positive family history for MSL-like features. Additionally, at least in some patients, a strong genetic factor, compatible with autosomal dominant inheritance, seems a possible major driver of MSL development. Alcohol consumption and MSL development has to be regarded as a controversial issue. Patients suffering from MSL have a clear decrease in quality of life and a marked wish for treatment. Full article

Measurements of XPS survey, core levels (N 1s, O 1s, Pb 4f, I 3d), and valence band (VB) spectra of CH₃NH₃PbI₃ (MAPbI₃) hybrid perovskite prepared on different substrates (glass, indium tin oxide (ITO), and TiO₂) aged under different light-soaking conditions at room temperature are presented. The results reveal that the photochemical stability of MAPbI₃ depends on the type of substrate and gradually decreases when glass is replaced by ITO and TiO₂. Also, the degradation upon exposure to visible light is accompanied by the formation of MAI, PbI₂, and Pb⁰ products as shown by XPS core levels spectra. According to XPS O 1s and VB spectra measurements, this degradation process is superimposed on the partial oxidation of lead atoms in ITO/MAPbI₃ and TiO₂/MAPbI₃, for which Pb–O bonds are formed due to the diffusion of the oxygen ions from the substrates. This unexpected interaction leads to additional photochemical degradation. Full article

Non-geminate recombination, as one of the most relevant loss mechanisms in organic and perovskite solar cells, deserves special attention in research efforts to further increase device performance. It can be subdivided into first, second, and third order processes, which can be elucidated by the effects that they have on the time-dependent open-circuit voltage decay. In this study, analytical expressions for the open-circuit voltage decay exhibiting one of the aforementioned recombination mechanisms were derived. It was possible to support the analytical models with experimental examples of three different solar cells, each of them dominated either by first (PBDBT:CETIC-4F), second (PM6:Y6), or third (irradiated CH₃NH₃PbI₃) order recombination. Furthermore, a simple approach to estimate the dominant recombination process was also introduced and tested on these examples. Moreover, limitations of the analytical models and the measurement technique itself were discussed. Full article

Anthropogenic lead pollution is an environmental problem that threatens the quality of soils and waters and endangers living organisms in numerous surface and subsurface habitats. Lead coprecipitation on mineral surfaces through dissolution-recrystallization processes has long-term effects on lead bioavailability. Gypsum and calcite are among the most abundant and reactive rock forming minerals present in numerous geological settings. In this work, we studied the interaction of slightly acidic (pH_i = 5.5) Pb-bearing aqueous solutions ([Pb]_i = 1 and 10 mM) with crystals of gypsum and/or calcite under atmospheric conditions. This interaction resulted in a reduction of the concentration of lead in the liquid phase due to the precipitation of newly formed Pb-bearing solid phases. The extent of this Pb removal mainly depended on the nature of the primary mineral phase involved in the interaction. Thus, when gypsum was the only solid phase initially present in the system, the Pb-bearing liquid-gypsum interaction resulted in Pb removals in the 98–99.8% range, regardless of [Pb]_i. In contrast, when the interaction took place with calcite, Pb removal strongly depended on [Pb]_i. It reached 99% when [Pb]_i = 1 mM, while it was much more modest (~13%) when [Pb]_i = 10 mM. Interestingly, Pb-removal was maximized for both [Pb]_i (99.9% for solutions with [Pb]_i = 10 mM and 99.7% for solutions with [Pb]_i = 1 mM) when Pb-polluted solutions simultaneously interacted with gypsum and calcite crystals. Despite the large Pb removals found in most of the cases studied, the final Pb concentration ([Pb]_f) in the liquid phase was always well above the maximum permitted in drinking water (0.01 ppm), with the minimum ([Pb]_f = 0.7 ppm) being obtained for solutions with [Pb]_i = 1 mM after their interaction with mixtures of gypsum and calcite crystals. This result suggests that integrating the use of mixtures of gypsum-calcite crystals might help to develop more efficient strategies for in-situ decontaminating Pb-polluted waters through mineral coprecipitation processes. Full article

Anion exchange blend membranes (AEBMs) were prepared for use in Vanadium Redox Flow Batteries (VRFBs). These AEBMs consisted of 3 polymer components. Firstly, PBI-OO (nonfluorinated PBI) or F6-PBI (partially fluorinated PBI) were used as a matrix polymer. The second polymer, a bromomethylated PPO, was quaternized with 1,2,4,5-tetramethylimidazole (TMIm) which provided the anion exchange sites. Thirdly, a partially fluorinated polyether or a non-fluorinated poly (ether sulfone) was used as an ionical cross-linker. While the AEBMs were prepared with different combinations of the blend polymers, the same weight ratios of the three components were used. The AEBMs showed similar membrane properties such as ion exchange capacity, dimensional stability and thermal stability. For the VRFB application, comparable or better energy efficiencies were obtained when using the AEBMs compared to the commercial membranes included in this study, that is, Nafion (cation exchange membrane) and FAP 450 (anion exchange membrane). One of the blend membranes showed no capacity decay during a charge-discharge cycles test for 550 cycles run at 40 mA/cm² indicating superior performance compared to the commercial membranes tested. Full article

The commonly used electron transport material (6,6)-phenyl-C61 butyric acid methyl ester (PCBM) for perovskite solar cells (PSC) with inverted planar structures suffers from properties such as poor film-forming. In this manuscript, we demonstrate a simple method to improve the film-forming properties of PCBM by doping PCBM with poly(9,9-dioctylfluorene-co-benzothiadiazole) (F8BT) as the electron transport layer (ETL), which effectively enhances the performance of CH₃NH₃PbI₃ based solar cells. With 5 wt % F8BT in PCBM, the short circuit current (J_SC) and fill factor (FF) of PSC both significantly increased from 17.21 ± 0.15 mA·cm⁻² and 71.1 ± 0.07% to 19.28 ± 0.22 mA·cm⁻² and 74.7 ± 0.21%, respectively, which led to a power conversion efficiency (PCE) improvement from 12.6 ± 0.24% to 15 ± 0.26%. The morphology investigation suggested that doping with F8BT facilitated the formation of a smooth and uniform ETL, which was favorable for the separation of electron-hole pairs, and therefore, an improved performance of PSC. Full article