The SAM layer which formed hydrogen-bonding to the methylammonium of the perovskite induced dipole moments at the interface, resulting in energy band bending and increased built-in voltage, and consequently, improved charge transfer of the PSC.

Solar energy conversion has emerged as an attractive pathway in the decomposition of hazardous organic pollutants. Herein, tridoped β-NaYF 4 :Yb 3+ ,Tm 3+ ,Gd 3+ upconversion (UC) nanorods were embedded in a carbon-doped mesostructured TiO 2 hybrid film using triblock copolymer P123 acting as a mesoporous template and carbon source. The photoactivity of our novel material was reflected in the degradation of nitrobenzene, as a representative organic waste. The broad-band absorption of our rationally designed UC nanorod-embedded C-doped TiO 2 in the UV to NIR range unveiled a remarkable increase in nitrobenzene degradation (83%) within 3 h compared with pristine TiO 2 (50%) upon light irradiation. These results establish for the first time a synergetic bridge between the effects of a creative photon trapping TiO 2 architecture, improved NIR light-harvesting efficiency upon UC nanorod incorporation, and a simultaneous decrease in the band gap energy and increased visible light absorption by C-doping of the oxide lattice. The resulting nanostructure was believed to favor efficient charge and energy transfer between the photocatalyst components and to reduce charge recombination. Our novel hybrid nanostructure and its underlined synthesis strategy reflect a promising route to improve solar energy utilization in environmental remediation and in a wide range of photocatalytic applications, e.g., water splitting, CO 2 reutilization, and production of fuels.

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Statin medications have been suggested for widespread use in patients with systemic lupus erythematosus (SLE). We studied the dose effectiveness and tolerability of pravastatin in SLE. We compared 41 SLE subjects in a two-month open-label dose-titration study of pravastatin to 22 SLE controls. Lipids, ALT, CPK, CRP, adverse effects were assessed. Linear mixed models assessed changes in lipids and CRP, comparing pravastatin subjects to controls. After 1 month of pravastatin 10 mg a day, total cholesterol decreased by 16% (+/-12.1%) and LDL by 24% (+/-17%), compared with 1.8% (+/-7.5%) and 2.6% (+/-8.6%) decreases in controls (P < 0.001). CRP did not decline. Glucocorticoids appeared to decrease pravastatin effectiveness. Serum CPK increased in one subject. Pravastatin reduced LDL and total cholesterol levels approximately the same degree observed in normal individuals, but the effect appeared blunted in those on modest doses of glucocorticoids and those with higher BMI.

Designing an efficient and stable hole transport layer (HTL) material is one of the essential ways to improve the performance of organic–inorganic perovskite solar cells (PSCs).

An efficient hole-transporting layer (HTL) based on functionalized two-dimensional (2D) MoS2-poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) composites has been developed for use in organic solar cells (OSCs). Few-layer, oleylamine-functionalized MoS2 (FMoS2) nanosheets were prepared via a simple and cost-effective solution-phase exfoliation method; then, they were blended into PEDOT:PSS, a conducting conjugated polymer, and the resulting hybrid film (PEDOT:PSS/FMoS2) was tested as an HTL for poly(3-hexylthiophene):[6,6]-phenyl-C61-butyric acid methyl ester (P3HT:PCBM) OSCs. The devices using this hybrid film HTL showed power conversion efficiencies up to 3.74%, which is 15.08% higher than that of the reference ones having PEDOT:PSS as HTL. Atomic force microscopy and contact angle measurements confirmed the compatibility of the PEDOT:PSS/FMoS2 surface for active layer deposition on it. The electrical impedance spectroscopy analysis revealed that their use minimized the charge-transfer resistance of the OSCs, consequently improving their performance compared with the reference cells. Thus, the proposed fabrication of such HTLs incorporating 2D nanomaterials could be further expanded as a universal protocol for various high-performance optoelectronic devices.

To harness the full potential of halide perovskite based optoelectronics, biological safety, compatibility with flexible/ stretchable platforms, and operational stability must be guaranteed. Despite substantial efforts, none has come close to providing a solution that encompasses all of these requirements. To address these issues, we devise a multifunctional encapsulation scheme utilizing hydrogen bond-based self-recovering polymeric nanomaterials as an alternative for conventional glass-based encapsulation. We show that Pb in physically damaged halide perovskite solar cells can be completely contained within the self-recovering encapsulation upon submersion in a simulated rain bath, as indicated by in vitro cytotoxicity tests. In addition, self-recovering encapsulation accommodates stable device operation upon casual bending and even stretching, which is in stark contrast to conventional glass-based encapsulation schemes. We also demonstrate the concept of assembling user-defined scalable modular optoelectronics based on halide perovskite solar cells and light emitting diodes through the use of self-recovering conductive nanocomposites. Finally, long-term operational stability of over 1000 h was achieved under harsh accelerated conditions (50 °C/50% RH and 85 °C/0% RH) with the incorporation of an ultrathin atomic layer deposited TiO 2 barrier underneath the multifunctional encapsulation. In light of these merits, the encapsulation scheme based on self-recovering polymeric nanomaterials is proposed as a simple, but practical solution to a multifaceted challenge in the field of halide perovskites.