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In recent years, tremendous growth has been seen for solution-processed bulk heterojunction solar cells (BHJSCs) using fullerene-free molecular acceptors. Herein, we report the synthesis, characterization of a coumarin-based organic semiconducting molecule C1, and its use in BHJSCs as an electron donor. The compound exhibited an absorption band at 472 nm in chloroform solution with an optical energy gap of 2.33 eV. The HOMO/LUMO energy levels of C1 were found to be ideal for use in BHJSCs. Using PC71BM and a fullerene-free acceptor IT-4F, the device generated power conversion efficiencies (PCEs) of 6.17 and 8.31%, respectively. The success of the device based on a fullerene-free acceptor is a result of complementary absorption and well-matched energy levels, resulting in an improved photocurrent and photovoltage in the device. Moreover, ternary solar cells fabricated by employing C1 (20 wt%) as a secondary donor, i.e., an active layer of C1PM6IT-4F (0.20.81.5), generated an enhanced PCE of 11.56% with a high short-circuit current density (JSC) of 16.42 mA cm-2, an open-circuit voltage (VOC) of 1.02 V, and a fill factor of 0.69 under 1 sun spectral illumination, which is ∼8% higher than that for the PM6IT-4F-based binary device (PCE = 10.70%). The increased PCE for the ternary organic solar cell may be related to the efficient exciton generation and its dissociation via Forster resonance energy transfer, which guarantees enough time for an exciton to diffuse toward the D/A interfaces.Fundamental understanding of the correlation between chemical bonding and lattice dynamics in intrinsically low thermal conductive crystalline solids is important to thermoelectrics, thermal barrier coating, and more recently to photovoltaics. Two-dimensional (2D) layered halide perovskites have recently attracted widespread attention in optoelectronics and solar cells. Here, we discover intrinsically ultralow lattice thermal conductivity (κL) in the single crystal of all-inorganic layered Ruddlesden-Popper (RP) perovskite, Cs2PbI2Cl2, synthesized by the Bridgman method. We have measured the anisotropic κL value of the Cs2PbI2Cl2 single crystal and observed an ultralow κL value of ∼0.37-0.28 W/mK in the temperature range of 295-523 K when measured along the crystallographic c-axis. First-principles density functional theory (DFT) analysis of the phonon spectrum uncovers the presence of soft (frequency ∼18-55 cm-1) optical phonon modes that constitute relatively flat bands due to localized vibrations of Cs and I atoms. https://www.selleckchem.com/products/oligomycin-a.html A further low energy optical mode exists at ∼12 cm-1 that originates from dynamic octahedral rotation around Pb caused by anharmonic vibration of Cl atoms induced by a 3s2 lone pair. We provide experimental evidence for such low energy optical phonon modes with low-temperature heat capacity and temperature-dependent Raman spectroscopic measurements. The strong anharmonic coupling of the low energy optical modes with acoustic modes causes damping of heat carrying acoustic phonons to ultrasoft frequency (maximum ∼37 cm-1). The combined effect of soft elastic layered structure, abundance of low energy optical phonons, and strong acoustic-optical phonon coupling results in an intrinsically ultralow κL value in the all-inorganic layered RP perovskite Cs2PbI2Cl2.The unprecedented synthesis of gem-difluoroalkenes through the Ramberg-Bäcklund reaction of alkyl triflones is described herein. Structurally diverse, fully substituted gem-difluoroalkenes that are difficult to prepare by other methods can be easily prepared from readily available triflones by treatment with specific Grignard reagents. Experimental and computational studies provide insight into the unique and critical role of the Grignard reagent, which serves both as a base to remove the α-proton and as a Lewis acid to assist C-F bond activation.Enzymes use a confined docking cavity and residual groups in the cavity to regulate substrate selectivity and catalytic activity. By mimicking enzymes, we herein report that metal-organic framework (MOF) KLASCC-1, with channels and inside-channel pyridyl groups, can promote orthoformate hydrolysis in basic solutions. By studying pH-dependent hydrolysis and using an analogue MOF that lacks inside-channel pyridyl groups, we proved protonated pyridyl groups as acid catalytic sites for orthoformate hydrolysis. By using MOFs with only open pyridyl groups, we demonstrated the necessity of the confined channels. X-ray diffraction structures of KLASCC-1 with encapsulated substrates confirmed that these channels can regulate activity and size selectivity. Recycling tests and crystallographic studies confirmed that KLASCC-1 kept its framework structure in catalysis. This work shows the potentials of using MOFs for host-guest catalysis that cannot be otherwise completed and underlines the advantages of using crystal engineering to identify active sites.Radiative cooling can alleviate urban heat island effects and passively improve personal thermal comfort. Among many emerging approaches, infrared (IR) transparent films and fabrics are promising because they can allow objects to directly radiate heat through bands of atmospheric transparency while blocking solar heating. However, achieving high solar reflectance while maintaining IR transmittance using scalable nanostructured materials requires control over the shape and size distribution of the nanoscale building blocks. Here, we investigate the scattering and transmission properties of electrospun polyacrylonitrile (PAN) nanofibers that feature spherical, ellipsoidal, and cylindrical morphologies. We find that nanofibers that have ellipsoidal beads exhibit the most efficient solar scattering, mainly due to the additive dielectric resonances of the ellipsoidal and cylindrical geometries, as confirmed through electromagnetic simulations. This favorable scattering decreases the amount of material needed to reach above 95% solar reflectance, which, in turn, enables high infrared transmittance (>70%) despite PAN's intrinsic IR absorption. We further show that these PAN nanofibers (nanoPAN) can enable cooling of surfaces with relatively low solar reflectance, which is demonstrated by covering a reference blackbody surface with beaded nanoPAN. During peak solar hours, this configuration lowers the temperature of the black surface by approximately 50 °C and is able to achieve as low as 3 °C below the ambient air temperature. More broadly, our demonstration using PAN, which is not as IR transparent as more commonly used polyethylene, provides a method for utilizing lower purity materials in radiative cooling.