The two-dimensional self-assembly behaviors of tetraphenylethylene (TPE) molecules are significant for further applications, but reports are rare. The self-assembled structures of two C2-symmetry TPE derivatives (H4TCPE and H4ETTC) possessing propeller structures and their stimulus responses to the addition of vinylpyridine derivatives were thoroughly studied with the assistance of scanning tunneling microscopy (STM) technique in combination with density functional theory (DFT) calculations. Although their chemical structures were similar, the H4TCPE and H4ETTC molecules self-assembled into closely packed lamellar and quadrilateral structures, respectively, at the 1-heptanoic acid/HOPG interface. After the addition of pyridine derivatives (DPE, PEBP-C4, and PEBP-C8), H4TCPE and H4ETTC showed different responsiveness resulting in different co-assembly structures. The results indicated that the structures of pyridine derivatives—including backbones and substituents—affected the intermolecular interactions of both H4TCPE/pyridine and H4ETTC/pyridine systems. The modification of the self-assembly behaviors of propeller-shaped H4TCPE and H4ETTC would contribute to the construction of more complex multilevel nanostructures.
With the great potential of the all-polymer solar cells for large-area wearable devices, both large-area device efficiency and mechanical flexibility are very critical but attract limited attention. In this work, from the perspective of the polymer configurations, two types of terpolymer acceptors PYTX-A and PYTX-B (X = Cl or H) are developed. The configuration difference caused by the replacement of non-conjugated units results in distinct photovoltaic performance and mechanical flexibility. Benefiting from a good match between the intrinsically slow film-forming of the active materials and the technically slow film-forming of the blade-coating process, the toluene-processed large-area (1.21 cm2) binary device achieves a record efficiency of 14.70%. More importantly, a new parameter of efficiency stretchability factor (ESF) is proposed for the first time to comprehensively evaluate the overall device performance. PM6:PYTCl-A and PM6:PYTCl-B yield significantly higher ESF than PM6:PY-IT. Further blending with non-conjugated polymer donor PM6-A, the best ESF of 3.12% is achieved for PM6-A:PYTCl-A, which is among the highest comprehensive performances. 相似文献
MODIS derived aerosol optical depths (AODs) at 550 nm are compared with sunphotometer CE318 measurements at 7 sites located at Yangtze River Delta (YRD) in China from July to October, 2007. The evaluation result indicates that MODIS AODs (Collection 5, C005) are in good agreement with those from CE318 in dense vegetation regions, but show more differences in those regions with complex underlying surface (such as at lake water and urban surface sites). Reasons for these differences are discussed after removing cases with significant errors caused by validation scheme. The final validation result shows that MODIS AODs are in good agreement with CE318 with a correlation coefficient of 0.85 and RMS of 0.15. 90% of MODIS cases fall in the range of Δτ = ± 0.05 ± 0.20τ, indicating MODIS aerosol retrieval algorithm, aerosol models and surface reflectance estimate are generally suitably reasonable for aerosol retrieval in YRD. However, MODIS AODs show a systemic errors with fitted line of y = 0.75x + 0.13, indicating underestimation of AOD when aerosol loadings are high. Aerosol models and surface reflectance estimations are dominant sources of MODIS aerosol retrieval errors. 相似文献
