We report on the fabrication of efficient annealing-free organic solar cells using co-solvent solution considered as a promising method for low-cost and time-saving manufacturing. Higher device efficiency could be obtained compared to the pure solvent casted device, resulting from the improved crystallinity, optical absorption and transport properties. The power conversion efficiency of 2.8% was obtained, demonstrating the feasibility of achieving low-cost and high-efficiency organic solar cells without any additional treatment and processing additives. 相似文献
Water transport is critical to the successful implementation of polymer electrolyte fuel cells (PEFC), especially in long-term and dynamic operation in automotives. Liquid water appears in the fuel cells not only from the water generated at the cathode catalyst layer but also as a result of condensation of water vapor from the humidified gases. In this study, we report a simple approach to prepare a superhydrophobic gas diffusion layer by chemical vapor deposition of polydimethylsiloxane without significant change in pore size of gas diffusion layer unlike other approach adding hydrophobic agent such as polytetrafluoroethylene. A superhydrophobic coating on the GDL can be obtained, leading to exceptionally enhanced power performance and stability of PEFC especially at a high current where water transport becomes more critical. 相似文献
Concise stereoselective syntheses of (?)-clavaminol A and deacetyl (+)-clavaminol H have been achieved from simple starting materials. Highlights of the synthesis for (?)-clavaminol A include a highly diastereoselective chelation-controlled hydride reduction of an amino ketone to give the anti amino alcohol directly, and NaBH4-mediated dehalogenation. The main synthetic approach for deacetyl (+)-clavaminol H features a highly diastereoselective chelation-controlled hydride reduction of the amino ketone to construct the anti amino alcohol and a palladium catalyzed hydrogenation reaction at the final step. 相似文献
It is shown that for the reported instances of “random” copolymerization in cationic systems, N values related to relative reactivity may be derived for monomers. The N values approximate reasonably well the values of the function, exp (-e) - 1.23, where e is the polarity e of the Q-e scheme for free-radical copolymerizations.
In a recent paper [1] it was shown that for the reported instances [2-4] of “random” copolymerization (r1,r2 = 1) in cationic systems, N values, related to relative reactivity, might be derived for monomers, employing styrene as a base monomer (N = 1). Thus d[M1]/d[M2] =N1[M1]/N2[M2] (1)
where d[M1]/d[M2] is the instantaneous copolymer composition, [M1]/[M2] is the ratio of unreacted monomers, and N1 and N2 are parameters related to general monomer reactivity of monomers 1 and 2, respectively, in cationic copolymerization. 相似文献
Interest in the copolymerizability of allyl glycidyl ether has been stimulated by recent industrial and academic interest in the monomer, because of its epoxy as well as allylic functionality, There is a paucity of information in the literature, however, concerning its copolymerization parameters with other monomers, and none, apparently, concerning its Q and e values. 相似文献
A m-xylene bridged imidazolium receptor 1 has been designed and synthesized. The receptor 1 utilizes two imidazole (C–H)+—anion hydrogen bonds and one aromatic hydrogen—anion hydrogen bond. The major driving force of complexation between the receptor 1 and anions comes from two imidazole (C–H)+—anion hydrogen bonding. However, some hydrogen bonding energy between aromatic hydrogen and anion exists, although it is expected to be much smaller than that of imidazole (C–H)+—anion hydrogen bonds. 相似文献
An arginine‐leucine block copolypeptide (R60L20) is synthesized, which is capable of forming vesicles with controllable sizes, able to transport hydrophilic cargo across the cell membrane, and exhibit relatively low cytotoxicity. The R60L20 vesicles also possess the ability to deliver DNA into mammalian cells for transfection. Although the transfection efficiency is lower than that of the commercially available transfection agent Lipofectamine 2000, the R60L20 vesicles are able to achieve transfection with significantly lower cytotoxicity and immunogenicity. This behavior is potentially due to its stronger interaction with DNA which subsequently provides better protection against anionic heparin.