RESUMEN
Both the regional isomerization and selenium-substitution of the small molecular acceptors (SMAs) play significant roles in developing efficient organic solar cells (OSCs), while their synergistic effects remain elusive. Herein, we developed three isomeric SMAs (S-CSeF, A-ISeF, and A-OSeF) via subtly manipulating the mono-selenium substituted position (central, inner, or outer) and type of heteroaromatic ring on the central core by synergistic strategies for efficient OSCs, respectively. Crystallography of asymmetric A-OSeF presents a closer intermolecular π-π stacking and more ordered 3-dimensional network packing and efficient charge-hopping pathways. With the successive out-shift of the mono-selenium substituted position, the neat films give a slightly wider band gap and gradually higher crystallinity and electron mobility. The PM1 : A-OSeF afford favourable fibrous phase separation morphology with more ordered molecular packing and efficient charge transportation compared to the other two counterparts. Consequently, the A-OSeF-based devices achieve a champion efficiency of 18.5 %, which represents the record value for the reported selenium-containing SMAs in binary OSCs. Our developed precise molecular engineering of the position and type of selenium-based heteroaromatic ring of SMAs provides a promising synergistic approach to optimizing crystal stacking and boosting top-ranked selenium-containing SMAs-based OSCs.
RESUMEN
In this work, TiO2 nanofiber membrane (NFM) with a complete surface microstructure was prepared through regulating the surface microstructure of TiO2 NFM by doping Zr. The crystal structures and morphological analyses indicated that the nanofiber membranes were consisted by disordered accumulation of Zr-doped TiO2 nanofibers with a crack-free surface, small grain size and high aspect ratio. When the doping amount of Zr was 0.8 mL, the tensile strength of the doped membranes reached 1.27 MPa, which was 60.7% higher than that of pure TiO2 NFM. The photocatalytic performance of Zr-doped TiO2 NFM was evaluated by the degradation performance of Methylene orange (MO) under simulated sunlight irradiation. Compared with the undoped TiO2 NFM, the 0.8-Zr/TiO2 NFM presented a higher catalytic degradation efficiency (improved by 69.6%), and the photocatalytic performance maintained stable after five circulating. It was found that the doping of Zr ions effectively limited the surface crack size and grain size of TiO2 nanofibers, thereby improving the tensile strength, and enhanced the surface area effect and carrier transfer efficiency of TiO2 NFM. On the other hand, a narrow band-gap was obtained by doping a small amount of Zr ions, which expanded the visible light response range to improve the photocatalytic performance of TiO2 nanofibers.
Asunto(s)
Nanofibras , Nanofibras/química , Luz , Titanio/químicaRESUMEN
Water was the source of life, in order to solve the serious water pollution problem facing the world, researchers have proposed many solutions. Among them, photoelectric catalytic technology based on semiconductor materials was an ideal and sustainable solution. Herein, by combining successive ionic layer adsorption and reaction (SILAR) with sol-gel electrospinning two strategies, a novel S-scheme heterojunction based on flexible and hierarchical BiOI/TiO2 nanofibrous membranes (BiOI/TiO2 NFM) was fabricated. The degradation rates of tetracycline (TC) and Rhodamine B (RHB) were 98.7% and 95.6%, respectively, under visible light irradiation. The main reason, except for the benefits offered by the hierarchical nanofiber structure, such as the large surface area, tightly connected interfaces and more exposed active sites, other advantages derived from photogenerated carrier transfer and superior redox ability were also momentous. To reveal the formed S-scheme heterojunction, a variety of test methods were used to characterize and test. These studies showed a significant increase in charge separation efficiency in the BiOI/TiO2 NFM, and the charge transport of S-scheme heterojunction was demonstrated. This study may offer new design ideas for the design and construction of novel structures of S-scheme heterojunctions.