RESUMEN
A polymer acceptor, named PX-1, is designed and synthesized using a polymerization strategy with grafted small molecule acceptors. This design approach allows for the freedom of end groups while maintaining efficient terminal packing, enhancing π-π interactions, and facilitating charge transport. All-polymer organic solar cells based on PM6: PX-1 demonstrate a promising efficiency of 13.55%. The result presents an alternative pathway for the design of high-efficiency polymer acceptors through the careful regulation of small molecule acceptor monomers and linker units.
Asunto(s)
Vendajes , Polímeros , PolimerizacionRESUMEN
All-weather personal thermal regulation has far been challenged by variable environments especially the regulatory failure caused by highly-dense solar radiation, low environmental radiation and the fluctuated epidermal moisture in different seasons. Herein, from the design of interface selectivity, dual-asymmetrically optical and wetting selective polylactic acid-based (PLA) Janus-type nanofabric is proposed to achieve on-demand radiative cooling and heating as well as sweat transportation. Hollow TiO2 particles are introduced in PLA nanofabric causing high interface scattering (â¼99%) and infrared emission (â¼91.2%) as well as surface hydrophobicity (CA > 140°). The strictly optical and wetting selectivity help achieve â¼12.8â of net cooling effect under > 1500 W/m2 of solar power and â¼5â of cooling advantage higher than cotton fabric and sweat resistance simultaneously. Contrarily, the semi-embedded Ag nanowires (AgNWs) with high conductivity (0.245 Ω/sq) endows the nanofabric with visible water permeability and excellent interface reflection for thermal radiation from body (>65%) thus causing â¼7â of thermal shielding. Through simple interface flipping, synergistical cooling-sweat reducing and warming-sweat resisting can be achieved to satisfy the thermal regulation in all weather. Compared with conventional fabrics, multi-functional Janus-type passive personal thermal management nanofabrics would be of great significance to achieve the personal health maintenance and energy sustainability.
RESUMEN
Suppressing intramolecular vibration of non-fullerene acceptors (NFAs) by molecular rigidification has been proven to be an effective way to reduce the non-radiative recombination loss and energetic disorder of organic solar cells (OSCs). Thus far, extensive attention has been drawn on rigidifying the fused-ring backbones of NFAs, whereas the highly flexible alkyl side chains are barely concerned. Herein, an effective strategy of side chain rigidification by introducing a spiro-ring is developed for the first time and applied to construct the NFA of Spiro-F. Compared to its counterpart F-2F, the rigid spirocyclic side chain can constrain the vibrational-rotational motion and control the orientation of two highly flexible n-octyl chains effectively. As a result, an optimal molecular packing with enhanced intermolecular actions and lower energetic disorder is achieved by Spiro-F, endowing the OSC based on the as cast blend of PM6:Spiro-F with a significantly improved PCE of 13.56% and much reduced recombination loss compared to that of PM6:F-2F. This work provides a feasible strategy to achieve efficient OSCs through the rigidification of the side chain and could boost the PCEs further if applied to some other efficient systems with smaller bandgaps.