The hierarchical photocatalysts of Ag/AgCl@plate-WO₃ have been synthesized by anchoring Ag/AgCl nanocrystals on the surfaces of single-crystalline WO₃ nanoplates that were obtained via an intercalation and topochemical approach. The heterogeneous precipitation process of the PVP-Ag⁺-WO₃ suspensions with a Cl⁻ solution added drop-wise was developed to synthesize AgCl@WO₃ composites, which were then photoreduced to form Ag/AgCl@WO₃ nanostructures in situ. WO₃ nanocrystals with various shapes (i.e., nanoplates, nanorods, and nanoparticles) were used as the substrates to synthesize Ag/AgCl@WO₃ photocatalysts, and the effects of the WO₃ contents and photoreduction times on their visible-light-driven photocatalytic performance were investigated. The techniques of TEM, SEM, XPS, EDS, XRD, N₂ adsorption-desorption and UV-vis DR spectra were used to characterize the compositions, phases and microstructures of the samples. The RhB aqueous solutions were used as the model system to estimate the photocatalytic performance of the as-obtained Ag/AgCl@WO₃ nanostructures under visible light (λ ≥ 420 nm) and sunlight. The results indicated that the hierarchical Ag/AgCl@plate-WO₃ photocatalyst has a higher photodegradation rate than Ag/AgCl, AgCl, AgCl@WO₃ and TiO₂ (P25). The contents and morphologies of the WO₃ substrates in the Ag/AgCl@plate-WO₃ photocatalysts have important effects on their photocatalytic performance. The related mechanisms for the enhancement in visible-light-driven photodegradation of RhB molecules were analyzed.

Single junction binary all-small-molecule (ASM) organic solar cells (OSCs) with power conversion efficiency (PCE) beyond 14% are achieved by using non-fullerene acceptor Y6 as the electron acceptor, but still lag behind that of polymer OSCs. Herein, an asymmetric Y6-like acceptor, BTP-FCl-FCl, is designed and synthesized to match the recently reported high performance small molecule donor BTR-Cl, and a record efficiency of 15.3% for single-junction binary ASM OSCs is achieved. BTP-FCl-FCl features a F,Cl disubstitution on the same end group affording locally asymmetric structures, and so has a lower total dipole moment, larger average electronic static potential, and lower distribution disorder than those of the globally asymmetric isomer BTP-2F-2Cl, resulting in improved charge generation and extraction. In addition, BTP-FCl-FCl based active layer presents more favorable domain size and finer phase separation contributing to the faster charge extraction, longer charge carrier lifetime, and much lower recombination rate. Therefore, compared with BTP-2F-2Cl, BTP-FCl-FCl based devices provide better performance with FF enhanced from 71.41% to 75.36% and J sc increased from 22.35 to 24.58 mA cm −2 , leading to a higher PCE of 15.3%. The locally asymmetric F, Cl disubstitution on the same end group is a new strategy to achieve high performance ASM OSCs.

Attributed to the rapid development of benzodithiophene (BDT) centered small molecule donors, all small molecule organic solar cells (ASM-OSCs) have achieved comparable power conversion efficiency (PCE) (>15%) along with high...