The synergy between H2-activation on atomically dispersed Pd and H-addition on Cu–O–Ce interfaces guarantees the highly active and selective hydrogenation of several α,β-unsaturated aldehydes via hydrogen spillover.
BA2PbI4 is selected to passivate the surface defects of MAPbBr3 SCFs. The addition of BA interacts with MA vacancy through chemical bonding, thus reducing surface defect density to achieve high performance photo-detector.
A functional group implantation strategy was proposed to significantly enhance the birefringent performance by replacing isotropic [S]2⁻ ions in the chalcogenide [Ba₃S][GeS₄] with anisotropic π-conjugated [CO₃]2⁻ groups in the oxychalcogenide [Ba₃CO₃][MS₄] (M = Ge and Sn). This implantation of functional groups does not alter the overall structure; however, both optical anisotropy and birefringence are greatly improved.
The neoteric phosphorization-controlled method for the in-situ immobilization of core/satellite-structureded RuP/RuP2 Heterojunctions onto N,P co-doped porous carbon nanosheets as a high-performance HER electrocatalyst.
This study presents a novel bimetallic CuGa2 catalyst, utilizing p-d orbital hybridization to enhance electrochemical nitrogen fixation, achieving 9.82 μg h⁻1 cm⁻2 NH3 yield and 38.25% Faradaic efficiency.
This review highlights the structural design strategies of multiple-resonance thermally activated delayed fluorescence (MR-TADF) materials to mitigate π-π stacking through steric modulation. It explores their progress in concentration-independent OLEDs and addresses future challenges, promoting advancements in narrow-emission OLED technologies.
Here we review the recent advances in the biomolecule-directed synthesis and geometry control of chiral plasmonic nanomaterials and widen the scope of their potential applications. It is envisioned that these studies will pave the way toward the rational design of chiral plasmonic nanomaterials with desired optical properties for emerging applications.