Orthogonal Holographic and Multicolor Fluorescent Images via Aggregation Caused Quenching and Aggregation Induced Emission Nanoparticles with Förster Resonance Energy Transfer.

Achieving crosstalk-free, multimodal photopatterning within a single material element is crucial for enhancing information storage capacity and security. Herein, we report composite dye nanoparticles constructed via supramolecular encapsulation of aggregation-caused quenching (ACQ) dyes by an aggregation-induced emission (AIE) matrix. This architecture enables efficient Förster resonance energy transfer (FRET) from tetraphenylethylene (TPE) to 2,5-bis(4-(diethylamino)-benzylidene)cyclopentanone (BDEA), resulting in dual-mode optical encoding.

Inclusion Complexes of Photosensitizers with Cyclodextrins for Enhancing the Fabrication of Volume Grating.

A supramolecule photosensitizer (supra-photosensitizer) based on the host-guest complexation of cyclodextrins and a bis-chalcone dye (BDEA) was prepared. Methyl-β-cyclodextrin (Me-β-CD), with the highest inclusion rate, was confirmed as the best host among the four cyclodextrins. The host-guest properties of Me-β-CD and BDEA were characterized by FTIR, XRD, H NMR, PLQY, SEM, Job's plot, Benesi-Hildebrand plot, and others.

Priority Occupation of C-Sites by N-Confining P-Implantation in Pyrrodic N-Sites in NCNT@P,N-MoC for Highly Efficient Electrocatalytic Hydrogen Evolution.

Optimizing the electronic configuration of MoC by activating heteroatom(s)-neighboring carbon atoms to enhance the activity of hydrogen evolution reaction (HER) has been demonstrated. However, the development of heteroatom-doped MoC to fabricate a water electrolyzer is still a challenge because of the limitation of a well-defined electronic structure of hybridization of Mo with heteroatom(s). Here, nitrogen (N) and phosphor (P) codoped MoC embedded carbon nanotubes (NCNT@P,N-MoC) with the priority occupation of C-sites by N, which well confines the P-implantation at the pyrrodic N-sites and brings out N-O bonding on the surface, which favorably modifies the electronic configuration of adjacent Mo, resulting in highly efficient pH-tolerant HER activity.