Red and Near-Infrared Thermally Activated Delayed Fluorescence Emitters Based on a Dibenzo[f,h]pyrido[2,3-b]quinoxaline Acceptor.

Recently, there has been growing interest in deep red (DR) and near-infrared (NIR) thermally activated delayed fluorescence (TADF) emitters due to their potential use in applications in bioimaging and night-vision displays. Herein, we designed and synthesized a series of red/NIR TADF emitters, DMAC, PXZ, and DPACz, that all contain the same electron-accepting PyBP (dibenzo [f, h] pyrido [2,3-b]quinoxaline) moiety. These compounds emit at 643 nm for DMACPyBP, 722 nm for DPACz PyBP, and 743 nm for PXZPyBP in toluene solution, while their thin films singlet-triplet energy gaps (ΔE) are <0.

Phosphinecarboxamide based InZnP QDs - an air tolerant route to luminescent III-V semiconductors.

We describe a new synthetic methodology for the preparation of high quality, emission tuneable InP-based quantum dots (QDs) using a solid, air- and moisture-tolerant primary phosphine as a group-V precursor. This presents a significantly simpler synthetic pathway compared to the state-of-the-art precursors currently employed in phosphide quantum dot synthesis which are volatile, dangerous and air-sensitive, P(Si(CH)).

Investigating the effect of N-doping on carbon quantum dots structure, optical properties and metal ion screening.

Carbon quantum dots (CQDs) derived from biomass, a suggested green approach for nanomaterial synthesis, often possess poor optical properties and have low photoluminescence quantum yield (PLQY). This study employed an environmentally friendly, cost-effective, continuous hydrothermal flow synthesis (CHFS) process to synthesise efficient nitrogen-doped carbon quantum dots (N-CQDs) from biomass precursors (glucose in the presence of ammonia). The concentrations of ammonia, as nitrogen dopant precursor, were varied to optimise the optical properties of CQDs.