Selenium atoms induce organic doped system to produce pure phosphorescence emission

A host-guest system is constructed using a guest containing two selenium atoms. The selenium atoms can increase the spin-orbit coupling constant and the conjugation degree, thereby increasing the emission wavelength,...

Emergence of Long Afterglow and Room Temperature Phosphorescence Emission from Ultra Small Sulfur Dots

Sulfur dots (S-dots) are one of the most recently developed non-metallic luminescent nanomaterials which possess several advantages over traditional inorganic Quantum dots (QDs). Here, we have synthesized highly luminescent ultra-small...

Structural, spectroscopic and DFT theoretical studies of phosphorescent CuIP2S-containing cuprous complexes

Luminescent cuprous complexes are important coordination compounds due to their relative abundance, low cost and ability to display excellent luminescence. The structures of two CuIP2S-type cuprous complexes, namely, iodido(thiourea-κS)bis(triphenylphosphane-κP)copper(I), [CuI(CH4N2S)(C18H15P)2] or [CuI(TU)(TPP)2] (I), and (2,3-dihydrobenzimidazole-2-thione-κS)iodidobis(triphenylphosphane-κP)copper(I), [CuI(C7H6N2S)(C18H15P)2] or [CuI(DHBIT)(TPP)2] (II), are described. In these two structures, the complex molecules of both are constructed by one copper(I) centre, one iodide ion, two TPP ligands and one thione ligand (TU for I and DHBIT for II). The copper(I) centres of I and II are both located in a distorted CuIP2S tetrahedron and are coordinated by two P atoms from two TPP ligands, one S atom from the thione ligand and the I atom. The UV–Vis absorption and photoluminescence properties of these CuIP2S-type cuprous complexes have been studied using crystalline powder samples. Detailed time-dependent density functional theory (TD-DFT) calculations and wavefunction analysis reveal that the pale-blue–green phosphorescence emission should originate from intra-ligand (TPP for I and DHBIT for II) charge transfer, with a small component of the metal-to-ligand charge transfer 3(IL+ML)CT excited state.

Simple Vanilla Derivatives for Long-Lived Room-Temperature Polymer Phosphorescence as Invisible Security Inks

Developing novel long-lived room-temperature polymer phosphorescence (RTPP) materials could significantly expand their application scope. Herein, a series of RTPP materials based on eight simple vanilla derivatives for security ink application are reported. Attributed to strong mutual hydrogen bonding with polyvinyl alcohol (PVA) matrix, vanilla-doped PVA films exhibit ultralong phosphorescence emission under ambient conditions observed by naked eyes, where methyl vanillate shows the longest emission time up to 7 s. Impressively, when vanilla-doped PVA materials are utilized as invisible security inks, and the inks not only present excellent luminescent emission stability under ambient conditions but also maintain perfect reversibility between room temperature and 65°C for multiple cycles. Owing to the unique RTPP performance, an advanced anticounterfeiting data encoding/reading strategy based on handwriting technology and complex pattern steganography is developed.

Novel ultrabright luminescent copper nanoclusters and application in light-emitting devices

Ultra-small tri/tetra-nuclear copper nanoclusters (Cu3/Cu4) exhibit ultrabright phosphorescence emission (Фem = 71.8 and 63.5%). Cu3 is firstly applied as a single component phosphor for white light-emitting diodes with favourable characteristics.

Pure room temperature phosphorescence emission of organic host-guest doped system with quantum efficiency of 64%

A new doped system with pure phosphorescent emission is constructed using four 1-(4-(diphenylamino)phenyl)-2-phenylethan-1-one derivatives containing halogen atoms as the guests and benzophenone as the host. That is, the doped system...

Ultrabright Au@Cu14 nanoclusters: 71.3% phosphorescence quantum yield in non-degassed solution at room temperature

The photoluminescence of metal nanoclusters is typically low, and phosphorescence emission is rare due to ultrafast free-electron dynamics and quenching by phonons. Here, we report an electronic engineering approach to achieving very high phosphorescence (quantum yield 71.3%) from a [Au@Cu14(SPhtBu)12(PPh(C2H4CN)2)6]+ nanocluster (abbreviated Au@Cu14) in non-degassed solution at room temperature. The structure of Au@Cu14 has a single-Au-atom kernel, which is encapsulated by a rigid Cu(I) complex cage. This core-shell structure leads to highly efficient singlet-to-triplet intersystem crossing and suppression of nonradiative energy loss. Unlike the phosphorescent organic materials and organometallic complexes—which require de-aerated conditions due to severe quenching by air (i.e., O2)—the phosphorescence from Au@Cu14 is much less sensitive to air, which is important for lighting and biomedical applications.