Browse
Submit Data
Databases
API
Help

Dataset Information

46 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Red-light excited efficient metal-free near-infrared room-temperature phosphorescent films.

ABSTRACT: A set of red-light-excited, metal-free room-temperature phosphorescence (RTP) systems was constructed with brominated phenolsulfonephthaleine derivatives. The best metal-free RTP system has the reddest near-infrared (NIR) RTP emission (λ_p = 819 nm) with the highest phosphorescence quantum yield (Φ_RTP = 3.0%) so far identified. The RTP emission can be switched ON-OFF by adding acid and alkali alternately. A logic operation with half-subtractor function and dual-channel response (visible light emission/NIR RTP emission) was also constructed based on these properties.

SUBMITTER: Sun S

PROVIDER: S-EPMC8866102 | biostudies-literature | 2022 Feb

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Publications

Red-light excited efficient metal-free near-infrared room-temperature phosphorescent films.

Sun Siyu S Ma Liangwei L Wang Jie J Ma Xiang X Tian He H

National science review 20210511 2

A set of red-light-excited, metal-free room-temperature phosphorescence (RTP) systems was constructed with brominated phenolsulfonephthaleine derivatives. The best metal-free RTP system has the reddest near-infrared (NIR) RTP emission (λ<sub>p</sub> = 819 nm) with the highest phosphorescence quantum yield (Φ<sub>RTP</sub> = 3.0%) so far identified. The RTP emission can be switched ON-OFF by adding acid and alkali alternately. A logic operation with half-subtractor function and dual-channel respo ...[more]

PMID: 35223047

Similar Datasets

Visible-Light-Excited Room Temperature Phosphorescent Carbon Dots.

Project description:Carbon dots (CDs) with a room temperature phosphorescent (RTP) feature have attracted considerable interest in recent years due to their fundamental importance and promising applications. However, the reported matrix-free RTP CDs only show short-wavelength (green to yellow) emissions and have to be triggered by ultraviolet (UV) light (below 400 nm), limiting their applications in certain fields. Herein, visible-light-excited matrix-free RTP CDs (named AA-CDs) with a long-wavelength (orange) emission are reported for the first time. The AA-CDs can be facilely prepared via a microwave heating treatment of L-aspartic acid (AA) in the presence of ammonia and they emit unique orange RTP in the solid state with visible light (420 nm) excitation just being switched off. Through the studies of the carbonization process, the C=O and C=N containing moieties in the AA-CDs are confirmed to be responsible for the observed RTP emission. Finally, the applications of AA-CDs in information encryption and anti-counterfeiting were preliminarily demonstrated.

| S-EPMC7153588 | biostudies-literature

Efficient Spin-Light-Emitting Diodes With Tunable Red to Near-Infrared Emission at Room Temperature.

Project description:Spin light-emitting diodes (spin-LEDs) are important for spin-based electronic circuits as they convert the carrier spin information to optical polarization. Recently, chiral-induced spin selectivity (CISS) has emerged as a new paradigm to enable spin-LED as it does not require any magnetic components and operates at room temperature. However, CISS-enabled spin-LED with tunable wavelengths ranging from red to near-infrared (NIR) has yet to be demonstrated. Here, chiral quasi-2D perovskites are developed to fabricate efficient spin-LEDs with tunable wavelengths from red to NIR region by tuning the halide composition. The optimized chiral perovskite films exhibit efficient circularly polarized luminescence from 675 to 788 nm, with a photoluminescence quantum yield (PLQY) exceeding 86% and a dissymmetry factor (glum) ranging from 8.5 × 10-3 to 2.6 × 10-2. More importantly, direct circularly polarized electroluminescence (CPEL) is achieved at room temperature in spin-LEDs. This work demonstrated efficient red and NIR spin-LEDs with the highest external quantum efficiency (EQE) reaching 12.4% and the electroluminescence (EL) dissymmetry factors (gEL) ranging from 3.7 × 10-3 to 1.48 × 10-2 at room temperature. The composition-dependent CPEL performance is further attributed to the prolonged spin lifetime as revealed by ultrafast transient absorption spectroscopy.

| S-EPMC11899487 | biostudies-literature

Metal ion-manipulated afterglow on rhodamine 6G derivative-doped room-temperature phosphorescent PVA films.

Project description:The long-lived room-temperature phosphorescence (RTP) originating from thiophene boronate polyvinyl alcohol (PVA) has enabled the creation of metal-ion-responsive RTP films doped with spirolactam ring-containing rhodamine 6G (1). In this study, RTP-active PVA films, namely, TDB@PVA and ATB@PVA, were prepared through boronate esterification of thiophene-2,5-diboronic acid (TDB) and 5-acetylthiophene-2-boronic acid (ATB) with the diol units of PVA. The delayed emission properties were evaluated, revealing an emission band at 477 nm with a turquoise afterglow for TDB@PVA and at 510 nm with a green afterglow for ATB@PVA after UV light irradiation ceased. The photophysical properties were assessed using TD-DFT and DFT calculations at the B3LYP/cc-pVDZ level. N-(rhodamine-6G)lactam dye with a salicylimine unit (1) was doped into the RTP-based PVA films, producing a multicolored afterglow upon the addition of metal ions. This phenomenon is explained by a triplet-to-singlet Förster-type resonance energy transfer process from the cross-linked thiophene boronate in PVA to the metal-ion-activated colored form of 1. This photophysical feature finds applicability in encryption techniques. Notably, the reversible metal-ligand coordination of 1 in the PVA system enabled a write/erase information process.

| S-EPMC11428105 | biostudies-literature

A facile way to obtain near-infrared room-temperature phosphorescent soft materials based on Bodipy dyes.

Project description:Research on pure organic room-temperature phosphorescent (RTP) materials has made great advances but near-infrared (NIR) RTP emitting materials are still rare. Novel amorphous acrylamide copolymers containing iodine substituted borondipyrromethene (Bodipy) were prepared to obtain strong absorption in the visible region and moderate RTP in the NIR region with much larger Stokes shift than the fluorescence emission of traditional Bodipy dyes. Expensive metals and crystallization were left out to avoid biotoxicity and strict preparation conditions. Monoiodo and diiodo-Bodipy derivatives were both designed to study the substitution effect of iodine atoms. Photophysical properties, phosphorescence quantum yield and lifetime were characterized. Gels with NIR RTP emission were facilely prepared with the incorporation of ureidopyrimidone (UPy) and N,N'-methylenebisacrylamide (MBAA). The mechanical properties of the gels were measured using a rheometer and the results showed that the gels displayed fast self-healing ability due to the strong quadruple hydrogen bonding between UPy moieties.

| S-EPMC7067252 | biostudies-literature

Clustering and halogen effects enabled red/near-infrared room temperature phosphorescence from aliphatic cyclic imides.

Project description:Pure organic room temperature phosphorescence (RTP) materials become increasingly important in advanced optoelectronic and bioelectronic applications. Current phosphors based on small aromatic molecules show emission characteristics generally limited to short wavelengths. It remains an enormous challenge to achieve red and near-infrared (NIR) RTP, particularly for those from nonaromatics. Here we demonstrate that succinimide derived cyclic imides can emit RTP in the red (665, 690 nm) and NIR (745 nm) spectral range with high efficiencies of up to 9.2%. Despite their rather limited molecular conjugations, their unique emission stems from the presence of the imide unit and heavy atoms, effective molecular clustering, and the electron delocalization of halogens. We further demonstrate that the presence of heavy atoms like halogen or chalcogen atoms in these systems is important to facilitate intersystem crossing as well as to extend through-space conjugation and to enable rigidified conformations. This universal strategy paves the way to the design of nonconventional luminophores with long wavelength emission and for emerging applications.

| S-EPMC9098632 | biostudies-literature

Excited-State Dynamics of Room-Temperature Phosphorescent Organic Materials Based on Monobenzil and Bisbenzil Frameworks.

Project description:Room-temperature phosphorescent (RTP) materials have been attracting tremendous interest, owing to their unique material characteristics and potential applications for state-of-the-art optoelectronic devices. Recently, we reported the synthesis and fundamental photophysical properties of new RTP materials based on benzil, i.e., fluorinated monobenzil derivative and fluorinated and non-fluorinated bisbenzil derivative analogues [Yamada, S. et al., Beilstein J. Org. Chem. 2020, 16, 1154-1162.]. To deeply understand their RTP properties, we investigated the excited-state dynamics and photostability of the derivatives by means of time-resolved and steady-state photoluminescence spectroscopies. For these derivatives, clear RTP emissions with lifetimes on the microsecond timescale were identified. Among them, the monobenzil derivative was found to be the most efficient RTP material, showing both the longest lifetime and highest amplitude RTP emission. Time-resolved photoluminescence spectra, measured at 77 K, and density functional theory calculations revealed the existence of a second excited triplet state in the vicinity of the first excited singlet state for the monobenzil derivative, indicative of the presence of a fast intersystem crossing pathway. The correlation between the excited state dynamics, emission properties, and conformational flexibility of the three derivatives is discussed.

| S-EPMC7504296 | biostudies-literature

Room-temperature phosphorescent transparent wood.

Project description:Transparent wood with high transmittance and versatility has attracted great attention as an energy-saving building material. Many studies have focused on luminescent transparent wood, while the research on organic afterglow transparent wood is an interesting combination. Here, we use luminescent difluoroboron β-diketonate (BF2bdk) compounds, methyl methacrylate (MMA), delignified wood, and initiators to prepare room-temperature phosphorescent transparent wood by thermal initiation polymerization. The resultant PMMA has been found to interact with BF2bdk via dipole-dipole interactions and consequently enhance the intersystem crossing of BF2bdk excited states. The transparent wood matrix can provide a rigid environment for BF2bdk triplets and serve as oxygen barrier to suppress non-radiative decay and oxygen quenching. The prepared afterglow material has the characteristics of diverse composition, long afterglow emission lifetimes, and high photoluminescence quantum yield. This afterglow transparent wood also demonstrates potential application value in areas such as high mechanical strength, good hydrophobicity, and high cost-effectiveness.

| S-EPMC11747176 | biostudies-literature

Room temperature phosphorescent wood hydrogel.

Project description:Room temperature phosphorescent (RTP) hydrogels exhibit great potential but show poor mechanical performance (Tensile strengthen <1 MPa) and non-tunable RTP performance, hindering their practical applications. Here, we develop wood hydrogel (W-hydrogel) by the in situ polymerization of acrylamide in the presence of delignified wood. As a result of the molecular interactions between the components of delignified wood and polyacrylamide, the W-hydrogel exhibit a tensile strengthen of 38.4 MPa and green RTP emission with a lifetime of 32.5 ms. Moreover, the tensile strength and RTP lifetime are increased to 153.8 MPa and 69.7 ms, upon treating W-hydrogel with ethanol. Significantly, the mechanical and RTP performance of W-hydrogel is switched by alternating "ethanol and water" treatments. Additionally, W-hydrogel is used as energy donor in order to produce red afterglow emission using RhB via an energy transfer process. Taking advantage of these properties, W-hydrogel is processed into multiple hydrogel-based luminescent materials.

| S-EPMC11618341 | biostudies-literature

Two-photon excited deep-red and near-infrared emissive organic co-crystals.

Project description:Two-photon excited near-infrared fluorescence materials have garnered considerable attention because of their superior optical penetration, higher spatial resolution, and lower optical scattering compared with other optical materials. Herein, a convenient and efficient supramolecular approach is used to synthesize a two-photon excited near-infrared emissive co-crystalline material. A naphthalenediimide-based triangular macrocycle and coronene form selectively two co-crystals. The triangle-shaped co-crystal emits deep-red fluorescence, while the quadrangle-shaped co-crystal displays deep-red and near-infrared emission centered on 668 nm, which represents a 162 nm red-shift compared with its precursors. Benefiting from intermolecular charge transfer interactions, the two co-crystals possess higher calculated two-photon absorption cross-sections than those of their individual constituents. Their two-photon absorption bands reach into the NIR-II region of the electromagnetic spectrum. The quadrangle-shaped co-crystal constitutes a unique material that exhibits two-photon absorption and near-infrared emission simultaneously. This co-crystallization strategy holds considerable promise for the future design and synthesis of more advanced optical materials.

| S-EPMC7493989 | biostudies-literature

Efficient Red/Near-Infrared-Emissive Carbon Nanodots with Multiphoton Excited Upconversion Fluorescence.

Project description:Red/near-infrared (NIR) emissive carbon nanodots (CNDs) with photoluminescence (PL) quantum yield (QY) of 57% are prepared via an in situ solvent-free carbonization strategy for the first time. 1-Photon and 2-photon cellular imaging is demonstrated by using the CNDs as red/NIR fluorescence agent due to the high PL QY and low biotoxicity. Further study shows that the red/NIR CNDs exhibit multiphoton excited (MPE) upconversion fluorescence under excitation of 800-2000 nm, which involves three NIR windows (NIR-I, 650-950 nm; NIR-II, 1100-1350; NIR-III, 1600-1870 nm). 2-Photon, 3-photon, and 4-photon excited fluorescence of the CNDs under excitation of different wavelengths is achieved. This study develops an in situ solvent-free carbonization method for efficient red/NIR emissive CNDs with MPE upconversion fluorescence, which may push forward the application of the CNDs in bioimaging.

| S-EPMC6724478 | biostudies-literature

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data