Red Molecules Research Articles

Efficient thermally activated delayed fluorescence materials from symmetric anthraquinone derivatives for high-performance red OLEDs

Constructing efficient red thermally activated delayed-fluorescence (TADF) materials for high-performance organic light-emitting diodes (OLEDs) remains challenging due to the formidable barrier of energy gap law. In this work, a design strategy of connecting two donor units to the adjacent positions of electron acceptor is proposed for creating red luminescent materials, and four Y-shaped TADF molecules consisting of strong electron-withdrawing anthraquinone (AQ) acceptor and triphenylamine or acridine-based donors are designed and synthesized. They exhibit strong red emissions (604−618 nm) in toluene solutions and orange/red emissions (566−608 nm) with good photoluminescence quantum yields (43−68%) in doped films, and enjoy small singlet-triplet energy gaps (0.02−0.10 eV) and fast reverse intersystem crossing processes (1.5–7.3 × 105 s−1), which are attributed to the unique Y-shape structure. A maximum external quantum efficiency of 19.5% with an electroluminescence peak at 616 nm is achieved for AQ-PTPA-based red doped device, representing the highest level for red TADF-OLEDs based on AQ acceptor in the literature. This work can provide guidance for the design of efficient red delayed-fluorescence molecules for the application in OLEDs.

Exploration of red and deep red Thermally activated delayed fluorescence molecules constructed via intramolecular locking strategy

Red and deep red (DR) organic light-emitting diodes (OLEDs) have garnered increasing attention due to their widespread applications in display technology and lighting devices. However, most red OLEDs exhibit low luminescence efficiency, severely limiting their practical applications. To address this challenge, we theoretically design four novel TADF molecules with red and DR luminescence using intramolecular locking strategies building upon the experimental findings of DCN-DLB and DCN-DSP, and their crystal structures are predicted with the lower energy and higher packing density. The photophysical properties and luminescence mechanism of six molecules in toluene and crystal are clarified using the first principles calculation and thermal vibration correlation function (TVCF) method. The proposed design strategy is anticipated to offer several advantages: enhanced electron-donating capabilities, more rigid structures, longer emission wavelengths and higher luminescence efficiency. Specifically, we introduce oxygen atoms and nitrogen atoms as intramolecular locks, and the newly developed DCN-DBF and DCN-PHC have redshifted emission, narrow singlet–triplet energy gap (ΔEST), fast reverse intersystem crossing rate and enhanced photoluminescence quantum yield (PLQY). Notably, DCN-DBF achieves both long wavelength emission and high efficiency, with emission peaks at 598 nm and 587 nm corresponding to PLQY of 52.13 % and 43.42 % in toluene and crystal, respectively. Our work not only elucidates the relationship between molecular structures and photophysical properties, but also proposes feasible intramolecular locking design strategies and four promising red and DR TADF molecules, which could provide a valuable reference for the design of more efficient red and DR TADF emitters.

Hierarchical Self-Assembly and Aggregation-Induced Emission Enhancement in Tetrabenzofluorene-Based Red Emitting Molecules.

The newly synthesized chiral active [5]helicene-like tetrabenzofluorene (TBF) based highly red-emitting molecules exhibit flower-like self-assembly. These molecules display photophysical and structural properties such as intramolecular charge transfer, dual state emission, large fluorescence quantum yield, and solvatochromism. In TBFID, the indandione functional group attached on both sides as the terminal group offers an A-D-A push-pull effect and acts as a strong acceptor to cause more redshift in solution as well as in solid state as compared to TBFPA (TBF with benzaldehyde functional group in terminal position). The self-assembly studies of TBFID demonstrate the aggregation-induced emission enhancement (AIEE) attributed to the restriction of intramolecular rotation at the aggregated state. Furthermore, TBFID shows high quantum yield and intense red emission, making the molecule fit for organic light-emitting diodes (OLED) and bioimaging applications.

Pressure-enhanced sensing of tissue oxygenation via endogenous porphyrin: Implications for dynamic visualization of cancer in surgery

Fluorescence guidance is routinely used in surgery to enhance perfusion contrast in multiple types of diseases. Pressure-enhanced sensing of tissue oxygenation (PRESTO) via fluorescence is a technique extensively analyzed here, that uses an FDA-approved human precursor molecule, 5-aminolevulinic acid (ALA), to stimulate a unique delayed fluorescence signal that is representative of tissue hypoxia. The ALA precontrast agent is metabolized in most tissues into a red fluorescent molecule, protoporphyrin IX (PpIX), which has both prompt fluorescence, indicative of the concentration, and a delayed fluorescence, that is amplified in low tissue oxygen situations. Applied pressure from palpation induces transient capillary stasis and a resulting transient PRESTO contrast, dominant when there is near hypoxia. This study examined the kinetics and behavior of this effect in both normal and tumor tissues, with a prolonged high PRESTO contrast (contrast to background of 7.3) across 5 tumor models, due to sluggish capillaries and inhibited vasodynamics. This tissue function imaging approach is a fundamentally unique tool for real-time palpation-induced tissue response in vivo, relevant for chronic hypoxia, such as vascular diseases or oncologic surgery.

Dendrophthoe falcata extract mediated Fe3O4 nanoparticles: A functional agent for dye degradation and inflammation mitigation

The synthesis of metal oxide nanoparticles through green methods using plant extracts has garnered significant interest for their sustainable and multifunctional applications. In this study, the leaf extracts of Dendrophthoe falcata (D'falcata), a medicinal plant known for its rich phytochemical composition was successfully utilized as a reducing and stabilizing agent to synthesize Fe3O4 nanoparticles through a co-precipitation method. The D'falcata-mediated Fe3O4 nanoparticles were characterized using XRD, FTIR, UV–vis, SEM, EDAX, and TEM. The prepared nanoproduct was employed to decompose Congo red dye molecules through photocatalysis. XRD and FTIR analyses confirmed the cubic spinel phase of Fe3O4 nanoparticles and the Fe-O peak around 600 cm-1, while the UV–vis spectrum exhibited an absorption peak around 350 nm. Morphological studies revealed that the synthesized D'Fe3O4 nanoparticles were slightly agglomerated and ranged in size from 25 to 35 nm. The EDAX profile confirmed the presence of expected elements like Fe, O, and N in the final product. VSM studies indicated that D'Fe3O4 displayed paramagnetic behavior. Moreover, the anti-inflammatory assay demonstrated its potential for tumor therapy, with a percentage inhibition of 95 %, surpassing the standard diclofenac sodium (89 %). The smaller size of the D'falcata-mediated Fe3O4 nanoparticles also makes them a viable option for magnetic resonance imaging. Furthermore, photocatalytic studies showed the increase in dye degradation efficiency over the time. The findings from XRD, SEM, FTIR, and VSM analyses were well corroborated, highlighting the enhanced photocatalytic and anti-inflammatory activities of the synthesized D'Fe3O4 sample.

Fabrication of Bi0.90Sm0.1Fe0.97Cr0.03O3@PANI core-shell and improvement of its photocatalyst properties

Bi0.90Sm0.1Fe0.97Cr0.03O3@PANI core-shell structures were made by a two-step method, first, bismuth ferrite nanoparticles by hydrothermal method and then, aniline core-shell by co-precipitation method. The bismuth ferrite (BFO) XRD pattern showed no impurities of Sm, Cr, or their compounds in the samples, indicating that Sm+3 and Cr+3 had been replaced in the BFO structure. The XRD pattern of the Bi0.90Sm0.1Fe0.97Cr0.03O3@PANI core-shell shows all peaks of Bi0.90Sm0.1Fe0.97Cr0.03O3 composition with lower intensity, as a result, the Bi0.90Sm0.1Fe0.97Cr0.03O3 composition is phase single. This lower intensity is attributed to the presence of amorphous polyaniline in the core-shell structure. Since there is in the FT-IR spectrum of the Bi0.90Sm0.1Fe0.97Cr0.03O3@PANI core-shell, characteristic peaks of both polyaniline and bismuth ferrite simultaneously so, the FT-IR spectrum of the Bi0.90Sm0.1Fe0.97Cr0.03O3@PANI core-shell is a perovskite structure. The synthesized samples exhibit weak magnetic properties and behave as a paramagnetic material. The absorption capability of core-shell compared to core nanoparticles has increased in the visible region, and this enhancement is attributed to the influence of the presence of polyaniline. All the peaks in the UV–visible absorption spectrum characterize the nano-sized bismuth ferrite and polyaniline in the UV–visible spectrum of the core-shell. The intensity of the photoluminescence spectrum in the doped sample is significantly higher compared to the core-shell sample. This indicates a much faster recombination rate in the doped nanoparticles compared to the core-shell nanocomposite. The doping of the core with Cr and Sm elements, as well as the coating of the core with a polymeric shell, has led to an increase in the degradation rate of the red dye. We also found that shell thickness plays a vital role in dye degradation efficiency and photocatalytic performance. The Bi0.90Sm0.1Fe0.97Cr0.03O3@PANI core-shell exhibits significant photocatalytic activity under visible light. The photocatalytic studies show that the best sample is Bi0.9Sm0.1Fe0.97Cr0.03O3@PANI core-shell with aniline concentration of 0.2 mL and a pH = 2 which was able to destroy 100 % of Congo red dye molecules.

Introducing Internal Host Component to Thermally Activated Delayed Fluorescence Emitter for Efficient NIR Nondoped Organic Light-Emitting Diodes.

Developing thermally activated delayed fluorescence (TADF) near-infrared (NIR) organic light-emitting diodes (OLEDs) based on nondoped emitting layers is intriguing yet challenging, limited by low exciton utilization and notorious concentration quenching. Herein, a facile strategy is proposed to address this issue by incorporating an internal host component onto a traditional donor (D)-acceptor (A)-type red TADF molecule. A proof-of-concept emitter with an internal host is accordingly developed as well as a control one without an internal host. In the case of their monomer states, both emitters exhibit similar emission spectra due to their identical D-A pairs. However, under nondoped conditions, significant improvement in exciton utilization and quenching-resistant features are observed for the molecule with the internal host. The corresponding nondoped OLED yielded a maximum external quantum efficiency of 2.4%, with NIR emission peaking at 765 nm, which was a nearly 10-fold improvement relative to the efficiency based on the control molecule without an internal host. To the best of our knowledge, this result is on par with those of state-of-the art nondoped NIR TADF OLEDs in a similar emission region. These results offer a feasible pathway for the design and development of high-efficiency NIR nondoped OLEDs.

Red Fluorescent Molecule with Aggregation-Induced Emission Based on Dehydroabietic Acid Diarylamine for Bioimaging.

In this paper, molecules with AIE red light properties were designed by coupling dehydroabietic acid diarylamine and 2,3-diphenylfumaronitrile, which were designated 2DTPA-CN and 2TPA-CN. The emission wavelengths were 683nm and 701nm, respectively. The 2DTPA-CN and 2TPA-CN showed typical AIE characteristics with large Stokes shifts of 7.4 × 104 cm-1 and 6.7 × 104 cm-1, respectively. The obvious solvatochromism and electron cloud distributions of HOMO/LUMO in the ground and excited states both reveal the intramolecular charge transfer (ICT) effect. The 2DTPA-CN, boasting exceptional biocompatibility, was successfully prepared into nanoparticles (NPs), which were applied to tumor cell imaging, showing good bioimaging effects both in vitro imaging in live cells and in vivo imaging in live mice. The results demonstrated that it possesses significant potential as an effective bioimaging reagent for the detection of tumor cells. Furthermore, the incorporation of 2,3-diphenylfumaronitrile moieties to dehydroabietic acid diarylamine emerged as a proficient approach to broaden the emission wavelengths of rosin-based fluorescent materials.

The neutral Red probe location in large unilamellar vesicles: Influence of membrane composition and phase states

Biological membranes are complex and dynamic self-assembled structures composed of lipids and proteins. They depict emergent properties that are heterogeneous in the membrane plane. Therefore, their study is currently one of the greatest challenges in biophysics.The versatility of spectroscopic techniques has encouraged the development of new fluorescent probes capable of sensing different membrane properties. The Neutral Red (NR) molecule is a dye that protonates at pH < 6.8 (pKa = 6.8), leading to the charged species (NRH+). NR is widely employed in molecular biology to assess cell viability and mitochondrial function, and to sense intracellular pH. However, the photophysical behavior of NR in complex media such as membranes were not systematically characterized even though of the wide application in molecular biology.In this work, the photophysical behavior of NNR (pH 8 neutral specie) and NRH+ (pH 4) was studied by employing large unilamellar vesicles (LUVs) with different compositions, membrane phase states.The results of this study show that the spectroscopic behavior of NNR is more sensitive to the membrane composition than that of NRH+. The wavelength of the maximum emission of NNR was at shorter wavelengths in liquid-disordered (Ld) membranes compared to gel or liquid-ordered (Lo) membranes. The Red-edge excitation shifts (REES) and Anisotropy magnitudes were lower in membranes in the gel or Lo, compared to membranes in Ld. The same tendency was observed for NRH+, although the spectral changes in this case were smaller, as well as the changes in the REES effect, and anisotropy magnitudes were lower related to the NR species. We suggest that NNR and NRH+ are localized in different regions of the membrane depending on the membrane phase estate. NR and NRH+ are located in more internal regions of the interface in membranes in Ld phase state, whereas in gel or Lo phase membranes, NR is located in a more external region, and NRH+ is adsorbed on the membrane surface. Consequently, the spectral signals of both, NNR and NRH+, correspond to the species distributed in different locations of the membrane in Ld compared to gel and Lo phase. Therefore, the information provided by the probe inserted in different membranes is not directly comparable.

Polymer Microspheres Copolymerized with Deep Red Fluorescent Molecules as a Label for Lateral Flow Immunochromatography.

The development of fluorescently labeled microspheres is a critical aspect of advancing the technology of lateral flow immunochromatography (LFIA) for biological detection. Nevertheless, potential interference posed by the background fluorescence originating from the nitrocellulose (NC) membrane would significantly impact the sensitivity and accuracy of microsphere-based detection in LFIA. In this work, an attempt was made to extend the π-conjugated system and asymmetric structure of rhodamine fluorophore, resulting in the synthesis of dye molecules (RB2) incorporating double bonds, which can reach an absolute photoluminescence quantum yield (PLQY) of 30.01% in EtOH. Subsequently, carboxyl group functionalized fluorescent microspheres were prepared in a two-step copolymerization via soap-free emulsion polymerization. The obtained microspheres were characterized by scanning electron microscopy, transmission electron microscopy, DLS, Fourier transform infrared spectroscopy, ultraviolet spectrophotometry, and fluorescence spectrophotometry. The results showed that RB2 was successfully copolymerized into the microspheres, and the resulting microspheres had good dispersion and stability with high red fluorescence intensity (λabs ∼ 610 nm, λem ∼ 660 nm). Utilizing these microspheres, the resulting lateral flow immunoassay was successfully found to detect SARS-CoV-2 N protein with a detection limit of 2.5 pg/mL and the linear concentration spanning from 2.5 pg/mL to 10 ng/mL. The results confirm the effectiveness of the synthetic fluorescent microspheres as the label for LFIA.

Inhibition of malaria and babesiosis parasites by putative red blood cell targeting small molecules.

Chemotherapies for malaria and babesiosis frequently succumb to the emergence of pathogen-related drug-resistance. Host-targeted therapies are thought to be less susceptible to resistance but are seldom considered for treatment of these diseases. Our overall objective was to systematically assess small molecules for host cell-targeting activity to restrict proliferation of intracellular parasites. We carried out a literature survey to identify small molecules annotated for host factors implicated in Plasmodium falciparum infection. Alongside P. falciparum, we implemented in vitro parasite susceptibility assays also in the zoonotic parasite Plasmodium knowlesi and the veterinary parasite Babesia divergens. We additionally carried out assays to test directly for action on RBCs apart from the parasites. To distinguish specific host-targeting antiparasitic activity from erythrotoxicity, we measured phosphatidylserine exposure and hemolysis stimulated by small molecules in uninfected RBCs. We identified diverse RBC target-annotated inhibitors with Plasmodium-specific, Babesia-specific, and broad-spectrum antiparasitic activity. The anticancer MEK-targeting drug trametinib is shown here to act with submicromolar activity to block proliferation of Plasmodium spp. in RBCs. Some inhibitors exhibit antimalarial activity with transient exposure to RBCs prior to infection with parasites, providing evidence for host-targeting activity distinct from direct inhibition of the parasite. We report here characterization of small molecules for antiproliferative and host cell-targeting activity for malaria and babesiosis parasites. This resource is relevant for assessment of physiological RBC-parasite interactions and may inform drug development and repurposing efforts.

A graft-modified sponge with COFs for wastewater treatment and iodine adsorption

Azo dyes, used in large quantities in drinks, have become a threat to human health. In the treatment of dyes, the method of chemical adsorption is often used due to its simple and efficient features. Covalent organic frameworks (COFs) material with the characteristics of stability and porosity has great potential for the adsorption of azo dyes. However, the application of COFs is severely limited by their poor mechanical properties and hard recovery. By the strategy of in situ growth using the original functional groups of the sponge, COFs are successfully grafted onto melamine sponges to give rise to a porous sponge@COFs material. The material can adsorb up to 621 mg g−1 of Congo red, a common azo dye. In addition, it exhibits strong adsorption of iodine solution with the saturated adsorption of 1504.76 mg g−1. More importantly, sponge@COFs can selectively adsorb azo dyes with S–O- bond. The adsorption mechanism is inferred as the connect of S–O- in the Congo red molecule with O atom of sponge@COFs. Also, the mechanism of iodine adsorption is explained to be due to the coordination of C atoms in COFs with I atom. In addition, as an adsorbent, the material is recoverable, stable and heat resistant. Relying on the stronger performance and lower cost, sponge@COFs is expected to be developed as a new adsorbent.

Adsorption of food dyes from aqueous solution on a sweet potato residue-derived carbonaceous adsorbent: Analytical interpretation of adsorption mechanisms via adsorbent characterization and statistical physics modeling

The adsorption of three food dyes, namely allura red AC, carmine and tartrazine, on a sweet potato residue-derived activated carbon (SPAC) was analyzed via experimental and theoretical tools. In a first step, SPAC was characterized by BET, FTIR and XRD to unravel its textural and surface properties. Adsorption isotherms of the three dyes were obtained at different temperatures ranging from 30 to 50 °C. Classical models were first applied to model the adsorption isotherms, but they were unable to describe the adsorption mechanisms. An alternative approach based on the application of mono- and multi-layer models from statistical physics theory was then used to better investigate the adsorption mechanisms. This alternative approach indicated that carmine and allura red AC adsorption followed a monolayer behavior, whereas the adsorption of tartrazine was a multi-layer process. These dyes were adsorbed via different configurations (horizontal, non-horizontal, horizontal and non-horizontal at the same time), depending on the system and the temperature. Tartrazine dye was removed via an aggregation process at different temperatures, while carmine was aggregated only at high temperatures. This aggregation process was absent for the allura red AC adsorption. Endothermic physisorption processes was observed for dye adsorption under these experimental conditions. The theoretical analysis indicated that SPAC is a promising material for the removal of these dyes, particularly in the case of allura red AC dye molecule. Overall, this study reports a combination of experimental and theoretical results to provide a new perspective at the molecular level of the removal of dye molecules using a low-cost activated carbon.

Green synthesis of magnetic chitosan composite hydrogel (Fe3O4@CS photocatalyst) for the solar light driven catalytic degradation of organic contaminants

Ecofriendly magnetic chitosan composite hydrogel (Fe3O4@CS photo-catalyst) was prepared by using an aqueous extract of Boerhevia procombens leaves for the solar light mediated catalytic degradation of lethal organic Congo red dye. The prepared composite hydrogel was structurally studied using Fourier transform infrared spectroscopy (FT-IR) which reveals the formation of the Fe3O4@CS photocatalyst. The X-ray diffraction (XRD) investigation of the composite hydrogel signified high crystallinity of photocatalyst and crystallite structure of 53 nm for magnetite nanoparticles (Fe3O4 NPs). The surface investigation suggests multilayered porous photocatalyst owing to the presence of cavities offering more photoactive sites for the photodecomposition of dye molecules. The energy dispersive X-ray (EDX) scanning supports the fabrication of Fe3O4@CS photocatalyst due to the perseverance of carbon, nitrogen, oxygen, and iron. The thermogravimetric analysis (TGA) together with vibrating sample magnetometry (VSM) certifies the preparation of thermally stable and magnetic composite hydrogel. The fabricated Fe3O4@CS photocatalyst possess low bandgap energy of 2.36 eV, supporting the excellent disintegration of dye molecules in the sunlight irradiations. The photocatalyst exhibited a maximum degradation efficacy of 99.1% for Congo red dye in the solar light irradiations with refined states of 70 min radiation time, dye concentration of 20 mg/L, pH 6, and 200 mg photocatalyst amount obeying the second-order kinetic model (R2 = 0.9959). The Fe3O4@CS photocatalyst displayed a little decrease in dissociation efficiency of dye molecules after five repeated cycles owing to the coverage or rupturing of photoactive sites. Conclusively, the results support Fe3O4@ CS to be an economical and biocompatible magnetic catalyst for the catalytic decontamination of Congo red dye molecules and other organic contaminants in domestic and industrial wastewater effluents.

Designing solution-processed thermally activated delayed fluorescence emitters via introducing bulky steric hindrance groups for pure red OLEDs

We introduced bulky spiro-fluorene groups into a newly designed pure red TADF molecule to reduce the triplet exciton quenching caused by intermolecular π–π stacking.

Red Propolis: Chemical and Mid-Infrared Spectroscopic Characterization and Classification by Geographic Origin

In this paper, we report the characterization of Brazilian red propolis from two origins. The commercial value of this product is due to its composition and bioactivity, which depend on geographical factors. Total and individual phenolic, antioxidant, and medium infrared spectroscopic (MIR) characterization of 72 red propolis samples from two origins (Bahia (BA) and Rio Grande do Norte (RN), Brazil) were performed. Samples from RN showed higher concentrations of biomarkers. The BA samples showed higher antioxidant capacity despite having lower concentrations of the red propolis biomarker molecules when compared to the RN samples. The MIRS showed differences regarding the origin. The principal component analysis confirmed the differences, generating well-defined groups. Linear discriminant analysis or discriminant analysis and and partial least squares discriminant analysis showed excellent model performance. The models with MIRS data from raw propolis have a high correct classification rate and require no sample preparation. These findings can affect red propolis production, boosting sustainable extractivism, and changing the reality of small communities.

A green cross-linking method for the preparation of renewable three-dimensional graphene sponges for efficient adsorption of Congo red dye

Graphene-based materials possess significant potential for the treatment of dye wastewater due to their exceptional adsorption properties toward stubborn pollutants. However, their utilization is hindered by high preparation costs, low yields, environmental pollution during synthesis, and challenges in regenerating the adsorbent. This study proposes a novel approach to address these limitations by developing nitrogen-doped three-dimensional (3D) polyvinyl alcohol cross-linked graphene sponges (N-PGA) using a cross-linking method with ammonium carbonate. This method offers a relatively mild and environmentally friendly approach. Ammonium carbonate serves as both a reducing and modifying agent, facilitating the formation of the intrinsic structure of N-PGA and acting as a nitrogen source. Meanwhile, polyvinyl alcohol (PVA) is utilized as the cross-linking agent. The results demonstrate that N-PGA exhibits a favorable internal 3D hierarchical porous structure and possesses robust mechanical properties. The measured specific surface area (BET) of N-PGA was as high as 406.538 m2·g–1, which was favorable for its efficient adsorption of Congo red dye molecules. At an initial concentration of 50 mg·L–1, N-PGA achieved an impressive removal rate of 89.6% and an adsorption capacity of 112 mg·g–1 for Congo red (CR) dye. Furthermore, it retained 79% of its initial adsorption capacity after 10 cycles, demonstrating excellent regeneration performance. In summary, the synthesized N-PGA displays remarkable efficacy in the adsorption of CR dye in wastewater, opening up new possibilities for utilizing 3D porous graphene nanomaterials as efficient adsorbents in wastewater treatment.

Green waste immobilized Ag/Cu feather like Bi-matrix on garment dye decomposes and their bio-efficacy

This paper describes a simple phyto-remediation of feather-like silver/copper bi-matrix (BMs) was constructed by employing pommagrant waste peel (PWP) extract as crucial role of reducing agent and chelating agents. Numerous strategies, including UV–Visible, XRD, SEM-EDX, and TEM and BET isotherm were used to analysis the optical, structural, surface area and functional properties. Ag/Cu BPNMs of TEM characterization shows feather-like architectural features with constrained size and shape. The Ag/Cu co-catalytic nanoparticles have a particle size of 34–64 nm. The photocatalytic efficiency of Ag/Cu BMs was investigated using a garment dye, Congo red (CR), at successive time intervals under halogen lamp exposure. For Ag/Cu bimetallic nanoparticles, the photocatalytic degradation rate was recorded to be 100% after 40 min which is caused by adsorption of Congo red dye molecules on Ag/Cu and their degradation by reactive oxygen species (ROS). ROS are free hydroxyl radicals such as •OH and O2• ions that have high oxidizing capacity. The developed Ag/Cu BMs shown effective bacteriostatic action against many infections.

V2O5/Cds as nanocomposite catalyst for Congo red dye photocatalytic degradation under visible light

V2O5/CdS nanocomposites were prepared using a facile method and utilized as photocatalysts for Congo red (CR) dye molecule degradation. CR is an azo-type dye, which is toxic with a complex structure. The toxicity brings harmful effects on ecotoxicological for aquatic bodies. This study investigated the feasibility of V2O5/CdS nanocomposite catalyst for CR degradation. The V2O5/CdS nanocomposite catalyst was prepared using chemical bath deposition method. The nanocomposite catalyst is evaluated based on the band gap energy using UV–Vis. The degradation of CR dyes was explored through the effect of pH, different catalyst loadings, and the effect on the initial CR dye concentration. It was found that the optimum pH for the CR degradation is pH 8, while the optimum loading and optimum initial CR dye concentration are found at 10 mg and 10 ppm, respectively.

Isomer engineering for red thermally activated delayed fluorescence molecules: Luminescence mechanism study and rational molecular design

Developing efficient red TADF molecules remains a great challenge and it is extremely urgent to reveal the luminescence mechanisms through theoretical perspectives. Herein, the photophysical properties of two pairs of red TADF isomers in toluene and solid phase have been theoretically studied. Results indicate that, compared with trans-isomers, cis-isomers possess smaller energy gaps which bring fast RISC processes. While for molecules in solid phase, decreased energy gaps and increased spin orbit coupling constants are determined, all these factors contribute to the remarkable RISC processes. Furthermore, previous experimental measurements are reasonably explained and three new red TADF molecules are theoretically proposed.