Photoinduced Electron Transfer Effect Research Articles

Fluorescence Sensing Properties of a Bibranched Cyanostilbene Derivative Containing -NH2 for Trace Water and Picric Acid Determination.

In order to design organic small molecule fluorescent materials with multiple sensing, a bibranched -NH2 modified cyanostilbene derivative (AM) was synthesized. It exhibits solvent and aggregation-induced emission effects, with a solid-state quantum yield of 28%, which is seven times higher than that in THF. The synthesized sample AM demonstrated high sensitivity to trace water via a fluorescence "turn-off" response, achieving a low detection limit of 0.41 µM in THF and 0.80 µM in EtOH. AM also exhibits a "turn-off" response to picric acid, attributed to the photo-induced electron transfer effect it induces. The recognition of picric acid by AM demonstrates specificity and resistance to interference from nitro explosives, with a detection limit of 300 ppb and a linear relationship (R2 = 0.9981) at the range of 0-4 equivalents AM. Such acid recognition can facilitate the design of qualitative test papers and safety inks. Additionally, AM can function as a temperature sensor with a linear relationship (R2 = 0.9976) within the temperature range of 25-110°C. Leveraging these unique characteristics, a series of methods were proposed for the direct quantitative determination of trace water in nonaqueous solvents, picric acid, and temperature.

A Novel Multi-Effect Photosensitizer for Tumor Destruction via Multimodal Imaging Guided Synergistic Cancer Phototherapy.

How to ingeniously design multi-effect photosensitizers (PSs), including multimodal imaging and multi-channel therapy, is of great significance for highly spatiotemporal controllable precise phototherapy of malignant tumors. Herein, a novel multifunctional zinc(II) phthalocyanine-based planar micromolecule amphiphile (ZnPc 1) was successfully designed and synthesized, in which N atom with photoinduced electron transfer effect was introduced to enhance the near-infrared absorbance and nonradiative heat generation. After simple self-assembling into nanoparticles (NPs), ZnPc 1 NPs would exhibit enhanced multimodal imaging properties including fluorescence (FL) imaging (FLI) /photoacoustic (PA) imaging (PAI) /infrared (IR) thermal imaging, which was further used to guide the combined photodynamic therapy (PDT) and photothermal therapy (PTT). It was that under the self-guidance of the multimodal imaging, ZnPc 1 NPs could precisely pinpoint the tumor from the vertical and horizontal boundaries achieving highly efficient and accurate treatment of cancer. Accordingly, the integration of FL/PA/IR multimodal imaging and PDT/PTT synergistic therapy pathway into one ZnPc 1 could provide a blueprint for the next generation of phototherapy, which offered a new paradigm for the integration of diagnosis and treatment in tumor and a promising prospect for precise cancer therapy.

Multidimensional detection of roxarsone via AIE-based sulfates

Improper abuse of roxarsone (ROX) in industrial production leads to harmful effects on water, soil, food, and living creatures. It is significant to detect its concentration in the environment and biosystem. Herein, two aggregation-induced emission (AIE)-active fluorescence probes, TPE-TPE and TPE-TPE-CN, are successfully synthesized via a sulfur (VI) fluoride exchange (SuFEx) click reaction and first employed to detect ROX in the environment and living 3T3 cells. These two probes can selectively detect ROX in water due to the synergistic effect of photoinduced electron transfer (PET) and fluorescence resonance energy transfer (FRET) between the probes and ROX. The detection limit of TPE-TPE and TPE-TPE-CN is 0.154 and 0.385 μmol/L, respectively, much lower than the safety concentration stipulated by the World Health Organization (WHO). In addition, with the aid of a color discrimination application in a smartphone, these two probes can also detect ROX in real samples (such as water, soil, and cabbage), demonstrating their excellent potential for monitoring ROX in a practical environment.

Hydrogen-bond tuned conjugated architectures for nitric oxide sensing in single-benzene framework: Advances and mechanistic insights

In contrast to the conventional fluorescence enhancement resulting from the cessation of the photoinduced electron transfer effect upon capturing nitric oxide (NO) by o-phenylenediamine, we found an interesting fluorescence quench within small molecule fluorophores characterized by intramolecular hydrogen bonding. Herein, the integration of a push-pull electron system with intramolecular hydrogen bonding onto an ultra-small fluorophore was employed to fabricate a hydrogen bond-tuned single benzene core fluorescent probe with an exceptional fluorescence quantum yield of 26 %, denoted as HSC-1. By virtue of its small size and low molecular weight (mere 192 g/mol), it demonstrated superior solubility and biocompatibility. Given the optimized conditions, HSC-1 manifested extraordinary linearity in detecting NO concentrations ranging from 0.5 to 60 μM, with an outstanding detection limit of 23.8 nM. Theoretical calculations unraveled the photophysical properties of hydrogen bonding-related probe molecules and highlighted the NO sensing mechanism. This pioneering work offers an important platform for the design of small fluorescence probes only with a single benzene core applied to NO sensing, which will potentially emerge as a new frontier in the area.

A lysosome-targeted fluorescent probe for fluorescence imaging of hypochlorous acid in living cells and in vivo

Lysosomes, as crucial acidic organelles in cells, play a significant role in cellular functions. The levels and distribution of hypochlorous acid (HOCl) within lysosomes can profoundly impact their biological functionality. Hence, real-time monitoring of the concentration of HOCl in lysosomes holds paramount importance for further understanding various physiological and pathological processes associated with lysosomes. In this study, we developed a bodipy-based fluorescent probe derived from pyridine and phenyl selenide for the specific detection of HOCl in aqueous solutions. Leveraging the probe's sensitive photoinduced electron transfer effect from phenyl selenide to the fluorophore, the probe exhibited satisfactory high sensitivity (with a limit of detection of 5.2 nM and a response time of 15 s) to hypochlorous acid. Further biological experiments confirmed that the introduction of the pyridine moiety enabled the probe molecule to selectively target lysosomes. Moreover, the probe successfully facilitated real-time monitoring of HOCl in cell models stimulated by N-acetylcysteine (NAC) and lipopolysaccharide (LPS), as well as in a normal zebrafish model. This provides a universal method for dynamically sensing HOCl in lysosomes.

Lignin based water-soluble fluorescent macromolecular probes for the detection of Fe3+ ion

Lignin is an abundant biomass material in the natural world, its application value and application scope ought to be enlarged. In this work, dealkalized lignin with good water-solubility was used to combine with water-insoluble boron-dipyrromethene (BODIPY) fluorophore to obtain readily water-soluble macromolecular probes. Firstly, a small molecular fluorescent BODIPY probe with two amino groups (-NH2) and another small molecular fluorescent probe with two chlorine groups (-Cl) were synthesized. Secondly, the small-molecular fluorescent probe with two -NH2 groups reacted with carbonyl groups in the lignin by Schiff base formation reaction. Meanwhile, the small-molecular fluorescent probe with two -Cl groups reacted with hydroxyl groups in the lignin by Williamson ether formation reaction. Eventually, two lignin-based fluorescent probes were obtained. The molecular weights of the two probes reached 22.4 kDa and 20.1 kDa. Moreover, these two fluorescent probes were readily soluble in H2O and DMF. Both of the fluorescent macromolecules have good recognition ability for Fe3+, with detection limits of 2.1 × 10−7 mol/L and 1.1 × 10−7 mol/L respectively. Fe3+ interacts with the fluorescent probe, and the imine bond (-CN-) reacts with Fe3+ to cause fluorescence response. The photo-induced electron transfer effect is enhanced, and the photo-induced electron transfer (PET) mechanism causes the fluorescent quenching. This work expands the application scope of lignin as a biomass material and lays a foundation for the development of lignin materials.

A bimetallic organic framework based fluorescent aptamer probe for the detection of zearalenone in cereals

In this work, a bimetallic organic framework (Cu/UiO-66) based “turn on” fluorescent aptamer probe was designed for the high-efficiency detection of zearalenone (ZEN). In the probe, the 6-carboxyfluorescein-labeled aptamer (FAM-Apt) was used as the recognition element, and the electrostatic interaction, coordination effect, and photoinduced electron transfer effect between FAM-Apt and Cu/UiO-66 caused fluorescence quenching. When ZEN existed, FAM-Apt recognized ZEN specifically, causing FAM-Apt to separate from the surface of Cu/UiO-66 and recovery of fluorescence. Under the optimal conditions, the probe had a linear detection range of 0.5 ng/mL–60 ng/mL, and the detection limit was 0.048 ng/mL. The application potential of the probe was verified by real detection of various cereals and their products, with a standard recovery from 83.67 %–106.8 %. The development of this efficient, rapid, and sensitive ZEN detection method provides a new platform for the quality control of cereals and their products.

Fluorescent Features and Applicable Biosensing of a Core-Shell Ag Nanocluster Shielded by a DNA Tetrahedral Nanocage.

The DNA frame structure as a natural shell to stably shield the sequence-templated Ag nanocluster core (csAgNC) is intriguing yet challenging for applicable fluorescence biosensing, for which the elaborate programming of a cluster scaffold inside a DNA-based cage to guide csAgNC nucleation might be crucial. Herein, we report the first design of a symmetric tetrahedral DNA nanocage (TDC) that was self-assembled in a one-pot process using a C-rich csAgNC template strand and four single strands. Inside the as-constructed soft TDC architecture, the template sequence was logically bridged from one side to another, not in the same face, thereby guiding the in situ synthesis of emissive csAgNC. Because of the strong electron-repulsive capability of the negatively charged TDC, the as-formed csAgNC displayed significantly improved fluorescence stability and superb spectral behavior. By incorporating the recognizable modules of targeted microRNAs (miRNAs) in one vertex of the TDC, an updated TDC (uTDC) biosensing platform was established via the photoinduced electron transfer effect between the emissive csAgNC reporter and hemin/G-quadruplex (hG4) conjugate. Because of the target-interrupted csAgNC switching in three states with the spatial proximity and separation to hG4, an "on-off-on" fluorescing signal response was executed, thus achieving a wide linear range to miRNAs and a limit of detection down to picomoles. Without complicated chemical modifications, this simpler and more cost-effective strategy offered accurate cell imaging of miRNAs, further suggesting possible therapeutic applications.

Fluorescence turn-off strategy for sensitive detection of DNA methyltransferase activity based on DNA-templated gold nanoclusters

DNA methylation results in a variety of human diseases and the DNA methylation process is mediated by DNA methyltransferases, which have therefore become potential targets for disease treatment. In this study, a turn-off nanogold biological probe system was successfully created for determining the activity of DNA methyltransferases (M.SssI MTase). A dumbbell-shaped DNA probe with a site-recognizable region of M. SssI MTase and a fluorescent signal probe based on a DNA-templated gold nanocluster (DNA-AuNC) probe combined for the quantitative detection of M. SssI MTase. This dumbbell-shaped DNA probe was methylated by M. SssI MTase, and the dumbbell-shaped DNA probe with a methyl group was recognized by an endonuclease (GlaI) and cleaved into hairpin DNA. The dGTP was added to the 3′-OH terminus of hairpin DNA fragments in the presence of terminal deoxynucleotidyl transferase (TdT), and the hairpin DNA was extended with a G-rich sequence that can be used as an inactivation probe. When the inactivation probe was combined with the signal probe, the fluorescent signal disappeared due to the photoinduced electron transfer effect. Methyltransferase activity was then detected based on the turn-off principle of the fluorescence signal from the DNA-AuNCs. The bioprobe enabled sensitive detection of M. SssI MTase with a detection limit of 0.178 U mL−1 and good specificity. The bioprobe demonstrated good detection efficiency in both human serum and cell lysates, and its unique fluorescence turn-off mechanism provided good resistance to interference, thus increasing its potential application in complex biological samples. Moreover, it is suitable for screening and assessing the inhibitory activity of M. SssI MTase inhibitors, and therefore has significant potential for disease diagnosis and drug discovery.

Concentration-regulated multi-color fluorescent carbon dots for the detection of rifampicin, morin and Al3+

Carbon dots have many new and interesting phenomena, and the concentration dependent luminescence wavelength is an intriguing one. Herein, nitrogen-sulfur co-doped carbon dots (NSCDs) diluted to different concentrations, the high concentration of G-NSCDs (0.2 mg mL−1) with green fluorescence and the low-concentration of B-NSCDs (0.01 mg mL−1) with blue fluorescence were obtained. Further, it was found that the detection behaviors are different for different concentrations. The “turn-off” fluorescent sensor of G-NSCDs can specifically recognize rifampicin in a linear range of 0.2–20 μM with a detection limit of 56.6 nM employing the mutual effect of photo-induced electron transfer and dynamic quenching. Meanwhile, a “turn-off” B-NSCDs fluorescence sensor was constructed to effectively identify morin based on the internal filtration effect and static quenching, achieving a suitable linearity of 0.2–30 μM and a detection limit of 51.2 nM. Due to the strong chelation of morin and Al3+, a “turn-on” fluorescent probe for sequential detection Al3+ was fabricated based on B-NSCDs-morin system, obtaining a good linearity of 0.1–2.0 μM with a satisfactory detection limit of 45.8 nM. These interesting behaviors indicate that NSCDs are expected to become novel sensing materials for the monitoring of rifampicin, morin and Al3+ in organisms, which is beneficial for our health.

A naphthalimide-based fluorescent probe for rapid detection of nitrite and its application in food quality monitoring

Nitrite (NO2−) is a widely used food additive and long-term aging of cooked leftovers may also contribute to the formation of NO2−, excessive consumption of NO2− is harmful to human health. Developing an effective sensing strategy for on-site monitoring of NO2− has attracted considerable attention. Herein, a novel colorimetric and fluorometric probe ND-1 based on photoinduced electron transfer effect (PET) was designed for highly selective and sensitive detection of nitrite (NO2−) in foods. The probe ND-1 was strategically constructed by employing naphthalimide as the fluorophore and o-phenylendiamine as the specific recognition site for NO2−. The triazole derivative ND-1-NO2- could be produced exclusively by reacting with NO2−, leading to a visible colorimetric change from yellow to colorless accompanied by a significantly enhanced fluorescence intensity at 440 nm. The probe ND-1 exhibited promising sensing performances towards NO2− including high selectivity, rapid response time (within 7 min), low detection limit (47.15 nM) and wide quantitative detection range (0–35 μM). In addition, probe ND-1 was capable of quantitative detecting of NO2− in real food samples (including pickled vegetables and cured meat products) with satisfactory recovery rates (97.61%–103.08%). Moreover, the paper device loaded by probe ND-1 could be utilized for visual monitoring of NO2− levels variation of stir-fried greens. This study provided a feasible method for the accurate, traceable and rapid on-site monitoring NO2− in foods.

Fluorescence sensitively sensing on antibiotic and nitrobenzene of two diverse 2D Zn-organic networks

Two 2D luminous zinc(II) coordination polymers have been synthesized hydrothermally with the formulas of [Zn(4-HDBB)(3-bibz)](1) and [Zn2(4-DBB) (OH)(4,4′-bbpy)1.5]·2H2O(2) (4-H3DBB = 4-(3,5-dicarboxylatobenloxy) benzoic acid, 3-bibz = 3-bis(imidazole-l-ylmethyl) benzene and 4,4′-bbpy = 4,4′-bis (imidazolyl) biphenyl), and characterized by single crystal X-ray diffraction, IR, TG and PXRD technologies. Structural analyses exhibit both of them crystallize in P-1 space group of triclinic crystal system with 2D network structures. 1 possesses the interpenetration of 2D (4,4) networks based on the cross of two kinds of 1D chains. The 2D networks of 2 featuring 1D tube-like structure are linked by the six-number-ring H-bonds clusters. Fluorescence sensing properties on antibiotic of two complexes display 1 could detect of chloramphenicol (LOD = 6.64 × 10−7 mol⋅ L-1) and the detection limit of polymer 2 for tetracycline is 1.22 × 10−7 mol⋅ L-1. Solvents detection show that nitrobenzene in water was completely quenched by all of them, and display the highly sensitive sensing for nitrobenzene with the limit of detection of 5.0 × 10−8 mol L-1(1) and 2.14 × 10−7mol·L-1(2), respectively. Through theoretical calculation, it is found that the sensing mechanism of two complexes on nitrobenzene could be mainly attributed to the photo-induced electron transfer effect (PET). The fact shows that the two complexes can be used multi-functional sensors in the future.

Enhancement of Coloring and Bleaching Rates of Photochromic WO<sub>3</sub> Composite Films by Adding Polyethylene Glycol

WO3-based photochromic composite films were fabricated using a translucent urethane resin and a peroxoisopolytungstic acid - methanol solution as raw materials. Moreover, and polyethylene glycol (PEG, molecular weight 1000) was added to the composite as a sensitizer. The WO3 mean particle sizes in the obtained composite were 46–55 nm, which implies that by PEG addition caused a slight reduction in the particle size. Additionally, the coloring/bleaching rate and the transmittance module of the composite films were drastically increased by PEG addition. These improvements in photochromic properties were previously considered to be due to the effect of the particle size of WO3 particles in the composite, but were mainly assumed the effect of photoinduced electron transfer, which is caused by the presence of PEG in the composites.

Red-emissive carbon dots based fluorescent and smartphone-integrated paper sensors for sensitive detection of carbendazim

Trace detection of carbendazim (CBZ), a worldwide used pesticide, in crops and foods is important and urgent to reduce risks to human health. Herein, newly red-emissive carbon dots (R-CDs) based fluorescent and smartphone-integrated paper sensors were developed for highly-selective, and -sensitive rapid sensing of CBZ. R-CDs were synthesized from citric acid and urea via a DMF solvothermal method, which showed excellent analytical performance due to abundant carboxyl groups on the surface and long emission wavelength to avoid autofluorescence interference of matrix. According to the red fluorescence quenching by CBZ via π-π interaction and photoinduced electron-transfer effect, the newly fluorescent nano sensor could realize CBZ sensing within 3 min with high selectivity out of the other six interfering pesticides, as well as fascinating sensitivity with an ultralow detection limit of 3.5 ng/mL. The practicable application in the spiked medicinal Lotus seeds samples exhibited satisfactory recoveries of 95.5%-108.3%. The portable paper-based sensor fabricated by depositing R-CDs on the filter paper enabled quantitative readout of test strip results assisted with a smartphone, providing a rapid on-site tool for CBZ detection in medicinal foods. This is the first report of a novel, sensitive, and portable R-CDs based sensing platform for simple, cost-effective, and rapid on-site detection of CBZ in the field of food safety with great application potential.

Application of a Dual-Probe Coloading Nanodetection System in the Process Monitoring and Efficacy Assessment of Photodynamic Therapy: An In Vitro Study.

The oxygen-consuming property of photodynamic therapy (PDT) affects its effects and aggravates tumor hypoxia, thus upregulating the vascular endothelial growth factor (VEGF) to exacerbate tumor metastasis and lead to treatment failure. Therefore, it is necessary to monitor the dynamic changes in the factors related to PDT and tumor development trends in real time, thus helping to improve PDT efficiency. This study fabricated a fluorescent probe, TPE-2HPro, and a fluorescein-labeled aptamer probe, FAM-AptamerVEGF, to detect hydrogen peroxide (H2O2) and VEGF through the photoinduced electron-transfer effect and the specific affinity of the aptamer to VEGF, respectively. The two probes were loaded into the inner pores and absorbed on the surface of polydopamine coating-wrapped mesoporous silica nanoparticles (MSN@PDA) to construct the dual-probe-loaded system, MSNTH@PDAApt, which was kept stable in fetal bovine serum (FBS) solution and achieved pH-responsive release behavior, thus helping to increase the accumulation of the two probes in tumor cells. The dichloroacetic acid-mediated in vitro antitumor tests showed that the changing trends of H2O2 and VEGF levels were consistent with the results of related mechanism studies and could be monitored by MSNTH@PDAApt. The in vitro chlorin e6 (Ce6)-mediated PDT treatment demonstrated that when the illumination condition was 650 nm, 50 mW/cm2 for 10 min, cells were more inclined to metastasis and invasion rather than death due to a substantial increase in VEGF expression at the low Ce6 concentrations. With the increase of the Ce6 concentration, the growth of the H2O2 level gradually exceeded that of VEGF, and the reactive oxygen species (ROS)-mediated cell death dominated when the Ce6 concentration was about 2 times its IC50 values. Besides, hypoxia also affected the H2O2 and VEGF changes. These results demonstrated that MSNTH@PDAApt could precisely monitor and assess the tumor development trends during PDT treatment, thus helping improve the treatment effect.

A highly efficient molecularly imprinted fluorescence sensor for assessing whole wheat grains by the rapid and sensitive detection of alkylresorcinols

To differentiate whole wheat foods from refined wheat foods is still challenging grain industry and confusing consumers. Alkylresorcinols (ARs), as biomarkers of whole wheat grains, can serve for assessing the authenticity of whole wheat foods. Herein, a highly efficient fluorescence sensing platform (CDs@MIP) for rapid and sensitive analysis of ARs was explored, using carbon dots (CDs) as fluorophores and 5-heneicosylresorcinol (C21:0 AR) as template molecules embedded in a molecularly imprinted polymer (MIP) coating. Benefiting from the specific cavities in the probe and a photo-induced electron transfer effect, the fluorescence intensity of CDs@MIP was significantly quenched in the presence of C21:0 AR, exhibiting a superior binding efficiency and selectivity. As a result, the fabricated optical sensor delivered a wide linear range of C21:0 AR from 0.015 to 60 μg mL−1 with an ultralow detection limit of 4 ng mL−1. It was noteworthy that the sensor was successfully applied for the rapid detection of C21:0 AR in commercial whole-wheat foods as well as visualization analysis on the test paper, comprehensively validating the practicality and efficacy of CDs@MIP based fluorescence assay. The study provides a rapid and sensitive detection method of C21:0 AR, paving a new way for guiding grain industry to effectively qualify the authenticity and to quantify the content of whole wheat in wheat-based foods.

A fluorescent covalent organic framework for visual detection of p-benzoquinone

P-benzoquinone (PBQ) is toxic and harmful for health. The development of portable sensor to realize the detection of PBQ is of great significance. Herein, a novel covalent organic framework (COFML-TFPB) with intramolecular charge transfer and aggregation induced emission properties was proposed via condensation reaction of melem (ML) and 1,3,5-tris (4-formylphenyl) benzene (TFPB). COFML-TFPB shows strong fluorescence in both solution and solid state and can be used for the fluorescence detection of PBQ. Due to the internal filtration effect and photoinduced electron transfer effect, PBQ can quench the fluorescence of COFML-TFPB. The developed COFML-TFPB fluorescent sensor displayed a wide linear range for PBQ from 0.138 ng mL−1 – 35 μg mL−1, and the detection limit was 0.046 ng mL−1. In addition, fluorescent test paper for rapid and portable detection of PBQ was also developed by depositing COFML-TFPB on filter paper directly. It reduces the cost and time of detection and realizes the semiquantitative detection of PBQ. Moreover, the fluorescence color was converted into digital RGB value to calculate the concentration of PBQ accurately by a smartphone. This method realizes the portable qualitative and semiquantitative determination of PBQ.

A Tumor-Targeting Dual-Stimuli-Activatable Photodynamic Molecular Beacon for Precise Photodynamic Therapy.

A multifunctional photodynamic molecular beacon (PMB) has been designed and synthesized which contains an epidermal growth factor receptor (EGFR)-targeting cyclic peptide and a trimeric phthalocyanine skeleton in which the three zinc(II) phthalocyanine units are each substituted with a glutathione (GSH)-responsive 2,4-dinitrobenzenesulfonate (DNBS) quencher and are linked via two cathepsin B-cleavable GFLG peptide chains. This tailor-made conjugate is fully quenched in the native form due to the photoinduced electron transfer effect of the DNBS moieties and the self-quenching of the phthalocyanine units. It can target the EGFR overexpressed in cancer cells, and after receptor-mediated endocytosis, it can be activated selectively by the co-existence of intracellular GSH and cathepsin B, both of which are also overproduced in cancer cells, in terms of fluorescence emission and singlet oxygen generation. The cell-selective behavior of this PMB has been demonstrated using a range of cancer cells with different expression levels of EGFR, while the stimuli-responsive properties have been studied both in vitro and in various aqueous media. The overall results show that this advanced PMB, which exhibits several levels of control of the tumor specificity, is a promising photosensitizer for precise antitumoral photodynamic therapy.

Integration of quantum dots with Zn2GeO4 nanoellipsoids to expand the dynamic detection range of uranyl ions in fluorescent test strips

Fluorescent colorimetric test strips normally have a narrow dynamic detection–range due to the limited responsive range from single responsive materials, which cannot meet the wide detection requirement in practical applications. Herein, we developed an approach to detect uranyl ions (UO22+) with a broad detection range using the synthesized ZnS:Mn quantum dots (QDs) modified Zn2GeO4 nanoellipsoids (Zn2GeO4 @ZnS:Mn NEs), containing two responsive materials with the opposite signal responses at different UO22+ concentrations. Specifically, a red to chocolate color change was observed at low analyte concentrations (0.01–100 μM) resulting from the photoinduced electron transfer effect from ZnS:Mn QDs to UO22+. A sequentially olive drab to green color change has been observed when further increasing the UO22+ concentration (100–1000 μM) as a result of the antenna effect between Zn2GeO4 nanoellipsoids and UO22+. In addition, a low-cost and portable fluorescent test strip has been further fabricated through embedding Zn2GeO4 @ZnS:Mn NEs on a microporous structure membrane, demonstrating a facile yet effective colorimetric response to UO22+ in lab water, lake water, and seawater with a wide dynamic range. Therefore, it is potentially attractive for real-time and on-site detection of UO22+ in sudden-onset situations.

Heterogeneous photosensitizers: Super-efficient dual functional polydopamine nanohybrid for epoxy photopolymerization

The photosensitivity of nanoparticulate polydopamine (PDA) and polydopamine coated multiwalled carbon nanotubes (PDA/MWCNT) and their effect on the photopolymerization of epoxy monomers were systematically investigated. PDA/MWCNT nanohybrid at only 0.625 wt% has been shown to photo-catalyse the polymerization speed and conversion when compared with the commercial free radical photoinitiator, BAPO or non-free radical enhanced cationic photoinitiating resin systems. More importantly, it substantially increased the conversion by more than 140% over the unfilled free radical promoted cationic photoinitiating resin system. Covalent coated PDA/MWCNT nanohybrids were fabricated by oxidative polymerization of dopamine on the surface of acid treated MWCNTs. The modified MWCNT nanofiller has a dual role as photosensitizer/co-initiator in the FRPCP photoinitiating system and as mechanical reinforcement for the epoxy matrix. The use of PDA nanoparticles also led to the improvement in the polymerization process, albeit a limited one. Further evaluation of the observation suggests that the increase in the polymerization speed could be due to the photoinduced electron transfer effect in the polydopamine domain of the hybrid. The super efficiency effect has been explained through the heterojunction formation at the interface of dissimilar semi-conductive/conductive materials, polydopamine, a bio conjugated molecule with UV sensitivity and MWCNT hybrids, in the curing of epoxy monomers. This type of hybridized sensitizers/co-initiators have the potential to be applied in vat type 3D printing technologies such as SLA and DLP enabling printing with light blocking additives which otherwise pose a challenge in UV–Vis enabled curing and printing.