Fluorescence Emission Research Articles

Recent Developments of Hybrid Fluorescence Techniques: Advances in Amyloid Detection Methods.

Amyloid fibrils are formed from various pathological proteins. Monitoring their aggregation process is necessary for early detection and treatment. Among the available detection techniques, fluorescence is simple, intuitive, and convenient due to its sensitive and selective mode of detection. It has certain disadvantages like poor photothermal stability and detection state limitation. Research has focused on minimising the limitation by developing hybrid fluorescence techniques. This review focuses on the two ways fluorescence (intrinsic and extrinsic) has been used to monitor amyloid fibrils. In intrinsic/label free fluorescence: i) The fluorescence emission through aromatic amino acid residues like phenylalanine (F), tyrosine (Y) and tryptophan (W) is present in amyloidogenic peptides/protein sequence. And ii) The structural changes from alpha helix to cross-β-sheet structures during amyloid formation contribute to the fluorescence emission. The second method focuses on the use of extrinsic fluorophores to monitor amyloid fibrils i) organic dyes/small molecules, ii) fluorescent tagged proteins, iii) nanoparticles, iv) metal complexes and v) conjugated polymers. All these fluorophores havetheir own limitations. Developing them into hybrid fluorescence techniques and converting it into biosensors can contribute to early detection of disease.

Multicolor emissive hyperbranched polysiloxanes from enhanced spatial electronic communication for security encryption and bacteria imaging

Unconventional fluorescent polymers with long-wavelength emission have attracted considerable attention due to their facile preparation, good biocompatibility, and excellent processability. However, their emission at long-wavelength is relative low. Herein, a series of aromatic amino acids functionalized hyperbranched polysiloxanes with deep red to cyan fluorescence were prepared. Experimental and theoretical calculation results show that the long-wavelength emission comes from the spatial electronic delocalization among conjugated π bonds and electron-rich functional groups. The balance between rigidity and flexibility is favorable for the strong long-wavelength emission. Moreover, the polymers’ fluorescence is sensitive to Fe3+ and OH– ions; and these polymers show potential applications in security encryption, fluorescent stamp inks and bacteria multicolor fluorescence imaging. This work provides an efficient method for the development of long-wavelength emissive unconventional fluorescence polymers

Preparation of fluorescent carbon dots by flow-assisted melt polymerization for tetracycline detection in medical wastewater

Tetracycline (TC) is one of the most important therapeutic drugs that is widely used in hospitals. However, its harmful effects on human health and various ecosystems cannot be ignored. Owing to its poor metabolic activity and low biodegradability, TC commonly discharges as the parent compound and accumulates readily in sludges and soils by precipitation from wastewater, which can induce the evolution of antibiotic-resistant bacteria; therefore, it has been listed as one of the new pollutants with potential ecotoxicological risk. The control measures and environmental management of TC pollutants in environmental water samples require precise determination of TC pollutant concentrations. Carbon dots (CDs) are an emerging type of fluorescent material with numerous advantages such as easy preparation, low cost, low toxicity, and good biocompatibility. Consequently, they have attracted widespread attention in the field of TC detection. Herein, we synthesized TE-CDs with good blue-fluorescence performance via flow-assisted melt polymerization using tricarboxylic acid and ethylenediamine as raw precursors. The morphology and structure of the prepared TE-CDs were characterized. The transmission electron microscopy (TEM) results showed that the prepared TE-CDs were well dispersed, with an average diameter of (2.43±0.48) nm. The X-ray diffraction (XRD) results showed that the TE-CDs had an amorphous carbon structure. Infrared spectroscopy and X-ray photoelectron spectroscopy (XPS) characterizations showed that the surface of the TE-CDs was rich in hydrophilic groups, such as amino, hydroxyl, and carboxyl groups, which indicated that TE-CDs had good water solubility and were advantageous for detecting TC in medical wastewater. Subsequently, the optical properties of the TE-CDs were investigated. The fluorescence emission spectra of the TE-CDs were recorded at various excitation wavelengths. The emission spectra of the TE-CDs exhibited excitation wavelength dependence and when the excitation wavelength changes from 300 nm to 400 nm, their fluorescence intensity decreased to varying degrees. The TE-CDs exhibited optimal fluorescence intensity at an excitation wavelength of 368 nm, while the emission wavelength was 448 nm. TC could effectively quench the blue fluorescence of the CDs, and by utilizing this property, the detection of TC concentration could be achieved. After the addition of TC, the fluorescence of the system immediately reached an extreme value, and no significant change was observed within 10 min. An incubation time of 20 s was selected to obtain precise results. Additionally, the TE-CDs exhibited stable fluorescence intensity over a wide pH range. The fluorescence stability of the TE-CDs was investigated, and no significant change in fluorescence intensity was observed after standing for 10 d, indicating that the prepared TE-CDs had excellent fluorescence stability. The fluorescence intensity of the TE-CDs decreased to varying degrees within the range of 2-200 mg/L TC until complete quenching occurred. TC mass concentration in the range of 4-20 mg/L showed a good linear relationship (R2=0.9978) with the fluorescence quenching intensity of the TE-CDs. The limit of detection was 0.2 mg/L. A preliminary investigation was undertaken to explore the quenching mechanism of the TE-CDs fluorescence by TC. Upon addition of TC, a significant reduction in the fluorescence lifetime of the TE-CDs was observed. During the quenching process, no new substances were observed by UV absorption spectroscopy. Additionally, no significant changes in the 1H NMR spectra of the TE-CDs were noted before and after the addition of TC, indicating the absence of an interaction between the TE-CDs and TC. Therefore, the quenching mechanism may involve dynamic quenching. The selectivity and anti-interference ability of the developed method were evaluated; in the presence of interfering substances, TC quenched the fluorescence of the TE-CDs, indicating that the TE-CDs had good selectivity and anti-interference performance towards TC. The method was applied to the quantitative detection of TC in medical wastewater, with recoveries of 96.5%-119.8% and relative standard deviations of 0.8%-2.6%. In conclusion, the analytical performance of the proposed method is comparable with that of previously reported detection methods; moreover, the method has the advantages of low operational cost, simple preparation process, time-saving, and good repeatability. Therefore, the TE-CDs can be used as chemical sensors for the detection of TC in medical wastewater and have good practical applications.

Assessing statistical neural networks potentiality to distinguish PDO Kalamata and Molaoi olive oil varieties

Several regional areas in Greece produce high quality olive oil by cultivating certain varieties. Olive oil varieties of Kalamata and Molaoi are of special interest, since they produce extra virgin olive oil. Concretely, Kalamata is a city located in southwestern Greece. Intuitively, Molaoi is a town located in southeastern Greece. Subsequently, both geographic locations are known for their famous olive oil quality. Continually, Protected Designation of Origin (PDO) Kalamata olive oil, established by Council regulation (EC) No 510/2006, is considered an exceptional extra virgin olive oil variety. Specifically, there is a need to distinguish PDO Kalamata olive oil from other olive oil varieties is Greece such as the Molaoi olive oil, since PDO Kalamata olive oil is the main variety exported in the global olive oil market. Distinguishing PDO Kalamata from Molaoi olive oil is possible by incorporating statistical neural networks. Concretely, applying neural network experimentation enables differentiation between variations of certain chemical characteristics observed in certain geographic locations of Greece. In this paper, we use statistical neural networks to distinguish the geographical origin of PDO Kalamata olive oil compared with Molaoi olive oil based on synchronous excitation−emission fluorescence spectroscopy of provided olive oils samples evaluated in the chemical laboratory. Evaluation based on certain experimentation phase and subsequent data visualization of the adopted statistical neural networks are promising for distinguishing the samples of PDO Kalamata olive oil with high values of prediction accuracy. Such ability enables olive oil industry to assess extra virgin olive oil profitable potentiality in global market.

Fluorescent emission and nondestructive 3D textural imaging in geologic materials by multiphoton microscopy

This work greatly expands the application of multiphoton microscopy to geological investigations by using a tightly focused femtosecond laser beam to excite fluorescent emissions among minimally prepared rock and mineral samples. This novel finding provides a tool for spatially resolving UV-visible fluorescent sources in minerals. Through a combination of harmonic generation and fluorescence, unique opportunities are made available for mineralogical investigations of terrestrial rocks and astromaterials. This report includes the first demonstrations for 3D imaging of fluid inclusions in minerals and radiation-induced luminescence imaging in meteorites. Nonlinear optical mineralogy, enabled by multiphoton microscopy, provides unique insights into mineralogic samples and holds the potential to revolutionize the analysis of geologic and astromaterials samples in the coming years.

Recent Advances of Organic-Inorganic Hybrid Fluorescent Hyperbranched Polymer: Synthesis, Performance Regulation Strategies and Applications.

The organic-inorganic hybrid fluorescent hyperbranched polymer, including hyperbranched polysiloxane and hyperbranched polyborate, have attracted much attention due to their excellent optical properties and wide range of applications. Hyperbranched polysiloxane and polyborates, prepared by introducing Si or B elements into organic polymer chains at the molecular level through rational molecular design and novel synthesis methods, exhibit outstanding photophysical properties as an indispensable branch of organic-inorganic hybrid fluorescent materials. Herein, this review highlights the recent research progress on hyperbranched polysiloxanes and hyperbranched polyborates, including strategies for regulating their emission wavelengths, quantum yields, and fluorescence lifetimes, potential emission mechanisms, and various applications. Finally, some challenges and promising future directions in the field of organic-inorganic hybrid fluorescent polymers are summarized.

New Pd(II)-pincer type complexes as potential antitumor drugs: synthesis, nucleophilic substitution reactions, DNA/HSA interaction, molecular docking study and cytotoxic activity.

Two new complexes of Pd(II), [Pd(L1)Cl]Cl (Pd1) and [Pd(L2)Cl]Cl (Pd2), (where L1 = N2,N6-bis(5-methylthiazol-2-yl)pyridine-2,6-dicarboxamide and L2 = N2,N6-di(benzo[d]thiazol-2-yl)pyridine-2.6-dicarboxamide) were synthesized. Characterization of the complexes was performed using elemental analysis, IR, 1H NMR spectroscopy and MALDI-TOF mass spectrometry. The nucleophilic substitution reactions of complexes with L-Methionine (L-Met), L-Cysteine (L-Cys) and guanosine-5'-monophosphate (5'-GMP) were studied by stopped-flow method at physiological conditions (pH = 7.2 and 37 °C). Complex Pd1 was more reactive than Pd2 in all studied reactions, while the order of reactivity of the selected ligands was: L-Met > L-Cys > 5'-GMP. The interaction of complexes with calf thymus-DNA (CT-DNA) was studied by Uv-Vis absorption and fluorescence emission spectroscopy. Competitive binding studies with intercalative agent ethidium bromide (EB) and minor groove binder Hoechst 33258 were performed as well. Both complexes interacted with DNA through intercalation and minor groove binding, where the latter was preferred. Additionally, the interaction of Pd1 and Pd2 complexes with human serum albumin (HSA) was studied employing fluorescence quenching spectroscopy. The results indicate a moderate binding affinity of complexes, with slightly stronger binding of the Pd1. Fluorescence competition experiments with site-markers (eosin Y and ibuprofen) for HSA were used to locate the binding site of Pd1 to the HSA. Additionally, the interaction with DNA and HSA was studied by molecular docking and the revealed results were in good agreement with the experimentally obtained ones. Pd1 complex exhibited cytotoxicity toward human (HCT116) and mouse cell lines (CT26) of colorectal cancer, mouse (4T1) and human (MDA-MB468) breast cancer lines and non-cancerous mouse mesenchymal stem cells (mMSC). In addition, Pd1 complex demonstrated significant selectivity towards cancer cells over non-cancerous mMSC, indicating a high potential to eliminate malignant cells without affecting normal cells. It induced apoptosis in CT26 cells, effectively arrested the cell cycle in the S phase, and selectively down-regulated cyclin D and cyclin E. Moreover, it can alter the expression of cell cycle regulators by increasing p21 and decreasing p-AKT. These findings confirm its ability to disrupt key tumor cell survival signals and suggest that the Pd1 complex is a potent candidate for effective cancer treatment.

A portable fluorescence sensing system for timely onsite perfluorooctane sulfonate detection based on an aggregate induced emission fluorescence sensor.

Perfluorooctane sulfonate (PFOS), a ubiquitous persistent organic pollutant, has aroused growing concern due to its adverse effects on human health. Timely onsite monitoring of PFOS in heavily contaminated areas is crucial for effective pollution management and prevention of its spread. However, relevant PFOS detection methods have rarely been reported. Herein, we developed a fluorescence sensing system capable of achieving timely onsite detection of PFOS under outdoor conditions. First, aggregate induced emission (AIE) fluorescence sensors, TPE-PAs, were synthesized. The optimized sensor could selectively interact with PFOS through electrostatic attraction and hydrogen bonding and exhibited prominent fluorescence enhancement after treating with PFOS. There was a good linear relationship between the fluorescence enhancement and PFOS concentration in the range of 0.05-30 ppm, and the limit of detection was measured to be 0.047 ppm. In addition, owing to the AIE fluorescence mechanism and high concentration of TPE-PAs in the sensing medium, the sensor demonstrated excellent anti-interference performance. Second, we developed a portable fluorometer, by modifying the power supply and sample cell of a tiny fluorometer, and further integrated this modified fluorometer, the prepared fluorescence sensor, standard PFOS solutions and other consumables into a portable test system. This test system showed good detection accuracy and reliability and successfully achieved timely onsite PFOS detection in real water samples.

Phosphorus Central Chiral Multiresonance Thermally Activated Delayed Fluorescence Emitter Towards Narrowband and Efficient Circularly Polarized Electroluminescence

Phosphorus Central Chiral Multiresonance Thermally Activated Delayed Fluorescence Emitter Towards Narrowband and Efficient Circularly Polarized Electroluminescence

A Novel Near-Infrared Tricyanofuran-Based Fluorophore Probe for Polarity Detection and LD Imaging

In this paper, LD-TCF, a targeting probe for lipid droplets (LDs) with a near-infrared emission wavelength and large Stokes shift, was fabricated for polarity detection by assembling a donor–π–acceptor (D–π–A) molecule with typical twisted intramolecular charge transfer (TICT) characteristics. Surprisingly, the fluorescence emission wavelength of the newly constructed probe LD-TCF was stretched to 703 nm, and the Stokes shift was amplified to 126 nm. Furthermore, LD-TCF could specifically answer the change in polarity efficiently and did not experience interference from other biologically active materials. Importantly, LD-TCF exhibited the ability to target lipid droplets, providing valuable insights for the early diagnosis and tracking of pathophysiological processes underlying LD polarity.

Mechanistic insights into the interaction of anxiolytic drugs with human serum albumin in a ternary system utilizing spectroscopic and molecular modeling approaches

In recent years, buspirone has been co-administered with sertraline to resolve sexual disorders caused by sertraline. Therefore, the present study was conducted to investigate the interaction effect of two antidepressants and anxiolytic drugs, sertraline and buspirone, on human serum albumin (HSA) using spectroscopic and molecular docking techniques. Fluorescence emission spectroscopy and molecular docking were used to calculate the binding affinity and determine the best binding sites for these two drugs. Additionally, UV-visible and circular dichroism spectroscopy were performed to investigate the effect of these drugs on the conformational changes of HSA. The results showed that both drugs have a strong ability to quench the fluorescence of HSA through a static mechanism, and cause structural changes in HSA. It was also found that binding of sertraline and buspirone to HSA is spontaneous (ΔG° <) and hydrophobic interactions, van der Waals forces and hydrogen bonds play a significant role in these interactions in the ternary system. In addition, molecular docking data showed that both drugs bind with high affinity to the Trp residue in subdomain IIA. The binding constants (Kb) for (HSA-SRH)-BSH and (HSA-BSH)-SRH were equal to 6.30 and 3.99, respectively, at 298 K. This study demonstrates that the presence of the second drug (buspirone/sertraline) affects the interaction and binding affinity of the first drug (sertraline/buspirone) to human serum albumin.

Stable Xanthene Radicals and Their Heavy Chalcogen Analogues Showing Tunable Doublet Emission from Green to Near‐infrared

Organic luminescent radicals, unlike traditional closed‐shell fluorescent emitters, exhibit distinct luminescence mechanisms, offering promising potential for optoelectronic devices. To date, stable luminescent radicals have predominantly been confined to polychlorinated triphenylmethyl radicals, underscoring the need for new platforms to expand their emission spectra. In this study, we report the synthesis of stable 9‐aryl‐substituted xanthene radicals and their heavy chalcogen analogues (1a‐c and 2a‐c), which exhibited excellent chemical stability and emission ranging from green to near‐infrared (527~714 nm). Notably, the selenium‐substituted radical (1c) demonstrates a significantly enhanced photoluminescence quantum yield of 41% when doped into its precursor solid. Additionally, the introduction of methoxyphenyl groups has largely enhanced the stability of the radical, showcasing an excellent photostability with the longest half‐life of around 1792 h. The high internal quantum efficiency of up to 81% was further validated in organic light‐emitting diode. This study introduces a novel class of stable carbon‐centered radicals with high tunability and functionality for photoelectric applications.

Stable Xanthene Radicals and Their Heavy Chalcogen Analogues Showing Tunable Doublet Emission from Green to Near-infrared.

Organic luminescent radicals, unlike traditional closed-shell fluorescent emitters, exhibit distinct luminescence mechanisms, offering promising potential for optoelectronic devices. To date, stable luminescent radicals have predominantly been confined to polychlorinated triphenylmethyl radicals, underscoring the need for new platforms to expand their emission spectra. In this study, we report the synthesis of stable 9-aryl-substituted xanthene radicals and their heavy chalcogen analogues (1a-c and 2a-c), which exhibited excellent chemical stability and emission ranging from green to near-infrared (527~714 nm). Notably, the selenium-substituted radical (1c) demonstrates a significantly enhanced photoluminescence quantum yield of 41% when doped into its precursor solid. Additionally, the introduction of methoxyphenyl groups has largely enhanced the stability of the radical, showcasing an excellent photostability with the longest half-life of around 1792 h. The high internal quantum efficiency of up to 81% was further validated in organic light-emitting diode. This study introduces a novel class of stable carbon-centered radicals with high tunability and functionality for photoelectric applications.

Sensing the Small Change of Intermolecular Distance in Supramolecular Assembly by Using the Tunable Emission Wavelength of AIE-Active Luminogens.

The distinct molecular states - single molecule, assembly, and aggregate - of two ionic macromolecules, TPPE-APOSS and TPE-APOSS, are easily distinguishable through their tunable fluorescence emission wavelengths, which reflect variations in intermolecular distances. Both ionic macromolecules contain aggregation-induced emission (AIE) active moieties whose emission wavelengths are directly correlated to their mutual distances in solution: far away from each other as individual molecules, maintaining a tunable and relatively long distance in electrostatic interactions-controlled blackberry-type assemblies (microphase separation), or approaching van der Waals close distance in aggregates (macrophase separation). Furthermore, within the blackberry assemblies, the emission wavelength decreases monotonically with increasing assembly size, indicative of shorter intermolecular distances at nanoscale. The emission changes of TPPE-APOSS blackberry assemblies can even be visually distinguishable by eyes when their sizes and intermolecular distances are tuned. Molecular dynamics simulations further revealed that macromolecules are confined in various conformations by controllable intermolecular distances within the blackberry structure, thereby resulting in fluorescence emission with tunable wavelength.

Pure room temperature phosphorescence emission in nondoped OLEDs: adjustable oxidation states and excited-state modulation.

Purely organic room temperature phosphorescence (RTP) materials are a new kind of triplet emitter, which can harvest both singlet and triplet excitons in theory, thus showing great application potential for organic light-emitting diodes (OLEDs). However, nondoped OLEDs based on RTP emitters have been rarely explored owing to challenges in realizing efficient phosphorescence in single-component systems. Herein, three donor-acceptor-type luminogens were designed and synthesized in which phenothiazine, with different oxidation degrees, acted as the electron donor and acetophenone as the acceptor. The adjustable oxidation states of phenothiazine enabled the modulation of excited states, facilitating the transition from dual RTP and thermally activated delayed fluorescence emissions to pure RTP. A nondoped OLED device was then fabricated based on the pure RTP emitter, achieving a high exciton utilization efficiency of 86%, clearly demonstrating the enhancement of electroluminescence performance through RTP properties.

Mitochondria-Targeted NIR Ratiometric and Colorimetric Fluorescent Probe for Biothiols Based on a Thiol-Chromene Click Reaction.

In this work, a mitochondria-targeted NIR ratiometric and colorimetric fluorescent probe 1 was tactfully designed and synthesized by a novel design strategy of modifying chromene to pyridine for the first time. 1 exhibited a maximum absorption peak at 508 nm and a maximum fluorescence emission peak at 650 nm. Under the stimulus of biothiols (cysteine (Cys), homocysteine (Hcy), and glutathione (GSH)), the maximum absorption and fluorescence emission peaks of 1 blue-shifted to 448 and 541 nm, respectively, along with color changes from red to yellow under visible light and from red to green under a 365 nm ultraviolet (UV) lamp, which can be ascribed to the click reaction of biothiols with the α,β-unsaturated ketone of the chromene moiety with pyran ring-opening, phenol formation, and 1,6-elimination of the p-hydroxybenzyl moiety. 1 detected biothiols (Cys, GSH, and Hcy) with high sensitivity (LODs of 29, 23, and 16 nM for Cys, GSH, and Hcy, respectively), excellent selectivity, and fast response. Moreover, 1 can target mitochondria and image the fluctuation of intracellular biothiols by dual-emission channels.

Red-emissive carbon dots from Hibiscus rosa-sinensis: a detailed appraisal of tartrazine dye sensing properties.

Aneconomically viable and greener approach is introduced to fabricate red emissive carbon dots (R@CQDs) via employing hydrothermal means on Hibiscus rosa-sinensis leaves as precursor source. The obtained R@CQDs displayed excitation-dependent behavior, with high aqueous stability, quantum yield of 56%, and outstanding fluorescence aptitude under the conditions of varied range of ionic strength and pH (1-12). The fluorescence emission behavior of R@CQDs displayed selective turn off fluorescenceresponse to tartrazine over other interfering species with alimit of detection of 0.09µM and quantitation limit of 0.30µM. Theoretical calculations employing density functional theory (DFT) were carried out to complement experimental findings and getting insights into the underlying mechanism governing the sensing of tartrazine. The developed sensor holds significant potential for tartrazine detection in real samples and offering wider prospective in the food safety assessment.

Lanthanide Functionalized Carbon Quantum Dots for White Light Emission, pH Sensing, and Co (II) Detection.

Carbon quantum dots (CQDs) with fluorescence emission have been widely studied for versatile applications, but facile tunability of the spectral properties of CQDs by doping remains to be further explored. Herein, employing lanthanide ion Eu3+ as a dopant and activator, a simple and efficient synthesis route for pure CQDs and Eu-CQDs was demonstrated using N, N-dimethylformamide, oleic acid, and oleylamine as precursors for carbon sources. In comparison, with the popular citric acid precursor, the as-prepared CQDs and Eu-CQDs exhibited an obviously smaller particle size (1.72 ± 0.29 nm) and a more uniform distribution. Through systematic optimization of Eu3+ doping for the Eu-CQD system, colorful light emissions in the visible range were first realized under excitation of ultraviolet (UV) ∼360 nm for promising application of UV-triggered light-emitting diodes. Most interestingly, this Eu-CQD solution with UV-excited colorful light emissions was utilized as a visual pH sensor, experimentally featuring good repeatabilities and stabilities (pH values switching between 7 and 14). Besides, the Eu-CQD solution exhibited highly sensitive detection characteristics for Co (II) ions. Due to the spectral overlapping, the quenching efficiency is as high as 96.3%, and the detection limit is obtained as 0.139 μM, which is much lower than the maximum concentration of Co (II) in the drinking water permitted by WHO. All of these relevant results significantly demonstrate the great potential of lanthanide doping in the multifunctionalization of CQDs for certain emerging applications like lighting, sensing, and detection.

Investigation of H-Bonding and pH on the Fluorescence Spectral Behavior of Valsartan.

The photophysical properties of valsartan (VAL), a potent phenyl tetrazole derivative sartan, were investigated. Valsartan has absorption bands at 230nm and 255nm and a fluorescence band at about [Formula: see text] = 346nm in butanol which is red shifted depending on the H-bonding capability of the solvent. The role of H-bonding in the excited state was approved through the linear correlation of the emission energy of VAL with Camlet-Taft acidity and basicity parameters, α and β, of polar protic solvents. The position and intensity of fluorescence emission bands of VAL are found to be pH dependent, shifting from 425nm at pH 2 to 375nm at pH 4 with enhancement of intermolecular H-bonding and fluorescence intensity depletion beyond pH 5 with formation of tetrazole anion. The results were supported by time-resolved fluorescence measurements which indicated the presence of different species with different lifetimes in the excited state depending on solution pH value. Computational results based on time dependent density functional methods (TDDFT) show that the tetrazole moiety is involved in the [Formula: see text] absorption transitions, while natural bond analysis (NBO) shows that VAL adopts a dimer conformation in water because of effective intermolecular H-bonding.

Responsive integration performed by laser-induced Er3+ structural doping and graphene nanoplatelets

Laser-induced preparation method has the advantages of high efficiency, high yield, no ionic diffusion restriction and competitive side reaction, which can prepare diversified composite materials based on small-scale and distributed characteristics. Besides, integrating multiple performance and conducting inductive feedback are helpful for the reliability and calibration of laser-induced materials in the precision field. Herein, responsive integration is designed based on graphene nanoplatelets/ZnSe:Er3+ composite with optical, electrical, thermal and visual properties for real-time feedback. Er3+ ions doped ZnSe is obtained by fast laser-induced method, combined with two-dimensional graphene nanoplatelets and assembled into temperature-sensitive polyimide and cellulose paper, realizing the characteristics of photoelectric conversion and photothermal conversion. Besides, red fluorescence guiding perceptual behavior can also be produced under the radiation of NIR laser. Based on the proposed composite, bionic flower is constructed, and exhibits good motion features in blooming. Meanwhile, large curvature bending, high thermal sensitivity and strong fluorescence emission are also revealed. Such performance combination design provides a convenient approach for multi signals cross feedback in soft actuator, which strengthens the monitoring and guidance of motion perceptions, and can be potentially applied in diversified fields.