Search

High energy density and enhanced rate capability are highly sought-after for supercapacitors in today’s mobile world. In this work, polyaniline/titanium carbide (MXene) (PANI/Ti3C2Tx) nanohybrid is synthesized through a facile and cost-effective self-assembly of one-dimensional (1D) PANI nanofibers and two-dimensional (2D) Ti3C2Tx nanosheets. PANI/Ti3C2Tx delivers greatly improved specific capacitance, ultrahigh rate capability (67% capacitance retention from 1 to 100 A·g−1) as well as good cycle stability. Electrochemical kinetic analysis reveals that PANI/Ti3C2Tx is featured with surface capacitance-dominated process and has a quasi-reversible kinetics at high scan rates, giving rise to an ultrahigh rate capability. By using PANI/Ti3C2Tx as positive electrode, an 1.8 V aqueous asymmetric supercapacitor (ASC) is successfully assembled, showing a maximum energy density of 50.8 Wh·kg−1 (at 0.9 kW·kg−1) and a power density of 18 kW·kg−1 (at 26 Wh·kg−1). Moreover, an 3.0 V organic ASC is also elaborately fabricated by using PANI/Ti3C2Tx, achieving an ultrahigh energy density of 67.2 Wh·kg−1 (at 1.5 kW·kg−1) and a power density of 30 kW·kg−1 (at 26.8 Wh·kg−1). The present work not only improves fundamental understanding of the structure-property relationship towards ultrahigh rate capability electrode materials, but also provides valuable guideline for the rational design of high-performance energy storage devices with both high energy and power densities.

Potassium-ion batteries (PIBs) are appealing alternatives to conventional lithium-ion batteries (LIBs) because of their wide potential window, fast ionic conductivity in the electrolyte, and reduced cost. However, PIBs suffer from sluggish K+ reaction kinetics in electrode materials, large volume expansion of electroactive materials, and the unstable solid electrolyte interphase. Various strategies, especially in terms of electrode design, have been proposed to address these issues. In this review, the recent progress on advanced anode materials of PIBs is systematically discussed, ranging from the design principles, and nanoscale fabrication and engineering to the structure-performance relationship. Finally, the remaining limitations, potential solutions, and possible research directions for the development of PIBs towards practical applications are presented. This review will provide new insights into the lab development and real-world applications of PIBs.

A simple, convenient and label-free approach was developed for detection of acetylcholine (ACh) based on competitive enzymatic hydrolysis by use of liquid crystals (LCs) as a sensing medium. Self-assembled monolayers of myristoylcholine (Myr) were obtained at the aqueous/LC interface when the surfactants were in contact with LCs, resulting in a perpendicular orientation of LCs at the interface. Thus, LCs displayed a dark optical image. However, enzymatic hydrolysis of Myr by acetylcholinesterase (AChE) disturbed the Myr monolayers, which led to a horizontal orientation of LCs at the interface, thereby inducing a dark-to-bright shift of the LCs optical appearance. Interestingly, as ACh was also a substrate of AChE, the bright appearance of LCs was prevented when incubating the mixture of AChE and ACh with Myr decorated aqueous/LC interface due to the competitive enzymatic hydrolysis between Myr and ACh by AChE. By using this strategy, ACh could be detected selectively and sensitively, with a broad linear range from 0.01 μmol/L to 1 mmol/L and a low detection limit of 14.5 nmol/L. The results showed that the competitive enzymatic hydrolysis-assisted LC-based sensor had potential applications in ACh detection.

Hexavalent chromium is highly toxic and regarded as one of the main pollutants in the environment. Sophisticated laboratory instruments are commercially available for the in-field determination of chromium. It is highly desirable to develop affordable, portable, sensitive and reliable methods for on-site Cr(VI) detection. For field analysis, we designed a smartphone-based absorbance device with an ultralong absorption path to improve sensitivity. The intensity of the transmission light was detected by the illumination sensor in the smartphone. The absorption path was enlarged to a maximum of 83.5 cm by 41 reflection cycles. The intensity of the reflected light in an empty colorimetric cell can be serviced as the internal references to correct the possible baseline drift due to light source intensity decay. The absorbance measured by the proposed device obeys the Lambert–Beer law in the range of 0–1.1. This device was used to determine Cr(VI) in water samples on-site by using 1,5-diphenylcarbazide as a colorimetric reagent, with the linear range of 1–18 μg L−1 and limit of detection of 0.26 μg L−1. This simple absorbance device offers the advantages of cost-effectiveness, ease of implementation, portability, sensitivity and reliability for field analysis.

Benzo[a]pyrene (Bap) is one of the main organic pollutants in the atmospheric haze that is rich in fine water drops and particulate matters. The understanding of the Bap's form in water is of great importance to unveil its real biological effects toward the respiratory system. To date, various reports have documented its toxicological effects in the molecular form. Herein, we found that Bap existed as self-aggregated nanoclusters of tunable sizes rather than as dissolved molecules in water and different sized nanoclusters illustrated varied cytotoxicity. These findings indicated that the size, which has been ignored in previous studies, is also a dominant parameter similar to the molecular concentration for determining Bap's cytotoxicity. Polystyrene (PS) nanoparticles, as a model for nanoplastics, could adsorb Bap nanoclusters and serve as carriers that enter the cells. The combination effect interestingly altered the cytotoxicity distinction of Bap of different sizes. The intracellular fate of the nanoparticles and subcellular organelle damages were studied to unveil the mechanisms of cytotoxic distinction. Small Bap nanoclusters entered cells faster than their large counterparts. The Bap of the PS@Bap complex was stably adsorbed on PS at the early stages of endocytosis until it was detached during the lysosomal transport and maturation process. The dissociated Bap may bypass the lysosome pathway and be released into the cytosol with a nanocluster structure or relocate into the endoplasmic reticulum. On the other hand, the detached PS preferred to bind to the mitochondria or be excreted out of the cell via the lysosomal pathway. Moreover, the PS@Bap complex resulted in a significant loss of the mitochondrial membrane potential and induced apoptosis through the mitochondria-involved apoptosis pathway. This study provides a new perspective towards the toxicological mechanism of insoluble hydrophobic organic compounds and reveals the environmental significance of nanoplastics for regulating the biological effects of conventional pollutants.

Adenosine triphosphate (ATP), as a high-energy phosphate compound that stores and releases energy in living cells, has an irreplaceable role in many physiological processes and maintenance of biological functions, and can be used as an indicator of many diseases. In this work, a composite nanoprobe, silver nanocluster (AgNC) @ molybdenum disulfide (MoS2), was designed to achieve in situ fluorescence imaging and quantitative analysis of intracellular ATP in HeLa cells by fluorescence spectrometry and inductively coupled plasma mass spectrometry (ICP-MS). The probe was constructed based on the adsorption of DNA-AgNCs by MoS2 nanosheets, and the DNA-AgNCs were prepared with the ATP aptamer as a template, whose fluorescence was initially quenched by MoS2. When the probe was incubated into the cells, intracellular ATP recognized the aptamer sequence and caused the DNA-AgNCs to fall off the MoS2 nanosheets, resulting in fluorescence recovery. Here, AgNCs not only acted as a fluorescence label for imaging, but also as an element tag for quantitative analysis of intracellular ATP with the detection of 107Ag by ICP-MS. The ATP in HeLa cells detected by this method was 24.6 ± 1.7 nmol L−1, which was in good agreement with the test result of the ATP test kit (20.4 ± 0.8 nmol L−1). The proposed method has potential application in medical clinical diagnosis and evaluation of the body’s metabolic level via fluorescence imaging and ICP-MS detection of intracellular ATP.

Molecularly imprinting polymers (MIPs), as artificial antibodies with high recognition selectivity to template molecules, are widely used in various biosensors. To improve further the selectivity of MIPs-based photoelectrochemical (PEC) biosensors, we report a differential strategy using non-imprinted polymers (NIPs) as the reference. In a proof-to-concept example for the determination of dopamine (DA), MIPs and NIPs membranes were fabricated by electrochemical polymerization of polypyrrole membranes on the surface of graphene quantum dots (GQDs)/TiO2 nanotubes (NTs). The photocurrent difference between the two PEC cells, MIPs@GQDs/TiO2 NTs−Pt and NIPs@GQDs/TiO2 NTs−Pt, was measured as the signal. As the non-specific adsorption of non-template molecules on the outside surface of MIPs and NIPs membranes is similar, the anti-interference ability for the determination of DA is much improved by using differential strategy. In the normal and differential PEC measurement models, 10.0 μM ascorbic acid is equivalent to 3.12 and 0.40 μM DA, respectively. Further, the smaller specific surface area in NIPs membrane was compensated by using a weight factor to correct the residual interference in a modified differential model. By using 10.0 μM ascorbic acid as the balance point, the presence of 10.0 μM H2O2, glutathione, uric acid or glucose is equivalent only to 0.090, 0.061,0.11 or 0.041 μM of DA, respectively, which are about 3–7% of their interference levels in the normal photocurrent model. The differential PEC method was applied in the determination of DA in serum samples in the linear range of 0.05–12.5 μM, with the detection limit of 0.018 μM.

Lithium-ion capacitors (LICs) could combine the virtues of high power capability of conventional super-3capacitors and high energy density of lithium-ion batteries. However, the lack of high-performance electrode materials and the kinetic imbalance between the positive and negative electrodes are the major challenge. In this study, Fe3O4 nanoparticles encapsulated in nitrogen-rich carbon (Fe3O4@NC) were prepared through a self-assembly of the colloidal FeOOH with polyaniline (PANI) followed by pyrolysis. Due to the well-designed nanostructure, conductive nitrogen-rich carbon shells, abundant micropores and high specific surface area, Fe3O4@NC-700 delivers a high capacity, high rate capability and long cycling stability. Kinetic analyses of the redox reactions reveal the pseudocapacitive mechanism and the feasibility as negative material in LIC devices. A novel LIC was constructed with Fe3O4@NC-700 as the negative electrode and expanded graphene (EGN) as the positive electrode. The well-matched two electrodes effectively alleviate the kinetic imbalance between the positive and negative electrodes. As a result, Fe3O4@NC-700//EGN LIC exhibits a wide operating voltage window, and thus achieves an ultrahigh energy density of 137.5 W h kg−1. These results provide fundamental insights into the design of pseudocapacitive electrode and show future research directions towards the next generation energy storage devices.

With high energy density and low material cost, lithium-sulfur batteries (LSBs) emerge quite expeditiously as a fascinating energy storage system over the past decade. Broad applications of LSBs ranging from electric vehicles to stationary grid storage seem rather bright in recent literatures. However, there still exist many pressing challenges to be addressed because we do not yet fully understand and control the electrode-electrolyte interface chemistries during battery operation, such as polysulfide shuttling and poor utilization of active sulfur. Single-atom catalysts (SACs) pave new possibilities of tackling the tough issues due to their decent applicability in the atomic-level identification of structure-activity relationships and reaction mechanism, as well as their structural tunability with atomic precision. This review comprehensively summarizes the very recent advances in utilization of highly active SACs for LSBs by stating and discussing the related publications, which involves catalyst synthesis routes, battery performance, catalytic mechanisms, optimization strategies, and promises to achieve long-life, high-energy LSBs. We see that endeavors to employ SACs to modify sulfur cathode have allowed efficient polysulfide conversion and confinement, leading to the minimization of shuttle effect. Parallel efforts are being devoted to extending the scope of SACs to cell separator and lithium metal anode in order to unlock the full potential of LSBs. We also obtain mechanistic insights into battery chemistries and nature of SACs in their strong interactions with polysulfides through advanced in situ characterizations documented. Overall, acceleration in the development of LSBs by introducing SACs is noticeable, and this cutting edge needs more attentions to further promoting the design of better LSBs.

Computational simulation methods are used for characterizing the detailed attachment, diffusion and desorption of halogen vapor molecules in zeolitic imidazolate framework-8 (ZIF-8). The attachment energies of Cl2, Br2 and I2 are −55.2, −48.5 and −43.0 kJ mol−1, respectively. The framework of ZIF-8 is disrupted by Cl2, which bonds with Zn either on the surface or by freely diffusing into the cage. A framework deformation on the surface of ZIF-8 can be caused by the attachment of Br2, but only reorientation of the 2-methylimidazolate linkers (mIms) for I2. In diffusion, the halogen molecules have a tendency to vertically permeate the apertures of cages followed with swing effect implemented by the mIms. Larger rotation angles of mIms are caused by Br2 because of its stronger interaction with mIms than I2. A maximum of 7 Br2 or 5 I2 molecules can be accommodated in one cage. Br2 are clinging to the mIms and I2 are arranged as crystal layout in the cages, therefore in desorption processes molecules attached to the surface and free inside are desorbed while some remained. These results are beneficial for better understanding the adsorption and desorption processes of halogen vapors in the porous materials.

In this work, we report a simple ratiometric electrochemiluminescence (ECL) method for ultra-sensitive immunoanalysis. A glassy carbon electrode (GCE) was modified by a mixture of porous g-C3N4 nanosheets and carbon nanotubes (CNTs). Secondary antibodies were labeled using CuS nanoparticles as the tags. After immune recognition, CuS nanoparticles in the immunocomplex were dissolved as Cu2+, which can quench the ECL of g-C3N4. The amount of Cu2+ was determined to quantify the concentration of the target antigen. To enhance the sensitivity, Cu2+ ions were firstly enriched and reduced to Cu on the surface of GCE/CNTs-g-C3N4, and the cathodic ECL of g-C3N4 was measured as the reference signal in the ratiometric ECL measurements. After applying a potential of 0.6 V (vs. Ag/AgCl) for 6 s, Cu was dissolved as Cu2+, which can quench the ECL of g-C3N4 with much higher efficiency because the freshly dissolved Cu2+ ions were distributed mainly within the Helmholtz layer of GCE/CNTs-g-C3N4. By using the ECL intensity ratio of GCE/CNTs-g-C3N4 (Cu2+) to GCE/CNTs-g-C3N4 (Cu) measured under the potentiostatic model as the signal indictor, the ratiometric ECL method was used to detect a biomarker of alpha fetoprotein with the limit of detection of 0.1 fg mL-1. It was shown that the influence of the difference in electrode modification and ECL measurement conditions on the determination of Cu2+ is suppressed greatly in the ratiometric ECL method. The combination of ratiometric ECL with electrochemical enrichment and biometallization is a useful strategy to enhance the sensitivity and reproducibility in immunoanalysis.

The continuous exploration of advanced electrode materials is of remarkable significance to revolutionize next-generation high-performance energy storage devices towards a green future. Benefiting from their electrochemically active sites and abundant redox centers, bimetallic selenides with desirable nanostructures recently have emerged as promising electrode alternatives for battery–supercapacitor hybrid (BSH) devices which demonstrate enormous potential in bridging the gap between electrochemical properties with high power densities (supercapacitors) and energy densities (batteries). Herein, employing the hydrothermal approach with solid Ni–Co spheres as precursors followed by the selenization process, selenide-rich bimetallic selenide spheres with a core–shell nanostructure were rationally designed and synthesized for use as the cathode electrode in superior BSH devices. The as-obtained (NiCo)9Se8/(NiCo)0.85Se (Ni–Co–Se) exhibits a high specific capacity of 164.44 mA h g−1 at a current density of 1 A g−1 with 85.72% capacity retention even after 5000 cycles at a current density of as high as 8 A g−1, suggesting its great promise in practical applications for BSH devices. By integrating activated carbon as the anode with the as-obtained bimetallic selenides as the cathode, an alkaline aqueous BSH device is fabricated and delivers a high energy density of 37.54 W h kg−1 at a high power density of 842.7 W kg−1. It is found that the excellent electrochemical performances can be ascribed to facile ion and electron transport pathways, high electrical conductivity and reliable structural robustness of the prepared selenides. Moreover, the synthetic strategy presented in this paper opens up an avenue to guide the synthesis of various anion doped bimetallic compounds towards high-performance energy conversion and storage devices.

The magnetic resonance imaging diagnosis and high-efficiency tumor targeting treatment are of notable importance for cancer therapy. In this study, starch-octanoic acid (ST-OA) micelles were successfully prepared to co-encapsulate the anti-tumor drug doxorubicin (DOX) and superparamagnetic iron oxide nanoparticles (SPIONs), taking advantage of the hydrophobic core of the core-shell micellar structure. Size distribution, morphology and in vitro release behaviors of micelles were investigated. In addition, magnetic properties and the anti-tumor theranostic performance were confirmed by conducting the cellular uptake, in vivo imaging and anti-tumor activity experiments. Therefore, co-encapsulation and specific delivery of the chemotherapeutic drug and contrast agent into tumor cells can realize the diagnosis and treatment of malignant tumor at the same time.

Oxidative stress is an important pathological mechanism for acute kidney injury (AKI). SS-31, as a mitochondria-targeted peptide with strong antioxidant activity, is a good candidate for the treatment of AKI. However, an efficient treatment of AKI requires frequent administration of SS-31, which is due to its poor specific biodistribution and low delivery efficiency. To overcome these deficiencies, we designed pH-responsive and AKI-kidney targeted nanopolyplexes (NPs) for effectively delivering SS-31, which is new frontier for formulation of HA and CS. NPs are electrostatically complexed using anionic hyaluronic acid and cationic chitosan as materials, which could increase the accumulation in injured areas and uptake into CD44-overexpressed cells. Electrostatic balance of NPs is broken in low pH environment of lysosomes to allow SS-31 releasing and subsequently targeting to mitochondria to represent therapeutic effect. In vitro studies indicate that NPs exhibited higher antioxidative and antiapoptotic effects as compared with free SS-31. AKI mouse model suggests that NPs have significantly higher therapeutic efficiency than bare SS-31. It was found that NPs had excellent ability to decrease oxidative stress, protect mitochondrial structure, reduce inflammatory response, reduce apoptosis and necrosis of tubular cells after intravenious administration. Overall, the results suggest that the NPs have significant potential to enhance the specific biodistribution and delivery of SS-31, therefore have good effects on reducing oxidative stress and inflammation, preventing tubular apoptosis and necrosis. We believe NPs are effective delivery system for AKI treatment in clinical application.

Cationic anticancer peptides, which can induce tumor cell immunogenic death and further promote systemic tumor-specific immune responses, have offered a promising solution to relieve the tumor immunosuppressive microenvironment. However, peptide drugs are easily degraded and lack of targeting ability when administered systemically, leading to limitations in their applications. Herein, we report a pH and thermal dual-sensitive bovine lactoferricin-loaded (one of the most widely studied cationic anticancer peptides) nanoparticles, which simultaneously exhibited antitumor and immune cell activated effects when applied with microwave thermotherapy, an auxiliary method of immunotherapy. The bovine lactoferricin could be delivered to the tumor site by nanoparticles, be immediately released from nanoparticles in the acidic environment of lysosomes and the thermal condition caused by microwave radiation, and ultimately induce tumor apoptosis with the release of damage-associated molecular patterns (DAMPs). It is worth noting that the strategy of bovine lactoferricin-loaded nanoparticles intravenous injection combined with local microwave thermotherapy not only showed excellent efficacy in relieving tumor growth but also resulted in strong antitumor immunities, which was due to the released bovine lactoferricin under stimulating conditions, and the pool of tumor-associated antigens generated by tumor destruction. In conclusion, this work presents a strategy for tumor treatment based on dual-sensitive bovine lactoferricin-loaded nanoparticles combined with microwave thermotherapy, which may provide a solution for cationic anticancer peptides delivery and improving antitumor immune responses.

This paper is an investigation on oscillation characteristics and transition routes of thermocapillary convection in an annular liquid pool in the space experiment carried out on SJ-10 recoverable scientific experiment satellite. Thermocapillary convection caused by non-uniformity of surface tension and the instability problem of the convection are introduced, and the measurement by thermocouples has been analyzed in detail. Through the relationship between the critical condition of start-oscillation in thermocapillary convection and the volume ratio, and the relationship between the oscillation frequency and the volume ratio, transition processes from steady flow to oscillatory flow and then to bifurcation are investigated. In addition, the acting mechanism of thermocapillary force has been discussed comparing with buoyant-thermocapillary convection on the ground.

Improvement of the sensitivity and selectivity is important in the development of an analytical method. Herein, we propose a differential photoelectrochemical (PEC) sensor to hydrogen peroxide based on the catalytic activity difference between two zeolitic imidazolate framework (ZIF) surface coatings. In the sensing and reference photoelectrodes, ZIF-67 and ZIF-8 films were grown on the surface of carboxylated carbon nanotubes-graphite-like carbon nitride/TiO2 nanotube array, respectively. The molecular sieve effect of ZIF-8 and ZIF-67 coatings can prevent the diffusion of molecules with size larger than the pores in coating layers (e.g. ascorbic acid), improving the selectivity of the PEC sensor to H2O2. The sensing photoelectrode offers higher sensitivity to H2O2 than the reference one due to the excellent catalytic activity of ZIF-67. The interference from the surfaces of the sensing and reference photoelectrodes can be eliminated effectively by the differential strategy, enhancing further the selectivity, reliability and stability of the sensor. Under optimized conditions, the as-prepared differential PEC sensor was applied to the detection of H2O2 with limit of detection of 1.5 nM, exhibiting high sensitivity and anti-interference ability.

Spinal cord injury (SCI) routinely causes the immediate loss and disruption of neurons followed by complicated secondary injuries, including inflammation, oxidative stress, and dense glial scar formation. Inhibitory factors in the lesion scar and poor intrinsic neural regeneration capacity restrict functional recovery after injury. Minocycline, which has neuroprotective activity, can alleviate secondary injury, but the long-term administration of this drug may cause toxicity. Polysialic acid (PSA) is a large cell-surface carbohydrate that is critical for central nervous system development and is capable of promoting precursor cell migration, axon path finding, and synaptic remodeling; thus, PSA plays a vital role in tissue repair and regeneration. Here, we developed a PSA-based minocycline-loaded nanodrug delivery system (PSM) for the synergistic therapy of spinal cord injury. The prepared PSM exerted marked anti-inflammatory and neuroprotective activities both in vitro and in vivo. The administration of PSM could significantly protect neurons and myelin sheaths from damage, reduce the formation of glial scar, recruit endogenous neural stem cells to the lesion site, and promote the regeneration of neurons and the extension of long axons throughout the glial scar, thereby largely improving the locomotor function of SCI rats and exerting a superior therapeutic effect. The findings might provide a novel strategy for SCI synergistic therapy and the utilization of PSA in other central nervous system diseases.

Photodynamic therapy (PDT) and photothermal therapy (PTT) are effective cancer treatments, and photosensitizers play the most important role in the treatment. However, photosensitizers are insufficient for in vivo tumor treatment. Herein, we develop a small molecule fluorophore Cy-HPT as a novel photosensitizer, which possesses the advantages of near-infrared (NIR) emission, high photothermal conversion efficiency and high singlet oxygen generation efficiency. Moreover, a nanoplatform of HSA@Cy-HPT was synthesized by self-assembly of Cy-HPT and human serum albumin (HSA) in aqueous solution. Compared to Cy-HPT, HSA@Cy-HPT possesses more stable spectral properties, enhances the effect of PDT/PTT, and exhibits more satisfactory in vivo metabolism. HSA@Cy-HPT demonstrates outstanding tumor targeting in subcutaneous tumor xenograft models owing to its enhanced permeability and retention in tumor tissue. Furthermore, HSA@Cy-HPT was successfully utilized in tumor xenograft models and tumor tissue growth was clearly inhibited without any regrowth, extending survival rate of the models. Also, no distinct damage of the normal tissue of tumor xenograft models was observed using hematoxylin & eosin staining. This study presents a promising therapeutic agent for the synergetic PDT and PTT cancer treatment.

Multiple drug resistance and the increase in the appearance of superbugs together with the exceedingly scant development of new potent antibiotic drugs pose an urgent global medical threat and imminent public security crisis. In the present study, we fabricated well-dispersed tocopherol polyethylene glycol succinate (TPGS)-capped silver nanoparticles (AgNPs) of about 10 nm in size. The hollow structure of the TPGS-capped AgNPs (TPGS/AgNPs) was confirmed and applied to load antibiotics. The TPGS/AgNPs proved to be able to cross the bacterial cell wall and penetrate into bacteria, thereby delivering more of the antibiotic to the interior of bacteria and thus enhancing the in vitro antibacterial effect of the antibiotic, even overcoming the drug-resistance in drug-resistant E. coli and Acinetobacter baumannii. It was found that the TPGS modification in the TPGS/AgNPs could decrease the activity of the efflux pumps AdeABC and AdeIJK in drug-resistant Acinetobacter baumannii via inhibiting the efflux pump genes adeB and adeJ, thus increasing the accumulation of the delivered antibiotic and overcoming the drug-resistance. Tigecycline delivered by TPGS/AgNPs could effectively antagonize drug-resistance in an acute peritonitis model mice, thereby increasing the survival rate and alleviating the inflammatory response. TPGS/AgNPs were developed as a novel and effective antibiotic delivery system and TPGS was demonstrated to have great potential as a pharmaceutical excipient for use in drug-resistant infection therapy.

A simple, low-cost and label-free strategy for detecting lithocholic acid (LCA) was designed at the liquid crystals (LCs)/aqueous interface via competitive host-guest inclusion. In this method, sodium dodecyl sulfate (SDS) was initially adsorbed on the fluid interface and induced LCs to adopt the homeotropic ordering. Inclusion complexation of SDS and β-cyclodextrin (β-CD) disturbed interaction between LCs and SDS and evoked LCs to keep a tilted alignment. When injecting LCA into the mixed solution of SDS and β-CD, SDS excluded from the cavity of β-CD by competitive host-guest inclusion and could be re-adsorbed at the LCs/aqueous interface, resulting in the orientational transition of LCs from tilted to homeotropic state. Correspondingly, a bright-to-dark optical response was observed under polarized optical microscope (POM). The as-prepared LCs-based sensor could detect LCA as low as about 2 μM in aqueous solution. Moreover, the practicability of the approach was validated by monitoring the known amount of LCA in human urine. This work offers an appealing approach for the detection of LCA which has a great potentiality in clinical diagnosis.

The sluggish redox kinetic and the severe shuttle effect remain the key issues for the application of lithium–sulfur batteries, resulting in low sulfur utilization and rapid capacity fading. Herein, a nanostructured VS4 anchored on defect-rich carbon nanofibers (CNF-VS4) was coated on the commercial separator as both physical blocks to mitigate the shuttle effects and as an electrocatalyst to enhance the reaction kinetics of polysulfides/Li2S. Besides, polar nanostructured VS4 shows a high affinity to polysulfides, and conductive CNF network serves as “second collector” to trap and reutilize the active materials. The functional coating layer also provides rich defects for the dispersion and stabilization of Li2S. When the CNF-VS4 functional separator based on a high-sulfur content (80 wt%) cathode was applied in Li–S batteries, a high initial capacity of 1135 mA h g−1 at 0.2C and a superior rate capacity of 780 mA h g−1 at 2C were achieved. Even under a higher rate (5C), it still delivered a stable capacity of 300 mA h g−1 over 1000 cycles with a high coulombic efficiency of 95%.

Ratiometric electrochemical sensors can provide a relatively accurate analysis of target analytes due to their self-calibration function. Herein, we report a simple ratiometric strategy for achieving the electrochemical detection of Cd(ii), Hg(ii), Pb(ii) and Zn(ii), as well as multiple cancer biomarkers by using metal sulfide nanoparticles as signal tags. A conductive polymer film of poly(2-amino terephthalic acid) (ATA) was electrochemically produced on a glassy carbon electrode (GCE) and doped with carbon nanotubes (CNTs) and mercaptosuccinic acid (MSA). Using Bi(iii) as an enhancer and internal reference in anodic stripping voltammetry, the MSA-CNT-ATA/GCE exhibited sensitive and distinguishable voltammetric responses to Cd(ii), Hg(ii), Pb(ii) and Zn(ii), with detection limits of 0.13, 0.49, 0.16 and 0.089 μg L-1, respectively. By using CdS, HgS, PbS and ZnS labeled secondary antibodies as the signal tags, alpha-fetoprotein, carbohydrate antigen 19-9, carbohydrate antigen 125, and carcinoembryonic antigen were determined simultaneously according to the amounts of metal sulfide in the sandwich-type complexes, with detection limits of 0.11 pg mL-1, 0.68 mU mL-1, 1.4 mU mL-1 and 0.23 pg mL-1, respectively. This ratiometric approach has a wide scope in the electrochemical detection of heavy metal ions as well as immunoassays with metal ions serving as signal tags.

A liquid crystals (LCs)-based sensing platform was constructed for simple, convenient, inexpensive and label-free detection of α-amylase, associated with disruption of host-guest interaction between sodium dodecyl sulphate (SDS) and β-cyclodextrin (β-CD). In the presence of SDS/β-CD solution, a bright optical image was observed corresponding to the tilted anchoring of LCs at the aqueous/LCs interface. While a black optical appearance was captured when the pre-incubated mixture containing SDS/β-CD complex and ≥0.0001 mg/mL α-amylase was transferred onto the fluid interface. The reason for this difference is that α-amylase could hydrolyze β-CD and subsequently destroy the host-guest interaction between SDS and β-CD. SDS molecules escaping from the cavity of β-CDs were adsorbed at the aqueous/LCs interface, which evoked the homeotropic state of LCs. In the case of α-amylase below 0.0001 mg/mL, a bright optical image was observed. Based on these, detection of α-amylase could be achieved and its detection limit was ∼0.0001 mg/mL (15 U/L). Moreover, this sensing platform was successfully utilized to monitor α-amylase in the body fluids, such as urine and saliva, indicating its potentiality in the relevant clinical diagnosis.

Lithium–sulfur (Li–S) batteries are widely regarded as some of the most promising next-generation energy storage systems due to their cost advantage and high theoretical energy density. However, the shuttle effect arising from the dissolution of polysulfides into organic electrolyte, the insulating nature of sulfur and their discharge products severely restrict the development of high-energy density Li–S batteries. Herein, a porous organic framework containing diketopyrrolopyrrole (DPP) building blocks is reasonably designed and it serves as a shuttle-inhibiting layer to bifunctionally increase the physical and chemical trapping of lithium polysulfides. The frameworks were synthesized through a bottom-up approach, allowing precise control of the network design at the molecular level. As a result, the framework-derived microscale networks with polar units effectively hinder the shuttle effect of polysulfides and promise excellent electrochemical performances with regard to improving kinetics and long-term cycling stability of Li–S batteries. DFT calculations demonstrate the charge transfer (CT) behavior and favorable binding energy between the DPP units and lithium polysulfides. This work not only provides a novel strategy to fabricate a bifunctional modified separator for high-performance Li–S batteries, but also inspires us to further develop advanced materials for emerging energy storage applications.

Effective treatment for acute lung injury (ALI) is in high demand. Lung-targeted ternary nanoparticles containing anti-intercellular adhesion molecule-1 (ICAM-1) antibody-conjugated simvastatin-loaded nanostructured lipid carrier (ICAM/NLC), protamine (Pro), and angiopoietin-1 (Ang-1) gene (ICAM-NLC/Pro/Ang) were developed for ALI therapy. The ternary nanoparticles with different weight ratios of ICAM-NLC to Ang-1 gene were prepared via charge interaction. The anti-ICAM-1 antibody-conjugated ternary nanoparticles exhibited higher cellular uptake and transfection efficiency (from 26.7% to 30.9%) in human vascular endothelial cell line EAhy926 than the non-targeted control. The largest size of ICAM-NLC/Pro/Ang (357.1 nm) was employed for further study, which significantly up-regulated in vitro and in vivo Ang-1 protein expression. In vivo i.v. administration of ICAM-NLC/Pro/Ang (357.1 nm) significantly attenuated pulmonary TNF-α and IL-6 levels, inflammatory cell infiltration, and led to positive histological improvements in lipopolysaccharide-induced ALI mice. Collectively, the ICAM-NLC/Pro/Ang that co-delivered simvastatin and Ang-1 gene may represent a potential treatment modality for ALI.

Glutathione (GSH) is of significance in human pathology due to its many cellular functions. γ-Glutamyl transpeptidase (γ-GT) plays a key role in the balance of GSH by breaking down extracellular GSH. In this study, we proposed a novel strategy for sensitive and selective detection of GSH based on LC sensing platform coupled with its inhibition of γ-GT. The γ-GT cleavable surfactant, dodecyl N-ethanamide N, N, N-trimethylammonium bromide (DAA), was synthesized and utilized to decorate the aqueous/LC interface. A black optical image of LCs was observed due to formation of the self-assembled DAA monolayer at the interface. Subsequently, the optical response of LCs returned to bright appearance after transferring γ-GT to the DAA-laden interface because DAA could be enzymatically hydrolyzed by γ-GT and the monolayer was disrupted. Interestingly, LCs remained dark images after the DAA-decorated interface in contact with the pre-incubated GSH and γ-GT. The detection limit of GSH reached 1 pg/mL, which demonstrates high competitiveness with the current assays. The detection mechanism of GSH was explained by Isothermal titration calorimetry (ITC) measurements and Fourier transform infrared (FTIR) spectroscopy. This work presents an appealing route to achieve ultrasensitive detection of GSH according to its hydrolysis by γ-GT and the as-prepared simple and robust LC-based sensing platform has potentials in the diagnosis of GSH-related diseases (e.g. cancer, liver damage, and malignant neoplasms).

Fabrications and applications of luminescent films have been an interesting and important challenge within the realm of academia and industry. Herein, a novel fluorescence-based strategy for the H2O2 detection has been developed by fabrication of stabilized, thin, transparent, and luminescent films composed of europium-containing polyoxometalates (Eu-POM) and environmentally friendly chitosan (CS) via a facile solution casting approach. In comparison with pure Eu-POM, enhanced fluorescent properties are obtained from the as-prepared Eu-POM/CS films in terms of prolonged fluorescence lifetime and a remarkable fluorescent quenching effect in the presence of hydrogen peroxide (H2O2). The fluorescence intensity of Eu-POM/CS films exhibits a linear correlation in response to the H2O2 concentration over a wide range of 1.1–66 μM, with a detection limit of 0.11 μM. Furthermore, the fluorescent films display a high detection selectivity which are capable of differentiating hydrogen peroxide (H2O2) from the interfering species, such as sugars, l -amino acids, and other metabolites. All these advances towards the development of Eu-POM/CS films open up new applications for luminescent films, but most importantly, they can help in the far-reaching technological implementations of a simple, cost-effective method for the detection of H2O2 in many fields.

The lithium sulfur battery is regarded as a promising energy solution because of its high energy density. However, the insulating nature and large volumetric expansion of sulfur and the high solubility of polysulfides restrict their practical applications. Here carbon nanotube (CNT)-induced yolk–shell carbon nanopolyhedra, with Co–N-doping, is used as host material for sulfur. The CNTs are used to create a conductive network which interweaves each carbon polyhedron and induces the formation of a yolk–shell structure during the sulfur melt-diffusion process due to the “perforation effect”. The CNT-connected Co–N-doped carbon nanopolyhedra containing sulfur yolk–shell structure (S@Co–N–C/CNTs-0.5) can achieve a capacity of 712.2 mAh g–1 at 1675 (1 C) mA g–1 after 300 cycles and 511.8 mAh g–1 at 3350 (2 C) mA g–1. The outstanding performance is attributed to the new paradigm, S@Co–N–C/CNTs-0.5 yolk–shell structure, which creates a conductive network allowing for improved electron transport and convenient ele...

Signal amplification for electrochemiluminescence (ECL) has conventionally been achieved by employing effective matrixes that can accelerate the electrochemical redox processes or carry more electr...

Herein, we developed a smartphone-based ratiometric resonance light scattering (RLS) device for portable field analysis and immunoassay. The RLS signal was detected by the camera in a smartphone controlled by a user-edited APP software. Except the smartphone, the total cost of the detection system itself is about 60 $, including a laser pointer and battery, a twin cuvette, a collective lens, and outside box. By using the RLS brightness ratio between the sample and reference channels in the twin cuvette as the signal indicator, the baseline drifts due to the variations in incident light intensity, ambient temperature, and shooting parameters of camera, can be eliminated efficiently. A new brightness indictor, (R − R0)/(Rmax − R), was proposed to linearize the calibration curve. Where R and R0 are the rightness ratio in sample and blank, Rmax is the maximum averaged brightness ratio, respectively. The applicability of the portable RLS device was demonstrated by the field analysis for Pb2+ in environmental water samples, using [CTA]2PbI4］(CAT = cetyltrimethyl ammonium) as the luminophore. The limit of detection for Pb2+ is 0.7 μg L−1. By using PbS nanoparticles conjugated second antibody as the signal tag, the RLS method was applied in immunoassay to determine alpha fetoprotein with the limit of detection of 0.1 pg mL−1. This smartphone-based ratiometric RLS device offers the advantages of good portability, low cost, high sensitivity and reliability.

The in vivo bio-behaviors and biosafety of nanoparticles were demonstrated to be closely correlated with particle sizes, which illustrated whether they could be used as the effective drug delivery carriers. Though tumor penetration capabilities of the small pore sized-mesoporous silica nanoparticles (MSNs) were reported to be in a particle size-dependent manner, the size effects of large pore sized-MSNs on the safe and effective cancer resistance treatment, especially at sub-50 nm, were not explicitly evaluated. In this study, we fabricate the 20 nm and 50 nm MSNs, and aim at investigating their difference in tumor accumulation, penetration, retention and toxicity both in vitro and in vivo. Our results showed that these two particle sized-MSNs possessed the excellent tumor penetration capabilities both in resistant human hepatocellular carcinoma cells-cultured spheroids and in the corresponding xenograft mice models, but the 50 nm MSNs seemed to have the better tumor accumulation and retention effects than the 20 nm MSNs. Moreover, the 50 nm MSNs displayed the lower toxicities than the 20 nm MSNs whatever on resistant cancer cell lines or on zebrafish embryos, indicating the greater systematic biosafety. In a word, our data provide the evidence that selection of the large pore-sized MSNs at the appropriate particle size (not the smaller the better) as bio-macromolecule nanocarriers will play a key role in the safe and effective treatment against cancer resistance.

The development of space experiment payload for studying thermocapillary convection in the liquid bridge with large Pr number on TG-2 space laboratory as well as the experiments are presented in detail in this paper, and the objectives of the space experiments are confirmed. The functions of the payload are analyzed, and the technical and engineering specifications are determined. Detailed designs and experimental verifications are performed on the structure of liquid bridge columns, the method of bubble removing in the liquid, the bridge cleaning system, the accurate control of aspect ratio and volume ratio, and the high-sensitivity measurement of fluid temperature. Matching experiments on the ground according to space experiment properties are carried out, 5cSt silicone oil is selected as the fluid medium in space experiments. And the states of liquid bridge and temperature oscillation signals obtained from space experiments are presented at the end of this paper. Specific summarizations and discussions to the experiment project on fluid science in space are conducted in this paper, which will provide a useful reference for scientists participating space experimental research in the future.

Boron nitride nanosheets (BNNSs) have gained significant attraction in energy and environment fields because of their two-dimensional (2D) nature, large band gap and high thermal/mechanical performance. However, the current low production efficiency of high-quality BNNSs is still a bottleneck limiting their applications. Herein, based on sonication-assisted liquid-phase exfoliation, we demonstrated a rapid, high-efficient and scalable production strategy of BNNSs and documented the effects of a spectrum of exfoliation factors (e.g., ultrasonic condition, solvent and bulk material feeding) on the yield of BNNSs. A record of yield of 72.5% was achieved while the exfoliated BNNSs have few-layer and defect-free feature. Thanks to the Lewis acid sites of the boron atoms, the BNNSs can interact with the polysulfide anions in liquid electrolyte and also can facilitate the uniform lithium deposition, which finally endow a lithium-sulfur (Li-S) battery with long life. This work provides a facile and rapid strategy for large scale preparation of high-quality BNNSs, also contributes a long-life strategy for dendrite-free Li-S battery, opens new avenues of BNNSs in energy application.

Near-infrared electrochemiluminescence (NIR ECL) luminophores are strongly anticipated in ECL bioimaging and spectrum-resolved multiplexing assays. Herein, bovine serum albumin-stabilized Ag nanoclusters (BSA-Ag NCs) are demonstrated promising NIR ECL performance, exhibiting strong anodic ECL spectrum peak at 904 nm in aqueous medium. The ECL intensity of BSA-Ag NCs-triethanolamine system was enhanced 3.2 times by adding TiO2 nanoparticles as co-reactant accelerator. In a spectrum-resolved triplex-color ECL multiplexing immunoassay, CdSe NCs, CdTe NCs and BSA-Ag NCs were used as the ECL tags, carbohydrate antigen 125 (CA125), carbohydrate antigen 19–9 (CA19-9) and cardiac troponin I (cTnI) were chosen as model analytes. The ECL peaks of three antigen-NCs pairs were simultaneously measured via one ECL potential scan. The composite of carbon nanotubes-TiO2 nanoparticles-chitosan was served as the conductivity and co-reactant accelerators, enhancing the ECL intensity by 16 folds. With the integral intensity over the ECL peaks as the analytical signal to improve further the signal-to-noise ratio, the limits of detection were 0.035 mU mL−1 for CA125, 0.087 mU mL−1 for CA19-9, and 0.016 pg mL−1 for cTnI, respectively.

A smartphone-based ratiometric fluorescence device was designed to monitor the reaction kinetic process under vigorous mixing conditions, demonstrated by the hydrolysis of Cs4PbBr6 nanocrystals (NCs). In the presence of trace water, part of Cs4PbBr6 NCs (non-fluorescent) was converted to CsPbBr3 NCs (strong fluorescent). Using anthracene as the reference fluorophore, the brightness ratio of the green (from CsPbBr3 NCs) to blue (from anthracene) components in the fluorescence image which was recorded in situ by the smartphone camera was measured as the signal for kinetic analysis. It was shown that the water-triggered conversion reaction from Cs4PbBr6 NCs to CsPbBr3 NCs follows the pseudo-second-order kinetic model in the early rapid hydrolysis stage (up to 4 min). With increasing water content, the hydrolysis of Cs4PbBr6 NCs is promoted to yield more CsPbBr3 NCs, which was used to determine trace water in n-hexane, dichloromethane, and toluene with detection limits of 0.031, 0.043, and 0.057 μL mL−1, respectively. The device offers the advantages of portability and low cost for rapid field determination of trace water in hydrophobic organic solvents.

The nicotinamide adenine dinucleotide (NAD+) is an important small biomolecule that participates in a variety of physiological functions, and it has been regarded as a potential biomarker for disease diagnosis and a promising target for disease treatment. The conventional methods for NAD+ assay often suffer from complicated procedures, expensive labeling, poor selectivity, and unsatisfactory sensitivity. Herein, we develop a label-free and sensitive method for NAD+ assay based on the integration of a trifunctional split dumbbell probe with ligation-triggered isothermal rolling circle amplification (RCA). We design a trifunctional split dumbbell probe that can act as a probe for NAD+ recognition, a template for RCA reaction, and a substrate for SYBR Green I binding. In the presence of target NAD+, it can serve as a cofactor to active E. coli DNA ligase which subsequently catalyzes the ligation of split dumbbell probe to form a circular template for RCA reaction, generating numerous dumbbell probe amplicons which can be easily and label-free monitored by using SYBR Green I as the fluorescent indicator. Due to the high fidelity of NAD+-dependent ligation and high amplification efficiency of RCA amplification, this method exhibits high sensitivity with a detection limit of 85.6 fM and good selectivity with the capability of discriminating target NAD+ from its analogs. Moreover, this method can be applied for accurate and sensitive detection of NAD+ in complex biological samples and cancer cells, holding great potential in NAD+-related biological researches and clinical diagnosis.

Hypoxic stress is a common concern in medicine and biology, which can induce the cellular injury and death by excess production of reactive oxygen species (ROS). Hypochlorous acid (HOCl), one of the ROS, plays a crucial role in the oxidative damage to tissue proteins in the pathogenesis of various diseases. Therefore, excess production of HOCl might be an important factor for the damage caused by hypoxic stress. However, most of the present methods cannot meet the demand of real-time detection on account of the labile and reactive chemical properties of HOCl. Herein, we designed a near-infrared fluorescent probe, Cy-HOCl, for the selective imaging of HOCl in cells and in vivo. Cy-HOCl includes two moieties: a 4-amino-3-nitrophenol group as the response unit and a near-infrared heptamethine cyanine fluorophore as the fluorescent modulator. Cy-HOCl exhibits excellent selectivity and sensitivity towards the detection of HOCl. The hypoxic response behavior of Cy-HOCl is evaluated in cells to clarify the relationship between HOCl and hypoxia. The probe is also applied to measure HOCl in ex vivo-dissected organs of an acute ischemia mouse model as well as for real-time monitoring the changes of HOCl in the hypoxic zebrafish model.

Although plenty of active materials could be used as supercapacitor electrodes, only limited ones have been engineered to construct transparent supercapacitors. Specially, it is a great challenge to make opaque metal oxides, which often own high energy density, into transparent films. Here, we demonstrate a novel approach to fabricate transparent MnO2 films for flexible transparent supercapacitors. By utilizing breath-figure polymer films with ordered pores as template, arrays of MnO2 islands were electrochemically deposited, with high light transmission. The thickness and interspace distance of MnO2 island arrays could be adjusted by tuning deposition time so that the capacitance and transparency of the electrodes are changed accordingly. Such island array structure can effectively eliminate the internal stress existing in the composite film to avoid cracks during bending operation. The assembled transparent supercapacitor shows a transmittance of 44% at 550 nm and can yield a high capacitance of 4.73 mF...

Supramolecular materials assembled by amide-functionalized surface active ionic liquid, N-dodecyl- N'-acetamido imidazolium bromide ([C12ImCONH2]Br), and europium-containing polyoxometalates (Eu-POM) were fabricated in aqueous solution by a one-step method via ionic self-assembly strategy. The [C12ImCONH2]Br/Eu-POM supramolecular structures exhibit favorable fluorescence properties and represent a 15-fold increase in quantum yield (∼13.68%) compared to Eu-POM. Besides, more fluorescence was quenched obviously with the increasing concentration of dopamine (DA) (within the range of 0-100 μM), based on which DA monitoring could be achieved. The detection limit was identified to be 0.1 μM. The supramolecular nanoparticles are highly specific for the detection of DA. In addition, the hybrid assemblies display not only low cytotoxicity but also excellent biocompatibility to MC3T3-E1 cells. As a result, as-prepared supramolecular materials with these superior properties show the promising application in some fields such as biochemistry and biomedical science.

Maintaining the redox balance of biological systems is a key point to maintain a healthy physiological environment. Excessive iron ions (Fe3+) can cause apoptosis, tissue damage and death. Fortunately, ascorbic acid (AA) as a reducing agent has been evaluated for the reduction of Fe3+. Moreover, AA plays an important role in relieving hypoxia-induced oxidative stress. Therefore, the real-time imaging of the Fe3+ and AA fluctuations is important for understanding their biofunctions in cells and in vivo. In this work, we developed a fluorescent nanoprobe carbon dot-desferrioxamine B (CD-DB) by the conjugate connection of CDs and desferrioxamine B (a complexing agent for Fe3+) for the associated detection of Fe3+ and AA. CD-DB exhibited excellent sensitivity and selectivity for the detection of Fe3+ and AA. The nanoprobe CDs-DB@Fe obtained by the reaction of CD-DB and Fe3+ was suitable for tracing the dynamic changes of AA in cells and in vivo. Therefore, CDs-DB@Fe was used for monitoring the fluctuation of AA in hypoxic cell models, hypoxic zebrafish models and liver ischemia mice models. These results exhibited the decrease in AA under hypoxic conditions because AA was consumed to neutralize free radicals and relieve hypoxia-induced oxidative stress damage. The ideal biocompatibility and low toxicity make our nanoprobe a potential candidate for the research of the physiological effects of AA in vivo.

Trypsin plays a central role in catalyzing the hydrolysis of peptide bonds, so a technique with simple operation is needed to monitor the activity of trypsin. Here a simple and label-free senor based on liquid crystals (LCs) was developed by employing bovine serum albumin (BSA) as the enzyme substrate and dodecyl trimethyl ammonium bromide (DTAB) as the controller for the alignment of LC. It was found that DTAB could form a self-assembled monolayer at the aqueous/LC interface to produce the dark optical images of LCs. And the addition of BSA could disturb the monolayer, so that the optical signal of LCs turned bright from dark. But the hydrolysis of BSA by trypsin resulted in the dark appearance. The sensing platform allows detection as low as 1 U/mL under the polarized light microscope based on at least three measurements. Moreover, this method was successfully applied in the detection of trypsin in human urines, suggesting its potential applications in clinic diagnosis.

Ratiometric fluorescence sensors can provide more accurate analysis of target objects because of their self-calibration function. Traditional methods often use steps of chemical coupling with two different fluorescent materials as the dual emission source, which make the construction process complicated and hard to control. Here, we report a convenient and effective way to construct a ratiometric fluorescence sensor based on dual-emission carbon dots-gold nanoclusters (C–AuNCs) functionalized with dithiothreitol (DTT) for the sensitive detection of mercury ions (Hg2+) in water samples. As a type of novel nanoparticle, C–AuNCs are synthesized via microwaving a mixture of gold seeds solution and carbon precursor. In the presence of Hg2+, the free thiol group of DTT would attract them around the surface of C–AuNCs, and owing to the strong 5d10–5d10 metallophilic interactions between Hg2+ and Au+, the fluorescence emission at 598 nm is quenched while the emission at 466 nm remains at a constant intensity. Thus, an obvious color change from orange-red to blue under ultraviolet irradiation can be observed by the naked eye. Moreover, the as-prepared fluorescence sensor has high sensitivity with a detection limit of 8.7 nM, and successfully applies to detect Hg2+ in real water samples with satisfactory recoveries at three spiking levels ranging from 95.9 − 103.5%. The good results imply that the developed DTT/C–AuNCs sensor is conducive to trace Hg2+ determination and possesses the great application potential for water-quality monitoring.

Molecular imprinting as a versatile technology has gained popularity in various fields for diverse species; however, protein imprinting still remains challenging due to some inherent problems but is potentially rewarding work. Herein, we reported a facile strategy to imprint phycocyanin (PC), as a template, using quantum dots (QDs) co-capped by thioglycollic acid and glutathione directly as functional monomer via dopamine self-polymerization, which effectively simplified the imprinting process and afforded easy accessibility to recognition sites. The resulting QDs based imprinting nanosensor showed significant fluorescence decrease of QDs within less than 16 s upon binding PC owing to the ultrathin imprinting layer (ca. 3 nm), leading to a high detectability down to 0.075 μM. An excellent linearity was found within the wide range of 0.8–8.0 μM ( R 2 = 0.9935). Good recognition selectivity toward PC was displayed over other possible competing molecules, with a high imprinting factor of 7.3. Seawater and lake water samples spiked with PC were also analyzed, presenting satisfactory recoveries ranging from 90.8–110.1% with precisions below 4.6%, indicating the practicality of the imprinting nanosensor for accurately rapid nanoscale monitoring of algae blooms. By using another protein, bovine haemoglobin (BHb), as a convincing support model, the present study can provide a simple and general imprinting strategy toward various concerned proteins through rationally utilizing diverse functionalization and interactions.

Low sulfur loading and content, as well as severe shuttle effects, remain the key issues for the application of lithium–sulfur (Li–S) batteries, resulting in a low areal capacity and fast capacity fade. Herein, a highly efficient conductive network is developed by growing herringbone structured carbon nanofibers (CNFs) on the surface of graphene aerogel (GA–CNFs–Ni) and is further applied as a functional coating layer in Li–S batteries. The conductive coating layer, serves as both a shield to trap the active materials detached from the cathode and a conductive “second current collector” to reactivate the trapped active materials. The herringbone structured CNFs enriched with defects and gaps enlarge the available reaction site for electrons, the electrolyte and sulfur species, ensuring the smooth operation of the sulfur cathode with high loading and high content. In addition, the uniformly distributed Ni nanoparticles also exert strong chemical bonding with polysulfides by first-principle calculations. Consequently, the GA–CNFs–Ni coated separator enables the “double high” sulfur cathode (5 mg cm−2, 90 wt%) to display an ultrastable cycle capability and superior rate performance. Moreover, a high sulfur loading of 10 mg cm−2 and a low electrolyte/sulfur (E/S) ratio (6 μL mg−1) are obtained, delivering a high areal capacity of 5.5 mA h cm−2 after 60 cycles.

Magnesium lithospermate B (MLB) is an active polyphenol acid with multiple pharmacological activities and poor oral bioavailability. The present research aimed to construct MLB loaded solid lipid nanoparticles (MLB-SLNs) for oral delivery to enhance its bioavailability. MLB-SLNs were prepared by solvent diffusion method and subsequently modified with polyethylene glycol monostearate (PEG-SA) superficially. The particle sizes of MLB-SLNs varied from 82.57 to 53.50nm with an improved drug loading capacity (up to 16.18%) after PEG-SA modification. Pharmacokinetic study indicated that Cmax (peak plasma MLB concentration) and AUC (area under curve) of MLB-SLNs increased significantly compared to that of MLB solution in male SD rats. The relative bioavailability of MLB-SLNs with PEG-SA modification was 753.98% compared to MLB solution administered by tail intravenous injection. The enhanced transport mechanism could be further illustrated by the results that MLB-SLNs showed higher permeability across Madin-Daby canine kidney (MDCK) epithelial cell monolayer and MLB-SLNs with smaller particle size distribution and PEG-SA modification manifested stronger cellular internalization ability on MDCK cells. Thus, PEG-SA modified solid lipid nanoparticles confirmed with enhanced cellular transport and improved oral bioavailability can be a promising oral MLB delivery system.

The intramolecular proton-transfer processes of thymine were investigated by the density functional theory method. It is shown that the mutation from keto (T) to enol (T′) form is affected by zeolitic imidazolate framework-8 (ZIF-8) fragments such as single 2-methylimidazole neutral crystals (M), and negatively charged 2-methylimidazole ligands (M−). Results show that with the number (n) of water (w) molecules that assist proton-transfer increasing from 1 to 4, the order of the tautomeric energy barriers (in kcal mol−1) is T-2w (16.3) < T-1w (17.6) < T-3w (17.8) < T-4w (20.5). In the presence of M, the order of energy barrier is MT-2w (16.6) < MT-1w (17.7) < MT-3w (18.9) < MT-4w (20.8). M− has a catalysis effect on the energy barrier and the order is M−T-2w (14.4) < M−T-3w (15.2) < M−T-1w (16.3) < M−T-4w (16.8). The attachment of the M− fragment slightly promotes the proton-transfer processes in some instances. The characterization of the proton-transfer processes is helpful to understand the genotoxicity of ZIF-8 during drug delivery applications.

Here, we report the experimental observation of negative differential resistance (NDR) and hysteresis phenomena in graphene-based OLEDs and their effects on device performance. Our results reveal that the NDR and hysteresis mainly originate from the poly(methyl methacrylate) residue resting on graphene. We further demonstrate that current annealing is a facile and effective technique to remove the polymeric residue and eliminate the NDR, leading to the dramatically enhanced luminous efficiency from 30.9 to 41.6 cd A−1, and to 89.2 cd A−1 when equipped with a high index half-ball lens. The demonstrated pretreatment process of graphene establishes a new path for the construction of a wide variety of high performance optoelectronic devices.

Zinc cation (Zn2+) plays an important role in the chemistry of DNA base pairs. In this work, the influence of isolated and penta-hydrated Zn2+ on some of the intramolecular proton-transfer processes of thymine (T) is investigated by the density functional theory method. It is shown that the calculated binding energies between Zn2+ and T are exothermic in vacuum. Compared to T, Zn2+ increases the stability of tautomer T′ by 28.7 kcal mol−1, promoting the intramolecular proton transfer of T. But in a micro-water environment, the attachment processes of Zn2+ to T hydrates, penta-hydrated Zn2+ to T, and penta-hydrated Zn2+ to T hydrates lead to the rearrangement of molecules and the redistribution of charges. The conventional T is still the most stable form and the influence of Zn2+ is much reduced and the proton transfer is thermodynamically unfavored. The detailed characterization is helpful to understand the genotoxicity of zinc ions.

Herein, we report a ratiometric photoelectrochemical (PEC) immunosensor coupled with secondary antibodies-Co3O4 nanoparticle conjugates (Ab2-Co3O4 NPs) for signal amplification. The Ab1-g-C3N4@TiO2 NTs and BSA-g-C3N4@TiO2 NTs act as the sensing and reference photoelectrodes, where Ab1, BSA and TiO2 NTs are the capture antibodies, bovine serum albumin and TiO2 nanotube arrays, respectively. In the presence of target Ag, the sensing PEC photocurrent decreases due to the steric hindrance of Ab1 molecules, which increases the inner resistance of the photoelectrode. The signal-off response is enhanced further using Ab2-Co3O4 NP conjugates due to their steric hindrance effect and the consumption of electron donors by the Co3O4 NPs. Furthermore, the performance of the ratiometric PEC platform is tested using alpha-fetoprotein (AFP) as a model antigen. Under the optimal conditions, the concentration of AFP is detected in the range of 0.4 pg mL-1 to 40 ng mL-1 with a detection limit of 0.2 pg mL-1. This ratiometric strategy is beneficial to improve the reliability and anti-interference ability of PEC immunosensors.