Ultrastable and ultrasensitive pH-switchable carbon dots with high quantum yield for water quality identification,glucose detection,and two starch-based solid-state fluorescence materials

It is attractive and encouraging to develop new fluorescent carbon dots(CDs)with excellent optical properties and promising applications prospects.Herein,highly-efficient green emissive CDs(m-CDs)with a high quantum yield(QY)of 71.7%in water are prepared through a facile solvothermal method.Interestingly,the m-CDs exhibit excellent fluorescence stability in the pH range of 1–9.However,the fluorescence intensity of the m-CDs is almost completely quenched as the pH is increased from 9 to 10.The mechanism of the unique pH-responsive behavior is discussed in detail and a plausible mechanism is proposed.Owing to the unique pH-responsive behavior,the m-CDs are used as a on-off fluorescent probe for water quality identification.By combining the reversible pH-ultrasensitive optical properties of the m-CDs in the pH range of 9–10 with the glucose oxidase-mimicking(GOx-mimicking)ability of Au nanoparticles(AuNPs),glucose can be quantitatively detected.Finally,two environment-friendly starch-based solid-state fluorescence materials(powder and film)are developed through green preparation routes.

Solid-state mechanochemistry advancing two dimensional materials for lithium-ion storage applications:A mini review

The vigorous development of two-dimensional(2D)materials brings about numerous opportunities for lithiumion batteries(LIBs)due to their unique 2D layered structure,large specific surface area,outstanding mechanical and flexibility properties,etc.Modern technologies for production of 2D materials include but are not limited to mechanochemical(solid-state/liquid-phase)exfoliation,the solvothermal method and chemical vapor deposition.In this review,strategies leading to the production of 2D materials via solid-state mechanochemistry featuring traditional high energy ball-milling and Sichuan University patented pan-milling are highlighted.The mechanism involving exfoliation,edge selective carbon radical generation of the 2D materials is delineated and this is followed by detailed discussion on representative mechanochemical techniques for tailored and improved lithium-ion storage performance.In the light of the advantages of the solid-state mechanochemical method,there is great promise for the commercialization of 2D materials for the next-generation high performance LIBs.

Rapid interrogation of special nuclear materials by combining scattering and transmission nuclear resonance fluorescence spectroscopy

The smuggling of special nuclear materials(SNMs)across national borders is becoming a serious threat to nuclear nonproliferation.This paper presents a feasibility study on the rapid interrogation of concealed SNMs by combining scattering and transmission nuclear resonance fluorescence(s NRF and t NRF)spectroscopy.In s NRF spectroscopy,SNMs such as^(235,238)U are excited by a wide-band photon beam of appropriate energy and exhibit unique NRF signatures.Monte Carlo simulations show that one-dimensional scans can realize isotopic identification of concealed^(235,238)U when the detector array used for interrogation has sufficiently high energy resolution.The simulated isotopic ratio^(235U/238)U is in good agreement with the theoretical value when the SNMs are enclosed in relatively thin iron.This interrogation is followed by t NRF spectroscopy using a narrow-band photon beam with the goal of obtaining tomographic images of the concealed SNMs.The reconstructed image clearly reveals the position of the isotope^(235)U inside an iron rod.It is shown that the interrogation time of s NRF and t NRF spectroscopy is one order of magnitude lower than that when only t NRF spectroscopy is used and results in a missed-detection rate of 10^(-3).The proposed method can also be applied for isotopic imaging of other SNMs such as^(239,240)Pu and^(237)Np.

XRD Analysis on the Fluorescence Material of Sm Doped Si-Ca-Mg System

Fluorescence material of Sm doped Si-Ca-Mg system was synthesized by using the method of solid phase reaction at high temperature. The phase composition and crystal structure of this material were analyzed with XRD method for its composition and the existence form of Sm atom. We aimed to exactly determine the phase composition of this fluorescence material and the doping position and environment of rare-earth Sm atom in the system because these factors have significant effects on the properties. The analytical results show that the Sm atoms dope in Ca2O26Si6Sm8 lattice in the form of atomic site-occupation in three different space positions with different occupancy rates. Therefore, based on the XRD analytical results, the fluorescence material of Sm doped Si-Ca-Mg system with high performance can be synthesized.

Synthesis and characterization of high-voltage cathode material LiNi0.5Mn1.5O4 by one-step solid-state reaction

LiNi0. 5 Mn1. 5 O4 was prepared under various conditions by one-step solid-state reaction in air and its properties were investigated by X-ray diffractormetry (XRD), scanning electron microscopy (SEM) and electrochemical measurement. XRD patterns show that LiNi0. 5 Mn1. 5 O4 synthesized under various conditions has cubic spinel structure. SEM images exhibit that the particle size increases with increasing calcination temperature and time. Electro chemical test shows that the LiNi0. 5 Mn1.5 O4 calcined at 700 ℃ for 24 h delivers up to 143 mA · h/g, and the capacity retains 132 mA · h/g after 30 cycles.

Preparation of Li[Ni_(1/3)Co_(1/3)Mn_(1/3)]O_2 powders for cathode material in secondary battery by solid-state method

Employing Li2CO3, NiO, Co3O4, and MnCO3 powders as starting materials, Li[Ni1/3Co1/3Mn1/3]O2 was synthesized by solid-state reaction method. Various grinding aids were applied during milling in order to optimize the synthesis process. After successive heat treatments at 650 and 950 ℃, the prepared powders were characterized by X-ray diffraction (XRD) analysis, scanning electron microscopy, and transmission electron microscopy. The powders prepared by adding salt (NaCl) as grinding aid exhibit a clear R3m layer structure. The powders by other grinding aids like heptane show some impurity peaks in the XRD pattern. The former powders show a uniform particle size distribution of less than 1 μm average size while the latter shows a wide distribution ranging from 1 to 10 μm. Energy dispersive X-ray (EDX) analysiss show that the ratio of Ni, Co, and Mn content in the powder is approximately 1/3, 1/3, and 1/3, respecively. The EDX data indicate no incorporation of sodium or chlorine into the powders. Charge-discharge tests gave an initial discharge capacity of 160 mAh·g-1 for the powders with NaCl addition while 70 mAh·g-1 for the powders with heptane.

First Principle Material Genome Approach for All Solid-State Batteries

Due to ever-increasing concern about safety issues in using alkali metal ionic batteries, all solid-state batteries (ASSBs) have attracted tremendous attention. The foundation to enable high-performance ASSBs lies in delivering ultra-fast ionic conductors that are compatible with both alkali anodes and high-voltage cathodes. Such a challenging task cannot be fulfilled, without solid understanding covering materials stability and properties, interfacial reactions, structural integrity, and electrochemical windows. Here in this work, we will review recent advances on fundamental modeling in the framework of material genome initiative based on the density functional theory (DFT), focusing on solid alkali batteries. Efforts are made in offering a dependable road chart to formulate competitive materials and construct "better" batteries.

Synthesis and Color-tunable Fluorescence Properties of Schiff Base Zinc (II) Complexes Used as Electroluminescent Materials

Four kinds of bis(N-alkylsalicylaldiminato) zinc(II) complexes were synthesized, and their molecular structures were determined by FT-IR and elemental analysis. Their photoluminescence properties were determined, which indicated that they could emit strong fluorescence varying from blue to yellow to reddish orange depending on their different molecular structures. They had good thermostability, solubility and film forming capability, and can be used as organic lectroluminescent materials. These new complexes may afford the feasibility to realize full-color display with materials based on similar molecular structures.

Giant mechanocaloric materials for solid-state cooling

This article reviews the research progress of measurement techniques and materials on the mechanocaloric effect over the past few decades.Mechanocaloric materials can be divided into elastocaloric and barocaloric materials depending on the applied uniaxial stress or hydrostatic pressure.Elastocaloric materials include non-magnetic shape memory alloys,polymers,and rare-earth compounds.Barocaloric materials include magnetic shape memory alloys,ferroelectric ceramics,superionic conductors,and oxyfluorides.The mechanocaloric effects of these classes of materials are systematically compared in terms of the isothermal entropy change and adiabatic temperature change.In addition to the thermal effects,other characteristics closely related to the application of mechanocaloric materials are also summarized.Finally,perspectives for further development of mechanocaloric materials in the solid-state cooling area are discussed.

Comparison of Sulfur Dioxide Residue in Chinese Me-dicinal Materials by Titration-fluorescence Spectrome-try and Pharmacopoeia Method

With sulphur-fumigated Chinese medicinal materials （Fritillaria thunbergii , Isatis #utigotica , Asparagus cochinchinensis and Poria cocos ） as the test materials, sulfur dioxide or sulfite residue was determined by the method in Chinese Pharmacopoeia （2015 edition） and titration-fluorescence spectrometry, respec- tively. The results showed that there were significant differences in measured value between titration-fluorescence spectrometry and phmmacopoeia method. The t result of titration-fluorescence spectrometry was much closer to the actual content of sulfur dioxide in Chinese medicinal materials. Thus, titration-fluo- rescence spectrometry had higher application value

Evaluating Acid Resistance Effect of Fluoride-Releasing Dental Materials Using Quantitative Light-Induced Fluorescence-Digital in Vitro

As erosion has become one of the serious oral health problems, some fluoride-releasing dental materials have been developed to protect enamel from demineralization. The purpose of this study was to evaluate the antidemineralization effect of PRG Barrier Coat® and FujiVII® (fluoride-releasing dental materials). Four square windows measuring 1 mm2 were prepared on the labial enamel surface of each bovine tooth using masking tape and nail varnish. The first and second windows were half covered by fluoride-releasing material and control material, respectively, whereas the third and fourth windows were left untreated. All windows were immersed into 0.1 M lactic acid and 6wt% CM-cellulose (pH 4.5) at 38℃ for 21 days. Subsequently, the first and second windows were covered with nail varnish after removal of the materials, and the third and fourth windows were immersed into ultrapure water at 38℃ for 28 days after being half covered with fluoride-releasing and control materials, respectively. The following procedure was performed separately during evaluations of the fluoride-releasing materials, PRG Barrier Coat, and FujiVII®, using eight and six bovine teeth, respectively. The first, second, third, and fourth windows were classified into DM-PRG;Demineralized-PRG or DM-FujiVII;Demineralized-FujiVII, DM-TCM;Demineralized-traditional cement or DM-TGIC;De-mineralized-traditional glass ionomer cement, RM-PRG;Remineralized-PRG or RM-FujiVII;Re-mineralized-FujiVII, and RM-TCM;Remineralized- traditional cement or RM-TGIC;Remineral-ized-traditional glass ionomer cement, respectively. After nail varnish was removed, △Q values (mean ± SD) of the windows were measured using QLF-D and were compared between DM-PRG and DM-TCM, RM-PRG and RM-TCM, DM-FujiVII and DM-TGIC, and RM-FujiVII and RM-TGIC groups. △Q values of RM-PRG (-60 ± 44) and RM-FujiVII (-5.0 ± 10) were significantly higher than that of RM-TCM (-315 ± 193) and RM-TGIC (-56 ± 43), respectively. The fluoride releasing materials provided remineralization effects to bovine enamel.

Double spatial confinement on ruthenium nanoparticles inside carbon frameworks as durable catalysts for a quasi-solid-state Li–O_(2) battery

The rational design of large-area exposure,nonagglomeration,and longrange dispersion of metal nanoparticles(NPs)in the catalysts is critical for the development of energy storage and conversion systems.Little attention has been focused on modulating and developing catalyst interface contact engineering between a carbon substrate and dispersed metal.Here,a highly dispersed ultrafine ruthenium(Ru)NP strategy by double spatial confinement is proposed,that is,incorporating directed growth of metal–organic framework crystals into a bacterial cellulose templating substrate to integrate their respective merits as an excellent electrocatalytic cathode catalyst for a quasi-solid-state Li–O_(2) battery.The porous carbon matrix with highly dispersed ultrafine Ru NPs is well designed and used as cathode catalysts in a Li–O_(2) battery,demonstrating a high discharge areal capacity of 6.82 mAh cm^(–2) at 0.02 mA cm^(–2),a high-rate capability of 4.93 mAh cm^(–2) at 0.2 mA cm^(–2),and stable discharge/charge cycling for up to 500 cycles(2000 h)with low overpotentials of~1.4 V.This fundamental understanding of the structure–performance relationship demonstrates a new and promising approach to optimize highly efficient cathode catalysts for solid-state Li–O_(2) batteries.

Detection of Lactobacillus acidophilus in Fermented Material by Real-time Fluorescent Quantitative PCR

The species distinctive PCR primer of Lactobacillus acidophilus （ L. acidophilus） was designed according to 16S rRNA gene sequences of conunon Lac- tobacillus species in fermented material. Bacterial genome DNA of separated L. acidophilus in fermented sample was taken as template, and L. acidophilus in fer- mented material was conducted the quantitative determination by real-time quantitative PCR （RT-PCR）. Analysis on RT-PCR results shown that contents of L. aci- dophilus in the test sample reached 1.5 billion CFU / g. Test results shown that contents of L. acidophilus in fermented material could be detected accurately by the established RT-PCR method in the test. indicating that the established RT-PCR method could be aookued to the detection of L. acidophilus in fermented material.

Overlooked impact of precursor mixing:Implications in the electrochemical performance of battery electrode materials

Solid-state reactions are an essential part of the synthesis of various cathode materials for lithium-ion batteries(LIBs).Despite the simplicity and effectiveness for mass production,a subtle variation in synthesis conditions can often give rise to unexpectedly different physical properties,significantly affecting the electrochemical performance of electrode materials.However,this aspect has long been overlooked in the LIB community,which should focus on advancement in understanding the influence of synthesis conditions.As solid-state reactions occur only at the interface of precursor materials,maximizing the interfacial contact area between mixed precursor powders is crucial.Mechanical milling and/or mixing are common practices that have been performed in both academia and industry for this purpose.Unlike the common belief that this pre-treatment before calcination would be of great benefit for the preparation of high-performance LIB materials,we revealed in this work that this practice is not always successful for this goal.In our case study of the preparation of LiCoO_(2),we demonstrated that mechanical mixing-a routinely implemented process for homogeneous mixing of precursors-can be harmful if it is performed without assuring optimal working conditions for mixing.The underlying reasons for this surprising result are elucidated in this work,and we hope that this new insight can help avoid the potential pitfall of routine implementations performed for LIB materials.

Preparation and Fluorescence Properties of TiO_2∶Eu Nano-Materia ls

A series of europium-doped titanium dioxide (TiO 2) fluorescent nano-material s prepared by sol-gel method is presented. The phase structure and crystalline sizes of TiO 2∶Eu, which is doped with different europium content and then he at-treated at different temperature, were investigated by XRD,TG,DTA and TEM. The results show that europium could be introduced into TiO 2 under high temper ature and it can suppress the structural phase transition from anatase to rutile and the crystal growth of TiO 2 in TiO 2∶Eu nano-materials. The fluorescenc e spectra were examined by fluorescence spectrophotometer, and the results show that the fluorescence intensity is the strongest when europium content is 2.68%( mole fraction) and the heat-treated temperature is 700 ℃. From the measurement results of the fluorescence lifetimes, it can be seen that the fluorescence lifetime c ould be prolonged when europium is incorporated in TiO 2.

Synthesis, Characterization of A Novel Polymeric Reaction Monomer for Preparing Highly Fluorescent Rare Earth Polymer Materials

A novel polymeric reaction monomer (NPRM) for preparing highly fluorescent rare earth polymer materials was synthesized via interface and coordinating reaction. The composition and structure of the NPRM and intermediate product (ligand) were characterized through the Fourier transform infrared spectroscopy (FT-IR), carbon-nuclear magnetic resonance spectrum (13CNMR), Mass spectra (MS), and element analysis data. The results showed that the composition and structure of NPRM agreed with that of anticipated product. The NPRM was composed of two important sections. Section 1 was able to provide excellent fluorescent properties for final rare earth polymer material through the effect energy transfer between ligand and rare earth ion; Section 2 would endow with the NPRM excellent polymeric active and form highly fluorescent rare earth polymer material. Fluorescent properties of the NPRM were also researched via a CARY ECLIPSE fluorescent spectrometer. The results showed that the NPRM possessed excellent luminescent properties. The corresponding emission peaks based on the 5D0→7F1(601.6 nm), 5D0→7F2(625.0 nm), 5D0→7F3(660.5 nm) and 5D0→7F4(706.3 nm) transitions for Eu3+ were observed. The strongest emission peak was at 625 nm, which belonged to 5D0→7F2 transition.

Chiral thermally activated delayed fluorescence materials for circularly polarized organic light-emitting diodes

Chirality is an important natural characteristic of organic molecules,and chiral organic molecules have shown extensive application in areas such as pharmaceutical development and material science.Benefiting from the ability to achieve circularly polarized luminescence(CPL),chiral luminescent materials have shown potential applications in anti-glare display,optical communication and,3D display,etc.Due to the ability to harvest both singlet and triplet excitons by a fast reverse intersystem crossing process without involving noble metals,chiral thermally activated delayed fluorescence(TADF)materials with point chirality,axial chirality,planar chirality and helical chirality are regarded as the state-of-the-art materials for circularly polarized organic light-emitting diodes(CP-OLEDs).In recent years,the chiral TADF materials and CP-OLEDs have rapidly developed,but unfortunately,the dissymmetry factors(g)are far from the requirement of practical applications.The ideal emitters and devices should have both high efficiency and a g factor,or at least a balance between these two elements.This review gives an overview of recent progress in chiral TADF materials,with a particular focus on the chiral skeleton,CPL property and device performance.Furthermore,the molecular design concept,device structure and methods to improve the g factors of chiral materials and CP-OLEDs are also discussed.

Chiral multiple-resonance thermally activated delayed fluorescence materials based on chiral spiro-axis skeleton for efficient circularly polarized electroluminescence

Chiral luminescence materials have potential applications in the field of three-dimensional displays due to their circularly polarized luminescence(CPL)characteristics.However,the further development of circularly polarized organic light-emitting diodes(CP-OLEDs)needs to meet the requirements of high efficiency,high color purity,low cost,and high dissymmetry factor(gPLor gEL),chiral multiple resonance thermally activated delayed fluorescence(MR-TADF)materials are considered as candidates in these aspects.Herein,based on a pair of chiral spirofluorene precursors,two pairs of high-performance chiral MR-TADF emitters((R/S)-p-Spiro-DtBuCzB and(R/S)-m-Spiro-DtBuCzB)are developed,which exhibit strong emissions peaking at 491 and 502 nm in toluene with full-width at half-maximum values of 25 and 33 nm,respectively.In addition,small singlet–triplet energy gaps of 0.15 and 0.10 eV with high absolute photoluminescence efficiencies of 95.0%and 96.7%are observed for p-Spiro-DtBuCzB and m-Spiro-DtBuCzB molecules,respectively.OLEDs based on p-Spiro-DtBuCzB and m-Spiro-DtBuCzB display high maximum external quantum efficiencies of 29.6%and 33.8%,respectively.Most importantly,CP-OLEDs present symmetric circularly polarized electroluminescence spectra with|gEL|factors of 3.36×10^(-4)and 7.66×10^(-4)for devices based on(R/S)-p-Spiro-DtBuCzB and(R/S)-m-Spiro-DtBuCzB enantiomers,respectively.