Heterothermic Cataluminescence Sensor System for Efficient Determination of Aldehyde Molecules.

A simple and stable cataluminescence (CTL) sensing platform based on a single sensing material for effective and rapid detection of aldehydes is an urgent need due to growing concerns for the environment, security, and health. Here, an effective and user-friendly identification method is successfully proposed to determine six common aldehydes of homologous compounds via a heterothermic CTL sensor system. Using Gd2O3 with excellent catalytic activity as a sensing material, thermodynamic and kinetic insights into the interactions between Gd2O3 and aldehydes at different temperatures were extracted and integrated to generate a unique constellation profile for each tested aldehyde, whereby achieving their effective and prompt determination. Moreover, the sensor system allowed the quantitative analysis of aldehydes with detection limits of 0.001, 0.009, 0.011, 0.011, 0.007, and 0.003 µg mL-1. Significantly, the sensor system had an excellent stability of up to 30 days. The CTL sensing platform was constructed based on a thermal regulation strategy that can provide a new approach to chemical agent identification.

Multisignals Sensing Platform for Highly Sensitive, Accurate, and Rapid Detection of p-Aminophenol Based on Adsorption and Oxidation Effects Induced by Defective NH2-Ag-nMOFs.

Labile toxic pollutants detection remains a challenge due to the problem that a single method is prone to producing false-negative/-positive signals. The construction of a multisignal sensing platform with the advantages of different strategies is an effective way to solve this problem. Herein, a novel resonant light scattering (RLS), fluorescent and rapid visual multisignals sensing strategy for p-aminophenol (p-AP) detection was designed based on the adsorption and oxidation effects of defective amino-functionalized Ag-based nano metal-organic frameworks (NH2-Ag-nMOFs). In this reaction process, NH2-Ag-nMOFs with incomplete coordination oxidize H2O2 to produce singlet oxygen (1O2) which rapidly oxidizes p-AP, leading to the reduction of Ag+ to Ag0, thereby disrupting the structure of NH2-Ag-nMOFs and resulting in fluorescence quenching of NH2-Ag-nMOFs. Synchronously, owing to Ag0 aggregation and p-AP oxidation, the color of the system changed from colorless to purplish-red and pale brown within 20 s. The assay has realized the rapid naked-eye detection of 5 µM p-AP rapidly. Additionally, thanks to the intermolecular hydrogen bonding, NH2-Ag-nMOFs-p-AP aggregates formed, which enhanced the RLS signal. With the RLS signal, the designed multisignals sensing platform can analyze p-AP at a concentration as low as 11 nM and yield a wider dynamic response range than any single signal strategy reported before, which can quickly meet the measurement requirement of different actual samples. Overall, the proposed strategy without assembling various signal indicators presented an accurate, rapid, cost-effective, and sensitive multisignals sensing platform for p-AP analysis and has great prospects in labile toxic pollutants monitoring.

Organic Semiconductor Nanosheets for Sulfite Detecting Based on Activation of Sulfite and a Synergetic Chemiluminescence Resonance Energy Transfer Process in a Mild System of Fe2+-SO32.

Sulfur dioxide (SO2) as one kind of air pollution not only causes extreme environmental pollution but also negatively affects human health. Chemiluminescence (CL) methods applied for sulfite analysis with high selectivity based on activating sulfite with oxidants are always implemented in acid media with a high background rise. In this work, we proposed to develop a mild CL system of Fe2+-SO32- to detect sulfite under neutral conditions and provide in situ CL spectral data for deeply studying the CL mechanism of Fe2+-SO32-. Herein, we first synthesized one type of water-soluble supramolecular nanosheets, APDI NSs, which had a strong oxidation potential (+2.9 V) due to a π-conjugated system for activation of sulfite to enhance the generation of SO3̇- and other active radicals, and strong a CL signal from the APDI NSs-Fe2+-SO32- system was generated. By studying the CL mechanism under acidic and neutral conditions, a new CL reaction pathway (path-1) and a key intermediate, S2O42-, from the reaction of Fe2+ and SO32- were found. The CL signal was emitted by SO2* after oxidation of S2O42- by strong oxidants like SO4•- and further amplified by APDI NSs through the CL resonance energy transfer (CRET) process. Based on the APDI NSs-Fe2+-SO32- system under neutral conditions, a CL method for detecting SO32- was established. The detection limit was 2.7 × 10-8 M (S/N = 3), and the recovery rates in spiked water samples were in the range of 87%-101%. This study strengthens the understanding of the CL reaction process of the Fe2+-SO32- system and provides a mild sulfite sensing platform for environmental samples.

Instant Fingerprint Discrimination for Military Explosive Vapors by Dy3+ Doping a La2O3-Based Cataluminescence Sensor System.

With the intensification of explosive-based terrorism attack and environmental concerns, the innovation of high-efficiency and portable sensors for facile, rapid, and reliable monitoring of explosives has become one of the major demands in societies. Herein, a reliable and easy-to-use cataluminescence sensor system based on Dy3+ doping La2O3 nanorod catalysts has been developed for the identification and detection of six types of military explosive vapors, including homologous compounds and even isomers. The efficient discrimination is to make full use of the thermodynamic and kinetic information that can be extracted from the catalytic oxidation process of explosive molecules on various sensing materials, that is, the response signal and response time to generate the fingerprint of each target compound, while the rapid detection of the strategy can be manifested in response toward six military explosive vapors within 2.5 s and recover within 4 s. Meanwhile, the quantitative analysis of the explosives by the sensor system was realized based on 0.8%Dy:La2O3 with optimal catalytic activity, and the detection limits of NB, m-MNT, m-DNB, PNT, DNT, and TNT can reach 0.62, 0.49, 0.63, 0.38, 0.023, and 0.067 µg mL-1. In this research, we also constructed a novel sensor device and detection platform for explosive monitoring, which is of great significance for providing a new sensing principle for the efficient identification of explosives.

New Perylene-Based Chemiluminescent Polymer Nanoparticles for Highly Selective Detection of the Superoxide Anion In Vivo.

The superoxide anion (O2•-) is one of the primary reactive oxygen species in biological systems. Developing a determination system for O2•- in vivo has attracted much attention thanks to its complex biological function. Herein, we proposed a new perylene-based chemiluminescence (CL) probe, the SH-PDI polymer, which was capable of generating strong CL signals with O2•- in comparison with other ROS. The CL mechanism involved was proposed to be a kind of oxidation reaction induced by the breakage of the S-S and S-H bonds into sulfoxide bonds by O2•-. Subsequently, a nanoprecipitation method was introduced, using cumene-terminated poly(styrene-co-maleic anhydride) as the amphiphilic agent, to obtain water-soluble nanoparticles, SPPS NPs, which exhibited not only stronger CL intensity but also higher selectivity toward O2•- than the SH-PDI polymer. Moreover, the CL wavelength of the SPPS-O2•- system was found to be located at 580 and 710 nm, which was conducive to CL imaging. By virtue of these advantages, SPPS NPs were utilized to evaluate the O2•- level in vitro in the range of 0.25-60 µM at pH 7.0, with a detection limit of 8.2 × 10-8 M (S/N = 3). Moreover, SPPS NPs were also capable of imaging O2•- in an LPS-induced acute inflammation mice model and drug-induced acute kidney injury (AKI).

Normal diet ameliorates obesity more safely and effectively than ketogenic diet does in high-fat diet-induced obesity mouse based on gut microbiota and lipid metabolism.

Growing evidence supports the efficacy of ketogenic diets for inducing weight loss, but there are also potential health risks due to their unbalanced nutrient composition. We aim at assessing relative effectiveness of a balanced diet and ketogenic diet for reversing metabolic syndrome in a diet-induced C57BL/6J mouse model. Mice were fed high-fat diet to induce obesity. Obese individuals were then fed either ketogenic or balanced diets as an obesity intervention. Serum, liver, fat and faecal samples were analysed. We observed that both diet interventions led to significant decrease in body weight. The ketogenic intervention was less effective in reducing adipocyte cell size and led to dyslipidaemia. The composition of the gut microbiome in the balanced diet intervention was more similar to the non-obese control group and had improved functional attributes. Our results indicate intervention with balanced diets ameliorates obesity more safely and effectively than ketogenic diets in diet-induced obesity mouse model.

Flower-like Gold Nanoparticles for In Situ Tailoring Luminescent Molecules for Synergistic Enhanced Chemiluminescence.

In recent years, gold nanoparticles (AuNPs) have attracted much attention due to their ease of surface modification, excellent biocompatibility, and extraordinary optoelectronic and catalytic activities. Herein, based on a AuNP-catalyzed reaction, a strategy for tailoring luminescent molecules in situ is proposed to trigger an ultrastrong chemiluminescence (CL). In the strategy, flower-like AuNPs are prepared using CL molecular probes (Probe-OH for NaClO/ONOO-) via one-pot synthesis and subsequently act as a tailor for Probe-OH to generate novel CL molecules, allowing a synergistic CL enhancement about 4 times that of initial Probe-OH. Furthermore, by modification with poly(vinylpyrrolidone) (PVP) on the surface, the CL signals (only for NaClO) are amplified by 100 times based on an intermolecular chemically initiated electron exchange luminescence (CIEEL) mechanism. Given the improved sensitivity and selectivity over Probe-OH, the thus-formed CIEEL nanoplatform (PVP-Au) is successfully developed for detecting NaClO in a wide range of 2.5-100 µM, and the detection limit is 10.68 nM. This work provides unprecedented perspectives for expanding this facile and effective strategy for CL amplification based on AuNP catalysis.

Efficient Photoinduced Thermocatalytic Chemiluminescence System Based on the Z-Scheme Heterojunction Ag3PO4/Ag/Bi4Ti3O12 for H2S Sensing.

Cataluminescence as a highly efficient gas transduction principle has attracted wide attention among research in environmental monitoring and clinical diagnosis with increasing awareness of human safety. Nowadays, the development of innovation sensing systems and the construction of the sensing mechanism to improve the analytical performance of compounds remain a major challenge. Herein, we construct an advanced photoinduced thermocatalytic chemiluminescence (PI-TC-CL) gas-sensing system via the introduction of a Z-scheme heterojunction Ag3PO4/Ag/Bi4Ti3O12 to achieve higher efficient detection of H2S. The unique electron transport path of the Z-scheme heterojunction and the LSPR effect of Ag nanoparticles fascinate the generation of the photoinduced electron-hole pair on the surface of catalysts when stimulated by LED lamps and slow down the recombination of electron-hole pairs under thermal conditions. Thus, based on the cooperative effect of the Z-scheme heterojunction AgPO/Ag/BTO and PI-TC-CL system, we have successfully established an efficient H2S CTL detection system, which has a response three times higher than that on the traditional CTL system and even 45 times higher than that on BTO and ranges among the best of the state-of-the-art CTL performance in H2S detection with the linear range of 0.095-8.87 µg mL-1 and a limit of detection of 0.0065 µg mL-1. Besides, to explore the gas-sensing mechanism, the synergetic effects of photoinduction and thermal catalysis are investigated thoroughly via conductivity and electrochemical experiments. This research provides a new perspective of engineering highly efficient catalysts and ingenious sensor systems through designing the nanostructure of materials and synergism catalytic mechanism.

Multiplex DNA Walking Machines for Lung Cancer-Associated miRNAs.

Biomimetic DNA walking machines have gained great success in scrutinizing the microscopic world and sensitive biosensing of disease biomarkers. Despite superb achievements, the research on DNA walking machines for simultaneous detection of multiple analytes is still rare, while the design and realization of multiplexing are considered as an important bottleneck. The multiplex detection of biomarkers can not only improve the specificity of bioassays but also avoid the squander of valuable biological specimens. Herein, we reported multiplex three-dimensional (3D) DNA walking machines based on high-resolution inductively coupled plasma mass spectrometry (HR-ICPMS) for lung cancer-associated miRNA detection. In the presence of lung cancer-associated target miRNAs (miR-21, miR-141, and miR-125b), DNA walking machines were stimulated and operated to liberate a large number of lanthanide elements (Tb, Ho, and Tm), and then the signals were collected simultaneously by HR-ICPMS. The recovery test of target miRNAs in human serum and the simultaneous monitoring experiment of three miRNAs in human lung cancer cell line (A549) and normal cell line (HBE) specimens display satisfactory analysis capabilities for complex biological samples. Thanks to the vast potential of lanthanide tags and the modular design, the proposed bioassay might flexibly detect different miRNA combinations with corresponding sets of DNA walking machines to meet the requirements of various tasks.

Dapagliflozin improves endothelial cell dysfunction by regulating mitochondrial production via the SIRT1/PGC-1α pathway in obese mice.

Obesity is closely related to the occurrence of cardiovascular diseases, and an important reason for this is the induction of endothelial cell dysfunction. Mitochondria play an important role in maintaining the function of endothelial cells. In the present study, we examined the effects of the sodium-dependent glucose transporters 2 inhibitor dapagliflozin (DAPA) on the vascular endothelium in obese mice in vivo and on the structure and function of human umbilical vein endothelial cells (HUVECs) in vitro. The results revealed that DAPA rescued vascular endothelial damage in obese mice. Moreover, DAPA reversed the effects of palmitic acid (PA) on the reduction in angiogenesis and the increase in apoptosis in HUVECs. Furthermore, DAPA rescued the reduced mitochondrial membrane potential, mitochondrial viability, energy metabolism, mitochondrial biogenesis and the mitochondrial structural injury caused by PA. DAPA also activated the SIRT1/PGC-1α signaling pathway, while the SIRT1 inhibitor EX-527 abrogated the effects of DAPA on the mitochondria of HUVECs. In summary, our study suggests that DAPA improves endothelial cell mitochondrial function in obese mice by activating the SIRT1/PGC-1α pathway.

Transient Chemiluminescence Assay for Real-Time Monitoring of the Processes of SO32--Based Advanced Oxidation Reactions.

The hydroxyl radical (·OH) is a strong oxidizing agent in situ generated in advanced oxidation processes (AOPs) and crucial for assessing the performances of AOPs toward organic contaminants' degradation. Herein, we developed a specific luminescent probe, APDI (N' N'-di(propylethylenediamine)-perylene-3,4,9,10-tetracarboxylic diimide), to selectively detect ·OH among diverse reactive oxygen species and other radicals. Based on the transient chemiluminescence (TCL) spectra, the in situ concentration profile of ·OH within 0.01 s interval time in classical Fenton reactions and four kinds of SO32--based AOPs was obtained, which provides insights into the high dynamic processes of the whole ·OH generation and consumption processes. Besides, compared with acidic conditions, reduced degradation efficiencies in Fe2+-SO32- and Fe2+-SO32--H2O2 systems were found under neutral conditions. The complete depletion of active free radicals due to SO2-̇ radicals generated from Fe2+ and SO32- should account most for decreased degradation efficiencies evidenced by a new SO2* TCL signal discovered in the TCL spectra. In addition, similar phenomena have also been found in other M(n-1)+-SO32--related AOPs. As SO32- and HSO3- often exist naturally in wastewater, more efforts are needed to improve the performance of Fe2+-H2O2 systems. This discovery has important significance for organic contaminant degradation in a natural environment.

Evaluating the Band Gaps of Semiconductors by Cataluminescence.

A rapid and efficient methodology for the evaluation of band gaps of semiconductors is highly desirable to analyze and assess the intrinsic properties and extending application scopes of semiconductor materials. Here, the negative correlation of the cataluminescence (CTL) signal in the presence of H2S and the band gap of Aurivillius-type perovskite oxide Bi4+nFenTi3O12+3n (n = 1-4) was confirmed, where the H2S-induced CTL signal acts as a probe to evaluate the band gaps of semiconductor materials. The related mechanism shows that the thermal energy obtained by heating makes the electrons in the valence band more easily excite into the conduction band of a narrower band gap material and further promotes electron transfer between the gaseous compounds and semiconductor materials, causing acceleration of the catalytic oxide process. In addition, the extensibility was further verified by exploring the layered perovskite containing other insertion structures, including Bi4+nConTi3O12+3n (n = 1-4), Bi5NiTi3O15, and Bi5MnTi3O15, which was also consistent with the results characterized by UV diffuse reflectance spectroscopy. The established CTL probe for band gap evaluation shows rapid response, is simple to operate, and is of low cost, which is expected to become an innovative alternative to the conventional band gap assessment approach.

Metal-Tagged CRISPR/Cas12a Bioassay Enables Ultrasensitive and Highly Selective Evaluation of Kanamycin Bioaccumulation in Fish Samples.

The abuse of antibiotics in modern life and aquaculture has become a worldwide problem. Trace amounts of antibiotics discharged into natural water are increased in organisms through bioaccumulation and ultimately harm human health. Herein, we report a metal-tagged CRISPR/Cas12a bioassay and apply it to an ultrasensitive and highly selective evaluation of antibiotics bioaccumulation in wild fish samples. We integrated an element-tagging report probe and collateral cleavage activity of CRISPR/Cas12a. With the recognition and capture of target kanamycin by a "locked-activated" system, the activator strand was subsequently released to activate the collateral cleavage activity of Cas12a, followed by the cleavage of free Tm-Rep. After SA-MB capture, the biotin terminal was modified, and the uncleaved probe of Tm-Rep was removed. The acidized supernate containing the element tag fragment could be directly detected with 169Tm isotope monitoring by inductively coupled plasma mass spectrometry (ICPMS). With CRISPR/Cas12a biosensing and metal isotope detection by ICPMS, ultrasensitive and fast antibiotics analysis was realized with multiplex detection potential. Taking kanamycin as a modal analyte, a limit of detection as low as 4.06 pM was provided in a 30 min detection workflow. Besides, the bioaccumulation effect of kanamycin in a wild fish sample was also evaluated using the proposed strategy. We investigated the geographical distribution with Pseudorasbora parva samples collected in four different locations along a 600 km stretch of the Yangtze River. In addition, the bioaccumulation kinetics of antibiotics was evaluated in serum, muscle, and liver tissues of Pseudorasbora parva with 7 days of continuous feeding in a kanamycin-enriched environment.

Lanthanide Nanoprobes for the Multiplex Evaluation of Breast Cancer Biomarkers.

Metal stable isotope tagging has demonstrated great and unique success in the multiplex and ratiometry-based accurate detection of biomolecules and single cells, while its sensitivity is regarded as an Achilles' heel. Although lanthanide nanoparticles remain the most promising tags for elemental mass spectrometry, there is no report on the lanthanide nanoparticle-based multiplex immunoassay of disease markers in clinical serum samples because of their tough synthesis and bioconjugation and a complex physiological sample matrix. Herein, to fill this gap, multiple lanthanide nanoparticle tags (NaEuF4, NaTbF4, and NaHoF4) were delicately designed and facilely synthesized with a one-pot solvothermal method for the multiplex evaluation of breast cancer biomarkers carcinoembryonic antigen (CEA), CA153, and CA125 in human serum samples. The proposed method exhibited wide linear ranges and low levels of the detection limit for all biomarkers. The test results were consistent with the routine electrochemiluminescence results in clinical serum samples, which proved the possibility of the early prognosis of breast cancer as well as improving the surgical outcome prediction.

Ratiometric Cataluminescence Sensor of Amine Vapors for Discriminating Meat Spoilage.

The freshness of meat has always been the focus of attention from consumers and suppliers for health and economic reasons. Usually, amine vapors, as one of the main components of the gas produced in the process of meat spoilage, can be used to monitor meat spoilage. Here, a new ratiometric cataluminescence (CTL) sensor based on energy transfer was developed to identify amine vapors and monitor meat freshness. After Tb doping, amine vapors exhibit a dual-wavelength (490 and 555 nm) property of CTL signals when reacted on the surface of Tb-doped La2O2CO3, and the ratio of I555 to I490 (R555/490) is a unique value for a given analyte within a wide range of concentrations. To illustrate the new sensor, 15 amine vapors were successfully identified using R555/490, including homologues and isomers. Besides, this sensor was used to monitor four meats, and the freshness of meats can be distinguished by cluster analysis successfully. Moreover, further discussion of energy-transfer phenomena and influence factors has facilitating effects on exploring the mechanism of energy transfer at the gas-solid interface.

Analysis of influencing factors and prognosis of early postoperative recurrence, secondary tumor and metastasis of oral squamous cell carcinoma.

Oral squamous cell carcinoma (OSCC) is one of the most common cancers in the world and it accounts for more than 90% of oral cancers. In this study, we tried to estimate the risk of early postoperative recurrence, secondary tumor and metastasis of OSCC to predict the patient's prognosis according to its clinical condition to help increase their survival by screening high-risk patients. 153 patients with OSCC who were over 40 years of age were studied during 1985-2020. The influencing factors included gender, race, stage of tumor progression, treatment method, histological grade and tumor location, date of diagnosis and death, which were analyzed by the Markov multi-state model. Also, their saliva was sampled to determine the amount of Matrix Metalloproteinase13 (MMP13). Following-up of patients for 60 months showed that one year after the end of treatment, the probability of death was almost the same for patients with early postoperative recurrence or secondary tumor, but after 5 years, patients with early postoperative recurrence are at higher risk of death. Also, the MMP13 amount in the saliva of patients showed that high levels of MMP13 belonged to metastasis of OSCC than early postoperative recurrence and secondary tumor. Therefore, patients with more amount of MMP13 are more involved in metastasis than early postoperative recurrence and secondary tumor. Approximate knowledge of OSCC patients' next state and time according to their clinical condition can be one of the ways of timely diagnosis and treatment and thus reduce their mortality rate.

Clinicopathological features and lymph node metastasis risk in early gastric cancer with WHO criteria in China: 304 cases analysis.

AIMS: The aim of this research was to identify the clinicopathological characteristics of early gastric cancer (EGC) based on the WHO criteria, and to analyze predictors for lymph node metastasis (LNM) in EGC in a Chinese study population. METHODS: We retrospectively collected data of 304 Chinese EGC patients, including 265 patients undergoing radical gastrectomy and 39 patients undergoing endoscopic resection. Histological features were accessed by three experienced pathologists. Univariate analysis and multivariate analysis were used to identify the correlation between clinicopathological features and LNM. RESULTS: Among the 304 cases with EGC, the rate of well differentiated tubular adenocarcinoma was 11.2%, significantly lower than that of Japanese and South Korean, which was 24.8% and 19.9% respectively (p<0.001 and p = 0.006), but similar to that of a Western result, which was 11.9% (p = 0.860). Among the 265 patients who underwent gastrectomy, 18.5% of the patients had LNM. Univariate analysis showed that macroscopic type, differentiation degree, invasion depth, infiltration pattern (INF), lymphovascular invasion and ulceration were related to LNM. Multivariate analysis revealed that lymphovascular invasion (p < 0.001, OR = 6.549), ulceration (p = 0.035, OR = 2.527) and INF c (p = 0.042, OR = 3.424) were the independent risk factors of LNM in EGC. CONCLUSIONS: The pathological diagnosis standard of well differentiated tubular adenocarcinoma in China significantly differs from that in Japan and South Korea, but is similar to western countries. LNM is more likely to occur in EGCs with lymphovascular invasion, ulceration and INF c.

Engineering Ratiometric Persistent Luminous Sensor Arrays for Biothiols Identification.

Thiols play vital roles in mediating physiological processes. However, it is difficult to discriminate one thiol from another because of the similarities among structures and reactivities of thiols. In light of the ultralow background and impressive discrimination power, a persistent luminescence-based sensing array has attracted increasing attention but still remains a huge challenge. Herein, we have thoroughly studied the chemistry involving dual-emission persistent luminescence nanoparticles (D-PLNPs) with metal ions (MIs) and for the first time proposed an MIs-triggered ratiometric persistent luminescence (R-PersL) sensor array for the discrimination of six thiols. To extract data-rich outputs from a single sensor element, three representative D-PLNPs with a core-shell structure and subsequent carboxyl functionalizations (CSD-PLNPs) were rationally fabricated. Interestingly, MIs revealed the different regulating efficiencies for the two main emission bands of CSD-PLNPs, resulting from MI-triggered R-PersL signal transductions. Inspired by the crucial roles of thiols in vivo, a proof-of-concept sensor array through the ensemble of CSD-PLNPs-COOH and certain MIs was developed and demonstrated aR-PersL "fingerprint" pattern identification for six thiols. Remarkably, because of the autofluorescence-free background and high-throughput signal output, this sensing array system enabled a highly sensitive and differentiable detection of thiols at various concentrations in human blood serums, paving a new way to develop multiparameters sensing for complex analytes.

Chemiluminescence of Oleic Acid Capped Black Phosphorus Quantum Dots for Highly Selective Detection of Sulfite in PM2.5.

Quantum dots (QDs), especially metal-free QDs with their unique optoelectronic properties, environmental friendliness, and excellent biocompatibility, have opened a new avenue to explore novel chemiluminescence (CL) systems for analytical applications. However, the unknown CL properties, relatively weak emission, and instability of some of them in water (e.g., black phosphorus QDs) often seriously hinder their further practical applications. Chemical modification trends have offered new properties for materials and have been proved to be desirable ways to establish sensing platforms with improved sensitivity and stability. Herein, oleic acid capped black phosphorus QDs (OA-BP QDs) with improved stability and optical properties were successfully synthesized. More importantly, an extraordinary CL emission when OA-BP QDs reacted with SO32- was first observed. In the CL process, OA-BP QDs acted as the catalyst to trigger singlet oxygen (1O2) generation in NaHSO3, and then a chemiluminescence resonance energy transfer (CRET) between (1O2)2* (1O2 dimeric aggregate) and OA-BP QDs was produced. On this basis, a new CL system for directly monitoring SO32- in airborne fine particulate matter (PM2.5) was fabricated. The study opens attractive perspectives of modified metal-free QDs for the practice of CL in monitoring the chemical species in PM2.5.

Ratiometric Cataluminescence for Rapid Recognition of Volatile Organic Compounds Based on Energy Transfer Process.

Recognition of volatile organic compounds (VOCs) is a hot topic full of challenge from the perspective of environmental protection and human security. Here, we developed a novel ratiometric cataluminescence (RCTL) method for fast identification and detection gas compounds at various concentrations based on the energy transfer process, by the means of introducing rare earth ions codoped metal oxide into cataluminescence (CTL) sensor system to work as sensing material. When the prepared stick-like Y2O3:Eu3+,Tb3+ is exposed to kinds of analytes, different energy transfer process take place to emit two new signals at the characteristic wavelength of Tb3+ (ITb) and Eu3+ (IEu), which is available for us to identify miscellaneous gaseous compounds rely on the ratio of ITb to IEu (ITb/IEu). To confirm the feasibility of the proposed method, seven kinds of gas compounds, including homologous series and even structural isomers, were investigated and successfully distinguished in a wide range of concentrations. Besides, further discussion of the CTL sensing and recognition mechanism in this paper has facilitating effects on exploring reactive intermediates and explaining the essential principle of catalytic oxidation process.