FOOD AND AGRICULTURAL IMMUNOLOGY
·
2018
·
IF 2.568
Zhi-Li Xiao,Wei Tian,Zhen-Lin Xu,Yuan-Ming Sun
In this study, we develop a sensitive indirect competitive chemiluminescent enzyme immunoassay (ic-CLEIA) to detect cadmium (Cd) in cereals. A luminol-hydrogen peroxide chemiluminescence system catalysed by horseradish peroxidase (HRP) was used as the signal detecting system. The method showed a half-maximal inhibition concentration (IC50) of 0.5 ng/mL and a limit of determination (LOD) of 0.06 ng/mL. The assay indicated an effective linear range from 0.16 to 1.56 ng/mL. There were no obvious cross-reactivities with other metal ions, including Hg2+, Pb2+, As2+, Ag+, Fe3+, Cu2+, Cr2+, Au3+, Ca2+, Mg2+, Mn2+ and Zn2+. Recovery rates ranged from 79.2% to 120.0% for rice, maize, wheat, brown rice and glutinous rice samples. Twenty-five practical cereal samples were analysed, and the comparative analysis of the results showed a strong correlation (r = 0.984) between the CLEIA and the GFAAS methods. The results indicated that the ic-CLEIA developed was acceptable to screen for cadmium in cereal samples.
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ADVANCED FUNCTIONAL MATERIALS
·
2018
·Vol. 28
·期 14
·1703369
·
IF 13.325
Youchen Gu,Heping Shen,Chen Ye,Xuezeng Dai,Qian Cui,Jianbao Li,Feng Hao,Xiaojing Hao,Hong Lin
The thin-film photovoltaic material Cu 2 ZnSnS 4 (CZTS) has drawn worldwide attention in recent years due to its earth-abundant, nontoxic element constitution, and remarkable photovoltaic performance. Although state-of-the-art power conversion efficiency is achieved by hydrazine-based methods, effort to fabricate such devices in a high throughput, environmental-friendly way is still highlydesired. Here a hydrazine-free all-solution-processed CZTS solar cell with Na 2 S self-depleted back contact modification layer for the first time is demonstrated, using a ball-milled CZTS as light absorber, low-temperature solution-processed ZnO electron-transport layer as well as silver-nanowire transparent electrode. The inserting of Na 2 S self-depleted layer is proven to effectively stabilize the CZTS/Mo interface by eliminating a detrimental phase segregation reaction between CZTS and Mo-coated soda lime glass, thus leading to a better crystallinity of CZTS light absorbing layer, enhanced carrier transportation at CZTS/Mo interface as well as a smaller series resistance. Furthermore, the self-depletion feature of the Na 2 S modification layer also averts hole-transportation barrier within the devices. The results show the vital importance of interfacial engineering for these CZST devices and the Na 2 S interface layer can be extended to other optoelectronic devices using Mo contact.
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ACS Nano
·
2024
·
IF 15.8
Kuo Wang,Yajie Luo,Hongtu Zhan,Xiao-Xia Liu,Xiaoqi Sun
Zn metal anodes experience dendritic growth and hydrogen evolution reactions (HER) in aqueous batteries. Herein, we propose an interface regulation strategy with a trace (1.4 × 10–4 mol kg–1) all-in-one epicatechin (EC) electrolyte additive to solve the above issues and reveal the roles of individual functional groups. By the disassembly of EC into simple molecules combined with entire molecule investigations, we show that phenol and ether sites preferentially anchor on the Zn surface, while the hydroxyl group pointing outward enters Zn2+ solvation shells at the interface. It modifies the following desolvation path, which not only enables uniform deposition with the thermodynamically favored plate morphology but also inhibits HER. With these synergistic effects of trace EC additive, the lifespan of symmetric cells extends to 8.5 times that of the baseline ZnSO4 electrolyte. The capacity retention of Zn//MnO2 full batteries with N/P = 3 also increases from 59.1 to 85.6% after 500 cycles.
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
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2024
·
IF 4.9
Jiankang Li,Liuquan Lin,Sen Zhou,Xiaoming Yang
Room-temperature phosphorescence carbon dots (CDs) show the highlighted advantages in chemical sensing and bioimaging owing to its long lifetime, however, acquiring the efficient phosphorescence of carbon dots is still encountering difficulty due to the spin prohibition. Here, we synthesized one type of CDs through one-step hydrothermal method. To be specific, the CDs displayed the blue fluorescence in aqueous, and emitted the bright green phosphorescence when being coated on the filter paper. Importantly, introducing coumarin to the CDs resulted in the distinct quenching of both its fluorescence and phosphorescence. Based on this phenomenon, we successfully established a dual-channel detection of coumarin. The fluorescence detection channel exhibited a linear range of 5–350 μM with a detection limit of 0.196 μM, while the phosphorescence detection channel achieved a linear range of 50–1000 μM with a detection limit of 0.268 μM. The further investigation revealed that IFE and SQE were mainly responsible for the fluorescence quenching of CDs, while the phosphorescence quenching was originated from the increased energy gap between the singlet and triplet states (ΔE ST ) of CDs, thus obstructing the ISC process. Moreover, we employed the CDs as the phosphorescent ink for anti-counterfeiting.
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MICROCHIMICA ACTA
·
2024
·Vol. 192
·期 1
·1-12
·
IF 5.3
Liu Xiang,Li Huijun,Sun Junjun,Shi Jianchao,Xu Zhouqing,Wang Yan
A HPU-23@Ru@Tb-NH 2 sensor array with light-driven oxidase-mimicking activity and triple-emission fluorescence was developed. It was composed of a Tb 3+ -functionalized metal organic framework and Ru(bpy) 3 2+ and applied to the simultaneous detection of Hg 2+ , ClO − , and PO 4 3− via differently responsive channels. HPU-23@Ru@Tb-NH 2 had a photoresponsive colorimetric response toward Hg 2+ with a LOD as low as 4.18 nM. In addition, the three emissions of the HPU-23@Ru@Tb-NH 2 sensor array were influenced by ClO − and PO 4 3− to varying degrees, causing remarkably distinguishable responses for the fluorescence channels to discriminate ClO − and PO 4 3− from each other. The detection limits of ClO − and PO 4 3− were 12.26 µM and 0.197 nM, respectively. Therefore, this work demonstrates the feasibility of multi-emission and multi-mode sensing platform, which is able to combine the advantages of different strategies for solving the problems of various toxic substances coexisting in the environment while meeting the needs of accurate and precise results and no side interferences. Graphical
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JOURNAL OF MOLECULAR STRUCTURE
·
2024
·
IF 4
Xueqi Duan,Guona Li,Zhijian Jia,Hongzhen Xie,Xing Li
Copper is an essential element in the human body. Excess accumulations of copper, however, would become a potential threat. Therefore, it is of great significance to detect copper ions. Owing to their controllable morphology, dispersal characteristics, high extinction coefficient, and easily functionalized surfaces, gold nanoparticles (AuNPs) have been highly employed as attractive sensing probes for environmental and biological analyses. We herein propose an eco-friendly colorimetric strategy based on AuNPs modified with 3-pyridinylboronic acid (PA) for sensitive and selective detection of copper ions (Cu 2+ ) in water at trace level. The color changes of the system from wine-red to gray-blue with increasing amounts of copper ions is due to the binding of AuNPs modified with 3-pyridinylboronic acid to copper ions, which in turn leads to the aggregation of AuNPs with fine anti-interference. Strengths of the work: 1) rapid response time without complex pre-treatment; 2) high sensitivity with low limit of detection (LOD) and the good linear relationship ( R 2 = 0.98, LOD = 3.0 μM by the naked eye and 72 nM by ultraviolet-visible spectroscopy); 3) high selectivity under other interfering ions. In addition, the detection mechanism of this work has been successfully confirmed by density functional theory (DFT), transmission electron microscopy (TEM), dynamic light scattering (DLS), X-ray diffraction (XRD), Zeta potential analysis and ultraviolet-visible spectroscopy (UV–vis).
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Analytical Methods
·
2012
·Vol. 4
·期 8
·2441-2446
·
IF 1.547
Qian Zhang,Tao Liang,Lingqing Wang,Hongying Cao
A selective pressurized liquid extraction (SPLE) method has been optimized for the determination of polycyclic aromatic hydrocarbons (PAHs) in soil samples. The method comprises a fully automated extraction and on-line clean-up procedure by inclusion of sorbents in the extraction cells. The contributing parameters of SPLE including type of solvent, static extraction time, number of extractions, extraction temperature, nature and amount of sorbents were investigated. The optimal extraction was performed at 70 °C for 10 min (static extraction time) cycled once using n-hexane/methylene chloride (50 : 50, v/v) and the sorbents in the extraction cells were 3 g of alumina and 2 g of silica gel. The collected extracts from the cells, after pre-concentration, were clean enough for direct injection into GC-MS. Validation of the SPLE technique was performed, with the recovery rates for 16 PAHs in the range of 75–103%, and the relative standard deviation (RSD) was generally less than 10%. Method detection limits (MDL) were in the ranges of 0.001–0.080 μg kg−1 for the GC-MS analyses. Finally, the method was successfully used to evaluate the cultivated soils in Beijing, China.
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CHEMICAL ENGINEERING JOURNAL
·
2025
·
IF 13.2
Guangyuan Chen,Linzhen Wu,Zeru Wang,Ruixi Liu,Chuan Tan,Yi Tan,Yawen Liu,Miaomiao He,Hao Zhang,Yikun Huang,Jiongzhi Zhu,Tao Duan,Lin Zhu
The capture of radioactive gaseous iodine is essential for the sustainable development of nuclear energy and the long-term safe supply of nuclear fuel. However, the presence of nitrogen oxides in the exhaust gas generated during spent fuel reprocessing poses significant challenges to the stability of iodine adsorbents. It is crucial to consider the impact of NOx on the structure and adsorption performance of the materials. We report here the development of an aluminum-based metal–organic framework (MOF), CAU-1, engineered for efficient iodine capture. Synthesized through a cost-effective and straightforward method, CAU-1 exhibits excellent structural stability and robust adsorption performance, with a maximum iodine vapor adsorption capacity of 1277.18 mg/g at 130 °C and methyl iodide adsorption capacity of 533.10 mg/g, highlighting its potential for efficient iodine vapor removal. Notably, CAU-1 retains its structural integrity and iodine adsorption performance even in the presence of 5 % NO 2 , maintaining high adsorption capacities for I 2 (1129.41 mg/g) and CH 3 I (436.79 mg/g). Mechanistic analysis revealed the key role of the –NH 2 group in the iodine adsorption process. Additionally, co-adsorption studies with I 2 and NO 2 showed that CAU-1 can still capture iodine in the form of both I 2 and I 3 - in the presence of NO 2 . This study illustrates the potential of CAU-1 as an effective industrial adsorbent for removing iodine from NO 2 -containing gas streams.
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Energy Storage Materials
·
2024
·
IF 18.9
Kuo Wang,Tong Qiu,Lu Lin,Hongtu Zhan,Xiao-Xia Liu,Xiaoqi Sun
Zn anode experiences dendrite issues in aqueous Zn batteries. They result from uneven Zn 2+ flux and Sand behavior depending on the current density. Herein, the amino alcohol of 2,2′,2′′-nitrilotriethanol (NTE) additive with chelation ability is introduced to achieve stable and parallel Zn deposition. NTE preferentially adsorbs on Zn surface, which chelates with Zn 2+ at interface upon geometry transformation. It not only homogenizes Zn 2+ flux to inhibit dendrites at low current densities, but also supply sufficient Zn 2+ to delay Sand behavior at high current densities. Parallel growth of Zn hexagonal plates is realized. Thus, Zn plating/stripping in symmetric cells at 10 mA cm −2 reaches >1600 h cycle life with the addition of 2.5% NTE in the ZnSO 4 electrolyte, corresponding to a high cumulative plated capacity of 8.5 Ah cm −2 . At the conditions of 5 °C or 70% depth of discharge, the lifespans of symmetric cells also extend to 6977 h and 230 h, respectively. In anode free full cells, a Zn 2+ pre-inserted V 6 O 13 ·H 2 O cathode retains 250 mAh g −1 capacity after 300 cycles at 6 A g −1 , superior to 83 mAh g −1 with NTE free electrolyte.
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JOURNAL OF FOOD SCIENCE
·
2024
·
IF 3.2
Xi Wu,Chenggang Geng,Weiwei Cheng,Zhenjiong Wang,Yan Zhang,Di Wu,Xiaozhi Tang
In this work, an ultrasensitive electrochemical sensor based on Zr-MOF-SH/rGA/NPG was developed for the first time for the rapid determination of mercury ions. First, nanoporous gold (NPG) film was covered on the glassy carbon electrode (GCE) to offer a desirable substrate. Then, Zr-MOF-SH/rGA composites were dropped on the NPG film to form a modified electrode. Mercapto functionalized MOFs (Zr-MOF-SH) showed strong adsorption capability toward mercury ions, and the unique structure of reduced graphene oxide aerogel (rGA) provided various sites for coupling with Zr-MOF-SH as well as improved the electrochemical activity. As a consequence of the synergistic effect of Zr-MOF-SH, rGA, and NPG, the optimized Zr-MOF-SH/rGA/NPG/GCE sensor showed excellent detection performance toward mercury ions with a linear range from 0 to 200 nM and a low limit of detection of 1.4 nM. Meanwhile, the fabricated electrochemical sensor exhibited outstanding stability, reproducibility, and anti-interference ability. To verify the practical applicability, the Zr-MOF-SH/rGA/NPG/GCE was applied for the determination of mercury ions in real rice samples with desirable recovery rates ranging from 98.8% to 108.3%.
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CHEMICAL ENGINEERING JOURNAL
·
2024
·
IF 13.3
Tao Wu,Hassan Karimi-Maleh,Yan Li,Zhouxiang Zhang,Dongxing Zhang,Yangping Wen,Li Fu,Nianbing Zhong,Elena Niculina Dragoi,Tejraj M. Aminabhavi
MOFs/MXene adsorbent was prepared by in-situ growth of MOFs(ZIF-67/ZIF-8) crystal particles onto the surface and between the layers of multi-layer MXene substrate. The method followed complex separation and recovery steps after completion of adsorption and there can be a risk of secondary contamination. To avoid this, DLP technique was used to print a series of 3D printed structures (3DS) with a specific topography, the prepared MOFs/MXene composites were loaded onto surface of the structure. Polydopamine (PDA) was then coated onto the surface to prepare monolithic adsorbent (PDA/MOFs/MXene/3DS) that was easily separated and recovered. The adsorbent was characterized by SEM, XRD, FTIR, TGA and XPS, while the batch adsorption of CR and Hg (II) was performed under different experimental conditions. The optimal removal rate and maximum adsorption of the monolithic adsorbent for CR and Hg (II) were 99.13/94.10 % and 75.76/464.48 mg/g, respectively and adsorption followed chemisorption onto the surface monolayer, which was spontaneous and exothermic. Multiple cycle tests showed excellent removal of CR (82.29 %) and Hg (78.47 %). In addition, adsorbent with synergistic effects of electrostatic interactions, H-bonding and π-π stacking shows a good adsorption effect. The study proved that that PDA/MOFs/MXene/3DS is a high-strength, structurally designable, green and promising adsorbent for large-scale remediation of real contaminants frpm wastewater.
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MICROCHEMICAL JOURNAL
·
2025
·
IF 5.1
Xueqi Duan,Xing Li,Qingya Yang
Due to the serious threat of excessive copper and magnesium ions to human health, it is crucial to detect copper and magnesium ions in aquatic environments. In this study, we propose a colorimetric strategy – gold nanoparticles (AuNPs) modified by 5-(3-aminophenyl)-1H-tetrazole (TA@AuNPs) for the rapid and portable identification of copper and magnesium ions in water. As the concentration of the target metal ions increases, the colorimetric principle (TA@AuNPs) causes the aggregation of the AuNPs system, shifts of the surface plasma resonance (SPR) absorption peak, and a change of system colors (wine-red to gray-blue). The advantages of this work: 1) the detection process is simple without complex pretreatment; 2) the concentration of the target ions could be quickly detected within 3 min by Standard Color Cards; 3) it can selectively detect two kinds of metal ions (Cu 2+ and Mg 2+ ) with high specificity in the presence of other interfering ions; 4) It eliminates the interference of calcium ions in the detection of magnesium ions; 5) It has excellent linearity and low detection limit (for Cu 2+ : R 2 = 0.94, LOD = 30.0 μM by the naked eye and 0.229 μM through ultraviolet–visible spectroscopy; for Mg 2+ : R 2 = 0.96, LOD = 300 μM by the naked eye and 0.653 μM through ultraviolet–visible spectroscopy). Furthermore, the colorimetric mechanism of the present work has been comprehensively demonstrated through DLS, TEM, zeta potential analysis, FT-IR, UV–vis and Gaussian calculations.
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