Green Chemical Engineering
·
2024
·
IF 9.1
Taihang Zhou,Fen Qiao,Sen Qian,Shoaib Muhammad,Haitao Li,Yanzhen Liu
In the contemporary context, tetracycline is widely utilized as a prevalent antibiotic in various facets of life. However, the excessive use of antibiotics has caused visible environmental consequences. Henceforth, the scientific community has increasingly focused on developing catalysts that exhibit exceptional efficacy in the proficient degradation of tetracycline. In this study, a novel nanomaterial was developed to encapsulate CdTe quantum dots (QDs) with a SiO 2 shell. The distinct synthesis approach generated a composite material that showed heterogeneity and considerably increased the contact area with contaminants. Consequently, the transfer of photoelectron to the SiO 2 spheres was significantly improved, leading to a more efficient separation during the catalytic process. The study investigated how different factors, such as the loading of the catalyst, the initial concentration of tetracycline, pH levels, and the wight ratio of CdTe QDs (SiO 2 + CdTe QDs) affected the effectiveness of photocatalytic tetracycline degradation. The findings indicated that the optimal degradation efficiency was observed at a catalyst concentration of 0.25 g/L and a solution pH of 9, leading to an impressive degradation rate of 96% within a mere 2 h timeframe.
研究领域:
环境科学
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材料科学
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高影响因子
DALTON TRANSACTIONS
·
2024
·Vol. 53
·期 18
·8011-8019
·
IF 3.5
Kai Liu,Mao-Jin Ran,Zhi-Rong Li,Yi-Fu Huang,Ze-Yu Jiang,Wan-Ying Li,Shokir Khojiev,Zhi-Yi Hu,Li-Hua Chen,Jing Liu,Yu Li,Bao-Lian Su
Designing efficient, inexpensive, and stable photocatalysts to degrade organic pollutants and antibiotics has become an effective way for environmental remediation. In this work, we successfully performed in situ growth of CdS QDs on the surface of elliptical BiVO4 to try to show the advantage of the binary heterojuncted photocatalyst (BVO@CdS) for the photocatalytic degradation of tetracycline (TC). The In situ growth of CdS QDs can provide a large number of reactive sites and also generate a larger contact area with BiVO4. In addition, compared with mechanical composite materials, in situ growth can significantly reduce the energy barrier at the interface between BiVO4 and CdS, providing more channels for the separation and migration of photogenerated charge carriers, and further improving reaction activity. As a result, BVO@CdS-0.05 shows the best degradation efficiency, with a degradation rate of 88% after 30 min under visible light. The TC photodegradation follows a pseudo-second-order reaction with a dynamic constant of 0.472 min−1, which is 6.47 times that of pure BiVO4, 7.24 times that of pure CdS QDs and 2 times that of the mechanical composite. The degradation rate of BVO@CdS-0.05 decreases to 77.8% with a retention rate of 88.5% after four cycles, demonstrating excellent stability. Through liquid chromatography-mass spectrometry (LC-MS) analysis, two possible pathways for TC degradation are proposed. Through free radical capture experiments, electron spin resonance measurements, and photoelectrochemical comprehensive analysis, it is confirmed that BVO@CdS composites have constructed an efficient Z-scheme heterojunction via in situ growth, thereby highly enhancing the separation and transport efficiency of charge carriers.
研究领域:
环境科学
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材料科学
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PubMed
高影响因子
Molecular BioSystems
·
2011
·Vol. 7
·期 8
·2452-2458
·
IF 3.825
Jianbo Xiao,Feijiu Wang,Jie Liu,Litong Wang,Guoyin Kai,Xibin Yu
Zero-dimensional nanostructures such as ZnO#ZnS QDs heterojunctures (QDHJs) are green nanoparticles and have gained a tremendous amount of attention. However, very little information is available on the effects of these heterojunctures on the transportation of drugs in blood. Herein, stilbenes were studied for their affinities for common bovine plasma proteins (CBPP) in the presence and absence of QDHJs with different diameters. The affinities of QDHJs for CBPP improved with increasing QDHJs size. QDHJs improved the affinities of resveratrol and polydatin for CBPP by 14.74% to 22.36% and 12.56% to 21.34% depending on the size of QDHJs. The number of binding sites (n) between resveratrol and polydatin for CBPP in the presence of QDHJs were 1.04 ± 0.03 and 1.06 ± 0.04, which were obviously higher than those in the absence of QDHJs (n = 0.89 and 0.92). QDHJs in blood will decrease the free concentration of stilbenes and weaken their pharmacological effects.
研究领域:
药理学
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纳米生物学
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PubMed
高影响因子
OPTICAL MATERIALS
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2019
·
IF 2.687
Changhong Li,Ye Li,Tianliang Zhou,Rong-Jun Xie
Mn-doped CsPbCl 3 (CsPbCl 3 :Mn) perovskite colloidal quantum dots (QDs) attract a great deal of interests, and have great potentials for various optoelectronics applications due to their outstanding optical and electrical properties. However, practical applications of CsPbCl 3 :Mn QDs are severely limited by the cumbersome preparation methods and low photoluminescence quantum efficiency (PLQY). Herein, we propose a single-step ultrasonic synthesis method to successfully synthesize CsPbCl 3 :Mn QDs with controlled size and morphology by changing the Mn:Pb ratio. Simultaneously, we introduce triethylamine (TETN) to passivate the surface of CsPbCl 3 :Mn QDs. The phase purity, microstructure, chemical composition and photoluminescence properties of the samples were investigated by means of various analytic techniques. The synthesized QDs exhibit dual emissions of 411 and 601 nm, ascribing to the excitonic emission of QDs and the characteristic Mn 2+ emission, respectively. The quantum yield of the CsPbCl 3 :Mn QDs could therefore be significantly improved from 17.49 to 41.15%. We believe that the facial synthesis method and the surface passivation of TETN can also be applied to other transition metal or lanthanide ions doped lead halide perovskite QDs.
研究领域:
材料科学
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光学工程
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化学工程
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高影响因子
Analytical Methods
·
2017
·Vol. 9
·期 6
·929-936
·
IF 1.9
Fan Zhang,Miaomiao Chen,Haiqing Zhang,Huayu Xiong,Wei Wen,Xiuhua Zhang,Shengfu Wang
A sensitive, convenient and rapid fluorescent sensor for effectively and directly detecting propranolol was proposed based on the fluorescence suppression of 3-mercaptopropionic acid stabilized CdTe quantum dots. The fluorescence suppression mechanism between CdTe QDs and propranolol was studied by time-resolved fluorescence spectroscopy, UV-Vis spectroscopy and fluorescence spectroscopy, and it was attributed to the simultaneous action of the inner filter effect (IFE) and dynamic quenching effect (DQE). The effects of the concentration of quantum dots, pH value of buffer solution and incubation time on the fluorescence signal of the propranolol/CdTe quantum dot system were also investigated. The results indicated that, when the experiment was conducted under optimal experimental conditions, the linear range of this assay was 0.1 μM to 2 μM and 5 μM to 200 μM, with a corresponding detection limit of 0.055 μM. Moreover, some common drug excipients and analogues of propranolol and stimulants had no apparent effect on the determination of propranolol. The proposed fluorescent sensor could be readily used for effectively and directly detecting propranolol in biological samples.
研究领域:
分析化学
·
生物医学
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高影响因子
ANALYTICAL CHEMISTRY
·
2014
·
IF 5.825
Chaoying Xu,Ronghui Zhou,Wenwei He,Lan Wu,Peng Wu,Xiandeng Hou
Fingerprints are unique characteristics of an individual, and their imaging and recognition is a top-priority task in forensic science. Fast LFP (latent fingerprint) acquirement can greatly help policemen in screening the potential criminal scenes and capturing fingerprint clues. Of the two major latent fingerprints (LFP), eccrine is expected to be more representative than sebaceous in LFP identification. Here we explored the heavy metal-free Mn-doped ZnS quantum dots (QDs) as a new imaging moiety for eccrine LFPs. To study the effects of different ligands on the LFP image quality, we prepared Mn-doped ZnS QDs with various surface-capping ligands using QDs synthesized in high-temperature organic media as starting material. The orange fluorescence emission from Mn-doped ZnS QDs clearly revealed the optical images of eccrine LFPs. Interestingly, N-acetyl-cysteine-capped Mn-doped ZnS QDs could stain the eccrine LFPs in as fast as 5 s. Meanwhile, the levels 2 and 3 substructures of the fingerprints could also be simultaneously and clearly identified. While in the absence of QDs or without rubbing and stamping the finger onto foil, no fluorescent fingerprint images could be visualized. Besides fresh fingerprint, aged (5, 10, and 50 days), incomplete eccrine LFPs could also be successfully stained with N-acetyl-cysteine-capped Mn-doped ZnS QDs, demonstrating the analytical potential of this method in real world applications. The method was also robust for imaging of eccrine LFPs on a series of nonporous surfaces, such as aluminum foil, compact discs, glass, and black plastic bags.
研究领域:
法医学
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材料科学
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化学
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PubMed
高影响因子
JOURNAL OF APPLIED POLYMER SCIENCE
·
2017
·Vol. 135
·期 6
·45831
·
IF 1.86
Jing Zhang,Liqun Chen,Jiada Chen,Dan Wu,Jie Feng
We demonstrated an extremely facile way to fabricate inorganic–organic microgels with pH sensitivity and fluorescence. Aqueous dextran microgels are crosslinked by ZnO quantum dots (QDs). The ZnO@Dextran microgels were synthesized by simply mixing amino-modified ZnO (ZnO QDs) with carboxymethyl dextran (CMD) while stirring. The hybrid microgels showed an average diameter of ∼5 μm and strong fluorescence under ultraviolet (365 nm) irradiation. Up to 79.3 wt % of ZnO QDs were loaded into microgels. The ZnO QDs crosslinkage in the hybrid microgels structure enabled the microgels to degrade under mild acidic environment due to pH sensitivity of ZnO QDs. After loading of doxorubicin (Dox), the microgels were used as drug carriers for pH-controlled release of Dox. The degradation of the microgels and the release of loaded cargos could be monitored by detecting fluorescence intensity of the microgels. Moreover, owing to the cytotoxicity of ZnO QDs at their destination, drug-loaded ZnO@Dextran microgels can be used for synergistic therapy. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135 , 45831.
研究领域:
材料科学
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生物医学工程
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纳米医学
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高影响因子
COLLOIDS AND SURFACES B-BIOINTERFACES
·
2022
·
IF 5.999
Qiang Zhang,Shengbao Duan,Yinong Huang,Jingjing Tian,Jia Hu
By integrating the fluorescence of quantum dots (QDs) and Mn 2+ -pefloxacin mesylate (Mn 2+ -pefloxacin), a new type of dual-band fluorescence biosensor for high-efficiency and sensitive determination of double-stranded DNA (dsDNA) is developed. The biosensor is based on the fluorescence "OFF-ON" mode of both QDs and QDs-Mn 2+ -pefloxacin. The Mn 2+ -pefloxacin complex can quench the QDs fluorescence via photoinduced electron transfer (PET), and its fluorescence is also quenched. Due to the specificity and strong binding affinity of dsDNA for the Mn 2+ -pefloxacin complex, it can break the low fluorescent QDs-Mn 2+ -pefloxacin and restore the fluorescence of QDs and Mn 2+ -pefloxacin complex in their respective bands. Therefore, the dual-band fluorescence quantitative detection of dsDNA by QDs-Mn 2+ -pefloxacin can be achieved, while bovine serum albumin , single-stranded DNA, and bio-related ions do not yield similar results. Furthermore, the possible reaction mechanisms are systematically discussed. The detection limits (3δ/K) of herring sperm (hs) DNA in the fluorescence recovery bands of QDs and Mn 2+ -pefloxacin complex are 0.0142 and 0.0465 μg/mL, respectively. The developed biosensor was used for dsDNA detection in synthetic samples, and desirable results are obtained.
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PubMed
高影响因子
MOLECULES
·
2022
·Vol. 27
·期 7
·2097
·
IF 4.927
Pu Li,Xiaoxiao Chen,Gaojun Wu,Zhe Wang,Chaobiao Huang
An ascorbic acid (AA) sensor was constructed based on the fluorescence resonance energy transfer (FRET) between CdS quantum dots (CdS QDs) and polydopamine (PDA) to detect trace AA sensitively. FRET occurred due to the broad absorption spectrum of PDA completely overlapped with the narrow emission spectrum of CdS QDs. The fluorescence of CdS QDs was quenched and in the “off” state. When AA was present, the conversion of DA to PDA was hindered and the FRET disappeared, resulting in the fluorescence of CdS QDs in an “on” state. Importantly, the degree of fluorescence recovery of CdS QDs displayed a desirable linear correlation with the concentration of AA in the range of 5.0–100.0 μmol/L, the linear equation isy=0.0119cAA+0.3113, and the detection limit is 1.16 μmol/L (S/N = 3,n= 9). There was almost no interference with common amino acid, glucose and biological sulfhydryl small molecules to AA. Trace amount of AA in vitamin C tablets were determined and satisfactory results were obtained; the recoveries were observed to be 98.01–100.7%.Keywords:CdS quantum dots;PDA;fluorescence resonance energy transfer;ascorbic acid
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2019
·
IF 4.084
Tao Wang,Xiqing Liu,Donglai Han,Yuxuan Sun,Changchang Ma,Yang Liu,Pengwei Huo,Yongsheng Yan
In this work, a biofiber was used as the natural polymer carrier to design a BiVO 4 QDs/cellulose fiber composite for photocatalytic application. The biofiber was obtained from bamboo, which was green, abundant and short growth cycle in Asia. Naturally rich groups of biofiber provided many sites to absorb the Bi 3+ to form the uniform distribution for BiVO 4 QDs . Moreover, a series of results indicated the strong connection was formed between biofiber and BiVO 4 QDs, which could increase the stability and electron transfer . Therefore, the new composite photocatalyst exhibited better stability and effectively photocatalytic activity . Moreover, the possible mechanism of synthesis and photocatalytic were discussed, which provided insight for synthesizing photocatalytic based on biomaterials.
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高影响因子
ANALYST
·
2020
·Vol. 146
·期 3
·949-955
·
IF 3.978
Fan Lu,Yeling Yang,Yucheng Liu,Fubing Wang,Xinghu Ji,Zhike He
High concentration of uric acid is usually related to cardiovascular and cerebrovascular diseases. Developing a simple method for the rapid and efficient detection of uric acid has a great significance in clinical diagnosis. In this work, alginate hydrogel microspheres embedded with CdZnTeS QDs and urate oxidase (Alg@QDs-UOx MSs) were prepared for the first time, and further used for point-of-care testing (POCT) of patients with a high concentration of uric acid. This strategy is mainly based on visual detection of H2O2, the product of uric acid after an enzymatic reaction. The proposed sensor (Alg@QDs-UOx MSs) has several advantages. First, it can reduce the interference of the proteins to the fluorescence of QDs. Second, Alg@QDs-UOx MSs help improve the stability of the CdZnTeS QDs as well as the activity of urate oxidase during storage. Third, it is easy to use, has fast response speed, and is of low cost. Therefore, the proposed sensor shows good application prospects. Simply through the built-in camera of a smartphone, we can visualize the urine samples from patients with a high concentration of uric acid within 10 minutes, and the accuracy rates were 100%. In the range of 100.0 μM to 900.0 μM, the I/I0 values and uric acid concentrations are in a great linear relationship (R2 = 0.9973), indicating that this method can be employed for quantitative analysis of uric acid in human urine (<10 mM). The limit of detection (LOD) is 20.3 μM.
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高影响因子
Nanoscale
·
2024
·Vol. 16
·期 28
·13654-13662
·
IF 5.8
Naiwei Wei,Hong Zhu,Danni Yan,Shuai Yang,Lili Xu,Shengli Zhang,Yuhui Dong,Yousheng Zou,Haibo Zeng
I–III–VI quantum dots (QDs) have gained widespread attention owing to their significant advantages of non-toxicity, large structural tolerance, and efficient photoluminescence potential. However, the disbalance of reactivity between the elements will result in undesired products and compromised optical properties. Reducing the activity of highly reactive group IB elements is the most common approach, but it will reduce the overall reactivity and lead to a wide dispersion of QD sizes. In this study, we propose a method to improve the overall reactivity of the reaction system using the highly active IIIA precursor InI3, which triggers rapid nucleation and promotes the formation of Ag(In,Ga)S2 (AIGS) QDs, resulting in monodisperse particle size distributions and a significantly improved photoluminescence quantum yield (PLQY) (from 12% to 72%). Furthermore, narrow band edge emission is realized by coating a gallium sulfide (GaSx) shell on the basis of obtaining high-quality AIGS QDs. The core/shell QDs exhibit a 90% PLQY with a full width at half maximum (FWHM) of only 31 nm at 530 nm. This study provides a viable design strategy to synthesize monodisperse AIGS QDs with a narrow peak width and efficient luminescence, promoting the application of AIGS QDs in the field of luminescent displays.
研究领域:
材料科学
·
纳米技术
·
光学
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PubMed
高影响因子