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JOURNAL OF LUMINESCENCE · 2015 · IF 2.719

Rapid fluorometric determination of perfluorooctanoic acid by its quenching effect on the fluorescence of quantum dots

Qi Liu,Aizhen Huang,Nan Wang,Guan Zheng,Lihua Zhu

Analysis of perfluorooctanoic acid (PFOA) usually requires a combination of high-performance liquid chromatography and mass spectrometry , which is expensive and time-consuming. In the present work, water-soluble CdS quantum dots (QDs) were employed to develop a simple and rapid fluorometric method for the determination of PFOA. Strongly fluorescent CdS QDs were prepared by using 3-mercaptopropionic acid (MPA) as a stabilizer . It was observed that PFOA strongly quenched the fluorescence emission of the MPA-CdS QDs because PFOA promotes the aggregation of MPA-CdS QDs through a fluorine–fluorine affinity interaction. Under optimum conditions, the fluorescence intensity of MPA-CdS QDs was observed to decrease linearly with an increase in the concentration of PFOA from 0.5 to 40   μmol   L −1 , with a limit of detection of 0.3   μmol   L −1 . This new method was successfully implemented for the analysis of PFOA-spiked textile samples, with recoveries ranging from 95% to 113%.

研究领域: 分析化学 · 环境科学
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JOURNAL OF CRYSTAL GROWTH · 2025 · IF 2

Cost-effective, hydride-free aqueous synthesis of CdTe quantum dots enabled by using ammonia as the reducing agent

Van-Thao Ta,Duy-Khanh Nguyen,Xuan-Bach Nguyen,Phuong-Nam Nguyen,Sinh-Hung Nguyen,Xuan-Dung Mai

The development of a simple, cost-effective, and green method to synthesize CdTe quantum dots (QDs), which are a key nanomaterial in sensing, bioimaging, and immunofluorescence analysis is highly desirable. In this study, we used ammonia in lieu of common hydride reductant to synthesize CdTe QDs by simple refluxing aqueous solutions of cadmium salt, sodium tellurite, and 3-mercaptopropionic acid (MPA). The obtained CdTe QDs were characterized by absorption and photoluminescent spectroscopies, X-ray diffraction (XRD), and transmission electron microscope (TEM). The absorption window and the emission color of QDs were facile controlled over the green–red range by varying the refluxing time. As the QD size increased the crystal structure transformed from CdTe to a CdTeS alloyed form. The results demonstrated herein suggest a cost-effective method for production of CdTe QDs.

研究领域: 材料科学 · 纳米技术
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SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY · 2020 · IF 3.232

MPA-CdTe quantum dots as “on-off-on” sensitive fluorescence probe to detect ascorbic acid via redox reaction

Meiling Ding,Kun Wang,Min Fang,Weiju Zhu,Longchao Du,Cun Li

Mercaptopropionic acid (MPA) capped CdTe quantum dots (MPA-CdTe QDs) were synthesized in aqueous medium by hydrothermal method , which modified by Fe 3+ could be used as a fluorescent probe to detect ascorbic acid (AA). MPA-CdTe QDs fluorescence probe could be used as successive sensor for metal ions and AA with “on-off-on” process. The fluorescence of QDs was quenched after adding Fe 3+ to MPA-CdTe QDs. Then, the fluorescence of the Fe 3+ @MPA-CdTe QDs can be sensitively turned on by AA to give an “on–off–on” fluorescence response according to the oxidation–reduction between Fe 3+ and AA. There was a linear relationship between fluorescence intensity quenching value and the concentration of Fe 3+ in the range of 2–10 μM since Fe 3+ sensitively reacted with CdTe QDs. The linear detection range for AA was 0.1–1 μM with a limit of detection of 6.6 nM. The principle is proved by fluorescence emission spectroscopy, nuclear magnetic resonance spectroscopy. The proposed method is successfully used to detect the AA in human plasma sample.

研究领域: 分析化学 · 生物化学
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JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY · 2015 ·Vol. 15 ·期 6 ·4462-4469 · IF 1.556

Photodegradation of Mercaptopropionic Acid- and Thioglycollic Acid-Capped CdTe Quantum Dots in Buffer Solutions

Miao Yanping,Yang Ping,Zhao Jie,Du Yingying,He Haiyan,Liu Yunshi

CdTe quantum dots (QDs) were synthesized by 3-mercaptopropionic acid (MPA) and thioglycollic acid (TGA) as capping agents. It is confirmed that TGA and MPA molecules were attached on the surface of the QDs using Fourier transform infrared (FT-IR) spectra. The movement of the QDs in agarose gel electrophoresis indicated that MPA-capped CdTe QDs had small hydrodynamic diameter. The photoluminescence (PL) intensity of TGA-capped QDs is higher than that of MPAcapped QDs at same QD concentration because of the surface passivation of TGA. To systemically investigate the photodegradation, CdTe QDs with various PL peak wavelengths were dispersed in phosphate buffered saline (PBS) and Tris-borate-ethylenediaminetetraacetic acid (TBE) buffer solutions. It was found that the PL intensity of the QDs in PBS decreased with time. The PL peak wavelengths of the QDs in PBS solutions remained unchanged. As for TGA-capped CdTe QDs, the results of PL peak wavelengths in TBE buffer solutions indicated that S2− released by TGA attached to Cd2+ and formed CdS-like clusters layer on the surface of aqueous CdTe QDs. In addition, the number of TGA on the CdTe QDs surface was more than that of MPA. When the QDs were added to buffer solutions, agents were removed from the surface of CdTe QDs, which decreased the passivation of agents thus resulted in photodegradation of CdTe QDs in buffer solutions.

研究领域: 材料科学 · 生物化学
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Surfaces and Interfaces · 2025 · IF 6.3

Value-added conversion of lignin based on inorganic−organic dual-ligand-regulated CdSe@CdS nanorods

Qiyi Gan,Huakang Yang,Zining Zhang,Jun Liu,Yudong Guo,Dongxiang Luo,Xiao Liu

In lignin valorization systems, CdSe@CdS nanorods exhibit exceptional photocatalytic performance, where precise control over the rates of oxidation and reduction reactions is crucial. This study introduces a ligand modulation strategy that involves the incorporation of mercaptopropionic acid (MPA) and hexafluorophosphate (PF₆⁻) onto the surface of the nanorods to achieve a balanced redox reaction profile. The inorganic PF₆⁻ ligand primarily promotes reduction reactions, whereas MPA enhances hole transfer. By optimizing the distribution ratio of these ligands, the study achieved a significant enhancement in photocatalytic efficiency, resulting in a 94 % conversion rate for 2-phenoxy-1-phenylethanol (PP-ol) and yields of 67 % and 66 % for phenol and acetophenone, respectively. The distinct roles of MPA and PF₆⁻ can be attributed to their respective spatial site resistances, electrostatic interactions, and surface passivation characteristics. MPA, with its larger spatial resistance, stabilizes and extends hole lifetimes, thereby enhancing hole transfer efficiency. In contrast, PF₆⁻ exhibits lower spatial resistance and stronger electrostatic effects, which facilitate accelerated electron transfer. Furthermore, the ligands optimize the transport pathways for both electrons and holes on the nanorod surface through passivation. This ligand design strategy provides valuable insights for the development of efficient nanorod photocatalysts aimed at biomass valorization.

研究领域: 化学工程 · 材料科学 · 生物质转化
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RSC Advances · 2014 ·Vol. 4 ·期 48 ·25183-25188 · IF 3.708

Fluorescence enhancement detection of uric acid based on water-soluble 3-mercaptopropionic acid-capped core/shell ZnS:Cu/ZnS

Meihua Wang,Weifen Niu,Xin Wu,Lixia Li,Jun Yang,Shaomin Shuang,Chuan Dong

3-Mercaptopropionic acid (MPA)-capped ZnS:Cu/ZnS core/shell quantum dots (QDs) have been synthesized via a facile aqueous coprecipitation method and characterized by fluorescence, UV-Vis absorption, infrared spectroscopy and transmission electron microscopy. The fluorescence of ZnS:Cu/ZnS could be increased in the presence of uric acid (UA). The affecting factors for the fluorescence of ZnS:Cu/ZnS were examined including pH, temperature and reacting time. Under the optimized conditions, the fluorescence intensity of the ZnS:Cu/ZnS QDs against the UA concentration showed a linear response in the range of 0.66 μM to 3.3 μM with the correlation coefficient (R2) 0.9973 and the limit of detection 0.044 μM. Most relevant molecules and physiological ions had no effect on the detection of UA. The feasibility of the developed method was further demonstrated by determining the concentration of uric acid in human urine samples and the recoveries were 95% ∼ 103%. Our work provides a sensitive, selective and convenient fluorescence method to determine UA in real samples.

研究领域: 分析化学 · 纳米医学 · 生物传感器 · 临床检验 · 分子诊断
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NANOTECHNOLOGY · 2018 ·Vol. 29 ·期 30 ·305707 · IF 3.404

Aqueous synthesis of L-cysteine and mercaptopropionic acid co-capped ZnS quantum dots with dual emissions

Yingkun Ren,Yongbo Wang,Min Yang,Enzhou Liu,Xiaoyun Hu,Xu Zhang,Jun Fan

In this paper, L-cysteine (L-cys) and mercaptopropionic acid (MPA) co-capped ZnS quantum dots (QDs) with dual emissions have been successfully synthesized by a one-pot aqueous-phase synthesis method. The intensities of the dual emissions could be controlled by regulating the molar ratio of L-cys to MPA, and the fluorescence color also turned from blue to yellow accordingly. The relationship between the ligands and fluorescence was investigated and the results indicated that L-cys could cause two emissions and MPA improved the emission intensity. In addition, the L-cys-MPA co-capped ZnS QDs showed high photostability under UV irradiation. Therefore, the L-cys-MPA co-capped ZnS QDs, which show the dual emissions and tunable emission intensities, have great potentials for use in ratiometric fluorescence sensors and multicolor bioimaging.

CAS / MDL: 70-18-8 107-96-0
研究领域: 材料科学 · 生物医学工程
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ACS ES&T Water · 2024 · IF 4.8

Bioactive Sulfide Stimulates Sulfur-Oxidizing and Denitrifying Bacteria to Accelerate Nitrogen Removal: A Novel Biological Approach to Water Purification

Wei Yang,Wei Li,Haixiao Zhao,Xiao Ma,Feiyang Xia,Qian Tan

Nitrogen pollution causes eutrophication and algal blooms worldwide. Algae-derived organic sulfides can interact with organisms to affect nitrogen cycling, but the associated patterns and mechanisms remain unclear. This study investigated the effects of dimethylsulfoniopropionate (DMSP), an important bioactive sulfide, on nitrogen transformation and removal at the water–sediment interface in microcosm systems (water–sediment and water–sediment–biofilm–benthos). Results showed that DMSP altered the dynamics of total nitrogen and dissolved inorganic nitrogen in overlying water, particularly promoting 74.39% reduction of nitrate in the system containing biofilm and benthos. The presence of DMSP in conjunction with biofilm and bioturbation affected the nitrogen transformation in the sediment. DMSP increased the content of dissolved organic carbon but decreased the content of dissolved oxygen in water. Moreover, it was converted to sulfate in water, enhancing the abundance of bacteria capable of denitrification and sulfur oxidation (such as Pseudomonas) as well as related genes, including narGHI, norBC, soxA, soxC, soxY, and soxZ, in the biofilm. This observation suggests that the process of sulfur oxidation promotes denitrification. The current study highlights the potential applications of DMSP in water purification systems and presents a novel biological approach to aquatic management.

CAS / MDL: 4337-33-1
研究领域: 环境微生物学 · 水污染治理
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JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY · 2020 · IF 4.192

Functionalized Copper Nanoclusters-Based Fluorescent Probe with Aggregation-Induced Emission Property for Selective Detection of Sulfide Ions in Food Additives

Dawei Wang,Zhiqiang Wang,Xiaobin Wang,Xuming Zhuang,Chunyuan Tian,Feng Luan,Xiuli Fu

In this paper, a novel and facile synthetic method of 3-mercaptopropionic acid functionalized copper nanoclusters with aggregation-induced emission (AIE) induced by Cu2+ (Cu2+@MPA-Cu NCs) was developed by a one-pot reaction as a fluorescent probe for the detection of sulfide ion (S2–). The prepared Cu2+@MPA-Cu NCs behaved as aggregated clusters and had strong pink fluorescence under 365 nm UV light with excellent fluorescence emission at 610 nm. The quantum yield increased from 0.56% to 4.8% before and after Cu2+ added. The presence of S2– would strongly bind to Cu2+, which caused the structure of the aggregated Cu2+@MPA-Cu NCs to be destroyed and then the fluorescence quenched. On the basis of this principle, a fluorescent probe was constructed for the detection of S2– with a very good linearity in the range 0–600 μM (R2 = 0.9843) and a detection limit of 26.3 nM. Finally, the nanohybrids were successfully demonstrated for the application in the selective detection of S2– in food additives. This study essentially paved a new avenue for effectively developing an easy sensor platform for S2– measurements in food additives.

CAS / MDL: 1313-82-2
研究领域: 分析化学 · 食品科学
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MICROCHEMICAL JOURNAL · 2023 · IF 4.8

Sensitive detection of furazolidone and nitrofurantoin by fluorescent nanoprobe coated with 3-mercaptopropionic acid on CdS quantum dots

Jia Liu,Bin Yang,Yuting Wang,Fengming Zhang,Xin Liu,Shiyue Niu,Yue Yuan,Shuyun Bi

Cadmium sulfide quantum dots (CdS QDs) were synthesized with 3-mercaptopropionic acid (MPA) as protective agent, which were characterized by TEM, UV–vis, fluorescence, XRD and TGA. Based on the fluorescence quenching of 3-MPA-CdS QDs, the indirect methods for the determination of furazolidone (FZD) and nitrofurantoin (NFT) were established. The interaction between FZD/NFT and CdS QDs was investigated by using fluorescence, resonance light scattering, UV–vis and FT-IR. The analyses of Stern-Volmer and fluorescence lifetime indicated that the two quenching systems were all static. The binding constant ( K a ) of FZD/NFT-CdS QDs was 1.20 × 10 4 /1.81 × 10 4 L/mol at 293 K, respectively. Hydrogen bond or van der Waals force was the main binding force between CdS QDs and drugs. Under optimum experimental conditions, the concentration of FZD/NFT was respectively highly correlated with the fluorescence intensity ratio in the range of 0.27 – 36.03/0.57 – 28.58 μg mL −1 . The interference experiments showed that the methods had good selectivity. The limit of detection (LOD) for FZD/NFT was 0.02/0.01 μg mL −1 . The contents of FZD and NFT in fish samples were determined, and the recoveries were 97.41–99.52 % and 96.64–100.49 %, respectively.

研究领域: 分析化学 · 药物分析 · 食品安全检测
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ACS Applied Materials & Interfaces · 2015 · IF 6.723

Small GSH-Capped CuInS2 Quantum Dots: MPA-Assisted Aqueous Phase Transfer and Bioimaging Applications

Chuanzhen Zhao,Zelong Bai,Xiangyou Liu,Yijia Zhang,Bingsuo Zou,Haizheng Zhong

An efficient ligand exchange strategy for aqueous phase transfer of hydrophobic CuInS2/ZnS quantum dots was developed by employing glutathione (GSH) and mercaptopropionic acid (MPA) as the ligands. The whole process takes less than 20 min and can be scaled up to gram amount. The material characterizations show that the final aqueous soluble samples are solely capped with GSH on the surface. Importantly, these GSH-capped CuInS2/ZnS quantum dots have small size (hydrodynamic diameter <10 nm), moderate fluorescent properties (up to 34%) as well as high stability in aqueous solutions (stable for more than three months in 4 °C without any significant fluorescence quenching). Moreover, this ligand exchange strategy is also versatile for the aqueous phase transfer of other hydrophobic quantum dots, for instance, CuInSe2 and CdSe/ZnS quantum dots. We further demonstrated that GSH-capped quantum dots could be suitable fluorescence markers to penetrate cell membrane and image the cells. In addition, the GSH-capped CuInS2 quantum dots also have potential use in other fields such as photocatalysis and quantum dots sensitized solar cells.

CAS / MDL: 70-18-8
研究领域: 材料科学 · 生物学 · 医学
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RESEARCH ON CHEMICAL INTERMEDIATES · 2025 · IF 3.5

The effect of small molecular linkers on the solar driven photoelectrochemical hydrogen production performance of CdS quantum dot-sensitized TiO2 photoanodes

Li Zhen,Guo Guizhang,Yu Zhou,Ma Zengyue,Yu Libo

In the pursuit of highly efficient hydrogen production through photoelectrochemical water splitting, expanding the utilization of the visible spectrum and extending the lifetime of photogenerated electrons are crucial challenges for improving the efficiency. To address these challenges, we prepared CdS sensitized TiO 2 photoanodes using a one-step hydrothermal method, employing thioglycolic acid (TGA) and mercaptopropionic acid (MPA) as linkers. The successful synthesis of CdS QDs and the CdS/TiO 2 photoanode was confirmed through various characterization techniques, including transmission electron microscopy (TEM), X-ray diffraction, and scanning electron microscopy. Performance evaluations revealed that the TGA-decorated CdS/TiO 2 photoanode exhibited superior photocurrent density and stability compared to the MPA-modified counterpart. Notably, its applied bias photo-to-current conversion efficiency was 1.7 times greater than that of the MPA-modified CdS/TiO 2 photoanode. Furthermore, UV–visible absorption spectrum analysis demonstrated that the incorporation of CdS QDs significantly broadened the spectral response of the TiO 2 photoanode, extending it from the ultraviolet to the visible range. This enhancement is crucial for improving light harvesting capabilities. Additionally, our analysis of electron lifetime indicated that the shorter molecular chains of TGA effectively minimize the transfer distance for photogenerated electrons from the CdS QDs to the TiO 2 , resulting in improved electron lifetimes and, consequently, enhanced photocurrent density.

研究领域: 材料科学 · 能源科学 · 光电化学
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