BIOSENSORS & BIOELECTRONICS
·
2013
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IF 5.437
Hongqi Chen,Fei Yuan,Shaozhen Wang,Juan Xu,YiYan Zhang,Lun Wang
In this work, we design a FRET system for sensitive and selective determination of thrombin in red region, in which NaYF 4 :Yb,Er upconversion nanoparticles (UCNPs) act as donor and gold nanorods (Au NRs) act as acceptor. NaYF 4 :Yb,Er UCNPs with a strong emission at 661 nm were successfully synthesized by tuning the doped ions ratio. Carboxyl-functionalized NaYF 4 :Yb,Er UCNPs and Au NRs were then prepared and conjugated with the thrombin aptamers, respectively. The fluorescence emission band of NaYF 4 :Yb,Er UCNPs ( λ max =661 nm) highly overlaps with the absorption band of Au NRs( λ max =666 nm), which benefits from the large tunability of the spectrum band of Au NRs. A FRET system was then formed when thrombin was added to the mixture of NaYF 4 :Yb,Er UCNPs and Au NRs, which were both modified thrombin aptamers. The fluorescence quenching efficiency of NaYF 4 :Yb,Er UCNPs was increased in a thrombin concentration-dependent manner, which built the principle of thrombin quantification. The linear range was 2.5–90 nM in an aqueous buffer, and 3.75–112.5 nM in spiked human serum samples for thrombin. It also demonstrates a high selectivity to other biological species due to the specific binding. The measurement of thrombin in human plasma is satisfying, suggesting that the FRET system is of practical value in a complex biological sample matrix in red region.
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高影响因子
Catalysts
·
2021
·Vol. 11
·期 2
·184
·
IF 4.146
Huang Zhou,Fengjiao He
β-NaYF4:Yb,Er,Gd fluorescent nanorods were successfully coupled to a reduced TiO2(UCNPs@R-TiO2) nanocomposite and applied to visible-light catalytic sterilization under 980 nm near-infrared (NIR) light illumination. The UCNPs (β-NaYF4:Yb,Er,Gd) absorb the NIR light and emit red and green light. The visible light can be absorbed by the R-TiO2(Eg = 2.8 eV) for the photocatalytic reaction. About 98.1% ofEscherichia coliwere effectively killed upon 12 min of NIR light irradiation at a minimum inhibitory concentration (MIC) of 40 μg/mL UCNPs@R-TiO2nanocomposite. The bactericidal properties were further evaluated by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) analysis. We found that the high bactericidal activity was due to the synergistic effect between the UCNPs and R-TiO2. Moreover, the UCNPs show excellent upconversion luminance properties, and the introduction of visible-light-absorbed R-TiO2nanoparticles (2.8 eV) was conducive to the efficient separation and utilization of photogenerated electron-hole pairs.
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JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY
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2019
·
IF 3.261
Huanxian Shi,Qiqi Nie,Min Yang,Cunjin Wang,Enzhou Liu,Zhen Ji,Jun Fan
In this paper, a novel ratiometric fluorescence probe for melamine detection based on luminescence resonance energy transfer (LRET) between the NaYF 4 :Yb, Er upconversion nanoparticles (UCNPs) and gold nanoparticles (AuNPs) was developed. The detection mechanism could be interpreted to the AuNPs quenched the fluorescence intensity (F 542 and F 654 ) of the UCNPs under 980 nm excitation. after melamine addition, the fluorescence intensity of the UCNPs was recovered due to the aggregation of Au NPs. A good linear relationship between the ratio of F 542 to F 654 nm (F 542 /F 654 ) was obtained in ranges of 20-200 μg/L of the melamine concentration and the limit of detection was 8.8 nM. Besides, The probe exhibited an excellent selectivity and good sensitivity to melamine, and achieved the melamine detection in real sample. This work paved a new avenue for the potential practice application for commercial instantaneous determination of the melamine.
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APPLIED SURFACE SCIENCE
·
2018
·
IF 4.439
Lele Qiu,Yulin Yang,Guohua Dong,Debin Xia,Mengru Li,Xiao Fan,Ruiqing Fan
As for the solution-processed MAPbI 3 film, the pinholes and gaps are an inevitable and undesirable phenomenon, which can usually lead to serious interface charge recombination due to the penetration of hole transport materials in perovskite solar cells (PSCs). Herein, a hydrophobic β-NaYF 4 :Yb,Er up-conversion ultrathin layer with particle size ca. 6 nm was first applied to modify the MAPbI 3 film for optimizing the surface of perovskite film. Thereby, the corresponding PSCs yield a significantly enhanced power conversion efficiency of 15.17% compared with that (13.32%) of the pristine PSCs. Furthermore, the PSCs also have a good stability in air atmosphere (relative humidity ≤45%) because of the introduction of this hydrophobic material. After a series of detailed investigations and comparison, it can be easily concluded that the filled pinholes and gaps in perovskite films via β-NaYF 4 :Yb,Er nanoparticles is the main reason for the performance enhancement of the β-NaYF 4 :Yb,Er based PSCs, which can result in an enhanced hole extraction efficiency and reduced interface charge recombination. As a conclusion, it is a feasible and effective approach for improving the photovoltaic performance of PSCs by filling up the pinholes and gaps in perovskite films with up-conversion ultrathin layers.
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APPLIED SURFACE SCIENCE
·
2024
·
IF 6.3
Guangdong Wu,Juanqin Xue,Dashi Lei,Yanyan Zhou,Zhaoyuan Cao,Kang Ren,Qiang Bi,Zhihua Leng
Currently, upconversion nanoparticles (UCNPs) based photocatalysts have been extensively developed to improve solar energy utilization. However, the mechanisms underlying interfacial energy migration of upconversion photocatalyst remain unclear. Herein, a promising composite photocatalyst with complementary properties is designed by integrating β -NaGdF 4 :Yb 3+ /Er 3+ (NGFYE), CdS and multi-walled carbon nanotubes (MWCNTs). The morphology, structure and chemical properties of NGFYE@CdS/MWCNTs ternary photocatalyst are characterized. In addition, the existence of Förster resonance energy transfer process in NGFYE@CdS/MWCNTs photocatalysts, i.e., the migration of excitation energy from Er 3+ − 4 S 3/2 excitation level and higher excitation level (e.g., Er 3+ − 2 H 11/2 ) to CdS nanoparticles, was further confirmed by density functional theory (DFT) calculations. The optimized NGFYE@CdS/MWCNTs photocatalyst presents 71.65 % and 35.29 % degradation of tetracycline hydrochloride (TCH) and ciprofloxacin (CIP) under λ ≥ 800 nm irradiation for 3 h, respectively. This work not only illustrates the interfacial energy migration mechanism between NGFYE and CdS, but also provides insights for the rapid construction of heterojunction materials with efficient energy transfer interfaces.
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高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2020
·
IF 10.652
Wei Wan,Xinxin Han,Yayun Zhou,Fangrui Chen,Xiping Jing,Shi Ye
Developing a secure and unclonable anti-counterfeiting technology with more dimensional encryptions is urgently demanded. All-inorganic halide perovskites hold great potential for applications in advanced fluorescence anti-counterfeiting owing to their superior optical properties, such as tunable emission colors, narrow emission peaks, etc. By further utilizing the feasibility of anion exchange for perovskite halides, this research successfully designs five-dimensional (5D) anti-counterfeiting barcodes with core–shell-like structured perovskite-like oxide and perovskite halide composites. The composites are prepared by a facile synthesis method, which includes adhesive growth of Cs(Pb x Mn 1-x )(Cl y Br 1-y ) 3 on the surface of CsCa 2 Ta 3 O 10 : Yb, Er (abbreviated as CCTO: Yb, Er@CsMX 3 ) via sharing Cs + at the interface. The unique structure makes it possess sensitivity to some additive decrypted inks, offering one more intriguing anti-counterfeiting dimension beyond the common dual-mode fluorescence and time-gating technique. The CCTO: Yb, Er@CsMX 3 composites exhibit typical green upconversion (UC) luminescence under a 980 nm laser, red or green or blue (RGB) emission under ultraviolet (UV) light irradiation, ns-ms emission decay time, and changeable emission color when treated with decrypted inks. The fluorescent inks and barcodes are simple for fabrication, efficient for coding, easy for viewing and difficult for cloning, making them promising for anti-counterfeiting applications.
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TALANTA
·
2026
·
IF 6.7
Yasheng Dai,Jie Yao,Shiyuan Wang,Changgan Lai,Jie Gong,Chenjie Gu,Tao Jiang,Kerong Wu
Exosomes are regarded as cancer-associated biomarkers for early diagnosis and prognosis in clinical bioassays. Nevertheless, it remains a challenge to develop an approach that can achieve ultra-sensitive and quantitative detection of exosomes. Herein, an innovative dual-mode immunoassay dependent on surface-enhanced Raman scattering (SERS) and upconversion luminescence (UCL) was developed to detect prostate cancer-derived exosomes. A novel SERS-active immunosubstrate was constructed by combining black phosphorus (BP) with Ag nanoparticles, which exhibited an enhancement factor (EF) of about 3.69 × 10 9 , due to the synergistic electromagnetic and chemical effects. Meanwhile, an immunoprobe with stable and visually distinguishable UCL was developed based on Yb/Er co-doped NaGdF 4 nanoparticles with an intrinsic two-photon process. The specific capture of exosomes was achieved through antigen-antibody binding within the sandwich immunostructure, achieving limits of detection (LOD) as low as 93 and 172 particles/mL based on the dual-modal detection, respectively. Furthermore, the recognition of different derived exosomes was simply realized by visually observing the green fluorescence with different intensities, which paves the way for efficient preliminary identification of prostate cancer. Finally, the validation with clinical serum samples proved that the proposed approach holds significant promise for rapid cancer screening and diagnosis.
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TALANTA
·
2019
·
IF 4.916
Leilei Sun,Tao Wang,Yuzhen Sun,Zexin Li,Haining Song,Bin Zhang,Guangjun Zhou,Haifeng Zhou,Jifan Hu
Dual-functional nanosensors based on small molecule regulation can be widely used due to their simplicity, high sensitivity and selectivity. Herein, glutathione (GSH) calibrated dual-functional system for GSH and cadmium ions (Cd 2+ ) detection based on fluorescence resonance energy transfer (FRET) between NH 2 –NaYF 4 :Yb,Er/NaYF 4 @SiO 2 upconversion nanoparticles (UCNPs) and gold nanoparticles (AuNPs) is designed. Unmodified AuNPs are easy to aggregate in high-salt solution and thereby quenching the red emission of UCNPs. The presence of GSH prevents the aggregation of AuNPs, so GSH can be detected by the changes in the color of solution and the recovery of red emission of UCNPs. However, Cd 2+ can interact with GSH, which makes AuNPs easy to aggregate, resulting in a gradual decrease in red emission of UCNPs. The fluorescence response of the system is linear with the concentrations of GSH and Cd 2+ in a wide range of concentrations, with low detection limits of 0.016 μM and 0.059 μM, respectively. Furthermore, the nanosensor demonstrates high selectivity for GSH and Cd 2+ detection and can be applied for the detection of GSH in human plasma and Cd 2+ in drinking water .
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ACS Applied Nano Materials
·
2025
·
IF 5.5
Hanqing Liu,Yifei Zhou,Jing Xu,Le Ding,Chuan Liao,Tao Wang,Haifeng Zhou,Guangjun Zhou
High-efficiency detection of cadmium ions (Cd2+) and mercury ions (Hg2+) is crucial due to their harmful effects on the environment and human health. Here, we developed a ratiometric upconversion fluorescence (UCF)-based nanosensor by incorporating lanthanide-doped upconversion nanoparticles (UCNPs) and gold nanoparticles modified with trithiocyanuric acid (TMT-AuNPs) as specific recognition elements for the highly sensitive and selective real-time detection of Cd2+ and Hg2+. The developed nanosensor exhibited selective absorbance enhancement and UCF quenching behavior with the addition of Cd2+ and Hg2+ based on the inner filter effect (IFE). The sensitivity of the nanosensor was significantly enhanced by converting the change in absorbance into an exponential variation in UCF intensity. Therefore, the quantitative detection of Cd2+ and Hg2+ was achieved by measuring the UCF ratio I654/I540. In order to distinguish between Cd2+ and Hg2+, two biomolecules, glutathione (GSH) and ascorbic acid (AA), were used based on their different interactions with Cd2+ and Hg2+. GSH formed a specific tetrahedral complex (GSH)4Cd with Cd2+, thereby preventing Cd2+ from inducing changes in UCF intensity. In contrast, AA specifically reduced Hg2+, thereby preventing Hg2+-induced UCF changes. Thus, GSH and AA could also be detected. The limits of detection (LODs) of Cd2+, Hg2+, GSH, and AA were 2.8, 5.2, 5.1, and 7.2 nM, respectively. The designed detection platform provides a sensitive and straightforward sensing strategy for the multiplex detection of heavy metal ions and biological small molecules.
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ELECTROCHIMICA ACTA
·
2022
·
IF 7.336
Siqi Zhang,Shuopan Dun,Xugeng Guo,Jinglai Zhang
Introducing upconversion nanoparticles (UCNPs) or fabricating TiO 2 hollow spheres (TiO 2 -HSs) are considered two feasible strategies to enhance the photovoltaic performance of dye-sensitized solar cells (DSSCs). However, studies investigating a combination of UCNPs and TiO 2 -HSs for the application in DSSCs are still scarce. In this contribution, NaYF 4 :Yb,Er@NaGdF 4 :Nd@SiO 2 UCNPs and TiO 2 -HSs were synthesized and respectively applied as upconversion layers and scattering layers on the TiO 2 photoanode of DSSCs. The influence of different doping ratios of UCNPs on cell performance was explored. The present results reveal that the DSSCs device based on conventional P25 photoanode films incorporating the UCNPs with 10% can achieve a photovoltaic efficiency of 6.65%, showing 29.63% enhancement in comparison to the device without UCNPs. When the TiO 2 -HSs are used as scattering layers above the P25 film, the DSSCs device obtains a higher photovoltaic efficiency of 6.97%. More importantly, combining the UCNPs and TiO 2 -HSs can further enhance the photoelectrical property of DSSCs, realizing an optimal efficiency of 8.17%. Such an improvement can be attributed to a synergistic mechanism arising from the upconversion effect of UCNPs and the light scattering effect of TiO 2 -HSs. This work opens a new way of preparing composite photoanode films to improve the photovoltaic performances of DSSCs.
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APPLIED SURFACE SCIENCE
·
2016
·
IF 3.15
Zhenli Qin,Sinan Du,Yang Luo,Zhijian Liao,Fang Zuo,Jianbin Luo,Dong Liu
We report the use of an efficient hydrothermal method to synthesize superparamagnetic and red luminescent bifunctional Fe 3 O 4 @Mn 2+ -doped NaYF 4 :Yb/Er nanoparticles (NPs) with core@shell structures via a seed-growth procedure. Oleic acid coated Fe 3 O 4 (OA-Fe 3 O 4 ) NPs were initially synthesized using a coprecipitation method. The as-synthesized OA-Fe 3 O 4 NPs were then used as seeds, on which the red upconversion luminescent shell (Mn 2+ -doped NaYF 4 :Yb/Er) was formed. Furthermore, hydrophobic to hydrophilic surface modification of the Fe 3 O 4 @Mn 2+ -doped NaYF 4 :Yb/Er NPs was achieved via a ligand exchange method where oleic acid was displaced by a PEG phosphate ligand [PEG = poly(ethylene glycol)]. These materials were characterized by means of transmission electron microscopy (TEM), X-ray diffraction (XRD), photoluminescence (PL) spectroscopy, and vibrating sample magnetometry (VSM). The Fe 3 O 4 cores were uniformly coated with a Mn 2+ -doped NaYF 4 :Yb/Er shell, and the bifunctional Fe 3 O 4 @Mn 2+ -doped NaYF 4 :Yb/Er NPs were monodispersed. Furthermore, the Fe 3 O 4 @Mn 2+ -doped NaYF 4 :Yb/Er NPs exhibited a saturated magnetization value of 6.2 emu/g and emitted red luminescence under a 980 nm laser. The obtained bifunctional Fe 3 O 4 @Mn 2+ -doped NaYF 4 :Yb/Er NPs may find potential applications in drug targeting, bioseparation, and diagnostic analysis. The synthetic method may be employed for the preparation of other bifunctional nanomaterials.
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TALANTA
·
2017
·
IF 4.162
Ling-Feng Jiang,Bo-Cheng Chen,Ben Chen,Xue-Jian Li,Hai-Lin Liao,Hong-Miao Huang,Zhan-Jing Guo,Wen-Yan Zhang,Lin Wu
A sensitive and stable bioassay for the detection of Aβ oligomer (Aβo), a potentially promising candidate biomarker for Alzheimer's disease (AD) diagnosis, was developed using Fe 3 O 4 magnetic nanoparticles (MNPs) as the recognition and concentration elements and BaYF 5 :Yb,Er upconversion nanoparticles (UCNPs) as highly sensitive labels, conjugated with the Aβo aptamer (DNA1) and the complementary oligonucleotide of the Aβo aptamer (DNA2), respectively. The DNA1 hybridized with DNA2 to form the duplex structure on the surface of the MNPs/UCNPs nanocomposites probe. When the target Aβo was introduced, the aptamer DNA1 preferentially bound with Aβo and caused the dissociation of some complementary DNA2, liberating some UCNP-labeled complementary DNA2 and leading to a decreased upconversion fluorescent intensity on the surface of MNPs. The decreased fluorescence intensity of UCNPs was related to the concentration of Aβo in the range of 0.2–15 nM with a detection limit of 36 pM. The developed method then was successfully applied to measure Aβo in artificial cerebrospinal fluid. Benefiting from the magnetic separation and concentration effect of MNPs, the high sensitivity of UCNPs, as well as the selectivity and stability of the aptamer, the present strategy offered valuable information related to early diagnosis of AD process.
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