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JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY · 2019 · IF 3.261

A ratiometric fluorescence probe for melamine detection based on luminescence resonance energy transfer between the NaYF4:Yb, Er upconversion nanoparticles and gold nanoparticles

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.

CAS / MDL: 108-78-1
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APPLIED SURFACE SCIENCE · 2018 · IF 4.439

Surfaces modification of MAPbI3 films with hydrophobic β-NaYF4:Yb,Er up-conversion ultrathin layers for improving the performance of perovskite solar cells

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.

CAS / MDL: 10025-75-9
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Nanomaterials · 2017 ·Vol. 7 ·期 12 ·448 · IF 3.553

Sequential Growth of Uniform β-NaYF4@β-NaLnF4 (Ln = Y, Lu, Yb) Microcrystals with Luminescent Properties of Multicolor Tuning and Dual-Mode Emission

Dandan Ju,Feng Song,Yingdong Han,Wenjing Cui,Aihua Zhou,Shujing Liu,Xueqin Wang,Ming Feng,Chengguo Ming

We synthesized the uniform core-shell microstructured compounds with hexagonal phase NaYF4:Er/Yb microrods as the core and hexagonal phase NaLnF4(NaYbF4, NaLuF4:Yb/Tm, NaYF4:Yb/Er, NaYF4:Eu) as the shell based on the hydrothermal reaction. These microscale core-shell structures provided a platform for the spatially confining optical process while possessing high luminescence efficiency. The thickness of the shell could be controlled by adjusting the amounts of shell precursor, which significantly affected the intensity of the shell dopant ions emission and the emission color of core-shell upconversion luminescence (UCL). The uniform NaYF4@NaLnF4(Ln = Y, Lu, Yb) microrods, with a series of rare-earth ions doped into the core and shell layer at various doping concentrations, achieved color-tuning of the upconversion (UC) emission and dual-mode emission at the single-microcrystal level, thus allowing the efficient utilization of core-shell microcrystals in the photonics and security labeling. This study suggests a new class of luminescent materials in the microscopic field.Keywords:NaYF4microcrystals;microscale core-shell structures;multicolor tuning;dual-mode emission

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MICROCHIMICA ACTA · 2017 ·Vol. 184 ·期 10 ·4021-4027 · IF 4.58

Homogeneous time-resolved FRET assay for the detection of Salmonella typhimurium using aptamer-modified NaYF4:Ce/Tb nanoparticles and a fluorescent DNA label

Wang Xiaole,Niazi Sobia,Yukun Huang,Sun Weijia,Wu Shijia,Duan Nuo,Hun Xu,Wang Zhouping

The authors describe an aptasensor based on time-resolved fluorescence resonance energy transfer (TR-FRET) for the identification of Salmonella typhimurium ( S. typhimurium ). Aptamer-functionalized nanoparticles (NPs) is used as the energy donor, and a complementary oligonucleotide (cDNA) labeled with carboxyfluorescein (FAM) acts as the acceptor. The detection scheme is based on the hybridization between aptamer and cDNA, upon which photonic energy is transferred from NPs to FAM unless aptamer interacts with S. typhimurium . Due to the highly specific recognition ability of aptamer and the strong fluorescence intensity of NPs, the method is highly sensitive and selective for S. typhimurium . Under the optimal conditions, at excitation wavelength of 273 nm, a delay time of 100 μs and a gating time of 1 ms, the integrated time-resolved fluorescence intensity ratio (FAM 520 /Tb 489 ) is linear in the 100 to 10 6  cfu·mL −1 range, and the limit of detection is as low as 25 cfu·mL −1 . The assay was applied to the analysis of eggs and chicken meat for S. typhimurium , and the results were consistent with those of a plate-counting method. Schematic of a homogeneous time-resolved FRET assay for the determination of Salmonella typhimurium by FRET between NaYF 4 :Ce/Tb nanoparticle-tagged aptamer and FAM-cDNA, with a good linearity and the limit of detection of 25 cfu mL −1 .

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SOLAR ENERGY · 2019 · IF 4.674

Application of TiO2 hollow microspheres incorporated with up-conversion NaYF4:Yb3+, Er3+ nanoparticles and commercial available carbon counter electrodes in dye-sensitized solar cells

Wanxian Cai,Zhaobin Zhang,Yuanzeng Jin,Yanqi Lv,Ling Wang,Koucheng Chen,Xingfu Zhou

In this work, the up-conversion phosphor NaYF 4 :Yb 3+ , Er 3+ nanocrystalline mixed with P 25 and TiO 2 hollow microspheres with high light scattering ability were fabricated as electrode for dye-sensitized solar cells (DSSCs). Meanwhile, we take advantage of the low cost feature of the carbon counter electrode to replace the precious metal Platinum (Pt) of DSSCs. SEM results show that the well-dispersed TiO 2 hollow microspheres size is 1.5 μm with surface consisting of a large number of rice-like nanorods. The particle size of the as-prepared NaYF 4 :Yb 3+ , Er 3+ nanoparticles is about 80 nm. The Photocurrent-Voltage curve of P 25 /NaYF 4 :Yb 3+ , Er 3+ cell under 980 nm infrared light has an obvious infrared photoresponse. The fabricated DSSCs using NaYF 4 :Yb 3+ , Er 3+ achieves power conversion efficiency (PCE) of 5.27% under one sun illumination, which shows an increase of 16% when compared with the benchmark P 25 cell (4.55%). In addition, the optimized DSSC using TiO 2 hollow microspheres as the top scattering layers with NaYF 4 :Yb 3+ , Er 3+ /P 25 exhibits a prominent PCE of 6.23%, which shows a 37% increase in conversion efficiency when compared with the commercial P 25 cell (4.55%). The increase in conversion efficiency should be contributed to the dual effects of the enhanced light harvesting of up-conversion NaYF 4 :Yb 3+ , Er 3+ and light utilization of the top light scattering TiO 2 hollow microsphere.

研究领域: 材料科学 · 光伏技术 · 纳米技术 · 能量转换
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ACS Sustainable Chemistry & Engineering · 2019 · IF 6.97

Near-Infrared Light-Sensitive Hole-Transport-Layer Free Perovskite Solar Cells and Photodetectors with Hexagonal NaYF4:Yb3+,Tm3+@SiO2 Upconversion Nanoprism-Modified TiO2 Scaffold

Huijie Zhang,Yuqing Xiao,Fei Qi,Pei Liu,Yuan Wang,Fangjie Li,Changlei Wang,Guojia Fang,Xingzhong Zhao

Hexagonal NaYF4:Yb3+,Tm3+@SiO2 upconversion nanoprism-mixed SiO2 passivation layers are introduced into hole-transport-layer free carbon-based perovskite solar cells to improve the power conversion efficiency. This layer on the top of the TiO2 scaffold has multiple functions: (i) upconversion units could transform near-infrared photons to visible region and thus extend the absorption range; (ii) nanoprisms act as light-scattering centers to prolong light-transmission distance and enhance light harvesting; (iii) SiO2 capping layer could suppress charge recombination at the interface of perovskite/TiO2 through passivation effect. The champion efficiency of our carbon-based device with an optimal amount of upconversion nanoprisms is 14.47%, which is 16.1% higher than that of the reference (12.46%). In addition, our unencapsulated solar cells exhibit good stability against moisture and thermal stressing in ambient condition. We also demonstrated another application of our device as a self-powered photodetector with NIR-sensitive features.

研究领域: 材料科学 · 光电子学
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ELECTROCHIMICA ACTA · 2022 · IF 7.336

A synergistic effect of NaYF4:Yb,Er@NaGdF4:Nd@SiO2 upconversion nanoparticles and TiO2 hollow spheres to enhance photovoltaic performance of dye-sensitized solar cells

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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TALANTA · 2018 · IF 4.244

A novel bioassay based on aptamer-functionalized magnetic nanoparticle for the detection of zearalenone using time resolved-fluorescence NaYF4: Ce/Tb nanoparticles as signal probe

Sobia Niazi,Xiaole Wang,Imran Pasha,Imran Mahmood Khan,Sen Zhao,Muhammad Shoaib,Shijia Wu,Zhouping Wang

Zearalenone (ZEN) is a non-steroidal estrogenic mycotoxin produced by fungi on stored grains. The earlier detection methods used for ZEN rely on expensive equipment, time-consuming sample preparation and temperature sensitive antibodies. The current work, proposed a novel strategy based on ZEN aptamer labeled with amine-functionalized magnetic nanoparticle (MNPs) as a capture probe and time-resolved fluorescence (TRFL) nanoparticles labeled with complementary DNA (cDNA) as a signal probe. Under the optimized conditions, TRFL intensity at 544 nm was used to measure ZEN (R 2 = 0.9920) in the range of 0.001–10 ng mL −1 and limits of detection (LOD) for proposed method was 0.21 pg mL −1 . The specificity of bioassay was also determined by using other mycotoxins (OTA, AFB 2 , DON and Patulin) and results showed that the aptamer are specific to recognize only ZEN. The analytical applications of the present bioassay in maize and wheat samples were also examined and results were compared with existing methods. Based on these findings, it is suggested to use current rapid and simple bioassay for the determination of ZEN in food and agricultural products.

✓ 已验证 产品关联 DOI PubMed 高影响因子
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APPLIED SURFACE SCIENCE · 2016 · IF 3.15

Hydrothermal synthesis of superparamagnetic and red luminescent bifunctional Fe3O4@Mn2+-doped NaYF4:Yb/Er core@shell monodisperse nanoparticles and their subsequent ligand exchange in water

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.

CAS / MDL: 9004-74-4 2258654-78-1
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MICROCHIMICA ACTA · 2017 ·Vol. 184 ·期 9 ·3469-3475 · IF 4.58

A NIR-responsive up-conversion nanoparticle probe of the NaYF4:Er,Yb type and coated with a molecularly imprinted polymer for fluorometric determination of enrofloxacin

Tang Yiwei,Li Min,Gao Xue,Liu Xiuying,Gao Jinwen,Ma Tao,Li Jianrong

The paper describes the preparation of a fluorescent probe based on the use of up-conversion particles (UCPs) of the type NaYF 4 : Er, Yb and shelled with a molecularly imprinted polymer (MIP) that is specific for the antibiotic enrofloxacin. The upconverted green luminescence emitted by the UCPs upon photoexcitation at 980 nm was used to locally generate a thin MIP shell around the UCPs via photopolymerization. Enrofloxacin is used as the template, and ethylene glycol dimethacrylate (EGDMA) as the cross-linking agent. It is found that enrofloxacin is well captured by the MIP and then quenches the fluorescence of the UCPs. Fluorescence decreases linearly in the 63 ng·L −1 to 60 μg·L −1 enrofloxacin concentration range, with a 8 ng·L −1 limit of detection. The method was applied to the determination of enrofloxacin in spiked fish samples. Recoveries ranged from 83.7 to 87.7%, with relative standard deviations between 2.0 and 5.5% (for n  = 3). Schematic of an NIR-responsive up-conversion nanoparticle probe of the NaYF 4 :Er,Yb type and coated with a MIP for fluorometric determination of enrofloxacin. The upconverted luminescence emitted by the UCPs was used to locally generate a thin MIP shell around the UCPs via photopolymerization.

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ANALYTICAL AND BIOANALYTICAL CHEMISTRY · 2019 ·Vol. 411 ·期 7 ·1453-1465 · IF 3.286

Simultaneous detection of fumonisin B1 and ochratoxin A using dual-color, time-resolved luminescent nanoparticles (NaYF4: Ce, Tb and NH2-Eu/DPA@SiO2) as labels

Niazi Sobia,Khan Imran Mahmood,Yan Lv,Khan Muhammad Issa,Mohsin Ali,Duan Nuo,Wu Shijia,Wang Zhouping

A rapid and highly sensitive time-resolved fluorescence (TRF)-based aptasensor for simultaneous recognition of mycotoxins ochratoxin A (OTA) and fumonisin B 1 (FB 1 ) was developed using multi-color, Ln 3+ -doped time-resolved fluorescence nanoparticles (TRF-NPs) (NaYF 4 : Ce, Tb and NH 2 -Eu/DPA@SiO 2 NPs) coupled with complementary strand DNA (cDNA) as luminescence probe and aptamers-conjugated amine-functionalized Fe 3 O 4 magnetic nanoparticles (MNPs) act as a capture probe. Under the optimized conditions, the time-resolved fluorescence intensities at 544 and 618 nm corresponded with Tb 3+ and Eu 3+ , respectively, were used to measure FB 1 ( Y  = 19,177.1 + (− 12,054.4) x , R 2  = 0.9917) and OTA ( Y  = 4138.8 + (− 11,182.6) x , R 2  = 0.9924), respectively. The limits of detection (LODs) for FB 1 and OTA were 0.019 pg mL −1 and 0.015 pg mL −1 , respectively, which were much lower than previously described methods for simultaneous recognition of mycotoxins OTA and FB 1 while detection range varied from 0.0001–0.5 ng mL −1 . This aptasensor was effectively applied to quantity FB 1 and OTA in maize samples and results were compared with ELISA method. This is the first reported time-resolved fluorescence (TRF)-based aptasensor to detect two agriculturally important toxins in the maize. The developed aptasensor has potential to be used for detection of toxins in food safety fields. Graphical abstract

✓ 已验证 产品关联 DOI PubMed 高影响因子
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LANGMUIR · 2014 · IF 4.384

Turn-On Detection of a Cancer Marker Based on Near-Infrared Luminescence Energy Transfer from NaYF4:Yb,Tm/NaGdF4 Core–Shell Upconverting Nanoparticles to Gold Nanorods

Hongqi Chen,Yingying Guan,Shaozhen Wang,Yuan Ji,Mengqi Gong,Lun Wang

A homogeneous immunoassay for the sensitive and selective determination of trace amounts of α-fetoprotein (AFP, a cancer marker) by detection in the near-infrared (NIR) region based on luminescence energy transfer (LET) from NaYF4:Yb,Tm/NaGdF4 core–shell upconverting nanoparticles to gold nanorods (GNRs) is presented. The carboxyl-functionalized NaYF4:Yb,Tm/NaGdF4 core–shell upconverting nanoparticles (UCNPs) were excited by a 980 nm continuous wavelength laser, and its emission peak appeared at a near-infrared wavelength (∼804 nm). The carboxyl-functionalized upconverting nanoparticles were conjugated with the anti-AFP (Ab1) and acted as donor. GNRs with a high absorption band around 790 nm, which was overlapped the UCNPs emission, were synthesized and acted as the acceptor. The donor (negatively charged) interacted with the acceptor (positively charged) via electrostatic interactions to bring them into close proximity. LET could occur, producing a quenching phenomenon. When the AFP antigens were added into the system, the binding affinity between AFP and Ab1 was stronger than the electrostatic interactions, which released the energy acceptors from the energy donors, interrupting luminescence energy transfer, and therefore, the luminescence was recovered. On the basis of the restored luminescence, a turn-on optical immunosening system was developed. Under the optimal conditions, the linear range of detection was from 0.18 to 11.44 ng/mL for AFP (R = 0.99), with a detection limit as low as 0.16 ng/mL. The proposed method has also been used to monitor AFP in human serum samples. Therefore, further study based on the NaYF4:Yb,Tm/NaGdF4 core–shell nanoparticles-GNRs construction may open the way for a new class of NIR-LET biosensors with wide applications.

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