RESEARCH ON CHEMICAL INTERMEDIATES
·
2018
·Vol. 44
·期 10
·6369-6385
·
IF 1.674
Chen Zhangxu,Fu Ming-Lai,Huang Xiao-Dan,Yuan Baoling,Yang Jia-Cheng E.
To enhance photocatalytic activity spectra area of the TiO 2 based photocatalyst, and to separate and recycle photocatalyst easily, magnetic photocatalyst was prepared with β-NaYF 4 :Yb 3+ ,Tm 3+ , TiO 2 , Fe 3 O 4 as carriers, and tetraethyl orthosilicate as precursor. The magnetic infrared responsive photocatalysts were thoroughly characterized by field emission scanning electron microscopy, X-ray diffraction, a fluorescence spectrometer and UV–Vis–NIR diffuse reflectance spectroscopy. They showed that the composite of β-NaYF 4 :Yb 3+ ,Tm 3+ /TiO 2 /Fe 3 O 4 @SiO 2 (UCTFS) emits visible luminescence upon 980 nm excitation, and energy transfer from β-NaYF 4 :Yb 3+ ,Tm 3+ to TiO 2 was verified. The photocatalytic activities of the UCTFS were studied by orthogonal experiments for photodegradating methylene blue (MB). The degradation rate of MB can reach 86.69% under the optimal conditions. After the four recycles, the degradation rate remained 52.72%. It also showed that 50.27% of the degradation efficiency of phenol can be obtained under the same experimental parameters. These results suggest that magnetic UCTFS composite is stable and a magnetic NIR-driven photocatalyst for degradation of organic pollutants. Moreover, the NIR driven photocatalytic mechanism of this reported composite was proposed. The strategy suggested here may be indicated for the effective fabrication of magnetic NIR-driven photocatalyst for application in the water purification by full spectra of solar energy.
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JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY
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2018
·Vol. 18
·期 12
·8258-8268
·
IF 1.354
Tong Chao,Xie Shaowen,Zhou Hu,Li Na,Gong Liang,Jian Jian,Zhang Changfan,Xu Lijian,Xu Jianxiong
In this study, well-defined PAA-coated NaYF4:Yb3+, Er3+ nanophosphors were synthesized via a poly(acrylic acid) (PAA) mediated hydrothermal process. The rational control of initial reaction conditions, such as hydrothermal temperature, pH value of precursor-solution,
added amount of PAA, and molecular weight of PAA ligand, resulted in upconversion of NaYF4:Yb3+, Er3+ phosphors with varying crystal phases (α and β) and morphologies (e.g., nanosphere, submicrorod, microrod, microtube, and microprism).
By assessing the upconversion luminescent properties of the synthesized NaYF4:Yb3+, Er3+ phosphors upon excitation by 980 nm infrared light, it was demonstrated that the β-phase NaYF4:Yb3+, Er3+ phosphors generally
presented stronger upconversion luminescent than α-phase NaYF4:Yb3+, Er3+ phosphors and orthorhombic phase of YF3:Yb3+, Er3+ sample. Additionally, the β-phase NaYF4:Yb3+, Er3+
phosphors with hollow microtube morphology presented higher upconversion luminescent intensity than phosphors of other morphologies. This may be due to microtubes having larger surface area (inner and outer surfaces), which promoted the absorption efficiency under similar excitation conditions,
therefore generating higher luminescent intensity. Findings form this study suggest for precisely controlled growth of other complex rare earth fluoride compounds and provide a reference for exploration of component-, phase- and morphology-dependent upconversion luminescence properties.
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ACS Applied Materials & Interfaces
·
2015
·
IF 6.723
Xia Xu,Zhuo Wang,Pengpeng Lei,Yingning Yu,Shuang Yao,Shuyan Song,Xiuling Liu,Yue Su,Lile Dong,Jing Feng,Hongjie Zhang
Novel flower-like α-NaYb(Mn)F4:Er3+/Tm3+@NaYF4 upconversion nanoparticles (UCNPs) as luminescent nanothermometers have been developed by combining liquid–solid solution hydrothermal strategy with thermal decomposition strategy. Under 980 nm excitation, they exhibit intense upconversion luminescence and temperature-dependent upconversion luminescence over a wide temperature range. The influence of temperature on “band-shape” upconversion luminescence (UCL) spectra and the intensity of emission bands are analyzed and discussed in detail. We further successfully test and verify that intensity ratios REr of 2H11/2 → 4I15/2 and 4S3/2 → 4I15/2 and RTm of 1G4 → 3H5 and 3H4 → 3H6 are sensitive to temperature, and the population of active ions follows Boltzmann-type population distribution very well. These luminescent nanothermometers could be applied over a wide temperature range from 123 to 423 K with high sensitivity, which enable them to be excellent candidates for temperature sensors.
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BIOSENSORS & BIOELECTRONICS
·
2015
·
IF 6.409
Jianguo Zhang,Shaozhen Wang,Ni Gao,Dexiang Feng,Lun Wang,Hongqi Chen
A new turn-on luminescence energy transfer (LET) system has been designed for the detection of prostate specific antigen (PSA, a cancer marker) that utilizes Mn 2+ -enhanced long wavelength luminescence NaYF 4 : Yb, Er upconversion nanorods as the donor and gold nanorods as the acceptor. The Mn 2+ -doped NaYF 4 :Yb,Er upconversion luminescence nanorods with an emission peak located in the red region were synthesized. The presence of Mn 2+ markedly increased the luminescence intensity over that of the NaYF 4 :Yb, Er upconversion nanomaterials (excited by a 980 nm continuous wavelength laser). The surfaces of Mn 2+ -doped NaYF 4 :Yb, Er upconversion nanorods were modified with poly(acrylic acid). Antibodies against prostate specific antigen were bound to the surface of the carboxyl-functionalized upconversion nanorods, which acted as the energy donor in this LET system. Gold nanorods with an absorption band at ~666 nm were synthesized by the seed growth method, acted as the energy acceptor. The emission band of the upconversion nanorods overlapped well with the absorption band of the gold nanorods. The luminescence was quenched because of the electrostatic interactions that shortened the distance between the donor (negatively charged) and the accepter (positively charged).When the PSA antigen was added into the system, the energy acceptor and the energy donors were separated because the binding affinity between PSA and anti-PSA was greater than the electrostatic interactions, and thereby the luminescence was recovered. The linear range of detecting PSA was from 0.1172 to 18.75 ng/mL ( R =0.995), with a limit of detection for PSA as low as 0.1129 ng/mL. The method was successfully applied to the sensing of PSA in human serum samples.
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JOURNAL OF ALLOYS AND COMPOUNDS
·
2017
·
IF 3.133
Qiqi Nie,Yongbo Wang,Licong Jia,Bei Liu,Enzhou Liu,Xiaoyun Hu,Jun Fan
In this paper, a novel detection method based on luminescence resonance energy transfer (LRET) system for sensitive detection of Mn 2+ ions has been proposed. The positively charged upconversion nanoparticles capped with polyethyleneimin (PEI-UCNPs) and negatively charged Ag NPs capped with tripolyphosphate (P 3 O 10 5− -Ag NPs) were bound through electrostatic interaction . They were used as energy donors and acceptors, respectively. The green upconversion luminescence could be quenched because of a good overlap between the UCNPs emission and the Ag NPs absorption spectra . Nevertheless, the LRET was disrupted and the green upconversion luminescence was restored in the presence of Mn 2+ because of the coagulation of P 3 O 10 5− -Ag NPs. Thus, the relative luminescence intensity increased as the concentrations of Mn 2+ increased. The response is linear to the concentrations of Mn 2+ in the range from 0.2 to 5 μM, and the detection limit is evaluated to be 150 nM (S/N = 3). This probe was easy to operate with satisfactory selectivity and excellent sensitivity, which would be able to satisfy the requirements of Mn 2+ -related detection.
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Nanoscale
·
2016
·Vol. 8
·期 45
·19014-19024
·
IF 7.76
Lijie Bai,Wenya Jiang,Chunxiao Gao,Shuxian Zhong,Leihong Zhao,Zhengquan Li,Song Bai
The combination of upconversion nanocrystals with a wide-bandgap semiconductor is an efficient strategy to develop near-infrared (NIR)-responsive photocatalysts. The photocatalytic activity of the hybrid structures is greatly determined by the efficiency of the energy transfer on the interface between upconversion nanocrystals and the semiconductor. In this work, we demonstrate the interface design of a NaYF4:Yb,Tm–BiOCl hybrid structure based on the choice of suitable BiOCl facets in depositing NaYF4:Yb,Tm upconversion nanocrystals. It was found that the selective deposition of NaYF4:Yb,Tm nanocrystals on the BiOCl(110) facet can greatly enhance the photocatalytic performance in dye degradation compared with the sample with NaYF4:Yb,Tm nanocrystals loaded on the BiOCl(001) facet. Two effects were believed to contribute to this enhancement: (1) a stronger UV emission absorption ability of the BiOCl(110) facet from NaYF4:Yb,Tm in generating more photo-induced charge carriers resulted from the narrower bandgap; (2) a shorter diffusion distance of photogenerated charge carriers to the BiOCl(110) reactive facet for surface catalytic reactions owing to the spatial charge separation between different facets. This work highlights the rational interfacial design of an upconversion nanocrystal–semiconductor hybrid structure for enhanced energy transfer in photocatalysis.
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JOURNAL OF ALLOYS AND COMPOUNDS
·
2024
·
IF 5.8
Guangliang Lu,Rao Qin,Dabiao Zhai,Tianqi Wan,Jiangang Jiang,Dan Zhang,Ping Zhang,Yiping Wang,He Wang
The development and comparison of Latent Fingerprint Patterns (LFPs) constitute critical components of research in fingerprint detection and identification. However, the development of nanomaterials visualization and digital algorithms for LFPs analysis are mostly studied independently, resulting in inaccurate LFPs. This research synthesized a series of efficient red-emitting NaYF 4 :20 %Yb, 2 %Er, x %Mn ( x = 0, 5, 10, 15, 20, 25, 30, 35, and 40) upconversion nanoparticles (UCNPs) for image development, which were combined with a digital algorithm for accurate LFP recognition. The eightfold increase in luminescence intensity of NaYF 4 :Yb, Er, 30 %Mn at 653 nm effectively avoids interference from biological tissue fluorescence. This improvement is credited to the efficient reverse energy transfer mechanism between Er 3+ and Mn 2+ ions, specifically the transition sequence 4 S 3/2 (Er 3+ ) → 4 T 1 (Mn 2+ ) → 4 F 9/2 (Er 3+ ). Furthermore, a MATLAB program was employed to process the fluorescent images of LFPs developed using the UCNPs nanophosphors, achieving a high matching score of 90.09 % for the optimized sample, significantly outperforming traditional benchmarks. These results demonstrate the superior effectiveness of the NaYF 4 :Yb, Er, 30 %Mn nanophosphor, combined with digital processing algorithms, for practical LFP recognition applications.
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INORGANIC CHEMISTRY
·
2024
·
IF 4.3
Jinjian Wei,Mengxin Liu,Xinan Shi,Daocheng Pan
NaYF4:Ce3+,Tb3+ down-conversion nanoparticles with a photoluminescence quantum yield (PLQY) of 54.8% are synthesized by using a ligand-assisted coprecipitation method in this study. The reaction is completed within 1 min at room temperature, and short-chain hexanoic acid and hexylamine serve as the binary ligands, which enable us to synthesize highly luminescent NaYF4:Ce3+,Tb3+ nanoparticles at room temperature. X-ray diffraction (XRD) and transmission electron microscopy (TEM) are used to characterize the as-prepared nanocrystals. The results reveal that the NaYF4:Ce3+,Tb3+ nanocrystals exhibit excellent dispersion and have a particle size of 2.7 nm. Our NaYF4:Ce3+,Tb3+ nanocrystals possess the advantages of room-temperature preparation, high PLQY, and ultrasmall particle size. These results reveal that the NaYF4:Ce3+,Tb3+ nanocrystals might have a high potential in the applications of lighting, display devices, and bioimaging.
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Analytical Methods
·
2020
·Vol. 12
·期 42
·5081-5085
·
IF 2.596
Hongqi Chen,Huihui Wang,Wanying Xia,Jianguo Zhang,Lun Wang
In this work, we developed a simple and selective luminescence sensing system for detecting ascorbic acid (AA) based on NaGdF4:Yb,Er@NaYF4 upconversion nanoparticles (UCNPs) and oxidase-like CoOOH nanoflakes. When p-phenylenediamine (PPD) and oxidase-like CoOOH nanoflakes were added to the UCNPs solutions, PPD, as a typical substrate of oxidase, could be oxidized to PPDox. The luminescence intensity of UCNPs was quenched because PPDox could play a role as an energy acceptor. When AA was added to the above solution mixture, the CoOOH nanoflakes were destroyed, and then, the luminescence intensity was recovered. Under the best experimental conditions, the linear range for detection of AA was 0.8 to 280 μM, and the detection limit was 0.25 μM. Furthermore, the system could be applied to real sample analysis with satisfactory results.
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MOLECULES
·
2026
·Vol. 31
·期 19
·3412
·
IF 5.1
Xinyao Su,Wen Guo,Qunming Zhou,Tingting Xie,Lingyan Wu,Shangyang Wang,You Fu,Shurong Li,Wei Peng,Peijun Meng
Cancer theranostics urgently demands multifunctional nanomaterials capable of simultaneously enabling high-sensitivity imaging and multimodal synergistic therapy. In this study, a three-layer core–shell nanocomposite, NaYF4:Yb,Tm@NaGdF4:Eu@NH2-MIL-53(Fe), was designed and synthesized. The NaYF4:Yb,Tm nanoparticle core provides upconversion luminescence upon near-infrared (NIR) excitation and can serve as an excitation source for photodynamic therapy. An epitaxially grown NaGdF4:Eu intermediate shell was introduced to enhance luminescence and provide T1-weighted magnetic resonance imaging (MRI) capability. The outermost NH2-MIL-53(Fe) metal–organic framework shell was subsequently coated to provide potential chemodynamic therapy (CDT) capability. The effects of the Eu3+doping concentration, reaction temperature, reaction time, and oleic acid (OA)/1-octadecene (ODE) ratio on the anisotropic growth into a dumbbell-like morphology were examined to determine the optimal conditions. Under the optimal conditions (10 mol% Eu3+, 300 °C, 60 min, OA/ODE = 4:16), core–shell nanocrystals with regular morphology, uniform size, and the strongest upconversion luminescence were obtained. Polyvinylpyrrolidone (PVP)-mediated surface functionalization successfully induced the in situ growth of the NH2-MIL-53(Fe) outer shell, thereby constructing a three-layer core–shell nanocomposite as a potential theranostic platform. Various characterizations confirmed that the resulting composite integrates upconversion luminescence, paramagnetism, and hydroxyl radical generation capability, suggesting potential for NIR-driven dual-modal imaging-guided synergistic therapy.
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ELECTROCHIMICA ACTA
·
2017
·
IF 4.798
Jiwei Liang,Huiping Gao,Mengji Yi,Wenjia Shi,Yuefeng Liu,Zhenlong Zhang,Yanli Mao
β-NaYF 4 :Yb 3+ , Tm 3+ @ TiO 2 core-shell upconversion nanoparticles (UCNPs) were synthesized and incorporated into the TiO 2 mesoporous layer of perovskite solar cells (PSCs). Changes of the upconversion spectra of the UCNPs suggest the existence of the electron injection from NaYF 4 :Yb 3+ , Tm 3+ to the conduction band (CB) of TiO 2 through the NaYF 4 :Yb 3+ , Tm 3+ /TiO 2 nano-heterojunctions. The core-shell UCNPs that incorporated into the TiO 2 mesoporous layer not only act as the upconversion centers to use the NIR light but also serve as the light scatter centers to enhance the light harvesting. When using mesoporous layer containing the core-shell UCNPs in PSCs, the efficiency of the best devices is 16.27%, which is about 16.38% higher than that of the devices without core-shell UCNPs (13.98%). The significant enhancement in the performance of the PSCs is attributed to light scattering, NIR light upconversion and electron injection from the UCNPs to the CB of TiO 2 .
研究领域:
材料科学
·
能源科学
·
纳米技术
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Journal of Physical Chemistry C
·
2018
·
IF 4.484
Raheel Ahmed Janjua,Chan Gao,Rucheng Dai,Zhilei Sui,Muhammad Aqeel Ahmad Raja,Zhongping Wang,Xianxu Zhen,Zengming Zhang
Ultrasmall pure hexagonal phase NaYF4:Yb,Er is successfully prepared via the solvothermal method. The upconversion (UC) luminescence of hexagonal phase NaYF4:Yb,Er nanocrystals is ten times stronger than that of cubic phase nanocrystals with the same size of 6 nm. XRD results reveal that heating above 673 K leads to conversion of the hexagonal phase to the high-temperature cubic phase, whereas the cubic nanocrystals undergo phase transformation from normal cubic at room temperature to hexagonal at 673 K and further to high-temperature cubic above 773 K. The hexagonal nanocrystals exhibit emission enhancement after heat treatment up to 573 K. Further heating above 773 K induces a decreasing trend in emission due to the phase transition to the high-temperature cubic phase. The cubic phase exhibits decreasing luminescence with temperature due to strong cross relaxation and then increasing luminescence above the temperature of 673 K due to the hexagonal phase transformation. The luminescent properties of both the normal cubic phase and high-temperature cubic phase indicate that different crystal fields exist in these two phases due to the rearrangement of ligands around Er3+ at high temperature.
研究领域:
材料科学
·
纳米技术
·
发光材料
·
无机化学
·
光学材料
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