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OPTICAL MATERIALS · 2025 · IF 4.2

Luminescent NaYF4:Yb,Er@UiO-66 composite based probe for the selective and sensitive detection of Cu2+

Haoran Zhang,Tianxi Feng,Song Ye,Deping Wang

In this research, the modified upconversion nanocrystals NaYF 4 :Yb,Er were adopted as the precursors for the synthesis of the NaYF 4 :Yb,Er@UiO-66 composite. The XRD, XPS and TEM characterizations indicated that the composite has good crystallinity and uniform morphology. Under 980 nm excitation, the NaYF 4 :Yb,Er@UiO-66 composite exhibits bright upconversion emission that characterized of Er 3+ : 2 H 11/2 → 4 I 15/2 , 4 S 3/2 → 4 I 15/2 , and 4 F 9/2 → 4 I 15/2 radiative transitions. After modified with BPEI (branched polyethyleneimine), the NaYF 4 :Yb,Er@UiO-66/BPEI fluorescence probe was constructed and was used for the detection of Cu 2+ . The results revealed that the integrated emission intensity of Er 3+ displayed a linear relationship with the concentration of Cu 2+ within the range of 5 to 45 μM with a LOD of 0.9615 μM. This study offered a feasible method for constructing UCNC@UiO-66 composites with regular morphology,which may have a potential application as fluorescent probes for the detection of various metal ions by adjusting the doping luminescent center.

✓ 已验证 产品关联 DOI 高影响因子
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DALTON TRANSACTIONS · 2013 ·Vol. 42 ·期 27 ·9852-9861 · IF 3.806

Core–shell structured luminescent and mesoporous β-NaYF4:Ce3+/Tb3+@mSiO2-PEG nanospheres for anti-cancer drug delivery

Yuan Wu,Dongmei Yang,Xiaojiao Kang,Ping'an Ma,Shanshan Huang,Yang Zhang,Chunxia Li,Jun Lin

Multifunctional nanocomposites integrating mesoporous and luminescence properties into a single entity are synthesized via a facile and effective approach. Oleic acid capped β-NaYF4:Ce3+/Tb3+ nanoparticles (NPs) are transferred into aqueous solution by cetyltrimethylammonium bromide (CTAB) surfactants, and further encapsulated with uniform mesoporous silica shell followed by the surface modification with poly(ethylene glycol) (PEG), leading to the formation of water-dispersible and biocompatible core–shell structured β-NaYF4:Ce3+/Tb3+@mSiO2-PEG (denoted as NPs@mSiO2-PEG) nanospheres. The as-synthesized nanospheres show a typical mesoporous structure and a green emission under UV irradiation. Doxorubicin hydrochloride (DOX), a widely used anti-cancer drug, is used as a model drug to evaluate the loading and controlled release behaviors of the NPs@mSiO2-PEG in phosphoric acidic buffer solutions (PBS) at different pH values (pH = 7.4 and 5.0). The composite carriers provide a pH-sensitive drug release pattern and the drug releases faster under lower pH value. The endocytosis process of fluorescein isothiocyanate (FITC)-labelled nanospheres is characterized using flow cytometry and confocal laser scanning microscopy (CLSM) against A549 cells. The in vitro cytotoxic effect against A549 cells of the DOX-loaded carriers is investigated in detail. In addition, the extent of drug release can be monitored by the variation of photoluminescence (PL) intensity of β-NaYF4:Ce3+/Tb3+. Considering the good biocompatibility and pH-dependent drug release pattern, such core–shell structured luminescent NPs@mSiO2-PEG nanospheres have potential applications in controlled drug delivery.

研究领域: 生物材料 · 纳米医学 · 肿瘤学
✓ 已验证 DOI PubMed 高影响因子
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ACS Sustainable Chemistry & Engineering · 2020 · IF 7.632

Promoting the Growth of Mung Bean Plants through Uptake and Light Conversion of NaYF4:Yb,Er@CDs Nanocomposites

Xiaokai Xu,Wei Li,Chaofan Hu,Bingfu Lei,Xuejie Zhang,Yadong Li,Qiuqiang Zhan,Yingliang Liu,Jianle Zhuang

In recent years, the application of nanomaterials in promoting plant growth and augmenting photosynthesis has aroused great interest. Herein, carbon dots (CDs) are combined with NaYF4:Yb,Er to achieve an enhanced upconversion red emission. The effects of the obtained NaYF4:Yb,Er@CDs nanocomposites on the growth of mung bean plants are investigated. It is found that an appropriate concentration of the NaYF4:Yb,Er@CDs nanocomposites (0.5 mg/mL) can enhance the water absorption ability of hydroponic mung beans and promote their growth after incubation for 7 days. Confocal imaging shows that the nanocomposites can transfer from the roots to the stems and leaves. Interestingly, after spraying the nanocomposite solution on the surface of the mung bean seedling leaves and placing them under sunlight for 2 weeks, the root/stem lengths and wet/dry weight clearly increase. Moreover, the photosynthetic rate of the mung bean seedling is found to increase by more than 2 times, while the transpiration rate and stomatal conductance are improved by 144 and 148%, respectively. Such a promoting effect is ascribed to the ability of the NaYF4:Yb,Er@CDs nanocomposites to convert near-infrared (NIR) radiation into red light, which is beneficial for plant photosynthesis. This work provides a promising strategy for promoting plant growth by the application of nanomaterials.

研究领域: 植物学 · 纳米生物学 · 农业科学
✓ 已验证 DOI 高影响因子
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Catalysis Science & Technology · 2025 · IF 4.2

Near-infrared-activated NaYF4:Yb3+,Tm3+@g-C3N4@WO3@MXene photocatalytic system for enhanced removal of tetracycline antibiotics

Dongfang Han,Li Niu,Yuangong Ma,Youlin Huang,Wen-Sheng Zhang

To utilize near-infrared (NIR) light within the solar energy spectrum, we have engineered an advanced composite of NaYF4:Yb3+,Tm3+@g-C3N4@WO3@MXene (denoted as NYT@g-C3N4@WO3@MXene) capable of absorbing NIR light to facilitate photocatalytic reactions. This environmentally benign system integrates semiconductor heterostructures (g-C3N4 and WO3) with upconversion nanoparticles (NaYF4:Yb3+,Tm3+, abbreviated as NYT) and Ti3C2 MXene nanosheets. Experimental validation demonstrated exceptional performance in antibiotic remediation, with the composite achieving 86.3% tetracycline decomposition over 12 hours under NIR irradiation through synergistic mechanisms, while also exhibiting good cycling stability. The enhanced photocatalytic activity arises from collaborative effects between upconversion luminescence, optimized charge transfer pathways within the heterojunction architecture, and the visible light absorption characteristics of MXene.

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JOURNAL OF ELECTRONIC MATERIALS · 2024 ·Vol. 53 ·期 5 ·2514-2523 · IF 2.2

Upconversion Spectral Modulation and Temperature Sensing of NaYF4:Yb3+/Ho3+/Tm3+/Gd3+ Nanorods with Resistance to Thermal Quenching

Zhou Wei,Yang Jian,Jin Xiangliang

Upconversion (UC) nanomaterials are of interest to researchers because of their excellent photostability, effective quantum efficiency and optical temperature dependence. However, most UC nanomaterials are thermally quenched, which causes optical nanothermometers to be susceptible to their own thermal effects, reducing the accuracy of temperature measurements. In this paper, NaYF 4 :Yb 3+ /Ho 3+ /Tm 3+ /Gd 3+ nanorods with UC luminescence and resistance to thermal quenching are prepared through a simple hydrothermal method. The UC luminescence intensity of NaYF 4 :Yb 3+ /Ho 3+ /Tm 3+ /Gd 3+ nanorods is adjusted by doping with Tm 3+ ions. The luminescence intensity at each location shows different temperature dependence as the temperature increases. When the temperature reaches 573 K, the integrated luminescence intensity is three times that at 293 K. At the same time, the intensity at all temperature points in the range of 293–573 K is greater than the intensity at 293 K, which shows that the nanorods have excellent resistance to thermal quenching. In addition, the relative sensitivity ( S r ) of LIR( I 696 / I 476 ), LIR( I 696 / I 541 ), LIR( I 696 /I 646 ), LIR( I 696 / I 802 ), and LIR( I 541 / I 476 ) is investigated based on the luminescence intensity ratio (LIR) technique. The S r of LIR( I 696 / I 802 ) is found to have larger values in the low-temperature range, while S r of LIR( I 696 / I 476 ) has larger values in the high-temperature range. The use of LIR( I 696 / I 802 ) and LIR( I 696 / I 476 ) in separate temperature bands allows S r to reach 0.93–1.67 %K −1 in the range of 293–573 K, confirming that the nanorods have high S r over a wide temperature interval. This study indicates that the NaYF 4 :Yb 3+ /Ho 3+ /Tm 3+ /Gd 3+ nanorods are promising candidates for optical thermometers with high sensitivity, wide temperature range, and resistance to thermal quenching.

研究领域: 材料科学 · 光学 · 纳米技术
✓ 已验证 DOI 高影响因子
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JOURNAL OF LUMINESCENCE · 2019 · IF 2.961

Selective enhancement of green upconversion luminescence from NaYF4:Yb, Er microparticles through Ga3+ doping for sensitive temperature sensing

Manli Zhang,Xuesong Zhai,Pengpeng Lei,Shuang Yao,Xia Xu,Lile Dong,Kaimin Du,Chengyu Li,Jing Feng,Hongjie Zhang

Temperature sensors based on upconversion luminescence (UCL) intensity ratio have attracted great attention due to the high sensitivity. The enhancement of UCL is helpful to improve the sensitivity of temperature sensor. Doping is an effective way to achieve the UCL enhancement. Ga 3+ ions doped NaYF 4 :18%Yb,2%Er have been prepared through a facile one-pot solvothermal method . Upconversion (UC) emission intensity was significantly enhanced by introducing Ga 3+ ions into the lattice of NaYF 4 :Yb,Er, especially the green UC emission. With Ga 3+ concentration increasing, the size of the resulting NaYF 4 :Yb,Er,x%Ga particles decreases gradually. By doping 25% Ga 3+ , the green UC emission is increased by 30 times, while the red emission is enhanced by only 8 times. The morphology of particles and local symmetry around Er 3+ ions have been changed, resulting in the selective enhancement of green UC emission. In addition, the temperature-dependent UCL properties of NaYF 4 :Yb,Er,25%Ga and NaYF 4 :Yb,Er were investigated. The maximum thermal sensitivity of NaYF 4 :Yb,Er,25%Ga could reach 0.0046 K −1  at 498 K. Therefore, NaYF 4 :Yb,Er,25%Ga with strong green UCL could be served as a potential candidate for sensitive temperature sensing.

研究领域: 材料科学 · 光学传感器 · 发光材料 · 纳米技术
✓ 已验证 DOI 高影响因子
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JOURNAL OF THE AMERICAN CERAMIC SOCIETY · 2017 ·Vol. 100 ·期 7 ·3061-3069 · IF 2.841

Efficient dual-mode up-conversion and down-shifting emission in β-NaYF4:Yb3+,Er3+ microcrystals via ion exchange

Shaohua Fan,Shikai Wang,Hongtao Sun,Shiyu Sun,Guojun Gao,Lili Hu

We report efficient dual-mode up-conversion (UC) and down-shifting (DS) emission in a single Yb 3+ /Er 3+ -co-doped β-NaYF 4 microcrystals with controlled morphology and size via a simple Na + ion-exchange modification (IEM) method. IEM well preserves the crystal structure and monodispersed morphology of hydrothermal-synthesized β-NaYF 4 . Meanwhile, IEM gives rise to the significant enhancement of UC emission intensity up to 3800 times and strongly enhanced DS emission intensity of Er 3+ and Yb 3+ by several times in β-NaYF 4 :Yb 3+ ,Er 3+ microcrystals. IEM also strongly prolongs the DS emission lifetimes of Er 3+ and Yb 3+ in visible and near-infrared region. The enhanced UC and DS emission intensities and prolonged lifetimes in β-NaYF 4 :Yb 3+ ,Er 3+ are mainly ascribed to the dispersing of localized Yb 3+ and Er 3+ clusters during IEM.

研究领域: 材料科学 · 光子学 · 纳米技术 · 光学材料
✓ 已验证 DOI 高影响因子
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Nanoscale · 2017 ·Vol. 9 ·期 22 ·7666-7673 · IF 7.367

Manipulating the emission intensity and lifetime of NaYF4:Yb3+,Er3+ simultaneously by embedding it into CdS photonic crystals

Xin Su,Xiaoqian Sun,Suli Wu,Shufen Zhang

Photonic crystals (PCs) have long been considered effective for tuning upconversion luminescence due to their photonic band gap (PBG) and the redistribution of density of optical states (DOS). Although the emission intensity can be changed obviously by the PC effect, rarely an obvious lifetime change consistent with theory is observed due to the low refractive index of PS or SiO2 spheres in the commonly used PCs. Herein, CdS/NaYF4:Yb3+,Er3+ composite PCs with a high refractive index contrast are fabricated in one step with upconversion nanoparticles filled inside CdS PCs. When the upconversion emission peak lies at the edge of the PBGs of the composite PCs, a dramatic decrease in lifetime by 28% and 41% is observed for the green and red emissions, respectively. At the same time, obvious emission intensity enhancements are also observed. In contrast, PS PCs with a low refractive index contrast show a slight effect on the lifetime of upconversion luminescence with their emission peak at the edge of the PBGs. Our results agree well with theory and prove that a sufficiently large refractive index contrast is necessary for PCs to dramatically tune the luminescence lifetime and intensity simultaneously.

研究领域: 材料科学 · 光学
✓ 已验证 DOI PubMed 高影响因子
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APPLIED SURFACE SCIENCE · 2023 · IF 6.7

Near-infrared-driven enhanced β-NaYF4:Yb3+, Tm3+@BiOCl heterostructured upconversion composites for efficient degradation of organic contaminants

Jinyuan Zhang,Tong Liu,Tian Shi,Zhiyuan Cheng,Fuhua Gao,Da Cai,Shenghong Yang,Yueli zhang

Constructing comprehensive performance-enhanced heterostructured composite using the synergistic effect of complementary advantages between heterogeneous materials has always been challenging. In this work, highly stable β-NaYF 4 :Yb 3+ , Tm 3+ @BiOCl (NYF@BiOCl) heterostructured upconversion composites were successfully prepared using a two-step hydrothermal method. Compared to NYF/BiOCl mechanical mixtures, NYF@BiOCl with intimate interface show a higher photocatalytic degradation rate of rhodamine B (RhB) aqueous solutions, achieving 99.9% in 18 min and 98% in 2 h under simulated sunlight and near-infrared (NIR) light, respectively. The construction of heterostructures has a broad-spectrum response, which improves the utilization of sunlight and achieves efficient photocatalytic degradation of organic contaminants. Upconversion luminescence mechanism, spectral overlap, and Förster resonance energy transfer (FRET) explain the high photocatalytic activity of NYF@BiOCl. Meanwhile, NYF@BiOCl exhibits good universality to efficiently degrade other organic contaminants (methyl orange (MO), methylene blue (MB), bisphenol A (BPA), p-chlorophenol (4-CP)). This study demonstrates the potential of synergistic effects between heterogeneous materials. It Enhanced the photocatalytic activity of the NYF@BiOCl heterostructured composites driven by NIR light, providing a new strategy for energy-efficient and degradation of hazardous organic contaminants to alleviate environmental pollution.

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RSC Advances · 2022 ·Vol. 12 ·期 18 ·11534-11542 · IF 4.036

A multi-color persistent luminescent phosphor β-NaYF4:RE3+ (RE = Sm, Tb, Dy, Pr) for dynamic anti-counterfeiting

Bohan Wang,Zhihao Wang,Peng Mao,Yu Wang

Conventional luminescent materials generally exhibit uni-color and transient emission under UV excitation, which makes them mediocre in the field of anti-counterfeiting. The high-level anti-counterfeiting techniques are always becoming more complicated and in need of multi-color and persistent luminescent materials. Herein, we report a series of β-NaYF4:RE3+ (RE = Sm, Tb, Dy, Pr) persistent luminescent phosphors with multi-color emitting and ultra-long persistent luminescence under the irradiation of X-rays. The effects of doping concentrations of RE3+ on the size, morphology, radioluminescence and afterglow performance of the products are investigated in detail. Hexagonal structured rod-like β-NaYF4:Tb3+ crystals show super strong X-ray response and the afterglow signal lasts for up to seven days after X-rays are turned off. Upon X-rays irradiation, some of the F− ions are expected to escape from the crystal lattice by elastic collisions, leading to the generation of Frenkel defects: the F vacancies and interstitials , which capture electrons and release them slowly to achieve different afterglow emission times. Taking advantages of the extraordinary radioluminescence performance of the β-NaYF4:RE3+ persistent luminescent phosphors, the dynamic anti-counterfeiting patterns that containing rich time-resolved information were successfully designed.

✓ 已验证 产品关联 DOI PubMed 高影响因子
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OPTICAL MATERIALS · 2020 · IF 2.779

Size-tunable β-NaYF4:Yb/Er up-converting nanoparticles with a strong green emission synthesized by thermal decomposition

Hua Li,Xiaobo Shi,Xia Li,Lingbo Zong

Size-tunable β-NaYF 4 : Yb/Er (50–400 nm) up-converting nanoparticles (UCNPs) with a strong green emission were successfully prepared by a facile thermal decomposition method in a short period of time. The effects of the reaction time, the oleic acid (OA) content, and the doped Gd 3+ concentration on the crystal structure, the size evolution mechanism and the luminescence mechanism of the β-NaYF 4 : Yb/Er nanoparticles were discussed in detail. Characterization was completed using X-ray diffraction (XRD), transmission electron microscopy (TEM), high-resolution (HR-TEM), scanning electron microscopy (SEM), and photoluminescence (PL). The results reveal that the phase transition was completed at 15 min and the morphology of the NaYF 4 : Yb/Er UCNPs changed from spherical to large hexagonal disks (200–400 nm) in non-doped Gd 3+ . An appropriate decrease in the volume ratio of oleic acid (OA) to 1-octadecene (ODE) promoted NaF production, resulting in the formation of the hexagonal phase crystals and the subsequent increase of luminous intensity by 30–40 times. More importantly, the size of the β-NaYF 4 : Yb/Er decreased with Gd 3+ doping, and the UCNPs ultimately transformed into small hexagonal prisms (50 nm) with high monodispersity when the doping concentration of Gd 3+ was 60 mmoL. The PL spectra confirmed that the luminous intensity of the UCNPs with doped Gd 3+ was much higher than that of the undoped UCNPs. The results show that this route for UCNP fabrication with high luminous efficiency and a small size could be extended to other UCNP systems for multifunctional biomedical applications.

CAS / MDL: 112-80-1 112-88-9
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SENSORS AND ACTUATORS B-CHEMICAL · 2019 · IF 6.393

Strand displacement dual amplification miRNAs strategy with FRET between NaYF4:Yb,Tm/Er upconversion nanoparticles and Ti3C2 nanosheets

Feng Chen,Qiujun Lu,Youyu Zhang,Shouzhuo Yao

Due to the low abundance of miRNAs and the coordinated regulation of multiple miRNAs toward some biological processes, a method that can sensitively and simultaneously detect multiple miRNAs is needed. Here, a strand displacement dual amplification (SDDA) strategy was developed for multiple miRNAs analyses using a unique single strand-double strand-single strand DNA (sdsDNA), which generated by the target recognition probe hybridizing with the site region probe. During the process of SDDA, miRNA hybridized to the target recognition domain of sdsDNA, thereby releasing the site, which triggered the first strand displacement reaction. This strand displacement event resulted in the release of the other site, triggering the second strand displacement reaction. Both two strand displacement reactions in each assembly circle were integrated for amplified signals, which were tested by a fluorescence resonance energy transfer (FRET) assay. NaYF 4 :Yb,Tm/Er UCNPs and Ti 3 C 2 nanosheets were used as the energy donor-acceptor pair. By employing 1:2 ratio of donor-acceptor, the energy transfer efficiency between NaYF 4 :Yb,Tm/Er UCNPs and Ti 3 C 2 nanosheets could reach 90%, which enhanced signal-to-background ratio. Combining the benefits of dual amplification and efficient energy transfer on miRNAs detection, this assay exhibited a linear range from 5 fM to 100 pM for miRNA-21 and miRNA-10b. Moreover, this assay was applied to estimate the expression of miRNA-21 and miRNA-10b in human hepatoma and hepatocyte cell lines. Therefore, this FRET-based SDDA strategy has been used for highly sensitive detection of multiple miRNAs in cell lysate and facilitates the development of efficient biosensor platform.

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