DALTON TRANSACTIONS
·
2013
·Vol. 42
·期 27
·9852-9861
·
IF 3.806
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
JOURNAL OF THE AMERICAN CERAMIC SOCIETY
·
2017
·Vol. 100
·期 7
·3061-3069
·
IF 2.841
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
OPTICAL MATERIALS
·
2020
·
IF 2.779
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.
研究领域:
材料科学
·
光学
·
生物医学工程
✓ 已验证
产品关联
DOI
高影响因子
RSC Advances
·
2022
·Vol. 12
·期 18
·11534-11542
·
IF 4.036
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.
研究领域:
材料科学
·
光学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
APPLIED SURFACE SCIENCE
·
2023
·
IF 6.7
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.
研究领域:
环境科学
·
材料科学
✓ 已验证
产品关联
DOI
高影响因子
Journal of Materials Chemistry C
·
2017
·Vol. 5
·期 37
·9770-9777
·
IF 5.256
Shaohua Fan,Guojun Gao,Dmitry Busko,Zhiquan Lin,Shikai Wang,Xue Wang,Shiyu Sun,Andrey Turshatov,Bryce S. Richards,Hongtao Sun,Lili Hu
Monodisperse β-NaYF4:Yb3+,Tm3+ (NYF) hexagonal microplates with efficient near-infrared (NIR)-to-NIR up-conversion (UC) developed via a new ion-exchange modified hydrothermal method are reported. Ion exchange modification (IEM) not only significantly increases the UC intensity by up to 1000 times and prolongs the emission lifetimes of Tm3+ and Yb3+, but also enables the monodisperse morphology and size of hexagonal microplates to be maintained. A high UC quantum efficiency (QE) of 3.1% is obtained for IEM β-NaYF4:20%Yb3+,1%Tm3+ when excited with 980 nm light at a power density of 10 W cm−2. The UC emission properties can be finely tailored by changing the NaF/NYF molar ratio (NYF represents lanthanide doped β-NaYF4) and the doping concentration of Tm3+. The two photon NIR UC emission centered at ∼803 nm (arising from Tm3+: 3H4 → 3H6) dominates the UC emission spectrum and high concentrations of Tm3+ favor NIR UC further. A proof-of-concept optical image of printed patterns is demonstrated to verify their applications in security. These results suggest the promising applications of the newly developed monodisperse β-NaYF4:Yb3+,Tm3+ hexagonal microplates in security, luminescent labels, solid-state lasers, amplifiers, and biomedicine.
研究领域:
材料科学
·
光子学
·
纳米技术
·
光学材料
·
发光学
·
稀土掺杂
·
生物医学工程
✓ 已验证
DOI
高影响因子
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
✓ 已验证
DOI
高影响因子
Materials Science and Engineering B-Advanced Functional Solid-State Materials
·
2020
·
IF 4.706
Yuzhen Sun,Huifang Bi,Tao Wang,Leilei Sun,Zexin Li,Haining Song,Fenglei Sun,Haifeng Zhou,Guangjun Zhou,Jifan Hu
NaYF 4 :10Er/0.5Ho/30Ca@NaYF 4 is designed to achieve up-conversion luminescence color adjustment under 980 nm excitation. Ho 3+ doping enhances the red emission level of the system and changes the characteristic green emission into red emission. Importantly, Ho 3+ doping increases the difference in pumping time between green and red excited states. Under short pulse-width laser excitation, the red excited state does not have enough time to be populated, which weakens the emission of red emission, and the ratio of green to red emission will change. It is an effective up-conversion luminescence enhancement method to change the symmetry of crystal field around lanthanide ions by doping Ca 2+ . The green and red emission intensities of NaYF 4 :10Er/0.5Ho/30Ca doped with 30% Ca 2+ ions are 9.0 and 6.3 times higher than those of Ca 2+ free samples, respectively.
研究领域:
材料科学
·
光学
✓ 已验证
DOI
高影响因子
Nanoscale Research Letters
·
2019
·Vol. 14
·期 1
·1-10
·
IF 3.159
Yuan Maohui,Wang Rui,Zhang Chaofan,Yang Zining,Yang Xu,Han Kai,Ye Jingfeng,Wang Hongyan,Xu Xiaojun
The presence of manganese ions (Mn 2+ ) in Yb/Er-co-doped nanomaterials results in suppressing green (545 nm) and enhancing red (650 nm) upconversion (UC) emission, which can achieve single-red-band emission to enable applications in bioimaging and drug delivery. Here, we revisit the tunable multicolor UC emission in a single Mn 2+ -doped β-NaYF 4 :Yb/Er microcrystal which is synthesized by a simple one-pot hydrothermal method. Excited by a 980 nm continuous wave (CW) laser, the color of the single β-NaYF 4 :Yb/Er/Mn microrod can be tuned from green to red as the doping Mn 2+ ions increase from 0 to 30 mol%. Notably, under a relatively high excitation intensity, a newly emerged emission band at 560 nm ( 2 H 9/2 → 4 I 13/2 ) becomes significant and further exceeds the traditional green (545 nm) emission. Therefore, the red-to-green (R/G) emission intensity ratio is subdivided into traditional (650 to 545 nm) and new (650 to 560 nm) R/G ones. As the doped Mn 2+ ions increase, these two R/G ratios are in lockstep with the same tunable trends at low excitation intensity, but the tunable regions become different at high excitation intensity. Moreover, we demonstrate that the energy transfer (ET) between Mn 2+ and Er 3+ contributes to the adjustment of R/G ratio and leads to tunable multicolor of the single microrod. The spectroscopic properties and tunable color from the single microrod can be potentially utilized in color display and micro-optoelectronic devices.
研究领域:
材料科学
·
生物医学工程
✓ 已验证
产品关联
DOI
PubMed
高影响因子
Nanoscale
·
2024
·Vol. 16
·期 17
·8661-8671
·
IF 5.8
Mingxing Li,Xiaoge Wang,Xiaofan Cao,Zhiqun He,Chunjun Liang,Jing Ju,Fangtian You
NaYF4 systems have been widely studied as up-conversion host matrices, and their phase transitions are flexible and worth investigating in great detail. Herein, the evolution of morphology and crystal structure of a Eu3+-doped β-NaYF4 single nanoparticle heated in an air atmosphere was investigated using in situ transmission electron microscopy (TEM). The annealing process revealed that the hexagonal β-NaYF4 phase undergoes sequential transformations into high-temperature cubic phases at both 350 °C and 500 °C. The emission characteristics of Eu3+ in the single nanoparticle after heating treatment were also analyzed using Correlative Cathodoluminescence Electron Microscopy (CCLEM). The results of CCLEM suggest a gradual decrease followed by a subsequent increase in structural symmetry. A comprehensive spectroscopic and structural analysis encapsulates the entire transformation process as NaYF4 → YOF → Y2O3. In situ energy dispersive spectroscopy analyses (EDS) support this reaction process. The aforementioned technique yields correlative lattice-resolved TEM images and nanoscale spectroscopic information, which can be employed to assess the structure–function relationships on the nanoscale.
研究领域:
材料科学
·
光学
·
纳米技术
✓ 已验证
DOI
高影响因子
Nano Research
·
2023
·Vol. 16
·期 7
·10026-10033
·
IF 9.9
Jiang Shihui,Ke Jianxi,Li Guowei,Liu Aijun,Li Xiaohan,Ye Lixiang,Jiang Feilong,Liu Yongsheng,Hong Maochun
Hexagonal-phase NaYF 4 (β-NaYF 4 ) has been acknowledged to be one of the most efficient doping hosts to prepare bright lanthanide-doped luminescent nano-bioprobes for various biomedical applications. However, to date, it remains a great challenge to synthesize ultra-bright lanthanide-doped β-NaYF 4 nano-bioprobes under a low reaction temperature by using conventional synthetic methods. Herein, we first develop an acetic acid (HAc)-mediated coprecipitation method for the preparation of ultra-bright lanthanide-doped β-NaYF 4 nanoprobes under a low reaction temperature at 200 °C. Based on a series of comparative spectroscopic investigations, we show that the use of HAc in the reaction environment can not only promote the rapid α–β phase transformation of NaYF 4 host at 200 °C within 1 h but also boost the absolute photoluminescence quantum yield (PLQY) of NaYF 4 nanocrystals to 30.68% for near-infrared emission and to 3.79% for upconversion luminescence, both of which are amongst the highest values for diverse lanthanide-doped luminescent nanocrystals ever reported. By virtue of their superior near-infrared luminescence, we achieve optical-guided dynamic vasculature imaging in vivo of the whole body at a high spatial resolution (23.8 µm) under 980 nm excitation, indicating its potential for the diagnosis and treatment evaluation of vasculature-related diseases.
研究领域:
材料科学
·
生物医学工程
·
光学
✓ 已验证
产品关联
DOI
高影响因子
MOLECULES
·
2019
·Vol. 24
·期 2
·
IF 3.06
Lili Xu,Man Wang,Qing Chen,Jiajia Yang,Wubin Zheng,Guanglei Lv,Zewei Quan,Chunxia Li
In recent years, rare earth doped upconversion nanocrystals have been widely used in different fields owing to their unique merits. Although rare earth chlorides and trifluoroacetates are commonly used precursors for the synthesis of nanocrystals, they have certain disadvantages. For example, rare earth chlorides are expensive and rare earth trifluoroacetates produce toxic gases during the reaction. To overcome these drawbacks, we use the less expensive rare earth hydroxide as a precursor to synthesize β-NaYF4nanoparticles with multiform shapes and sizes. Small-sized nanocrystals (15 nm) can be obtained by precisely controlling the synthesis conditions. Compared with the previous methods, the current method is more facile and has lower cost. In addition, the defects of the nanocrystal surface are reduced through constructing core–shell structures, resulting in enhanced upconversion luminescence intensity.
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）