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CRYSTENGCOMM · 2018 ·Vol. 20 ·期 40 ·6351-6357 · IF 3.304

Synthesis and photoluminescence properties of novel core–shell–shell SiO2@CePO4:Tb@SiO2 submicro-spheres

Kui-Suo Yang,Yi-Lian Li,Yang-Yang Ma,Li-Na Feng,An-Ping Wu,Yan Qiao,Jin-Rong Bao,Wen-Xian Li,Xiao-Wei Zhu,Ran-Bo Yu

A novel core–shell–shell SiO2@CePO4:Tb@SiO2 submicro-sphere was controllably synthesized by a bridging ligand organosilane HOOCC6H4N(CONH(CH2)3Si(OCH2CH3)3)2 (MABA-Si) connecting the silica core and rare earth ions. The as-synthesized samples were investigated using scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and infrared spectroscopy (IR). It is found that SiO2@CePO4:Tb@SiO2 has a ∼25 nm outermost shell, a ∼4 nm intermediate shell, and a ∼200 nm core. SiO2@CePO4:Tb@SiO2 exhibits stable photoluminescence properties in aqueous solution: its photoluminescence intensity was unquenched even after 15 days. The core–shell–shell submicro-spheres were found to have better photoluminescence than the core–shell submicro-spheres because the SiO2 shell protected the phosphor materials and then improved its photoluminescence intensity and biocompatibility. A formation mechanism of the core–shell–shell SiO2@CePO4:Tb@SiO2 submicro-spheres was proposed. Thus, the low-cost preparation of the core–shell–shell SiO2@CePO4:Tb@SiO2 submicro-spheres could be rationally achieved using SiO2.

CAS / MDL: 99-05-8 24801-88-5
研究领域: 材料科学 · 纳米技术 · 光学 · 化学
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ACS Applied Materials & Interfaces · 2013 · IF 5.008

Boronic Acid-Functionalized Core–Shell–Shell Magnetic Composite Microspheres for the Selective Enrichment of Glycoprotein

Miaorong Pan,Yangfei Sun,Jin Zheng,Wuli Yang

In this work, core–shell–shell-structured boronic acid-functionalized magnetic composite microspheres Fe3O4@SiO2@poly (methyl methacrylate-co-4-vinylphenylbornoic acid) (Fe3O4@SiO2@P(MMA-co-VPBA)) with a uniform size and fine morphology were synthesized. Here, Fe3O4 magnetic particles were prepared by a solvothermal reaction, whereas the Fe3O4@SiO2 microspheres with a core–shell structure were obtained by a sol–gel process. 3-(Trimethoxysilyl) propyl methacrylate (MPS)-modified Fe3O4@SiO2 was used as the seed in the emulsion polymerization of MMA and VPBA to form the core–shell–shell-structured magnetic composite microspheres. As the boronic acid groups on the surface of Fe3O4@SiO2@P(MMA-co-VPBA) could form tight yet reversible covalent bonds with the cis-1,2-diols groups of glycoproteins, the magnetic composite microspheres were applied to enrich a standard glycoprotein, horseradish peroxidase (HRP), and the results demonstrated that the composite microspheres have a higher affinity for the glycoproteins in the presence of the nonglycoprotein bovine serum albumin (BSA) over HRP. Additionally, different monomer mole ratios of MMA/VPBA were studied, and the results implied that using MMA as the major monomer could reduce the amount of VPBA with a similar glycoprotein enrichment efficiency but a lower cost.

CAS / MDL: 9003-99-0 9007-43-6
研究领域: 分析化学 · 材料科学 · 生物化学
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ACS Applied Materials & Interfaces · 2024 · IF 8.3

Surface-Enhanced Raman Spectroscopy Sensor Integrated with Ag@ZIF-8@Au Core–Shell–Shell Nanowire Membrane for Enrichment, Ultrasensitive Detection, and Inactivation of Bacteria in the Environment

Guanwen Su,Yue Liu,Yulin Hou,Rui Zhang,Wei Wang,Jie Zhang,Leping Dang

A core–shell–shell sandwich material is developed with silver nanowires as the core, ZIF-8 as an inner shell, and gold nanoparticles as the outer shell, namely, Ag@ZIF-8@Au nanowires (AZA-NW). Then, the synthesized AZA-NW is transformed into a surface-enhanced Raman spectroscopy (SERS) sensor (named M-AZA) by the vacuum filtration method and used to enrich, detect, and inactivate traces of bacteria in the environment. The M-AZA sensor has three main functions: (1) trace bacteria are effectively enriched, with an enrichment efficiency of 91.4%; (2) ultrasensitive detection of trace bacteria is realized, with a minimum detectable concentration of 1 × 101 CFU/mL; (3) bacteria are effectively killed up to 92.4%. The shell thickness of ZIF-8 (5–75 nm) is controlled by adjusting the synthesis conditions. At an optimum shell thickness of 15 nm, the effect of gold nanoparticles and ZIF-8 shell on the sensor’s stability, SERS activity, and antibacterial performance is investigated. The simulation of the SERS sensor using the finite difference time domain (FDTD) method is consistent with the experimental results, theoretically demonstrating the role of the gold nanoparticles and the ZIF-8 shell. The sensor also shows excellent stability, safety, and generalizability. The campus water sample is then tested on-site by the M-AZA SERS sensor, indicating its potential for practical applications.

研究领域: 材料科学 · 纳米技术 · 环境科学 · 分析化学 · 生物技术
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CRYSTENGCOMM · 2020 ·Vol. 22 ·期 46 ·8110-8117 · IF 3.117

A novel one-pot strategy to rapidly synthesize bright red emitting upconversion nanocrystals with core–shell–shell structure

Zhiyuan Cheng,Hao Lin,Tong Liu,Yongjin Li,Shenghong Yang,Yueli Zhang

β-NaErF4:0.005Tm upconversion nanocrystals (UCNCs) with core–shell structure are quite popular due to efficient red upconversion luminescence. However, the traditional seed-mediated growth method is not continuous and quite time consuming, while the successive layer-by-layer strategy is unfriendly because of the usage of toxic sodium trifluoroacetate (Na-TFA). In this work, we utilized a novel one-pot strategy to synthesize β-NaErF4:0.005Tm with core–shell–shell structure. The morphology of the core could be significantly regulated. NaYbF4 and NaYF4 shells could be epitaxially grown on the core by simply adding fresh raw materials and heating to 300 °C, successively. Thanks to the suppression of surface quenching and energy back transfer from Yb3+ to Er3+, the population density of excited states of Er3+ (4I13/2, 4I11/2 and 4I9/2) was much improved, resulting in the tremendously enhanced upconversion intensity of β-NaErF4:0.005Tm@NaYbF4@NaYF4. This one-pot protocol could supply core–shell–shell red UCNCs with regular morphology, enhanced intensity and long-lasting decay lifetime, offering promising opportunities for applications such as bioprobing, anti-counterfeiting, photodynamic therapy, etc.

研究领域: 材料科学 · 纳米技术 · 光学 · 生物医学工程
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Journal of Physical Chemistry C · 2021 · IF 4.126

Filtering Strategy of Colloidal Quantum Dots for Improving Performance of Light-Emitting Diodes

Zhiwei Yao,Chenghao Bi,Jianjun Tian

Quantum dot light-emitting diodes (QLEDs) show great potential in high-definition displays due to their narrow emission and high color purity. However, the imperfect quantum dots (QDs) with high trap density are difficult to be removed from QD solution, which could cause serious nonradiative recombination, thereby suppressing the improvement of QLEDs. Here, we devise a novel chemical filtering strategy with a bidentate coordination to remove the imperfect QDs. The bidentate ligand of ethanolamine (EA) with an amidogen and a carboxyl was directly added into the CdSe/CdS/ZnS core/shell/shell QD solution. Then, uncoordinated sites such as S2– and Zn2+ on the surface of QDs were bonded with the amidogen and carboxyl of EA, respectively, resulting in aggregations of the imperfect QDs with high defect density, which were precipitated from the solution. As a result, the photoluminescence quantum yield (PLQY) of the filtered QD solution increased to 93% because of the decrease in trap density. The size distribution of QDs was also improved after filtration. QLEDs fabricated with filtered QDs show a high external quantum efficiency (EQE) of 15.76% and luminance of 19,640 cd/m2, greater than those of the control devices. This strategy shows a great potential to be used in the large-scale treatment and production of QDs and QLEDs.

研究领域: 材料科学 · 纳米技术 · 光电子学 · 显示技术
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Materials Today Chemistry · 2024 · IF 6.7

Confined growth with particle attachment driven self-sieving for enhanced cascade reaction via versatile core-shell-shell nanocomposites

ZhaoGuo Wu,XueZhi Zhou,Hao Chen,AiWu Zhao,Jin Wang

Controlling formation of metal organic frameworks (MOFs) with embedded enzymes on magnetic surface has been achieved by a confined growth with particle attachment driven self-sieving approach for the first time. Specifically, a versatile route of silica encapsulation guided enzyme assembly for formation of ZIF-8 shell has been successfully demonstrated by shaped-controllable Fe 3 O 4 nanoparticles , e.g., nanorod and nanocube. Interestingly, silica encapsulation can lead to structural diversity of ZIF-8 shell on the shaped-controllable Fe 3 O 4 nanoparticles for affecting properties of the nanocomposites. Furthermore, embedded enzymes confined between silica endoskeleton and ZIF-8 exoskeleton can participate in cascade reaction with different activities and stabilities in the terms of plasmonic assemblies fabrication and cancer cell catalytic therapy. As a result, a circulation plasmonic fabrication and cancer therapy can be achieved via the magnetic nanocomposites. It can be expected that the confined growth with particle attachment driven self-sieving method can be versatile to generate diverse MOFs shell encapsulated shaped-controllable nanoparticles for efficiently embedding enzyme in the nanocomposites.

研究领域: 材料科学 · 纳米技术 · 生物技术 · 癌症治疗
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RSC Advances · 2021 ·Vol. 11 ·期 40 ·24843-24851 · IF 3.361

Fabrication of a novel core–shell–shell temperature-sensitive magnetic composite with excellent performance for papain adsorption

Pengfei Chen,Shun Yao,Dongmei Zheng,Zhiyuan Xu,Jinling Yu,Tingting Liang

Herein, a novel temperature-sensitive magnetic composite (Fe3O4@SiO2@P(NIPAM-co-VI)/Cu2+) with a uniform core–shell–shell structure was successfully prepared via a layer-by-layer method. The resulting magnetic composite revealed good magnetic properties and remarkable affinity to papain with a maximum adsorption capacity of 199.17 mg g−1. The adsorption equilibrium data fitted the pseudo-second-order kinetic and Freundlich models well, and the major thermodynamics parameters indicated that adsorption was an endothermic and spontaneous process. Fe3O4@SiO2@P(NIPAM-co-VI)/Cu2+ could thermally protect papain, which is attributed to the reversible hydrophilic–hydrophobic transition of the composite at temperatures below and above the lower critical solution temperature. More importantly, the magnetic composite could be recycled at least six times without a remarkable loss in its adsorption capacity, and the process of adsorption and elution had no significant effect on the activity and structure of papain. This work could provide a novel separation method for papain without loss of its activity.

研究领域: 材料科学 · 化学工程 · 生物技术
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