Flower-like ceria (CeO2) architectures consisting of well aligned nanosheets were first synthesized by a glycol solvothermal method. The size of CeO2 architectures is about 5?μm in width and 10?μm in length, with the nanosheets thickness below 100?nm. Subsequently, the adsorbed Ag ions on the surface of CeO2 were in situ reduced to form Ag nanoparticles (NPs), leading to the fabrication of Ag/CeO2 hybrid architectures (HAs). The formed Ag NPs with sizes of 20–40?nm were uniformly loaded on the surface of the CeO2 sheets. The antibacterial properties of Ag/CeO2 HAs against Gram-negative E. coli and Gram-positive S. aureus were evaluated by minimum inhibitory concentration (MIC), minimum bactericidal concentration (MBC), and a filter paper inhibition zone method. The results demonstrated that Ag/CeO2 HAs displayed excellent antibacterial activity toward S. aureus and E. coli, which were attributed to the synergistic antibacterial effect between Ag NPs and CeO2 in HAs. Here, CeO2 nanoflowers as a new substrate could restrict Ag NPs aggregations and improve their antibacterial activities. Therefore, the resulted Ag/CeO2 HAs would be considered as a promising antibacterial agent.
In this study, we report a novel and simple solution-phase route for one-dimensional metal nanocrystals. BiIn nanocrystals were prepared by directly dispersing melting BiIn alloy at an appropriate solvent. The as-obtained BiIn nanocrystals with a dendritic shape possess a good crystalline phase. The morphology of the nanocrystals can be greatly modified by changing the reaction parameters. This strong UV emission might arise from the quantum-confined In2O3 particles. 相似文献
Assembly of Sn on Cu Nanorods as anode for Li-ion microbatteries was prepared by a two-step electrodeposition design. Firstly, Cu nanorods arrays were grown on copper substrate by anodic aluminum oxide template-assisted growth method. Then, Sn was deposited onto Cu nanorods arrays by galvanostatic deposition. X-ray diffraction and scanning electron microscopy measurements reveal that Cu nanorod arrays are covered with Sn. Electrochemical performances of prepared electrodes were evaluated by charge/discharge cycle measurement. The assembly of Sn on Cu nanorods electrode exhibited highly reversible specific capacity and superior capacity retention resulting from the three-dimensionally nano-architectured design, which exhibits a large surface area, shortened Li-ion diffusion distance, Cu–Sn alloying, and can accommodate the volume expansion of Sn during cycling. Deposition time is an important parameter for fabricating the assembly of Sn on Cu nanorods electrode with suitable structure and morphology.
The authors describe a highly sensitive and selective photoelectrochemical (PEC) assay for mercury(II) ions. It is based on a dual signal amplification strategy. The first enhancement results from the surface plasmon resonance (SPR) of Au@Ag nanoparticles (NPs) absorbed on MoS2 nanosheets. Here, the injection of hot electrons of Au@Ag NPs into MoS2 nanosheets produces a strong photocurrent, while background signals are strongly reduced. The second enhancement results from the use of a thymine rich ct-DNA aptamer attached to the Au@Ag-MoS2 nanohybrid. The DNA specifically binds Hg(II) ions to form thymine-Hg(II)-thymine (T-Hg-T) complexes. This leads to the formation of a hairpin-shaped dsDNA structure. The use of a CdSe quantum dot label at the terminal end of the ct-DNA further facilitates electron–hole separation. The photocurrent of the detector is measured as a function of Hg(II) concentration at a bias voltage of 0.1 V and under irradiation of 430 nm light. Due to the two-fold amplification strategy presented here, the linear range extends from 10 pmol·L?1 to 100 nmol·L?1, with a detection limit of 5 pmol·L?1 (at S/N?=?3).
Graphical Abstract The injection of hot electrons of Au@Ag into MoS2 produces a strong photocurrent, and the formation of thymine-Hg(II)-thymine further facilitates electron–hole separation by CdSe. This dual signal amplification strategy is used to detect Hg(II) ions via a photoelectrochemical assay.
In this paper, we describe a surfactant-assisted solution dispersion method to obtain metal nanoparticles, which involves dispersing and stabilizing metal droplets in an appropriate solvent. This method has been successfully used to prepare Pb nanoparticles from bulk Pb. The X-ray powder diffraction and transmission electron microscopy investigations show the formation of Pb nanoparticles possessing the same crystal structure as bulk metal and an average particle diameter of 40 nm. Thermal analysis indicates that Pb nanoparticles have organic shell, which is in agreement with the excellent oil-solubility. In addition, the tribological properties of Pb nanoparticles as additive in oil are discussed. 相似文献
The electrochemical properties and overcharge protection mechanism of xylene as a new polymerizable electrolyte additive for overcharge protection of lithium ion batteries were studied by cyclic voltammetry tests, charge- discharge performance and battery power capacity measurements. It was found that when the battery was overcharged, xylene could electrochemically polymerize at the overcharge potential of 4.3—4.7 V (vs. Li/Li+) to form a thin polymer film on the surface of the cathode, thus preventing voltage runaway. On the other hand, the use of xylene as an overcharge protection electrolyte additive did not influence the normal performance of lithium ion batteries. 相似文献
Carbon nanotube (CNT)-doped liquid crystals (LCs) have attracted intensive research studies as prospective materials in optic display devices, microfluidic sensors, and lubricants due to their unique molecular structures and properties. In this paper, the interaction between the doped CNTs and the hosting 4-cyano-4$^{\prime }$-pentylbiphenyl (5CB) molecules (in both nematic and isotropic phases) was investigated and we focused on the boundary layer rheological properties of the CNT-doped 5CB under external electric field. The experiments were performed by using a quartz crystal microbalance (for boundary layer viscosity investigation) and a rheometer (for bulk viscosity measurement). The results indicate that the bulk viscosity of the CNT-doped 5CB presents an obvious electroviscous effect in its nematic phase while no electroviscous effect in its isotropic phase. Additionally, we found that the boundary layer viscosity of the CNT-doped 5CB demonstrated significant electroviscous effects both in its nematic phase and isotropic phase. The enhanced electroviscous effects on the boundary layer viscosity of CNT-doped 5CB can be attributed to the highly ordered structures of LC molecules and CNTs on the substrate under external electric field. The unique properties of the boundary layer rheology of CNT-doped 5CB LC were further discussed in view of the ordering of LC molecules induced by the electric field, the polarity of CNTs, and the aligning interaction between CNTs and LC molecules. 相似文献