Fabrication and simulation studies on D-shaped optical fiber sensor via surface plasmon resonance

This paper describes simulation and experimental methods for designing a D-shaped surface plasmon resonance (SPR) fibre sensor. The sensor consists of two set-up approaches. Finite element method is used in simulation on the fibre sensor device. Two experimental methods for detecting relative intensity are used by varying the wavelength of the optical signal sources and the thickness of gold layer coated on the D-shaped fibre. In the first method, the sensor device works by detecting the relative intensity of two optical signal sources having different wavelengths. In the second set-up, the relative intensity between two D-shaped fibres coated with different thicknesses of gold is measured when a single signal source is launched at the input. The difference in intensities of the signal outputs is used to estimate the refractive index at the sensing region. A prototype SPR D-shaped fibre sensor has been fabricated and the experimental results show good agreement with simulation.     

Rational Design of Functional Peptide–Gold Hybrid Nanomaterials for Molecular Interactions

Gold nanoparticles (AuNPs) have been extensively used for decades in biosensing-related development due to outstanding optical properties. Peptides, as newly realized functional biomolecules, are promising candidates of replacing antibodies, receptors, and substrates for specific molecular interactions. Both peptides and AuNPs are robust and easily synthesized at relatively low cost. Hence, peptide–AuNP-based bio-nano-technological approaches have drawn increasing interest, especially in the field of molecular targeting, cell imaging, drug delivery, and therapy. Many excellent works in these areas have been reported: demonstrating novel ideas, exploring new targets, and facilitating advanced diagnostic and therapeutic technologies. Importantly, some of them also have been employed to address real practical problems, especially in remote and less privileged areas. This contribution focuses on the application of peptide–gold hybrid nanomaterials for various molecular interactions, especially in biosensing/diagnostics and cell targeting/imaging, as well as for the development of highly active antimicrobial/antifouling coating strategies. Rationally designed peptide–gold nanomaterials with functional properties are discussed along with future challenges and opportunities.     

Gold nanocages in cancer diagnosis,therapy, and theranostics: A brief review

Regarding the increasing number of cancer patients, the global burden of this disease is continuing to grow. Despite a considerable improvement in the diagnosis and treatment of various types of cancer, new diagnosis and treatment strategies are required. Nanotechnology, as an interesting and advanced field in medicine, is aimed to further advance both cancer diagnosis and treatment. Gold nanocages (AuNCs), with hollow interiors and porous walls, have received a great deal of interest in various biomedical applications such as diagnosis, imaging, drug delivery, and hyperthermia therapy due to their special physicochemical characteristics including the porous structure and surface functionalization as well as optical and photothermal properties. This review is focused on recent developments in therapeutic and diagnostic and applications of AuNCs with an emphasis on their theranostic applications in cancer diseases.     

硅钛杂化介孔球负载金纳米粒子及其催化性能调控

以能源开发(如光解水制氢)及环境保护(如有机物降解)应用为目标, 负载型贵金属催化剂在设计、制备及理论研究方面已取得了长足的发展。本工作以具有特异形貌及结构的树枝状二氧化硅纳米球载体为基础, 通过溶胶-凝胶法在其孔道引入二氧化钛纳米颗粒形成硅钛杂化结构。通过有机改性技术, 在树枝状硅钛杂化纳米球表面接枝氨基官能团。然后, 通过浸渍法和硼氢化钠还原手段, 在杂化纳米球孔道负载超细金纳米粒子。不同手段表征结果显示实验成功制备了树枝状硅钛杂化纳米球负载金纳米颗粒复合材料。在模拟太阳光下, 所得催化剂光解水产氢量及速率为69.08 μmol·g^-1和13.82 μmol·g^-1·h^-1, 约为对比样催化剂(树枝状二氧化硅纳米球负载金纳米粒子)的7倍。在无光条件下, 其降解对硝基苯酚的表观动力学常数为6.540×10^-3 s^-1, 约为对比样的17倍(0.372×10^-3 s^-1)。由此可见, 设计合成的新型催化剂展现出优越的多功能催化活性。     

Controllable Formation of Luminescent Carbon Quantum Dots Mediated by the Fano Resonances Formed in Oligomers of Gold Nanoparticles

Rapid and controllable formation of fluorescent carbon quantum dots (CQDs) is highly desirable in the fields of nanophotonics and biophotonics. Here, a novel strategy for creating CQDs, which emit white light efficiently under the excitation of either laser light or a mercury lamp, is proposed and demonstrated. The luminescent CQDs are generated by irradiating a poly(vinyl alcohol) (PVA) film doped with dense gold nanoparticles (AuNPs) with femtosecond laser pulses. The creation of CQDs from PVA is a two‐step dehydration process mediated by AuNPs which act not only as heat sources but also as catalytic agents. The formation of C?C, C? C, and C? O bonds is confirmed by infrared Fourier transformation spectroscopy and X‐ray photoelectron spectroscopy. It is revealed both numerically and experimentally that a spatially localized temperature distribution at the deep subwavelength scale can be achieved in oligomers of AuNPs by resonantly exciting the Fano resonances formed in the oligomers of AuNPs, enabling the generation of CQDs with small diameters. As one of the potential applications, it is demonstrated that optical display and optical data storage with ultralow energy can be realized by selectively introducing luminescent CQDs in the AuNP/PVA film.     

In Situ Self-Assembly of Nanoscale Particles into Macroscale Ordered Monolayers with Enhanced Memory Performance

In situ fabrication of macroscale ordered monolayers of nanoparticles (NPs) on targeted substrates is highly desirable for precision electronic and optical devices, while it remains a great challenge. In this study, a solution is provided to address this challenge by developing a colloidal ink formulation and employing the direct-ink-writing (DIW) technique, where on-demand delivery of ink at a targeted location and directional evaporation with controllable rate are leveraged to precisely guide the deposition of polystyrene-grafted gold NPs (Au@PS NPs) into a macroscale monolayer with an ordered Au NP array embedded in a PS thin film. A 2D steady-state diffusion-controlled evaporation model, which explains the parameter dependence of the experimental results and gives semiquantitative agreement with the experimental evaporation kinetics is proposed. The ordered monolayer is used as both nanocrystal floating gates and the tunneling layer for nonvolatile memory devices. It shows significantly enhanced performance compared with a disordered NP film prepared by spin coating. This approach allows for fine control of NP self-assembly to print macroscaleordered monolayers directly onto substrates, which has great promise for application in broad fields, including microelectronic and photoelectronic devices, sensors, and functional coatings.     

Large-Area Arrays of Polymer-Tethered Gold Nanorods with Controllable Orientation and Their Application in Nano-Floating-Gate Memory Devices

In this work, it is reported that large-area (centimeter-scale) arrays of non-close-packed polystyrene-tethered gold nanorod (AuNR@PS) can be prepared through a liquid–liquid interfacial assembly method. Most importantly, the orientation of AuNRs in the arrays can be controlled by changing the intensity and direction of electric field applied in the solvent annealing process. The interparticle distance of AuNR can be tuned by varying the length of polymer ligands. Moreover, the AuNR@PS with short PS ligand are favorited to form orientated arrays with the assistance of electric field, while long PS ligands make the orientation of AuNRs difficult. The orientated AuNR@PS arrays are employed as the nano-floating gate of field-effect transistor memory device. Tunable charge trapping and retention characteristics in the device can be realized by electrical pulse with visible light illumination. The memory device with orientated AuNR@PS array required less illumination time (1 s) at the same onset voltage in programming operation, compared to the control device with disordered AuNR@PS array (illumination time: 3 s). Moreover, the orientated AuNR@PS array-based memory device can maintain the stored data for more than 9000 s, and exhibits stable endurance characteristic without significant degradation in 50 programming/reading/erasing/reading cycles.     

Injectable Bone Cement Reinforced with Gold Nanodots Decorated rGO-Hydroxyapatite Nanocomposites,Augment Bone Regeneration

Interest in the development of new generation injectable bone cements having appropriate mechanical properties, biodegradability, and bioactivity has been rekindled with the advent of nanoscience. Injectable bone cements made with calcium sulfate (CS) are of significant interest, owing to its compatibility and optimal self-setting property. Its rapid resorption rate, lack of bioactivity, and poor mechanical strength serve as a deterrent for its wide application. Herein, a significantly improved CS-based injectable bone cement (modified calcium sulfate termed as CS_mod), reinforced with various concentrations (0–15%) of a conductive nanocomposite containing gold nanodots and nanohydroxyapatite decorated reduced graphene oxide (rGO) sheets (AuHp@rGO), and functionalized with vancomycin, is presented. The piezo-responsive cement exhibits favorable injectability and setting times, along with improved mechanical properties. The antimicrobial, osteoinductive, and osteoconductive properties of the CS_mod cement are confirmed using appropriate in vitro studies. There is an upregulation of the paracrine signaling mediated crosstalk between mesenchymal stem cells and human umbilical vein endothelial cells seeded on these cements. The ability of CS_mod to induce endothelial cell recruitment and augment bone regeneration is evidenced in relevant rat models. The results imply that the multipronged activity exhibited by the novel-CS_mod cement would be beneficial for bone repair.