A dense SERS substrate of the AgNPs@GO compound film for detecting homocysteine molecules.

This study focuses on the development of a highly sensitive surface-enhanced Raman scattering (SERS) sensor for detecting homocysteine (Hcy) molecules. The Hcy sensor was created by depositing silver nanoparticles (AgNPs) onto the surface of graphene oxide (GO) film to form a dense AgNPs@GO composite film. The AgNPs on the composite film interacted with sulfur atoms (S) of Hcy molecules to form Ag-S bonds, which boosted the chemisorption of Hcy molecules and enabled them to be specifically recognized. The SERS sensor exhibited a maximum enhancement factor of up to 1.1 × 104, with a reliable linear response range from 1 to 60 ng mL-1. The limit of detection (LOD) for Hcy molecules was as low as 1.1 × 10-9 M. Moreover, Hcy molecules were successfully distinguished in a mixed solution of γ-aminobutyric acid and Hcy molecules. In this study, a simple preparation process of SERS substrate and a novel detection method for Hcy molecules provided a new pathway for the rapid and effective detection of Hcy molecules in the food and biomedicine fields.

A highly sensitive electrochemical sensor by growing Ag nanoparticles on the surface of PPy@PEDOT:PSS film for detecting sodium hydroxymethanesulfinate molecules.

A high-sensitivity electrochemical sensor was fabricated via in situ growth of Ag nanoparticles (AgNPs) on the surface of a polypyrrole@poly(3,4-ethylenedioxythiophene):polystyrene sulfonic acid (PPy@PEDOT:PSS) film for detecting sodium hydroxymethanesulfinate (SHF) molecules in milk and rice flour samples. The sensor fabrication process involved randomly decorating Ag seed points on the porous PPy@PEDOT:PSS film via a chemical reduction process using a AgNO3 solution. Next, AgNPs were anchored on the PPy@PEDOT:PSS film surface using an electrochemical deposition method to prepare a sensor electrode. Under optimal conditions, the sensor exhibits a good linear relation within a range of 1-130 ng/mL for real milk and rice flour samples and its limit-of-detection values were up to 0.58 and 0.29 ng/mL, respectively. Additionally, Raman spectroscopy was used to identify the byproducts of the chemical reaction, such as formaldehyde. This AgNP/PPy@PEDOT:PSS film-based electrochemical sensor offers a simple and rapid method for detecting SHF molecules in food products.

A Multilayer Interlaced Ag Nanosheet Film Prepared by an Electrodeposition Method on a PPy@PEDOT:PSS Film: A Strategy to Prepare Sensitive Surface-Enhanced Raman Scattering Substrates.

A highly sensitive multilayer interlaced silver (Ag) nanosheet (MISN) film was prepared on a PPy@PEDOT:PSS film via an electrodeposition method for surface-enhanced Raman scattering (SERS) applications. After the PPy@PEDOT:PSS film was pretreated with ascorbic acid solution, many sparse Ag nanoparticles (NPs) could be directly reduced on the surface of the PPy@PEDOT:PSS film in AgNO3 solution. Then, the MISN film was directionally grown along the surface of sparse Ag NPs by using an electrochemical galvanostatic method to form a Ag/PPy@PEDOT:PSS film for a SERS substrate. The results indicated that with the increase in electrodeposition time, the density of Ag nanosheets was also increased for boosting the SERS effect. Accordingly, owing to the directional growth of Ag NPs, the increase in the length-width ratio of single Ag nanosheets would further promote the SERS signal of the substrate. Moreover, the maximum enhancement factor of the SERS substrate could reach to 12,478, and the minimum limit of detection of melamine solution was down to 5.42 ng/mL. The SERS sensitivity of the Ag nanosheet film reached 100.65. This method of preparing the SERS substrate provides a novel and robust strategy for the low-cost and high-sensitivity detection in biomedicine, drugs, and food.

Research on the photoluminescence properties of Cu2+-doped perovskite CsPbCl3 quantum dots.

CsPbX3 (X = Cl, Br, and I) quantum dots (QDs) and Cu2+-doped CsPbCl3 QDs with different Cu-to-Pb molar ratios were synthesized via a solvent-based thermal synthesis method. The photoluminescence (PL) properties of these Cu2+-doped CsPbCl3 QDs were also investigated in this study. The results showed that with the increase in the Cl- concentration the surface defects of CsPb(Cl/Br)3 QDs increased, which resulted in an increase in the non-radiative recombination of excitons and weakened the PL intensity. Moreover, Cu2+-doped CsPbCl3 QDs maintained the cubic crystal structure of the initial phases. Owing to the doping of Cu2+ ions, the surface defects of CsPbCl3 QDs were effectively eliminated, which facilitated the excitonic recombination via a radiative pathway. The PL quantum yields (PLQYs) of Cu2+-doped CsPbCl3 QDs were increased to 51%, showing great photostability. From the results, it is believed that Cu:CsPbCl3 QDs can be widely used in optoelectronic devices.

Triple-band black-phosphorus-based absorption using critical coupling.

Black phosphorus (BP) is an important two-dimensional material that plays a key role in new photoelectric devices. In this work, a triple-band BP-based absorber was proposed, in which a monolayer BP is coupled with the missing angle rectangular structure. Due to the critical coupling of the guided resonance, the BP absorber achieves a triple-band absorption. The results showed that the absorption spectra at 2901.76 nm, 3810.71 nm, and 4676.97 nm under TM polarization achieve a high absorption of 95.45%, 98.68%, and 98.06%, respectively. In addition, the absorption peak and resonance wavelength can be flexibly adjusted by the electron doping of BP, the geometrical parameters of the structure, and the refractive index of the dielectric substrate. Because of the anisotropy properties of BP, the structure exhibits polarization-dependent absorption characteristics. Thus, the missing angle rectangular structure will provide a potential to design mid-infrared absorbers and shows a significant practical application in many photoelectric devices such as photodetectors, modulators, and optical switches.

Translational Informatics for Parkinson's Disease: from Big Biomedical Data to Small Actionable Alterations.

Parkinson's disease (PD) is a common neurological disease in elderly people, and its morbidity and mortality are increasing with the advent of global ageing. The traditional paradigm of moving from small data to big data in biomedical research is shifting toward big data-based identification of small actionable alterations. To highlight the use of big data for precision PD medicine, we review PD big data and informatics for the translation of basic PD research to clinical applications. We emphasize some key findings in clinically actionable changes, such as susceptibility genetic variations for PD risk population screening, biomarkers for the diagnosis and stratification of PD patients, risk factors for PD, and lifestyles for the prevention of PD. The challenges associated with the collection, storage, and modelling of diverse big data for PD precision medicine and healthcare are also summarized. Future perspectives on systems modelling and intelligent medicine for PD monitoring, diagnosis, treatment, and healthcare are discussed in the end.

Enhanced and broadened fluorescence of ZnSe quantum dots enabled by the fluorescence energy transfer system of ZnSe quantum dots and gold nanoparticles.

The enhanced and broadened fluorescence of ZnSe quantum dots (QDs) were studied by using a fluorescence energy transfer system (FETS) of ZnSe QDs and gold nanoparticles (NPs). The FETS were prepared via uniformly dispersing the gold nanoparticles into ZnSe QD solution in the condition of magnetic stirring. Enhanced and broadened fluorescence was observed on the film of the FETS due to the transfer of photo-generated carriers between the ZnSe QDs and the gold NPs, instead of the surface plasma resonance effect. The excitonic and enhanced fluorescence on the FETS film depended on the competition of electron-hole recombination and electron transfer from the ZnSe QDs to the gold NPs. In addition, because of the excitonic fluorescence of the ZnSe QDs absorbed by the gold NPs, the electrons of the s-p band of the gold NPs were further increased to facilitate its energy level shift toward the conduction band of the ZnSe QDs in order to create a blueshift in the enhanced fluorescence. This enhanced and broadened fluorescence method can be applied for controlling fluorescence in photoelectric detection, photodiodes, lightshows, and sensor devices.

Preparation of porous Fe2O3 nanorods-reduced graphene oxide nanohybrids and their excellent microwave absorption properties.

In this paper, α-Fe2O3 nanoparticles (NPs)-reduced graphene oxide (RGO), α-FeOOH nanorods (NRs)-RGO and porous α-Fe2O3 NRs-RGO could be selectively synthesized by hydrothermal method. The investigations indicated that the obtained α-Fe2O3 NPs, α-FeOOH NRs and porous α-Fe2O3 NRs were either attached on the surface of RGO sheets or coated uniformly by the RGO sheets. And the as-prepared nanohybrids exhibited excellent microwave absorption performance, which was proved to be ascribed to the quarter-wavelength matching model. The optimum reflection loss (RL) values for α-Fe2O3 NPs-RGO, α-FeOOH NRs-RGO and porous α-Fe2O3 NRs-RGO were ca. -32.3, -37.4 and -71.4 dB, respectively. Moreover, compared to the obtained α-Fe2O3 NPs-RGO and α-FeOOH NRs-RGO, the as-prepared porous α-Fe2O3 NRs-RGO nanohybrids exhibited enhanced microwave absorption properties because of their special structure and synergetic effect. The possible enhanced microwave absorption mechanisms were discussed in details. Our results confirmed that the geometrical morphology had a great influence on their microwave absorption properties, which provided a promising approach to exploit high performance microwave absorbing materials.

Water-assisted and controllable synthesis of core/shell/shell structured carbon-based nanohybrids, and their magnetic and microwave absorption properties.

By controlling the pyrolysis temperature, core/shell/shell structured Fe/Fe5C2/carbon nanotube bundles (Fe/Fe5C2/CNTBs), Fe/Fe3C/helical carbon nanotubes (Fe/Fe3C/HCNTs) and Fe/Fe3C/chain-like carbon nanospheres (Fe/Fe3C/CCNSs) with high encapsulation efficiency could be selectively synthesized in large-scale by water-assisted chemical vapor deposition method. Water vapor was proved to play an important role in the growth process. Because of α-Fe nanoparticles tightly wrapped by two layers, the obtained core/shell/shell structured nanohybrids showed high stabilities and good magnetic properties. The minimum reflection loss values of the as-prepared nanohybrids reached approximately -15.0, -46.3 and -37.1 dB, respectively. The excellent microwave absorption properties of the as-prepared core/shell/shell structured nanohybrids were considered to the quarter-wavelength matching model. Moreover, the possible enhanced microwave absorption mechanism of the as-prepared Fe/Fe3C/HCNTs and Fe/Fe3C/CCNSs were discussed in details. Therefore, we proposed a simple, inexpensive and environment-benign strategy for the synthesis of core/shell/shell structured carbon-based nanohybrids, exhibiting a promising prospect as high performance microwave absorbing materials.

Enhancement effect of defect fluorescence of ZnSe quantum dots on a heterojuction of ZnSe quantum dots and gold nanoparticles.

We studied an enhancement effect of defect fluorescence of ZnSe quantum dots (QDs) on a heterojunction of ZnSe QDs and gold nanoparticles. The photoluminescence (PL) of Au/ZnSe heterojunction is excited by using a 150 nm diameter ultraviolet laser spot of a scanning near-field optical microscope. Owing to the charge transfer of photon-generated carriers from ZnSe QDs, the enhanced PL effect is observed, which results from the increase of the built-in electric field to hinder the electron transfer to gold nanoparticles and is trapped by the defect states of ZnSe QDs. The broadening of defect fluorescence spectra and the reduction of excitonic fluorescence in multi-heterojunction of ZnSe QDs and gold nanoparticles are also observed which is attributed to an increase of their contact areas. We believe that enhanced defect fluorescence method described in this paper have potential applications in forming uniform optoelectronic heterojunction in controlling and boosting fluorescent efficiency of weak PL devices.

Enhanced photoluminescence of corrugated Al2O3 film assisted by colloidal CdSe quantum dots.

We present the enhanced photoluminescence (PL) of a corrugated Al2O3 film enabled by colloidal CdSe quantum dots. The colloidal CdSe quantum dots are fabricated directly on a corrugated Al2O3 substrate using an electrochemical deposition (ECD) method in a microfluidic system. The photoluminescence is excited by using a 150 nm diameter ultraviolet laser spot of a scanning near-field optical microscope. Owing to the electron transfer from the conduction band of the CdSe quantum dots to that of Al2O3, the enhanced photoluminescence effect is observed, which results from the increase in the recombination rate of electrons and holes on the Al2O3 surface and the reduction in the fluorescence of the CdSe quantum dots. A periodically-fluctuating fluorescent spectrum was exhibited because of the periodical wire-like corrugated Al2O3 surface serving as an optical grating. The spectral topographic map around the fluorescence peak from the Al2O3 areas covered with CdSe quantum dots was unique and attributed to the uniform deposition of CdSe QDs on the corrugated Al2O3 surface. We believe that the microfluidic ECD system and the surface enhanced fluorescence method described in this paper have potential applications in forming uniform optoelectronic films of colloidal quantum dots with controllable QD spacing and in boosting the fluorescent efficiency of weak PL devices.

Heteronanostructured Co@carbon nanotubes-graphene ternary hybrids: synthesis, electromagnetic and excellent microwave absorption properties.

In order to explore high efficiency microwave absorption materials, heteronanostructured Co@carbon nanotubes-graphene (Co@CNTs-G) ternary hybrids were designed and produced through catalytic decomposition of acetylene at the designed temperature (400, 450, 500 and 550 °C) over Co3O4/reduced graphene oxide (Co3O4/RGO). By regulating the reaction temperatures, different CNT contents of Co@CNTs-G ternary hybrids could be synthesized. The investigations indicated that the as-prepared heteronanostructured Co@CNTs-G ternary hybrids exhibited excellent microwave absorption properties, and their electromagnetic and microwave absorption properties could be tuned by the CNT content. The minimum reflection loss (RL) value reached approximately -65.6, -58.1, -41.1 and -47.5 dB for the ternary hybrids synthesized at 400, 450, 500 and 550 °C, respectively. And RL values below -20 dB (99% of electromagnetic wave attenuation) could be obtained over the as-prepared Co@CNTs-G ternary hybrids in the large frequency range. Moreover, based on the obtained results, the possible enhanced microwave absorption mechanisms were discussed in details. Therefore, a simple approach was proposed to explore the high performance microwave absorbing materials as well as to expand the application field of graphene-based materials.