Freemansantiago4691

Surface enhanced Raman scattering (SERS)-based nanoprobes have been used as well-established analytical tools enabling single-molecule detection. In this work, we report a facile method to decorate sea urchin-like gold nanoparticles (SUGNPs) on the surface of PMMA/P4VP nanofibers. Firstly, PMMA/P4VP nanofibers within the submicrometer size range were prepared by applying the electrospinning technique. Then, the incorporation of SUGNPs on the surface of PMMA/P4VP nanofiber was achieved by immersing PMMA/P4VP nanofiber into freshly prepared SUGNP aqueous solution through the specific Au-N interactions. The as-fabricated SUGNP-coated PMMA/P4VP nanofibers exhibited good sensitivity and reproducibility in SERS measurements with the relative standard deviation down to 6.6%, by employing 4-mercaptobenzoic acid as a probe molecule with 30 min of soaking time. Hence, we envisage that the SUGNP-coated PMMA/P4VP nanofibers can act as efficient and stable SERS substrates for potential applications in molecular detection as well as chemical and biological analysis.

The anisotropic nature of colloidal particles results in orientation-dependent interactions that organize the particles into peculiar structures different from those formed by isotropic colloids. Particles with a hydrophilic hemisphere are expected to assemble in hydrophobic solvents due to the contribution of hydrophobic interactions as observed for molecular amphiphiles.

Asymmetrically decorated silica-based Janus particles are dispersed in an apolar solvent, chloroform, and their structure and dynamics are studied by light scattering and compared with computer simulations.

Gelation of amphiphilic Janus particles with asymmetric surface decoration is observed in a hydrophobic medium. The influence of particle asymmetry on gel structure and dynamics is discussed. Unlike particles with long-range repulsive interactions in water, these systems rapidly form rather compact structures that are nevertheless more ramified than those made of isotropic hydrophobic particles. Comparison with computer simulations allows visualization of the gel and reveals a contribution of asymmetric short-range attractions and cross-term repulsions to the net effective interaction potential.

Gelation of amphiphilic Janus particles with asymmetric surface decoration is observed in a hydrophobic medium. The influence of particle asymmetry on gel structure and dynamics is discussed. Unlike particles with long-range repulsive interactions in water, these systems rapidly form rather compact structures that are nevertheless more ramified than those made of isotropic hydrophobic particles. Comparison with computer simulations allows visualization of the gel and reveals a contribution of asymmetric short-range attractions and cross-term repulsions to the net effective interaction potential.The intrinsic faradic reactivity is the uppermost factor determining the charge storage capability of battery material, the construction of p-n junction composing of different faradic components is a rational tactics to enhance the faradic activity. Herein, a reduced graphene oxide@cobalt nickle sulfide@nickle cobalt layered double hydroxide composite (rGO@CoNi2S4@NiCo LDH) with p-n junction structure is designed by deposition of n-type nickle cobalt layered double hydroxide (NiCo LDH) around p-type reduced graphene oxide@cobalt nickle sulfide (rGO@CoNi2S4), the charge redistribution across the p-n junction enables enhanced faradic activities of both components and further the overall charge storage capacity of the resultant rGO@CoNi2S4@NiCo LDH battery electrode. As expected, the rGO@CoNi2S4@NiCo LDH electrode can deliver high specific capacity (Cs, 1310 ± 26 C g-1 at 1 A g-1) and good cycleability (77% Cs maintaining ratio undergoes 5000 charge-discharge cycles). Furthermore, the hybrid supercapacitor (HSC) based on the rGO@CoNi2S4@NiCo LDH p-n junction battery electrode exports high energy density (Ecell, 57.4 Wh kg-1 at 323 W kg-1) and good durability, showing the prospect of faradic p-n junction composite in battery typed energy storage.The self-healing mechanism and bioelectrochemical interface properties of supramolecular gels have been rarely explored. In this context, we propose a constitutive "fibril-reorganization" model to reveal the self-healing mechanism of a series of core-shell structured guanosine-borate (GB) hydrogels and emphasize that interfibrillar interactions at the supramolecular polymer scale (G-quadruplex nanowires) drive the self-healing process of GB hydrogels. Structure-electrochemical sensing performance studies reveal that GB hydrogel nanofibers with relatively strong biomolecular affinity such as -SH modified GB hydrogel (GB-SH) show a high sensitivity of response and low limit of detection for tumour marker alpha-fetoprotein sensing (AFP; 0.076 pg mL-1). Guanosine/ferroceneboronic acid (GB-Fc) hydrogel nanofibers with superior conductivity and redox activity display the widest linear detection range for AFP (0.0005-100 ng mL-1). Structure-property correlations of GB hydrogels provide useful insight for the future design of advanced self-healing materials and electrochemical biosensors.G-quadruplex (G4) is a non-canonical structure that is formed in G-rich sequences of nucleic acids. G4s play important roles in vivo, such as telomere maintenance, transcription, and DNA replication. β-Aminopropionitrile in vitro There are three typical topologies of G4 parallel, anti-parallel, and hybrid. In general, metal cations, such as potassium and sodium, stabilize G4s through coordination in the G-quartet. While G4s have some functions in vivo, there are many reports of developed applications that use G4s. As various conformations of G4s could form from one sequence depending on varying conditions, many researchers have developed G4-based sensors. Furthermore, G4 is a great scaffold of aptamers since many aptamers folded into G4s have also been reported. However, there are some challenges about its practical use due to the difference between practical sample conditions and experimental ones. G4 conformations are dramatically altered by the surrounding conditions, such as metal cations, pH, and crowding. Many studies have been conducted to characterize G4 conformations under various conditions, not only to use G4s in practical applications but also to reveal its function in vivo.