김주훈 교수

We demonstrate the feasible use of Pt nanoparticles encapsulated inside amine-terminated fourth-generation polyamidoamine dendrimers as peroxidase-mimetic labels for sensitive colorimetric assays. This was performed by utilizing intrinsic dual functionalities of the dendrimer-encapsulated Pt nanoparticles, i.e. peroxidase-like activity and multiple conjugation sites.

Recent advances in metasurface lenses (metalenses) have shown great potential for opening a new era in compact imaging, photography, light detection, and ranging (LiDAR) and virtual reality/augmented reality applications. However, the fundamental trade-off between broadband focusing efficiency and operating bandwidth limits the performance of broadband metalenses, resulting in chromatic aberration, angular aberration, and a relatively low efficiency. A deep-learning-based image restoration frame

This article describes a method for the global profiling of the substrate specificities of DNA ligases and illustrates examples using the Taq and T4 DNA ligases. The method combines oligonucleotide arrays, which offer the benefits of high throughput and multiplexed assays, with mass spectrometry to permit label-free assays of ligase activity. Arrays were prepared by immobilizing ternary biotin-tagged DNA substrates to a self-assembled monolayer presenting a layer of streptavidin protein. The arr

Turn-on type fluorescence sensing of O₂ is considered a promising approach to developing ways to measure O₂ in microenvironments with spatially distributed O₂ levels. As a class of nanomaterials with a high degree of control over composition and structure, dendrimer-encapsulated nanoparticles (DENs) are promising candidates to mimic biological enzymes. Here, we report a strategy to monitor spatially distributed O₂ across a three-dimensional (3D) human

We demonstrate a method for constructing bifunctional nanostructures, which conjugate biochemical and electrocatalytic activities, on glassy carbon surfaces by decorating the carbon surfaces with both biologically active glucose oxidases and size-monodisperse Pt nanoparticles (less than 2 nm in diameter) utilizing only a single dendrimer layer.

A chemosensor compound (1) consisting of a central ferrocene with two butylaminomethyl arms showed unexpected facile electrochemical oxidation of the secondary amines in proximity to the ferrocene, which was utilized for electrochemical discrimination of phthalic acid selectively over two other isomers, isophthalic acid and terephthalic acid.

In this study, we report the controllable synthesis of dendrimer-encapsulated Pt nanoparticles (Pt DENs) utilizing repetitively coupled chemical reduction and galvanic exchange reactions. The synthesis strategy allows the expansion of the applicable number of Pt atoms encapsulated inside dendrimers to more than 1000 without being limited by the fixed number of complexation sites for Pt²⁺ precursor ions in the dendrimers. The synthesis of Pt DENs is achieved in a short period of time (

We report the electrochemical grafting of amine-terminated dendrimers encapsulating nanoparticles onto indium tin oxide (ITO) surfaces.

Abstract Enhanced electrochemiluminescence (ECL) of luminol was reported with the use of dendrimer‐encapsulated Au nanoparticle (Au DEN)‐modified ITOs in the presence of hydrogen peroxide, which was applied for sensitive ECL‐based electroanalysis of hydrogen peroxide. The enhanced ECL of luminol in the presence of hydrogen peroxide was attributed to facile electrochemical oxidation of luminol/hydrogen peroxide on the Au DEN‐modified ITOs at potentials as low as ∼0.4 V (vs. Ag/AgCl). Spooling ECL

Abstract We report the electrochemiluminescence (ECL) of water‐soluble individual Au nanoclusters (Au NCs) fractionated by polyacrylamide gel electrophoresis of Au NCs synthesized using glutathione. The individual Au NCs demonstrated unique and significant differences in ECL. Interestingly, they exhibited near‐infrared (near‐IR) ECL that became dominant when the ratio of Au(I) to Au(0) decreased in the individual Au NCs. This indicated that the oxidation states of Au NCs primarily affected the E

In this work, we report a bipolar electrode (BPE) array system with self-driven optical readouts of the faradic current flowing through the BPEs. The BPE array system is based on the spontaneous redox reactions that are respectively occurring at opposite poles of the BPEs with appropriate electrocatalysts on the poles; this system is analogous to one consisting of galvanic electrochemical cells. The galvanic BPE array system operates in a self-powered mode that requires there to be neither a dir