Jeong-Hoon Choi
Hanyang University · 材料科学
研究室紹介
Professor Jeong-Hoon Choi's research lab specializes in advanced 2D materials and environmental chemistry, with a focus on MXene-based nanomaterials for sensing and stability enhancement, and the formation mechanisms of hazardous disinfection by-products like N-nitrosodimethylamine (NDMA) in water treatment processes. The lab employs in situ characterization techniques such as RHEED and atomic-force microscopy to study epitaxial growth dynamics and surface reactions, while also developing innovative surface engineering strategies—like iCVD-deposited hydrophobic coatings—to improve the environmental stability of MXenes. A key research direction involves elucidating alternative pathways for NDMA formation that bypass traditional nitrosation mechanisms, particularly under chlorination and chloramination conditions.
Research Overview
Research Output Trend
Figures are computed from collected data and may differ slightly.
Selected Papers
15Abstract The main gas‐sensing mechanisms of 2D materials are surface charge transfer by analytes and Schottky barrier (SB) modulation at the interface between the metallic and semiconducting surfaces. In particular, dramatic differences in the gas‐sensing performances of 2D materials originate from SB modulation. However, SB sites typically exist only at the interface between the semiconducting channel material and the metal electrode. Herein, in situ formed multiple SBs in a single gas‐sensing
The formation of N-nitrosodimethylamine (NDMA) by the nitrosation of dimethylamine (DMA) is greatly enhanced by the presence of free chlorine (HOCl). The effect of HOCl appears at first to be contrary because HOCl rapidly oxidizes nitrite and hence should reduce NDMA formation from a mechanism involving classical nitrosation. The enhanced nitrosation by the presence of HOCl is, however, consistent with a mechanism that involves the formation of a highly reactive nitrosating intermediate such as
We have observed the growth mode transition from two-dimensional (2D) layer-by-layer to step-flow in the earliest stage growth of heteroepitaxial SrRuO3 thin films on TiO2-terminated (001) SrTiO3 substrates by in situ high pressure reflective high energy electron diffraction (RHEED) and atomic-force microscopy. There is no RHEED intensity recovery after each laser pulse in the first oscillation when the growth mode is 2D layer-by-layer. On the other hand, it is getting more pronounced in the sec
Developing a methodology to enhance long-term stability is one of the most important issues in MXene research, since they are prone to oxidation in the ambient environment. Although various approaches have been suggested to improve the stability of MXene, they have suffered from complicated processes and limited applicability to various types of MXene nanostructures. Herein, we report a simple and versatile technique to enhance the environmental stability of MXenes. Ti 3 C 2 T x MXene films were
Experiments were conducted to investigate the hypothesis that N-nitrosodimethylamine (NDMA) is a potential disinfection by-product. NDMA was formed by the reaction of dimethylamine (DMA) with monochloramine and also with free chlorine in the presence of ammonia. We proposed a mechanism for NDMA formation which does not require the presence of nitrite as in N-nitrosation. The critical NDMA formation reactions consist of i) the formation of monochloramine by combination of free chlorine with ammon
Studies were conducted to investigate the hypothesis that N-nitrosodimethylamine (NDMA) is a potential disinfection by-product specifically produced during chlorination or chloramination. Experiments were conducted using dimethylamine (DMA) as a model precursor. NDMA was formed by the reaction of DMA with free chlorine in the presence of ammonia and also with monochloramine. We proposed a mechanism for NDMA formation in chlorinated or chloraminated water, which does not require nitrite as in N-n
Covalent organic frameworks (COFs) are attracting increasing interest in various applications due to their ability to capture molecules originating from their highly crystallized porous structures. However, most types of COFs are non-conductive and cannot be directly applied to electronic devices. Herein, we utilize non-conductive COFs in chemiresistor sensors by forming composite structures with conductive reduced graphene oxide (rGO). The composites rGO@COF exhibit low-enough resistance to be
Research Areas
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