• Bulletin of the Korean Chemical Society
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• 제31권11호
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• pp.3212-3216
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• 2010

A new rhodamine-based sensor 1 was designed and synthesized by incorporating rhodamine B and benzimidazole moieties. Sensor 1 exhibits high selectivity and sensitivity to $Cu^{2+}$ in $CH_3CN$-water solution (HEPES buffer, pH = 7.0) with an obvious color change from colorless to pink. Other metal ions such as $Hg^{2+}$, $Ag^+$, $Pb^{2+}$, $Sr^{2+}$, $Ba^{2+}$, $Cd^{2+}$, $Ni^{2+}$, $Co^{2+}$, $Fe^{2+}$, $Mn^{2+}$, $Cu^{2+}$, $Zn^{2+}$, $Ce^{3+}$, $Mg^{2+}$, $K^+$ and $Na^+$ had no such color change and have no significant influence on $Cu^{2+}$ recognition process. The interaction of $Cu^{2+}$ and sensor 1 was proven to adopt a 1:1 binding stoichiometry and the recognition process is reversible.

• 전기전자학회논문지
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• 제22권4호
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• pp.1062-1067
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• 2018

본 연구에서는 화학센서의 개발에 있어서 감지 대상 물질을 정확히 선택적으로 인식하고 그 결과를 물리적 신호로서 발산할 수 있는 분자시스템이 화학센서의 감지부에 도입되고 이러한 기술을 바탕으로 효율적인 감지기술의 개발이 요청되고 있어 미량의 중금속 이온 측정용 화학센서의 연구를 하였다. 본 연구에서는 감지 대상 물질로서 저 농도의 $Ag^+$, $Cu^{2+}$ 이온들을 통하여 이들에 대한 선택적인 감지 결과를 SPR 센서를 응용한 인식 기능성 감지 막 제조를 하여 측정대상 금속이온들에 대한 선택적인 측정을 하여 저 농도에서 매우 정밀 하게 감지 가능한 센서시스템을 구현하였다. 이 결과 DTSQ-dye를 이용한 감지 막 측정 결과의 경우 저 농도 $Ag^+$이온에 따른 공명각의 변화는 $Ag^+$ 이온의 최고농도인 $10^{-4}M$ 까지 공명각의 변화는 $2.17[^{\circ}]$이며, 다른 금속과 비교 시 약 4.3배나 되는 큰 공명각의 변화를 보였고, SQ-dye를 이용한 감지막 측정 결과의 경우 저 농도 $Cu^{2+}$ 이온에 따른 공명각의 변화는 $Cu^{2+}$의 최고농도인 $10^{-4}M$ 까지 공명각의 변화는 $2.3[^{\circ}]$이며 다른 금속과의 비교시 약 4.5배나 되는 큰 공명각의 변화를 보였다.

• Bulletin of the Korean Chemical Society
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• 제31권3호
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• pp.615-619
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• 2010

A new coumarin-thiazolobenzo-crown ether based fluorogenic chemosensor BTC (1) was reported. The ion-selective binding properties of 1 with different alkali, alkaline earth metals and transitional metals were investigated in an ethanol-DMSO system. BTC (1) showed the highest binding constant toward $Hg^{2+}$ over $Ag^+$, $Pb^{2+}$ and $Cu^{2+}$.

• Bulletin of the Korean Chemical Society
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• 제34권10호
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• pp.3088-3092
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• 2013

A novel PVC membrane sensor for perindopril based on perindopril-phosphotungstate ion pair complex was prepared. The influence of membrane composition (i.e. percent of PVC, plasticizer, ion-pair complex, and kind of plasticizer), inner solution, pH of test solution and foreign cations on the electrode performance was investigated. The optimized membrane demonstrates Nernstian response ($30.9{\pm}1.0$ mV per decade) for perindopril cations over a wide linear range from $9.0{\times}10^{-7}$ to $1{\times}10^{-2}$ M at $25^{\circ}C$. The potentiometric response is independent of the pH in the range of 4.0-9.5. The proposed sensor has the advantages of easy preparation, fast response time. The selectivity coefficients indicate excellent selectivity for perindopril over many common cations (e.g., $Na^+$, $K^+$, $Mg^{2+}$, $Cu^{2+}$, $Ni^{2+}$, rhamnose, maltose, glycine and benzamide. The practical applications of this electrode was demonstrated by measuring the concentrations of perindopril in pure solutions and pharmaceutical preparations with satisfactory results.

• 센서학회지
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• 제33권5호
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• pp.366-372
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• 2024

In this study, we present a novel approach to improve electrochemical heavy metal ion (HMI) sensing responses via post-synthetic modification of carbon nanotube-based metal-organic framework (MOF) nanocomposites with a Schiff base. UiO66-NH₂ was employed as the MOF and incorporated with multi-walled carbon nanotubes (MWCNT) through in-situ growth, enhancing the electrical conductivity of the MWCNT-UiO66-NH₂ composite. Subsequently, the Schiff base, which has been proven to be an excellent ligand for metal ion detection, was functionalized onto MWCNT-UiO66-NH₂ via post-synthetic modification to improve its HMI absorption capacity. To evaluate the effect of the Schiff base on HMI detection capacity, electrochemical sensing of Cd²⁺, Pb²⁺, Cu²⁺, and Hg²⁺ was performed in an aqueous solution utilizing the MWCNT-UiO66-Schiff modified electrode as well as the bare electrode. Individual differential pulse anodic stripping voltammetry results revealed that the modified electrode with MWCNT-UiO66-Schiff exhibited increased HMI sensing properties, especially with 1.82-fold improvement in average oxidation currents toward 10 µM of Cu²⁺ compared to that for a bare glassy carbon electrode. The selective Cu²⁺-sensing properties of MWCNT-UiO66-Schiff were reflected in the highly selective Cu²-binding affinity of the Schiff base-containing model molecules compared to those of Cd²⁺, Hg²⁺, and Pb²⁺. Our work provides a new strategy for improving the sensing properties of electrochemical HMI sensors by the post-synthetic modification of MWCNT-UiO66 with a Schiff base.

• EDISON SW 활용 경진대회 논문집
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• 제3회(2014년)
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• pp.275-285
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• 2014

Dipyrene-based fluorescent chemosensor(분자 1)가 개발되었다. 분자 1은 여러 금속이온 중 $Cu^{2+}$와 $Hg^{2+}$의 fluorescent chemosensor로서 센싱할 수 있고, excimer-switch off mechanism에 따라 $Cu^{2+}$와 $Hg^{2+}$ 금속이온을 감지한다. Ground state와 excited state에 대한 DFT와 TD-DFT 방법을 통해 분자 1의 $Hg^{2+}$에 대한 형광 turn on/off을 확인하고, 구조변화에 따른 molecular orbital을 계산하였다. 계산결과 분자 1은 excited state에서 excimer를 형성할 수 있으나 $1+Hg^{2+}$는 excimer를 형성하지 못함을 알 수 있었다. 여기서 우리는 분자 1과 $Hg^{2+}$ 금속이온 결합에 대하여 실험값과 비교 분석하여 그 메커니즘 조사하였다.

• 한국자기학회지
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• 제22권5호
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• pp.173-177
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• 2012

미크론 자성비드 검출용 바이오센서에 활용하는 GMR-SV 박막을 이온빔 스퍼터링 증착법으로 glass/Ta(5.8 nm)/NiFe(5 nm)/Cu(t nm)/NiFe(3 nm)/FeMn(12 nm)/Ta(5.8 nm)의 구조를 갖도록 증착하였다. 비자성체 Cu의 두께가 3.0 nm에서 2.2 nm까지 얇아질수록 교환결합력은 증가하였고 자기저항비는 다소 감소하였다. 비자성체의 두께가 얇으면 반강자성체의 층간 교환작용이 강자성체의 고정층뿐만 아니라 자유층의 스핀배열에도 영향을 주고 있음을 확인할 수 있었다. 또한 리소그래피 공정 과정을 거쳐 GMR-SV 소자를 제작하여 미크론 자기비드를 검출하였다. 여기서 자기비드를 떨어뜨리기 전과 후의 자기저항비, 교환결합력, 보자력은 각각 0.9%, 3Oe, 2 Oe의 값을 나타내었다. 이러한 결과로 나노 단위의 바이오센서에 활용할 수 있는 가능성을 보여주었다.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2013년도 제44회 동계 정기학술대회 초록집
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• pp.85-85
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• 2013

Label-free, sensitive and selective detection methods with high spatial resolution are critically required for future applications in chemical sensor, biological sensor, and nanospectroscopic imaging. Here I describe the development of Plasmon Resonance Energy Transfer (PRET)-based molecular imaging in living cells as the first demonstration of intracellular imaging with PRET-based nanospectroscopy. In-vivo PRET imaging relied on the overlap between plasmon resonance frequency of gold nanoplasmonic probe (GNP) and absorption peak frequencies of conjugated molecules, which leads to create 'quantized quenching dips' in Rayleigh scattering spectrum of GNP. The position of these dips exactly matched with the absorption peaks of target molecules. As another innovative application of PRET, I present a highly selective and sensitive detection of metal ions by creating conjugated metal-ligand complexes on a single GNP. In addition to conferring high spatial resolution due to the small size of the metal ion probes (50 nm in diameter), this method is 100 to 1,000 folds more sensitive than organic reporter-based methods. Moreover, this technique achieves high selectivity due to the selective formation of Cu2+complexes and selective resonant quenching of GNP by the conjugated complexes. Since many metal ion ligand complexes generate new absorption peak due to the d-d transition in the metal ligand complex when a specific metal ion is inserted into the complex, we can match with the scattering frequency of nanoplasmonic metal ligand systems and the new absorption peak.

• 센서학회지
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• 제22권1호
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• pp.89-94
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• 2013

In this paper, we developed a beam of MEMS probe card using a BeCu sheet. Silicon wafer thickness of $400{\mu}m$ was fabricated by using deep reactive ion etching (RIE) process. After forming through silicon via (TSV), the silicon wafer was bonded with BeCu sheet by soldering process. We made BeCu beam stress-free owing to removing internal stress by using joule heating. BeCu beam was fused by using joule heating caused by high current. The fabricated BeCu beam measured length of 1.75 mm and width of 0.44 mm, and thickness of $15{\mu}m$. We measured fusing current as a function of the cutting planes. Maximum current was 5.98 A at cutting plane of $150{\mu}m^2$. The proposed low-cost and simple fabrication process is applicable for producing MEMS probe beam.

• Current Applied Physics
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• 제18권11호
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• pp.1255-1260
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• 2018

In this work, a green and simple one-pot route was developed for the synthesis of highly fluorescent aminofunctionalized graphene quantum dots (a-GQDs) via hydrothermal process without any further modification or surface passivation. We synthesized the a-GQDs using glucose as the carbon source and ammonium as a functionalizing agent without the use of a strong acid, oxidant, or other toxic chemical reagent. The as-obtained aGQDs have a uniform size of 3-4 nm, high contents of amino groups, and show a bright green emission with high quantum yield of 32.8%. Furthermore, the a-GQDs show effective fluorescence quenching for $Cu^{2+}$ ions which can serve as effective fluorescent probe for the detection of $Cu^{2+}$. The fluorescent probe using the obtained aGQDs exhibits high sensitivity and selectivity toward $Cu^{2+}$ with the limit of detection as low as 5.6 nM. The mechanism of the $Cu^{2+}$ induced fluorescence quenching of a-GQDs can be attributed to the electron transfer by the formation of metal complex between $Cu^{2+}$ and the amino groups on the surface of a-GQDs. These results suggest great potential for the simple and green synthesis of functionalized GQDs and a practical sensing platform for $Cu^{2+}$ detection in environmental and biological applications.