In this work, a nanocomposite containing gold (Au) nanofibers decorated iron-metal–organic framework (Fe-MOF) was successfully synthesized for electrochemical detection of acetaminophen (AAP). The as-synthesized Au@Fe-MOF nanocomposite was confirmed by various characterization techniques. Morphological analysis showed that the Au nanofibers with an average size of less than 10 nm were dispersed on the Fe-MOF. Cyclic voltammetric analysis showed that the Au@Fe-MOF nanocomposite showed well-defined redox peaks with higher current than that of GCE and Fe-MOF. The Au@Fe-MOF/ GCE exhibited a linear range, sensitivity, and detection limit of 0.5–18 μM, 4.95 μM/μA/cm2, and 0.12 μM, respectively. The Au@Fe-MOF/GCE showed a very low response for the interference materials. The real sample analysis revealed that the Au@Fe-MOF/GCE showed good recovery towards the AAP in urine and paracetamol. Therefore, the developed sensor can be used for quality control of AAP.

Herein, a new and generic strategy has been proposed to introduce uniformly distributed graphitic carbon into the nanostructured metal oxide. A facile and generic synthetic protocol has been proposed to introduce uniformly distributed conducting graphitic carbon into the Co3O4 nanoparticles ( Co3O4 NPs@graphitic carbon). The prepared Co3O4 NPs@graphitic carbon has been drop casted onto the portable screen-printed electrode (SPE) to realize its potential application in the individual and simultaneous quantification of toxic Pb(II) and Cd(II) ions present in aqueous solution. The proposed Co3O4 NPs@graphitic carbon-based electrochemical sensor exhibits a wide linear range from 0 to 120 ppb with limit of detection of 3.2 and 3.5 ppb towards the simultaneous detection of Pb(II) and Cd(II), which falls well below threshold limit prescribed by WHO.

본 연구는 나노섬유를 제조하는데 빠르고 효과적인 전기방사법을 이용하여 PVA(Polyvinyl alcohol)와 AgNO3를 혼합하여 제조한 용액을 금속산화물 기반 나노 섬유로 이루어진 투명 전극을 제조하고 그 특성을 분석하였다. PVA/AgNO3 혼합 용액을 전기방사법을 이용하여 유리기판 위에 나노 섬유 구조체 형태로 방사하여 250 ℃에서 2 시간 동안 열처리 과정을 통해 전기 전도성이 향상된 은 나노 섬유 기반 투명 전극을 제조하였다. 제조된 투명전극은 four-point probe 장비를 이용하여 전기적 특성을 분석하였으며, UV - Vis spectrophotometer 를 이용하여 제조된 투명전극의 투과도를 확인하였다. 또한, Scanning Electron Microscopy (SEM)과 Energy Dispersive Spectrometer(EDS)를 통해 은 나노 섬유의 표면 특성과 성분을 확인하였다. 이러한 분석들을 통해, 전기 방사 시간에 따른 면 저항과 투과도의 최적화된 조건을 확인할 수 있었으며, 은 나노 섬유로 이루어진 투명 전극은 전기적, 광학적, 기계적 특성이 우수하여 태양전지, 디스플레이, 터치스크린과 같은 차세대 유연 디스플레이에 적용 가능성을 보여주었다.

리튬금속전지(LMB)는 매우 큰 이론 용량을 갖지만 단락(short circuit), 수명 감소 등을 야기하는 덴드라이트(dendrite) 가 형성되는 큰 문제점을 갖고 있다. 본 연구에서는 poly(dimethylsiloxane) (PDMS)에 graphene oxide (GO) nanosheet를 고르게 분산시킨 PDMS/GO 복합체를 합성하였고 이를 박막 형태로 코팅하여 덴드라이트의 형성을 물리적으로 억제할 수 있는 막의 효과를 이끌어내었다. PDMS의 경우, 그 자체로는 이온 전도체가 아니기 때문에 리튬 이온의 통로를 형성시켜 리튬 이온의 이동을 원활하게 하기 위하여 5wt% 불산(HF)으로 에칭하여 PDMS/GO 박막이 이온전도성을 가질 수 있도록 하였다. 주사전자현미경(scanning electron microscopy, SEM)을 통해 전면 및 단면을 관찰하여 PDMS/GO 박막의 형상을 확인하였다. 그리고 PDMS/GO 박막을 리튬금속전지에 적용하여 실시한 배터리 테스트 결과, 100번째 사이클까지 쿨롱 효율(columbic efficiency) 이 평균 87.4%로 유지되었고, 박막이 코팅되지 않은 구리 전극보다 과전압이 감소되었음을 전압 구배(voltage profile) 를 통해 확인하였다.

리튬 덴드라이트의 효과적인 억제를 위해 유/무기 복합체를 리튬메탈 전극의 보호층으로 사용하였다. 유기물로는 PVDF-HFP가 사용되었으며 무기물로는 TiO2가 사용되었다. 유기물로 사용된 PVDF-HFP는 높은 유연성을 가지는 고분자로서 무기물의 matrix 역할을 하며, 무기물로 사용된 TiO2 나노입자는 보호막의 기계적 강도와 이온전도성을 향상시켜주는 역할을 하였다. 합성된 보호막은 SEM, AFM, XRD를 통하여 PVDF-HFP matrix에 TiO2가 잘 분산되어 있는 형태인 것을 확인할 수 있 었다. 또한 전기화학적 분석 결과, 향상된 기계적 물성과 이온전도성으로 인해 polymer-inorganic composite은 비교 샘플(untreated 와 PVDF-HFP 보호층) 대비 100번째 사이클까지 80%의 높은 쿨롱 효율 및 20 mV 미만의 낮은 과전압을 나타내었다.

A metal mesh TCE film is fabricated using a series of processes such as UV imprinting of a transparent trench pattern (with a width of 2-5 μm) onto a PET film, filling it with silver paste, wiping of the surface, and heatcuring the silver paste. In this work nanosized (40-50 nm) silver particles are synthesized and mixed with submicron (250-300 nm)-sized silver particles to prepare silver paste for the fabrication of metal mesh-type TCE films. The filling of these silver pastes into the patterned trench layer is examined using a specially designed filling machine and the rheological testing of the silver pastes. The wiping of the trench layer surface to remove any residual silver paste or particles is tested with various mixture solvents, and ethyl cellosolve acetate (ECA):DI water = 90:10 wt% is found to give the best result. The silver paste with 40-50 nm Ag:250-300 nm Ag in a 10:90 wt% mixture gives the highest electrical conductance. The metal mesh TCE film obtained with this silver paste in an optimized process exhibits a light transmittance of 90.4% and haze at 1.2%, which is suitable for TSP application.

The electrochemical performances of an asymmetric hybrid capacitor were investigated using LiFePO4 as the positive electrode and active carbon fibers(ACF) as the negative electrode. The electrochemical behaviors of a nonaqueous hybrid capacitor were characterized by constant current charge/discharge test. The specific capacitance using LiFePO4/ACF electrode turned out to be 0.87F/cm2 and the unit cell showed excellent cycling performance. This hybrid capacitor was able to deliver a specific energy as high as 178 Wh/kg at a specific power of 1,068 W/kg.

The power capacitors used as vehicle inverters must have a small size, high capacitance, high voltage, fast response and wide operating temperature. Our thin film capacitor was fabricated by alumina layers as a dielectric material and a metal electrode instead of a liquid electrolyte in an aluminum electrolytic capacitor. We analyzed the micro structures and the electrical properties of the thin film capacitors fabricated by nano-channel alumina and metal electrodes. The metal electrode was filled into the alumina nano-channel by electroless nickel plating with polyethylene glycol and a palladium catalyst. The spherical metals were formed inside the alumina nano pores. The breakdown voltage and leakage current increased by the chemical reaction of the alumina layer and PdCl2 solution. The thickness of the electroless plated nickel layer was 300 nm. We observed the nano pores in the interface between the alumina layer and the metal electrode. The alumina capacitors with nickel electrodes had a capacitance density of 100 nF/cm2, dielectric loss of 0.01, breakdown voltage of 0.7MV/cm and leakage current of 104μA.

반도체 메모리 소자에 이용되는 하부전극의 Pt 박막을 MOCVD 증착방법을 이용하여 SiO2(100nm)/Si 기판위에 증착하였다. 반응개스로 O2개스를 사용하였을 경우에 순수한 Pt 박막을 얻었으며 증착층은(11)우선방향을 가지고 성장하였다. 증착온도가 450˚C에서는 결정립 경계에 많은 hole이 형성되어 박막의 비저항을 증가시켰다. MOCVD에 의해 얻어진 Pt 박막은 전 증착온도범위에서 인장응력을 가지고 있었으며 400˚C이상의 온도에서 hole이 형성되면서 응력은 감소하였다. MOCVD-Pt 위에 PEMOCVD로 증착한 강 유전체 SrBi2Ta2O9박막은 균일하고 치밀한 미세구조를 보였다.

As industry continues to develop, the contents of various recalcitrant substances that are not removed by conventional wastewater treatment have increased in modern society. The metal working fluids (MWFs) used in the metal working process contain chemical substances, such as mineral oils, anticorrosive agents, extreme-pressure additives, and stabilizers, as well as high concentrations of organics and ammonia-nitrogen. Accordingly, MWFs are required to develop advanced treatments to conserve hydro-ecological resources. This study investigated the removal efficiency of ammonia nitrogen from MWFs according to operating time, applied voltage, and NaCl concentration using a Ti/IrO2 electrode in a batch-type reactor. The experimental results showed that ammonia-nitrogen removal efficiencies without NaCl were 89% and 92% when voltage was adjusted to 15 and 20 V for 60 min and removal efficiency was 90% at 25 V for 40 min. Removal efficiencies of 10 mM NaCl were 4% and 2% greater than those of not adding NaCl at 15 V for 50 min and 20 V for 30 min.

1900년대 초부터 금속 가공 장비의 수명 연장 및 가공물의 품질 향상을 위해 금속 가공 공정에 절삭유가 이용되어 왔다. 금속 가공 특성에 따라 절삭효율 향상을 위해 각종 첨가제를 포함시켜 여러 종류의 절삭유가 제조되고 있으며, 일반적으로 수용성과 비수용성으로 분류된다. 비수용성 절삭유의 경우, 폐유처리과정에서 유독성 물질 발생, 발연･발화 등의 문제로 수용성 절삭유의 사용이 점차 증가해 왔으며, 국내에서 이용되는 절삭유의 60% 이상이 수용성 절삭유이다. 사용된 수용성 절삭유는 비수용성 절삭유와 같이 소각처리 하기에는 비용이 크며, 수계로 유출시 COD 약 30,000~100,000ppm의 고농도 유기성분에 의해 인근 수계를 오염시킬 수 있으므로 각별한 처리가 필요하다. 따라서 본 연구에서는 Ti-IrO2전극을 이용하여 NaCl 첨가, 인가전압 변화를 통해 수용성 절삭유 내 오염물질의 전기화학적 처리에 미치는 영향을 검토하고, 수용성 절삭유의 전기화학적 처리에 대한 기초자료를 제공하고자 한다. 시료는 U사의 W1-1종 수용성 절삭유를 이용하였으며 증류수와 혼합하여 5% 농도의 인공 시료를 제조하였다. 시료의 특성은 Table 1, 실험 조건은 Table 2에 나타내었다.

Generally, metal working fluids (MWFs) are used to reduce friction in metalworking processes. In addition to mineral oils, MWFs contain many chemical substances, such as anticorrosive agents, extreme-pressure additives, and stabilizers, as well as high concentrations of organics and ammonia nitrogen. Accordingly, MWFs must be managed to advanced treatment for hydro-ecological conservation. This study investigated the removal efficiency of ammonia nitrogen from MWFs according to operating time, applied voltage, distance between electrodes, and NaCl concentration using aluminum in a batch-type reactor. The experimental results were as follows: First, without NaCl, removal efficiencies of ammonia nitrogen were 69.6%, 37.9%, and 22.7%, when the distance between electrodes was adjusted to 1, 4, and 7 cm, respectively, at 15 V for 60 min. Secondly, without NaCl, removal efficiencies of ammonia nitrogen were 49.5 and 90.9% when the voltage was adjusted to 5 V and 10 V, respectively, for 60 min and 94.6% at 15 V for 40 min. Lastly, with the addition of NaCl 10 mM, the removal efficiency of ammonia nitrogen was 40.3% and 11.5% greater than that of no addition of NaCl at 5 V for 60 min and at 10 V for 30 min.

Varing the flow velocity of solution and particle diameter, the mass transfer coefficient of the local electrode on current feeder has been measured in an empty flow reactor, an inert fluidized bed electrode reactor, and an active fluidized bed electrode reactor. It had its maximium value when the bed porosity was 0.6 to 0.65 and decreased with increasing the height of local electrode. The mass transfer coefficient was found to be high especially when bigger particle was fluidized. Electrochemical deposition of copper dissolved in the synthesized wastewater has been performed in the active fluidized bed electrode reactor. The deduction rate was higher than 90% and the residual concentration of copper decreased to less than 5ppm.