• 한국진공학회:학술대회논문집
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• 한국진공학회 2004년도 제27회 학술발표회 초록집
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• pp.146-146
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• 2004

• 분석과학
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• 제8권4호
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• pp.569-574
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• 1995

In-situ spectroelectrochemical studies have been carried out on the oxidation of Mn(II) at platinum, gold, lead dioxide, and bismuth doped lead dioxide electrodes. The Mn(III), $MnO_2$, and/or ${MnO_4}^-$ species are produced depending on experimental conditions employed during electrolysis. Mn(III) is shown to be produced from a very early stage during the anodic potential scan and undergo disproportionation-conproportionation reactions depending on the relative concentration of each species near the electrode surface. An oxidation mechanism consistent with these observations is proposed.

• 대한치과기공학회지
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• 제31권1호
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• pp.55-61
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• 2009

Passive fitting of meso-structure and super-structures is a predominant requirement for the longevity and clinical success of osseointegrated dental implants. However, precision and passive fitting has been unpredictable with conventional methods of casting as well as for corrective techniques. Alternative to conventional techniques, electro discharge machining(EDM) is an advanced method introduced to dental technology to improve the passive fitting of implant prosthesis. In this technique material is removed by melting and vaporization in electric sparks. Regarding the efficacy of EDM, the application of this technique induces severe surface morphological and elemental alterations due to the high temperatures developed during machining, which vary between $10,000{\sim}20,000^{\circ}C$. The aim of this study was to investigate the morphological and elemental alterations induced by EDM process of casting dental gold alloy and non-precious alloy used for the production of implant-supported prosthesis. A conventional clinical dental casting alloys were used for experimental specimens patterns, which were divided in three groups, high fineness gold alloy(Au 75%, HG group), low fineness gold alloy(Au 55%, LG group) and nonprecious metal alloy(Ni-Cr, NP group). The UCLA type plastic abutment patterns were invested with conventional investment material and were cast in a centrifugal casting machine. Castings were sandblasted with $50{\mu}m\;Al_2O_3$. One casting specimen of each group was polished by conventional finishing(HGCON, LGCON, NPCON) and one specimen of each group was subjected to EDM in a system using Cu electrodes, kerosene as dielectric fluid in 10 min for gold alloy and 20 min for Ni-Cr alloy(HGEDM. LGEDM, NOEDM). The surface morphology of all specimens was studied under an energy dispersive X-ray spectrometer (EDS). The quantitative results from EDS analysis are presented on the HGEDM and LGEDM specimens a significant increase in C and Cu concentrations was found after EDM finishing. The different result was documented for C on the NPEDM with a significant uptake of O after EDM finishing, whereas Al, Si showed a significant decrease in their concentrations. EDS analysis showed a serious uptake of C and Cu after the EDM procedure in the alloys studied. The C uptake after the EDM process is a common finding and it is attributed to the decomposition of the dielectric fluid in the plasma column, probably due to the development of extremely high temperatures. The Cu uptake is readily explained from the decomposition of Cu electrodes, something which is also a common finding after the EDM procedure. However, all the aforementioned mechanisms require further research. The clinical implication of these findings is related with the biological and corrosion resistance of surfaces prepared by the EDM process.

• Bulletin of the Korean Chemical Society
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• 제27권5호
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• pp.672-678
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• 2006

A new approach to fabricate an enzyme electrode was described based on the immobilization of horseradish peroxidase (HRP) on dithiobis-N-succinimidyl propionate (DTSP) self-assembled monolayer (SAM) formed on gold-nanoparticles (Au-NPs) which were electrochemically deposited onto glassy carbon electrode (GCE) surface. The overall surface area and average size of Au-NPs could be controlled by varying deposition time and were examined by Field Emission-Scanning Electron Microscope (FE-SEM). The $O_2$ reduction capability of the surface demonstrated that Au-NPs were thermodynamically stable enough to stay on GCE surface. The immobilized HRP electrode based on Au-NPs/GCE presented faster, more stable and sensitive amperometric response in the reduction of hydrogen peroxide than a HRP immobilized on DTSP/gold plate electrode not containing Au-NPs. The effects of operating potential, mediator concentration, and pH of buffer electrolyte solution on the performance of the HRP biosensor were investigated. In the optimized experimental conditions, the HRP immobilized GCE incorporating smaller-sized Au-NPs showed higher electrocatalytic activity due to the high surface area to volume ratio of Au-NPs in the biosensor. The HRP electrode showed a linear response to $H_2O_2$ in the concentration range of 1.4 $\mu$M-3.1 mM. The apparent Michaelis-Menten constant ($K _M\; ^{app}$) determined for the immobilized HRP electrodes showed a trend to be decreased by decreasing size of Au-NPs electrodeposited onto GCE.

• 대한화학회지
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• 제66권6호
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• pp.436-441
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• 2022

나노 다공성 구조를 가지는 전극은 매우 큰 전기화학적 표면적을 지니기 때문에 그 형성 방법에 대한 연구가 다양하게 이루어져 왔다. 본 논문에서는 정전위 양극 산화를 이용하여 초미세전극(ultramicroelectrode, UME) 표면에 나노 다공성 금(nanoporous gold, NPG) 구조를 도입하는 방법을 연구하였다. 1M KCl을 포함하는 0.1M 인산완충용액(pH 8)에서 1.3 V의 정전위를 가해 주면 잘 정의된 NPG 구조가 UME 표면에 도입되었다. NPG-UME 형성에서 인가 전위와 반응 시간, 그리고 전극의 크기가 형성된 NPG 전극의 거칠기 인자(roughness factor, R_f)에 미치는 영향을 관찰하여 양극 산화 효율을 조사하였다. 10분 정도의 짧은 시간에 2000정도의 큰 R_f 값을 가지는 NPG-UME를 만들 수 있었는데, 전기화학적 글루코오스 검출에 효과적으로 활용 가능하였다. 본 연구 결과는 적은 시료양으로 전기화학적 분석을 수행하는 경우 응용성이 클 것으로 기대한다.

• 전기화학회지
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• 제11권3호
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• pp.176-183
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• 2008

본 연구에서는 8족 금속 원소인 osmium을 중심금속으로 4가지의 착물을 합성하였다. 합성한 착물은 ${[Os(bpy)}_2{(ap-im)Cl]}^{+/2+}$, ${[Os(dme-bpy)}_2{(ap-im)Cl]}^{+/2+}$, ${[Os(dmo-bpy)}_2{(ap-im)Cl]}^{+/2+}$, ${[Os(dcl-bpy)}_2{(ap-im)Cl]}^{+/2+}$이다. 합성된 착물을 순환전압전류법을 포함한 다양한 전기화학분석방법을 이용하여 전기적 성질을 조사하여 작용기에 따른 전위의 변화를 다음의 전위구간에서 $E_p$:$-0.06\;V{\sim}0.313\;V$ vs. Ag/AgCl 확인하였다. 합성한 화합물을 전기적 흡착방법으로 고정된 금나노입자(gold nano-particles)를 전극 위에 자기조립방식으로 고정화를 시켰다. 당과 당 분해효소(Glucose Oxidase, GOx)에 의한 촉매반응의 전류를 확인하였고, glucose농도에 따른 변화하는 전류의 양도 확인하였다. 마지막으로 고정된 4가지의 osmium complex는 서로 다른 전위로 인하여 촉매전류의 양이 달라지는 것을 알 수 있었고, 이로 인해 redox complex의 전위가 촉매반응에 미치는 영향을 확인 할 수 있었다.

• Journal of Electrical Engineering and Technology
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• 제4권4호
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• pp.546-551
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• 2009

In this paper, we describe a self-aligned fabrication method for a nano-patterned bottom electrode using flood exposure from the backside. Misalignments between layers could cause the final devices to fail after the fabrication of the nano-scale bottom electrodes. A self-alignment was exploited to embed the bottom electrode inside the glass substrate. Aluminum patterns act as a dry etching mask to fabricate glass trenches as well as a self-aligned photomask during the flood exposure from the backside. The patterned photoresist (PR) has a negative sidewall slope using the flood exposure. The sidewall slopes of the glass trench and the patterned PR were $54.00^{\circ}$ and $63.47^{\circ}$, respectively. The negative sidewall enables an embedment of a gold layer inside $0.7{\mu}m$ wide glass trenches. Gold residues on the trench edges were removed by the additional flood exposure with wet etching. The sidewall slopes of the patterned PR are related to the slopes of the glass trenches. Nano-scale bottom electrodes inside the glass trenches will be used in beam resonators operating at high resonant frequencies.

• 대한화학회지
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• 제19권2호
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• pp.104-115
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• 1975

요오드의 전기화학적 환원과정을 여러가지 특성을 가진 물아닌 용매 속에서 polarography, chronopotentiometry, cyclic voltammetry, controlled potential coulometry 등의 전기분석적 방법을 이용하여 적하수은전극, 백금, 금 및 백금아말감전극등을 사용하여 상세히 조사하였다. 메탄올, 에탄올, 이소프로판올 및 피리딘과 같은 양쪽성 용매 속에서는 $I_2{\longrightarrow}I^-$의 I단계 환원과정을 거치며 아세톤, 디메틸포름아미드, 메틸에틸케톤, 디메틸술폭시드, 아세토니릴과 같은 반양성자 용매속에서는 $I_2{\longrightarrow}I_3^-{\longrightarrow}I^-$의 2단계 환원과정을 거쳤다. 적하수은전극, 고인 수은전극, 백금, 금 그리고 백금아말감전극등 전극조건을 다르게 하였을 때에도 $^'I_2$의 환원과정은 같았으며 사용한 모든 전극에서 확산지배적이었다. 반양성자용매에 물을 첨가하여 그 영향을 걸토한 결과 물의 첨가량이 약 $50v/v{\%}$ 이상일때 2단계의 환원과정이 1단계의 환원과정으로 줄어들었다. 또 chronopotentiometric data와 Send의 식으로부터 계산한 각 용매 속에서의 요오드의 확산계수는 $D_{I2}^{AN}=5.96{\times}10^{-6}cm^2/sec,\;D_{13-}^{AN}=9.63{\times}10^{-6}cm^2/sec,\;D_{I2}^{MeOH}=5.30{\times}10^{-6}cm^2/sec$이였다. 전기화학적 환원과정의 stoichiometry를 알아 보고저 controlled potential coulometry로 使用하였으며, 얻은 생성물은 은법적정으로 확인 및 정량하였다.

• Bulletin of the Korean Chemical Society
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• 제16권9호
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• pp.819-823
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• 1995

Thin films of two kinds of Prussian Blue (PB)-modified, using iron(Ⅲ) complex instead of conventional FeCl3, were prepared on a gold substrate and these films were able to be electrochemically reduced in potassium nitrate solution. In case of PB-modified films prepared from Fe(Ⅲ)-ethylenediamine-N,N'-diacetic acid (FeEN3+)/K3Fe(CN)6 solution, the mid-peak potential was 0.156 V in 0.1 M KNO3 and it was found that potassium ion migrates into or out of the film during the electrolysis. These films were shown to be electrochromic. These films exhibited smaller peak separation than those formed from Fe(Ⅲ)-tartaric acid (FeTA3+)/K3Fe(CN)6 system. The diffusion coefficient of Fe(CN)63-/4- redox couple, evaluated using the fabricated Au rotating disc electrode(rde) previously reported, was in good agreement with the existing data. Two experimental procedures, including the voltammetry at relatively low scan rates and the rde study, have been used in order to characterize the electrode kinetics. The electrode kinetics of some redox couples (FeEN2+-FeEN3+ and FeTA2+-FeTA3+) on both PB-modified thin films and bare Au electrode were studied using a Au rde. In all cases the rate constants of electron transfer obtained with the PB-modified film electrodes were only slightly less than those obtained for the same reaction on bare Au disc electrodes. The conductivities, as determined from the slopes of the i-V curves for a ca. 1 mm sample for dried PB-modified potassium-rich and deficient bulk samples pressed between graphite electrodes, were 6.21 × 10-7 and 2.03 × 10-7(Ω·cm)-1, respectively.

• 대한기계학회:학술대회논문집
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• 대한기계학회 2007년도 춘계학술대회A
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• pp.1450-1454
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• 2007

A Contact-type Linear Encoder-like Capacitive Displacement Sensor (CLECDiS) has been developed to measure displacements at high accuracy within a long measurement range. In this paper, we have worked on improving the performance and reliability of the sensor. The performance increase can be done by introducing the smaller electrode patterns of $4{\mu}m$ width. In order to improve the reliability of the sensor we have changed the electrode layers from chrome-gold to chrome-gold-chrome and re-design its supporting structure. The newly-designed sensor is fabricated and tested to show that its sensitivity is $35pF/{\mu}m$, which implies that its resolution may be 0.36nm if SNR (Signal-to-Noise-Ratio) is 80.1dB. It is about ten times of that $(3.14pF/{\mu}m)$ of its previous version with 10${\mu}m$ electrodes. The total measurement range remains the same as the previous one; 15mm. The calibration experiments show its improved performance and reliability.