• 분석과학
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• 제5권1호
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• pp.7-15
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• 1992

게르마늄을 Phenylfluorone과 착물을 만들어 과염소산 지지전해질에서 Linear Sweep Voltammetry에 의해 정량하고, 염산용액 중에서 형성된 착물을 UV-VIS Spectrophotometry로 정량한 결과를 비교하였다. 이때 전기화학적인 방법의 경우 정량범위가 $2.5{\sim}80{\mu}g/L$이었고, 분광광도법의 경우는 $10{\sim}300{\mu}g/L$이었다.

• Korean Chemical Engineering Research
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• 제56권2호
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• pp.151-155
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• 2018

고분자전해질 연료전지(PEMFC)의 고분자막 열화정도는 주로 수소투과전류밀도로 평가한다. 수소투과전류밀도는 선형주사전압전류측정법(Linear Sweep Voltammetry, LSV)으로 측정하는데 DOE프로토콜과 NEDO프로토콜이 분석방법에 차이가 있다. 본 연구에서는 PEMFC 구동 및 가속 열화 시험 과정에서 두 프로토콜을 적용해 수소투과 전류밀도를 비교하였다. DOE 방법에 의한 LSV 방법에서는 주사속도(scan rate) 변화가 수소투과 전류밀도에 영향을 주지만 NEDO 방법에서는 주사속도가 수소투과전류밀도에 영향을 주지 않았다. 고분자막 가습/건조 15,000사이클 평가과정에서 DOE 방법은 막의 열화를 민감하게 측정하였으나 NEDO방법은 DOE방법에 비해 막의 열화가 덜 민감하게 나타났다.

• Korean Chemical Engineering Research
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• 제57권4호
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• pp.507-511
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• 2019

고분자전해질 연료전지(PEMFC)의 고분자막 내구성을 평가하는데 수소투과도가 많이 사용되고 있다. 수소투과도를 쉽게 측정하는 방법으로 선형 주사 전압 측정법(Linear Sweep Voltammetry, LSV)이 주로 사용된다. 연구자마다 LSV 측정 방법에 차이가 있어 연구 결과를 비교하기가 어려울 때가 많다. 그래서 본 연구에서는 측정하기 어렵지만 정확한 값이라고 할 수 있는 기체 크로마토그래프에 의한 수소투과도와 DOE와 NEDO의 LSV 방법을 비교하여 정확성을 확인하고자 하였다. 온도와 상대습도를 변화시키며 수소투과도를 측정해 비교했을 때, DOE LSV 방법이 GC 방법과 비교해 오차 범위 5%이하의 정확성을 보였다. NEDO LSV 방법은 DOE방법과 같이 0.3V의 전류 값으로 수소투과전류밀도를 결정했을 때 오차는 감소하였다.

• Journal of Electrochemical Science and Technology
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• 제11권4호
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• pp.379-383
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• 2020

The novel voltammetry using a semi-circular potential wave for quasi-reversible charge transfer system on electrode is theoretically investigated. Compared with conventional voltammetry based on linear sweep such as linear sweep voltammetry (LSV), semi-circular potential sweep voltammetry (SCV) may decrease the charging current outside the center of potential range and increase the faradaic current at the midpoint due to variable scan rate. In this paper, we investigate the system based on macroelectrode where simple 1 dimensional (1 D) diffusion system is valid with various charge transfer rate constant (k₀). In order to observe the amplification at midpoint, voltammetric response with different midpoint ranging from -200 mV to 200 mV are studied. SCVs shows both the shift of peak potential and the amplification of peak current for quasi-reversible electrode reaction while only higher peak current is observed for reversible reaction. Moreover, the higher current at midpoint enable the amplification of current at low overpotential region which may assist the determination of onset potential as a figure-of-merit in electrocatalyst.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2008년도 하계학술대회 논문집 Vol.9
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• pp.123-123
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• 2008

본 논문에서는 Cu의 ECMP 적용을 위해 $HNO_3$ 전해액의 active, passive, transient, trans-passive 영역을 I-V 특성 곡선을 통해 알아보았고, LSV (Linear sweep voltammetry)와 CV (Cyclic voltammetry)법을 통하여 전기화학적 특성을 비교 분석하였다.

• Korean Journal of Chemical Engineering
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• 제35권11호
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• pp.2290-2295
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• 2018

An acceleration stress test (AST) was performed to evaluate the durability of a polymer membrane in a polymer electrolyte membrane fuel cell (PEMFC) for 500 hours. Previous studies have shown that hydrogen crossover measured by linear sweep voltammetry (LSV) increases when the polymer membrane deteriorates in the AST process. On the other hand, hydrogen crossover of the membrane often decreases in the early stages of the AST test. To investigate the cause of this phenomenon, we analyzed the MEA operated for 50 hours using the AST method (OCV, RH 30% and $90^{\circ}C$). Cyclic voltammetry and transmission electron showed that the electrochemical surface area (ECSA) decreased due to the growth of electrode catalyst particles and that the hydrogen crossover current density measured by LSV could be reduced. Fourier transform infrared spectroscopy and thermogravimetric/differential thermal analysis showed that -S-O-S- crosslinking occurred in the polymer after the 50 hour AST. Gas chromatography showed that the hydrogen permeability was decreased by -S-O-S- crosslinking. The reduction of the hydrogen crossover current density measured by LSV in the early stages of AST could be caused by both reduction of the electrochemical surface area of the electrode catalyst and -S-O-S- crosslinking.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2009년도 하계학술대회 논문집
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• pp.486-486
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• 2009

In this paper, the current-voltage (I-V) curves, such as linear sweep voltammetry (LSV) and cyclic voltammetry (CV), were employed to evaluate the effect of electrolyte concentration on the electrochemical reaction trend. From the I-V curve, the electrochemical states of active, passive, transient and trans-passive could be characterized. And then, we investigated that how this chemical affect the process of voltage-induced material removal in electrochemical mechanical polishing (ECMP) of Copper. The scanning electron microscopy (SEM) and energy dispersive spectroscopy EDS) analyses were used to observe the surface profile. Finally, we monitored the oxidation and reduction process of the Cu surface by the repetition of anodic and cathodic potential from cyclic voltammetry (CV) method in acid- and alkali-based electrolyte. From these analyses, it was important to understand the electrochemical mechanisms of the ECMP technology.

• Journal of Electrochemical Science and Technology
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• 제11권4호
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• pp.346-351
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• 2020

The removal characteristics of copper (Cu) from electrochemical surface by voltage-activated reaction were reviewed to assess the applicability of electrochemical-mechanical polishing (ECMP) process in three types of electrolytes, such as HNO₃, KNO₃ and NaNO₃. Electrochemical surface conditions such as active, passive, transient and trans-passive states were monitored from its current-voltage (I-V) characteristic curves obtained by linear sweep voltammetry (LSV) method. In addition, the oxidation and reduction process of the Cu surface by repetitive input of positive and negative voltages were evaluated from the I-V curve obtained using the cyclic voltammetry (CV) method. Finally, the X-ray diffraction (XRD) patterns and energy dispersive spectroscopy (EDS) analyses were used to observe the structural surface states of a Cu electrode. The electrochemical analyses proposed in this study will help to accurately control the material removal rate (MRR) from the actual ECMP process because they are a good methodology for predicting optimal electrochemical process parameters such as current density, operating voltage, and operating time before performing the ECMP process.

• Korean Chemical Engineering Research
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• 제52권4호
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• pp.425-429
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• 2014

최근까지 대부분의 PEMFC MEA(Membrnae and Electrode Assembly) 열화 연구는 전극과 전해질 막 각각 분리되어 연구되었다. 그런데 실제 PEMFC 운전조건에서는 전극과 전해질 막은 동시에 열화된다. 동시열화과정에서 전극열화와 전해질 막 열화는 상호 작용한다. 전해질 막의 열화정도를 측정하는데 수소투과도가 많이 사용되고 있다. 그런데 동시 열화가 발생했을 때 선형 쓸음 전기량 측정법(Linear Sweep Voltammetry, LSV)에 의해 수소투과도를 측정하면 전극열화가 수소투과전류를 감소시키는데, LSV 방법이 전극 촉매의 활성 면적에 의존하기 때문이다. 본 연구에서는 전극과 막 동시 열화과정에서 기체 크로마토그래프에 의한 PEMFC 전해질막의 수소투과도를 측정하였다. 기체 크로마토그래프 측정 방법은 전극 상태와 무관하기 때문에 전극과 막 동시 열화 과정에서 수소투과도가 전극 열화 영향을 받지 않음을 확인하였다.

• Bulletin of the Korean Chemical Society
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• 제34권5호
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• pp.1462-1466
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• 2013

We demonstrate that ruthenium oxide ($RuO_2$) nanotubes with controlled dimensions can be synthesized using facile electrochemical means and anodic aluminum oxide (AAO) templates. $RuO_2$ nanotubes were formed using a cyclic voltammetric deposition technique and an aqueous plating solution composed of $RuCl_3$. Linear sweep voltammetry (LSV) was used to determine the effective electrochemical oxidation potential of $Ru^{3+}$ to $RuO_2$. The length and wall thickness of $RuO_2$ nanotubes can be adjusted by varying the range and cycles of the electrochemical cyclic voltammetric potentials. Thick-walled $RuO_2$ nanotubes were obtained using a wide electrochemical potential range (-0.2~1 V). In contrast, an electrochemical deposition potential range from 0.8 to 1 V produced thin-walled and longer $RuO_2$ nanotubes in an identical number of cycles. The dependence of wall thickness and length of $RuO_2$ nanotubes on the range of cyclic voltammetric electrochemical potentials was attributed to the distinct ionic diffusion times. This significantly improves the ratio of surface area to mass of materials synthesized using AAO templates. Furthermore, this study is directive to the controlled synthesis of other metal oxide nanotubes using a similar strategy.