• 분석과학
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• 제8권4호
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• pp.597-601
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• 1995

The transfer of chloride ion across an anion exchange membrane (AEM) was investigated by cyclic voltammetry (CV) and electrochemical impedance spectra. In CV experiment, when the size of the hole in membrane was much smaller than the distance between membrane holes, the Cl anion transfer showed steady state voltammetric behavior. Each hole in membrane can be regarded as a microelectrode and the membrane was equivalent to a microelectrode array in this condition. When the hole in membrane was large or the distance between membrane holes was small, the CV curve of the Cl anion transfer across membrane showed peak shape, which attributed to linear diffusion. In ac impedance measurement, the impedance spectrum of the membrane system was composed of two semicircles at low de bias, corresponding to the bulk characteristics of the membrane and the kinetic process of ion transfer, respectively. The bulk membrane resistance increases with increasing dc bias and only one semicircle was observed at higher dc bias. The parameters related to kinetic and membrane properties were discussed.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2009년도 하계학술대회 논문집
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• pp.5-6
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• 2009

In this paper, plasma ion implant is performed with $PH_3$ gas diluted by helium gas on P-type Si wafer (100). Spike Rapid Thermal Processing(RTP) annealing performed for 30~60 sec from $800\;^{\circ}C$ to $1000\;^{\circ}C$ in $N_2+O_2$ ambient. Crystalline defect is analyzed by Transmission Electron Microscope(TEM) and Double crystal X-ray Diffraction(DXRD). Contact resistivity($\rho c$), contact resistance(Rc) and sheet resistance(Rs) are analyzed by measuring Transfer Length Method(TLM) using 4155C analysis. As annealing temperature increase, Rs decrease and ${\rho}c$ and Rc increase at temperature higher than $850\;^{\circ}C$. We achieve low Rs, ${\rho}c$ and Rc with Plasma ion implant and spike RTP.

• 전기화학회지
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• 제2권4호
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• pp.195-201
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• 1999

탈기된 0.1 M $Na_2SO_4$ 수용액에서 Fe-Cr강의 재부동태 특성을 Cr함량, 인가전위 그리고 염소이온의 농도를 변화시키면서 관찰하였다. 염소이온이 없는 경우 재부동태 속도를 나타내는 식 log i=k-n log t에서 -n값은 Cr함량에 관계없이 -1에 수렴하였으나 Cr함량이 증가할수록 재부동태 전류밀도는 낮아졌다. A. C. impedance spectroscopy측정 결과, Cr 함량과 인가전위가 증가할수록 형성된 재부동태 피막의 charge transfer resistance$(R_{ct})$ 값은 상승하였다. 또한 재부동태 동안 흐르는 전류밀도를 Faraday식을 이용하여 피막의 두께를 계산해보면 Cr함량이 증가할수록 얇은 부동태 피막이 형성된다는 것을 알 수 있었다. 그러나 염소이온이 존재하는 경우, 염소이온이 Fe-Cr강의 재부동태를 방해하는 효과는 인가전위가 증가할수록 상승하였다.

• 멤브레인
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• 제32권5호
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• pp.357-365
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• 2022

최근 전기자동차용 이차전지 등의 수요가 급증하면서 효율적인 리튬 화합물의 생산이 큰 주목을 받고 있다. 바이폴라막 전기투석은 친환경적이며 경제성 및 효율성이 우수한 전기화학적 리튬 화합물 생산공정으로 알려져 있다. 바이폴라막 전기투석 공정의 효율은 바이폴라막의 성능에 의해 좌우되기 때문에 바이폴라막의 선택이 매우 중요하다. 본 연구에서는 세계적으로 가장 널리 사용되고 있는 대표적인 상용 BPM인 Astom사의 BP-1E 및 Fumatech사의 FBM을 비교 분석함으로써 전기화학적 LiOH 생산을 위한 BPED 공정에 적합한 BPM의 특성을 도출하고자 하였다. 체계적인 평가를 통해 BPM의 특성중 막의 이온전달저항 및 co-ion leakage를 줄이는 것이 가장 중요하고 이러한 관점에서 BP-1E가 FBM보다 더 우수한 성능을 가지고 있음을 확인하였다.

• Carbon letters
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• 제12권3호
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• pp.180-183
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• 2011

Li metal is accepted as a good counter electrode for electrochemical impedance spectroscopy (EIS) as the active material in Li-ion and Li-ion polymer batteries. We examined the existence of signal noise from a Li-metal counter quantitatively as a preliminary study. We suggest an electrochemical cell with one switchable electrode to obtain the exact impedance signal of active materials. To verify the effectiveness of the switchable electrode, EIS measurements of the solid electrolyte interphase (SEI) before severe $Li^+$ intercalation to SFG6 graphite (at > ca. 0.25 V vs. Li/$Li^+$) were taken. As a result, the EIS spectra without the signal of Li metal were obtained and analyzed successfully for the following parameters i) $Li^+$ conduction in the electrolyte, ii) the geometric resistance and constant phase element of the electrode (insensitive to the voltage), iii) the interfacial behavior of the SEI related to the $Li^+$ transfer and residence throughout the near-surface (sensitive to voltage), and iv) the term reflecting the differential limiting capacitance of $Li^+$ in the graphite lattice.

• Journal of Electrochemical Science and Technology
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• 제7권2호
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• pp.179-184
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• 2016

The interface between the surface of a cathode material and the electrolyte gives rise to surface reactions such as solid electrolyte interface (SEI) and chemical side reactions. These reactions lead to increased surface resistance and charge transfer resistance. It is consequently necessary to improve the electrochemical characteristics by suppressing these reactions. In order to suppress unnecessary surface reactions, we coated cathode material using polypropylene (PP). The PP coating layer effectively reduced the SEI film that is generated after a 4.3 V initial charging process. By mitigating the formation of the SEI film, the PP-coated Li[(Ni_0.6Co_0.1Mn_0.3)_0.36(Ni_0.80Co_0.15Al0.05)_0.64)]O₂(NCS) electrode provided enhanced transport of Li⁺ ions due to reduced SEI resistance (R_SEI) and charge transfer resistance (R_ct). The initial charge and discharge efficiency of the PP-coated NCS electrode was 96.2 % at a current density of 17 mA/g in a voltage range of 3.0 ~ 4.3 V, whereas the efficiency of the NCS electrode was only 94.7 %. The presence of the protective PP layer on the cathode improved the thermal stability by reducing the generated heat, and this was confirmed via DSC analysis by an increased exothermic peak.

• 한국가시화정보학회지
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• 제20권2호
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• pp.13-20
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• 2022

An effective capacitive deionization process termed membrane capacitive deionization (MCDI) is newly designed and experimentally tested for seawater desalination. By preventing co-ions to be expelled, MCDI can improve the ion removal performance, but there is a trade-off between blocking co-ion transfer and increasing contact resistance. The conventional MCDI uses 2D-shaped films which increase contact resistance and reduce desalination performance in the trade-off. In this paper, with the 3-D shape of Nafion coated activated carbon cloth, the mentioned problems are expected to be solved making the desalination performance better. We visualized ion concentration and fluid flows with half-MCDI cell that can measure only efficiency of cathode. We found the optimal number of coatings which have the better efficiency than CMX, commercial cation exchange membrane in fixed current conditions of 100uA.

• Bulletin of the Korean Chemical Society
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• 제30권2호
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• pp.319-322
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• 2009

Gel polymer electrolytes were prepared by immersing a porous poly(vinylidene fluoride-co-hexafluoropropylene) membrane in an electrolyte solution containing small amounts of polymerizable additive (3,4-ethylenedioxythiophene, thiophene, biphenyl). The organic additives were electrochemically oxidized to form conductive polymer films on the electrode at high potential. With the gel polymer electrolytes containing different organic additive, lithium-ion polymer cells composed of carbon anode and LiCo$O_2$ cathode were assembled and their cycling performances were evaluated. Adding small amounts of thiophene or 3,4-ethylenedioxythiophene to the gel polymer electrolyte was found to reduce the charge transfer resistance in the cell and it thus exhibited less capacity fading and better high rate performance.

• Journal of Electrochemical Science and Technology
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• 제7권2호
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• pp.170-178
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• 2016

Composited molybdenum oxide and amorphous carbon (MoO₃/C) as anode material for lithium ion batteries has been successfully synthesized by calcining polyaniline (PANI) doped with ammonium heptamolybdate tetrahydrate (AMo). The as prepared electrode material was characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR) and field emission scanning electron microscopy (FE-SEM). The electrochemical performance of the anode was investigated by galvanostatic charge/discharge, cyclic voltammetry (CV), and electrochemical impedance spectroscopy (EIS). The MoO₃/C shows higher specific capacity, better cyclic performance and rate performance than pristine MoO₃ at room temperature. The electrochemical of MoO₃/C properties at various temperatures were also investigated. At elevated temperature, MoO₃/C exhibited higher specific capacity but suffered rapidly declines. While at low temperature, the electrochemical performance was mainly limited by the low kinetics of lithium ion diffusion and the high charge transfer resistance.

• 한국초전도ㆍ저온공학회논문지
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• 제5권2호
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• pp.41-45
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• 2003

Resistance distribution in thin film type SFCL elements of different shunt layer thickness was investigated. The 300 nm thick film of 2 inch diameter was coated with a gold layer and patterned into 2 mm wide meander lines. The shunt layer thickness was varied by ion milling the shunt layer with Ar ions, and also by having the shunt layer grown in different thickness. The SFCL element was subjected to simulated AC fault current for measurements. It was immersed in liquid nitrogenduring the experiment. The resistance distribution was not affected by the shunt layer thickness at applied voltages that brought the temperature of the elements to similar values. This result could be explained with the concept of heat transfer from the film to the surroundings. The resistance distribution was independent of the shunt layer thickness because thick sapphire substrates of high thermal conductivity dominated the thermal conductance of the elements.