• 제목/요약/키워드: Randles-Sevcik equation

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비양자성 매개물에서 (2, 4-difluoro-phenyl)-(2-phenyl-1H-quinolin-4-ylidene)-amine의 전기화학적 반응 (Electrochemical Behaviour of (2,4-difluoro-phenyl)-(2-phenyl-1H-quinolin-4-ylidene)-amine in Aprotic Media)

  • Kumari, Mamta;Sharma, D.K.
    • 대한화학회지
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    • 제55권1호
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    • pp.50-56
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    • 2011
  • (2, 4-difluoro-phenyl)-(2-phenyl-1H-quinolin-4-ylidene)-amine의 전기화학적 환원에 대하여 실온에서 순환전압전류 기술을 사용한 유리탄소전극(GCE)에서 N,N-dimethylformamide 하에서 0.1 M tetrabutylammoniumbromide로 조사하였다. 이민의 환원은 각각 한 전자를 포함하면서 2단계의 성공적인 단계로 일어난다. 이 매개물에서 처음 피크는 유리탄소전극 표면에서 약 -0.793 V(vs Ag/$Ag^+$)로 관측되었다. 그리고 그것은 더욱 안정하고 2번째 피크와 비교하여 명확하게 설명된다. 연구된 용매 매개물에서 이민의 확산계수($D_0$)는 수정된 Randles-Sevcik 식을 이용해 계산되었다. 반응 종들의 전자 이동 계수($\alpha$) 또한 계산되었다.

Application of Fractal Geometry to Interfacial Electrochemistry - I. Diffusion Kinetics at Fractal Electrodes

  • Shin Heon-Cheol;Pyun Su-Il
    • 전기화학회지
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    • 제4권1호
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    • pp.21-25
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    • 2001
  • 프랙탈 기하학의 계면 전기화학에로의 응용과 관련하여 프랙탈 표면을 향한 이온/원자 확산의 속도론에 대하여 다루었다. 우선 프랙탈 기하학의 기본 개념에 대하여 설명하였고, 이를 바탕으로 이온/원자의 확산 현상과 관련하여 다양한 전기적 입력하에서 전극 표면의 프랙탈 특성에 기인하는 특수한 반응 양상이 설명되었다 Chronoamperometry, chronopotentiometry및 linear sweep/cyclic voltammetry 실험시에 각각 관찰되는, 전극의 프랙탈 차원이 포함된 일 반화된 Cottrell, Sand 및 Randles-Sevcik 관계를 이론적으로 유도하였고, 그 의미에 대하여 설명하였다

Rate Capability of LiFePO4 Cathodes and the Shape Engineering of Their Anisotropic Crystallites

  • Alexander, Bobyl;Sang-Сheol, Nam;Jung-Hoon, Song;Alexander, Ivanishchev;Arseni, Ushakov
    • Journal of Electrochemical Science and Technology
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    • 제13권4호
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    • pp.438-452
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    • 2022
  • For cuboid and ellipsoid crystallites of LiFePO4 powders, by X-ray diffraction (XRD) and microscopic (TEM) studies, it is possible to determine the anisotropic parameters of the crystallite size distribution functions. These parameters were used to describe the cathode rate capability within the model of averaging the diffusion coefficient D over the length of the crystallite columns along the [010] direction. A LiFePO4 powder was chosen for testing the developed model, consisting of big cuboid and small ellipsoid crystallites (close to them). When analyzing the parts of big and small rate capabilities, the fitting values D = 2.1 and 0.3 nm2/s were obtained for cuboids and ellipsoids, respectively. When analyzing the results of cyclic voltammetry using the Randles-Sevcik equation and the total area of projections of electrode crystallites on their (010) plane, slightly different values were obtained, D = 0.9 ± 0.15 and 0.5 ± 0.15 nm2/s, respectively. We believe that these inconsistencies can be considered quite acceptable, since both methods of determining D have obvious sources of error. However, the developed method has a clearly lower systematic error due to the ability to actually take into account the shape and statistics of crystallites, and it is also useful for improving the accuracy of the Randles-Sevcik equation. It has also been demonstrated that the shape engineering of crystallites, among other tasks, can increase the cathode capacity by 15% by increasing their size correlation coefficients.

Electrochemical Impedance Spectroscopy and Cyclic Voltammetry Methods for Monitoring SmCl3 Concentration in Molten Eutectic LiCl-KCl

  • Shaltry, Michael R.;Allahar, Kerry N.;Butt, Darryl P.;Simpson, Michael F.;Phongikaroon, Supathorn
    • 방사성폐기물학회지
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    • 제18권1호
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    • pp.1-18
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    • 2020
  • Molten salt solutions consisting of eutectic LiCl-KCl and concentrations of samarium chloride (0.5 to 3.0 wt%) at 500℃ were analyzed using both cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). The CV technique gave the average diffusion coefficient for Sm3+ over the concentration range. Equipped with Sm3+ diffusion coefficient, the Randles-Sevcik equation predicted Sm3+ concentration values that agree with the given experimental values. From CV measurements; the anodic, cathodic, and half-peak potentials were identified and subsequently used as a parameter to acquire EIS spectra. A six-element Voigt model was used to model the EIS data in terms of resistance-time constant pairs. The lowest resistances were observed at the half-peak potential with the associated resistance-time constant pairs characterizing the reversible reaction between Sm3+ and Sm2+. By extrapolation, the Voigt model estimated the polarization resistance and established a polarization resistance-concentration relationship.