• 제목/요약/키워드: Potential sweep rate

검색결과 11건 처리시간 0.023초

Semi-Circular Potential Sweep Voltammetry: Electrochemically Quasi-Reversible System

  • Park, Kyungsoon;Hwang, Seongpil
    • 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.

Polythiophene의 전기화학적 도핑과 변색 스위치에 관한 연구 (A study on the color change switch and electrochemical doping of polythiophene)

  • 구할본;김주승;김현철;김종욱
    • E2M - 전기 전자와 첨단 소재
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    • 제9권2호
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    • pp.165-173
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    • 1996
  • We prepared polythiophene and poly(3-methylthiophene) films, known as conducting polymer, by electrochemical method. Polythiophene and poly(3-methylthiophene) films were doped and undoped dopant for the studing the understanding of doping mechanism and possible application to the color change switch. We observed that the anodic, cathodic wave and absorption spectra were slightly changed during doping and undoping process in polythiophene. It shows that doping and undoping process were showed some difference by the appearance and disappearance of polaron and bi-polaron. In the relation of the peak of oxidative current density and potential sweep rate of cyclic voltammograms, the amount of dopant in polythiophene film was homogeneously increased at low scan rate. This also can be applied to the poly(3-methlythiophene).

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수열 합성된 나노구조를 갖는 ZnO 에 대한 표면 및 계면 결함의 상대적인 영향 (Relative Influence of Surface and Interfacial Defects in Hydrothermally Grown Nanostructured ZnO)

  • 박철민;이지혜;소혜미;장원석
    • 대한기계학회논문집B
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    • 제38권10호
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    • pp.831-835
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    • 2014
  • 온도를 달리하여 수열합성 시킨 두 ZnO nanostructure 의 자외선 검출 소자에 대해 표면 결함과 기판과의 계면 결함의 상대적인 영향을 분석했다. 실험은 laser 가 인가된 상태에서 bias voltage sweep rate을 조절하여, 그에 따른 전류-전압 곡선을 통해 이루어졌다. 수열 성장이 적게 된 ZnO nanostructure의 경우 405, 355 nm laser 인가시, bias voltage sweep rate 을 느리게 할 수록, 전류-전압 기울기가 낮아졌으며, 대조적으로 성장이 크게 된 시료의 경우 기울기가 높아졌다. 이에 대한 이유는 계면과 표면 결함 영향의 차이로 발생됨이 고려됐다. 이와 같이 laser 가 인가된 상태에서 bias voltage sweep rate 에 따른 전류-전압 곡선 분석 실험은 M-S-M (Metal-Semiconductor-Metal) 구조를 갖는 수열 성장된 ZnO 의 표면 및 계면 결함을 관찰하는데 도움을 줄 것으로 생각된다.

중크롬산이온의 음극 환원반응 (Cathodic Reduction of Dichromate Ion)

  • 이주성
    • 대한화학회지
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    • 제21권4호
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    • pp.276-283
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    • 1977
  • 산성용액중에서 백금음극을 사용하여 중크롬산이온의 환원을 전위주사법 및 정전위전해에 의하여 검토하였다. 지지전해질로서 황산나트륨(pH 1.5∼4.0)을 사용한 비완충용액중의 중크롬산칼륨의 분극곡선은 3단파가 생기며 첫째파 및 둘째파의 파고는 각각 크롬(Ⅵ)농도 및 수소이온의 활동도에 비례하나 셋째파는 어느 것에도 비례하지 않았다. 첫째 및 둘째 peak이 전류는 전위주사속도(${\nu}$)에 비례하나 셋째 peak는 50mV/sec이하의 늦은 주사속도에서 ${\nu}^{1/2}$에 비례하였다. 정전위전해에 의하면, 크롬(Ⅵ)의 환원은 셋째 peak보다 더 base이고 초기 pH가 약 2.3 이상이 되면 완전히 억제되었다. 그러므로 이 세 peak는 각각 $Cr_2O_7^{\to}Cr^{3+},\;2H^+{\to}H_2$ 및 음극피막의 형성으로 간주하였다.

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Electrochemical Behavior of Mordant Red 19 and its Complexes with Light Lanthanides

  • Sang Kwon Lee;Taek Dong Chung;Song-Ju Lee;Ki-Hyung Chjo;Young Gu Ha;Ki-Won Cha;Hasuck Kim
    • Bulletin of the Korean Chemical Society
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    • 제14권5호
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    • pp.567-574
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    • 1993
  • Mordant Red 19(MR19) is reduced at mercury electrode at -0.67 V vs. Ag/AgCl with two electrons per molecule in pH 9.2 buffer by differential pulse polarography and linear sweep voltammetry. The peak potential is dependent on the pH of solution. The exhaustive electrolysis, however, gives 4 electrons per molecule because of the disproportionation of the unstable hydrazo intermediate. The electrochemical reduction of lanthanide-MR19 complexes is observed at more cathodic potential than that of free ligand. The difference in peak potentials between complex and free ligand varies from 75 mV for $La^{3+}$ to 165 mV for $Tb^{3+}$ and increases with increasing the atomic number of lanthanide. The electrochemical reduction of lanthanide complexes with MR19 is due to the reduction of ligand itself, and it can be potentially useful as an indirect method for the determination of lanthanides. The shape of i-E curves and the scan rate dependence indicates the presence of adsorption and the adsorption was confirmed by potential double-step chronocoulometry and the effect of standing time. Also the surface excess of the adsorbed species and diffusion coefficients are determined. The composition of the complex is determined to be 1 : 2 by spectrophotometric and electrochemical methods.

Electro-Catalytic Behavior of an Antiarrhythmic Drug, Procainamide and its Electro-Analytical Applications

  • Abbar, Jyothi C.;Meti, Manjunath D.;Nandibewoor, Sharanappa T.
    • Journal of Electrochemical Science and Technology
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    • 제9권4호
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    • pp.292-300
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    • 2018
  • The electrocatalytic oxidative behavior of an antiarrhythmic drug, procainamide hydrochloride (PAH) at the gold electrode surface has been examined using different voltammetric methods like cyclic, linear-sweep and differential pulse voltammetry. Voltammograms obtained in this study reveal that the electrode exhibit excellent electrocatalytic activity towards oxidation of the drug. The parameters that can affect the peak current at different pH, scan rate and concentration were evaluated. The number of electrons transferred was calculated. The current displayed a wide linear response ranging from 0.5 to $30.0{\mu}M$ with a limit of detection of 56.4 nM. The impact of potential interfering agents was also studied. The electrode displayed wide advantages such as simple sample preparation, appreciable repeatability, reproducibility and also high sensitivity. Furthermore, the feasibility of the proposed method was successfully demonstrated by determining PAH in the spiked human biological sample.

Growth and Electrochemical Behavior of Poly[Ni(saldMp)] on Carbon Nanotubes as Potential Supercapacitor Materials

  • Zhang, Yakun;Li, Jianling;Kang, Feiyu;Wang, Xindong;Ye, Feng;Yang, Jun
    • Bulletin of the Korean Chemical Society
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    • 제33권6호
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    • pp.1972-1978
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    • 2012
  • The polymer of (2,2-dimethyl-1,3-propanediaminebis(salicylideneaminato))-nickel(II), Ni(saldMp), was deposited on multi-walled carbon nanotubes (MWCNTs) substrate by the route of potential linear sweep. The nano structures of poly[Ni(saldMp)] have been obtained by adjusting the monomer concentration of 0.1, 0.2, 0.5, 1.0 and 1.5 mmol $L^{-1}$. The poly[Ni(saldMp)] prepared in acetonitrile solution with monomer concentration of 1.0 mmol $L^{-1}$ shows the fastest growth rate. The effects of potential window on charge-discharge efficiency and electrodeposition scan number on capacitance performance were discussed. Poly[Ni(saldMp)] prepared with less electrodeposition scans exhibits higher capacitance, but this goes against the improvement of the whole electrode capacitance. Sample with 8 deposition scans is the best compromise with the geometric specific capacitance 3.53 times as high as that of pure MWCNTs, and 1.24 times for the gravimetric specific capacitance under the test potential window 0.0-1.0 V.

Electrochemical Investigation of Acetaminophen with a Carbon Nano-tube Composite Film Electrode

  • Li, Chunya;Zhan, Guoqing;Yang, Qingdan;Lu, Jianjie
    • Bulletin of the Korean Chemical Society
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    • 제27권11호
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    • pp.1854-1860
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    • 2006
  • Electrochemical behaviors of acetaminophen at a muti-wall carbon nano-tube composite film modified glassy carbon electrode were investigated by cyclic voltammetry, linear sweep voltammetry and chronocoulometry. Compared with that obtained at the unmodified electrode, the peak currents were enhanced significantly, and the oxidation peak shifted towards more negative potential with the reduction peak shifted positively. The peak-to-peak separation turned narrow, and suggested that the reversibility was improved greatly. Experimental parameters, such as scan rate, pH and accumulation conditions were optimized. It was found that a maximum current response can be obtained at pH = 5.0 after accumulation at -0.50 V for 80 s. The oxidation peak current was found to be linearly related to acetaminophen concentration over the range of $5.0{\times}10^{-7}\;\sim\;1.0{\times}10^{-4}$ mol $L^{-1}$ with a detection limit of $5.0{\times}10^{-8} $mol $L^{-1}$. A convenient and sensitive electrochemical method was developed for the determination of acetaminophen in a commercial paracetamol oral solution. Its practical application demonstrated that it has good selectivity and high sensitivity.

치과용 아말감의 산화환원에 관한 전기화학적 연구 (AN ELECTROCHEMICAL STUDY ON THE OXIDATION' AND REDUCTION OF DENTAL AMALGAM)

  • 이인복;이명종
    • Restorative Dentistry and Endodontics
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    • 제18권2호
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    • pp.431-445
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    • 1993
  • The purpose of this study was to observe corrosion characteristics of six dental amalgams and was to analyse corrosion products electrochemically. After each amalgam alloy and Hg was triturated as the direction of the manufacturer by using mechanical amalgamator, the triturated mass was inserted into the cylinderical metal mold ($12{\times}10mm$) and was condensed with 160kg/$cm^2$ by using the hydrolic press. The specimen was removed from the mold and was stored at room temperature for 1 week, and was polished with amalgam polishing kit. The anodic and cathodic polarization curve was obtained by using cyclic voltammetric method with 3-electrode potentiostat in saline for each amalgam and Ag, Sn, Cu plate specimen at $37{\pm}0.5^{\circ}C$. The potential sweep range was -1.7V~0. 4V(vs SCE) in working electrode and scan rate was 50mV/s and the exposed surface area of each specimen to the electrolytic solution was $0.79cm^2$. The results were as follows. 1. In anodic-cathodic polarization curve of amalgam specimens, two anodic current rising areas and two cathodic current peaks were obtained at the low Cu amalgam(CF, CS) specimen and three anodic current rising areas and three cathodic current peaks were obtained at the high Cu amalgam (TY, DS, HV) specimen. 2. As this compared with the anodic and cathodic current peak potentials of Sn, Cu and Ag specimen, the first cathodic current peak I c was caused by the reduction of divalent tin salt, second cathodic current peak IIIc results from the reduction of quadravalent tin salt, and third cathodic current peak me results from the reduction of copper salt. 3. As reverse potential sweeping was done repeatedly, anodic current was decreased slightly in all amalgam specimens.

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Aliphatic Acetylenic Alcohol의 電極反應過程 (Electorchemical Reduction Behavior of Aliphatic Acetylenic Alcohol)

  • 김원택;김진일;곽태영;이주성
    • 대한화학회지
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    • 제23권3호
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    • pp.180-185
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    • 1979
  • 각종 陰極, 卽 Ti, Zr, Ni, Pt, Cu, Ag, Au, Zn, Hg, Pb 및 흑연의 사용으로 2-butyne-1, 4-diol (BID)로부터 2-butene-1,4-diol (BED)까지의 電氣化學的 還元擧動에 관하여 연구하였다. IB族 金屬을 陰極으로 사용한 陰極分極曲線은 알칼리용액중에서 BID에 對해 한개의 還元波가 생기나 BED의 경우는 지지전해질내에서와 마찬가지로 還元波가 생기지 않았다. 고로 BID환원반응에 가장 적당한 陰極은 Cu, Ag, Au임을 알았다. 알칼리性 BID용액에서 銀電極을 사용한 電位走査法에서 peak電流는 電位走査速度의 제곱근과 BID농도에 比例하였다. 限界電流의 對數와 絶對溫度의 逆數의 관계로부터 구한 BID의 活性化에너지는 3.75kcal/mole였다. 고로 알칼리용액중 銀電極을 사용한 BID의 還元電流는 自己擴散에 의한 擴散電流임을 알았다.

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