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Voltammetry

Voltammetry. 伏安分析法. Read: pp. 716 –753 Problems: 25-1,2,3,6,13. Basic principle of v oltammetry. Voltammetry: A group of electrochemical methods based on measuring current (i)- applied potential curve during electrolysis

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Voltammetry

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  1. Voltammetry 伏安分析法

  2. Read: pp. 716 –753 Problems: 25-1,2,3,6,13 Basic principle of voltammetry Voltammetry: A group of electrochemical methods based on measuring current (i)- appliedpotential curve during electrolysis - only a small amount of sample (analyte) is used Polarography: Invented by J. Heyrovsky (Nobel Prize 1959). Differs from voltammetry in that it employs a dropping mercury electrode (DME) as Working electrodeto continuously renew the electrode surface.

  3. 1. Polarographic analysis process and the conditions for polarographic wave formation Polarographic analysis ： Electrolytic analysis carried out under special conditions. specific characteristics： A、a polarized electrode and a depolarized electrode are used as working electrode B、No stirring Incomplete electrolysis (only a small amount of analyte is consumed)

  4. Polarized electrode and depolarized electrode If the electrode potential has great changes when infinite small current flow through the electrode, such electrode is referred to as polarized electrode. eg. DME ; If the electrode potential does not change with current , such electrode is called ideal depolarized electrode. eg. SCE

  5. Three electrode cell:Working • Reference • Counter/auxilliary • current flows between working and counter electrodes. • Potential controlled by potentiostat between working and reference electrodes.

  6. Two special electrodes Supporting electrolyte : Usually relatively higher concentration of strong electrolytes (alkali metal salts) serves as supporting electrolyte Dissolved oxygen is usually removed by bubbling nitrogen through the solution Voltage scanning Under unstirred state, recording voltage - current curve

  7. ①～ ②residual current ③ electrolytic current ④～⑤limiting diffusion current Cd 2+ +2e + Hg = Cd(Hg) 2Hg + 2Cl- -2e = Hg2Cl2

  8. Electrode become more and more reducing and capable of reducing Cd2+ Cd2+ + 2e- Cd Current starts to be registered at the electrode All Cd2+ around the electrode has already been reduced. Current at the electrode becomes limited by the diffusion rate of Cd2+ from the bulk solution to the electrode. Thus, current stops rising and levels off at a plateau Working electrode is no yet capable of reducing Cd2+ only small residual current flow through the electrode Current at the working electrode continue to rise as the electrode become more reducing and more Cd2+ around the electrode are being reduced. Diffusion of Cd2+ does not limit the current yet 0.001 M Cd2+ in 0.1 M KNO3 supporting electrolyte i (A) E½ id Base line of residual current -0.2 -0.4 -0.6 -0.8 -1.0 -1.2 -1.4 V vs SCE

  9. Limiting current Related to concentration E½ at ½ i

  10. 0.5mmol镉离子极谱图

  11. Limiting diffusion current -- A basis of polarographically quantitative analysis When the applied voltage exceeds the decomposition voltage, diffusion-controlled current is expressed as: i = K(C-C0) When the applied voltage gets more negative, C0 →0, current becomes only diffusion limited, then id = KC Id reaches a limiting value proportional to ion concentration C in bulk solution, and do not changes with applied voltage longer

  12. Half-wave potential —polarographic qualitative analysis The potential at which the current is equal to one half the limiting current is called the half-wave potential and given the symbol E1/2.

  13. How it works? ▲ The applied voltage is gradually increased, typically by going to a more positive( more negative decomposing potential) ▲ A small residual current is observed. ▲ When the voltage becomes great enough, reduction occurs at the analytical electrode causing a current. ▲ The electrode is rapidly saturated so current production is limited – based on diffusion of the analyte to the small electrode.

  14. How it works ? The reduced species alters the surface of the mercury electrode. To prevent problems, the mercury surface is renewed by “ knocking off ” a drop –providing a fresh surface. This results in an oscillation of the data as it is collected.

  15. 2. The diffusion current theory and polarographic wave equation We have already known: id = KC In above equations, K is called Ilkovic constant, it is expressed as follows: K = 607 n D1/2m2/3t1/6 Thus, id = 607nD1/2m2/3t1/6C

  16. id = 607nD1/2m2/3t1/6C Concentration of electro-active analyte(mmol.L-1) Drop time (sec) Mercury mass flow rate(mg.sec-1) Diffusion coefficient of electroactive analyte in solution(cm2.sec-1) Average limiting diffusion current denoting average current on mercury drop from drop forming to falling (mA) Number of transferring electrons in electrode reaction(e/mol) From above equation, we can find thatwhen temperature, matrix solution and capillary characteristic are kept constant, id is proportional to C

  17. polarographic wave equation： When i = ½ id , log term in above equation is equal to zero, corresponding potential is calledhalfwave potential E1/2 ●E1/2 independent on the concentration ●basis of qualitative analysis

  18. 3. Interference current in classical DC polarography ● Residual current (1) redox reactions of impurities in solution (2) charging of Hg drop (non-faradaic current / non-redox current) ● Migration current The current produced by static attraction of the electrode to sought-for ions

  19. ●Polarographic Maximum (or malformed peak ) • Complex artifactual phenomenon • Less likely at low drop rates, in concentrated electrolyte, or low concentration of electroactive species • Lessened by inclusion of surfactants in medium

  20. ●Oxygen wave Dissolved oxygen is easily reduced at many working electrodes. Thus an aqueous solution saturated with air exhibits two distinct oxygen waves. The first results from the reduction of oxygen to hydrogen peroxide: O2 + 2H+ + 2e- H2O2 The second wave corresponds to the further reduction of hydrogen peroxide: H2O2 + 2H+ + 2e- 2H2O • Sparge solutions with high purity N2 or Ar for 5-20 min

  21. Factors that affect limiting diffusion current Characteristics of capillary – hight of Hg Potential of dropping Hg electrode Composition of solution Temperature Factors that affect half-wave potential Type and concentration of supporting electrolyte Temperature Forming complex Acidic of solution

  22. Question Why a reference electrode with large area and a dropping mercury electrode with very small area are used to electrolyze in polarographic analysis ? Why large amount of supporting electrolyte is added to sample solution? Why does nitrogen gas pass through the solution before electrolysis ? In the process of polarographic analysis whether or not to carry out stirring the solution? Why?

  23. 4. Polarographically quantitative analytical methods （id）avg = K·c ●Direct comparison method ●Calibration curve method ●Standard addition method

  24. 5. Applications Fundamental studies Inorganic applications Organic applications Applications in pharmaceutical and biochem fields

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